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RESEARCH

Jerome Rotter, M.D.

Contact Information:

Fax Number:

310-423-0238

Office Phone Number:

310-423-6467

Mailing Address:

UCLA Cedars-Sinai Medl Cntr- GenMed
BOX 950000, 8700 Beverly Blvd Rm 4221 N
Los Angeles, CA 90048
UNITED STATES

Email Address:

jerome.rotter@cshs.org

Website:

Home Page.

Director, Division of Medical Genetics

Co-Leader, Center for Translational Technologies

Professor, Department of Medicine

Department of Medicine

Division for Biomedical Sciences and Medicine

Research Director, Medical Genetics Research Institute

Professor in Residence, Human Genetics

Member, Internal Advisory Board

Genetics

ACCESS Program

Access Genetics and Genomics Home Area

CTSI

Research Education, Training, and Career Development Program (CTSI-ED)


A Short Biography:

Jerome I. Rotter, MD, FACP, FACMG is Director of Research and Co-Director of the Medical Genetics Institute, Director of the Division of Medical Genetics (Department of Medicine) and Director of the Common Diseases Genetics Program at Cedars-Sinai. He holds the Cedars-Sinai Board of Governors Chair in Medical Genetics. Dr. Rotter is also Principal Investigator of the National Heart Lung and Blood Institute's (NHLBI) MESA (Multi-Ethnic Study of Atherosclerosis) Family Study and Associate Director of National Institutes of Health (NIH) projects and center grants on inflammatory bowel diseases, coronary artery diseases and treatment of lipid disorders. Dr. Rotter received his bachelor's and medical degrees from University of California, Los Angeles (UCLA). He completed his internship in medicine at Harbor-UCLA Medical Center, followed by a residency in internal medicine at Wadsworth VA Hospital in Los Angeles and a fellowship in medical genetics at Harbor-UCLA Medical Center.
Selected Publications:

