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Cites articles 49

Date

Title

Authors

2019-01-16

Psychiatric disorders in children with 16p11.2 deletion and duplication

Maria Niarchou, Samuel Chawner, Anne M Maillard, David Skuse, Jeremy Hall, Michael Owen
2018-01-09

Psychiatric genetics and the structure of psychopathology

Ole A. Andreassen, Howard J Edenberg, Stephen Faraone, Jordan W Smoller
2018-06-11

Genetics of attention deficit hyperactivity disorder

Stephen Faraone
2018-09-01

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights

Itaru Kushima, Masahiro Nakatochi, Tomoko Shiino, Yuko Arioka, Emiko Shishido, Masashi Ikeda, Walid Yassin, Nakao Iwata, Norio Ozaki, Tomoko Toyota, Shusuke Numata, Yuka Yasuda, Hidenaga Yamamori, Branko Aleksic, Naoko Kawano, Yukako Nakamura, Masanari Itokawa, Akira Yoshimi, Tsukasa Sasaki, Ayako Nunokawa, Tetsuro Ohmori, Ichiro Kusumi, Mamoru Tochigi, Kiyoto Kasai, Maeri Yamamoto, Teppei Shimamura, Yasuko Funabiki, Ryo Kimura, Kazuhiro Yamakawa, Hiroki Kimura, Yuto Takasaki, Shohko Kunimoto, Yota Uno, Shuji Iritani, Hitoshi Kuwabara, Masahide Usami, Masaki Kodaira, Tetsuya Iidaka, Kanako Ishizuka, Hidenori Yamasue, Naohiro Okada, Makoto Ishitobi, Toshio Munesue, Hirotaka Kosaka, Tokio Uchiyama, Mitsuhiro Miyashita
2018-02-06

The nature of social cognitive deficits in children and adults with Klinefelter syndrome (47,XXY).

Sophie van Rijn
2018-08-14

The noncoding RNA AK127244 in 2p16.3 locus: A new susceptibility region for neuropsychiatric disorders

Ambra Rizzo, Marica Eoli, Chiara Pantaleoni
2018-04-27

Executive Functions in Children and Adolescents with Turner Syndrome: A Systematic Review and Meta-Analysis

Claire Mauger, Céline Lancelot
2018-01-01

A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data.

Brett Trost, Ryan Yuen, Stephen W. Scherer, Sergio L Pereira, Jeffrey R MacDonald, Daniele Merico, Giovanna Pellecchia, Christian Marshall, Zhuozhi Wang, Wilson W L Sung, Joe Whitney, Miriam S Reuter
2018-02-16

Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing.

M Stephen Meyn, Stephen W. Scherer, Roberto Mendoza-Londono, Christian Marshall, Rosanna Weksberg
2017-03-06

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

Ryan Yuen, Daniele Merico, Matt Bookman, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Zhuozhi Wang, Richard Jonathan Bingham, Giovanna Pellecchia, Christian Marshall, Eric Deneault, Lia D'Abate, Tara A Paton, Sergio L Pereira, Worrawat Engchuan, Edward J Higginbotham, Sylvia Lamoureux, Jeffrey R MacDonald, Thomas Nalpathamkalam, Wilson W L Sung, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael J Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury-Smith, Isabel M. Smith, Edwin H Cook, Stephen R Dager, Annette Estes, Louise Gallagher, Jeremy R Parr, Jacob A S Vorstman, Brendan J. Frey, Bridget A. Fernandez, Mayada Elsabbagh, Bartha Knoppers, Evdokia Anagnostou, Peter Szatmari, Robert H. Ring, David Glazer, Mathew T Pletcher, Stephen W. Scherer
2017-11-30

Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.

