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Journal of Personalized Medicine
|
December 23, 2022
The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population
Anurag Verma, Scott M Damrauer, Nawar Naseer, et al.
Nature Communications
|
June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders
Xinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.
Nature Communications
|
April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
Anton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
JAMA Network Open
|
May 28, 2024
Progesterone for Neurodevelopment in Fetuses With Congenital Heart Defects: A Randomized Clinical Trial
J William Gaynor, Julie S Moldenhauer, Erin E Zullo, et al.
Blood
|
March 17, 2026
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia: Data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)
Hanny Al-Samkari, Cassi Friday, Raj S Kasthuri, et al.
Nature Medicine
|
January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations
Joseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
Atlas Khan, Poppy A Gould, Yiming Luo, et al.
European Journal of Human Genetics : EJHG
|
June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
Theodore G Drivas, Dong Li, Divya Nair, et al.
Science (New York, N.Y.)
|
February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants
Hongbo Liu, Amin Abedini, Eunji Ha, et al.
Science Advances
|
March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
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of 4
Search research articles
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Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 40 results.
Journal of Personalized Medicine
|
December 23, 2022
The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population
Anurag Verma, Scott M Damrauer, Nawar Naseer, et al.
Nature Communications
|
June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders
Xinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.
Nature Communications
|
April 1, 2025
A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations
Anton Safonov, Tomoki T Nomakuchi, Elizabeth Chao, et al.
JAMA Network Open
|
May 28, 2024
Progesterone for Neurodevelopment in Fetuses With Congenital Heart Defects: A Randomized Clinical Trial
J William Gaynor, Julie S Moldenhauer, Erin E Zullo, et al.
Blood
|
March 17, 2026
Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia: Data from the Comprehensive HHT Outcomes Registry of the US (CHORUS)
Hanny Al-Samkari, Cassi Friday, Raj S Kasthuri, et al.
Nature Medicine
|
January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations
Joseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 6, 2025
The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
Atlas Khan, Poppy A Gould, Yiming Luo, et al.
European Journal of Human Genetics : EJHG
|
June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
Theodore G Drivas, Dong Li, Divya Nair, et al.
Science (New York, N.Y.)
|
February 6, 2025
Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants
Hongbo Liu, Amin Abedini, Eunji Ha, et al.
Science Advances
|
March 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara, et al.
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of 4