| Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase A Ramirez, A Heimbach, J Gründemann, B Stiller, D Hampshire, LP Cid, ... Nature genetics 38 (10), 1184-1191, 2006 | 1480 | 2006 |
| Bystander CD8+ T cells are abundant and phenotypically distinct in human tumour infiltrates Y Simoni, E Becht, M Fehlings, CY Loh, SL Koo, KWW Teng, JPS Yeong, ... Nature 557 (7706), 575-579, 2018 | 1211 | 2018 |
| Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors H Li, ET Courtois, D Sengupta, Y Tan, KH Chen, JJL Goh, SL Kong, ... Nature genetics 49 (5), 708-718, 2017 | 1014 | 2017 |
| Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes ZJ Zang, I Cutcutache, SL Poon, SL Zhang, JR McPherson, J Tao, ... Nature genetics 44 (5), 570-574, 2012 | 712 | 2012 |
| A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer KP Ng, AM Hillmer, CTH Chuah, WC Juan, TK Ko, ASM Teo, ... Nature medicine 18 (4), 521-528, 2012 | 679 | 2012 |
| G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth SM Pasternack, I von Kügelgen, KA Aboud, YA Lee, F Rüschendorf, ... Nature genetics 40 (3), 329-334, 2008 | 476 | 2008 |
| Genomic landscape of lung adenocarcinoma in East Asians J Chen, H Yang, ASM Teo, LB Amer, FG Sherbaf, CQ Tan, JJS Alvarez, ... Nature genetics 52 (2), 177-186, 2020 | 367 | 2020 |
| Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia J Schumacher, H Anthoni, F Dahdouh, IR König, AM Hillmer, N Kluck, ... The American Journal of Human Genetics 78 (1), 52-62, 2006 | 366 | 2006 |
| Methionine is a metabolic dependency of tumor-initiating cells Z Wang, LY Yip, JHJ Lee, Z Wu, HY Chew, PKW Chong, CC Teo, ... Nature medicine 25 (5), 825-837, 2019 | 337 | 2019 |
| Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia AM Hillmer, S Hanneken, S Ritzmann, T Becker, J Freudenberg, ... The American Journal of Human Genetics 77 (1), 140-148, 2005 | 296 | 2005 |
| A genome-wide association study for late-onset Alzheimer's disease using DNA pooling R Abraham, V Moskvina, R Sims, P Hollingworth, A Morgan, L Georgieva, ... BMC medical genomics 1, 1-13, 2008 | 236 | 2008 |
| Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin E Levy-Nissenbaum, RC Betz, M Frydman, M Simon, H Lahat, T Bakhan, ... Nature genetics 34 (2), 151-153, 2003 | 221 | 2003 |
| A genome-wide association study in 574 schizophrenia trios using DNA pooling G Kirov, I Zaharieva, L Georgieva, V Moskvina, I Nikolov, S Cichon, ... Molecular psychiatry 14 (8), 796-803, 2009 | 220 | 2009 |
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| Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia S Cichon, M Anker, IR Vogt, H Rohleder, M Pützstück, A Hillmer, ... Human molecular genetics 7 (11), 1671-1679, 1998 | 202 | 1998 |
| Susceptibility variants for male-pattern baldness on chromosome 20p11 AM Hillmer, FF Brockschmidt, S Hanneken, S Eigelshoven, M Steffens, ... Nature genetics 40 (11), 1279-1281, 2008 | 186 | 2008 |
| Large-scale whole-genome sequencing of three diverse Asian populations in Singapore D Wu, J Dou, X Chai, C Bellis, A Wilm, CC Shih, WWJ Soon, N Bertin, ... Cell 179 (3), 736-749. e15, 2019 | 170 | 2019 |
| Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing R Nahar, W Zhai, T Zhang, A Takano, AJ Khng, YY Lee, X Liu, CH Lim, ... Nature communications 9 (1), 216, 2018 | 168 | 2018 |
| Recurrent fusion genes in gastric cancer: CLDN18-ARHGAP26 induces loss of epithelial integrity F Yao, JP Kausalya, YY Sia, ASM Teo, WH Lee, AGM Ong, Z Zhang, ... Cell reports 12 (2), 272-285, 2015 | 153 | 2015 |
| Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci T Aung, M Ozaki, MC Lee, U Schlötzer-Schrehardt, G Thorleifsson, ... Nature genetics 49 (7), 993-1004, 2017 | 150 | 2017 |
