36280734 | Create Study | Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. | Nature genetics | Weiner, Daniel J; Ling, Emi; Erdin, Serkan; Tai, Derek J C; Yadav, Rachita; Grove, Jakob; Fu, Jack M; Nadig, Ajay; Carey, Caitlin E; Baya, Nikolas; Bybjerg-Grauholm, Jonas; iPSYCH Consortium; ASD Working Group of the Psychiatric Genomics Consortium; ADHD Working Group of the Psychiatric Genomics Consortium; Berretta, Sabina; Macosko, Evan Z; Sebat, Jonathan; O'Connor, Luke J; Hougaard, David M; Børglum, Anders D; Talkowski, Michael E; McCarroll, Steven A; Robinson, Elise B | November 1, 2022 | Not Determined |
35982160 | Create Study | Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. | Nature genetics | Fu, Jack M; Satterstrom, F Kyle; Peng, Minshi; Brand, Harrison; Collins, Ryan L; Dong, Shan; Wamsley, Brie; Klei, Lambertus; Wang, Lily; Hao, Stephanie P; Stevens, Christine R; Cusick, Caroline; Babadi, Mehrtash; Banks, Eric; Collins, Brett; Dodge, Sheila; Gabriel, Stacey B; Gauthier, Laura; Lee, Samuel K; Liang, Lindsay; Ljungdahl, Alicia; Mahjani, Behrang; Sloofman, Laura; Smirnov, Andrey N; Barbosa, Mafalda; Betancur, Catalina; Brusco, Alfredo; Chung, Brian H Y; Cook, Edwin H; Cuccaro, Michael L; Domenici, Enrico; Ferrero, Giovanni Battista; Gargus, J Jay; Herman, Gail E; Hertz-Picciotto, Irva; Maciel, Patricia; Manoach, Dara S; Passos-Bueno, Maria Rita; Persico, Antonio M; Renieri, Alessandra; Sutcliffe, James S; Tassone, Flora; Trabetti, Elisabetta; Campos, Gabriele; Cardaropoli, Simona; Carli, Diana; Chan, Marcus C Y; Fallerini, Chiara; Giorgio, Elisa; Girardi, Ana Cristina; Hansen-Kiss, Emily; Lee, So Lun; Lintas, Carla; Ludena, Yunin; Nguyen, Rachel; Pavinato, Lisa; Pericak-Vance, Margaret; Pessah, Isaac N; Schmidt, Rebecca J; Smith, Moyra; Costa, Claudia I S; Trajkova, Slavica; Wang, Jaqueline Y T; Yu, Mullin H C; Autism Sequencing Consortium (ASC); Broad Institute Center for Common Disease Genomics (Broad-CCDG); iPSYCH-BROAD Consortium; Cutler, David J; De Rubeis, Silvia; Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J; Talkowski, Michael E | September 1, 2022 | Not Determined |
31410696 | Create Study | Early Second Trimester Maternal Serum Steroid-Related Biomarkers Associated with Autism Spectrum Disorder. | Journal of autism and developmental disorders | Bilder, Deborah A; Esplin, M Sean; Coon, Hilary; Burghardt, Paul; Clark, Erin A S; Fraser, Alison; Smith, Ken R; Worsham, Whitney; Chappelle, Katlin; Rayner, Thomas; Bakian, Amanda V | November 2019 | Not Determined |
30545852 | Create Study | Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. | Science (New York, N.Y.) | An, Joon-Yong; Lin, Kevin; Zhu, Lingxue; Werling, Donna M; Dong, Shan; Brand, Harrison; Wang, Harold Z; Zhao, Xuefang; Schwartz, Grace B; Collins, Ryan L; Currall, Benjamin B; Dastmalchi, Claudia; Dea, Jeanselle; Duhn, Clif; Gilson, Michael C; Klei, Lambertus; Liang, Lindsay; Markenscoff-Papadimitriou, Eirene; Pochareddy, Sirisha; Ahituv, Nadav; Buxbaum, Joseph D; Coon, Hilary; Daly, Mark J; Kim, Young Shin; Marth, Gabor T; Neale, Benjamin M; Quinlan, Aaron R; Rubenstein, John L; Sestan, Nenad; State, Matthew W; Willsey, A Jeremy; Talkowski, Michael E; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J | December 2018 | Not Determined |
