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First glimpses of the neurobiology of autism spectrum disorder
First glimpses of the neurobiology of autism spectrum disorder
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First glimpses of the neurobiology of autism spectrum disorder

Sanders, Stephan J

Current opinion in genetics & development, 2015-08, Vol.33, p.80-92 [Periódico revisado por pares]

England: Elsevier Ltd

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2
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
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Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families

Leppa, Virpi M. ; Kravitz, Stephanie N. ; Martin, Christa Lese ; Andrieux, Joris ; Le Caignec, Cedric ; Martin-Coignard, Dominique ; DyBuncio, Christina ; Sanders, Stephan J. ; Lowe, Jennifer K. ; Cantor, Rita M. ; Geschwind, Daniel H.

American journal of human genetics, 2016-09, Vol.99 (3), p.540-554 [Periódico revisado por pares]

United States: Elsevier Inc

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3
The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex
The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex
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The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex

Spratt, Perry W.E. ; Ben-Shalom, Roy ; Keeshen, Caroline M. ; Burke, Kenneth J. ; Clarkson, Rebecca L. ; Sanders, Stephan J. ; Bender, Kevin J.

Neuron (Cambridge, Mass.), 2019-08, Vol.103 (4), p.673-685.e5 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
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Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

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

Nature genetics, 2017-04, Vol.49 (4), p.504-510 [Periódico revisado por pares]

United States: Nature Publishing Group

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5
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Robinson, Elise B ; St Pourcain, Beate ; Anttila, Verneri ; Kosmicki, Jack A ; Bulik-Sullivan, Brendan ; Grove, Jakob ; Maller, Julian ; Samocha, Kaitlin E ; Sanders, Stephan J ; Ripke, Stephan ; Martin, Joanna ; Hollegaard, Mads V ; Werge, Thomas ; Hougaard, David M ; Neale, Benjamin M ; Evans, David M ; Skuse, David ; Mortensen, Preben Bo ; Børglum, Anders D ; Ronald, Angelica ; Smith, George Davey ; Daly, Mark J

Nature genetics, 2016-05, Vol.48 (5), p.552-555 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
A framework for the interpretation of de novo mutation in human disease
A framework for the interpretation of de novo mutation in human disease
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A framework for the interpretation of de novo mutation in human disease

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

Nature genetics, 2014-09, Vol.46 (9), p.944-950 [Periódico revisado por pares]

United States: Nature Publishing Group

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7
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
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The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

Cotney, Justin ; Muhle, Rebecca A ; Sanders, Stephan J ; Liu, Li ; Willsey, A Jeremy ; Niu, Wei ; Liu, Wenzhong ; Klei, Lambertus ; Lei, Jing ; Yin, Jun ; Reilly, Steven K ; Tebbenkamp, Andrew T ; Bichsel, Candace ; Pletikos, Mihovil ; Sestan, Nenad ; Roeder, Kathryn ; State, Matthew W ; Devlin, Bernie ; Noonan, James P

Nature communications, 2015-03, Vol.6 (1), p.6404-6404, Article 6404 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism
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Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

Willsey, A. Jeremy ; Sanders, Stephan J. ; Li, Mingfeng ; Dong, Shan ; Tebbenkamp, Andrew T. ; Muhle, Rebecca A. ; Reilly, Steven K. ; Lin, Leon ; Fertuzinhos, Sofia ; Miller, Jeremy A. ; Murtha, Michael T. ; Bichsel, Candace ; Niu, Wei ; Cotney, Justin ; Ercan-Sencicek, A. Gulhan ; Gockley, Jake ; Gupta, Abha R. ; Han, Wenqi ; He, Xin ; Hoffman, Ellen J. ; Klei, Lambertus ; Lei, Jing ; Liu, Wenzhong ; Liu, Li ; Lu, Cong ; Xu, Xuming ; Zhu, Ying ; Mane, Shrikant M. ; Lein, Ed S. ; Wei, Liping ; Noonan, James P. ; Roeder, Kathryn ; Devlin, Bernie ; Sestan, Nenad ; State, Matthew W.

Cell, 2013-11, Vol.155 (5), p.997-1007 [Periódico revisado por pares]

United States: Elsevier Inc

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9
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
A Chromatin Accessibility Atlas of the Developing Human Telencephalon
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A Chromatin Accessibility Atlas of the Developing Human Telencephalon

Markenscoff-Papadimitriou, Eirene ; Whalen, Sean ; Przytycki, Pawel ; Thomas, Reuben ; Binyameen, Fadya ; Nowakowski, Tomasz J. ; Kriegstein, Arnold R. ; Sanders, Stephan J. ; State, Matthew W. ; Pollard, Katherine S. ; Rubenstein, John L.

Cell, 2020-08, Vol.182 (3), p.754-769.e18 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority
Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority
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Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority

Halladay, Alycia K ; Bishop, Somer ; Constantino, John N ; Daniels, Amy M ; Koenig, Katheen ; Palmer, Kate ; Messinger, Daniel ; Pelphrey, Kevin ; Sanders, Stephan J ; Singer, Alison Tepper ; Taylor, Julie Lounds ; Szatmari, Peter

Molecular autism, 2015-06, Vol.6 (1), p.36-36, Article 36 [Periódico revisado por pares]

England: BioMed Central Ltd

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