Tanaka Toshiko, Ngwa Julius S, van Rooij Frank Ja, Zillikens M Carola, Wojczynski Mary K, Frazier-Wood Alexis C, Houston Denise K, Kanoni Stavroula, Lemaitre Rozenn N, Luan Jian'an, Mikkilä Vera, Renstrom Frida, Sonestedt Emily, Zhao Jing Hua, Chu Audrey Y, Qi Lu, Chasman Daniel I, de Oliveira Otto Marcia C, Dhurandhar Emily J, Feitosa Mary F, Johansson Ingegerd, Khaw Kay-Tee, Lohman Kurt K, Manichaikul Ani, McKeown Nicola M, Mozaffarian Dariush, Singleton Andrew, Stirrups Kathleen, Viikari Jorma, Ye Zheng, Bandinelli Stefania, Barroso Inês, Deloukas Panos, Forouhi Nita G, Hofman Albert, Liu Yongmei, Lyytikäinen Leo-Pekka, North Kari E, Dimitriou Maria, Hallmans Goran, Kähönen Mika, Langenberg Claudia, Ordovas Jose M, Uitterlinden André G, Hu Frank B, Kalafati Ioanna-Panagiota, Raitakari Olli, Franco Oscar H, Johnson Andrew, Emilsson Valur, Schrack Jennifer A, Semba Richard D, Siscovick David S, Arnett Donna K, Borecki Ingrid B, Franks Paul W, Kritchevsky Stephen B, Lehtimäki Terho, Loos Ruth Jf, Orho-Melander Marju, Rotter Jerome I, Wareham Nicholas J, Witteman Jacqueline Cm, Ferrucci Luigi, Dedoussis George, Cupples L Adrienne, Nettleton Jennifer A Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake. The American journal of clinical nutrition. 2013; 97(6): 1395-402.
Tang Weihong, Teichert Martina, Chasman Daniel I, Heit John A, Morange Pierre-Emmanuel, Li Guo, Pankratz Nathan, Leebeek Frank W, Paré Guillaume, de Andrade Mariza, Tzourio Christophe, Psaty Bruce M, Basu Saonli, Ruiter Rikje, Rose Lynda, Armasu Sebastian M, Lumley Thomas, Heckbert Susan R, Uitterlinden André G, Lathrop Mark, Rice Kenneth M, Cushman Mary, Hofman Albert, Lambert Jean-Charles, Glazer Nicole L, Pankow James S, Witteman Jacqueline C, Amouyel Philippe, Bis Joshua C, Bovill Edwin G, Kong Xiaoxiao, Tracy Russell P, Boerwinkle Eric, Rotter Jerome I, Trégouët David-Alexandre, Loth Daan W, Stricker Bruno H Ch, Ridker Paul M, Folsom Aaron R, Smith Nicholas L A Genome-Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Genetic epidemiology. 2013; 97(6): .
Li Xiaohui, Bykhovskaya Yelena, Tang Yongming G, Picornell Yoana, Haritunians Talin, Aldave Anthony J, Szczotka-Flynn Loretta, Iyengar Sudha K, Rotter Jerome I, Taylor Kent D, Rabinowitz Yaron S An association between the calpastatin (CAST) gene and keratoconus. Cornea. 2013; 32(5): 696-701.
Reiner Alexander P, Hartiala Jaana, Zeller Tanja, Bis Joshua C, Dupuis Josée, Fornage Myriam, Baumert Jens, Kleber Marcus E, Wild Philipp S, Baldus Stephan, Bielinski Suzette J, Fontes João D, Illig Thomas, Keating Brendan J, Lange Leslie A, Ojeda Francisco, Müller-Nurasyid Martina, Munzel Thomas F, Psaty Bruce M, Rice Kenneth, Rotter Jerome I, Schnabel Renate B, Tang W H Wilson, Thorand Barbara, Erdmann Jeanette, Consortium Cardiogram, Jacobs David R, Wilson James G, Koenig Wolfgang, Tracy Russell P, Blankenberg Stefan, März Winfried, Gross Myron D, Benjamin Emelia J, Hazen Stanley L, Allayee Hooman Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Human molecular genetics. 2013; 97(6): .
Dubinsky Marla C, Kugathasan Subra, Kwon Soonil, Haritunians Talin, Wrobel Iwona, Wahbeh Ghassan, Quiros Antonio, Bahar Ron, Silber Gary, Farrior Sharmayne, Stephens Michael, Teleten Nick, Panikkath Deepa, Ippoliti Andrew, Vasiliauskas Eric, Fleshner Phillip, Williams Chadwick, Landers Carol, Rotter Jerome I, Targan Stephan R, Taylor Kent D, McGovern Dermot P B Multidimensional Prognostic Risk Assessment Identifies Association Between IL12B Variation and Surgery in Crohn's Disease. Inflammatory bowel diseases. 2013; 97(6): .
Gao Xiaoyi, Gauderman W James, Liu Yutao, Marjoram Paul, Torres Mina, Haritunians Talin, Kuo Jane Z, Chen Yii-Der I, Allingham R Rand, Hauser Michael A, Taylor Kent D, Rotter Jerome I, Varma Rohit A genome-wide association study of central corneal thickness in Latinos. Investigative ophthalmology & visual science. 2013; 54(4): 2435-43.
Hek Karin, Demirkan Ayse, Lahti Jari, Terracciano Antonio, Teumer Alexander, Cornelis Marilyn C, Amin Najaf, Bakshis Erin, Baumert Jens, Ding Jingzhong, Liu Yongmei, Marciante Kristin, Meirelles Osorio, Nalls Michael A, Sun Yan V, Vogelzangs Nicole, Yu Lei, Bandinelli Stefania, Benjamin Emelia J, Bennett David A, Boomsma Dorret, Cannas Alessandra, Coker Laura H, de Geus Eco, De Jager Philip L, Diez-Roux Ana V, Purcell Shaun, Hu Frank B, Rimm Eric B, Hunter David J, Jensen Majken K, Curhan Gary, Rice Kenneth, Penman Alan D, Rotter Jerome I, Sotoodehnia Nona, Emeny Rebecca, Eriksson Johan G, Evans Denis A, Ferrucci Luigi, Fornage Myriam, Gudnason Vilmundur, Hofman Albert, Illig Thomas, Kardia Sharon, Kelly-Hayes Margaret, Koenen Karestan, Kraft Peter, Kuningas Maris, Massaro Joseph M, Melzer David, Mulas Antonella, Mulder Cornelis L, Murray Anna, Oostra Ben A, Palotie Aarno, Penninx Brenda, Petersmann Astrid, Pilling Luke C, Psaty Bruce, Rawal Rajesh, Reiman Eric M, Schulz Andrea, Shulman Joshua M, Singleton Andrew B, Smith Albert V, Sutin Angelina R, Uitterlinden André G, Völzke Henry, Widen Elisabeth, Yaffe Kristine, Zonderman Alan B, Cucca Francesco, Harris Tamara, Ladwig Karl-Heinz, Llewellyn David J, Räikkönen Katri, Tanaka Toshiko, van Duijn Cornelia M, Grabe Hans J, Launer Lenore J, Lunetta Kathryn L, Mosley Thomas H, Newman Anne B, Tiemeier Henning, Murabito Joanne A genome-wide association study of depressive symptoms. Biological psychiatry. 2013; 73(7): 667-78.
Li Xiaohui, Bykhovskaya Yelena, Canedo Ana Laura Caiado, Haritunians Talin, Siscovick David, Aldave Anthony J, Szczotka-Flynn Loretta, Iyengar Sudha K, Rotter Jerome I, Taylor Kent D, Rabinowitz Yaron S Genetic Association of COL5A1 Variants in Keratoconus Patients Suggests a Complex Connection between Corneal Thinning and Keratoconus. Investigative ophthalmology & visual science. 2013; 54(4): 2696-704.
Powell Rhea, Davidson Duncan, Divers Jasmin, Manichaikul Ani, Carr J Jeffrey, Detrano Robert, Hoffman Eric A, Jiang Rui, Kronmal Richard A, Liu Kiang, Punjabi Naresh M, Shahar Eyal, Watson Karol E, Rotter Jerome I, Taylor Kent D, Rich Stephen S, Barr R Graham Genetic ancestry and the relationship of cigarette smoking to lung function and per cent emphysema in four race/ethnic groups: a cross-sectional study. Thorax. 2013; 54(4): .
Frazier-Wood Alexis C, Manichaikul Ani, Aslibekyan Stella, Borecki Ingrid B, Goff David C, Hopkins Paul N, Lai Chao-Qiang, Ordovas Jose M, Post Wendy S, Rich Stephen S, Sale Michèle M, Siscovick David, Straka Robert J, Tiwari Hemant K, Tsai Michael Y, Rotter Jerome I, Arnett Donna K Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity. Human genetics. 2013; 132(4): 405-13.
Sheu Wayne H-H, Kuo Jane Z, Lee I-Te, Hung Yi-Jen, Lee Wen-Jane, Tsai Hin-Yeung, Wang J-S, Goodarzi Mark O, Klein Ronald, Klein Barbara E K, Ipp Eli, Lin Shin-Yi, Guo Xiuqing, Hsieh Chang-Hsun, Taylor Kent D, Fu Chia-Po, Rotter Jerome I, Chen Yii-Der I Genome-wide association study in a Chinese population with diabetic retinopathy. Human molecular genetics. 2013; 32(5): .
Lee C Christine, Haffner Steven M, Wagenknecht Lynne E, Lorenzo Carlos, Norris Jill M, Bergman Richard N, Stefanovski Darko, Anderson Andrea M, Rotter Jerome I, Goodarzi Mark O, Hanley Anthony J Insulin clearance and the incidence of type 2 diabetes in Hispanics and African Americans: the IRAS Family Study. Diabetes care. 2013; 36(4): 901-7.
Huertas-Vazquez Adriana, Nelson Christopher P, Guo Xiuqing, Reinier Kyndaron, Uy-Evanado Audrey, Teodorescu Carmen, Ayala Jo, Jerger Katherine, Chugh Harpriya, Wtccc Harpriya, Braund Peter S, Deloukas Panos, Hall Alistair S, Balmforth Anthony J, Jones Michelle, Taylor Kent D, Pulit Sara L, Newton-Cheh Christopher, Gunson Karen, Jui Jonathan, Rotter Jerome I, Albert Christine M, Samani Nilesh J, Chugh Sumeet S Novel Loci associated with increased risk of sudden cardiac death in the context of coronary artery disease. PloS one. 2013; 8(4): e59905.
An S Sandy, Palmer Nicholette D, Hanley Anthony J G, Ziegler Julie T, Brown W Mark, Freedman Barry I, Register Thomas C, Rotter Jerome I, Guo Xiuqing, Chen Y-D Ida, Wagenknecht Lynne E, Langefeld Carl D, Bowden Donald W Genetic analysis of adiponectin variation and its association with type 2 diabetes in african americans. Obesity (Silver Spring, Md.). 2013; 54(4): .
Hruby Adela, Ngwa Julius S, Renström Frida, Wojczynski Mary K, Ganna Andrea, Hallmans Göran, Houston Denise K, Jacques Paul F, Kanoni Stavroula, Lehtimäki Terho, Lemaitre Rozenn N, Manichaikul Ani, North Kari E, Ntalla Ioanna, Sonestedt Emily, Tanaka Toshiko, van Rooij Frank J A, Bandinelli Stefania, Djoussé Luc, Grigoriou Efi, Johansson Ingegerd, Lohman Kurt K, Pankow James S, Raitakari Olli T, Riserus Ulf, Yannakoulia Mary, Zillikens M Carola, Hassanali Neelam, Liu Yongmei, Mozaffarian Dariush, Papoutsakis Constantina, Syvänen Ann-Christine, Uitterlinden André G, Viikari Jorma, Groves Christopher J, Hofman Albert, Lind Lars, McCarthy Mark I, Mikkilä Vera, Mukamal Kenneth, Franco Oscar H, Borecki Ingrid B, Cupples L Adrienne, Dedoussis George V, Ferrucci Luigi, Hu Frank B, Ingelsson Erik, Kähönen Mika, Kao W H Linda, Kritchevsky Stephen B, Orho-Melander Marju, Prokopenko Inga, Rotter Jerome I, Siscovick David S, Witteman Jacqueline C M, Franks Paul W, Meigs James B, McKeown Nicola M, Nettleton Jennifer A Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies. The Journal of nutrition. 2013; 143(3): 345-53.
