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Harald Surowy
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Association analysis identifies 65 new breast cancer risk loci
K Michailidou, S Lindström, J Dennis, J Beesley, S Hui, S Kar, A Lemaçon, ...
Nature 551 (7678), 92-94, 2017
13092017
Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
K Michailidou, J Beesley, S Lindstrom, S Canisius, J Dennis, MJ Lush, ...
Nature genetics 47 (4), 373-380, 2015
6492015
Breast cancer risk genes—association analysis in more than 113,000 women
Breast Cancer Association Consortium
New England Journal of Medicine 384 (5), 428-439, 2021
6112021
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
RL Milne, KB Kuchenbaecker, K Michailidou, J Beesley, S Kar, ...
Nature genetics 49 (12), 1767-1778, 2017
3532017
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer
L Wu, W Shi, J Long, X Guo, K Michailidou, J Beesley, MK Bolla, XO Shu, ...
Nature genetics 50 (7), 968-978, 2018
2132018
Age-and tumor subtype–specific breast cancer risk estimates for CHEK2* 1100delC carriers
MK Schmidt, F Hogervorst, R Van Hien, S Cornelissen, A Broeks, ...
Journal of clinical oncology 34 (23), 2750, 2016
2092016
Plasma DNA integrity as a biomarker for primary and metastatic breast cancer and potential marker for early diagnosis
D Madhavan, M Wallwiener, K Bents, M Zucknick, J Nees, S Schott, K Cuk, ...
Breast cancer research and treatment 146, 163-174, 2014
1892014
Blood-based DNA methylation as biomarker for breast cancer: a systematic review
Q Tang, J Cheng, X Cao, H Surowy, B Burwinkel
Clinical epigenetics 8, 1-18, 2016
1642016
Height and breast cancer risk: evidence from prospective studies and Mendelian randomization
B Zhang, XO Shu, RJ Delahanty, C Zeng, K Michailidou, MK Bolla, ...
Journal of the National Cancer Institute 107 (11), djv219, 2015
1462015
No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing
DF Easton, F Lesueur, B Decker, K Michailidou, J Li, J Allen, C Luccarini, ...
Journal of medical genetics 53 (5), 298-309, 2016
1342016
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
WE Ek, A Reznichenko, S Ripke, B Niesler, M Zucchelli, NV Rivera, ...
Gut 64 (11), 1774-1782, 2015
1302015
Plasma miR‐122 and miR‐200 family are prognostic markers in colorectal cancer
M Maierthaler, A Benner, M Hoffmeister, H Surowy, L Jansen, P Knebel, ...
International journal of cancer 140 (1), 176-187, 2017
1102017
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor
P Peterlongo, I Catucci, M Colombo, L Caleca, E Mucaki, M Bogliolo, ...
Human molecular genetics 24 (18), 5345-5355, 2015
1052015
Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis
X Shu, L Wu, NK Khankari, XO Shu, TJ Wang, K Michailidou, MK Bolla, ...
International journal of epidemiology 48 (3), 795-806, 2019
1002019
Combined genetic and splicing analysis of BRCA1 c.[594-2A> C; 641A> G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant …
M de La Hoya, O Soukarieh, I López-Perolio, A Vega, LC Walker, ...
Human molecular genetics 25 (11), 2256-2268, 2016
942016
Fine-scale mapping of the 5q11. 2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1
DM Glubb, MJ Maranian, K Michailidou, KA Pooley, KB Meyer, S Kar, ...
The American Journal of Human Genetics 96 (1), 5-20, 2015
922015
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
WY Lin, NJ Camp, M Ghoussaini, J Beesley, K Michailidou, JL Hopper, ...
Human molecular genetics 24 (1), 285-298, 2015
842015
Capture and Amplification by Tailing and Switching (CATS) An ultrasensitive ligation-independent method for generation of DNA libraries for deep sequencing from picogram …
A Turchinovich, H Surowy, A Serva, M Zapatka, P Lichter, B Burwinkel
RNA biology 11 (7), 817-828, 2014
772014
Predisposition for TMPRSS2-ERG Fusion in Prostate Cancer by Variants in DNA Repair Genes
M Luedeke, CM Linnert, MD Hofer, HM Surowy, AE Rinckleb, J Hoegel, ...
Cancer epidemiology, biomarkers & prevention 18 (11), 3030-3035, 2009
722009
Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype
NC Bramswig, O Caluseriu, HJ Lüdecke, FV Bolduc, NCL Noel, T Wieland, ...
Human genetics 136, 297-305, 2017
682017
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