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Shaping the Future

Rita M. Cantor

Contact Information:

Lab Number:

(310)267-2440

Office Phone Number:

310-267-2440

Work Address:

Office
Gonda Ctr
Los Angeles, CA 90095
UNITED STATES

Work Email Address:

rcantor@mednet.ucla.edu

Professor in Residence, Human Genetics

Member, ACCESS Program: Dept. of Human Genetics

Access Bioinformatics Home Area

Access Genetics and Genomics Home Area

Center for Neurobehavioral Genetics

Human Genetics

Faculty, BWF-IT-MD

Center for Metabolic Disease Prevention


Detailed Biography:

Statistical Genetics With the advent of new molecular genetic technologies, the mapping and identification of complex disease genes and their interactions has become feasible. Statistical analyses are often a necessary component of these gene mapping efforts. The statistical approaches needed to map disease genes vary with the particular research question, the population and disease under analysis. These are the design issues which are a focus of this research effort. We are applying statistical methodologies to identify genes contributing to lipid disorders which result in coronary artery disease, and in particular Familial Combined Hyperlipidemia, a common complex genetic disorder which often leads to premature death. We have conducted a genome scan to identify chromosomal regions likely to harbor the disease causing genes. Additionally we are looking at candidate genes in the linked and other chromosomal regions for association with the disease. We have also been analyzing Single Nucleotide Polymorphism(SNP) data from a chromosomal region of a gene family linked to the disorder. Patterns of linkage disequilibrium illustrate the research paradigms which may be necessary to identify the disease causing variants. We are also applying statistical methods to map genes contributing to Systemic Lupus Erythematosus(SLE). We have capitalized upon mouse-human synteny and conducted linkage analysis to identify a human chromosomal region likely to harbor an SLE gene. The positional candidate PARP has been shown to have a distorted allele transmission pattern in this sample, implicating it in the development of SLE. Future endeavors are to apply similar methodologies to infectious disease syndromes such as Kawasaki disease and birth defects such as spina bifida.

Publications:

Jasinska Anna J, Lin Michelle K, Service Susan, Choi Oi-Wa, Deyoung Joseph, Grujic Olivera, Kong Sit-Yee, Jung Yoon, Jorgensen Mathew J, Fairbanks Lynn A, Turner Trudy, Cantor Rita M, Wasserscheid Jessica, Dewar Ken, Warren Wesley, Wilson Richard K, Weinstock George, Jentsch J David, Freimer Nelson B   A non-human primate system for large-scale genetic studies of complex traits Human molecular genetics, 2012; .
Stein Jason L, Medland Sarah E, Vasquez Alejandro Arias, Hibar Derrek P, Senstad Rudy E, Winkler Anderson M, Toro Roberto, Appel Katja, Bartecek Richard, Bergmann Orjan, Bernard Manon, Brown Andrew A, Cannon Dara M, Chakravarty M Mallar, Christoforou Andrea, Domin Martin, Grimm Oliver, Hollinshead Marisa, Holmes Avram J, Homuth Georg, Hottenga Jouke-Jan, Langan Camilla, Lopez Lorna M, Hansell Narelle K, Hwang Kristy S, Kim Sungeun, Laje Gonzalo, Lee Phil H, Liu Xinmin, Loth Eva, Lourdusamy Anbarasu, Mattingsdal Morten, Mohnke Sebastian, Maniega Susana Muñoz, Nho Kwangsik, Nugent Allison C, O'Brien Carol, Papmeyer Martina, Pütz Benno, Ramasamy Adaikalavan, Rasmussen Jerod, Rijpkema Mark, Risacher Shannon L, Roddey J Cooper, Rose Emma J, Ryten Mina, Shen Li, Sprooten Emma, Strengman Eric, Teumer Alexander, Trabzuni Daniah, Turner Jessica, van Eijk Kristel, van Erp Theo G M, van Tol Marie-Jose, Wittfeld Katharina, Wolf Christiane, Woudstra Saskia, Aleman Andre, Alhusaini Saud, Almasy Laura, Binder Elisabeth B, Brohawn David G, Cantor Rita M, Carless Melanie A, Corvin Aiden, Czisch Michael, Curran Joanne E, Davies Gail, de Almeida Marcio A A, Delanty Norman, Depondt Chantal, Duggirala Ravi, Dyer Thomas D, Erk Susanne, Fagerness Jesen, Fox Peter T, Freimer Nelson B, Gill Michael, Göring Harald H H, Hagler Donald J, Hoehn David, Holsboer Florian, Hoogman Martine, Hosten Norbert, Jahanshad Neda, Johnson Matthew P, Kasperaviciute Dalia, Kent Jack W, Kochunov Peter, Lancaster Jack L, Lawrie Stephen M, Liewald David C, Mandl René, Matarin Mar, Mattheisen Manuel, Meisenzahl Eva, Melle Ingrid, Moses Eric K, Mühleisen Thomas W, Nauck Matthias, Nöthen Markus M, Olvera Rene L, Pandolfo Massimo, Pike G Bruce, Puls Ralf, Reinvang Ivar, Rentería Miguel E, Rietschel Marcella, Roffman Joshua L, Royle Natalie A, Rujescu Dan, Savitz Jonathan, Schnack Hugo G, Schnell Knut, Seiferth Nina, Smith Colin, Steen Vidar M, Valdés Hernández Maria C, Van den Heuvel Martijn, van der Wee Nic J, Van Haren Neeltje E M, Veltman Joris A, Völzke Henry, Walker Robert, Westlye Lars T, Whelan Christopher D, Agartz Ingrid, Boomsma Dorret I, Cavalleri Gianpiero L, Dale Anders M, Djurovic Srdjan, Drevets Wayne C, Hagoort Peter, Hall Jeremy, Heinz Andreas, Jack Clifford R, Foroud Tatiana M, Le Hellard Stephanie, Macciardi Fabio, Montgomery Grant W, Poline Jean Baptiste, Porteous David J, Sisodiya Sanjay M, Starr John M, Sussmann Jessika, Toga Arthur W, Veltman Dick J, Walter Henrik, Weiner Michael W, Weiner Michael W, Weiner Michael W, Weiner Michael W, Weiner Michael W, Bis Joshua C, Ikram M Arfan, Smith Albert V, Gudnason Vilmundur, Tzourio Christophe, Vernooij Meike W, Launer Lenore J, Decarli Charles, Seshadri Sudha, Seshadri Sudha, Seshadri Sudha, Andreassen Ole A, Apostolova Liana G, Bastin Mark E, Blangero John, Brunner Han G, Buckner Randy L, Cichon Sven, Coppola Giovanni, de Zubicaray Greig I, Deary Ian J, Donohoe Gary, de Geus Eco J C, Espeseth Thomas, Fernández Guillén, Glahn David C, Grabe Hans J, Hardy John, Hulshoff Pol Hilleke E, Jenkinson Mark, Kahn René S, McDonald Colm, McIntosh Andrew M, McMahon Francis J, McMahon Katie L, Meyer-Lindenberg Andreas, Morris Derek W, Müller-Myhsok Bertram, Nichols Thomas E, Ophoff Roel A, Paus Tomas, Pausova Zdenka, Penninx Brenda W, Potkin Steven G, Sämann Philipp G, Saykin Andrew J, Schumann Gunter, Smoller Jordan W, Wardlaw Joanna M, Weale Michael E, Martin Nicholas G, Franke Barbara, Wright Margaret J, Thompson Paul M   Identification of common variants associated with human hippocampal and intracranial volumes Nature genetics, 2012; 44(5): 552-561.
Casey Jillian P, Magalhaes Tiago, Conroy Judith M, Regan Regina, Shah Naisha, Anney Richard, Shields Denis C, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Cali Phil, Correia Catarina, Corsello Christina, Coutanche Marc, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Foley Suzanne, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Holt Richard, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Lamb Janine A, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lord Catherine, Lund Sabata C, Maestrini Elena, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Miller Judith, Minopoli Fiorella, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Nygren Gudrun, Oliveira Guiomar, Pagnamenta Alistair T, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Pickles Andrew, Pinto Dalila, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Ragoussis Jiannis, Roge Bernadette, Rutter Michael L, Sequeira Ana F, Soorya Latha, Sousa Inês, Sykes Nuala, Stoppioni Vera, Tancredi Raffaella, Tauber Maïté, Thompson Ann P, Thomson Susanne, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Vorstman Jacob A S, Wallace Simon, Wang Kai, Wassink Thomas H, White Kathy, Wing Kirsty, Wittemeyer Kerstin, Yaspan Brian L, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Geschwind Daniel H, Haines Jonathan L, Hallmayer Joachim, Monaco Anthony P, Nurnberger John I, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vieland Veronica J, Wijsman Ellen M, Green Andrew, Gill Michael, Gallagher Louise, Vicente Astrid, Ennis Sean   A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder Human genetics, 2012; 131(4): 565-79.
Loo Sandra K, Shtir Corina, Doyle Alysa E, Mick Eric, McGough James J, McCracken James, Biederman Joseph, Smalley Susan L, Cantor Rita M, Faraone Stephen V, Nelson Stanley F   Genome-wide association study of intelligence: additive effects of novel brain expressed genes Journal of the American Academy of Child and Adolescent Psychiatry, 2012; 51(4): 432-440.e2.
