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Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencing Merico, Daniele; Sharfe, Nigel; Dadi, Harjit; Thiruvahindrapuram, Bhooma; de Rijke, Jill; Dahi, Zakia; Zarrei, Mehdi; Al Ghamdi, Abdulrahman; Al Shaqaq, Azhar; Vong, Linda; Roifman, Chaim M. Share Save
FUNCTIONAL-BASED ASSOCIATION STUDY OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IN EUROPEAN, AFRICAN, AND EAST ASIAN POPULATIONS Engchuan, Worrawat; Shanta, Omar; Macdonald, Jeffrey R.; Thiruvahindrapuram, Bhooma; Kumar, Kuldeep; Huguet, Guillaume; Wang, Zhuozhi; Pellecchia, Giovanna; Yuen, Ryan K. C.; Merico, Daniele; Jacquemont, Sebastien; Scherer, Stephen W.; Sebat, Jonathan Share Save
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy Fehlings, Darcy L.; Zarrei, Mehdi; Engchuan, Worrawat; Sondheimer, Neal; Thiruvahindrapuram, Bhooma; MacDonald, Jeffrey R.; Higginbotham, Edward J.; Thapa, Ritesh; Behlim, Tarannum; Aimola, Sabrina; Switzer, Lauren; Ng, Pamela; Wei, John; Danthi, Prakroothi S.; Pellecchia, Giovanna; Lamoureux, Sylvia; Ho, Karen; Pereira, Sergio L.; de Rijke, Jill; Sung, Wilson W. L.; Mowjoodi, Alireza; Howe, Jennifer L.; Nalpathamkalam, Thomas; Manshaei, Roozbeh; Ghaffari, Siavash; Whitney, Joseph; Patel, Rohan V.; Hamdan, Omar; Shaath, Rulan; Trost, Brett; Knights, Shannon; Samdup, Dawa; McCormick, Anna; Hunt, Carolyn; Kirton, Adam; Kawamura, Anne; Mesterman, Ronit; Gorter, Jan Willem; Dlamini, Nomazulu; Merico, Daniele; Hilali, Murto; Hirschfeld, Kyle; Grover, Kritika; Bautista, Nelson X.; Han, Kara; Marshall, Christian R.; Yuen, Ryan K. C.; Subbarao, Padmaja; Azad, Meghan B.; Turvey, Stuart E.; Mandhane, Piush; Moraes, Theo J.; Simons, Elinor; Maxwell, George; Shevell, Michael; Costain, Gregory; Michaud, Jacques L.; Hamdan, Fadi F.; Gauthier, Julie; Uguen, Kevin; Stavropoulos, Dimitri J.; Wintle, Richard F.; Oskoui, Maryam; Scherer, Stephen W. Share Save
GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA Engchuan, Worrawat; Thiruvahindrapuram, Bhooma; MacDonald, Jeffrey R.; Shanta, Omar; Kumar, Kuldeep; Klein, Marieke; Huguet, Guillaume; Wang, Zhuozhi; Pellecchia, Giovanna; Yuen, Ryan K. C.; Merico, Daniele; Jacquemont, Sebastien; Scherer, Stephen W.; Sebat, Jonathan Share Save
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Gene copy number variation and pediatric mental health/neurodevelopment in a general population Zarrei, Mehdi; Burton, Christie L.; Engchuan, Worrawat; Higginbotham, Edward J.; Wei, John; Shaikh, Sabah; Roslin, Nicole M.; MacDonald, Jeffrey R.; Pellecchia, Giovanna; Nalpathamkalam, Thomas; Lamoureux, Sylvia; Manshaei, Roozbeh; Howe, Jennifer; Trost, Brett; Thiruvahindrapuram, Bhooma; Marshall, Christian R.; Yuen, Ryan K. C.; Wintle, Richard F.; Strug, Lisa J.; Stavropoulos, Dimitri J.; Vorstman, Jacob A. S.; Arnold, Paul; Merico, Daniele; Woodbury-Smith, Marc; Crosbie, Jennifer; Schachar, Russell J.; Scherer, Stephen W. Share Save
Whole Genome Sequencing to Resolve the Genomic Architecture of Cerebral Palsy in a Canadian Cohort Oskoui, Maryam; Zarrei, Mehdi; Engchuan, Worrawat; Sondheimer, Neal; Thiruv, Bhooma; Higginbotham, Edward; Thapa, Ritesh; Behlim, Tarannum; Aimola, Sabrina; Wei, John; Danthi, Prakroothi; Pellecchia, Giovanna; Ho, Karen; de Rijke, Jill; Howe, Jennifer; Nalpathamkalam, Thomas; Manshaei, Roozbeh; Whitney, Joseph; Patel, Rohan; Hamdan, Omar; Shaath, Rulan; Knights, Shannon; Trost, Brett; Samdup, Dawa; Mccormick, Anna; Hunt, Carolyn; Kirton, Adam; Kawamura, Anne; Mesterman, Ronit; Gorter, Jan Willem; Dlamini, Nomazulu; Merico, Daniele; Yuen, Ryan; Shevell, Michael; Stavropoulos, Dimitri; Wintle, Richard; Fehlings, Darcy; Scherer, Stephen Share Save
