38699304 | Create Study | Contribution of autosomal rare and de novo variants to sex differences in autism. | medRxiv : the preprint server for health sciences | Koko, Mahmoud; Kyle Satterstrom, F; Autism Sequencing Consortium; APEX consortium; Warrier, Varun; Martin, Hilary | April 16, 2024 | Not Determined |
38402414 | Create Study | Evaluating and improving health equity and fairness of polygenic scores. | HGG advances | Zhang, Tianyu; Zhou, Geyu; Klei, Lambertus; Liu, Peng; Chouldechova, Alexandra; Zhao, Hongyu; Roeder, Kathryn; G'Sell, Max; Devlin, Bernie | April 11, 2024 | 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 |
35438146 | Create Study | Robust and accurate estimation of cellular fraction from tissue omics data via ensemble deconvolution. | Bioinformatics (Oxford, England) | Cai, Manqi; Yue, Molin; Chen, Tianmeng; Liu, Jinling; Forno, Erick; Lu, Xinghua; Billiar, Timothy; Celedón, Juan; McKennan, Chris; Chen, Wei; Wang, Jiebiao | May 26, 2022 | Not Determined |
34112972 | Create Study | Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. | Molecular psychiatry | DeMichele-Sweet, Mary Ann A; Klei, Lambertus; Creese, Byron; Harwood, Janet C; Weamer, Elise A; McClain, Lora; Sims, Rebecca; Hernandez, Isabel; Moreno-Grau, Sonia; Tárraga, Lluís; Boada, Mercè; Alarcón-Martín, Emilio; Valero, Sergi; NIA-LOAD Family Based Study Consortium, Alzheimer’s Disease Genetics Consortium (ADGC); Liu, Yushi; Hooli, Basavaraj; Aarsland, Dag; Selbaek, Geir; Bergh, Sverre; Rongve, Arvid; Saltvedt, Ingvild; Skjellegrind, Håvard K; Engdahl, Bo; Stordal, Eystein; Andreassen, Ole A; Djurovic, Srdjan; Athanasiu, Lavinia; Seripa, Davide; Borroni, Barbara; Albani, Diego; Forloni, Gianluigi; Mecocci, Patrizia; Serretti, Alessandro; De Ronchi, Diana; Politis, Antonis; Williams, Julie; Mayeux, Richard; Foroud, Tatiana; Ruiz, Agustin; Ballard, Clive; Holmans, Peter; Lopez, Oscar L; Kamboh, M Ilyas; Devlin, Bernie; Sweet, Robert A | October 1, 2021 | Not Determined |
32268104 | Create Study | Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. | Cell reports | Werling, Donna M; Pochareddy, Sirisha; Choi, Jinmyung; An, Joon-Yong; Sheppard, Brooke; Peng, Minshi; Li, Zhen; Dastmalchi, Claudia; Santpere, Gabriel; Sousa, André M M; Tebbenkamp, Andrew T N; Kaur, Navjot; Gulden, Forrest O; Breen, Michael S; Liang, Lindsay; Gilson, Michael C; Zhao, Xuefang; Dong, Shan; Klei, Lambertus; Cicek, A Ercument; Buxbaum, Joseph D; Adle-Biassette, Homa; Thomas, Jean-Leon; Aldinger, Kimberly A; O'Day, Diana R; Glass, Ian A; Zaitlen, Noah A; Talkowski, Michael E; Roeder, Kathryn; State, Matthew W; Devlin, Bernie; Sanders, Stephan J; Sestan, Nenad | April 2020 | Not Determined |
31981491 | Create Study | Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. | Cell | Satterstrom, F Kyle; Kosmicki, Jack A; Wang, Jiebiao; Breen, Michael S; De Rubeis, Silvia; An, Joon-Yong; Peng, Minshi; Collins, Ryan; Grove, Jakob; Klei, Lambertus; Stevens, Christine; Reichert, Jennifer; Mulhern, Maureen S; Artomov, Mykyta; Gerges, Sherif; Sheppard, Brooke; Xu, Xinyi; Bhaduri, Aparna; Norman, Utku; Brand, Harrison; Schwartz, Grace; Nguyen, Rachel; Guerrero, Elizabeth E; Dias, Caroline; Autism Sequencing Consortium; iPSYCH-Broad Consortium; Betancur, Catalina; Cook, Edwin H; Gallagher, Louise; Gill, Michael; Sutcliffe, James S; Thurm, Audrey; Zwick, Michael E; Børglum, Anders D; State, Matthew W; Cicek, A Ercument; Talkowski, Michael E; Cutler, David J; Devlin, Bernie; Sanders, Stephan J; Roeder, Kathryn; Daly, Mark J; Buxbaum, Joseph D | February 2020 | Not Determined |
31551426 | Create Study | CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. | Scientific data | Hoffman, Gabriel E; Bendl, Jaroslav; Voloudakis, Georgios; Montgomery, Kelsey S; Sloofman, Laura; Wang, Ying-Chih; Shah, Hardik R; Hauberg, Mads E; Johnson, Jessica S; Girdhar, Kiran; Song, Lingyun; Fullard, John F; Kramer, Robin; Hahn, Chang-Gyu; Gur, Raquel; Marenco, Stefano; Lipska, Barbara K; Lewis, David A; Haroutunian, Vahram; Hemby, Scott; Sullivan, Patrick; Akbarian, Schahram; Chess, Andrew; Buxbaum, Joseph D; Crawford, Greg E; Domenici, Enrico; Devlin, Bernie; Sieberts, Solveig K; Peters, Mette A; Roussos, Panos | September 2019 | Not Determined |
31455887 | Create Study | Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia. | Nature neuroscience | Breen, Michael S; Dobbyn, Amanda; Li, Qin; Roussos, Panos; Hoffman, Gabriel E; Stahl, Eli; Chess, Andrew; Sklar, Pamela; Li, Jin Billy; Devlin, Bernie; Buxbaum, Joseph D; CommonMind Consortium | September 2019 | Not Determined |
31424081 | Create Study | Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth. | Schizophrenia bulletin | Jalbrzikowski, Maria; Liu, Fuchen; Foran, William; Roeder, Kathryn; Devlin, Bernie; Luna, Beatriz | February 2020 | Not Determined |
31400192 | Create Study | Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression. | Bioinformatics (Oxford, England) | Wang, Jiebiao; Devlin, Bernie; Roeder, Kathryn | February 2020 | Not Determined |
