Jacob A S Vorstman (Jacob Vorstman, Jacob A Vorstman)

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 36

Top Venues

Research square

American journal of speech-language pathology

Molecular psychiatry

NPJ genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz, Katrina Palad, Nishi Patel, Sarah McGaughey, Louise Gallagher, Stephen W Scherer, Peter Szatmari, Jacob A S Vorstman
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure. Journal of neurodevelopmental disorders 16 (1) (2024)
Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz, Katrina Palad, Nishi Patel, Sarah McGaughey, Louise Gallagher, Stephen W Scherer, Peter Szatmari, Jacob A S Vorstman
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure. Journal of neurodevelopmental disorders 16 (1) (2024)
Jacob A S Vorstman, Jonathan Sebat, Vincent-Raphaël Bourque, Sebastien Jacquemont
Integrative genetic analysis: cornerstone of precision psychiatry. Molecular psychiatry (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M D'Gama, Katherine Howell, Nicole S Y Liang, Amy McTague, Annapurna H Poduri, Kimberly Wiltrout, null null, Anne Susan Bassett, John Chrisodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A S Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. NPJ genomic medicine 9 (1) (2024)
Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz, Katrina Palad, Nishi Patel, Sarah McGaughey, Louise Gallagher, Stephen W Scherer, Peter Szatmari, Jacob A S Vorstman
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure. Journal of neurodevelopmental disorders 16 (1) (2024)
Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz, Katrina Palad, Nishi Patel, Sarah McGaughey, Louise Gallagher, Stephen W Scherer, Peter Szatmari, Jacob A S Vorstman
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure. Journal of neurodevelopmental disorders 16 (1) (2024)
Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M D'Gama, Katherine Howell, Nicole S Y Liang, Amy McTague, Annapurna H Poduri, Kimberly Wiltrout, null null, Anne Susan Bassett, John Chrisodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A S Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. NPJ genomic medicine 9 (1) (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M McDonald-McGinn, T Blaine Crowley, Daniel E McGinn, Oanh T Tran, Daniella Miller, Jhih-Rong Lin, Elaine H Zackai, H Richard Johnston, Eva W C Chow, Jacob A S Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris Robert Vermeesch, Stephan Eliez, Maude Schneider, Marianne B M van den Bree, Michael J Owen, Wendy R Kates, Gabriela M Repetto, Vandana Shashi, Kelly Schoch, Carrie E Bearden, M Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C Murphy, Declan G M Murphy, Sixto García-Miñaúr, Luis Fernández, null null, Zhengdong D Zhang, Elizabeth Goldmuntz, Raquel E Gur, Beverly S Emanuel, Deyou Zheng, Christian R Marshall, Anne Susan Bassett, Tao Wang, Bernice E Morrow
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ genomic medicine 8 (1) (2023)
Emma Everaert, Tessel Boerma, Iris Selten, Ellen Gerrits, Michiel Houben, Jacob A S Vorstman, Frank N K Wijnen
Nonverbal Executive Functioning in Relation to Vocabulary and Morphosyntax in Preschool Children With and Without Developmental Language Disorder. Journal of speech, language, and hearing research : JSLHR (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Ada J S Chan, Worrawat Engchuan, Miriam S Reuter, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Brett Trost, Thomas Nalpathamkalam, Carol Negrijn, Sylvia Lamoureux, Giovanna Pellecchia, Rohan V Patel, Wilson W L Sung, Jeffrey R MacDonald, Jennifer L Howe, Jacob A S Vorstman, Neal Sondheimer, Nicole Takahashi, Judith H Miles, Evdokia Anagnostou, Kristiina Tammimies, Mehdi Zarrei, Daniele Merico, Dimitri J Stavropoulos, Ryan K C Yuen, Bridget A Fernandez, Stephen W Scherer
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Nature communications 13 (1) (2022)
Ania M Fiksinski, Gil D Hoftman, Jacob A S Vorstman, Carrie E Bearden