Stambolian Dwight, Wojciechowski Robert, Oexle Konrad, Pirastu Mario, Li Xiaohui, Raffel Leslie J, Cotch Mary Frances, Chew Emily Y, Klein Barbara, Klein Ronald, Wong Tien Y, Simpson Claire L, Klaver Caroline C W, van Duijn Cornelia M, Verhoeven Virginie J M, Baird Paul N, Vitart Veronique, Paterson Andrew D, Mitchell Paul, Saw Seang Mei, Fossarello Maurizio, Kazmierkiewicz Krista, Murgia Federico, Portas Laura, Schache Maria, Richardson Andrea, Xie Jing, Wang Jie Jin, Rochtchina Elena, Rochtchina Elena, Viswanathan Ananth C, Hayward Caroline, Wright Alan F, Polasek Ozren, Campbell Harry, Rudan Igor, Oostra Ben A, Uitterlinden André G, Hofman Albert, Rivadeneira Fernando, Amin Najaf, Karssen Lennart C, Vingerling Johannes R, Hosseini S M, Döring Angela, Bettecken Thomas, Vatavuk Zoran, Gieger Christian, Wichmann H-Erich, Wilson James F, Fleck Brian, Foster Paul J, Topouzis Fotis, McGuffin Peter, Sim Xueling, Inouye Michael, Holliday Elizabeth G, Attia John, Scott Rodney J, Rotter Jerome I, Meitinger Thomas, Bailey-Wilson Joan E Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Human molecular genetics. 2013; 54(4): .
Wu Ying, Waite Lindsay L, Jackson Anne U, Sheu Wayne H-H, Buyske Steven, Absher Devin, Arnett Donna K, Boerwinkle Eric, Bonnycastle Lori L, Carty Cara L, Cheng Iona, Cochran Barbara, Croteau-Chonka Damien C, Dumitrescu Logan, Eaton Charles B, Franceschini Nora, Guo Xiuqing, Henderson Brian E, Hindorff Lucia A, Kim Eric, Kinnunen Leena, Komulainen Pirjo, Lee Wen-Jane, Le Marchand Loic, Lin Yi, Lindström Jaana, Lingaas-Holmen Oddgeir, Mitchell Sabrina L, Narisu Narisu, Robinson Jennifer G, Schumacher Fred, Stančáková Alena, Sundvall Jouko, Sung Yun-Ju, Swift Amy J, Wang Wen-Chang, Wilkens Lynne, Wilsgaard Tom, Young Alicia M, Adair Linda S, Ballantyne Christie M, Bůžková Petra, Chakravarti Aravinda, Collins Francis S, Duggan David, Feranil Alan B, Ho Low-Tone, Hung Yi-Jen, Hunt Steven C, Hveem Kristian, Juang Jyh-Ming J, Kesäniemi Antero Y, Kuusisto Johanna, Laakso Markku, Lakka Timo A, Lee I-Te, Leppert Mark F, Matise Tara C, Moilanen Leena, Njølstad Inger, Peters Ulrike, Quertermous Thomas, Rauramaa Rainer, Rotter Jerome I, Saramies Jouko, Tuomilehto Jaakko, Uusitupa Matti, Wang Tzung-Dau, Boehnke Michael, Haiman Christopher A, Chen Yii-Der I, Kooperberg Charles, Assimes Themistocles L, Crawford Dana C, Hsiung Chao A, North Kari E, Mohlke Karen L Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. PLoS genetics. 2013; 9(3): e1003379.
Ng Maggie C Y, Saxena Richa, Li Jiang, Palmer Nicholette D, Dimitrov Latchezar, Xu Jianzhao, Rasmussen-Torvik Laura J, Zmuda Joseph M, Siscovick David S, Patel Sanjay R, Crook Errol D, Sims Mario, Chen Yii-Der I, Bertoni Alain G, Li Mingyao, Grant Struan F A, Dupuis Josée, Meigs James B, Psaty Bruce M, Pankow James S, Langefeld Carl D, Freedman Barry I, Rotter Jerome I, Wilson James G, Bowden Donald W Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Diabetes. 2013; 62(3): 965-76.
Porcu Eleonora, Medici Marco, Pistis Giorgio, Volpato Claudia B, Wilson Scott G, Cappola Anne R, Bos Steffan D, Deelen Joris, den Heijer Martin, Freathy Rachel M, Lahti Jari, Liu Chunyu, Lopez Lorna M, Nolte Ilja M, O'Connell Jeffrey R, Tanaka Toshiko, Trompet Stella, Arnold Alice, Bandinelli Stefania, Beekman Marian, Böhringer Stefan, Brown Suzanne J, Buckley Brendan M, Camaschella Clara, de Craen Anton J M, Davies Gail, de Visser Marieke C H, Ford Ian, Forsen Tom, Frayling Timothy M, Fugazzola Laura, Gögele Martin, Hattersley Andrew T, Hermus Ad R, Hofman Albert, Houwing-Duistermaat Jeanine J, Jensen Richard A, Kajantie Eero, Kloppenburg Margreet, Lim Ee M, Masciullo Corrado, Mariotti Stefano, Minelli Cosetta, Mitchell Braxton D, Nagaraja Ramaiah, Netea-Maier Romana T, Palotie Aarno, Persani Luca, Piras Maria G, Psaty Bruce M, Räikkönen Katri, Richards J Brent, Rivadeneira Fernando, Sala Cinzia, Sabra Mona M, Sattar Naveed, Shields Beverley M, Soranzo Nicole, Starr John M, Stott David J, Sweep Fred C G J, Usala Gianluca, van der Klauw Melanie M, van Heemst Diana, van Mullem Alies, Vermeulen Sita H, Visser W Edward, Walsh John P, Westendorp Rudi G J, Widen Elisabeth, Zhai Guangju, Cucca Francesco, Deary Ian J, Eriksson Johan G, Ferrucci Luigi, Fox Caroline S, Jukema J Wouter, Kiemeney Lambertus A, Pramstaller Peter P, Schlessinger David, Shuldiner Alan R, Slagboom Eline P, Uitterlinden André G, Vaidya Bijay, Visser Theo J, Wolffenbuttel Bruce H R, Meulenbelt Ingrid, Rotter Jerome I, Spector Tim D, Hicks Andrew A, Toniolo Daniela, Sanna Serena, Peeters Robin P, Naitza Silvia A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function. PLoS genetics. 2013; 9(2): e1003266.
Divers Jasmin, Palmer Nicholette D, Lu Lingyi, Register Thomas C, Carr J Jeffrey, Hicks Pamela J, Hightower R Caresse, Smith S Carrie, Xu Jianzhao, Cox Amanda J, Hruska Keith A, Bowden Donald W, Lewis Cora E, Heiss Gerardo, Province Michael A, Borecki Ingrid B, Kerr Kathleen F, Chen Y-D Ida, Palmas Walter, Rotter Jerome I, Wassel Christina L, Bertoni Alain G, Herrington David M, Wagenknecht Lynne E, Langefeld Carl D, Freedman Barry I Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus. Circulation. Cardiovascular genetics. 2013; 6(1): 97-105.
Yu Bing, Barbalic Maja, Brautbar Ariel, Nambi Vijay, Hoogeveen Ron C, Tang Weihong, Mosley Thomas H, Rotter Jerome I, deFilippi Christopher R, O'Donnell Christopher J, Kathiresan Sekar, Rice Ken, Heckbert Susan R, Ballantyne Christie M, Psaty Bruce M, Boerwinkle Eric, Boerwinkle Eric Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. Circulation. Cardiovascular genetics. 2013; 6(1): 82-8.
Thanassoulis George, Campbell Catherine Y, Owens David S, Smith J Gustav, Smith Albert V, Peloso Gina M, Kerr Kathleen F, Pechlivanis Sonali, Budoff Matthew J, Harris Tamara B, Malhotra Rajeev, O'Brien Kevin D, Kamstrup Pia R, Nordestgaard Børge G, Tybjaerg-Hansen Anne, Allison Matthew A, Aspelund Thor, Criqui Michael H, Heckbert Susan R, Hwang Shih-Jen, Liu Yongmei, Sjogren Marketa, van der Pals Jesper, Kälsch Hagen, Mühleisen Thomas W, Nöthen Markus M, Cupples L Adrienne, Caslake Muriel, Di Angelantonio Emanuele, Danesh John, Rotter Jerome I, Sigurdsson Sigurdur, Wong Quenna, Erbel Raimund, Kathiresan Sekar, Melander Olle, Gudnason Vilmundur, O'Donnell Christopher J, Post Wendy S, Post Wendy S Genetic associations with valvular calcification and aortic stenosis. The New England journal of medicine. 2013; 368(6): 503-12.
Lu Yi, Vitart Veronique, Burdon Kathryn P, Khor Chiea Chuen, Bykhovskaya Yelena, Mirshahi Alireza, Hewitt Alex W, Koehn Demelza, Hysi Pirro G, Ramdas Wishal D, Zeller Tanja, Vithana Eranga N, Cornes Belinda K, Tay Wan-Ting, Tai E Shyong, Cheng Ching-Yu, Liu Jianjun, Foo Jia-Nee, Saw Seang Mei, Thorleifsson Gudmar, Stefansson Kari, Dimasi David P, Mills Richard A, Mountain Jenny, Ang Wei, Hoehn René, Verhoeven Virginie J M, Grus Franz, Wolfs Roger, Castagne Raphaële, Lackner Karl J, Springelkamp Henriët, Yang Jian, Jonasson Fridbert, Leung Dexter Y L, Chen Li J, Tham Clement C Y, Rudan Igor, Vatavuk Zoran, Hayward Caroline, Gibson Jane, Cree Angela J, MacLeod Alex, Ennis Sarah, Polasek Ozren, Campbell Harry, Wilson James F, Viswanathan Ananth C, Fleck Brian, Li Xiaohui, Siscovick David, Taylor Kent D, Rotter Jerome I, Yazar Seyhan, Ulmer Megan, Li Jun, Yaspan Brian L, Ozel Ayse B, Richards Julia E, Moroi Sayoko E, Haines Jonathan L, Kang Jae H, Pasquale Louis R, Allingham R Rand, Ashley-Koch Allison, Ashley-Koch Allison, Mitchell Paul, Wang Jie Jin, Wright Alan F, Pennell Craig, Spector Timothy D, Young Terri L, Klaver Caroline C W, Martin Nicholas G, Montgomery Grant W, Anderson Michael G, Aung Tin, Willoughby Colin E, Wiggs Janey L, Pang Chi P, Thorsteinsdottir Unnur, Lotery Andrew J, Hammond Christopher J, van Duijn Cornelia M, Hauser Michael A, Rabinowitz Yaron S, Pfeiffer Norbert, Mackey David A, Craig Jamie E, Macgregor Stuart, Wong Tien Y Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature genetics. 2013; 45(2): 155-63.
Richardson Kris, Nettleton Jennifer A, Rotllan Noemi, Tanaka Toshiko, Smith Caren E, Lai Chao-Qiang, Parnell Laurence D, Lee Yu-Chi, Lahti Jari, Lemaitre Rozenn N, Manichaikul Ani, Keller Margaux, Mikkilä Vera, Ngwa Julius, van Rooij Frank J A, Ballentyne Christie M, Borecki Ingrid B, Cupples L Adrienne, Garcia Melissa, Hofman Albert, Ferrucci Luigi, Mozaffarian Dariush, Perälä Mia-Maria, Raitakari Olli, Tracy Russell P, Arnett Donna K, Bandinelli Stefania, Boerwinkle Eric, Eriksson Johan G, Franco Oscar H, Kähönen Mika, Nalls Michael, Siscovick David S, Houston Denise K, Psaty Bruce M, Viikari Jorma, Witteman Jacqueline C M, Goodarzi Mark O, Lehtimäki Terho, Liu Yongmei, Zillikens M Carola, Chen Yii-Der I, Uitterlinden André G, Rotter Jerome I, Fernandez-Hernando Carlos, Ordovas Jose M Gain-of-function lipoprotein lipase variant rs13702 modulates lipid traits through disruption of a microRNA-410 seed site. American journal of human genetics. 2013; 92(1): 5-14.
