| Inherited causes of clonal haematopoiesis in 97,691 whole genomes AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ... Nature 586 (7831), 763-768, 2020 | 474 | 2020 |
| GATES: a rapid and powerful gene-based association test using extended Simes procedure MX Li, HS Gui, JSH Kwan, PC Sham The American Journal of Human Genetics 88 (3), 283-293, 2011 | 436 | 2011 |
| Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases PCS HC So, AHS Gui, SS Cherny genetic epidemiology 35 (5), 310-317, 2011 | 318 | 2011 |
| A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases MX Li, HS Gui, JSH Kwan, SY Bao, PC Sham Nucleic acids research 40 (7), e53-e53, 2012 | 285 | 2012 |
| Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies Nature communications 9 (1), 5269, 2018 | 246 | 2018 |
| Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies RJL Anney, A Avbersek, D Balding, L Baum, F Becker, SF Berkovic, ... The Lancet Neurology, 2014 | 171 | 2014 |
| Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis J Waage, M Standl, JA Curtin, LE Jessen, J Thorsen, C Tian, N Schoettler, ... Nature genetics 50 (8), 1072-1080, 2018 | 134 | 2018 |
| Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function AB Wyss, T Sofer, MK Lee, N Terzikhan, JN Nguyen, L Lahousse, ... Nature communications 9 (1), 2976, 2018 | 99 | 2018 |
| Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes H Gui, D Schriemer, WW Cheng, RK Chauhan, G Antiňolo, C Berrios, ... Genome biology 18, 1-13, 2017 | 84 | 2017 |
| Correction of Hirschsprung-associated mutations in human induced pluripotent stem cells via clustered regularly interspaced short palindromic repeats/Cas9, restores neural … FPL Lai, ST Lau, JKL Wong, H Gui, RX Wang, T Zhou, WH Lai, HF Tse, ... Gastroenterology 153 (1), 139-153. e8, 2017 | 84 | 2017 |
| Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset H Gui, M Li, PC Sham, SS Cherny BMC research notes 4, 1-9, 2011 | 80 | 2011 |
| Identification of GLI mutations in patients with Hirschsprung disease that disrupt enteric nervous system development in mice JAJ Liu, FPL Lai, HS Gui, MH Sham, PKH Tam, MM Garcia-Barcelo, ... Gastroenterology 149 (7), 1837-1848. e5, 2015 | 57 | 2015 |
| RET and NRG1 interplay in Hirschsprung disease H Gui, WK Tang, MT So, P Proitsi, PC Sham, PK Tam, E Sau-Wai Ngan, ... Human genetics 132, 591-600, 2013 | 56 | 2013 |
| Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction F Guan, T Ni, W Zhu, LK Williams, LB Cui, M Li, J Tubbs, PC Sham, H Gui Molecular psychiatry 27 (1), 113-126, 2022 | 53 | 2022 |
| A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits Y Guo, B Tomlinson, T Chu, YJ Fang, H Gui, CS Tang, BH Yip, SS Cherny, ... PloS one 7 (2), e31489, 2012 | 49 | 2012 |
| Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients M McCormack, H Gui, A Ingason, D Speed, GEB Wright, EJ Zhang, ... Neurology 90 (4), e332-e341, 2018 | 47 | 2018 |
| Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet P Basil, Q Li, H Gui, TCK Hui, VHM Ling, CCY Wong, J Mill, GM McAlonan, ... Translational psychiatry 8 (1), 125, 2018 | 45 | 2018 |
| Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed MA Taub, MP Conomos, R Keener, KR Iyer, JS Weinstock, LR Yanek, ... Cell Genomics 2 (1), 2022 | 44 | 2022 |
| Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease CS Tang, H Gui, A Kapoor, JH Kim, B Luzón-Toro, A Pelet, G Burzynski, ... Human molecular genetics 25 (23), 5265-5275, 2016 | 44 | 2016 |
| Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease B Luzón-Toro, H Gui, M Ruiz-Ferrer, C Sze-Man Tang, RM Fernández, ... Scientific reports 5 (1), 16473, 2015 | 35 | 2015 |
Pak ShamDepartment of Psychiatry, The University of Hong Kong在 hku.hk 的电子邮件经过验证
