Publications:
A selected list of 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, StanÄáková 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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