Jensen Richard A, Sim Xueling, Li Xiaohui, Cotch Mary Frances, Ikram M Kamran, Holliday Elizabeth G, Eiriksdottir Gudny, Harris Tamara B, Jonasson Fridbert, Klein Barbara E K, Launer Lenore J, Smith Albert Vernon, Boerwinkle Eric, Cheung Ning, Hewitt Alex W, Liew Gerald, Mitchell Paul, Wang Jie Jin, Attia John, Scott Rodney, Glazer Nicole L, Lumley Thomas, McKnight Barbara, Psaty Bruce M, Taylor Kent, Hofman Albert, de Jong Paulus T V M, Rivadeneira Fernando, Uitterlinden Andre G, Tay Wan-Ting, Teo Yik Ying, Seielstad Mark, Liu Jianjun, Cheng Ching-Yu, Saw Seang-Mei, Aung Tin, Ganesh Santhi K, O'Donnell Christopher J, Nalls Mike A, Wiggins Kerri L, Kuo Jane Z, Kuo Jane Z, Kuo Jane Z, van Duijn Cornelia M, Gudnason Vilmundur, Klein Ronald, Siscovick David S, Rotter Jerome I, Tai E Shong, Vingerling Johannes, Wong Tien Y Genome-wide association study of retinopathy in individuals without diabetes. PloS one. 2013; 8(2): e54232.
Holliday Elizabeth G, Smith Albert V, Cornes Belinda K, Buitendijk Gabriëlle H S, Jensen Richard A, Sim Xueling, Aspelund Thor, Aung Tin, Baird Paul N, Boerwinkle Eric, Cheng Ching Yu, van Duijn Cornelia M, Eiriksdottir Gudny, Gudnason Vilmundur, Harris Tamara, Hewitt Alex W, Inouye Michael, Jonasson Fridbert, Klein Barbara E K, Launer Lenore, Li Xiaohui, Liew Gerald, Lumley Thomas, McElduff Patrick, McKnight Barbara, Mitchell Paul, Psaty Bruce M, Rochtchina Elena, Rotter Jerome I, Scott Rodney J, Tay Wanting, Taylor Kent, Teo Yik Ying, Uitterlinden André G, Viswanathan Ananth, Xie Sophia, Xie Sophia, Vingerling Johannes R, Klaver Caroline C W, Tai E Shyong, Siscovick David, Klein Ronald, Cotch Mary Frances, Wong Tien Y, Attia John, Wang Jie Jin Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. PloS one. 2013; 8(1): e53830.
An S Sandy, Hanley Anthony J G, Ziegler Julie T, Brown W Mark, Haffner Steven M, Norris Jill M, Rotter Jerome I, Guo Xiuqing, Chen Y-D Ida, Wagenknecht Lynne E, Langefeld Carl D, Bowden Donald W, Palmer Nicholette D Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study. Molecular genetics and metabolism. 2012; 107(4): 721-8.
Mangino Massimo, Hwang Shih-Jen, Spector Timothy D, Hunt Steven C, Kimura Masayuki, Fitzpatrick Annette L, Christiansen Lene, Petersen Inge, Elbers Clara C, Harris Tamara, Chen Wei, Srinivasan Sathanur R, Kark Jeremy D, Benetos Athanase, El Shamieh Said, Visvikis-Siest Sophie, Christensen Kaare, Berenson Gerald S, Valdes Ana M, Viñuela Ana, Garcia Melissa, Arnett Donna K, Broeckel Ulrich, Province Michael A, Pankow James S, Kammerer Candace, Liu Yongmei, Nalls Michael, Tishkoff Sarah, Thomas Fridtjof, Ziv Elad, Psaty Bruce M, Bis Joshua C, Rotter Jerome I, Taylor Kent D, Smith Erin, Schork Nicholas J, Levy Daniel, Aviv Abraham Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Human molecular genetics. 2012; 21(24): 5385-94.
Smith J Gustav, Avery Christy L, Evans Daniel S, Nalls Michael A, Meng Yan A, Smith Erin N, Palmer Cameron, Tanaka Toshiko, Mehra Reena, Butler Anne M, Young Taylor, Buxbaum Sarah G, Kerr Kathleen F, Berenson Gerald S, Schnabel Renate B, Li Guo, Ellinor Patrick T, Magnani Jared W, Chen Wei, Bis Joshua C, Curb J David, Hsueh Wen-Chi, Rotter Jerome I, Liu Yongmei, Newman Anne B, Limacher Marian C, North Kari E, Reiner Alexander P, Quibrera P Miguel, Schork Nicholas J, Singleton Andrew B, Psaty Bruce M, Soliman Elsayed Z, Solomon Allen J, Srinivasan Sathanur R, Alonso Alvaro, Wallace Robert, Redline Susan, Zhang Zhu-Ming, Post Wendy S, Zonderman Alan B, Taylor Herman A, Murray Sarah S, Ferrucci Luigi, Arking Dan E, Evans Michele K, Fox Ervin R, Sotoodehnia Nona, Heckbert Susan R, Whitsel Eric A, Newton-Cheh Christopher, Newton-Cheh Christopher Impact of ancestry and common genetic variants on QT interval in African Americans. Circulation. Cardiovascular genetics. 2012; 5(6): 647-55.
Butler Anne M, Yin Xiaoyan, Evans Daniel S, Nalls Michael A, Smith Erin N, Tanaka Toshiko, Li Guo, Buxbaum Sarah G, Whitsel Eric A, Alonso Alvaro, Arking Dan E, Benjamin Emelia J, Berenson Gerald S, Bis Josh C, Chen Wei, Deo Rajat, Ellinor Patrick T, Heckbert Susan R, Heiss Gerardo, Hsueh Wen-Chi, Keating Brendan J, Kerr Kathleen F, Li Yun, Limacher Marian C, Liu Yongmei, Lubitz Steven A, Marciante Kristin D, Mehra Reena, Meng Yan A, Newman Anne B, Newton-Cheh Christopher, North Kari E, Palmer Cameron D, Psaty Bruce M, Quibrera P Miguel, Redline Susan, Reiner Alex P, Rotter Jerome I, Schnabel Renate B, Schork Nicholas J, Singleton Andrew B, Smith J Gustav, Soliman Elsayed Z, Srinivasan Sathanur R, Zhang Zhu-ming, Zonderman Alan B, Ferrucci Luigi, Murray Sarah S, Evans Michele K, Sotoodehnia Nona, Magnani Jared W, Avery Christy L Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. Circulation. Cardiovascular genetics. 2012; 5(6): 639-46.
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Franceschini Nora, van Rooij Frank J A, Prins Bram P, Feitosa Mary F, Karakas Mahir, Eckfeldt John H, Folsom Aaron R, Kopp Jeffrey, Vaez Ahmad, Andrews Jeanette S, Baumert Jens, Boraska Vesna, Broer Linda, Hayward Caroline, Ngwa Julius S, Okada Yukinori, Polasek Ozren, Westra Harm-Jan, Wang Ying A, Del Greco M Fabiola, Glazer Nicole L, Kapur Karen, Kema Ido P, Lopez Lorna M, Schillert Arne, Smith Albert V, Winkler Cheryl A, Zgaga Lina, Zgaga Lina, Bandinelli Stefania, Bergmann Sven, Boban Mladen, Bochud Murielle, Chen Y D, Davies Gail, Dehghan Abbas, Ding Jingzhong, Doering Angela, Durda J Peter, Ferrucci Luigi, Franco Oscar H, Franke Lude, Gunjaca Grog, Hofman Albert, Hsu Fang-Chi, Kolcic Ivana, Kraja Aldi, Kubo Michiaki, Lackner Karl J, Launer Lenore, Loehr Laura R, Li Guo, Meisinger Christa, Nakamura Yusuke, Schwienbacher Christine, Starr John M, Takahashi Atsushi, Torlak Vesela, Uitterlinden André G, Vitart Veronique, Waldenberger Melanie, Wild Philipp S, Kirin Mirna, Zeller Tanja, Zemunik Tatijana, Zhang Qunyuan, Ziegler Andreas, Blankenberg Stefan, Boerwinkle Eric, Borecki Ingrid B, Campbell Harry, Deary Ian J, Frayling Timothy M, Gieger Christian, Harris Tamara B, Hicks Andrew A, Koenig Wolfgang, O' Donnell Christopher J, Fox Caroline S, Pramstaller Peter P, Psaty Bruce M, Reiner Alex P, Rotter Jerome I, Rudan Igor, Snieder Harold, Tanaka Toshihiro, van Duijn Cornelia M, Vollenweider Peter, Waeber Gerard, Wilson James F, Witteman Jacqueline C M, Wolffenbuttel Bruce H R, Wright Alan F, Wu Qingyu, Liu Yongmei, Jenny Nancy S, North Kari E, Felix Janine F, Alizadeh Behrooz Z, Cupples L Adrienne, Perry John R B, Morris Andrew P Discovery and fine mapping of serum protein loci through transethnic meta-analysis. American journal of human genetics. 2012; 91(4): 744-53.
An S Sandy, Palmer Nicholette D, Hanley Anthony J G, Ziegler Julie T, Brown W Mark, Haffner Steven M, Norris Jill M, Rotter Jerome I, Guo Xiuqing, Chen Y-D Ida, Wagenknecht Lynne E, Langefeld Carl D, Bowden Donald W Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin. Genetic epidemiology. 2012; 91(4): .
Wilk Jemma B, Shrine Nick R G, Loehr Laura R, Zhao Jing Hua, Manichaikul Ani, Lopez Lorna M, Smith Albert Vernon, Heckbert Susan R, Smolonska Joanna, Tang Wenbo, Loth Daan W, Curjuric Ivan, Hui Jennie, Cho Michael H, Latourelle Jeanne C, Henry Amanda P, Aldrich Melinda, Bakke Per, Beaty Terri H, Bentley Amy R, Borecki Ingrid B, Brusselle Guy G, Burkart Kristin M, Chen Ting-hsu, Couper David, Crapo James D, Davies Gail, Dupuis Josée, Franceschini Nora, Gulsvik Amund, Hancock Dana B, Harris Tamara B, Hofman Albert, Imboden Medea, James Alan L, Khaw Kay-Tee, Lahousse Lies, Launer Lenore J, Litonjua Augusto, Liu Yongmei, Lohman Kurt K, Lomas David A, Lumley Thomas, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, Musk Arthur W, Myers Richard H, North Kari E, Postma Dirkje S, Psaty Bruce M, Rich Stephen S, Rivadeneira Fernando, Rochat Thierry, Rotter Jerome I, Artigas María Soler, Starr John M, Uitterlinden André G, Wareham Nicholas J, Wijmenga Cisca, Zanen Pieter, Province Michael A, Silverman Edwin K, Deary Ian J, Palmer Lyle J, Cassano Patricia A, Gudnason Vilmundur, Barr R Graham, Loos Ruth J F, Strachan David P, London Stephanie J, Boezen H Marike, Probst-Hensch Nicole, Gharib Sina A, Hall Ian P, O'Connor George T, Tobin Martin D, Stricker Bruno H Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American journal of respiratory and critical care medicine. 2012; 186(7): 622-32.
Kaufman Joel D, Adar Sara D, Allen Ryan W, Barr R Graham, Budoff Matthew J, Burke Gregory L, Casillas Adrian M, Cohen Martin A, Curl Cynthia L, Daviglus Martha L, Roux Ana V Diez, Jacobs David R, Kronmal Richard A, Larson Timothy V, Liu Sally Lee-Jane, Lumley Thomas, Navas-Acien Ana, O'Leary Daniel H, Rotter Jerome I, Sampson Paul D, Sheppard Lianne, Siscovick David S, Stein James H, Szpiro Adam A, Tracy Russell P Prospective Study of Particulate Air Pollution Exposures, Subclinical Atherosclerosis, and Clinical Cardiovascular Disease: The Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air). American journal of epidemiology. 2012; 91(4): .
Ong Frank S, Vakil Hana, Xue Yuan, Kuo Jane Z, Shah Kandarp H, Lee Rand B, Bernstein Kenneth E, Rimoin David L, Getzug Terri, Das Kingshuk, Deignan Joshua L, Rotter Jerome I, Grody Wayne W The M694V Mutation in Armenian-Americans: A Ten-Year Retrospective Study of MEFV Mutation Testing for Familial Mediterranean Fever at UCLA. Clinical genetics. 2012; 91(4): .
