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Bernie Devlin

Showing results (91-100 of 165) with videos related to

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American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
American Journal of Human Genetics|July 9, 2013
Intellectual disability is associated with increased runs of homozygosity in simplex autismEce D Gamsiz, Emma W Viscidi, Abbie M Frederick, et al.
Molecular Autism|October 7, 2021
How rare and common risk variation jointly affect liability for autism spectrum disorderLambertus Klei, Lora Lee McClain, Behrang Mahjani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
Heterogeneous association between engrailed-2 and autism in the CPEA networkCamille W Brune, Elena Korvatska, Kristina Allen-Brady, et al.
Human Molecular Genetics|November 30, 2007
A network of dopaminergic gene variations implicated as risk factors for schizophreniaMichael E Talkowski, George Kirov, Mikhil Bamne, et al.
Molecular Autism|October 7, 2021
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorderBehrang Mahjani, Silvia De Rubeis, Christina Gustavsson Mahjani, et al.
The International Journal of Eating Disorders|February 1, 2008
The genetics of anorexia nervosa collaborative study: methods and sample descriptionWalter H Kaye, Cynthia M Bulik, Katherine Plotnicov, et al.
Nature Communications|March 11, 2015
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopmentJustin Cotney, Rebecca A Muhle, Stephan J Sanders, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics|July 21, 2014
Most genetic risk for autism resides with common variationTrent Gaugler, Lambertus Klei, Stephan J Sanders, et al.
Pageof 17

Showing results (91-100 of 165) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|March 6, 2021
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 familiesJonathan R Belyeu, Harrison Brand, Harold Wang, et al.
American Journal of Human Genetics|July 9, 2013
Intellectual disability is associated with increased runs of homozygosity in simplex autismEce D Gamsiz, Emma W Viscidi, Abbie M Frederick, et al.
Molecular Autism|October 7, 2021
How rare and common risk variation jointly affect liability for autism spectrum disorderLambertus Klei, Lora Lee McClain, Behrang Mahjani, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
Heterogeneous association between engrailed-2 and autism in the CPEA networkCamille W Brune, Elena Korvatska, Kristina Allen-Brady, et al.
Human Molecular Genetics|November 30, 2007
A network of dopaminergic gene variations implicated as risk factors for schizophreniaMichael E Talkowski, George Kirov, Mikhil Bamne, et al.
Molecular Autism|October 7, 2021
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorderBehrang Mahjani, Silvia De Rubeis, Christina Gustavsson Mahjani, et al.
The International Journal of Eating Disorders|February 1, 2008
The genetics of anorexia nervosa collaborative study: methods and sample descriptionWalter H Kaye, Cynthia M Bulik, Katherine Plotnicov, et al.
Nature Communications|March 11, 2015
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopmentJustin Cotney, Rebecca A Muhle, Stephan J Sanders, et al.
Nature Genetics|February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samplesJack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Nature Genetics|July 21, 2014
Most genetic risk for autism resides with common variationTrent Gaugler, Lambertus Klei, Stephan J Sanders, et al.
Pageof 17