30276537 | Create Study | Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder. | Human genetics | Chapman, N H; Bernier, R A; Webb, S J; Munson, J; Blue, E M; Chen, D-H; Heigham, E; Raskind, W H; Wijsman, Ellen M | October 2018 | Not Determined |
30246047 | Create Study | Autism Spectrum Disorder and Neonatal Serum Magnesium Levels in Preterm Infants. | Child neurology open | Bakian, Amanda V; Bilder, Deborah A; Korgenski, E Kent; Bonkowsky, Joshua L | January 2018 | Not Determined |
29523860 | Create Study | Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes. | Scientific reports | Lin, Chun-Yen; Chang, Kai-Wei; Lin, Chia-Yi; Wu, Jia-Ying; Coon, Hilary; Huang, Pei-Hsin; Ho, Hong-Nerng; Akbarian, Schahram; Gau, Susan Shur-Fen; Huang, Hsien-Sung | March 2018 | Not Determined |
29389935 | Create Study | Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk. | PLoS genetics | Waller, Rosalie G; Darlington, Todd M; Wei, Xiaomu; Madsen, Michael J; Thomas, Alun; Curtin, Karen; Coon, Hilary; Rajamanickam, Venkatesh; Musinsky, Justin; Jayabalan, David; Atanackovic, Djordje; Rajkumar, S Vincent; Kumar, Shaji; Slager, Susan; Middha, Mridu; Galia, Perrine; Demangel, Delphine; Salama, Mohamed; Joseph, Vijai; McKay, James; Offit, Kenneth; Klein, Robert J; Lipkin, Steven M; Dumontet, Charles; Vachon, Celine M; Camp, Nicola J | February 1, 2018 | Not Determined |
29267877 | Create Study | GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data. | Bioinformatics (Oxford, England) | Kunji, Khalid; Ullah, Ehsan; Nato Jr, Alejandro Q; Wijsman, Ellen M; Saad, Mohamad | May 2018 | Not Determined |
29266823 | Create Study | Mid-life social outcomes for a population-based sample of adults with ASD. | Autism research : official journal of the International Society for Autism Research | Farley M, Cottle KJ, Bilder D, Viskochil J, Coon H, Mcmahon W | January 2018 | Not Determined |
28968627 | Create Study | Association score testing for rare variants and binary traits in family data with shared controls. | Briefings in bioinformatics | Saad, Mohamad; Wijsman, Ellen M | January 2019 | Not Determined |
28540026 | Create Study | Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. | Molecular autism | Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium | January 1, 2017 | Not Determined |
28504703 | Create Study | Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. | Nature genetics | Weiner, Daniel J; Wigdor, Emilie M; Ripke, Stephan; Walters, Raymond K; Kosmicki, Jack A; Grove, Jakob; Samocha, Kaitlin E; Goldstein, Jacqueline I; Okbay, Aysu; Bybjerg-Grauholm, Jonas; Werge, Thomas; Hougaard, David M; Taylor, Jacob; iPSYCH-Broad Autism Group; Psychiatric Genomics Consortium Autism Group; Skuse, David; Devlin, Bernie; Anney, Richard; Sanders, Stephan J; Bishop, Somer; Mortensen, Preben Bo; Børglum, Anders D; Smith, George Davey; Daly, Mark J; Robinson, Elise B | July 2017 | Not Determined |
28289475 | Create Study | Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families. | Journal of neurodevelopmental disorders | Woodbury-Smith, M; Bilder, D A; Morgan, J; Jerominski, L; Darlington, T; Dyer, T; Paterson, A D; Coon, H | January 2017 | Not Determined |