Miller Melissa R, Pereira Rocio I, Langefeld Carl D, Lorenzo Carlos, Rotter Jerome I, Chen Yii-Der Ida, Bergman Richard N, Wagenknecht Lynne E, Norris Jill M, Fingerlin Tasha E Levels of Free Fatty Acids (FFA) Are Associated with Insulin Resistance But Do Not Explain the Relationship between Adiposity and Insulin Resistance in Hispanic Americans: The IRAS Family Study. The Journal of clinical endocrinology and metabolism. 2012; 97(9): 3285-91.
Fedorowski Artur, Franceschini Nora, Brody Jennifer, Liu Chunyu, Verwoert Germaine C, Boerwinkle Eric, Couper David, Rice Kenneth M, Rotter Jerome I, Mattace-Raso Francesco, Uitterlinden Andre, Hofman Albert, Almgren Peter, Sjögren Marketa, Hedblad Bo, Larson Martin G, Newton-Cheh Christopher, Wang Thomas J, Rose Kathryn M, Psaty Bruce M, Levy Daniel, Witteman Jacqueline, Melander Olle Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium. European heart journal. 2012; 33(18): 2331-41.
Murdoch Travis B, Xu Wei, Stempak Joanne M, Landers Carol, Targan Stephan R, Rotter Jerome I, Silverberg Mark S Pattern recognition receptor and autophagy gene variants are associated with development of antimicrobial antibodies in Crohn's disease. Inflammatory bowel diseases. 2012; 18(9): 1743-8.
Jones Michelle R, Chazenbalk Gregorio, Xu Ning, Chua Angela K, Eigler Tamar, Mengesha Emebet, Chen Yen-Hao, Lee Jung-Min, Pall Marita, Li Xiaohui, Chen Yii-Der I, Taylor Kent D, Mathur Ruchi, Krauss Ronald M, Rotter Jerome I, Legro Richard S, Azziz Ricardo, Goodarzi Mark O Steroidogenic Regulatory Factor FOS Is Underexpressed in Polycystic Ovary Syndrome (PCOS) Adipose Tissue and Genetically Associated with PCOS Susceptibility. The Journal of clinical endocrinology and metabolism. 2012; 97(9): E1750-7.
Chiang Charleston W K, Liu Ching-Ti, Lettre Guillaume, Lange Leslie A, Jorgensen Neal W, Keating Brendan J, Vedantam Sailaja, Nock Nora L, Franceschini Nora, Reiner Alex P, Demerath Ellen W, Boerwinkle Eric, Rotter Jerome I, Wilson James G, North Kari E, Papanicolaou George J, Cupples L Adrienne, Cupples L Adrienne, Murabito Joanne M, Hirschhorn Joel N Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms. Genetics. 2012; 192(1): 253-66.
Williams Jonathan S, Chamarthi Bindu, Goodarzi Mark O, Pojoga Luminita H, Sun Bei, Garza Amanda E, Raby Benjamin A, Adler Gail K, Hopkins Paul N, Brown Nancy J, Jeunemaitre Xavier, Ferri Claudio, Fang Rui, Leonor Thiago, Cui Jinrui, Guo Xiuqing, Taylor Kent D, Ida Chen Yii-Der, Xiang Anny, Raffel Leslie J, Buchanan Thomas A, Rotter Jerome I, Williams Gordon H, Shi Yujiang Lysine-specific demethylase 1: an epigenetic regulator of salt-sensitive hypertension. American journal of hypertension. 2012; 25(7): 812-7.
Ong Frank S, Das Kingshuk, Wang Jay, Vakil Hana, Kuo Jane Z, Blackwell Wendell-Lamar B, Lim Stephen W, Goodarzi Mark O, Bernstein Kenneth E, Rotter Jerome I, Grody Wayne W Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing. Expert review of molecular diagnostics. 2012; 12(6): 593-602.
Bykhovskaya Yelena, Li Xiaohui, Epifantseva Irina, Haritunians Talin, Siscovick David, Aldave Anthony, Szczotka-Flynn Loretta, Iyengar Sudha K, Taylor Kent D, Rotter Jerome I, Rabinowitz Yaron S Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies. Investigative ophthalmology & visual science. 2012; 53(7): 4152-7.
Iliev Iliyan D, Funari Vincent A, Taylor Kent D, Nguyen Quoclinh, Reyes Christopher N, Strom Samuel P, Brown Jordan, Becker Courtney A, Fleshner Phillip R, Dubinsky Marla, Rotter Jerome I, Wang Hanlin L, McGovern Dermot P B, Brown Gordon D, Underhill David M Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis. Science (New York, N.Y.). 2012; 336(6086): 1314-7.
Wassel Christina L, Lamina Claudia, Nambi Vijay, Coassin Stefan, Mukamal Kenneth J, Ganesh Santhi K, Jacobs David R, Franceschini Nora, Papanicolaou George J, Gibson Quince, Yanek Lisa R, van der Harst Pim, Ferguson Jane F, Crawford Dana C, Waite Lindsay L, Allison Matthew A, Criqui Michael H, McDermott Mary M, Mehra Reena, Cupples L Adrienne, Hwang Shih-Jen, Redline Susan, Kaplan Robert C, Heiss Gerardo, Rotter Jerome I, Boerwinkle Eric, Taylor Herman A, Eraso Luis H, Haun Margot, Li Mingyao, Meisinger Christa, O'Connell Jeffrey R, Shuldiner Alan R, Tybjærg-Hansen Anne, Frikke-Schmidt Ruth, Kollerits Barbara, Rantner Barbara, Dieplinger Benjamin, Stadler Marietta, Mueller Thomas, Haltmayer Meinhard, Klein-Weigel Peter, Summerer Monika, Wichmann H-Erich, Asselbergs Folkert W, Navis Gerjan, Mateo Leach Irene, Brown-Gentry Kristin, Goodloe Robert, Assimes Themistocles L, Becker Diane M, Cooke John P, Absher Devin M, Olin Jeffrey W, Mitchell Braxton D, Reilly Muredach P, Mohler Emile R, North Kari E, Reiner Alexander P, Kronenberg Florian, Murabito Joanne M Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium. Atherosclerosis. 2012; 222(1): 138-47.
Scott Robert A, Chu Audrey Y, Grarup Niels, Manning Alisa K, Hivert Marie-France, Shungin Dmitry, Tönjes Anke, Yesupriya Ajay, Barnes Daniel, Bouatia-Naji Nabila, Glazer Nicole L, Jackson Anne U, Kutalik Zoltán, Lagou Vasiliki, Marek Diana, Rasmussen-Torvik Laura J, Stringham Heather M, Tanaka Toshiko, Aadahl Mette, Arking Dan E, Bergmann Sven, Boerwinkle Eric, Bonnycastle Lori L, Bornstein Stefan R, Brunner Eric, Bumpstead Suzannah J, Brage Soren, Carlson Olga D, Chen Han, Chen Yii-Der Ida, Chines Peter S, Collins Francis S, Couper David J, Dennison Elaine M, Dowling Nicole F, Egan Josephine S, Ekelund Ulf, Erdos Michael R, Forouhi Nita G, Fox Caroline S, Goodarzi Mark O, Grässler Jürgen, Gustafsson Stefan, Hallmans Göran, Hansen Torben, Hingorani Aroon, Holloway John W, Hu Frank B, Isomaa Bo, Jameson Karen A, Johansson Ingegerd, Jonsson Anna, Jørgensen Torben, Kivimaki Mika, Kovacs Peter, Kumari Meena, Kuusisto Johanna, Laakso Markku, Lecoeur Cécile, Lévy-Marchal Claire, Li Guo, Loos Ruth J F, Lyssenko Valeri, Marmot Michael, Marques-Vidal Pedro, Morken Mario A, Müller Gabriele, North Kari E, Pankow James S, Payne Felicity, Prokopenko Inga, Psaty Bruce M, Renström Frida, Rice Ken, Rotter Jerome I, Rybin Denis, Sandholt Camilla H, Sayer Avan A, Shrader Peter, Schwarz Peter E H, Siscovick David S, Stancáková Alena, Stumvoll Michael, Teslovich Tanya M, Waeber Gérard, Williams Gordon H, Witte Daniel R, Wood Andrew R, Xie Weijia, Boehnke Michael, Cooper Cyrus, Ferrucci Luigi, Froguel Philippe, Groop Leif, Kao W H Linda, Vollenweider Peter, Walker Mark, Watanabe Richard M, Pedersen Oluf, Meigs James B, Ingelsson Erik, Barroso Inês, Florez Jose C, Franks Paul W, Dupuis Josée, Wareham Nicholas J, Langenberg Claudia No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels. Diabetes. 2012; 61(5): 1291-6.
Kuo Jane Z, Guo Xiuqing, Klein Ronald, Klein Barbara E, Cui Jinrui, Rotter Jerome I, Ipp Eli, Chen Yii-Der Ida Systemic soluble tumor necrosis factor receptors 1 and 2 are associated with severity of diabetic retinopathy in Hispanics. Ophthalmology. 2012; 119(5): 1041-6.
Ebong Imo A, Bertoni Alain G, Soliman Elsayed Z, Guo Mengye, Sibley Christopher T, Chen Yii-Der I, Rotter Jerome I, Chen Yi-Chun, Goff David C Electrocardiographic abnormalities associated with the metabolic syndrome and its components: the multi-ethnic study of atherosclerosis. Metabolic syndrome and related disorders. 2012; 10(2): 92-7.
Ong Frank S, Deignan Joshua L, Kuo Jane Z, Bernstein Kenneth E, Rotter Jerome I, Grody Wayne W, Das Kingshuk Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation. Pharmacogenomics. 2012; 13(4): 465-75.
Saxena Richa, Elbers Clara C, Guo Yiran, Peter Inga, Gaunt Tom R, Mega Jessica L, Lanktree Matthew B, Tare Archana, Castillo Berta Almoguera, Li Yun R, Johnson Toby, Bruinenberg Marcel, Gilbert-Diamond Diane, Rajagopalan Ramakrishnan, Voight Benjamin F, Balasubramanyam Ashok, Barnard John, Bauer Florianne, Baumert Jens, Bhangale Tushar, Böhm Bernhard O, Braund Peter S, Burton Paul R, Chandrupatla Hareesh R, Clarke Robert, Cooper-DeHoff Rhonda M, Crook Errol D, Davey-Smith George, Day Ian N, de Boer Anthonius, de Groot Mark C H, Drenos Fotios, Ferguson Jane, Fox Caroline S, Furlong Clement E, Gibson Quince, Gieger Christian, Gilhuijs-Pederson Lisa A, Glessner Joseph T, Goel Anuj, Gong Yan, Grant Struan F A, Grobbee Diederick E, Hastie Claire, Humphries Steve E, Kim Cecilia E, Kivimaki Mika, Kleber Marcus, Meisinger Christa, Kumari Meena, Langaee Taimour Y, Lawlor Debbie A, Li Mingyao, Lobmeyer Maximilian T, Maitland-van der Zee Anke-Hilse, Meijs Matthijs F L, Molony Cliona M, Morrow David A, Murugesan Gurunathan, Musani Solomon K, Nelson Christopher P, Newhouse Stephen J, O'Connell Jeffery R, Padmanabhan Sandosh, Palmen Jutta, Patel Sanjey R, Pepine Carl J, Pettinger Mary, Price Thomas S, Rafelt Suzanne, Ranchalis Jane, Rasheed Asif, Rosenthal Elisabeth, Ruczinski Ingo, Shah Sonia, Shen Haiqing, Silbernagel Günther, Smith Erin N, Spijkerman Annemieke W M, Stanton Alice, Steffes Michael W, Thorand Barbara, Trip Mieke, van der Harst Pim, van der A Daphne L, van Iperen Erik P A, van Setten Jessica, van Vliet-Ostaptchouk Jana V, Verweij Niek, Wolffenbuttel Bruce H R, Young Taylor, Zafarmand M Hadi, Zmuda Joseph M, Zmuda Joseph M, Zmuda Joseph M, Boehnke Michael, Altshuler David, McCarthy Mark, Kao W H Linda, Pankow James S, Cappola Thomas P, Sever Peter, Poulter Neil, Caulfield Mark, Dominiczak Anna, Shields Denis C, Bhatt Deepak L, Bhatt Deepak, Zhang Li, Curtis Sean P, Danesh John, Casas Juan P, van der Schouw Yvonne T, Onland-Moret N Charlotte, Doevendans Pieter A, Dorn Gerald W, Farrall Martin, FitzGerald Garret A, Hamsten Anders, Hegele Robert, Hingorani Aroon D, Hofker Marten H, Huggins Gordon S, Illig Thomas, Jarvik Gail P, Johnson Julie A, Klungel Olaf H, Knowler William C, Koenig Wolfgang, März Winfried, Meigs James B, Melander Olle, Munroe Patricia B, Mitchell Braxton D, Bielinski Susan J, Rader Daniel J, Reilly Muredach P, Rich Stephen S, Rotter Jerome I, Saleheen Danish, Samani Nilesh J, Schadt Eric E, Shuldiner Alan R, Silverstein Roy, Kottke-Marchant Kandice, Talmud Philippa J, Watkins Hugh, Asselbergs Folkert W, Asselbergs Folkert, de Bakker Paul I W, McCaffery Jeanne, Wijmenga Cisca, Sabatine Marc S, Wilson James G, Reiner Alex, Bowden Donald W, Hakonarson Hakon, Siscovick David S, Keating Brendan J Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. American journal of human genetics. 2012; 90(3): 410-25.