30911161 | Create Study | Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. | Nature genetics | Huckins, Laura M; Dobbyn, Amanda; Ruderfer, Douglas M; Hoffman, Gabriel; Wang, Weiqing; Pardiñas, Antonio F; Rajagopal, Veera M; Als, Thomas D; T Nguyen, Hoang; Girdhar, Kiran; Boocock, James; Roussos, Panos; Fromer, Menachem; Kramer, Robin; Domenici, Enrico; Gamazon, Eric R; Purcell, Shaun; CommonMind Consortium; Schizophrenia Working Group of the Psychiatric Genomics Consortium; iPSYCH-GEMS Schizophrenia Working Group; Demontis, Ditte; Børglum, Anders D; Walters, James T R; O'Donovan, Michael C; Sullivan, Patrick; Owen, Michael J; Devlin, Bernie; Sieberts, Solveig K; Cox, Nancy J; Im, Hae Kyung; Sklar, Pamela; Stahl, Eli A | April 2019 | Not Determined |
29112194 | Create Study | Genome-wide association study identifies a novel locus for cannabis dependence. | Molecular psychiatry | Agrawal, A; Chou, Y-L; Carey, C E; Baranger, D A A; Zhang, B; Sherva, R; Wetherill, L; Kapoor, M; Wang, J-C; Bertelsen, S; Anokhin, A P; Hesselbrock, V; Kramer, J; Lynskey, M T; Meyers, J L; Nurnberger, J I; Rice, J P; Tischfield, J; Bierut, L J; Degenhardt, L; Farrer, L A; Gelernter, J; Hariri, A R; Heath, A C; Kranzler, H R; Madden, P A F; Martin, N G; Montgomery, G W; Porjesz, B; Wang, T; Whitfield, J B; Edenberg, H J; Foroud, T; Goate, A M; Bogdan, R; Nelson, E C | May 2018 | Not Determined |
29100626 | Create Study | Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden. | Biological psychiatry | Yip, Benjamin Hon Kei; Bai, Dan; Mahjani, Behrang; Klei, Lambertus; Pawitan, Yudi; Hultman, Christina M; Grice, Dorothy E; Roeder, Kathryn; Buxbaum, Joseph D; Devlin, Bernie; Reichenberg, Abraham; Sandin, Sven | April 2018 | Not Determined |
28569757 | Create Study | Fetal and postnatal metal dysregulation in autism. | Nature communications | Arora, Manish; Reichenberg, Abraham; Willfors, Charlotte; Austin, Christine; Gennings, Chris; Berggren, Steve; Lichtenstein, Paul; Anckarsäter, Henrik; Tammimies, Kristiina; Bölte, Sven | June 2017 | Relevant |
28461698 | Create Study | Genetic risk for schizophrenia and psychosis in Alzheimer disease. | Molecular psychiatry | DeMichele-Sweet, M A A; Weamer, E A; Klei, L; Vrana, D T; Hollingshead, D J; Seltman, H J; Sims, R; Foroud, T; Hernandez, I; Moreno-Grau, S; Tárraga, L; Boada, M; Ruiz, A; Williams, J; Mayeux, R; Lopez, O L; Sibille, E L; Kamboh, M I; Devlin, B; Sweet, R A | April 2018 | Not Determined |
28191890 | Create Study | Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. | Nature genetics | Kosmicki, Jack A; Samocha, Kaitlin E; Howrigan, Daniel P; Sanders, Stephan J; Slowikowski, Kamil; Lek, Monkol; Karczewski, Konrad J; Cutler, David J; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph D; Neale, Benjamin M; MacArthur, Daniel G; Wall, Dennis P; Robinson, Elise B; Daly, Mark J | April 2017 | Not Determined |
27087321 | Create Study | A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies. | American journal of human genetics | Bodea, Corneliu A; Neale, Benjamin M; Ripke, Stephan; International IBD Genetics Consortium; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn | May 2016 | Not Determined |
26834510 | Create Study | The huge Package for High-dimensional Undirected Graph Estimation in R. | Journal of machine learning research : JMLR | Zhao, Tuo; Liu, Han; Roeder, Kathryn; Lafferty, John; Wasserman, Larry | April 2012 | Not Relevant |
26806987 | Create Study | Localized Functional Principal Component Analysis. | Journal of the American Statistical Association | Chen, Kehui; Lei, Jing | 2015 | Not Determined |
26402605 | Create Study | Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. | Neuron | Sanders, Stephan J; He, Xin; Willsey, A Jeremy; Ercan-Sencicek, A Gulhan; Samocha, Kaitlin E; Cicek, A Ercument; Murtha, Michael T; Bal, Vanessa H; Bishop, Somer L; Dong, Shan; Goldberg, Arthur P; Jinlu, Cai; Keaney 3rd, John F; Klei, Lambertus; Mandell, Jeffrey D; Moreno-De-Luca, Daniel; Poultney, Christopher S; Robinson, Elise B; Smith, Louw; Solli-Nowlan, Tor; Su, Mack Y; Teran, Nicole A; Walker, Michael F; Werling, Donna M; Beaudet, Arthur L; Cantor, Rita M; Fombonne, Eric; Geschwind, Daniel H; Grice, Dorothy E; Lord, Catherine; Lowe, Jennifer K; Mane, Shrikant M; Martin, Donna M; Morrow, Eric M; Talkowski, Michael E; Sutcliffe, James S; Walsh, Christopher A; Yu, Timothy W; Autism Sequencing Consortium; Ledbetter, David H; Martin, Christa Lese; Cook, Edwin H; Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn; State, Matthew W | September 23, 2015 | Not Determined |
25843333 | Create Study | DSM-5 and psychiatric genetics - round hole, meet square peg. | Biological psychiatry | Buxbaum, Joseph D | May 1, 2015 | Not Relevant |
25382957 | Create Study | Positive Semidefinite Rank-based Correlation Matrix Estimation with Application to Semiparametric Graph Estimation. | Journal of computational and graphical statistics : a joint publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America | Zhao, Tuo; Roeder, Kathryn; Liu, Han | October 20, 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 |
