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Translational Psychiatry
|
February 25, 2023
Comorbidities in autism spectrum disorder and their etiologies
Vahe Khachadourian, Behrang Mahjani, Sven Sandin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 18, 2026
Directional genetic relationships between obsessive-compulsive disorder and bipolar disorder and schizophrenia
Maria Niarchou, Marina Natividad Avila, Behrang Mahjani, et al.
Behavioural Brain Research
|
May 10, 2008
Increased locomotor activity in mice lacking the low-density lipoprotein receptor
Gregory A Elder, Andre Ragnauth, Nathan Dorr, et al.
Biorxiv : the Preprint Server for Biology
|
August 8, 2025
A framework to infer <i>de novo</i> exonic variants when parental genotypes are missing enhances association studies of autism
Haeun Moon, Laura Sloofman, Marina Natividad Avila, et al.
American Journal of Human Genetics
|
November 6, 2020
Not All Autism Genes Are Created Equal: A Response to Myers et al
Joseph D Buxbaum, David J Cutler, Mark J Daly, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
February 18, 2011
Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions
Takeshi Sakurai, Nathan P Dorr, Nagahide Takahashi, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
July 27, 2021
Reduced brain volume and white matter alterations in Shank3-deficient rats
Carla E M Golden, Victoria X Wang, Hala Harony-Nicolas, et al.
Journal of Neurochemistry
|
June 22, 2006
Calsenilin interacts with transcriptional co-repressor C-terminal binding protein(s)
Nikhat F Zaidi, Kristy G Kuplast, Kevin J Washicosky, et al.
Frontiers in Psychiatry
|
March 11, 2025
Adolescents and adults with FOXP1 syndrome show high rates of anxiety and externalizing behaviors but not psychiatric decompensation or skill loss
Tess Levy, Hailey Silver, Renee Soufer, et al.
Bioinformatics (Oxford, England)
|
May 4, 2026
A framework to infer de novo exonic variants when parental genotypes are missing enhances association studies of autism
Haeun Moon, Laura Sloofman, Marina Natividad Avila, et al.
Page
of 38
Search research articles
Search
Showing results (71-80 of 375) with videos related to
Sort By:
Page
of 38
Translational Psychiatry
|
February 25, 2023
Comorbidities in autism spectrum disorder and their etiologies
Vahe Khachadourian, Behrang Mahjani, Sven Sandin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 18, 2026
Directional genetic relationships between obsessive-compulsive disorder and bipolar disorder and schizophrenia
Maria Niarchou, Marina Natividad Avila, Behrang Mahjani, et al.
Behavioural Brain Research
|
May 10, 2008
Increased locomotor activity in mice lacking the low-density lipoprotein receptor
Gregory A Elder, Andre Ragnauth, Nathan Dorr, et al.
Biorxiv : the Preprint Server for Biology
|
August 8, 2025
A framework to infer <i>de novo</i> exonic variants when parental genotypes are missing enhances association studies of autism
Haeun Moon, Laura Sloofman, Marina Natividad Avila, et al.
American Journal of Human Genetics
|
November 6, 2020
Not All Autism Genes Are Created Equal: A Response to Myers et al
Joseph D Buxbaum, David J Cutler, Mark J Daly, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
February 18, 2011
Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions
Takeshi Sakurai, Nathan P Dorr, Nagahide Takahashi, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
July 27, 2021
Reduced brain volume and white matter alterations in Shank3-deficient rats
Carla E M Golden, Victoria X Wang, Hala Harony-Nicolas, et al.
Journal of Neurochemistry
|
June 22, 2006
Calsenilin interacts with transcriptional co-repressor C-terminal binding protein(s)
Nikhat F Zaidi, Kristy G Kuplast, Kevin J Washicosky, et al.
Frontiers in Psychiatry
|
March 11, 2025
Adolescents and adults with FOXP1 syndrome show high rates of anxiety and externalizing behaviors but not psychiatric decompensation or skill loss
Tess Levy, Hailey Silver, Renee Soufer, et al.
Bioinformatics (Oxford, England)
|
May 4, 2026
A framework to infer de novo exonic variants when parental genotypes are missing enhances association studies of autism
Haeun Moon, Laura Sloofman, Marina Natividad Avila, et al.
Page
of 38