Stephen W. Scherer, Marsha D Speevak, Daniele Merico, Anath C. Lionel, Christian Marshall, Gregory Costain, Chelsea Lowther
2017-08-03

De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy

Bhooma Thiruvahindrapuram, Stephen W. Scherer, Jeffrey R MacDonald, Daniele Merico, Edward J Higginbotham, Richard F Wintle, Christian Marshall, Matthew J Gazzellone, Darcy Fehlings
2017-09-20

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
2017-04-20

Cross-disorder comparative analysis of comorbid conditions reveals novel autism candidate genes
2016-11-21

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Sarah E Bergen, Enrico Domenici, Patrik K E Magnusson, Joseph Buxbaum, Erik G Jönsson, Vahram Haroutunian, Tiina Paunio, Thomas Werge, Bhooma Thiruvahindrapuram, Lieuwe de Haan, Inez Myin-Germeys, Benedicto Crespo-Facorro, Sophie E Legge, Stephen W. Scherer, Paola Giusti-Rodríguez, Tracey L Petryshen, Morten Mattingsdal, Joshua L Roffman, Bradley T Webb, Inge Joa, Tune H Pers, Jennifer L. Moran, Elvira Bramon, Murray J Cairns, Rolf Adolfsson, George Kirov, Donald W. Black, David Curtis, Danielle Posthuma, Sven Cichon, Michael C O'Donovan, Peter M. Visscher, Tõnu Esko, Andres Metspalu, Veikko Salomaa, Andrew Pocklington, Brian Kelly, Igor Nenadic, Srdjan Djurovic, Franziska Degenhardt, Ingrid Melle, Juha Veijola, Valentina Escott-Price, Aarno Palotie, Ingrid Agartz, Ole A. Andreassen, Christina M. Hultman, Larry J. Seidman, Kenneth Kendler, Mark Joseph Daly, Frank Dudbridge, Ina Giegling, Ann Olincy, René S. Kahn, Wiepke Cahn, Dan Rujescu, Raquelle I Mesholam-Gately, Jouko Lönnqvist, Jaana Suvisaari, Christos Pantelis, C. Robert Cloninger, Dominique Campion, Naomi R. Wray, Jordan W Smoller, Patrick F. Sullivan, Juha Karjalainen, Nakao Iwata, Jeffrey Lieberman, Johan G. Eriksson, Pamela Sklar, Stephan Ripke, Luba Kalaydjieva, Benjamin M. Neale, Daniele Merico, Rita M. Cantor, Dermot Walsh, Joel N Hirschhorn, John L Waddington, Douglas Blackwood, David St Clair, Michele T Pato, Nancy G. Buccola, James J. Crowley, Gary J. Donohoe, Per Hoffmann, Matthew C Keller, Robert McCarley, Derek W. Morris, Alkes Price, Douglas M. Ruderfer, Thomas G. Schulze, Stephanie H Witt, Aaron R Wolen, Steven A McCarroll, Markus M Nöthen, James Walters, Olli P H Pietiläinen, Nelson A. Freimer, Roel Ophoff, Annette M Hartmann, Eric Strengman, Nick Craddock, Christian Marshall, Daniel P Howrigan, Aniket Shetty, Peter Holmans, Madhusudan Gujral, William M Brandler, Zhouzhi Wang, Karin V Fuentes Fajarado, Margot Albus, Farooq Amin, Joshua R Atkins, Silviu-Alin Bacanu, Richard A Belliveau, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B. Bigdeli, Richard Bruggeman, Brendan Bulik-Sullivan, Guiqing Cai, Vaughan Carr, Noa Carrera, Stanley V Catts, Kimberley D Chambert, Jurgen Del Favero, Dimitris Dikeos, Elodie Drapeau, Jubao Duan, Peter Eichhammer, Laurent Essioux, Kyle Kai-How Farh, Martilias Farrell, Robert Freedman, Andreas J Forstner, Menachem Fromer, Elliot S Gershon, Stephanie Godard, Jacqueline I Goldstein, Jacob Gratten, Marian L Hamshere, Frans A. Henskens, Stefan Herms, Andrea Hofman, Masashi Ikeda, Bettina Konte, Claudine Laurent-Levinson, Deborah M Levy, Carmel M Loughland, Brion S. Maher, Colm Mcdonald, Carin J Meijer, Patricia T Michie, Vihra Milanova, Younes Mokrab, Deborah A Nertney, Gerald Nestadt, Kristin K Nicodemus, Laura Nisenbaum, Annelie Nordin, Colm O'Dushlaine, Jonathan Pimm, Ann E Pulver, Digby Quested, Abraham Reichenberg, Panos Roussos, Alan R. Sanders, Adam J Savitz, Ulrich Schall, Sibylle G Schwab, Edward M Scolnick, Jeremy Silverman, Chris C A Spencer, Eli A Stahl, Jana Strohmaier, T. Scott Stroup, Jin P Szatkiewicz, Srinivas Thirumalai, Paul A Tooney, Mark Weiser, Dieter B Wildenauer, Brandon K Wormley, Clement C. Zai, Aiden Corvin, Pablo V Gejman, Assen V Jablensky, Douglas F Levinson, Andrew McQuillin, Bryan Mowry, Brien P. Riley, Jonathan Sebat, Shaun M Purcell, David Collier, Phil H Lee, Kieran Murphy, Dheeraj Malhotra, Psychosis Endophenotypes International Consortium, James L. Kennedy
2016-10-18

Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation

Stephen W. Scherer, Christie Burton, Daniele Merico, Gregory L. Hanna, Christian Marshall, Matthew J Gazzellone, Noam Soreni, Kate D Fitzgerald
2016-05-19

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

Chelsea Lowther, Elaine S Goh, Lee-Anne Schultz, Antonella Morra, Rob Nicolson, Jack H Jung, Sharan Goobie, Mark A Tarnopolsky, Chitra Prasad, Margreet Walinga, Renske G Reijenga, Stephen W. Scherer, Anne S Bassett, Malgorzata J. M. Nowaczyk
2016-05-10

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

Marco Bellinzoni, Thomas Bourgeron, Thomas Rolland, Julien Buratti, Ryan Yuen, Yasushi Shimoda, Dominique Bonneau, Marion Leboyer, Stephen W. Scherer, Richard Delorme
2016-01-27

A Cross-Disorder Method to Identify Novel Candidate Genes for Developmental Brain Disorders

Christa Lese Martin, Andres Moreno-De-Luca, David H. Ledbetter
2016-08-01

Genome-wide characteristics of de novo mutations in autism

Lonnie Zwaigenbaum, Bhooma Thiruvahindrapuram, Peter Szatmari, Evdokia Anagnostou, Stephen W. Scherer, Tao Zhang, Mingbang Wang, Jeffrey R MacDonald, Kristiina Tammimies, Yang Huanming, Wendy Roberts, Ryan Yuen, Daniele Merico, Rosanna Weksberg, Bridget A. Fernandez, Robert H. Ring, Thomas Nalpathamkalam, Giovanna Pellecchia, Brendan J. Frey, Christian Marshall, Lia D'Abate, Dandan Cao, Zhuozhi Wang, Eric Deneault, Matt Bookman, Richard Jonathan Bingham, Mathew T Pletcher
2016-02-01

Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells

Pei-Chi Wei, Robin M Meyers
2016-08-18

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects

Rhys H Thomas, George Kirov, Mark Einon, Kimberley Kendall, Elliott Rees, Michael C O'Donovan, Valentina Escott-Price
2016-08-17

Analysis of protein-coding genetic variation in 60,706 humans

Michael Boehnke, Sekar Kathiresan, Jaakko Tuomilehto, Markku Laakso, Karol Estrada, Aarno Palotie, Taru Tukiainen, Danish Saleheen, Gad Getz, Roberto Elosua, Adam Kiezun, Joanne Berghout, Pradeep Natarajan, James Ware, Hong-Hee Won, Douglas M. Ruderfer, Hugh Christian Watkins, Kaitlin E Samocha, Dongmei Yu, Eric Minikel, Christina M. Hultman, Mark Joseph Daly, Stacey Gabriel, Steven A McCarroll, Dermot McGovern, Patrick F. Sullivan, James G. Wilson, Pamela Sklar, John Danesh, Lorena Orozco, Benjamin M. Neale, Valentin Ruano Rubio, Eric Banks, Laura D. Gauthier, Namrata Gupta, Grace Tiao, Jeremiah M Scharf, Diego Ardissino, David Altshuler, Gina M Peloso, Konrad J. Karczewski, Timothy R Fennell, Anne H O'Donnell-Luria, David N. Cooper, Daniel P Howrigan, Mark McCarthy, Shaun M Purcell, Daniel G. MacArthur, Mark DePristo, Monkol Lek, Jason Flannick, Jack A Kosmicki, Menachem Fromer, Mitja Kurki, Ami Levy Moonshine, Khalid Shakir, Christine Stevens, Ruth McPherson, Ryan Poplin
2015-03

