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Joseph Park, MD, PhD
Joseph Park, MD, PhD
New York Presbyterian - Weill Cornell
Verified email at nyp.org
Title
Cited by
Cited by
Year
Rapid upregulation and clearance of distinct circulating microRNAs after prolonged aerobic exercise
AL Baggish, J Park, PK Min, S Isaacs, BA Parker, PD Thompson, ...
Journal of applied physiology 116 (5), 522-531, 2014
2272014
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
M Vujkovic, S Ramdas, KM Lorenz, X Guo, R Darlay, HJ Cordell, J He, ...
Nature genetics 54 (6), 761-771, 2022
772022
Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease
H Liu, T Doke, D Guo, X Sheng, Z Ma, J Park, HMT Vy, GN Nadkarni, ...
Nature genetics 54 (7), 950-962, 2022
712022
Influence of statins on distinct circulating microRNAs during prolonged aerobic exercise
PK Min, J Park, S Isaacs, BA Taylor, PD Thompson, C Troyanos, ...
Journal of Applied Physiology 120 (6), 711-720, 2016
532016
Disrupting upstream translation in mRNAs is associated with human disease
DSM Lee, J Park, A Kromer, A Baras, DJ Rader, MD Ritchie, LR Ghanem, ...
Nature Communications 12 (1), 1515, 2021
492021
A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes
J Park, MG Levin, CM Haggerty, DN Hartzel, R Judy, RL Kember, N Reza, ...
Genetics in Medicine 22 (1), 102-111, 2020
452020
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations
J Park, AM Lucas, X Zhang, K Chaudhary, JH Cho, G Nadkarni, A Dobbyn, ...
Nature medicine 27 (1), 66-72, 2021
402021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severity
X Gu, H Yang, X Sheng, YA Ko, C Qiu, J Park, S Huang, R Kember, ...
Science translational medicine 13 (576), eaaz1458, 2021
352021
Whole genome sequence analysis of blood lipid levels in> 66,000 individuals
MS Selvaraj, X Li, Z Li, A Pampana, DY Zhang, J Park, S Aslibekyan, ...
Nature communications 13 (1), 5995, 2022
322022
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
G Hindy, P Dornbos, MD Chaffin, DJ Liu, M Wang, MS Selvaraj, D Zhang, ...
The American Journal of Human Genetics 109 (1), 81-96, 2022
262022
Endothelial lipase mediates efficient lipolysis of triglyceride-rich lipoproteins
SA Khetarpal, C Vitali, MG Levin, D Klarin, J Park, A Pampana, JS Millar, ...
PLoS genetics 17 (9), e1009802, 2021
252021
A genome-first approach to mortality and metabolic phenotypes in MTARC1 p. Ala165Thr (rs2642438) heterozygotes and homozygotes
CV Schneider, KM Schneider, DM Conlon, J Park, M Vujkovic, I Zandvakili, ...
Med 2 (7), 851-863. e3, 2021
242021
Brief report: coordinated modulation of circulating miR-21 in HIV, HIV-associated pulmonary arterial hypertension, and HIV/hepatitis C virus Coinfection
VN Parikh, J Park, I Nikolic, R Channick, BY Paul, T De Marco, PY Hsue, ...
JAIDS Journal of Acquired Immune Deficiency Syndromes 70 (3), 236-241, 2015
212015
Epidemiology of DYT1 dystonia: Estimating prevalence via genetic ascertainment
J Park, SM Damrauer, A Baras, JG Reid, JD Overton, P Gonzalez-Alegre
Neurology: Genetics 5 (5), e358, 2019
162019
A genome-wide association study for nonalcoholic fatty liver disease identifies novel genetic loci and trait-relevant candidate genes in the Million Veteran Program
M Vujkovic, S Ramdas, KM Lorenz, CV Schneider, J Park, KM Lee, ...
medRxiv, 2021
152021
A novel minimally-invasive method to sample human endothelial cells for molecular profiling
SW Waldo, DA Brenner, JM McCabe, M Dela Cruz, B Long, VA Narla, ...
PloS one 10 (2), e0118081, 2015
122015
Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection
C Zhang, A Verma, Y Feng, MCR Melo, M McQuillan, M Hansen, A Lucas, ...
Proceedings of the National Academy of Sciences 119 (21), 2022
82022
Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults
S Ahmadmehrabi, B Li, J Park, B Devkota, M Vujkovic, YA Ko, ...
Human Genetics 140, 957-967, 2021
62021
Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort
D Hui, S Mehrabi, AE Quimby, T Chen, S Chen, J Park, B Li, ...
PLoS Genetics 19 (1), e1010584, 2023
42023
A genome-first approach to rare variants in hypertrophic cardiomyopathy genes MYBPC3 and MYH7 in a medical biobank
J Park, EA Packard, MG Levin, RL Judy, Regeneron Genetics Center, ...
Human Molecular Genetics 31 (5), 827-837, 2022
42022
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Articles 1–20