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Human Molecular Genetics
|
May 24, 2018
Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich's ataxia patients
Daniel Nachun, Fuying Gao, Charles Isaacs, et al.
Genome Medicine
|
March 16, 2022
Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes
Michael J Gloudemans, Brunilda Balliu, Daniel Nachun, et al.
Brain, Behavior, & Immunity - Health
|
November 29, 2021
Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression
Amy Lin, Jennifer K Forsyth, Gil D Hoftman, et al.
Acta Neuropathologica Communications
|
November 30, 2022
Methylation differences in Alzheimer's disease neuropathologic change in the aged human brain
Anna-Lena Lang, Tiffany Eulalio, Eddie Fox, et al.
Biorxiv : the Preprint Server for Biology
|
March 3, 2025
Mapping the regulatory effects of common and rare non-coding variants across cellular and developmental contexts in the brain and heart
Andrew R Marderstein, Soumya Kundu, Evin M Padhi, et al.
European Heart Journal
|
January 17, 2024
Clonal haematopoiesis of indeterminate potential and atrial fibrillation: an east Asian cohort study
Hyo-Jeong Ahn, Hong Yul An, Gangpyo Ryu, et al.
Nature Communications
|
July 15, 2024
PRC2-AgeIndex as a universal biomarker of aging and rejuvenation
Mahdi Moqri, Andrea Cipriano, Daniel J Simpson, et al.
Nature Genetics
|
June 15, 2026
Decoding common and rare noncoding variant effects across cellular and developmental contexts
Andrew R Marderstein, Soumya Kundu, Evin M Padhi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Long-read genome sequencing and multi-omics in aging and neurodegeneration
Tanner D Jensen, Yann Le Guen, Lia Talozzi, et al.
Nature Cardiovascular Research
|
August 28, 2024
Loss-of-function mutations in Dnmt3a and Tet2 lead to accelerated atherosclerosis and concordant macrophage phenotypes
Philipp J Rauch, Jayakrishnan Gopakumar, Alexander J Silver, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Human Molecular Genetics
|
May 24, 2018
Peripheral blood gene expression reveals an inflammatory transcriptomic signature in Friedreich's ataxia patients
Daniel Nachun, Fuying Gao, Charles Isaacs, et al.
Genome Medicine
|
March 16, 2022
Integration of genetic colocalizations with physiological and pharmacological perturbations identifies cardiometabolic disease genes
Michael J Gloudemans, Brunilda Balliu, Daniel Nachun, et al.
Brain, Behavior, & Immunity - Health
|
November 29, 2021
Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression
Amy Lin, Jennifer K Forsyth, Gil D Hoftman, et al.
Acta Neuropathologica Communications
|
November 30, 2022
Methylation differences in Alzheimer's disease neuropathologic change in the aged human brain
Anna-Lena Lang, Tiffany Eulalio, Eddie Fox, et al.
Biorxiv : the Preprint Server for Biology
|
March 3, 2025
Mapping the regulatory effects of common and rare non-coding variants across cellular and developmental contexts in the brain and heart
Andrew R Marderstein, Soumya Kundu, Evin M Padhi, et al.
European Heart Journal
|
January 17, 2024
Clonal haematopoiesis of indeterminate potential and atrial fibrillation: an east Asian cohort study
Hyo-Jeong Ahn, Hong Yul An, Gangpyo Ryu, et al.
Nature Communications
|
July 15, 2024
PRC2-AgeIndex as a universal biomarker of aging and rejuvenation
Mahdi Moqri, Andrea Cipriano, Daniel J Simpson, et al.
Nature Genetics
|
June 15, 2026
Decoding common and rare noncoding variant effects across cellular and developmental contexts
Andrew R Marderstein, Soumya Kundu, Evin M Padhi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 24, 2025
Long-read genome sequencing and multi-omics in aging and neurodegeneration
Tanner D Jensen, Yann Le Guen, Lia Talozzi, et al.
Nature Cardiovascular Research
|
August 28, 2024
Loss-of-function mutations in Dnmt3a and Tet2 lead to accelerated atherosclerosis and concordant macrophage phenotypes
Philipp J Rauch, Jayakrishnan Gopakumar, Alexander J Silver, et al.
Page
of 3