Jones Michelle R, Chua Angela K, Mengesha Emebet A, Taylor Kent D, Chen Yii-Der I, Li Xiaohui, Krauss Ronald M, Rotter Jerome I, Rotter Jerome I, Legro Richard S, Azziz Ricardo, Goodarzi Mark O Metabolic and cardiovascular genes in polycystic ovary syndrome: a candidate-wide association study (CWAS). Steroids. 2012; 77(4): 317-22.
Ranganathan Gouri, Unal Resat, Pokrovskaya Irina D, Tripathi Preeti, Rotter Jerome I, Goodarzi Mark O, Kern Philip A The lipoprotein lipase (LPL) S447X gain of function variant involves increased mRNA translation. Atherosclerosis. 2012; 221(1): 143-7.
Manichaikul Ani, Chen Wei-Min, Williams Kayleen, Wong Quenna, Sale Michèle M, Pankow James S, Tsai Michael Y, Rotter Jerome I, Rich Stephen S, Mychaleckyj Josyf C Analysis of family- and population-based samples in cohort genome-wide association studies. Human genetics. 2012; 131(2): 275-87.
Goodarzi Mark O, Jones Michelle R, Li Xiaohui, Chua Angela K, Garcia Obed A, Chen Yii-Der I, Krauss Ronald M, Rotter Jerome I, Ankener Wendy, Legro Richard S, Azziz Ricardo, Strauss Jerome F, Dunaif Andrea, Urbanek Margrit Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts. Journal of medical genetics. 2012; 49(2): 90-5.
Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqing A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics. 2012; 2012(2): .
Li Xiaohui, Bykhovskaya Yelena, Haritunians Talin, Siscovick David, Aldave Anthony, Szczotka-Flynn Loretta, Iyengar Sudha K, Rotter Jerome I, Taylor Kent D, Rabinowitz Yaron S A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Human molecular genetics. 2012; 21(2): 421-9.
Kenny Eimear E, Pe'er Itsik, Karban Amir, Ozelius Laurie, Mitchell Adele A, Ng Sok Meng, Erazo Monica, Ostrer Harry, Abraham Clara, Abreu Maria T, Atzmon Gil, Barzilai Nir, Brant Steven R, Bressman Susan, Burns Edward R, Chowers Yehuda, Clark Lorraine N, Darvasi Ariel, Doheny Dana, Duerr Richard H, Eliakim Rami, Giladi Nir, Gregersen Peter K, Hakonarson Hakon, Jones Michelle R, Marder Karen, McGovern Dermot P B, Mulle Jennifer, Orr-Urtreger Avi, Proctor Deborah D, Pulver Ann, Rotter Jerome I, Silverberg Mark S, Ullman Thomas, Warren Stephen T, Waterman Matti, Zhang Wei, Bergman Aviv, Mayer Lloyd, Katz Seymour, Desnick Robert J, Cho Judy H, Peter Inga A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. PLoS genetics. 2012; 8(3): e1002559.
Elbers Clara C, Guo Yiran, Tragante Vinicius, van Iperen Erik P A, Lanktree Matthew B, Castillo Berta Almoguera, Chen Fang, Yanek Lisa R, Wojczynski Mary K, Li Yun R, Ferwerda Bart, Ballantyne Christie M, Buxbaum Sarah G, Chen Yii-Der Ida, Chen Wei-Min, Cupples L Adrienne, Cushman Mary, Duan Yanan, Duggan David, Evans Michele K, Fernandes Jyotika K, Fornage Myriam, Garcia Melissa, Garvey W Timothy, Glazer Nicole, Gomez Felicia, Harris Tamara B, Halder Indrani, Howard Virginia J, Keller Margaux F, Kamboh M Ilyas, Kooperberg Charles, Kritchevsky Stephen B, LaCroix Andrea, Liu Kiang, Liu Yongmei, Musunuru Kiran, Newman Anne B, Onland-Moret N Charlotte, Ordovas Jose, Peter Inga, Post Wendy, Redline Susan, Reis Steven E, Saxena Richa, Schreiner Pamela J, Volcik Kelly A, Wang Xingbin, Yusuf Salim, Zonderland Alan B, Anand Sonia S, Becker Diane M, Psaty Bruce, Rader Daniel J, Reiner Alex P, Rich Stephen S, Rotter Jerome I, Sale Michèle M, Tsai Michael Y, Borecki Ingrid B, Hegele Robert A, Kathiresan Sekar, Nalls Michael A, Taylor Herman A, Hakonarson Hakon, Sivapalaratnam Suthesh, Asselbergs Folkert W, Drenos Fotios, Wilson James G, Keating Brendan J Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations. PloS one. 2012; 7(12): e50198.
Fox Caroline S, White Charles C, Lohman Kurt, Heard-Costa Nancy, Cohen Paul, Zhang Yingying, Johnson Andrew D, Emilsson Valur, Liu Ching-Ti, Chen Y-D Ida, Taylor Kent D, Allison Matthew, Budoff Matthew, Budoff Matthew, Rotter Jerome I, Carr J Jeffrey, Hoffmann Udo, Ding Jingzhong, Cupples L Adrienne, Liu Yongmei Genome-wide association of pericardial fat identifies a unique locus for ectopic fat. PLoS genetics. 2012; 8(5): e1002705.
Gao Xiaoyi, Haritunians Talin, Marjoram Paul, McKean-Cowdin Roberta, Torres Mina, Taylor Kent D, Rotter Jerome I, Gauderman William J, Varma Rohit Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels. Frontiers in genetics. 2012; 3(2): 117.
Suchy-Dicey Astrid M, Enquobahrie Daniel A, Heckbert Susan R, Rotter Jerome I, Psaty Bruce M, McKnight Barbara Hemodynamic fluid shear stress response genes and carotid intima-media thickness: a candidate gene association analysis in the cardiovascular health study. International journal of molecular epidemiology and genetics. 2012; 3(2): 174-8.
Agarwal Subhashish, Jacobs David R, Vaidya Dhananjay, Sibley Christopher T, Jorgensen Neal W, Rotter Jerome I, Chen Yii-Der Ida, Liu Yongmei, Andrews Jeanette S, Kritchevsky Stephen, Goodpaster Bret, Kanaya Alka, Newman Anne B, Simonsick Eleanor M, Herrington David M Metabolic Syndrome Derived from Principal Component Analysis and Incident Cardiovascular Events: The Multi Ethnic Study of Atherosclerosis (MESA) and Health, Aging, and Body Composition (Health ABC). Cardiology research and practice. 2012; 2012(2): 919425.
Musunuru Kiran, Romaine Simon P R, Lettre Guillaume, Wilson James G, Volcik Kelly A, Tsai Michael Y, Taylor Herman A, Schreiner Pamela J, Rotter Jerome I, Rich Stephen S, Redline Susan, Psaty Bruce M, Papanicolaou George J, Ordovas Jose M, Liu Kiang, Krauss Ronald M, Glazer Nicole L, Gabriel Stacey B, Fornage Myriam, Cupples L Adrienne, Buxbaum Sarah G, Boerwinkle Eric, Ballantyne Christie M, Kathiresan Sekar, Rader Daniel J Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project. PloS one. 2012; 7(5): e36473.
Manichaikul Ani, Palmas Walter, Rodriguez Carlos J, Peralta Carmen A, Divers Jasmin, Guo Xiuqing, Chen Wei-Min, Wong Quenna, Williams Kayleen, Kerr Kathleen F, Taylor Kent D, Tsai Michael Y, Goodarzi Mark O, Sale Michèle M, Diez-Roux Ana V, Rich Stephen S, Rotter Jerome I, Mychaleckyj Josyf C Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis. PLoS genetics. 2012; 8(4): e1002640.
Aslibekyan Stella, Goodarzi Mark O, Frazier-Wood Alexis C, Yan Xiaofei, Irvin Marguerite R, Kim Eric, Tiwari Hemant K, Guo Xiuqing, Straka Robert J, Taylor Kent D, Tsai Michael Y, Hopkins Paul N, Korenman Stanley G, Borecki Ingrid B, Chen Yii-Der I, Ordovas Jose M, Rotter Jerome I, Arnett Donna K Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate. PloS one. 2012; 7(10): e48663.
Kwon Soonil, Yan Xiaofei, Cui Jinrui, Yao Jie, Yang Kai, Tsiang Donald, Li Xiaohui, Rotter Jerome I, Guo Xiuqing Application of Bayesian regression with singular value decomposition method in association studies for sequence data. BMC proceedings. 2011; 5 Suppl 9(7376): S57.
Lichtenstein Gary R, Targan Stephan R, Dubinsky Marla C, Rotter Jerome I, Barken Derren M, Princen Fred, Carroll Susan, Brown Michelle, Stachelski Jordan, Chuang Emil, Landers Carol J, Stempak Joanne M, Singh Sharat, Silverberg Mark S Combination of genetic and quantitative serological immune markers are associated with complicated Crohn's disease behavior. Inflammatory bowel diseases. 2011; 17(12): 2488-96.
Irvin Marguerite Ryan, Shrestha Sadeep, Chen Yii-Der I, Wiener Howard W, Haritunians Talin, Vaughan Laura K, Tiwari Hemant K, Taylor Kent D, Scherzer Rebecca, Saag Michael S, Grunfeld Carl, Rotter Jerome I, Arnett Donna K Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men. Pharmacogenetics and genomics. 2011; 21(12): 798-807.
Dauber Andrew, Yu Yongguo, Turchin Michael C, Chiang Charleston W, Meng Yan A, Demerath Ellen W, Patel Sanjay R, Rich Stephen S, Rotter Jerome I, Schreiner Pamela J, Wilson James G, Shen Yiping, Wu Bai-Lin, Hirschhorn Joel N Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. American journal of human genetics. 2011; 89(6): 751-9.
