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The Journal of Allergy and Clinical Immunology
|
September 2, 2008
ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry
Patrick M A Sleiman, Kiran Annaiah, Marcin Imielinski, et al.
Nature
|
July 17, 2007
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakon Hakonarson, Struan F A Grant, Jonathan P Bradfield, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 14, 2023
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study
Patrick M Sleiman, Hui-Qi Qu, John J Connolly, et al.
Nature Genetics
|
May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
Mario Capasso, Marcella Devoto, Cuiping Hou, et al.
Cell Reports
|
November 14, 2023
The molecular genetic landscape of human brain size variation
Jakob Seidlitz, Travis T Mallard, Jacob W Vogel, et al.
The New England Journal of Medicine
|
May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
John M Maris, Yael P Mosse, Jonathan P Bradfield, et al.
Circulation Research
|
September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data
Joseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis
Jin Li, Yun R Li, Joseph T Glessner, et al.
Nature
|
June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastoma
Sharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophrenia
Joseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
Page
of 13
Search research articles
Search
Showing results (81-90 of 124) with videos related to
Sort By:
Page
of 13
The Journal of Allergy and Clinical Immunology
|
September 2, 2008
ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry
Patrick M A Sleiman, Kiran Annaiah, Marcin Imielinski, et al.
Nature
|
July 17, 2007
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Hakon Hakonarson, Struan F A Grant, Jonathan P Bradfield, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
July 14, 2023
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium study
Patrick M Sleiman, Hui-Qi Qu, John J Connolly, et al.
Nature Genetics
|
May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
Mario Capasso, Marcella Devoto, Cuiping Hou, et al.
Cell Reports
|
November 14, 2023
The molecular genetic landscape of human brain size variation
Jakob Seidlitz, Travis T Mallard, Jacob W Vogel, et al.
The New England Journal of Medicine
|
May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma
John M Maris, Yael P Mosse, Jonathan P Bradfield, et al.
Circulation Research
|
September 11, 2014
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data
Joseph T Glessner, Alexander G Bick, Kaoru Ito, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
March 29, 2022
Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis
Jin Li, Yun R Li, Joseph T Glessner, et al.
Nature
|
June 19, 2009
Copy number variation at 1q21.1 associated with neuroblastoma
Sharon J Diskin, Cuiping Hou, Joseph T Glessner, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophrenia
Joseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
Page
of 13