27980662 | Create Study | Estimating relationships between phenotypes and subjects drawn from admixed families. | BMC proceedings | Blue, Elizabeth M; Brown, Lisa A; Conomos, Matthew P; Kirk, Jennifer L; Nato Jr, Alejandro Q; Popejoy, Alice B; Raffa, Jesse; Ranola, John; Wijsman, Ellen M; Thornton, Timothy | January 2016 | Not Relevant |
27980652 | Create Study | Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data. | BMC proceedings | Saad, Mohamad; Nato Jr, Alejandro Q; Grimson, Fiona L; Lewis, Steven M; Brown, Lisa A; Blue, Elizabeth M; Thornton, Timothy A; Thompson, Elizabeth A; Wijsman, Ellen M | January 2016 | Not Relevant |
27956748 | Create Study | Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism. | Molecular psychiatry | Rubinstein, M; Patowary, A; Stanaway, I B; McCord, E; Nesbitt, R R; Archer, M; Scheuer, T; Nickerson, D; Raskind, W H; Wijsman, E M; Bernier, R; Catterall, W A; Brkanac, Z | February 1, 2018 | Relevant |
27562213 | Create Study | VARPRISM: incorporating variant prioritization in tests of de novo mutation association. | Genome medicine | Hu, Hao; Coon, Hilary; Li, Man; Yandell, Mark; Huff, Chad D | August 2016 | Not Determined |
27535846 | Create Study | Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders. | Human genetics | Truong DT, Shriberg LD, Smith SD, Chapman KL, Scheer-Cohen AR, Demille MM, Adams AK, Nato AQ, Wijsman EM, Eicher JD, Gruen JR | December 2016 | Not Relevant |
27178863 | Create Study | Early event-related potentials to emotional faces differ for adults with autism spectrum disorder and by serotonin transporter genotype. | Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | Faja, Susan; Dawson, Geraldine; Aylward, Elizabeth; Wijsman, Ellen M; Webb, Sara Jane | June 2016 | Not Determined |
27120335 | Create Study | Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech. | PloS one | Peter B, Wijsman EM, Nato AQ, Matsushita MM, Chapman KL, Stanaway IB, Wolff J, Oda K, Gabo VB, Raskind WH | January 2016 | Not Determined |
26866700 | Create Study | Family-based approaches: design, imputation, analysis, and beyond. | BMC genetics | Wijsman EM | 2016 | Not Relevant |
26231429 | Create Study | PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers. | Bioinformatics (Oxford, England) | Nato Jr, Alejandro Q; Chapman, Nicola H; Sohi, Harkirat K; Nguyen, Hiep D; Brkanac, Zoran; Wijsman, Ellen M | December 1, 2015 | Not Relevant |
26204995 | Create Study | Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes. | Human genetics | Chapman, Nicola H; Nato Jr, Alejandro Q; Bernier, Raphael; Ankenman, Katy; Sohi, Harkirat; Munson, Jeff; Patowary, Ashok; Archer, Marilyn; Blue, Elizabeth M; Webb, Sara Jane; Coon, Hilary; Raskind, Wendy H; Brkanac, Zoran; Wijsman, Ellen M | October 2015 | Not Determined |
25640677 | Create Study | Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. | American journal of human genetics | Maier, Robert; Moser, Gerhard; Chen, Guo-Bo; Ripke, Stephan; Cross-Disorder Working Group of the Psychiatric Genomics Consortium; Coryell, William; Potash, James B; Scheftner, William A; Shi, Jianxin; Weissman, Myrna M; Hultman, Christina M; Landén, Mikael; Levinson, Douglas F; Kendler, Kenneth S; Smoller, Jordan W; Wray, Naomi R; Lee, S Hong | February 5, 2015 | Not Relevant |