O'Donnell Christopher J, Kavousi Maryam, Smith Albert V, Kardia Sharon L R, Feitosa Mary F, Hwang Shih-Jen, Sun Yan V, Province Michael A, Aspelund Thor, Dehghan Abbas, Hoffmann Udo, Bielak Lawrence F, Zhang Qunyuan, Eiriksdottir Gudny, van Duijn Cornelia M, Fox Caroline S, de Andrade Mariza, Kraja Aldi T, Sigurdsson Sigurdur, Elias-Smale Suzette E, Murabito Joanne M, Launer Lenore J, van der Lugt Aad, Kathiresan Sekar, Kathiresan Sekar, Krestin Gabriel P, Herrington David M, Howard Timothy D, Liu Yongmei, Post Wendy, Mitchell Braxton D, O'Connell Jeffrey R, Shen Haiqing, Shuldiner Alan R, Altshuler David, Elosua Roberto, Salomaa Veikko, Schwartz Stephen M, Siscovick David S, Voight Benjamin F, Bis Joshua C, Glazer Nicole L, Psaty Bruce M, Boerwinkle Eric, Heiss Gerardo, Blankenberg Stefan, Zeller Tanja, Wild Philipp S, Schnabel Renate B, Schillert Arne, Ziegler Andreas, Münzel Thomas F, White Charles C, Rotter Jerome I, Nalls Michael, Oudkerk Matthijs, Johnson Andrew D, Newman Anne B, Uitterlinden Andre G, Massaro Joseph M, Cunningham Julie, Harris Tamara B, Hofman Albert, Peyser Patricia A, Borecki Ingrid B, Cupples L Adrienne, Gudnason Vilmundur, Witteman Jacqueline C M Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation. 2011; 124(25): 2855-64.
Walter Stefan, Atzmon Gil, Demerath Ellen W, Garcia Melissa E, Kaplan Robert C, Kumari Meena, Lunetta Kathryn L, Milaneschi Yuri, Tanaka Toshiko, Tranah Gregory J, Völker Uwe, Yu Lei, Arnold Alice, Benjamin Emelia J, Biffar Reiner, Buchman Aron S, Boerwinkle Eric, Couper David, De Jager Philip L, Evans Denis A, Harris Tamara B, Hoffmann Wolfgang, Hofman Albert, Karasik David, Kiel Douglas P, Kocher Thomas, Kuningas Maris, Launer Lenore J, Lohman Kurt K, Lutsey Pamela L, Mackenbach Johan, Marciante Kristin, Psaty Bruce M, Reiman Eric M, Rotter Jerome I, Seshadri Sudha, Shardell Michelle D, Smith Albert V, van Duijn Cornelia, Walston Jeremy, Zillikens M Carola, Bandinelli Stefania, Baumeister Sebastian E, Bennett David A, Ferrucci Luigi, Gudnason Vilmundur, Kivimaki Mika, Liu Yongmei, Murabito Joanne M, Newman Anne B, Tiemeier Henning, Franceschini Nora A genome-wide association study of aging. Neurobiology of aging. 2011; 32(11): 2109.e15-28.
Schmidt Helena, Zeginigg Marion, Wiltgen Marco, Freudenberger Paul, Petrovic Katja, Cavalieri Margherita, Gider Pierre, Enzinger Christian, Fornage Myriam, Debette Stephanie, Rotter Jerome I, Ikram Mohammad A, Launer Lenore J, Schmidt Reinhold, Schmidt Reinhold Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. Brain : a journal of neurology. 2011; 134(Pt 11): 3384-97.
Avery Christy L, He Qianchuan, North Kari E, Ambite Jose L, Boerwinkle Eric, Fornage Myriam, Hindorff Lucia A, Kooperberg Charles, Meigs James B, Pankow James S, Pendergrass Sarah A, Psaty Bruce M, Ritchie Marylyn D, Rotter Jerome I, Taylor Kent D, Wilkens Lynne R, Heiss Gerardo, Lin Dan Yu A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains. PLoS genetics. 2011; 7(10): e1002322.
Burdon Kathryn P, Macgregor Stuart, Bykhovskaya Yelena, Javadiyan Sharhbanou, Li Xiaohui, Laurie Kate J, Muszynska Dorota, Lindsay Richard, Lechner Judith, Haritunians Talin, Henders Anjali K, Dash Durga, Siscovick David, Anand Seema, Aldave Anthony, Coster Douglas J, Szczotka-Flynn Loretta, Mills Richard A, Iyengar Sudha K, Taylor Kent D, Phillips Tony, Montgomery Grant W, Rotter Jerome I, Hewitt Alex W, Sharma Shiwani, Rabinowitz Yaron S, Willoughby Colin, Craig Jamie E Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Investigative ophthalmology & visual science. 2011; 52(11): 8514-9.
Schnabel Renate B, Kerr Kathleen F, Lubitz Steven A, Alkylbekova Ermeg L, Marcus Gregory M, Sinner Moritz F, Magnani Jared W, Wolf Philip A, Deo Rajat, Lloyd-Jones Donald M, Lunetta Kathryn L, Mehra Reena, Levy Daniel, Fox Ervin R, Arking Dan E, Mosley Thomas H, Müller-Nurasyid Martina, Young Taylor R, Wichmann H-Erich, Seshadri Sudha, Farlow Deborah N, Rotter Jerome I, Soliman Elsayed Z, Glazer Nicole L, Wilson James G, Breteler Monique M B, Sotoodehnia Nona, Newton-Cheh Christopher, Kääb Stefan, Ellinor Patrick T, Alonso Alvaro, Benjamin Emelia J, Heckbert Susan R, Heckbert Susan R Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project. Circulation. Cardiovascular genetics. 2011; 4(5): 557-64.
Sobrin Lucia, Green Todd, Sim Xueling, Jensen Richard A, Tai E Shyong, Tay Wan Ting, Wang Jie Jin, Mitchell Paul, Sandholm Niina, Liu Yiyuan, Hietala Kustaa, Iyengar Sudha K, Iyengar Sudha K, Brooks Matthew, Buraczynska Monika, Van Zuydam Natalie, Smith Albert V, Gudnason Vilmundur, Doney Alex S F, Morris Andrew D, Leese Graham P, Palmer Colin N A, Palmer Colin N A, Swaroop Anand, Taylor Herman A, Wilson James G, Penman Alan, Chen Ching J, Groop Per-Henrik, Saw Seang-Mei, Aung Tin, Klein Barbara E, Rotter Jerome I, Siscovick David S, Cotch Mary Frances, Klein Ronald, Daly Mark J, Wong Tien Y Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe). Investigative ophthalmology & visual science. 2011; 52(10): 7593-602.
Bhatia Gaurav, Patterson Nick, Pasaniuc Bogdan, Zaitlen Noah, Genovese Giulio, Pollack Samuela, Mallick Swapan, Myers Simon, Tandon Arti, Spencer Chris, Palmer Cameron D, Adeyemo Adebowale A, Akylbekova Ermeg L, Cupples L Adrienne, Divers Jasmin, Fornage Myriam, Kao W H Linda, Lange Leslie, Li Mingyao, Musani Solomon, Mychaleckyj Josyf C, Ogunniyi Adesola, Papanicolaou George, Rotimi Charles N, Rotter Jerome I, Ruczinski Ingo, Salako Babatunde, Siscovick David S, Tayo Bamidele O, Yang Qiong, McCarroll Steve, Sabeti Pardis, Lettre Guillaume, De Jager Phil, Hirschhorn Joel, Zhu Xiaofeng, Cooper Richard, Reich David, Wilson James G, Price Alkes L Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. American journal of human genetics. 2011; 89(3): 368-81.
Goodarzi Mark O, Cui Jinrui, Chen Yii-Der I, Hsueh Willa A, Guo Xiuqing, Rotter Jerome I Fasting insulin reflects heterogeneous physiological processes: role of insulin clearance. American journal of physiology. Endocrinology and metabolism. 2011; 301(2): E402-8.
Haritunians Talin, Jones Michelle R, McGovern Dermot P B, Shih David Q, Barrett Robert J, Derkowski Carrie, Dubinsky Marla C, Dutridge Debra, Fleshner Phillip R, Ippoliti Andrew, King Lily, Leshinsky-Silver Esther, Levine Arie, Melmed Gil Y, Mengesha Emebet, Vasilauskas Eric A, Ziaee Shabnam, Rotter Jerome I, Targan Stephan R, Taylor Kent D Variants in ZNF365 isoform D are associated with Crohn's disease. Gut. 2011; 60(8): 1060-7.
Pojoga Luminita H, Underwood Patricia C, Goodarzi Mark O, Williams Jonathan S, Adler Gail K, Jeunemaitre Xavier, Hopkins Paul N, Raby Benjamin A, Lasky-Su Jessica, Sun Bei, Cui Jinrui, Guo Xiuqing, Taylor Kent D, Chen Yii-Der Ida, Xiang Anny, Raffel Leslie J, Buchanan Thomas A, Rotter Jerome I, Williams Gordon H Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension. The Journal of clinical endocrinology and metabolism. 2011; 96(8): E1288-92.
Hixson James E, Shimmin Lawrence C, Montasser May E, Kim Do-Kyun, Zhong Yu, Ibarguen Heladio, Follis Jack, Malcom Gray, Strong Jack, Howard Tim, Langefeld Carl, Liu Yongmei, Rotter Jerome I, Johnson Craig, Herrington David Common variants in the periostin gene influence development of atherosclerosis in young persons. Arteriosclerosis, thrombosis, and vascular biology. 2011; 31(7): 1661-7.
Smith Nicholas L, Rice Kenneth M, Bovill Edwin G, Cushman Mary, Bis Joshua C, McKnight Barbara, Lumley Thomas, Glazer Nicole L, van Hylckama Vlieg Astrid, Tang Weihong, Dehghan Abbas, Strachan David P, O'Donnell Christopher J, Rotter Jerome I, Heckbert Susan R, Psaty Bruce M, Rosendaal Frits R Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis. Blood. 2011; 117(22): 6007-11.
Marciante Kristin D, Durda Jon P, Heckbert Susan R, Lumley Thomas, Rice Ken, McKnight Barbara, Totah Rheem A, Tamraz Bani, Kroetz Deanna L, Fukushima Hisayo, Kaspera Rüdiger, Bis Joshua C, Glazer Nicole L, Li Guo, Austin Thomas R, Taylor Kent D, Rotter Jerome I, Jaquish Cashell E, Kwok Pui-Yan, Tracy Russell P, Psaty Bruce M Cerivastatin, genetic variants, and the risk of rhabdomyolysis. Pharmacogenetics and genomics. 2011; 21(5): 280-8.
Kraja Aldi T, Vaidya Dhananjay, Pankow James S, Goodarzi Mark O, Assimes Themistocles L, Kullo Iftikhar J, Sovio Ulla, Mathias Rasika A, Sun Yan V, Franceschini Nora, Absher Devin, Li Guo, Zhang Qunyuan, Feitosa Mary F, Glazer Nicole L, Haritunians Talin, Hartikainen Anna-Liisa, Knowles Joshua W, North Kari E, Iribarren Carlos, Kral Brian, Yanek Lisa, O'Reilly Paul F, McCarthy Mark I, Jaquish Cashell, Couper David J, Chakravarti Aravinda, Psaty Bruce M, Becker Lewis C, Province Michael A, Boerwinkle Eric, Quertermous Thomas, Palotie Leena, Jarvelin Marjo-Riitta, Becker Diane M, Kardia Sharon L R, Rotter Jerome I, Chen Yii-Der Ida, Borecki Ingrid B A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Diabetes. 2011; 60(4): 1329-39.
Wagenknecht Lynne E, Palmer Nicholette D, Bowden Donald W, Rotter Jerome I, Norris Jill M, Ziegler Julie, Chen Yii-Der I, Haffner Steven, Scherzinger Ann, Langefeld Carl D Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study. Liver international : official journal of the International Association for the Study of the Liver. 2011; 31(3): 412-6.
Jones Michelle R, Chua Angela, Chen Yii-Der I, Li Xiaohui, Krauss Ronald M, Rotter Jerome I, Legro Richard S, Azziz Ricardo, Goodarzi Mark O Harnessing expression data to identify novel candidate genes in polycystic ovary syndrome. PloS one. 2011; 6(5): e20120.