25284784 | Create Study | De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. | Cell reports | Dong, Shan; Walker, Michael F; Carriero, Nicholas J; DiCola, Michael; Willsey, A Jeremy; Ye, Adam Y; Waqar, Zainulabedin; Gonzalez, Luis E; Overton, John D; Frahm, Stephanie; Keaney 3rd, John F; Teran, Nicole A; Dea, Jeanselle; Mandell, Jeffrey D; Hus Bal, Vanessa; Sullivan, Catherine A; DiLullo, Nicholas M; Khalil, Rehab O; Gockley, Jake; Yuksel, Zafer; Sertel, Sinem M; Ercan-Sencicek, A Gulhan; Gupta, Abha R; Mane, Shrikant M; Sheldon, Michael; Brooks, Andrew I; Roeder, Kathryn; Devlin, Bernie; State, Matthew W; Wei, Liping; Sanders, Stephan J | October 9, 2014 | Not Determined |
25152607 | Create Study | Stability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models. | Advances in neural information processing systems | Liu H, Roeder K, Wasserman L | December 31, 2010 | Not Determined |
25086666 | Create Study | A framework for the interpretation of de novo mutation in human disease. | Nature genetics | Samocha, Kaitlin E; Robinson, Elise B; Sanders, Stephan J; Stevens, Christine; Sabo, Aniko; McGrath, Lauren M; Kosmicki, Jack A; Rehnström, Karola; Mallick, Swapan; Kirby, Andrew; Wall, Dennis P; MacArthur, Daniel G; Gabriel, Stacey B; DePristo, Mark; Purcell, Shaun M; Palotie, Aarno; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Gibbs, Richard A; Schellenberg, Gerard D; Sutcliffe, James S; Devlin, Bernie; Roeder, Kathryn; Neale, Benjamin M; Daly, Mark J | September 2014 | Not Determined |
25038753 | Study (346) | Most genetic risk for autism resides with common variation. | Nature genetics | Gaugler, Trent; Klei, Lambertus; Sanders, Stephan J; Bodea, Corneliu A; Goldberg, Arthur P; Lee, Ann B; Mahajan, Milind; Manaa, Dina; Pawitan, Yudi; Reichert, Jennifer; Ripke, Stephan; Sandin, Sven; Sklar, Pamela; Svantesson, Oscar; Reichenberg, Abraham; Hultman, Christina M; Devlin, Bernie; Roeder, Kathryn; Buxbaum, Joseph D | August 2014 | Relevant |
24796725 | Create Study | The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparison. | European child & adolescent psychiatry | Atladottir, Hjordis O; Gyllenberg, David; Langridge, Amanda; Sandin, Sven; Hansen, Stefan N; Leonard, Helen; Gissler, Mika; Reichenberg, Abraham; Schendel, Diana E; Bourke, Jenny; Hultman, Christina M; Grice, Dorothy E; Buxbaum, Joseph D; Parner, Erik T | February 2015 | Not Relevant |
24794370 | Create Study | The familial risk of autism. | JAMA | Sandin, Sven; Lichtenstein, Paul; Kuja-Halkola, Ralf; Larsson, Henrik; Hultman, Christina M; Reichenberg, Abraham | May 7, 2014 | Not Determined |
24587841 | Create Study | REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING. | The annals of applied statistics | Crossett, Andrew; Lee, Ann B; Klei, Lambertus; Devlin, Bernie; Roeder, Kathryn | June 27, 2013 | Not Determined |
24094742 | Create Study | Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder. | American journal of human genetics | Poultney, Christopher S; Goldberg, Arthur P; Drapeau, Elodie; Kou, Yan; Harony-Nicolas, Hala; Kajiwara, Yuji; De Rubeis, Silvia; Durand, Simon; Stevens, Christine; Rehnström, Karola; Palotie, Aarno; Daly, Mark J; Ma'ayan, Avi; Fromer, Menachem; Buxbaum, Joseph D | October 3, 2013 | Not Determined |
23966865 | Create Study | Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. | PLoS genetics | He, Xin; Sanders, Stephan J; Liu, Li; De Rubeis, Silvia; Lim, Elaine T; Sutcliffe, James S; Schellenberg, Gerard D; Gibbs, Richard A; Daly, Mark J; Buxbaum, Joseph D; State, Matthew W; Devlin, Bernie; Roeder, Kathryn | 2013 | Not Determined |
23743231 | Create Study | Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. | Genomics | Schafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B, Sutcliffe JS, Buxbaum JD, Roeder K | October 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 |
23555798 | Create Study | Clustering and alignment of polymorphic sequences for HLA-DRB1 genotyping. | PloS one | Ringquist, Steven; Bellone, Gaia; Lu, Ying; Roeder, Kathryn; Trucco, Massimo | 2013 | Not Determined |
23352160 | Create Study | Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. | Neuron | Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, et al. | January 23, 2013 | Not Determined |
23143602 | Create Study | Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. | Nature genetics | Whitcomb, David C; LaRusch, Jessica; Krasinskas, Alyssa M; Klei, Lambertus; Smith, Jill P; Brand, Randall E; Neoptolemos, John P; Lerch, Markus M; Tector, Matt; Sandhu, Bimaljit S; Guda, Nalini M; Orlichenko, Lidiya; Alzheimer's Disease Genetics Consortium; Alkaade, Samer; Amann, Stephen T; Anderson, Michelle A; Baillie, John; Banks, Peter A; Conwell, Darwin; Coté, Gregory A; Cotton, Peter B; DiSario, James; Farrer, Lindsay A; Forsmark, Chris E; Johnstone, Marianne; Gardner, Timothy B; Gelrud, Andres; Greenhalf, William; Haines, Jonathan L; Hartman, Douglas J; Hawes, Robert A; Lawrence, Christopher; Lewis, Michele; Mayerle, Julia; Mayeux, Richard; Melhem, Nadine M; Money, Mary E; Muniraj, Thiruvengadam; Papachristou, Georgios I; Pericak-Vance, Margaret A; Romagnuolo, Joseph; Schellenberg, Gerard D; Sherman, Stuart; Simon, Peter; Singh, Vijay P; Slivka, Adam; Stolz, Donna; Sutton, Robert; Weiss, Frank Ulrich; Wilcox, C Mel; Zarnescu, Narcis Octavian; Wisniewski, Stephen R; O'Connell, Michael R; Kienholz, Michelle L; Roeder, Kathryn; Barmada, M Michael; Yadav, Dhiraj; Devlin, Bernie | December 2012 | 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 |