25599223 | Create Study | Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways. | Nature neuroscience | Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium | February 1, 2015 | Not Determined |
25519371 | Create Study | Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analyses. | BMC proceedings | Blue, Elizabeth Marchani; Cheung, Charles Yk; Glazner, Christopher G; Conomos, Matthew P; Lewis, Steven M; Sverdlov, Serge; Thornton, Timothy; Wijsman, Ellen M | 2014 | Not Determined |
25519330 | Create Study | Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing. | BMC proceedings | Thornton, Timothy; Conomos, Matthew P; Sverdlov, Serge; Blue, Elizabeth M; Cheung, Charles Yk; Glazner, Christopher G; Lewis, Steven M; Wijsman, Ellen M | 2014 | Not Determined |
25392729 | Create Study | The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. | Molecular autism | Buxbaum JD, Bolshakova N, Brownfeld JM, Anney RJ, Bender P, Bernier R, Cook EH, Coon H, Cuccaro M, Freitag CM, Hallmayer J, Geschwind D, Klauck SM, Nurnberger JI, Oliveira G, Pinto D, Poustka F, Scherer SW, Shih A, Sutcliffe JS, Szatmari P, Vicente AM, Vieland V, Gallagher L | 2014 | Not Determined |
25363760 | Create Study | Synaptic, transcriptional and chromatin genes disrupted in autism. | Nature | De Rubeis, Silvia; He, Xin; Goldberg, Arthur P; Poultney, Christopher S; Samocha, Kaitlin; Cicek, A Erucment; Kou, Yan; Liu, Li; Fromer, Menachem; Walker, Susan; Singh, Tarinder; Klei, Lambertus; Kosmicki, Jack; Shih-Chen, Fu; Aleksic, Branko; Biscaldi, Monica; Bolton, Patrick F; Brownfeld, Jessica M; Cai, Jinlu; Campbell, Nicholas G; Carracedo, Angel; Chahrour, Maria H; Chiocchetti, Andreas G; Coon, Hilary; Crawford, Emily L; Curran, Sarah R; Dawson, Geraldine; Duketis, Eftichia; Fernandez, Bridget A; Gallagher, Louise; Geller, Evan; Guter, Stephen J; Hill, R Sean; Ionita-Laza, Juliana; Jimenz Gonzalez, Patricia; Kilpinen, Helena; Klauck, Sabine M; Kolevzon, Alexander; Lee, Irene; Lei, Irene; Lei, Jing; Lehtimäki, Terho; Lin, Chiao-Feng; Ma'ayan, Avi; Marshall, Christian R; McInnes, Alison L; Neale, Benjamin; Owen, Michael J; Ozaki, Noriio; Parellada, Mara; Parr, Jeremy R; Purcell, Shaun; Puura, Kaija; Rajagopalan, Deepthi; Rehnström, Karola; Reichenberg, Abraham; Sabo, Aniko; Sachse, Michael; Sanders, Stephan J; Schafer, Chad; Schulte-Rüther, Martin; Skuse, David; Stevens, Christine; Szatmari, Peter; Tammimies, Kristiina; Valladares, Otto; Voran, Annette; Li-San, Wang; Weiss, Lauren A; Willsey, A Jeremy; Yu, Timothy W; Yuen, Ryan K C; DDD Study; Homozygosity Mapping Collaborative for Autism; UK10K Consortium; Cook, Edwin H; Freitag, Christine M; Gill, Michael; Hultman, Christina M; Lehner, Thomas; Palotie, Aaarno; Schellenberg, Gerard D; Sklar, Pamela; State, Matthew W; Sutcliffe, James S; Walsh, Christiopher A; Scherer, Stephen W; Zwick, Michael E; Barett, Jeffrey C; Cutler, David J; Roeder, Kathryn; Devlin, Bernie; Daly, Mark J; Buxbaum, Joseph D | November 13, 2014 | Not Relevant |
25313507 | Create Study | SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking. | Translational psychiatry | Bowton E, Saunders C, Reddy IA, Campbell NG, Hamilton PJ, Henry LK, Coon H, Sakrikar D, Veenstra-VanderWeele JM, Blakely RD, Sutcliffe J, Matthies HJ, Erreger K, Galli A | 2014 | Not Determined |
