| InterVar: clinical interpretation of genetic variants by the 2015 ACMG-AMP guidelines Q Li, K Wang The American Journal of Human Genetics 100 (2), 267-280, 2017 | 860 | 2017 |
| Understanding type 1 diabetes through genetics: advances and prospects C Polychronakos, Q Li Nature Reviews Genetics 12 (11), 781-792, 2011 | 299 | 2011 |
| The definition of insulin resistance using HOMA-IR for Americans of Mexican descent using machine learning HQ Qu, Q Li, AR Rentfro, SP Fisher-Hoch, JB McCormick PloS one 6 (6), e21041, 2011 | 297 | 2011 |
| Long-read sequencing and de novo assembly of a Chinese genome L Shi, Y Guo, C Dong, J Huddleston, H Yang, X Han, A Fu, Q Li, N Li, ... Nature communications 7 (1), 12065, 2016 | 285 | 2016 |
| Organoid cultures as preclinical models of non–small cell lung cancer R Shi, N Radulovich, C Ng, N Liu, H Notsuda, M Cabanero, ... Clinical Cancer Research 26 (5), 1162-1174, 2020 | 196 | 2020 |
| Genetic variability of human angiotensin‐converting enzyme 2 (hACE2) among various ethnic populations Q Li, Z Cao, P Rahman Molecular genetics & genomic medicine 8 (8), e1344, 2020 | 70 | 2020 |
| Adiponectin/leptin ratio and metabolic syndrome in a Mexican American population S Mirza, HQ Qu, Q Li, PJ Martinez, AR Rentfro, JB McCormick, ... Clinical and investigative medicine 34 (5), E290-E297, 2011 | 70 | 2011 |
| PNPLA3 polymorphisms and liver aminotransferase levels in a Mexican American population Q Li, HQ Qu, AR Rentfro, ML Grove, S Mirza, Y Lu, CL Hanis, MB Fallon, ... Clinical and Investigative Medicine 35 (4), E237-E245, 2012 | 46 | 2012 |
| Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants MM He, Q Li, M Yan, H Cao, Y Hu, KY He, K Cao, MM Li, K Wang Genome medicine 11, 1-14, 2019 | 43 | 2019 |
| Characterization of distinct populations of carcinoma-associated fibroblasts from non–small cell lung carcinoma reveals a role for ST8SIA2 in cancer cell invasion J Hao, C Zeltz, M Pintilie, Q Li, S Sakashita, T Wang, M Cabanero, ... Neoplasia 21 (5), 482-493, 2019 | 40 | 2019 |
| BRAF V600E mutation and MET amplification as resistance pathways of the second-generation anaplastic lymphoma kinase (ALK) inhibitor alectinib in lung cancer R Shi, SN Martins Filho, M Li, A Fares, J Weiss, NA Pham, O Ludkovski, ... Lung Cancer 146, 78-85, 2020 | 30 | 2020 |
| Gene-specific function prediction for non-synonymous mutations in monogenic diabetes genes Q Li, X Liu, RA Gibbs, E Boerwinkle, C Polychronakos, HQ Qu PLoS One 9 (8), e104452, 2014 | 30 | 2014 |
| Quantifying differences in heritability among psoriatic arthritis (PsA), cutaneous psoriasis (PsC) and psoriasis vulgaris (PsV) Q Li, V Chandran, L Tsoi, D O’Rielly, RP Nair, D Gladman, JT Elder, ... Scientific reports 10 (1), 4925, 2020 | 29 | 2020 |
| Fragment‐based local statistical potentials derived by combining an alphabet of protein local structures with secondary structures and solvent accessibilities Q Li, C Zhou, H Liu Proteins: Structure, Function, and Bioinformatics 74 (4), 820-836, 2009 | 29 | 2009 |
| Missense variants in TAF1 and developmental phenotypes: Challenges of determining pathogenicity H Cheng, S Capponi, E Wakeling, E Marchi, Q Li, M Zhao, C Weng, ... Human mutation 41 (2), 449-464, 2020 | 26 | 2020 |
| Ancestral effect on HOMA-IR levels quantitated in an American population of Mexican origin HQ Qu, Q Li, Y Lu, CL Hanis, SP Fisher-Hoch, JB McCormick Diabetes care 35 (12), 2591-2593, 2012 | 26 | 2012 |
| Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies distinct proteotypes associated with patient outcomes S Mirhadi, S Tam, Q Li, N Moghal, NA Pham, J Tong, BJ Golbourn, ... Nature communications 13 (1), 1811, 2022 | 24 | 2022 |
| Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome GJ Lyon, M Vedaie, T Beisheim, A Park, E Marchi, L Gottlieb, TC Hsieh, ... European Journal of Human Genetics 31 (7), 824-833, 2023 | 23 | 2023 |
| CancerVar: An artificial intelligence–empowered platform for clinical interpretation of somatic mutations in cancer Q Li, Z Ren, K Cao, MM Li, K Wang, Y Zhou Science Advances 8 (18), 13, 2022 | 22 | 2022 |
| A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect JA Pater, T Benteau, A Griffin, C Penney, SG Stanton, S Predham, ... Human Genetics 136 (1), 107-118, 2017 | 22 | 2017 |
Kai WangChildren's Hospital of Philadelphia在 email.chop.edu 的电子邮件经过验证