22511880 | Create Study | Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. | PLoS genetics | Chahrour, Maria H; Yu, Timothy W; Lim, Elaine T; Ataman, Bulent; Coulter, Michael E; Hill, R Sean; Stevens, Christine R; Schubert, Christian R; ARRA Autism Sequencing Collaboration; Greenberg, Michael E; Gabriel, Stacey B; Walsh, Christopher A | 2012 | Not Determined |
22499558 | Create Study | Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability. | American journal of medical genetics. Part C, Seminars in medical genetics | Kou, Yan; Betancur, Catalina; Xu, Huilei; Buxbaum, Joseph D; Ma'ayan, Avi | May 15, 2012 | Not Determined |
22495311 | Create Study | Patterns and rates of exonic de novo mutations in autism spectrum disorders. | Nature | Neale, Benjamin M; Kou, Yan; Liu, Li; Ma'ayan, Avi; Samocha, Kaitlin E; Sabo, Aniko; Lin, Chiao-Feng; Stevens, Christine; Wang, Li-San; Makarov, Vladimir; Polak, Paz; Yoon, Seungtai; Maguire, Jared; Crawford, Emily L; Campbell, Nicholas G; Geller, Evan T; Valladares, Otto; Schafer, Chad; Liu, Han; Zhao, Tuo; Cai, Guiqing; Lihm, Jayon; Dannenfelser, Ruth; Jabado, Omar; Peralta, Zuleyma; Nagaswamy, Uma; Muzny, Donna; Reid, Jeffrey G; Newsham, Irene; Wu, Yuanqing; Lewis, Lora; Han, Yi; Voight, Benjamin F; Lim, Elaine; Rossin, Elizabeth; Kirby, Andrew; Flannick, Jason; Fromer, Menachem; Shakir, Khalid; Fennell, Tim; Garimella, Kiran; Banks, Eric; Poplin, Ryan; Gabriel, Stacey; DePristo, Mark; Wimbish, Jack R; Boone, Braden E; Levy, Shawn E; Betancur, Catalina; Sunyaev, Shamil; Boerwinkle, Eric; Buxbaum, Joseph D; Cook Jr, Edwin H; Devlin, Bernie; Gibbs, Richard A; Roeder, Kathryn; Schellenberg, Gerard D; Sutcliffe, James S; Daly, Mark J | April 4, 2012 | Not Determined |
22463983 | Create Study | Genetic architecture in autism spectrum disorder. | Current opinion in genetics & development | Devlin B, Scherer SW | June 2012 | Not Determined |
22170232 | Create Study | Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis. | Genes and immunity | Achkar JP, Klei L, de Bakker PI, Bellone G, Rebert N, Scott R, Lu Y, Regueiro M, Brzezinski A, Kamboh MI, Fiocchi C, Devlin B, Trucco M, Ringquist S, Roeder K, Duerr RH | April 2012 | Not Determined |
22005930 | Create Study | Genome-wide association study of Alzheimer''s disease with psychotic symptoms. | Molecular psychiatry | Hollingworth, P; Sweet, R; Sims, R; Harold, D; Russo, G; Abraham, R; Stretton, A; Jones, N; Gerrish, A; Chapman, J; Ivanov, D; Moskvina, V; Lovestone, S; Priotsi, P; Lupton, M; Brayne, C; Gill, M; Lawlor, B; Lynch, A; Craig, D; McGuinness, B; Johnston, J; Holmes, C; Livingston, G; Bass, N J; Gurling, H; McQuillin, A; GERAD Consortium; National Institute on Aging Late-Onset Alzheimer's Disease Family Study Group; Holmans, P; Jones, L; Devlin, B; Klei, L; Barmada, M M; Demirci, F Y; DeKosky, S T; Lopez, O L; Passmore, P; Owen, M J; O'Donovan, M C; Mayeux, R; Kamboh, M I; Williams, J | December 2012 | Not Determined |
21996756 | Create Study | A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. | Human genetics | 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 Jr, 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 | April 2012 | Not Determined |
21982423 | Create Study | Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees. | Biological psychiatry | Melhem, Nadine; Middleton, Frank; McFadden, Kathryn; Klei, Lambertus; Faraone, Stephen V; Vinogradov, Sophia; Tiobech, Josepha; Yano, Victor; Kuartei, Stevenson; Roeder, Kathryn; Byerley, William; Devlin, Bernie; Myles-Worsley, Marina | December 15, 2011 | Not Determined |
21892380 | Create Study | STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE. | The annals of applied statistics | Percival, Daniel; Roeder, Kathryn; Rosenfeld, Roni; Wasserman, Larry | June 1, 2011 | Not Determined |
21703496 | Create Study | Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders. | Journal of the American Academy of Child and Adolescent Psychiatry | Liu, Xiao-Qing; Georgiades, Stelios; Duku, Eric; Thompson, Ann; Devlin, Bernie; Cook, Edwin H; Wijsman, Ellen M; Paterson, Andrew D; Szatmari, Peter | July 2011 | Not Determined |
21685912 | Create Study | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. | Nature genetics | Höglinger, Günter U; Melhem, Nadine M; Dickson, Dennis W; Sleiman, Patrick M A; Wang, Li-San; Klei, Lambertus; Rademakers, Rosa; de Silva, Rohan; Litvan, Irene; Riley, David E; van Swieten, John C; Heutink, Peter; Wszolek, Zbigniew K; Uitti, Ryan J; Vandrovcova, Jana; Hurtig, Howard I; Gross, Rachel G; Maetzler, Walter; Goldwurm, Stefano; Tolosa, Eduardo; Borroni, Barbara; Pastor, Pau; PSP Genetics Study Group; Cantwell, Laura B; Han, Mi Ryung; Dillman, Allissa; van der Brug, Marcel P; Gibbs, J Raphael; Cookson, Mark R; Hernandez, Dena G; Singleton, Andrew B; Farrer, Matthew J; Yu, Chang-En; Golbe, Lawrence I; Revesz, Tamas; Hardy, John; Lees, Andrew J; Devlin, Bernie; Hakonarson, Hakon; Müller, Ulrich; Schellenberg, Gerard D | June 2011 | Not Determined |
21658581 | Create Study | Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. | Neuron | 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 Jr, Edwin H; Geschwind, Daniel; Roeder, Kathryn; Devlin, Bernie; State, Matthew W | June 9, 2011 | Not Determined |