Cantor Rita M   Model-based linkage analysis of a binary trait Methods in molecular biology (Clifton, N.J.), 2012; 850(4): 285-300.
Lu Ake Tzu-Hui, Bakker Steven, Janson Esther, Cichon Sven, Cantor Rita M, Ophoff Roel A   Prediction of serotonin transporter promoter polymorphism genotypes from single nucleotide polymorphism arrays using machine learning methods Psychiatric genetics, 2012; 44(5): .
Ripke Stephan, Sanders Alan R, Kendler Kenneth S, Levinson Douglas F, Sklar Pamela, Holmans Peter A, Lin Dan-Yu, Duan Jubao, Ophoff Roel A, Andreassen Ole A, Scolnick Edward, Cichon Sven, St Clair David, Corvin Aiden, Gurling Hugh, Werge Thomas, Rujescu Dan, Blackwood Douglas H R, Pato Carlos N, Malhotra Anil K, Purcell Shaun, Dudbridge Frank, Neale Benjamin M, Rossin Lizzy, Visscher Peter M, Posthuma Danielle, Ruderfer Douglas M, Fanous Ayman, Stefansson Hreinn, Steinberg Stacy, Mowry Bryan J, Golimbet Vera, De Hert Marc, Jönsson Erik G, Bitter István, Pietiläinen Olli P H, Collier David A, Tosato Sarah, Agartz Ingrid, Albus Margot, Alexander Madeline, Amdur Richard L, Amin Farooq, Bass Nicholas, Bergen Sarah E, Black Donald W, Børglum Anders D, Brown Matthew A, Bruggeman Richard, Buccola Nancy G, Byerley William F, Cahn Wiepke, Cantor Rita M, Carr Vaughan J, Catts Stanley V, Choudhury Khalid, Cloninger C Robert, Cormican Paul, Craddock Nicholas, Danoy Patrick A, Datta Susmita, de Haan Lieuwe, Demontis Ditte, Dikeos Dimitris, Djurovic Srdjan, Donnelly Peter, Donohoe Gary, Duong Linh, Dwyer Sarah, Fink-Jensen Anders, Freedman Robert, Freimer Nelson B, Friedl Marion, Georgieva Lyudmila, Giegling Ina, Gill Michael, Glenthøj Birte, Godard Stephanie, Hamshere Marian, Hansen Mark, Hansen Thomas, Hartmann Annette M, Henskens Frans A, Hougaard David M, Hultman Christina M, Ingason Andrés, Jablensky Assen V, Jakobsen Klaus D, Jay Maurice, Jürgens Gesche, Kahn René S, Keller Matthew C, Kenis Gunter, Kenny Elaine, Kim Yunjung, Kirov George K, Konnerth Heike, Konte Bettina, Krabbendam Lydia, Krasucki Robert, Lasseter Virginia K, Laurent Claudine, Lawrence Jacob, Lencz Todd, Lerer F Bernard, Liang Kung-Yee, Lichtenstein Paul, Lieberman Jeffrey A, Linszen Don H, Lönnqvist Jouko, Loughland Carmel M, Maclean Alan W, Maher Brion S, Maier Wolfgang, Mallet Jacques, Malloy Pat, Mattheisen Manuel, Mattingsdal Morten, McGhee Kevin A, McGrath John J, McIntosh Andrew, McLean Duncan E, McQuillin Andrew, Melle Ingrid, Michie Patricia T, Milanova Vihra, Morris Derek W, Mors Ole, Mortensen Preben B, Moskvina Valentina, Muglia Pierandrea, Myin-Germeys Inez, Nertney Deborah A, Nestadt Gerald, Nielsen Jimmi, Nikolov Ivan, Nordentoft Merete, Norton Nadine, Nöthen Markus M, O'Dushlaine Colm T, Olincy Ann, Olsen Line, O'Neill F Anthony, Orntoft Torben F, Owen Michael J, Pantelis Christos, Papadimitriou George, Pato Michele T, Peltonen Leena, Petursson Hannes, Pickard Ben, Pimm Jonathan, Pulver Ann E, Puri Vinay, Quested Digby, Quinn Emma M, Rasmussen Henrik B, Réthelyi János M, Ribble Robert, Rietschel Marcella, Riley Brien P, Ruggeri Mirella, Schall Ulrich, Schulze Thomas G, Schwab Sibylle G, Scott Rodney J, Shi Jianxin, Sigurdsson Engilbert, Silverman Jeremy M, Spencer Chris C A, Stefansson Kari, Strange Amy, Strengman Eric, Stroup T Scott, Suvisaari Jaana, Terenius Lars, Thirumalai Srinivasa, Thygesen Johan H, Timm Sally, Toncheva Draga, van den Oord Edwin, van Os Jim, van Winkel Ruud, Veldink Jan, Walsh Dermot, Wang August G, Wiersma Durk, Wildenauer Dieter B, Williams Hywel J, Williams Nigel M, Wormley Brandon, Zammit Stan, Sullivan Patrick F, O'Donovan Michael C, Daly Mark J, Gejman Pablo V, Gejman Pablo V   Genome-wide association study identifies five new schizophrenia loci Nature genetics, 2011; 43(10): 969-76.
Sanders Stephan J, Ercan-Sencicek A Gulhan, Hus Vanessa, Luo Rui, Murtha Michael T, Moreno-De-Luca Daniel, Chu Su H, Moreau Michael P, Gupta Abha R, Thomson Susanne A, Mason Christopher E, Bilguvar Kaya, Celestino-Soper Patricia B S, Choi Murim, Crawford Emily L, Davis Lea, Wright Nicole R Davis, Dhodapkar Rahul M, DiCola Michael, DiLullo Nicholas M, Fernandez Thomas V, Fielding-Singh Vikram, Fishman Daniel O, Frahm Stephanie, Garagaloyan Rouben, Goh Gerald S, Kammela Sindhuja, Klei Lambertus, Lowe Jennifer K, Lund Sabata C, McGrew Anna D, Meyer Kyle A, Moffat William J, Murdoch John D, O'Roak Brian J, Ober Gordon T, Pottenger Rebecca S, Raubeson Melanie J, Song Youeun, Wang Qi, Yaspan Brian L, Yu Timothy W, Yurkiewicz Ilana R, Beaudet Arthur L, Cantor Rita M, Curland Martin, Grice Dorothy E, Günel Murat, Lifton Richard P, Mane Shrikant M, Martin Donna M, Shaw Chad A, Sheldon Michael, Tischfield Jay A, Walsh Christopher A, Morrow Eric M, Ledbetter David H, Fombonne Eric, Lord Catherine, Martin Christa Lese, Brooks Andrew I, Sutcliffe James S, Cook Edwin H, Geschwind Daniel, Roeder Kathryn, Devlin Bernie, State Matthew W   Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism Neuron, 2011; 70(5): 863-85.
Voineagu Irina, Wang Xinchen, Johnston Patrick, Lowe Jennifer K, Tian Yuan, Horvath Steve, Mill Jonathan, Cantor Rita M, Blencowe Benjamin J, Geschwind Daniel H   Transcriptomic analysis of autistic brain reveals convergent molecular pathology Nature, 2011; 474(7351): 380-4.
Zhao Jian, Wu Hui, Khosravi Melanie, Cui Huijuan, Qian Xiaoxia, Kelly Jennifer A, Kaufman Kenneth M, Langefeld Carl D, Williams Adrienne H, Comeau Mary E, Ziegler Julie T, Marion Miranda C, Adler Adam, Glenn Stuart B, Alarcón-Riquelme Marta E, Alarcón-Riquelme Marta E, Alarcón-Riquelme Marta E, Pons-Estel Bernardo A, Harley John B, Bae Sang-Cheol, Bang So-Young, Cho Soo-Kyung, Jacob Chaim O, Vyse Timothy J, Niewold Timothy B, Gaffney Patrick M, Moser Kathy L, Kimberly Robert P, Edberg Jeffrey C, Brown Elizabeth E, Alarcon Graciela S, Petri Michelle A, Ramsey-Goldman Rosalind, Vilá Luis M, Reveille John D, James Judith A, Gilkeson Gary S, Kamen Diane L, Freedman Barry I, Anaya Juan-Manuel, Merrill Joan T, Criswell Lindsey A, Scofield R Hal, Stevens Anne M, Guthridge Joel M, Chang Deh-Ming, Song Yeong Wook, Park Ji Ah, Lee Eun Young, Boackle Susan A, Grossman Jennifer M, Hahn Bevra H, Goodship Timothy H J, Cantor Rita M, Yu Chack-Yung, Shen Nan, Tsao Betty P   Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility PLoS genetics, 2011; 7(5): e1002079.