Song Youngsup, Altarejos Judith, Goodarzi Mark O, Inoue Hiroshi, Guo Xiuqing, Berdeaux Rebecca, Kim Jeong-Ho, Goode Jason, Igata Motoyuki, Paz Jose C, Hogan Meghan F, Singh Pankaj K, Goebel Naomi, Vera Lili, Miller Nina, Cui Jinrui, Jones Michelle R, Jones Michelle R, Jones Michelle R, Chen Yii-Der I, Taylor Kent D, Hsueh Willa A, Rotter Jerome I, Montminy Marc CRTC3 links catecholamine signalling to energy balance. Nature. 2010; 468(7326): 933-9.
Haritunians Talin, Taylor Kent D, Targan Stephan R, Dubinsky Marla, Ippoliti Andrew, Kwon Soonil, Guo Xiuqing, Melmed Gil Y, Berel Dror, Mengesha Emebet, Psaty Bruce M, Glazer Nicole L, Vasiliauskas Eric A, Rotter Jerome I, Fleshner Phillip R, McGovern Dermot P B Genetic predictors of medically refractory ulcerative colitis. Inflammatory bowel diseases. 2010; 16(11): 1830-40.
Chalasani Naga, Guo Xiuqing, Loomba Rohit, Goodarzi Mark O, Haritunians Talin, Kwon Soonil, Cui Jinrui, Taylor Kent D, Wilson Laura, Cummings Oscar W, Chen Yii-Der Ida, Rotter Jerome I, Rotter Jerome I Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. Gastroenterology. 2010; 139(5): 1567-76, 1576.e1-6.
Levin Gregory, Kestenbaum Bryan, Ida Chen Yii-Der, Jacobs David R, Psaty Bruce M, Rotter Jerome I, Siscovick David S, de Boer Ian H Glucose, insulin, and incident hypertension in the multi-ethnic study of atherosclerosis. American journal of epidemiology. 2010; 172(10): 1144-54.
Engelman Corinne D, Meyers Kristin J, Ziegler Julie T, Taylor Kent D, Palmer Nicholette D, Haffner Steven M, Fingerlin Tasha E, Wagenknecht Lynne E, Rotter Jerome I, Bowden Donald W, Langefeld Carl D, Norris Jill M Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study. The Journal of steroid biochemistry and molecular biology. 2010; 122(4): 186-92.
Bowden Donald W, An S Sandy, Palmer Nicholette D, Brown W Mark, Norris Jill M, Haffner Stephen M, Hawkins Gregory A, Guo Xiuqing, Rotter Jerome I, Chen Y-D Ida, Wagenknecht Lynne E, Langefeld Carl D Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study. Human molecular genetics. 2010; 19(20): 4112-20.
McGovern Dermot P B, Jones Michelle R, Taylor Kent D, Marciante Kristin, Yan Xiaofei, Dubinsky Marla, Ippoliti Andy, Vasiliauskas Eric, Berel Dror, Derkowski Carrie, Dutridge Deb, Fleshner Phil, Shih David Q, Melmed Gil, Mengesha Emebet, King Lily, Pressman Sheila, Haritunians Talin, Guo Xiuqing, Targan Stephan R, Rotter Jerome I, Rotter Jerome I Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. Human molecular genetics. 2010; 19(17): 3468-76.
Ippoliti Andrew, Devlin Shane, Mei Ling, Yang Huiying, Papadakis Konstantinos A, Vasiliauskas Eric A, McGovern Dermot P B, Abreu Maria T, Melmed Gil, Shaye Omid, Enayati Pedram, Chen Gary, Choi Jennifer, Taylor Kent, Landers Carol J, Rotter Jerome I, Targan Stephan R Combination of innate and adaptive immune alterations increased the likelihood of fibrostenosis in Crohn's disease. Inflammatory bowel diseases. 2010; 16(8): 1279-85.
Dubinsky Marla C, Mei Ling, Friedman Madison, Dhere Tanvi, Haritunians Talin, Hakonarson Hakon, Kim Cecilia, Glessner Joseph, Targan Stephan R, McGovern Dermot P, Taylor Kent D, Rotter Jerome I Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease. Inflammatory bowel diseases. 2010; 16(8): 1357-66.
Mangravite Lara M, Medina Marisa Wong, Cui Jinrui, Pressman Sheila, Smith Joshua D, Rieder Mark J, Guo Xiuqing, Nickerson Deborah A, Rotter Jerome I, Krauss Ronald M Combined influence of LDLR and HMGCR sequence variation on lipid-lowering response to simvastatin. Arteriosclerosis, thrombosis, and vascular biology. 2010; 30(7): 1485-92.
Van Hee Victor C, Adar Sara D, Szpiro Adam A, Barr R Graham, Diez Roux Ana, Bluemke David A, Sheppard Lianne, Gill Edward A, Bahrami Hossein, Wassel Christina, Sale Michele M, Siscovick David S, Rotter Jerome I, Rich Stephen S, Kaufman Joel D Common genetic variation, residential proximity to traffic exposure, and left ventricular mass: the multi-ethnic study of atherosclerosis. Environmental health perspectives. 2010; 118(7): 962-9.
Smith Nicholas L, Felix Janine F, Morrison Alanna C, Demissie Serkalem, Glazer Nicole L, Loehr Laura R, Cupples L Adrienne, Dehghan Abbas, Lumley Thomas, Rosamond Wayne D, Lieb Wolfgang, Rivadeneira Fernando, Bis Joshua C, Folsom Aaron R, Benjamin Emelia, Aulchenko Yurii S, Haritunians Talin, Couper David, Murabito Joanne, Wang Ying A, Stricker Bruno H, Gottdiener John S, Chang Patricia P, Wang Thomas J, Rice Kenneth M, Hofman Albert, Heckbert Susan R, Fox Ervin R, O'Donnell Christopher J, Uitterlinden Andre G, Rotter Jerome I, Willerson James T, Levy Daniel, van Duijn Cornelia M, Psaty Bruce M, Witteman Jacqueline C M, Boerwinkle Eric, Vasan Ramachandran S Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Circulation. Cardiovascular genetics. 2010; 3(3): 256-66.
Bertoni Alain G, Burke Gregory L, Owusu James A, Carnethon Mercedes R, Vaidya Dhananjay, Barr R Graham, Jenny Nancy S, Ouyang Pamela, Rotter Jerome I Inflammation and the incidence of type 2 diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA). Diabetes care. 2010; 33(4): 804-10.
Benjamin Emelia J, Rice Kenneth M, Arking Dan E, Pfeufer Arne, van Noord Charlotte, Smith Albert V, Schnabel Renate B, Bis Joshua C, Boerwinkle Eric, Sinner Moritz F, Dehghan Abbas, Lubitz Steven A, D'Agostino Ralph B, Lumley Thomas, Ehret Georg B, Heeringa Jan, Aspelund Thor, Newton-Cheh Christopher, Larson Martin G, Marciante Kristin D, Soliman Elsayed Z, Rivadeneira Fernando, Wang Thomas J, Eirksdottir Gudny, Levy Daniel, Psaty Bruce M, Li Man, Chamberlain Alanna M, Hofman Albert, Vasan Ramachandran S, Harris Tamara B, Rotter Jerome I, Kao W H Linda, Agarwal Sunil K, Stricker Bruno H Ch, Wang Ke, Launer Lenore J, Smith Nicholas L, Chakravarti Aravinda, Uitterlinden Andr G, Wolf Philip A, Sotoodehnia Nona, Kttgen Anna, van Duijn Cornelia M, Meitinger Thomas, Mueller Martina, Perz Siegfried, Steinbeck Gerhard, Wichmann H-Erich, Lunetta Kathryn L, Heckbert Susan R, Gudnason Vilmundur, Alonso Alvaro, Kb Stefan, Ellinor Patrick T, Witteman Jacqueline C M Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nature genetics. 2009; 41(8): 879-81.
Levy Daniel, Ehret Georg B, Rice Kenneth, Verwoert Germaine C, Launer Lenore J, Dehghan Abbas, Glazer Nicole L, Morrison Alanna C, Johnson Andrew D, Aspelund Thor, Aulchenko Yurii, Lumley Thomas, Kttgen Anna, Vasan Ramachandran S, Rivadeneira Fernando, Eiriksdottir Gudny, Guo Xiuqing, Arking Dan E, Mitchell Gary F, Mattace-Raso Francesco U S, Smith Albert V, Taylor Kent, Scharpf Robert B, Hwang Shih-Jen, Sijbrands Eric J G, Bis Joshua, Harris Tamara B, Ganesh Santhi K, O'Donnell Christopher J, Hofman Albert, Rotter Jerome I, Coresh Josef, Benjamin Emelia J, Uitterlinden Andr G, Heiss Gerardo, Fox Caroline S, Witteman Jacqueline C M, Boerwinkle Eric, Wang Thomas J, Gudnason Vilmundur, Larson Martin G, Chakravarti Aravinda, Psaty Bruce M, van Duijn Cornelia M Genome-wide association study of blood pressure and hypertension. Nature genetics. 2009; 41(6): 677-87.
Newton-Cheh Christopher, Eijgelsheim Mark, Rice Kenneth M, de Bakker Paul I W, Yin Xiaoyan, Estrada Karol, Bis Joshua C, Marciante Kristin, Rivadeneira Fernando, Noseworthy Peter A, Sotoodehnia Nona, Smith Nicholas L, Rotter Jerome I, Kors Jan A, Witteman Jacqueline C M, Hofman Albert, Heckbert Susan R, O'Donnell Christopher J, Uitterlinden Andr G, Psaty Bruce M, Lumley Thomas, Larson Martin G, Stricker Bruno H Ch Common variants at ten loci influence QT interval duration in the QTGEN Study. Nature genetics. 2009; 41(4): 399-406.
Psaty Bruce M, O'Donnell Christopher J, Gudnason Vilmundur, Lunetta Kathryn L, Folsom Aaron R, Rotter Jerome I, Uitterlinden Andr G, Harris Tamara B, Witteman Jacqueline C M, Boerwinkle Eric, Boerwinkle Eric Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts. Circulation. Cardiovascular genetics. 2009; 2(1): 73-80.
Krauss Ronald M, Mangravite Lara M, Smith Joshua D, Medina Marisa W, Wang Dai, Guo Xiuqing, Rieder Mark J, Simon Joel A, Hulley Steven B, Waters David, Saad Mohammed, Williams Paul T, Taylor Kent D, Yang Huiying, Nickerson Deborah A, Rotter Jerome I Variation in the 3-hydroxyl-3-methylglutaryl coenzyme a reductase gene is associated with racial differences in low-density lipoprotein cholesterol response to simvastatin treatment. Circulation. 2008; 117(12): 1537-44.
Goodarzi Mark O, Lehman Donna M, Taylor Kent D, Guo Xiuqing, Cui Jinrui, Quiones Manuel J, Clee Susanne M, Yandell Brian S, Blangero John, Hsueh Willa A, Attie Alan D, Stern Michael P, Rotter Jerome I SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse. Diabetes. 2007; 56(7): 1922-9.
Duerr Richard H, Taylor Kent D, Brant Steven R, Rioux John D, Silverberg Mark S, Daly Mark J, Steinhart A Hillary, Abraham Clara, Regueiro Miguel, Griffiths Anne, Dassopoulos Themistocles, Bitton Alain, Yang Huiying, Targan Stephan, Datta Lisa Wu, Kistner Emily O, Schumm L Philip, Lee Annette T, Gregersen Peter K, Barmada M Michael, Rotter Jerome I, Nicolae Dan L, Cho Judy H A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science (New York, N.Y.). 2006; 314(5804): 1461-3.
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