21480485 | Create Study | Using linkage information to weight a genome-wide association of bipolar disorder. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Howrigan, D P; Laird, N M; Smoller, J W; Devlin, B; McQueen, M B | June 2011 | Not Determined |
21408211 | Create Study | Testing for an unusual distribution of rare variants. | PLoS genetics | Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ | March 2011 | Not Determined |
21078308 | Create Study | Do common variants play a role in risk for autism? Evidence and theoretical musings. | Brain research | Devlin B, Melhem N, Roeder K | March 22, 2011 | Not Determined |
21067556 | Create Study | Shedding new light on genetic dark matter. | Genome medicine | Melhem N, Devlin B | 2010 | Not Determined |
20862653 | Create Study | Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies. | Statistics in medicine | Crossett A, Kent BP, Klei L, Ringquist S, Trucco M, Roeder K, Devlin B | December 10, 2010 | Not Determined |
20711421 | Create Study | Genome-Wide Significance Levels and Weighted Hypothesis Testing. | Statistical science : a review journal of the Institute of Mathematical Statistics | Roeder K, Wasserman L | November 2009 | Not Determined |
20689656 | Create Study | A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY. | The annals of applied statistics | Lee, Ann B; Luca, Diana; Roeder, Kathryn | 2010 | Not Determined |
20663923 | Create Study | A genome-wide scan for common alleles affecting risk for autism. | Human molecular genetics | 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 Jr, 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 | October 15, 2010 | Not Determined |
20531469 | Create Study | Functional impact of global rare copy number variation in autism spectrum disorders. | Nature | 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 Jr, 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 | July 15, 2010 | Not Determined |
20435442 | Create Study | Consanguinity and increased risk for schizophrenia in Egypt. | Schizophrenia research | Mansour, Hader; Fathi, Warda; Klei, Lambertus; Wood, Joel; Chowdari, Kodavali; Watson, Annie; Eissa, Ahmed; Elassy, Mai; Ali, Ibtihal; Salah, Hala; Yassin, Amal; Tobar, Salwa; El-Boraie, Hala; Gaafar, Hanan; Ibrahim, Nahed E; Kandil, Kareem; El-Bahaei, Wafaa; El-Boraie, Osama; Alatrouny, Mohamed; El-Chennawi, Farha; Devlin, Bernie; Nimgaonkar, Vishwajit L | July 2010 | Not Determined |
20088021 | Create Study | Screen and clean: a tool for identifying interactions in genome-wide association studies. | Genetic epidemiology | Wu J, Devlin B, Ringquist S, Trucco M, Roeder K | April 2010 | Not Determined |
19784398 | Create Study | HIGH DIMENSIONAL VARIABLE SELECTION. | Annals of statistics | Wasserman, Larry; Roeder, Kathryn | January 1, 2009 | Not Determined |
19625980 | Create Study | Neural correlates of symptom dimensions in pediatric obsessive-compulsive disorder: a functional magnetic resonance imaging study. | Journal of the American Academy of Child and Adolescent Psychiatry | Gilbert AR, Akkal D, Almeida JR, Mataix-Cols D, Kalas C, Devlin B, Birmaher B, Phillips ML | September 2009 | Not Determined |
19513023 | Create Study | Phenotypic and genotypic characteristics of inflammatory bowel disease in French Canadians: comparison with a large North American repository. | The American journal of gastroenterology | Bhat M, Nguyen GC, Pare P, Lahaie R, Deslandres C, Bernard EJ, Aumais G, Jobin G, Wild G, Cohen A, Langelier D, Brant S, Dassopoulos T, McGovern D, Torres E, Duerr R, Regueiro M, Silverberg MS, Steinhart H, Griffiths AM, Elkadri A, Cho J, Proctor D, Goyette P, Rioux J, et al. | September 2009 | Not Determined |
19455578 | Create Study | Discovering genetic ancestry using spectral graph theory. | Genetic epidemiology | Lee AB, Luca D, Klei L, Devlin B, Roeder K | January 2010 | Not Determined |
19404257 | Create Study | Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. | Nature | Glessner, Joseph T; Wang, Kai; Cai, Guiqing; Korvatska, Olena; Kim, Cecilia E; Wood, Shawn; Zhang, Haitao; Estes, Annette; Brune, Camille W; Bradfield, Jonathan P; Imielinski, Marcin; Frackelton, Edward C; Reichert, Jennifer; Crawford, Emily L; Munson, Jeffrey; Sleiman, Patrick M A; Chiavacci, Rosetta; Annaiah, Kiran; Thomas, Kelly; Hou, Cuiping; Glaberson, Wendy; Flory, James; Otieno, Frederick; Garris, Maria; Soorya, Latha; Klei, Lambertus; Piven, Joseph; Meyer, Kacie J; Anagnostou, Evdokia; Sakurai, Takeshi; Game, Rachel M; Rudd, Danielle S; Zurawiecki, Danielle; McDougle, Christopher J; Davis, Lea K; Miller, Judith; Posey, David J; Michaels, Shana; Kolevzon, Alexander; Silverman, Jeremy M; Bernier, Raphael; Levy, Susan E; Schultz, Robert T; Dawson, Geraldine; Owley, Thomas; McMahon, William M; Wassink, Thomas H; Sweeney, John A; Nurnberger, John I; Coon, Hilary; Sutcliffe, James S; Minshew, Nancy J; Grant, Struan F A; Bucan, Maja; Cook, Edwin H; Buxbaum, Joseph D; Devlin, Bernie; Schellenberg, Gerard D; Hakonarson, Hakon | May 28, 2009 | Not Determined |