Fears Scott C, Scheibel Kevin, Abaryan Zvart, Lee Chris, Service Susan K, Jorgensen Matthew J, Fairbanks Lynn A, Cantor Rita M, Freimer Nelson B, Woods Roger P   Anatomic brain asymmetry in vervet monkeys PloS one, 2011; 6(12): e28243.
Cantor Rita M, Wilcox Marsha   Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes Genetic epidemiology, 2011; 35 Suppl 1(3): S85-91.
Zhang Yafeng, Cantor Rita M, MacGibbon Kimber, Romero Roberto, Goodwin Thomas M, Mullin Patrick M, Fejzo Marlena S   Familial aggregation of hyperemesis gravidarum American journal of obstetrics and gynecology, 2011; 204(3): 230.e1-7.
Anney Richard, Klei Lambertus, Pinto Dalila, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Sykes Nuala, Pagnamenta Alistair T, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chu Su H, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Melhem Nadine M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Devlin Bernie, Ennis Sean, Hallmayer Joachim   A genome-wide scan for common alleles affecting risk for autism Human molecular genetics, 2010; 19(20): 4072-82.
Shen Nan, Fu Qiong, Deng Yun, Qian Xiaoxia, Zhao Jian, Kaufman Kenneth M, Wu Yee Ling, Yu C Yung, Tang Yuanjia, Chen Ji-Yih, Yang Wanling, Wong Maida, Kawasaki Aya, Tsuchiya Naoyuki, Sumida Takayuki, Kawaguchi Yasushi, Howe Hwee Siew, Mok Mo Yin, Bang So-Young, Liu Fei-Lan, Chang Deh-Ming, Takasaki Yoshinari, Hashimoto Hiroshi, Harley John B, Guthridge Joel M, Grossman Jennifer M, Cantor Rita M, Song Yeong Wook, Bae Sang-Cheol, Chen Shunle, Hahn Bevra H, Lau Yu Lung, Tsao Betty P   Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus Proceedings of the National Academy of Sciences of the United States of America, 2010; 107(36): 15838-43.
Pinto Dalila, Pagnamenta Alistair T, Klei Lambertus, Anney Richard, Merico Daniele, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Almeida Joana, Bacchelli Elena, Bader Gary D, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Bryson Susan E, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chung Brian H Y, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Cytrynbaum Cheryl, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Andrew, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Pilorge Marion, Piven Joseph, Ponting Chris P, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Sequeira Ana F, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stein Olaf, Sykes Nuala, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Webber Caleb, Weksberg Rosanna, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Wu Jing, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Devlin Bernie, Ennis Sean, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Hallmayer Joachim, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Scherer Stephen W, Sutcliffe James S, Betancur Catalina   Functional impact of global rare copy number variation in autism spectrum disorders Nature, 2010; 466(7304): 368-72.
Ingason Andrés, Giegling Ina, Cichon Sven, Hansen Thomas, Rasmussen Henrik B, Nielsen Jimmi, Jürgens Gesche, Muglia Pierandrea, Hartmann Annette M, Strengman Eric, Vasilescu Catalina, Mühleisen Thomas W, Djurovic Srdjan, Melle Ingrid, Lerer Bernard, Möller Hans-Jürgen, Francks Clyde, Pietiläinen Olli P H, Lonnqvist Jouko, Suvisaari Jaana, Tuulio-Henriksson Annamari, Walshe Muriel, Vassos Evangelos, Di Forti Marta, Murray Robin, Bonetto Chiara, Tosato Sarah, Tosato Sarah, Cantor Rita M, Rietschel Marcella, Craddock Nick, Owen Michael J, Peltonen Leena, Andreassen Ole A, Nöthen Markus M, St Clair David, Ophoff Roel A, O'Donovan Michael C, Collier David A, Werge Thomas, Rujescu Dan   A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia Human molecular genetics, 2010; 19(7): 1379-86.
Rullo Ornella J, Woo Jennifer M P, Wu Hui, Hoftman Alice D C, Maranian Paul, Brahn Brittany A, McCurdy Deborah, Cantor Rita M, Tsao Betty P   Association of IRF5 polymorphisms with activation of the interferon alpha pathway Annals of the rheumatic diseases, 2010; 69(3): 611-7.
Weissglas-Volkov Daphna, Plaisier Christopher L, Huertas-Vazquez Adriana, Cruz-Bautista Ivette, Riaño-Barros Daniela, Herrera-Hernandez Miguel, Riba Laura, Cantor Rita M, Sinsheimer Janet S, Aguilar-Salinas Carlos A, Tusie-Luna Teresa, Pajukanta Päivi   Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans Arteriosclerosis, thrombosis, and vascular biology, 2010; 30(2): 353-9.
Weissglas-Volkov Daphna, Aguilar-Salinas Carlos A, Sinsheimer Janet S, Riba Laura, Huertas-Vazquez Adriana, Ordoñez-Sánchez Maria L, Rodriguez-Guillen Rosario, Cantor Rita M, Tusie-Luna Teresa, Pajukanta Päivi   Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples Circulation. Cardiovascular genetics, 2010; 3(1): 31-8.
Cantor Rita M, Lange Kenneth, Sinsheimer Janet S   Prioritizing GWAS results: A review of statistical methods and recommendations for their application American journal of human genetics, 2010; 86(1): 6-22.
Brouwers Martijn C G J, van Greevenbroek Marleen M J, Cantor Rita M   Heritability of nonalcoholic fatty liver disease Gastroenterology, 2009; 137(4): 1536.
