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ZHIHAO DING
ZHIHAO DING
Head of Human Genetics - Biberach, Boehringer Ingelheim
Verified email at boehringer-ingelheim.com
Title
Cited by
Cited by
Year
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
58712012
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
6632023
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
4202014
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
3552012
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
3442022
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
1842014
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
802014
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
732016
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
612018
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
352017
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
23
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
152023
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
132023
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
122023
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
102015
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
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