19278733 | Create Study | Replicable differences in preferred circadian phase between bipolar disorder patients and control individuals. | Psychiatry research | Wood, Joel; Birmaher, Boris; Axelson, David; Ehmann, Mary; Kalas, Catherine; Monk, Kelly; Turkin, Scott; Kupfer, David J; Brent, David; Monk, Timothy H; Nimgainkar, Vishwajit L | April 30, 2009 | Not Determined |
19152378 | Create Study | Consanguinity associated with increased risk for bipolar I disorder in Egypt. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Mansour, Hader; Klei, Lambertus; Wood, Joel; Talkowski, Michael; Chowdari, Kodavali; Fathi, Warda; Eissa, Ahmed; Yassin, Amal; Salah, Hala; Tobar, Salwa; El-Boraie, Hala; Gaafar, Hanan; Elassy, Mai; Ibrahim, Nahed E; El-Bahaei, Wafaa; Elsayed, Mohamed; Shahda, Mohamed; El Sheshtawy, Eman; El-Boraie, Osama; El-Chennawi, Farha; Devlin, Bernie; Nimgaonkar, Vishwajit L | September 5, 2009 | Not Determined |
19122664 | Create Study | Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. | Nature genetics | Silverberg MS, Cho JH, Rioux JD, McGovern DP, Wu J, Annese V, Achkar JP, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, Bossa F, Griffiths AM, Ippoliti AF, Lahaie RG, Latiano A, Paré P, Proctor DD, Regueiro MD, Steinhart AH, Targan SR, et al. | February 2009 | Not Determined |
18519160 | Create Study | Searching for disease susceptibility variants in structured populations. | Genomics | Roeder K, Luca D | January 2009 | Not Determined |
18252225 | Create Study | On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. | American journal of human genetics | Luca, Diana; Ringquist, Steven; Klei, Lambertus; Lee, Ann B; Gieger, Christian; Wichmann, H-Erich; Schreiber, Stefan; Krawczak, Michael; Lu, Ying; Styche, Alexis; Devlin, Bernie; Roeder, Kathryn; Trucco, Massimo | February 2008 | Not Determined |
17922480 | Create Study | Pleiotropy and principal components of heritability combine to increase power for association analysis. | Genetic epidemiology | Klei L, Luca D, Devlin B, Roeder K | January 2008 | Not Determined |
17561376 | Create Study | Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk. | Schizophrenia research | Shirts BH, Kim JJ, Reich S, Dickerson FB, Yolken RH, Devlin B, Nimgaonkar VL | August 2007 | Not Determined |
17549760 | Create Study | Improving power in genome-wide association studies: weights tip the scale. | Genetic epidemiology | Roeder K, Devlin B, Wasserman L | November 2007 | Not Determined |
17453677 | Create Study | Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia? | Annals of medicine | Kim JJ, Shirts BH, Dayal M, Bacanu SA, Wood J, Xie W, Zhang X, Chowdari KV, Yolken R, Devlin B, Nimgaonkar VL | 2007 | Not Determined |
17436020 | Create Study | Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation. | Human genetics | Devlin, Bernie; Klei, Lambertus; Myles-Worsley, Marina; Tiobech, Josepha; Otto, Caleb; Byerley, William; Roeder, Kathryn | July 2007 | Not Determined |
17434289 | Create Study | Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association. | Genomics | Yu CE, Seltman H, Peskind ER, Galloway N, Zhou PX, Rosenthal E, Wijsman EM, Tsuang DW, Devlin B, Schellenberg GD | June 2007 | Not Determined |
17342507 | Create Study | Testing for association based on excess allele sharing in a sample of related cases and controls. | Human genetics | Klei, Lambertus; Roeder, Kathyrn | June 2007 | Not Determined |
17322880 | Create Study | Mapping autism risk loci using genetic linkage and chromosomal rearrangements. | Nature genetics | Autism Genome Project Consortium; 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 | March 2007 | Not Determined |
16893532 | Create Study | Novel, replicated associations between dopamine D3 receptor gene polymorphisms and schizophrenia in two independent samples. | Biological psychiatry | Talkowski ME, Mansour H, Chowdari KV, Wood J, Butler A, Varma PG, Prasad S, Semwal P, Bhatia T, Deshpande S, Devlin B, Thelma BK, Nimgaonkar VL | September 15, 2006 | Not Determined |
16631129 | Create Study | Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. | Biological psychiatry | Talkowski, Michael E; Seltman, Howard; Bassett, Anne S; Brzustowicz, Linda M; Chen, Xiangning; Chowdari, Kodavali V; Collier, David A; Cordeiro, Quirino; Corvin, Aiden P; Deshpande, Smita N; Egan, Michael F; Gill, Michael; Kendler, Kenneth S; Kirov, George; Heston, Leonard L; Levitt, Pat; Lewis, David A; Li, Tao; Mirnics, Karoly; Morris, Derek W; Norton, Nadine; O'Donovan, Michael C; Owen, Michael J; Richard, Christian; Semwal, Prachi; Sobell, Janet L; St Clair, David; Straub, Richard E; Thelma, B K; Vallada, Homero; Weinberger, Daniel R; Williams, Nigel M; Wood, Joel; Zhang, Feng; Devlin, Bernie; Nimgaonkar, Vishwajit L | July 15, 2006 | Not Determined |
16507006 | Create Study | Association study of eight circadian genes with bipolar I disorder, schizoaffective disorder and schizophrenia. | Genes, brain, and behavior | Mansour HA, Wood J, Logue T, Chowdari KV, Dayal M, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL | March 2006 | Not Determined |
16400608 | Create Study | Using linkage genome scans to improve power of association in genome scans. | American journal of human genetics | Roeder, Kathryn; Bacanu, Silvi-Alin; Wasserman, Larry; Devlin, B | February 2006 | Not Determined |