Stefansson Hreinn, Ophoff Roel A, Steinberg Stacy, Andreassen Ole A, Cichon Sven, Rujescu Dan, Werge Thomas, Pietiläinen Olli P H, Mors Ole, Mortensen Preben B, Sigurdsson Engilbert, Gustafsson Omar, Nyegaard Mette, Tuulio-Henriksson Annamari, Ingason Andres, Hansen Thomas, Suvisaari Jaana, Lonnqvist Jouko, Paunio Tiina, Børglum Anders D, Hartmann Annette, Fink-Jensen Anders, Nordentoft Merete, Hougaard David, Norgaard-Pedersen Bent, Böttcher Yvonne, Olesen Jes, Breuer René, Möller Hans-Jürgen, Giegling Ina, Rasmussen Henrik B, Timm Sally, Mattheisen Manuel, Bitter István, Réthelyi János M, Magnusdottir Brynja B, Sigmundsson Thordur, Olason Pall, Masson Gisli, Gulcher Jeffrey R, Haraldsson Magnus, Fossdal Ragnheidur, Thorgeirsson Thorgeir E, Thorsteinsdottir Unnur, Ruggeri Mirella, Tosato Sarah, Franke Barbara, Strengman Eric, Kiemeney Lambertus A, Kiemeney Lambertus A, Melle Ingrid, Djurovic Srdjan, Abramova Lilia, Kaleda Vasily, Sanjuan Julio, de Frutos Rosa, Bramon Elvira, Vassos Evangelos, Fraser Gillian, Ettinger Ulrich, Picchioni Marco, Walker Nicholas, Toulopoulou Timi, Need Anna C, Ge Dongliang, Yoon Joeng Lim, Shianna Kevin V, Freimer Nelson B, Cantor Rita M, Murray Robin, Kong Augustine, Golimbet Vera, Carracedo Angel, Arango Celso, Costas Javier, Jönsson Erik G, Terenius Lars, Agartz Ingrid, Petursson Hannes, Nöthen Markus M, Rietschel Marcella, Matthews Paul M, Muglia Pierandrea, Peltonen Leena, St Clair David, Goldstein David B, Stefansson Kari, Collier David A   Common variants conferring risk of schizophrenia Nature, 2009; 460(7256): 744-7.
Bucan Maja, Abrahams Brett S, Wang Kai, Glessner Joseph T, Herman Edward I, Sonnenblick Lisa I, Alvarez Retuerto Ana I, Imielinski Marcin, Hadley Dexter, Bradfield Jonathan P, Kim Cecilia, Gidaya Nicole B, Lindquist Ingrid, Hutman Ted, Sigman Marian, Kustanovich Vlad, Lajonchere Clara M, Singleton Andrew, Kim Junhyong, Wassink Thomas H, McMahon William M, Owley Thomas, Sweeney John A, Coon Hilary, Nurnberger John I, Li Mingyao, Cantor Rita M, Minshew Nancy J, Sutcliffe James S, Cook Edwin H, Dawson Geraldine, Buxbaum Joseph D, Grant Struan F A, Schellenberg Gerard D, Geschwind Daniel H, Hakonarson Hakon   Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes PLoS genetics, 2009; 5(6): e1000536.
Wang Kai, Zhang Haitao, Ma Deqiong, Bucan Maja, Glessner Joseph T, Abrahams Brett S, Salyakina Daria, Imielinski Marcin, Bradfield Jonathan P, Sleiman Patrick M A, Kim Cecilia E, Hou Cuiping, Frackelton Edward, Chiavacci Rosetta, Takahashi Nagahide, Sakurai Takeshi, Rappaport Eric, Lajonchere Clara M, Munson Jeffrey, Estes Annette, Korvatska Olena, Piven Joseph, Sonnenblick Lisa I, Alvarez Retuerto Ana I, Herman Edward I, Dong Hongmei, Hutman Ted, Sigman Marian, Ozonoff Sally, Klin Ami, Owley Thomas, Sweeney John A, Brune Camille W, Cantor Rita M, Bernier Raphael, Gilbert John R, Cuccaro Michael L, McMahon William M, Miller Judith, State Matthew W, Wassink Thomas H, Coon Hilary, Levy Susan E, Schultz Robert T, Nurnberger John I, Haines Jonathan L, Sutcliffe James S, Cook Edwin H, Minshew Nancy J, Buxbaum Joseph D, Dawson Geraldine, Grant Struan F A, Geschwind Daniel H, Pericak-Vance Margaret A, Schellenberg Gerard D, Hakonarson Hakon   Common genetic variants on 5p14.1 associate with autism spectrum disorders Nature, 2009; 459(7246): 528-33.
Cantor Rita M   Molecular genetics of autism Current psychiatry reports, 2009; 11(2): 137-42.
Fears Scott C, Melega William P, Service Susan K, Lee Chris, Chen Kelly, Tu Zhuowen, Jorgensen Matthew J, Fairbanks Lynn A, Cantor Rita M, Freimer Nelson B, Woods Roger P   Identifying heritable brain phenotypes in an extended pedigree of vervet monkeys The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009; 29(9): 2867-75.
Alvarez Retuerto Ana I, Cantor Rita M, Gleeson Joseph G, Ustaszewska Anna, Schackwitz Wendy S, Pennacchio Len A, Geschwind Daniel H   Association of common variants in the Joubert syndrome gene (AHI1) with autism Human molecular genetics, 2008; 17(24): 3887-96.
Lu Ake T, Ogdie Matthew N, Järvelin Marjo-Ritta, Moilanen Irma K, Loo Sandra K, McCracken James T, McGough James J, Yang May H, Peltonen Leena, Nelson Stanley F, Cantor Rita M, Smalley Susan L   Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008; 147B(8): 1488-94.
Schaffer Barbara A J, Bertram Lars, Miller Bruce L, Mullin Kristina, Weintraub Sandra, Johnson Nancy, Bigio Eileen H, Mesulam Marsel, Wiedau-Pazos Martina, Jackson George R, Cummings Jeffrey L, Cantor Rita M, Levey Allan I, Tanzi Rudolph E, Geschwind Daniel H   Association of GSK3B with Alzheimer disease and frontotemporal dementia Archives of neurology, 2008; 65(10): 1368-74.
Lee Jenny C, Weissglas-Volkov Daphna, Kyttälä Mira, Dastani Zari, Cantor Rita M, Sobel Eric M, Plaisier Christopher L, Engert James C, van Greevenbroek Marleen M J, Kane John P, Malloy Mary J, Pullinger Clive R, Huertas-Vazquez Adriana, Aguilar-Salinas Carlos A, Tusie-Luna Teresa, de Bruin Tjerk W A, Aouizerat Bradley E, van der Kallen Carla C J, Croce Carlo M, Aqeilan Rami I, Marcil Michel, Viikari Jorma S A, Lehtimäki Terho, Raitakari Olli T, Kuusisto Johanna, Laakso Markku, Taskinen Marja-Riitta, Genest Jacques, Pajukanta Päivi   WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels American journal of human genetics, 2008; 83(2): 180-92.
Mar-Heyming Rebecca, Miyazaki Makoto, Weissglas-Volkov Daphna, Kolaitis Nicholas A, Sadaat Narimaan, Plaisier Christopher, Pajukanta Päivi, Cantor Rita M, de Bruin Tjerk W A, Ntambi James M, Lusis Aldons J   Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia Arteriosclerosis, thrombosis, and vascular biology, 2008; 28(6): 1193-9.
Cantor Rita M, Geschwind Daniel H   Schizophrenia: genome, interrupted Neuron, 2008; 58(2): 165-7.
Chin Mark H, Qian Wei-Jun, Wang Haixing, Petyuk Vladislav A, Bloom Joshua S, Sforza Daniel M, Laćan Goran, Liu Dahai, Khan Arshad H, Cantor Rita M, Bigelow Diana J, Melega William P, Camp David G, Smith Richard D, Smith Desmond J   Mitochondrial dysfunction, oxidative stress, and apoptosis revealed by proteomic and transcriptomic analyses of the striata in two mouse models of Parkinson's disease Journal of proteome research, 2008; 7(2): 666-77.
Alarcón Maricela, Abrahams Brett S, Stone Jennifer L, Duvall Jacqueline A, Perederiy Julia V, Bomar Jamee M, Sebat Jonathan, Wigler Michael, Martin Christa L, Ledbetter David H, Nelson Stanley F, Cantor Rita M, Geschwind Daniel H   Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene American journal of human genetics, 2008; 82(1): 150-9.
