| 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 | 243 | 2014 |
| 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 | 127 | 2022 |
| 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 | 120 | 2022 |
| 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 | 64 | 2021 |
| 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 | 58 | 2016 |
| 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 | 55 | 2020 |
| 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 | 48 | 2021 |
| 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 | 47 | 2022 |
| 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 | 41 | 2021 |
| 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 | 36 | 2021 |
| 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 | 33 | 2022 |
| 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 | 31 | 2021 |
| 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 | 20 | 2019 |
| 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 | 20 | 2015 |
| 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 | 16 | 2021 |
| 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 | 13 | 2022 |
| 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 | 12 | 2022 |
| 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 | 12 | 2015 |
| Regeneron Genetics Center; Ritchie, MD; Owens, AT; et al. A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record … J Park, MG Levin, CM Haggerty, DN Hartzel, R Judy, RL Kember, N Reza Genet. Med 22, 102-111, 2020 | 10 | 2020 |
| Large-scale identification of undiagnosed hepatic steatosis using natural language processing CV Schneider, T Li, D Zhang, AI Mezina, P Rattan, H Huang, KT Creasy, ... EClinicalMedicine 62, 2023 | 8 | 2023 |
Marylyn D RitchieUniversity of Pennsylvaniaupenn.edu의 이메일 확인됨