16152575 | Create Study | Selection of eating-disorder phenotypes for linkage analysis. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Bulik, Cynthia M; Bacanu, Silviu-Alin; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Keel, Pamela; Kaplan, Allan S; Mitchell, James E; Rotondo, Alessandro; Strober, Michael; Treasure, Janet; Woodside, D Blake; Sonpar, Vibhor A; Xie, Weiting; Bergen, Andrew W; Berrettini, Wade H; Kaye, Walter H; Devlin, Bernie | November 5, 2005 | Not Determined |
16152574 | Create Study | Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Bacanu, Silviu-Alin; Bulik, Cynthia M; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Keel, Pamela; Kaplan, Allan S; Mitchell, James E; Rotondo, Alessandro; Strober, Michael; Treasure, Janet; Woodside, D Blake; Sonpar, Vibhor A; Xie, Weiting; Bergen, Andrew W; Berrettini, Wade H; Kaye, Walter H; Devlin, Bernie | November 5, 2005 | Not Determined |
16103890 | Create Study | Autism and the serotonin transporter: the long and short of it. | Molecular psychiatry | Devlin B, Cook EH, Coon H, Dawson G, Grigorenko EL, McMahon W, Minshew N, Pauls D, Smith M, Spence MA, Rodier PM, Stodgell C, Schellenberg GD, CPEA Genetics Network | December 2005 | Not Determined |
16094613 | Create Study | Multipoint linkage analysis for a very dense set of markers. | Genetic epidemiology | Bacanu SA | November 2005 | Not Determined |
16076655 | Create Study | Circadian phase variation in bipolar I disorder. | Chronobiology international | Mansour HA, Wood J, Chowdari KV, Dayal M, Thase ME, Kupfer DJ, Monk TH, Devlin B, Nimgaonkar VL | 2005 | Not Determined |
16027741 | Create Study | Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease. | Molecular psychiatry | Sweet RA, Devlin B, Pollock BG, Sukonick DL, Kastango KB, Bacanu SA, Chowdari KV, DeKosky ST, Ferrell RE | November 2005 | Not Determined |
16009739 | Create Study | Heritability of psychosis in Alzheimer disease. | The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry | Bacanu, Silviu-Alin; Devlin, Bernie; Chowdari, Kodavali V; DeKosky, Steven T; Nimgaonkar, Vishwajit L; Sweet, Robert A | July 2005 | Not Determined |
15920508 | Create Study | Association of multiple DRD2 polymorphisms with anorexia nervosa. | Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | Bergen AW, Yeager M, Welch RA, Haque K, Ganjei JK, van den Bree MB, Mazzanti C, Nardi I, Fichter MM, Halmi KA, Kaplan AS, Strober M, Treasure J, Woodside DB, Bulik CM, Bacanu SA, Devlin B, Berrettini WH, Goldman D, Kaye WH | September 2005 | Not Determined |
15915326 | Create Study | Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia. | Human genetics | Klei, Lambertus; Bacanu, Silviu-Alin; Myles-Worsley, Marina; Galke, Brandi; Xie, Weiting; Tiobech, Josepha; Otto, Caleb; Roeder, Kathyrn; Devlin, Bernie; Byerley, William | August 2005 | Not Determined |
15637716 | Create Study | Characterization of multilocus linkage disequilibrium. | Genetic epidemiology | Rinaldo A, Bacanu SA, Devlin B, Sonpar V, Wasserman L, Roeder K | April 2005 | Not Determined |
15637715 | Create Study | Analysis of single-locus tests to detect gene/disease associations. | Genetic epidemiology | Roeder K, Bacanu SA, Sonpar V, Zhang X, Devlin B | April 2005 | Not Determined |
15601530 | Create Study | Integration of association statistics over genomic regions using Bayesian adaptive regression splines. | Human genomics | Zhang X, Roeder K, Wallstrom G, Devlin B | November 2003 | Not Determined |
15514657 | Create Study | Genomic Control to the extreme. | Nature genetics | Devlin B, Bacanu SA, Roeder K | November 2004 | Not Determined |
15498468 | Create Study | ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR. | Genomics | Yu CE, Devlin B, Galloway N, Loomis E, Schellenberg GD | September 2004 | Not Determined |
15372617 | Create Study | Robust estimation of critical values for genome scans to detect linkage. | Genetic epidemiology | Bacanu SA | January 2005 | Not Determined |
15048647 | Create Study | Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Devlin, Bernie; Bennett, Pamela; Dawson, Geraldine; Figlewicz, Denise A; Grigorenko, Elena L; McMahon, William; Minshew, Nancy; Pauls, David; Smith, Moyra; Spence, M Anne; Rodier, Patricia M; Stodgell, Chris; Schellenberg, Gerard D; CPEA Genetics Network | April 1, 2004 | Not Determined |
14755456 | Create Study | Haplotypes of the monoamine oxidase genes and the risk for substance use disorders. | American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | Vanyukov, Michael M; Maher, Brion S; Devlin, Bernie; Tarter, Ralph E; Kirillova, Galina P; Yu, Ling-Mei; Ferrell, Robert E | February 15, 2004 | Not Determined |
14571259 | Create Study | False discovery or missed discovery? | Heredity | Devlin B, Roeder K, Wasserman L | December 2003 | Not Determined |
12933562 | Create Study | Genomic control for association studies: a semiparametric test to detect excess-haplotype sharing. | Biostatistics (Oxford, England) | Devlin B, Roeder K, Wasserman L | December 2000 | Not Relevant |
12813726 | Create Study | Evolutionary-based association analysis using haplotype data. | Genetic epidemiology | Seltman H, Roeder K, Devlin B | July 2003 | Not Determined |