Belmonte Matthew K, Mazziotta John C, Minshew Nancy J, Evans Alan C, Courchesne Eric, Dager Stephen R, Bookheimer Susan Y, Aylward Elizabeth H, Amaral David G, Cantor Rita M, Chugani Diane C, Dale Anders M, Davatzikos Christos, Gerig Guido, Herbert Martha R, Lainhart Janet E, Murphy Declan G, Piven Joseph, Reiss Allan L, Schultz Robert T, Zeffiro Thomas A, Levi-Pearl Susan, Lajonchere Clara, Colamarino Sophia A   Offering to share: how to put heads together in autism neuroimaging Journal of autism and developmental disorders, 2008; 38(1): 2-13.
Freimer Nelson B, Service Susan K, Ophoff Roel A, Jasinska Anna J, McKee Kevin, Villeneuve Amelie, Belisle Alexandre, Bailey Julia N, Breidenthal Sherry E, Jorgensen Matthew J, Mann J John, Cantor Rita M, Dewar Ken, Fairbanks Lynn A   A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species Proceedings of the National Academy of Sciences of the United States of America, 2007; 104(40): 15811-6.
Forsman Eva, Cantor Rita M, Lu Ake, Eriksson Aldur, Fellman Johan, Järvelä Irma, Forsius Henrik   Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish population Acta ophthalmologica Scandinavica, 2007; 85(5): 500-7.
Ribeiro Luciana, Busnello João V, Cantor Rita M, Whelan Fiona, Whittaker Pamela, Deloukas Panos, Wong Ma-Li, Licinio Julio   The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans Neuroreport, 2007; 18(12): 1291-3.
Lin Yi-Wen, Hsu Lea Chia-Ling, Kuo Pao-Lin, Huang William J, Chiang Han-Sun, Yeh Shauh-Der, Hsu Tuan-Yi, Yu Yueh-Hsiang, Hsiao Kuang-Nan, Cantor Rita M, Yen Pauline H   Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan Human mutation, 2007; 28(5): 486-94.
Lu Ake Tzu-Hui, Cantor Rita M   Weighted variance FBAT: a powerful method for including covariates in FBAT analyses Genetic epidemiology, 2007; 31(4): 327-37.
Duvall Jacqueline A, Lu Ake, Cantor Rita M, Todd Richard D, Constantino John N, Geschwind Daniel H   A quantitative trait locus analysis of social responsiveness in multiplex autism families The American journal of psychiatry, 2007; 164(4): 656-62.
Wu Hui, Boackle Susan A, Hanvivadhanakul Punchong, Ulgiati Daniela, Grossman Jennifer M, Lee Youngho, Shen Nan, Abraham Lawrence J, Mercer Timothy R, Park Elly, Hebert Lee A, Rovin Brad H, Birmingham Dan J, Chang Deh-Ming, Chen Chung Jen, McCurdy Deborah, Badsha Humeira M, Thong Bernard Y H, Chng Hiok H, Arnett Frank C, Wallace Daniel J, Yu C Yung, Hahn Bevra H, Cantor Rita M, Tsao Betty P   Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosus Proceedings of the National Academy of Sciences of the United States of America, 2007; 104(10): 3961-6.
Kerner Berit, Bailey Julia N, Cantor Rita M   Co-regulation and multilocus determinants of gene expression in humans BMC proceedings, 2007; 1 Suppl 1(3): S88.
Stone Jennifer L, Merriman Barry, Cantor Rita M, Geschwind Daniel H, Nelson Stanley F   High density SNP association study of a major autism linkage region on chromosome 17 Human molecular genetics, 2007; 16(6): 704-15.
Tsao Betty P, Szatmari Peter, Paterson Andrew D, Zwaigenbaum Lonnie, Roberts Wendy, Brian Jessica, Liu Xiao-Qing, Vincent John B, Skaug Jennifer L, Thompson Ann P, Senman Lili, Feuk Lars, Qian Cheng, Bryson Susan E, Jones Marshall B, Marshall Christian R, Scherer Stephen W, Vieland Veronica J, Bartlett Christopher, Mangin La Vonne, Goedken Rhinda, Segre Alberto, Pericak-Vance Margaret A, Cuccaro Michael L, Gilbert John R, Wright Harry H, Abramson Ruth K, Betancur Catalina, Bourgeron Thomas, Gillberg Christopher, Leboyer Marion, Buxbaum Joseph D, Davis Kenneth L, Hollander Eric, Silverman Jeremy M, Hallmayer Joachim, Lotspeich Linda, Sutcliffe James S, Haines Jonathan L, Folstein Susan E, Piven Joseph, Wassink Thomas H, Sheffield Val, Geschwind Daniel H, Bucan Maja, Brown W Ted, Cantor Rita M, Constantino John N, Gilliam T Conrad, Herbert Martha, Lajonchere Clara, Ledbetter David H, Lese-Martin Christa, Miller Janet, Nelson Stan, Samango-Sprouse Carol A, Spence Sarah, State Matthew, Tanzi Rudolph E, Coon Hilary, Dawson Geraldine, Devlin Bernie, Estes Annette, Flodman Pamela, Klei Lambertus, McMahon William M, Minshew Nancy, Munson Jeff, Korvatska Elena, Rodier Patricia M, Schellenberg Gerard D, Smith Moyra, Spence M Anne, Stodgell Chris, Tepper Ping Guo, Wijsman Ellen M, Yu Chang-En, Rogé Bernadette, Mantoulan Carine, Wittemeyer Kerstin, Poustka Annemarie, Felder Bärbel, Klauck Sabine M, Schuster Claudia, Poustka Fritz, Bölte Sven, Feineis-Matthews Sabine, Herbrecht Evelyn, Schmötzer Gabi, Tsiantis John, Papanikolaou Katerina, Maestrini Elena, Bacchelli Elena, Blasi Francesca, Carone Simona, Toma Claudio, Van Engeland Herman, de Jonge Maretha, Kemner Chantal, Koop Frederieke, Koop Frederike, Langemeijer Marjolein, Langemeijer Marjolijn, Hijmans Channa, Hijimans Channa, Staal Wouter G, Baird Gillian, Bolton Patrick F, Rutter Michael L, Weisblatt Emma, Green Jonathan, Aldred Catherine, Wilkinson Julie-Anne, Pickles Andrew, Le Couteur Ann, Berney Tom, McConachie Helen, Bailey Anthony J, Francis Kostas, Honeyman Gemma, Hutchinson Aislinn, Parr Jeremy R, Wallace Simon, Monaco Anthony P, Barnby Gabrielle, Kobayashi Kazuhiro, Lamb Janine A, Sousa Ines, Sykes Nuala, Cook Edwin H, Guter Stephen J, Leventhal Bennett L, Salt Jeff, Lord Catherine, Corsello Christina, Hus Vanessa, Weeks Daniel E, Volkmar Fred, Tauber Maïté, Fombonne Eric, Shih Andy, Meyer Kacie J   Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics, 2007; 39(3): 319-28.
Brouwers Martijn C G J, Cantor Rita M, Kono Naoko, Yoon Jeong Lim, van der Kallen Carla J H, Bilderbeek-Beckers Monique A L, van Greevenbroek Marleen M J, Lusis Aldons J, de Bruin Tjerk W A   Heritability and genetic loci of fatty liver in familial combined hyperlipidemia Journal of lipid research, 2006; 47(12): 2799-807.
Wong Ma-Li, Whelan Fiona, Deloukas Panagiotis, Whittaker Pamela, Delgado Marcos, Cantor Rita M, McCann Samuel M, Licinio Julio   Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response Proceedings of the National Academy of Sciences of the United States of America, 2006; 103(41): 15124-9.
