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Sleep|February 13, 2025
Big data approaches for novel mechanistic insights on sleep and circadian rhythms: a workshop summaryLawrence Baizer, Regina Bures, Girish Nadkarni, et al.Science Translational Medicine|January 14, 2021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severityXiangchen Gu, Hongliu Yang, Xin Sheng, et al.Journal of the American College of Cardiology|June 6, 2020
Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery DiseaseKrishna G Aragam, Amanda Dobbyn, Renae Judy, et al.JAMA|December 11, 2019
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryScott M Damrauer, Kumardeep Chaudhary, Judy H Cho, et al.Epilepsia|July 15, 2023
In-hospital outcomes in patients with and without epilepsy diagnosed with COVID-19-A cohort studyClaire Ufongene, Grace Van Hyfte, Parul Agarwal, et al.Nature Communications|April 20, 2023
Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patientsYiming Wu, Kyle Gettler, Meltem Ece Kars, et al.Medrxiv : the Preprint Server for Health Sciences|October 13, 2021
Acute COVID-19 gene-expression profiles show multiple etiologies of long-term sequelaeRyan C Thompson, Nicole W Simons, Lillian Wilkins, et al.Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.Nature Medicine|December 9, 2022
Molecular states during acute COVID-19 reveal distinct etiologies of long-term sequelaeRyan C Thompson, Nicole W Simons, Lillian Wilkins, et al.Pageof 11