12813725 | Create Study | Analysis of multilocus models of association. | Genetic epidemiology | Devlin B, Roeder K, Wasserman L | July 2003 | Not Determined |
12675687 | Create Study | Cladistic analysis of human apolipoprotein a4 polymorphisms in relation to quantitative plasma lipid risk factors of coronary heart disease. | Annals of human genetics | Wang, G Q; DiPietro, M; Roeder, K; Heng, C-K; Bunker, C H; Hamman, R F; Kamboh, M I | March 2003 | Not Determined |
12610778 | Create Study | On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. | American journal of human genetics | Tzeng, Jung-Ying; Devlin, B; Wasserman, Larry; Roeder, Kathryn | April 2003 | Not Determined |
12476400 | Create Study | Significant linkage on chromosome 10p in families with bulimia nervosa. | American journal of human genetics | Bulik, Cynthia M; Devlin, B; Bacanu, Silviu-Alin; Thornton, Laura; Klump, Kelly L; Fichter, Manfred M; Halmi, Katherine A; Kaplan, Allan S; Strober, Michael; Woodside, D Blake; Bergen, Andrew W; Ganjei, J Kelly; Crow, Scott; Mitchell, James; Rotondo, Alessandro; Mauri, Mauro; Cassano, Giovanni; Keel, Pamela; Berrettini, Wade H; Kaye, Walter H | January 2003 | Not Determined |
12210285 | Create Study | No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network. | American journal of medical genetics | Devlin B, Bennett P, Cook EH, Dawson G, Gonen D, Grigorenko EL, McMahon W, Pauls D, Smith M, Spence MA, Schellenberg GD, Collaborative Programs of Excellence in Autism (CPEA) Genetics Network | August 8, 2002 | Not Determined |
12192612 | Create Study | Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau. | Molecular psychiatry | Devlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B, Novasad D, Chu A, TCuenco K, Tiobek S, Otto C, Byerley W | 2002 | Not Determined |
12105318 | Create Study | Linkage analysis of Alzheimer disease with psychosis. | Neurology | Bacanu, S A; Devlin, B; Chowdari, K V; DeKosky, S T; Nimgaonkar, V L; Sweet, R A | July 9, 2002 | Not Determined |
12023979 | Create Study | Association and linkage analyses of RGS4 polymorphisms in schizophrenia. | Human molecular genetics | Chowdari, Kodavali V; Mirnics, Karoly; Semwal, Prachi; Wood, Joel; Lawrence, Elizabeth; Bhatia, Triptish; Deshpande, Smita N; B K, Thelma; Ferrell, Robert E; Middleton, Frank A; Devlin, Bernie; Levitt, Pat; Lewis, David A; Nimgaonkar, Vishwajit L | June 1, 2002 | Not Determined |
11914406 | Create Study | Increased familial risk of the psychotic phenotype of Alzheimer disease. | Neurology | Sweet, R A; Nimgaonkar, V L; Devlin, B; Lopez, O L; DeKosky, S T | March 26, 2002 | Not Determined |
11912184 | Create Study | Linkage analysis of anorexia nervosa incorporating behavioral covariates. | Human molecular genetics | Devlin, Bernie; Bacanu, Silviu-Alin; Klump, Kelly L; Bulik, Cynthia M; Fichter, Manfred M; Halmi, Katherine A; Kaplan, Allan S; Strober, Michael; Treasure, Janet; Woodside, D Blake; Berrettini, Wade H; Kaye, Walter H | March 15, 2002 | Not Determined |
11855950 | Create Study | Genomic control, a new approach to genetic-based association studies. | Theoretical population biology | Devlin, B; Roeder, K; Wasserman, L | November 2001 | Not Determined |
11754475 | Create Study | Association studies for quantitative traits in structured populations. | Genetic epidemiology | Bacanu SA, Devlin B, Roeder K | January 2002 | Not Determined |
11754473 | Create Study | Mixture models for linkage analysis of affected sibling pairs and covariates. | Genetic epidemiology | Devlin B, Jones BL, Bacanu SA, Roeder K | January 2002 | Not Determined |
11754464 | Create Study | Unbiased methods for population-based association studies. | Genetic epidemiology | Devlin, B; Roeder, K; Bacanu, S A | December 2001 | Not Determined |
11499679 | Create Study | Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania. | Human genetics | Devlin, B; Roeder, K; Otto, C; Tiobech, S; Byerley, W | June 2001 | Not Determined |
11318178 | Create Study | Flexible parametric measurement error models. | Biometrics | Carroll RJ, Roeder K, Wasserman L | March 1999 | Not Determined |
11315092 | Create Study | Genomic control for association studies. | Biometrics | Devlin, B; Roeder, K | December 1999 | Not Relevant |
11309689 | Create Study | Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes. | American journal of human genetics | Seltman, H; Roeder, K; Devlin, B | May 2001 | Not Determined |
11119294 | Create Study | A Bayesian hierarchical model for allele frequencies. | Genetic epidemiology | Lockwood JR, Roeder K, Devlin B | January 2001 | Not Determined |
10801388 | Create Study | The power of genomic control. | American journal of human genetics | Bacanu, S A; Devlin, B; Roeder, K | June 2000 | Not Relevant |
10677324 | Create Study | Haplotype fine mapping by evolutionary trees. | American journal of human genetics | Lam, J C; Roeder, K; Devlin, B | February 2000 | Not Relevant |
10657297 | Create Study | Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. | Science (New York, N.Y.) | Baysal, B E; Ferrell, R E; Willett-Brozick, J E; Lawrence, E C; Myssiorek, D; Bosch, A; van der Mey, A; Taschner, P E; Rubinstein, W S; Myers, E N; Richard 3rd, C W; Cornelisse, C J; Devilee, P; Devlin, B | February 4, 2000 | Not Determined |