25241009 | Create Study | Spatial relative risk patterns of autism spectrum disorders in Utah. | Journal of autism and developmental disorders | Bakian, Amanda V; Bilder, Deborah A; Coon, Hilary; McMahon, William M | April 2015 | Not Determined |
25132070 | Create Study | Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigrees. | Genetic epidemiology | Saad M, Wijsman EM | November 2014 | Not Determined |
25112184 | Create Study | Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond. | Genetic epidemiology | Blue EM, Sun L, Tintle NL, Wijsman EM | September 2014 | Not Determined |
24958436 | Create Study | Psychiatric comorbidity and medication use in adults with autism spectrum disorder. | Journal of autism and developmental disorders | Buck, Tara R; Viskochil, Joseph; Farley, Megan; Coon, Hilary; McMahon, William M; Morgan, Jubel; Bilder, Deborah A | December 2014 | Not Determined |
24837662 | Create Study | A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. | Nature biotechnology | Hu H, Roach JC, Coon H, Guthery SL, Voelkerding KV, Margraf RL, Durtschi JD, Tavtigian SV, Shankaracharya , Wu W, Scheet P, Wang S, Xing J, Glusman G, Hubley R, Li H, Garg V, Moore B, Hood L, Galas DJ, Srivastava D, Reese MG, Jorde LB, Yandell M, Huff CD | July 2014 | Not Determined |
24768552 | Create Study | Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. | American journal of human genetics | Pinto, Dalila; Delaby, Elsa; Merico, Daniele; Barbosa, Mafalda; Merikangas, Alison; Klei, Lambertus; Thiruvahindrapuram, Bhooma; Xu, Xiao; Ziman, Robert; Wang, Zhuozhi; Vorstman, Jacob A S; Thompson, Ann; Regan, Regina; Pilorge, Marion; Pellecchia, Giovanna; Pagnamenta, Alistair T; Oliveira, Bárbara; Marshall, Christian R; Magalhaes, Tiago R; Lowe, Jennifer K; Howe, Jennifer L; Griswold, Anthony J; Gilbert, John; Duketis, Eftichia; Dombroski, Beth A; De Jonge, Maretha V; Cuccaro, Michael; Crawford, Emily L; Correia, Catarina T; Conroy, Judith; Conceição, Inês C; Chiocchetti, Andreas G; Casey, Jillian P; Cai, Guiqing; Cabrol, Christelle; Bolshakova, Nadia; Bacchelli, Elena; Anney, Richard; Gallinger, Steven; Cotterchio, Michelle; Casey, Graham; Zwaigenbaum, Lonnie; Wittemeyer, Kerstin; Wing, Kirsty; Wallace, Simon; van Engeland, Herman; Tryfon, Ana; Thomson, Susanne; Soorya, Latha; Rogé, Bernadette; Roberts, Wendy; Poustka, Fritz; Mouga, Susana; Minshew, Nancy; McInnes, L Alison; McGrew, Susan G; Lord, Catherine; Leboyer, Marion; Le Couteur, Ann S; Kolevzon, Alexander; Jiménez González, Patricia; Jacob, Suma; Holt, Richard; Guter, Stephen; Green, Jonathan; Green, Andrew; Gillberg, Christopher; Fernandez, Bridget A; Duque, Frederico; Delorme, Richard; Dawson, Geraldine; Chaste, Pauline; Café, Cátia; Brennan, Sean; Bourgeron, Thomas; Bolton, Patrick F; Bölte, Sven; Bernier, Raphael; Baird, Gillian; Bailey, Anthony J; Anagnostou, Evdokia; Almeida, Joana; Wijsman, Ellen M; Vieland, Veronica J; Vicente, Astrid M; Schellenberg, Gerard D; Pericak-Vance, Margaret; Paterson, Andrew D; Parr, Jeremy R; Oliveira, Guiomar; Nurnberger, John I; Monaco, Anthony P; Maestrini, Elena; Klauck, Sabine M; Hakonarson, Hakon; Haines, Jonathan L; Geschwind, Daniel H; Freitag, Christine M; Folstein, Susan E; Ennis, Sean; Coon, Hilary; Battaglia, Agatino; Szatmari, Peter; Sutcliffe, James S; Hallmayer, Joachim; Gill, Michael; Cook, Edwin H; Buxbaum, Joseph D; Devlin, Bernie; Gallagher, Louise; Betancur, Catalina; Scherer, Stephen W | May 1, 2014 | Not Determined |