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome. Molecular psychiatry (2022)
Justo Pinzón-Espinosa, Marte van der Horst, Janneke R Zinkstok, Jehannine C Austin, Cora Aalfs, Albert Batalla, Patrick Sullivan, Jacob A S Vorstman, Jurjen J Luykx
Barriers to genetic testing in clinical psychiatry and ways to overcome them: from clinicians' attitudes to sociocultural differences between patients across the globe. Translational psychiatry 12 (1) (2022)
Emma Everaert, Iris Selten, Tessel Boerma, Michiel Houben, Jacob A S Vorstman, Hester de Wilde, Desiree Derksen, Sarah Haverkamp, Frank N K Wijnen, Ellen Gerrits
The Language Profile of Preschool Children With 22q11.2 Deletion Syndrome and the Relationship With Speech Intelligibility. American journal of speech-language pathology 32 (1) (2022)
Emma Everaert, Iris Selten, Tessel Boerma, Michiel Houben, Jacob A S Vorstman, Hester de Wilde, Desiree Derksen, Sarah Haverkamp, Frank N K Wijnen, Ellen Gerrits
The Language Profile of Preschool Children With 22q11.2 Deletion Syndrome and the Relationship With Speech Intelligibility. American journal of speech-language pathology 32 (1) (2022)
Dorinde Korteling, Marco P M Boks, Ania M Fiksinski, Ilja N van Hoek, Jacob A S Vorstman, Hanneke W M van Deutekom, Judith J M Jans, Janneke R Zinkstok
Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome. Translational psychiatry 12 (1) (2022)
Emma Everaert, Iris Selten, Tessel Boerma, Michiel Houben, Jacob A S Vorstman, Hester de Wilde, Desiree Derksen, Sarah Haverkamp, Frank N K Wijnen, Ellen Gerrits
The Language Profile of Preschool Children With 22q11.2 Deletion Syndrome and the Relationship With Speech Intelligibility. American journal of speech-language pathology 32 (1) (2022)
Marijn Muurling, Lianne Maria Reus, Casper de Boer, Sterre C Wessels, Raj R Jagesar, Jacob A S Vorstman, Martien J H Kas, Pieter Jelle Visser
Assessment of Social Behavior Using a Passive Monitoring App in Cognitively Normal and Cognitively Impaired Older Adults: Observational Study. JMIR aging 5 (2) (2022)
Emma Everaert, Iris Selten, Tessel Boerma, Michiel Houben, Jacob A S Vorstman, Hester de Wilde, Desiree Derksen, Sarah Haverkamp, Frank N K Wijnen, Ellen Gerrits
The Language Profile of Preschool Children With 22q11.2 Deletion Syndrome and the Relationship With Speech Intelligibility. American journal of speech-language pathology 32 (1) (2022)
Danielle A Baribeau, Ny Hoang, Thanuja Selvanayagam, D James Stavropoulos, Gregory Costain, Stephen W Scherer, Jacob A S Vorstman
Developmental implications of genetic testing for physical indications. European journal of human genetics : EJHG 30 (11) (2022)
Emma Everaert, Iris Selten, Tessel Boerma, Michiel Houben, Jacob A S Vorstman, Hester de Wilde, Desiree Derksen, Sarah Haverkamp, Frank N K Wijnen, Ellen Gerrits
The Language Profile of Preschool Children With 22q11.2 Deletion Syndrome and the Relationship With Speech Intelligibility. American journal of speech-language pathology (2022)
Raj R Jagesar, Jacob A S Vorstman, Martien J H Kas
Requirements and Operational Guidelines for Secure and Sustainable Digital Phenotyping: Design and Development Study. Journal of medical Internet research 23 (4) (2021)
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, Alana Iaboni, Kristina Calli, Delnaz Roshandel, Iva Pritišanac, Alan Moses, Julie D Forman-Kay, Brett Trost, Mehdi Zarrei, Olivia Rennie, Lynette Y S Lau, Christian R Marshall, Siddharth Srivastava, Brianna Godlewski, Elizabeth D Buttermore, Mustafa Sahin, Dean Hartley, Thomas Frazier, Jacob A S Vorstman, Stelios Georgiades, Suzanne M E Lewis, Peter Szatmari, Clarrisa A Lisa Bradley, Anne-Claude Tabet, Marjolaine Willems, Serge Lumbroso, Amélie Piton, James Lespinasse, Richard Delorme, Thomas Bourgeron, Evdokia Anagnostou, Stephen W Scherer
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder. NPJ genomic medicine 6 (1) (2021)
Niels Jongs, Raj Jagesar, Neeltje E M van Haren, Brenda W J H Penninx, Lianne Reus, Pieter Jelle Visser, Nic J A van der Wee, Ina M Koning, Celso Arango, Iris E C Sommer, Marinus J C Eijkemans, Jacob A S Vorstman, Martien J H Kas