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Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder Chan, Ada J. S.; Engchuan, Worrawat; Reuter, Miriam S.; Wang, Zhuozhi; Thiruvahindrapuram, Bhooma; Trost, Brett; Nalpathamkalam, Thomas; Negrijn, Carol; Lamoureux, Sylvia; Pellecchia, Giovanna; Patel, Rohan, V; Sung, Wilson W. L.; MacDonald, Jeffrey R.; Howe, Jennifer L.; Vorstman, Jacob; Sondheimer, Neal; Takahashi, Nicole; Miles, Judith H.; Anagnostou, Evdokia; Tammimies, Kristiina; Zarrei, Mehdi; Merico, Daniele; Stavropoulos, Dimitri J.; Yuen, Ryan K. C.; Fernandez, Bridget A.; Scherer, Stephen W. Share Save
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A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment Breetvelt, Elemi J.; Smit, Karel C.; van Setten, Jessica; Merico, Daniele; Wang, Xiao; Vaartjes, Ilonca; Bassett, Anne S.; Boks, Marco P. M.; Szatmari, Peter; Scherer, Stephen W.; Kahn, Rene S.; Vorstman, Jacob A. S. Share Save
Transcriptome-Wide Off-Target Effects of Steric-Blocking Oligonucleotides Holgersen, Erle M.; Gandhi, Shreshth; Zhou, Yongchao; Kim, Jinkuk; Vaz, Brandon; Bogojeski, Jovanka; Bugno, Magdalena; Shalev, Zvi; Cheung-Ong, Kahlin; Goncalves, Joao; O'Hara, Matthew; Kron, Ken; Verby, Marta; Sun, Mark; Kakaradov, Boyko; Delong, Andrew; Merico, Daniele; Deshwar, Amit G. Share Save
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia Mojarad, Bahareh A.; Yin, Yue; Manshaei, Roozbeh; Backstrom, Ian; Costain, Gregory; Heung, Tracy; Merico, Daniele; Marshall, Christian R.; Bassett, Anne S.; Yuen, Ryan K. C. Share Save
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B cell acute lymphoblastic leukemia cells mediate RANK-RANKL-dependent bone destruction Rajakumar, Sujeetha A.; Papp, Eniko; Lee, Kathy K.; Grandal, Ildiko; Merico, Daniele; Liu, Careesa C.; Allo, Bedilu; Zhang, Lucia; Grynpas, Marc D.; Minden, Mark D.; Hitzler, Johann K.; Guidos, Cynthia J.; Danska, Jayne S. Share Save
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion Cleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aaron M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex, V; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold, I; Oanh Tran; Holmans, Peter; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Monica E.; Gallagher, Robert S.; Gur, Ruben C.; Tang, Sunny X.; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, Maria C.; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E.; McCabe, Kathryn L.; Hooper, Stephen R.; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Fraguas, David; Garcia-Minaur, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suner, Damia H.; Raventos-Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S. Share Save
Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons (vol 11, pg 1211, 2018) Deneault, Eric; White, Sean H.; Rodrigues, Deivid C.; Ross, P. Joel; Faheem, Muhammad; Zaslavsky, Kirill; Wang, Zhuozhi; Alexandrova, Roumiana; Pellecchia, Giovanna; Wei, Wei; Piekna, Alina; Kaur, Gaganjot; Howe, Jennifer L.; Kwan, Vickie; Thiruvahindrapuram, Bhooma; Walker, Susan; Lionel, Anath C.; Pasceri, Peter; Merico, Daniele; Yuen, Ryan K. C.; Singh, Karun K.; Ellis, James; Scherer, Stephen W. Share Save
Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap Reimand, Juri; Isserlin, Ruth; Voisin, Veronique; Kucera, Mike; Tannus-Lopes, Christian; Rostamianfar, Asha; Wadi, Lina; Meyer, Mona; Wong, Jeff; Xu, Changjiang; Merico, Daniele; Bader, Gary D. Share Save
COPY NUMBER VARIANTS IN BRAIN-RELATED GENES ARE ASSOCIATED WITH NEUROPSYCHIATRIC TRAITS IN CHILDHOOD Burton, Christie; Zarrei, Mehdi; Enghuan, Worrawat; Merico, Daniele; MacDonald, Jeff; Xiao, Bowei; Paterson, Andrew; Strug, Lisa; Marshall, Christian; Crosbie, Jennifer; Arnold, Paul; Schachar, Russell; Scherer, Stephen Share Save
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