24718985 | Create Study | Detection of Mendelian consistent genotyping errors in pedigrees. | Genetic epidemiology | Cheung CY, Thompson EA, Wijsman EM | May 2014 | Not Determined |
24600472 | Create Study | A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism. | Frontiers in genetics | Carayol, Jérôme; Schellenberg, Gerard D; Dombroski, Beth; Amiet, Claire; Génin, Bérengère; Fontaine, Karine; Rousseau, Francis; Vazart, Céline; Cohen, David; Frazier, Thomas W; Hardan, Antonio Y; Dawson, Geraldine; Rio Frio, Thomas | January 2014 | Not Determined |
24507777 | Create Study | A statistical framework to guide sequencing choices in pedigrees. | American journal of human genetics | Cheung, Charles Y K; Marchani Blue, Elizabeth; Wijsman, Ellen M | February 6, 2014 | Not Determined |
24243664 | Create Study | Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes. | Genetic epidemiology | Saad, Mohamad; Wijsman, Ellen M | January 2014 | Not Determined |
24167172 | Create Study | Maternal prenatal weight gain and autism spectrum disorders. | Pediatrics | Bilder DA, Bakian AV, Viskochil J, Clark EA, Botts EL, Smith KR, Pimentel R, McMahon WM, Coon H | November 2013 | Not Determined |
23943636 | Create Study | DRAW+SneakPeek: analysis workflow and quality metric management for DNA-seq experiments. | Bioinformatics (Oxford, England) | Lin CF, Valladares O, Childress DM, Klevak E, Geller ET, Hwang YC, Tsai EA, Schellenberg GD, Wang LS | October 1, 2013 | Not Determined |
23933821 | Create Study | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. | Nature genetics | Cross-Disorder Group of the Psychiatric Genomics Consortium; Lee, S Hong; Ripke, Stephan; Neale, Benjamin M; Faraone, Stephen V; Purcell, Shaun M; Perlis, Roy H; Mowry, Bryan J; Thapar, Anita; Goddard, Michael E; Witte, John S; Absher, Devin; Agartz, Ingrid; Akil, Huda; Amin, Farooq; Andreassen, Ole A; Anjorin, Adebayo; Anney, Richard; Anttila, Verneri; Arking, Dan E; Asherson, Philip; Azevedo, Maria H; Backlund, Lena; Badner, Judith A; Bailey, Anthony J; Banaschewski, Tobias; Barchas, Jack D; Barnes, Michael R; Barrett, Thomas B; Bass, Nicholas; Battaglia, Agatino; Bauer, Michael; Bayés, Mònica; Bellivier, Frank; Bergen, Sarah E; Berrettini, Wade; Betancur, Catalina; Bettecken, Thomas; Biederman, Joseph; Binder, Elisabeth B; Black, Donald W; Blackwood, Douglas H R; Bloss, Cinnamon S; Boehnke, Michael; Boomsma, Dorret I; Breen, Gerome; Breuer, René; Bruggeman, Richard; Cormican, Paul; Buccola, Nancy G; Buitelaar, Jan K; Bunney, William E; Buxbaum, Joseph D; Byerley, William F; Byrne, Enda M; Caesar, Sian; Cahn, Wiepke; Cantor, Rita M; Casas, Miguel; Chakravarti, Aravinda; Chambert, Kimberly; Choudhury, Khalid; Cichon, Sven; Cloninger, C Robert; Collier, David A; Cook, Edwin H; Coon, Hilary; Cormand, Bru; Corvin, Aiden; Coryell, William H; Craig, David W; Craig, Ian W; Crosbie, Jennifer; Cuccaro, Michael L; Curtis, David; Czamara, Darina; Datta, Susmita; Dawson, Geraldine; Day, Richard; De Geus, Eco J; Degenhardt, Franziska; Djurovic, Srdjan; Donohoe, Gary J; Doyle, Alysa