Publications:
A selected list of 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, RenterÃa 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.
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.
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.
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.
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
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The SLC6A14 gene shows evidence of association with obesity
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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
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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
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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
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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,
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Birth defects research. Part A, Clinical and molecular teratology,
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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
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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
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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,
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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
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A susceptibility locus for migraine with aura, on chromosome 4q24
American journal of human genetics,
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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,
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Aouizerat, BE, Allayee, H, Cantor, RM, Dallinga-Thie, GM, Lanning, CD, de Bruin, TWA, Rotter, JI, Lusis, AJ
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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
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