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Medrxiv : the Preprint Server for Health Sciences
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November 26, 2025
APOL1 Monoallelic and Biallelic genotypes and CKD, Proteinuria and FSGS in African Americans from the Vanderbilt Biobank (BioVU)
Steven W Clapp, Jefferson L Triozzi, Zhihong Yu, et al.
Cell Genomics
|
April 21, 2023
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, et al.
Nature Communications
|
June 14, 2020
Functional annotation of rare structural variation in the human brain
Lide Han, Xuefang Zhao, Mary Lauren Benton, et al.
The American Journal of Psychiatry
|
May 15, 2024
Genome-Wide Association Study of Treatment-Resistant Depression: Shared Biology With Metabolic Traits
JooEun Kang, Victor M Castro, Michael Ripperger, et al.
Research Square
|
September 2, 2025
Persistent Tic Disorders Are Associated With 17q12 Duplications
Matthew Halvorsen, Sheng Wang, Tyne Miller-Fleming, et al.
The Journal of Allergy and Clinical Immunology
|
August 13, 2013
Genome-wide association study of lung function phenotypes in a founder population
Tsung-Chieh Yao, Gaixin Du, Lide Han, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2024
Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systems
Nick Strayer, Tess Vessels, Karmel Choi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcare
Cecile Avery, Mojgan Babanejad, James Baker, et al.
Cell
|
August 2, 2022
A cross-disorder dosage sensitivity map of the human genome
Ryan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
APOL1 Monoallelic and Biallelic genotypes and CKD, Proteinuria and FSGS in African Americans from the Vanderbilt Biobank (BioVU)
Steven W Clapp, Jefferson L Triozzi, Zhihong Yu, et al.
Cell Genomics
|
April 21, 2023
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
Calwing Liao, Mariana Moyses-Oliveira, Celine E F De Esch, et al.
Nature Communications
|
June 14, 2020
Functional annotation of rare structural variation in the human brain
Lide Han, Xuefang Zhao, Mary Lauren Benton, et al.
The American Journal of Psychiatry
|
May 15, 2024
Genome-Wide Association Study of Treatment-Resistant Depression: Shared Biology With Metabolic Traits
JooEun Kang, Victor M Castro, Michael Ripperger, et al.
Research Square
|
September 2, 2025
Persistent Tic Disorders Are Associated With 17q12 Duplications
Matthew Halvorsen, Sheng Wang, Tyne Miller-Fleming, et al.
The Journal of Allergy and Clinical Immunology
|
August 13, 2013
Genome-wide association study of lung function phenotypes in a founder population
Tsung-Chieh Yao, Gaixin Du, Lide Han, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 8, 2024
Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systems
Nick Strayer, Tess Vessels, Karmel Choi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Genome sequencing of 35,024 predominantly African ancestry persons addresses gaps in genomics and healthcare
Cecile Avery, Mojgan Babanejad, James Baker, et al.
Cell
|
August 2, 2022
A cross-disorder dosage sensitivity map of the human genome
Ryan L Collins, Joseph T Glessner, Eleonora Porcu, et al.
Page
of 4