A copy number variation map of the human genome

Stephen W. Scherer, Jeffrey R MacDonald, Daniele Merico
2015-01-26

Whole-genome sequencing of quartet families with autism spectrum disorder

Lonnie Zwaigenbaum, Bhooma Thiruvahindrapuram, Peter Szatmari, Stephen W. Scherer, Kristiina Tammimies, Robert H. Ring, Wendy Roberts, Daniele Merico, Rosanna Weksberg, Bridget A. Fernandez, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan Yuen, Christian Marshall, Matthew J Gazzellone, Lia D'Abate, Eric Deneault
2015-11-09

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family.

Niels Tommerup, Thomas Werge
2015-08-03

Clinically relevant copy number variations detected in cerebral palsy

Bhooma Thiruvahindrapuram, Richard F Wintle, Stephen W. Scherer, Rosanna Weksberg, Christian Marshall, Matthew J Gazzellone, Zhuozhi Wang, Darcy Fehlings
2015-02-19

Integrative analysis of 111 reference human epigenomes

Ronald Harris
2014-06-24

Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study

Fabio Macciardi, Dan J. Stein, Guy A. Rouleau, Jeremy Veenstra-VanderWeele, Humberto Nicolini, Bhooma Thiruvahindrapuram, Nuria Lanzagorta, Tracey L Petryshen, Eske M Derks, Gregory L. Hanna, Jack Samuels, Paul Sandor, Gary A Heiman, Cathy L. Barr, Homero Vallada, Helena Paula Brentani, Susanne Walitza, Edna Grünblatt, Victor I Reus, Marion Leboyer, Danielle Posthuma, Jay A. Tischfield, Donald W. Black, Richard Delorme, Peter Falkai, Damiaan Denys, Edwin H Cook, Stephen W. Scherer, Joseph Jankovic, Peter Heutink, Nancy J Cox, Euripedes Constantino Miguel, Carol A Mathews, Maria C Rosario, Benjamin M. Neale, Ben A Oostra, Michele T Pato, Danielle C Cath, Jeremiah M Scharf, Nelson A. Freimer, Christian Marshall, Bernadette A Cullen, Gerald Nestadt, Cornelia Illmann, Lisa Osiecki, Cathy L Budman, Roger Kurlan, Rainald Moessner, Laura Bellodi, Fortu Benarroch, Maria Cristina Cavallini, Beatriz Camarena, Sylvain Chouinard, Christine Lochner, Wolfgang Maier, Michael Wagner, Sian Hemmings
2014-12-11

A high-resolution copy-number variation resource for clinical and population genetics

Zhuozhi Wang, Pingzhao Hu, John Wei, Jeffrey R MacDonald, Giovanna Pellecchia, Chao Lu, John R McLaughlin, Richard F Wintle, Stephen W. Scherer, Irene L Andrulis
2013-04-20

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Michael C O'Donovan, Ingrid Agartz, Stanley Zammit, Gerard Van Grootheest, Jonna Kuntsi, Barbara Franke, Peter Holmans, Matthew C Keller, Engilbert Sigurdsson
2013-06-27

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays

Stephen W. Scherer, Marsha D Speevak, Daniele Merico, Anath C. Lionel, Christian Marshall, Gregory Costain, Tracy Yuen, Eva W C Chow, Chelsea Lowther

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