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Dirk S. Paul
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Genomic atlas of the human plasma proteome
BB Sun, JC Maranville, JE Peters, D Stacey, JR Staley, J Blackshaw, ...
Nature 558 (7708), 73-79, 2018
14422018
The allelic landscape of human blood cell trait variation and links to common complex disease
WJ Astle, H Elding, T Jiang, D Allen, D Ruklisa, AL Mann, D Mead, ...
Cell 167 (5), 1415-1429. e19, 2016
12012016
Risk thresholds for alcohol consumption: combined analysis of individual-participant data for 599 912 current drinkers in 83 prospective studies
AM Wood, S Kaptoge, AS Butterworth, P Willeit, S Warnakula, T Bolton, ...
The Lancet 391 (10129), 1513-1523, 2018
11972018
PhenoScanner: a database of human genotype-phenotype associations
JR Staley, J Blackshaw, MA Kamat, S Ellis, P Surendran, BB Sun, ...
Bioinformatics 32 (20), 3207-3209, 2016
11952016
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
10832023
Genetic drivers of epigenetic and transcriptional variation in human immune cells
L Chen, B Ge, FP Casale, L Vasquez, T Kwan, D Garrido-Martín, S Watt, ...
Cell 167 (5), 1398-1414. e24, 2016
6662016
The International Human Epigenome Consortium: a blueprint for scientific collaboration and discovery
HG Stunnenberg, International Human Epigenome Consortium, M Hirst
Cell 167 (5), 1145-1149, 2016
5222016
Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome
CA Albers, DS Paul, H Schulze, K Freson, JC Stephens, PA Smethurst, ...
Nature Genetics 44 (4), 435-439, 2012
4662012
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
3962022
Seventy-five genetic loci influencing the human red blood cell
P van der Harst, W Zhang, IM Leach, A Rendon, N Verweij, J Sehmi, ...
Nature 492 (7429), 369-375, 2012
3902012
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
JMM Howson, W Zhao, DR Barnes, WK Ho, R Young, DS Paul, LL Waite, ...
Nature Genetics 49 (7), 1113-1119, 2017
3002017
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Q Wang, RS Dhindsa, K Carss, AR Harper, A Nag, I Tachmazidou, ...
Nature 597 (7877), 527-532, 2021
2672021
Quantitative comparison of DNA methylation assays for biomarker development and clinical applications
C Bock, F Halbritter, FJ Carmona, S Tierling, P Datlinger, Y Assenov, ...
Nature Biotechnology 34 (7), 726-737, 2016
2462016
Correlation of an epigenetic mitotic clock with cancer risk
Z Yang, A Wong, D Kuh, DS Paul, VK Rakyan, RD Leslie, SC Zheng, ...
Genome Biology 17 (1), 205, 2016
2382016
Deciphering the genomic, epigenomic, and transcriptomic landscapes of pre-invasive lung cancer lesions
VH Teixeira, CP Pipinikas, A Pennycuick, H Lee-Six, D Chandrasekharan, ...
Nature Medicine 25 (3), 517-525, 2019
2092019
Increased DNA methylation variability in type 1 diabetes across three immune effector cell types
DS Paul, AE Teschendorff, MAN Dang, R Lowe, MI Hawa, S Ecker, ...
Nature Communications 7, 13555, 2016
1592016
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P Surendran, EV Feofanova, N Lahrouchi, I Ntalla, S Karthikeyan, J Cook, ...
Nature Genetics 52 (12), 1314-1332, 2020
1342020
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection
SM Zekavat, SH Lin, AG Bick, A Liu, K Paruchuri, C Wang, MM Uddin, ...
Nature Medicine 27 (6), 1012-1024, 2021
1252021
eFORGE: a tool for identifying cell type-specific signal in epigenomic data
CE Breeze, DS Paul, J van Dongen, LM Butcher, JC Ambrose, JE Barrett, ...
Cell Reports 17 (8), 2137-2150, 2016
1202016
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types
S Ecker, L Chen, V Pancaldi, FO Bagger, JM Fernandez, ...
Genome Biology 18 (1), 18, 2017
1172017
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