A framework for assessing neuropsychiatric phenotypes by using smartphone-based location data. Translational psychiatry 10 (1) (2020)
Bochao Danae Lin, Fabrice Colas, Isaac J Nijman, Jelena Medic, William Brands, Jeremy R Parr, Kristel R van Eijk, Sabine M Klauck, Andreas G Chiocchetti, Christine Margarete Freitag, Elena Maestrini, Elena Bacchelli, Hilary Coon, Astrid M Vicente, Guiomar Oliveira, Alistair T Pagnamenta, Louise Gallagher, Sean Ennis, Richard Anney, Thomas Bourgeron, Jurjen J Luykx, Jacob A S Vorstman
The role of rare compound heterozygous events in autism spectrum disorder. Translational psychiatry 10 (1) (2020)
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, Tracy Heung, Aaron M Holleman, H Richard Johnston, Thomas Monfeuga, Donna M McDonald-McGinn, Raquel E Gur, Bernice E Morrow, Ann Swillen, Jacob A S Vorstman, Carrie E Bearden, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Stephen T Warren, Michael J Owen, Pankaj Chopra, David J Cutler, Richard Duncan, Alex V Kotlar, Jennifer G Mulle, Anna J Voss, Michael E Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I Salmons, Oanh Tran, Peter Holmans, Antonio F Pardinas, James T R Walters, Wolfram Demaerel, Erik Boot, Nancy J Butcher, Gregory A Costain, Chelsea Lowther, Rens Evers, Therese A M J van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koen Devriendt, Elfi Vergaelen, Annick Vogels, Terrence Blaine Crowley, Daniel E McGinn, Edward M Moss, Robert J Sharkus, Marta Unolt, Elaine H Zackai, Monica E Calkins, Robert S Gallagher, Ruben C Gur, Sunny X Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M Repetto, Elemi Breetvelt, Sasja N Duijff, Ania M Fiksinski, Hayley Moss, Maria Niarchou, Kieran C Murphy, Sarah E Prasad, Eileen M Daly, Maria Gudbrandsen, Clodagh M Murphy, Declan G M Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria C Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F Cubells, Opal Y Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori-Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider, Frédérique Sloan Béna, Kevin M Antshel, Wanda Fremont, Wendy R Kates, Raoul Belzeaux, Tiffany Busa, Nicole Philip, Linda E Campbell, Kathryn L McCabe, Stephen R Hooper, Kelly Schoch, Vandana Shashi, Tony J Simon, Flora Tassone, Celso Arango, David Fraguas, Sixto García-Miñaúr, Jaume Morey-Canyelles, Jordi Rosell, Damià H Suñer, Jasna Raventos-Simic, null null, Michael P Epstein, Nigel M Williams, Anne S Bassett
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion. Molecular psychiatry 26 (8) (2020)
Robert William Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne Susan Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow, Donna M McDonald-McGinn, Ann Swillen, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Therese van Amelsvoort, Celso Arango, Marco Armando, Linda E Campbell, Joseph F Cubells, Stephan Eliez, Sixto Garcia-Minaur, Doron Gothelf, Wendy R Kates, Kieran C Murphy, Clodagh M Murphy, Declan G M Murphy, Nicole Philip, Gabriela M Repetto, Vandana Shashi, Tony J Simon, Damiàn Heine Suñer, Stefano Vicari, Stephen W Scherer, null null, Carrie E Bearden, Jacob A S Vorstman
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature medicine 26 (12) (2020)
Christian Patrick Schaaf, Catalina Betancur, Ryan K C Yuen, Jeremy R Parr, David H Skuse, Louise Gallagher, Raphael A Bernier, Janet A Buchanan, Joseph D Buxbaum, Chun-An Chen, Kira A Dies, Mayada Elsabbagh, Helen V Firth, Thomas Frazier, Ny Hoang, Jennifer Howe, Christian R Marshall, Jacques L Michaud, Olivia Rennie, Peter Szatmari, Wendy K Chung, Patrick F Bolton, Edwin H Cook, Stephen W Scherer, Jacob A S Vorstman
A framework for an evidence-based gene list relevant to autism spectrum disorder. Nature reviews. Genetics 21 (6) (2020)

Jacob A S Vorstman.css-eqlu8i{font-size:small;padding-left:4px;} (Jacob Vorstman, Jacob A Vorstman)

Publication Activity (10 Years)

Top Topics

Top Venues

Jacob A S Vorstman (Jacob Vorstman, Jacob A Vorstman)