Search research articles
Contact Us
Filters
Showing results (11-20 of 33) with videos related to
Page
of 4
Sort By:
G3 (Bethesda, Md.)
|
June 8, 2022
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomics
Si Lok, Timothy N H Lau, Brett Trost, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire
|
March 14, 2018
Copy number variation in fetal alcohol spectrum disorder
Mehdi Zarrei, Geoffrey G Hicks, James N Reynolds, et al.
Nature Genetics
|
April 27, 2004
Functional variants of OCTN cation transporter genes are associated with Crohn disease
Vanya D Peltekova, Richard F Wintle, Laurence A Rubin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 25, 2023
Clinical actionability of genetic findings in cerebral palsy
Sara A Lewis, Maya Chopra, Julie S Cohen, et al.
Arthritis and Rheumatism
|
June 30, 2005
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations
Mark van Oene, Richard F Wintle, Xiangdong Liu, et al.
JAMA Pediatrics
|
December 2, 2024
Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-Analysis
Sara A Lewis, Maya Chopra, Julie S Cohen, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
The EMBO Journal
|
January 24, 2004
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans
Suparna Sanyal, Richard F Wintle, Katie S Kindt, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
G3 (Bethesda, Md.)
|
June 8, 2022
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomics
Si Lok, Timothy N H Lau, Brett Trost, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue Program
Richard F Wintle, Anath C Lionel, Pingzhao Hu, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire
|
March 14, 2018
Copy number variation in fetal alcohol spectrum disorder
Mehdi Zarrei, Geoffrey G Hicks, James N Reynolds, et al.
Nature Genetics
|
April 27, 2004
Functional variants of OCTN cation transporter genes are associated with Crohn disease
Vanya D Peltekova, Richard F Wintle, Laurence A Rubin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 25, 2023
Clinical actionability of genetic findings in cerebral palsy
Sara A Lewis, Maya Chopra, Julie S Cohen, et al.
Arthritis and Rheumatism
|
June 30, 2005
Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations
Mark van Oene, Richard F Wintle, Xiangdong Liu, et al.
JAMA Pediatrics
|
December 2, 2024
Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-Analysis
Sara A Lewis, Maya Chopra, Julie S Cohen, et al.
Nature Communications
|
August 4, 2015
Clinically relevant copy number variations detected in cerebral palsy
Maryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
The EMBO Journal
|
January 24, 2004
Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans
Suparna Sanyal, Richard F Wintle, Katie S Kindt, et al.
BMC Genomics
|
April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome
Christian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Page
of 4