| The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups C Curtis, SP Shah, SF Chin, G Turashvili, OM Rueda, MJ Dunning, ... Nature 486 (7403), 346-352, 2012 | 5995 | 2012 |
| FinnGen provides genetic insights from a well-phenotyped isolated population MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ... Nature 613 (7944), 508-518, 2023 | 985 | 2023 |
| POT1 loss-of-function variants predispose to familial melanoma CD Robles-Espinoza, M Harland, AJ Ramsay, LG Aoude, V Quesada, ... Nature genetics 46 (5), 478-481, 2014 | 426 | 2014 |
| FinnGen: Unique genetic insights from combining isolated population and national health register data MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ... MedRxiv, 2022.03. 03.22271360, 2022 | 371 | 2022 |
| Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer EP Murchison, OB Schulz-Trieglaff, Z Ning, LB Alexandrov, MJ Bauer, ... Cell 148 (4), 780-791, 2012 | 362 | 2012 |
| Estimating telomere length from whole genome sequence data Z Ding, M Mangino, A Aviv, UK10K Consortium, T Spector, R Durbin Nucleic acids research 42 (9), e75-e75, 2014 | 199 | 2014 |
| Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association Z Ding, Y Ni, SW Timmer, BK Lee, A Battenhouse, S Louzada, F Yang, ... PLoS genetics 10 (11), e1004798, 2014 | 80 | 2014 |
| Germline TERT promoter mutations are rare in familial melanoma M Harland, M Petljak, CD Robles-Espinoza, Z Ding, NA Gruis, ... Familial cancer 15, 139-144, 2016 | 77 | 2016 |
| Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes GJ Maher, HK Ralph, Z Ding, N Koelling, H Mlcochova, E Giannoulatou, ... Genome research 28 (12), 1779-1790, 2018 | 62 | 2018 |
| Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germline E Giannoulatou, GJ Maher, Z Ding, AJM Gillis, LCJ Dorssers, A Hoischen, ... PLoS One 12 (5), e0178169, 2017 | 36 | 2017 |
| Genetic risk factors associated with preeclampsia and hypertensive disorders of pregnancy JS Tyrmi, T Kaartokallio, AI Lokki, T Jääskeläinen, E Kortelainen, ... JAMA cardiology 8 (7), 674-683, 2023 | 28 | 2023 |
| FinnGen: Unique genetic insights from combining isolated population and national health register data. medRxiv 2022 MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ... Google Scholar, 0 | 26 | |
| Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ... Nature 615 (7952), E19-E19, 2023 | 17 | 2023 |
| The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections SE Jones, FI Maisha, SJ Strausz, V Lammi, BE Cade, A Tervi, ... EBioMedicine 93, 2023 | 12 | 2023 |
| Pathway-based factor analysis of gene expression data produces highly heritable phenotypes that associate with age A Anand Brown, Z Ding, A Viñuela, D Glass, L Parts, T Spector, J Winn, ... G3: Genes, Genomes, Genetics 5 (5), 839-847, 2015 | 10 | 2015 |
| Comprehensive inherited risk estimation for risk-based breast cancer screening in women N Mars, S Kerminen, M Tamlander, M Pirinen, E Jakkula, K Aaltonen, ... Journal of Clinical Oncology, JCO. 23.00295, 2024 | 5 | 2024 |
| Assessing the landscape of selfish de novo mutations in human testes GJ Maher, HK Ralph, Z Ding, N Koelling, H Mlcochova, E Giannoulatou, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 825-825, 2019 | | 2019 |
| The Genetics of Cellular Phenotypes Z Ding University of Cambridge, 2015 | | 2015 |
| POT1 mutations predispose to familial melanoma CD Robles-Espinoza, M Harland, AJ Ramsay, LG Aoude, V Quesada, ... Cancer Research 74 (23_Supplement), 20-20, 2014 | | 2014 |
Richard DurbinDept of Genetics, University of CambridgeVerified email at cam.ac.uk