E; Duan, Jubao; Dudbridge, Frank; Duketis, Eftichia; Ebstein, Richard P; Edenberg, Howard J; Elia, Josephine; Ennis, Sean; Etain, Bruno; Fanous, Ayman; Farmer, Anne E; Ferrier, I Nicol; Flickinger, Matthew; Fombonne, Eric; Foroud, Tatiana; Frank, Josef; Franke, Barbara; Fraser, Christine; Freedman, Robert; Freimer, Nelson B; Freitag, Christine M; Friedl, Marion; Frisén, Louise; Gallagher, Louise; Gejman, Pablo V; Georgieva, Lyudmila; Gershon, Elliot S; Geschwind, Daniel H; Giegling, Ina; Gill, Michael; Gordon, Scott D; Gordon-Smith, Katherine; Green, Elaine K; Greenwood, Tiffany A; Grice, Dorothy E; Gross, Magdalena; Grozeva, Detelina; Guan, Weihua; Gurling, Hugh; De Haan, Lieuwe; Haines, Jonathan L; Hakonarson, Hakon; Hallmayer, Joachim; Hamilton, Steven P; Hamshere, Marian L; Hansen, Thomas F; Hartmann, Annette M; Hautzinger, Martin; Heath, Andrew C; Henders, Anjali K; Herms, Stefan; Hickie, Ian B; Hipolito, Maria; Hoefels, Susanne; Holmans, Peter A; Holsboer, Florian; Hoogendijk, Witte J; Hottenga, Jouke-Jan; Hultman, Christina M; Hus, Vanessa; Ingason, Andrés; Ising, Marcus; Jamain, Stéphane; Jones, Edward G; Jones, Ian; Jones, Lisa; Tzeng, Jung-Ying; Kähler, Anna K; Kahn, René S; Kandaswamy, Radhika; Keller, Matthew C; Kennedy, James L; Kenny, Elaine; Kent, Lindsey; Kim, Yunjung; Kirov, George K; Klauck, Sabine M; Klei, Lambertus; Knowles, James A; Kohli, Martin A; Koller, Daniel L; Konte, Bettina; Korszun, Ania; Krabbendam, Lydia; Krasucki, Robert; Kuntsi, Jonna; Kwan, Phoenix; Landén, Mikael; Långström, Niklas; Lathrop, Mark; Lawrence, Jacob; Lawson, William B; Leboyer, Marion; Ledbetter, David H; Lee, Phil H; Lencz, Todd; Lesch, Klaus-Peter; Levinson, Douglas F; Lewis, Cathryn M; Li, Jun; Lichtenstein, Paul; Lieberman, Jeffrey A; Lin, Dan-Yu; Linszen, Don H; Liu, Chunyu; Lohoff, Falk W; Loo, Sandra K; Lord, Catherine; Lowe, Jennifer K; Lucae, Susanne; MacIntyre, Donald J; Madden, Pamela A F; Maestrini, Elena; Magnusson, Patrik K E; Mahon, Pamela B; Maier, Wolfgang; Malhotra, Anil K; Mane, Shrikant M; Martin, Christa L; Martin, Nicholas G; Mattheisen, Manuel; M (see original citation for additional authors) | September 2013 | Not Determined |
23593035 | Create Study | Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. | PLoS genetics | Liu, Li; Sabo, Aniko; Neale, Benjamin M; Nagaswamy, Uma; Stevens, Christine; Lim, Elaine; Bodea, Corneliu A; Muzny, Donna; Reid, Jeffrey G; Banks, Eric; Coon, Hillary; Depristo, Mark; Dinh, Huyen; Fennel, Tim; Flannick, Jason; Gabriel, Stacey; Garimella, Kiran; Gross, Shannon; Hawes, Alicia; Lewis, Lora; Makarov, Vladimir; Maguire, Jared; Newsham, Irene; Poplin, Ryan; Ripke, Stephan; Shakir, Khalid; Samocha, Kaitlin E; Wu, Yuanqing; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Devlin, Bernie; Schellenberg, Gerard D; Sutcliffe, James S; Daly, Mark J; Gibbs, Richard A; Roeder, Kathryn | April 2013 | Not Determined |
23561844 | Create Study | GIGI: an approach to effective imputation of dense genotypes on large pedigrees. | American journal of human genetics | Cheung, Charles Y K; Thompson, Elizabeth A; Wijsman, Ellen M | April 4, 2013 | Not Determined |
23453885 | Create Study | Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. | Lancet (London, England) | Cross-Disorder Group of the Psychiatric Genomics Consortium | April 20, 2013 | Not Determined |