Spence Sarah J, Cantor Rita M, Chung Lien, Kim Sharon, Geschwind Daniel H, Alarcón Maricela   Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2006; 141B(6): 591-8.
Brouwers Martijn C G J, Kono Naoko, van Greevenbroek Marleen M J, van der Kallen Carla J H, Lusis Aldons J, de Bruin Tjerk W A, Cantor Rita M   Longitudinal differences in familial combined hyperlipidemia quantitative trait loci Arteriosclerosis, thrombosis, and vascular biology, 2006; 26(6): e118-9.
Suviolahti Elina, Reue Karen, Cantor Rita M, Phan Jack, Gentile Massimiliano, Naukkarinen Jussi, Soro-Paavonen Aino, Oksanen Laura, Kaprio Jaakko, Rissanen Aila, Salomaa Veikko, Kontula Kimmo, Taskinen Marja-Riitta, Pajukanta Päivi, Peltonen Leena   Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism Human molecular genetics, 2006; 15(3): 377-86.
Lee Grace S, Liao Xiaoyan, Cantor Rita M, Collins Michael D   Interactive effects of cadmium and all-trans-retinoic acid on the induction of forelimb ectrodactyly in C57BL/6 mice Birth defects research. Part A, Clinical and molecular teratology, 2006; 76(1): 19-28.
Ylisaukko-oja Tero, Alarcón Maricela, Cantor Rita M, Auranen Mari, Vanhala Raija, Kempas Elli, von Wendt Lennart, Järvelä Irma, Geschwind Daniel H, Peltonen Leena   Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families Annals of neurology, 2006; 59(1): 145-55.
Huertas-Vazquez Adriana, Aguilar-Salinas Carlos, Lusis Aldons J, Cantor Rita M, Canizales-Quinteros Samuel, Lee Jenny C, Mariana-Nuñez Lizzette, Riba-Ramirez Roopa-Metha Laura, Jokiaho Anne, Tusie-Luna Teresa, Pajukanta Päivi   Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1 Arteriosclerosis, thrombosis, and vascular biology, 2005; 25(9): 1985-91.
Wu Hui, Cantor Rita M, Graham Deborah S Cunninghame, Lingren Cecilia M, Farwell Lisa, Jager Philip L De, Bottini Nunzio, Grossman Jennifer M, Wallace Daniel J, Hahn Bevra H, Julkunen Heikki, Hebert Lee A, Rovin Brad H, Birmingham Dan J, Rioux John D, Yu C Yung, Kere Juha, Vyse Timothy J, Tsao Betty P   Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease Arthritis and rheumatism, 2005; 52(8): 2396-402.
Cantor Rita M, Kono Naoko, Duvall Jackie A, Alvarez-Retuerto Ana, Stone Jennifer L, Alarcón Maricela, Nelson Stanley F, Geschwind Daniel H   Replication of autism linkage: fine-mapping peak at 17q21 American journal of human genetics, 2005; 76(6): 1050-6.
Lee Grace S, Cantor Rita M, Abnoosian Arin, Park Euisun, Yamamoto Mitsuko L, Hovland David N, Collins Michael D   A gene(s) for all-trans-retinoic acid-induced forelimb defects mapped and confirmed to murine chromosome 11 Genetics, 2005; 170(1): 345-53.
Smalley Susan L, Loo Sandra K, Yang May H, Cantor Rita M   Toward localizing genes underlying cerebral asymmetry and mental health American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2005; 135B(1): 79-84.
Cantor Rita M, Chen Gary K, Pajukanta Päivi, Lange Kenneth   Association testing in a linked region using large pedigrees American journal of human genetics, 2005; 76(3): 538-42.
Stone Jennifer L, Merriman Barry, Cantor Rita M, Yonan Amanda L, Gilliam T Conrad, Geschwind Daniel H, Nelson Stanley F   Evidence for sex-specific risk alleles in autism spectrum disorder American journal of human genetics, 2004; 75(6): 1117-23.
Ogdie Matthew N, Fisher Simon E, Yang May, Ishii Janeen, Francks Clyde, Loo Sandra K, Cantor Rita M, McCracken James T, McGough James J, Smalley Susan L, Nelson Stanley F   Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11 American journal of human genetics, 2004; 75(4): 661-8.
Cantor Rita M, de Bruin Tjerk, Kono Naoko, Napier Susan, van Nas Atila, Allayee Hooman, Lusis Aldons J   Quantitative trait loci for apolipoprotein B, cholesterol, and triglycerides in familial combined hyperlipidemia pedigrees Arteriosclerosis, thrombosis, and vascular biology, 2004; 24(10): 1935-41.
Cantor Rita M, Yuan Jinying, Napier Susan, Kono Naoko, Grossman Jennifer M, Hahn Bevra H, Tsao Betty P   Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23 Arthritis and rheumatism, 2004; 50(10): 3203-10.
Mar Rebecca, Pajukanta Päivi, Allayee Hooman, Groenendijk Martine, Dallinga-Thie Geesje, Krauss Ronald M, Sinsheimer Janet S, Cantor Rita M, de Bruin Tjerk W A, Lusis Aldons J   Association of the APOLIPOPROTEIN A1/C3/A4/A5 gene cluster with triglyceride levels and LDL particle size in familial combined hyperlipidemia Circulation research, 2004; 94(7): 993-9.
Pajukanta Päivi, Lilja Heidi E, Sinsheimer Janet S, Cantor Rita M, Lusis Aldons J, Gentile Massimiliano, Duan Xiaoqun Joyce, Soro-Paavonen Aino, Naukkarinen Jussi, Saarela Janna, Laakso Markku, Ehnholm Christian, Taskinen Marja-Riitta, Peltonen Leena   Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1) Nature genetics, 2004; 36(4): 371-6.
Schanen Carolyn, Houwink Elisa J F, Dorrani Naghmeh, Lane Jane, Everett Ruth, Feng Alice, Cantor Rita M, Percy Alan   Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome American journal of medical genetics. Part A, 2004; 126A(2): 129-40.
Suviolahti Elina, Oksanen Laura J, Ohman Miina, Cantor Rita M, Ridderstrale Martin, Tuomi Tiinamaija, Kaprio Jaakko, Rissanen Aila, Mustajoki Pertti, Jousilahti Pekka, Vartiainen Erkki, Silander Kaisa, Kilpikari Riika, Salomaa Veikko, Groop Leif, Kontula Kimmo, Peltonen Leena, Pajukanta Päivi   The SLC6A14 gene shows evidence of association with obesity The Journal of clinical investigation, 2003; 112(11): 1762-72.
Yonan Amanda L, Alarcón Maricela, Cheng Rong, Magnusson Patrik K E, Spence Sarah J, Palmer Abraham A, Grunn Adina, Juo Suh-Hang Hank, Terwilliger Joseph D, Liu Jianjun, Cantor Rita M, Geschwind Daniel H, Gilliam T Conrad   A genomewide screen of 345 families for autism-susceptibility loci American journal of human genetics, 2003; 73(4): 886-97.
Allayee Hooman, Castellani Lawrence W, Cantor Rita M, de Bruin Tjerk W A, Lusis Aldons J   Biochemical and genetic association of plasma apolipoprotein A-II levels with familial combined hyperlipidemia Circulation research, 2003; 92(11): 1262-7.
Ogdie Matthew N, Macphie I Laurence, Minassian Sonia L, Yang May, Fisher Simon E, Francks Clyde, Cantor Rita M, McCracken James T, McGough James J, Nelson Stanley F, Monaco Anthony P, Smalley Susan L   A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11 American journal of human genetics, 2003; 72(5): 1268-79.
Pajukanta Päivi, Allayee Hooman, Krass Kelly L, Kuraishy Ali, Soro Aino, Lilja Heidi E, Mar Rebecca, Taskinen Marja-Riitta, Nuotio Ilpo, Laakso Markku, Rotter Jerome I, de Bruin Tjerk W A, Cantor Rita M, Lusis Aldons J, Peltonen Leena   Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q American journal of human genetics, 2003; 72(4): 903-17.
Martin Lisa J, Machado Antonio F, Loza M Angelica, Mao Gloria E, Lee Grace S, Hovland David N, Cantor Rita M, Collins Michael D   Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse Birth defects research. Part A, Clinical and molecular teratology, 2003; 67(4): 231-9.
Tsao Betty P, Cantor Rita M, Grossman Jennifer M, Kim Sung K, Strong Noel, Lau Chak S, Chen Chung-Jen, Shen Nan, Ginzler Ellen M, Goldstein Rose, Kalunian Kenneth C, Arnett Frank C, Wallace Daniel J, Hahn Bevra H   Linkage and interaction of loci on 1q23 and 16q12 may contribute to susceptibility to systemic lupus erythematosus Arthritis and rheumatism, 2002; 46(11): 2928-36.
Ehtesham Nadia, Cantor Rita M, King Lily M, Reinker Kent, Powell Berkley R, Shanske Alan, Unger Sheila, Rimoin David L, Cohn Daniel H   Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12 American journal of human genetics, 2002; 71(4): 947-51.
Tsao Betty P, Grossman Jennifer M, Riemekasten Gabriela, Strong Noel, Kalsi Jatinderpal, Wallace Daniel J, Chen Chung-Jen, Lau Chak S, Ginzler Ellen M, Goldstein Rose, Kalunian Kenneth C, Harley John B, Arnett Frank C, Hahn Bevra H, Cantor Rita M   Familiality and co-occurrence of clinical features of systemic lupus erythematosus Arthritis and rheumatism, 2002; 46(10): 2678-85.
Smalley Susan L, Kustanovich Vlad, Minassian Sonia L, Stone Jennifer L, Ogdie Matthew N, McGough James J, McCracken James T, MacPhie I Laurence, Francks Clyde, Fisher Simon E, Cantor Rita M, Monaco Anthony P, Nelson Stanley F   Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism American journal of human genetics, 2002; 71(4): 959-63.
Vakkilainen Juha, Pajukanta Päivi, Cantor Rita M, Nuotio Ilpo O, Lahdenperä Sanni, Ylitalo Kati, Pihlajamäki Jussi, Kovanen Petri T, Laakso Markku, Viikari Jorma S A, Peltonen Leena, Taskinen Marja-Riitta   Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia European journal of human genetics : EJHG, 2002; 10(9): 547-52.
Soro Aino, Pajukanta Päivi, Lilja Heidi E, Ylitalo Kati, Hiekkalinna Tero, Perola Markus, Cantor Rita M, Viikari Jorma S A, Taskinen Marja-Riitta, Peltonen Leena   Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families American journal of human genetics, 2002; 70(5): 1333-40.
Allayee Hooman, Krass Kelly L, Pajukanta Päivi, Cantor Rita M, van der Kallen Carla J H, Mar Rebecca, Rotter Jerome I, de Bruin Tjerk W A, Peltonen Leena, Lusis Aldons J   Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia Circulation research, 2002; 90(8): 926-31.
Wessman Maija, Kallela Mikko, Kaunisto Mari A, Marttila Pia, Sobel Eric, Hartiala Jaana, Oswell Greg, Leal Suzanne M, Papp Jeanette C, Hämäläinen Eija, Broas Petra, Joslyn Geoffrey, Hovatta Iiris, Hiekkalinna Tero, Kaprio Jaakko, Ott Jürg, Cantor Rita M, Zwart John-Anker, Ilmavirta Matti, Havanka Hannele, Färkkilä Markus, Peltonen Leena, Palotie Aarno   A susceptibility locus for migraine with aura, on chromosome 4q24 American journal of human genetics, 2002; 70(3): 652-62.
Quasney Michael W, Waterer Grant W, Dahmer Mary K, Turner Dawn, Zhang Qing, Cantor Rita M, Wunderink Richard G   Intracellular adhesion molecule Gly241Arg polymorphism has no impact on ARDS or septic shock in community-acquired pneumonia Chest, 2002; 121(3 Suppl): 85S-86S.
Wunderink Richard G, Waterer Grant W, Cantor Rita M, Quasney Michael W   Tumor necrosis factor gene polymorphisms and the variable presentation and outcome of community-acquired pneumonia Chest, 2002; 121(3 Suppl): 87S.
Ro Kyung M, Cantor Rita M, Lange Kenneth L, Ahn Samuel S   Palmar hyperhidrosis: evidence of genetic transmission Journal of vascular surgery : official publication, the Society for Vascular Surgery [and] International Society for Cardiovascular Surgery, North American Chapter, 2002; 35(2): 382-6.
Alarcón Maricela, Cantor Rita M, Liu Jianjun, Gilliam T Conrad, Geschwind Daniel H, Geschwind Daniel H   Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families American journal of human genetics, 2002; 70(1): 60-71.
Hovland, DN Cantor, RM Lee, GS Machado, AF Collins, MD   Identification of a murine locus conveying susceptibility to cadmium-induced forelimb malformations Genomics. , 2000; 63(2): 193-201.
Aouizerat, BE, Allayee, H, Cantor, RM, Dallinga-Thie, GM, Lanning, CD, de Bruin, TWA, Rotter, JI, Lusis, AJ   A genome scan for Familial Combined Hyperlipidemia reveals evidence of linkage with a locus on chromosme 11, American Journal of Human Genetics, 1999; 65: 397-412.
Cantor, RM, Lanning, CD   Analysis of Evidence for an alcoholism gene on chromosome 6, Genetic Epidemiology, 1999; .
Groenenjijk, M, Cantor, RM, Blom, NHHC, Rotter, JI, De Bruin, TWA, Dallinga-Thie, GM   Association of plasma lipids and apolipoproteins with the insulin response element in the apo ciii promoter region in Familial Combined Hyperlipidemia, Jounal of Lipids Research, 1999; 40: 1036-1044.
Tsao, BP Cantor, RM Grossman, JM Shen, N Teophilov, NT Wallace, DJ Arnett, FC Hartung, K Goldstein, R Kalunian, KC Hahn, BH Rotter, JI   PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosus The Journal of clinical investigation. , 1999; 103(8): 1135-40.
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