23259942 | Create Study | The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders. | Neuron | Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Lehner, Thomas; Roeder, Kathryn; State, Matthew W; Autism Sequencing Consortium | December 20, 2012 | Not Determined |
23008058 | Create Study | Excess mortality and causes of death in autism spectrum disorders: a follow up of the 1980s Utah/UCLA autism epidemiologic study. | Journal of autism and developmental disorders | Bilder D, Botts EL, Smith KR, Pimentel R, Farley M, Viskochil J, McMahon WM, Block H, Ritvo E, Ritvo RA, Coon H | May 2013 | Not Determined |
22843504 | Create Study | Individual common variants exert weak effects on the risk for autism spectrum disorders. | Human molecular genetics | Anney, Richard; Klei, Lambertus; Pinto, Dalila; Almeida, Joana; Bacchelli, Elena; Baird, Gillian; Bolshakova, Nadia; Bölte, Sven; Bolton, Patrick F; Bourgeron, Thomas; Brennan, Sean; Brian, Jessica; Casey, Jillian; Conroy, Judith; Correia, Catarina; Corsello, Christina; Crawford, Emily L; de Jonge, Maretha; Delorme, Richard; Duketis, Eftichia; Duque, Frederico; Estes, Annette; Farrar, Penny; Fernandez, Bridget A; Folstein, Susan E; Fombonne, Eric; Gilbert, John; Gillberg, Christopher; Glessner, Joseph T; Green, Andrew; Green, Jonathan; Guter, Stephen J; Heron, Elizabeth A; Holt, Richard; Howe, Jennifer L; Hughes, Gillian; Hus, Vanessa; Igliozzi, Roberta; Jacob, Suma; Kenny, Graham P; Kim, Cecilia; Kolevzon, Alexander; Kustanovich, Vlad; Lajonchere, Clara M; Lamb, Janine A; Law-Smith, Miriam; Leboyer, Marion; Le Couteur, Ann; Leventhal, Bennett L; Liu, Xiao-Qing; Lombard, Frances; Lord, Catherine; Lotspeich, Linda; Lund, Sabata C; Magalhaes, Tiago R; Mantoulan, Carine; McDougle, Christopher J; Melhem, Nadine M; Merikangas, Alison; Minshew, Nancy J; Mirza, Ghazala K; Munson, Jeff; Noakes, Carolyn; Nygren, Gudrun; Papanikolaou, Katerina; Pagnamenta, Alistair T; Parrini, Barbara; Paton, Tara; Pickles, Andrew; Posey, David J; Poustka, Fritz; Ragoussis, Jiannis; Regan, Regina; Roberts, Wendy; Roeder, Kathryn; Roge, Bernadette; Rutter, Michael L; Schlitt, Sabine; Shah, Naisha; Sheffield, Val C; Soorya, Latha; Sousa, Inês; Stoppioni, Vera; Sykes, Nuala; Tancredi, Raffaella; Thompson, Ann P; Thomson, Susanne; Tryfon, Ana; Tsiantis, John; Van Engeland, Herman; Vincent, John B; Volkmar, Fred; Vorstman, J A S; Wallace, Simon; Wing, Kirsty; Wittemeyer, Kerstin; Wood, Shawn; Zurawiecki, Danielle; Zwaigenbaum, Lonnie; Bailey, Anthony J; Battaglia, Agatino; Cantor, Rita M; Coon, Hilary; Cuccaro, Michael L; Dawson, Geraldine; Ennis, Sean; Freitag, Christine M; Geschwind, Daniel H; Haines, Jonathan L; Klauck, Sabine M; McMahon, William M; Maestrini, Elena; Miller, Judith; Monaco, Anthony P; Nelson, Stanley F; Nurnberger Jr, John I; Oliveira, Guiomar; Parr, Jeremy R; Pericak-Vance, Margaret A; Piven, Joseph; Schellenberg, Gerard D; Scherer, Stephen W; Vicente, Astrid M; Wassink, Thomas H; Wijsman, Ellen M; Betancur, Catalina; Buxbaum, Joseph D; Cook, Edwin H; Gallagher, Louise; Gill, Michael; Hallmayer, Joachim; Paterson, Andrew D; Sutcliffe, James S; Szatmari, Peter; Vieland, Veronica J; Hakonarson, Hakon; Devlin, Bernie | November 1, 2012 | Not Determined |