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Katri Pylkäs
Katri Pylkäs
Researcher
Verified email at oulu.fi
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Year
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
13142017
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
K Michailidou, P Hall, A Gonzalez-Neira, M Ghoussaini, J Dennis, ...
Nature genetics 45 (4), 353-361, 2013
12612013
Breast-Cancer Risk in Families with Mutations in PALB2
AC Antoniou, S Casadei, T Heikkinen, D Barrowdale, K Pylkäs, J Roberts, ...
New England Journal of Medicine 371 (6), 497-506, 2014
10712014
Polygenic risk scores for prediction of breast cancer and breast cancer subtypes
N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ...
The American Journal of Human Genetics 104 (1), 21-34, 2019
9012019
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
XR Yang, J Chang-Claude, EL Goode, FJ Couch, H Nevanlinna, RL Milne, ...
Journal of the National Cancer Institute 103 (3), 250-263, 2011
8392011
Prediction of breast cancer risk based on profiling with common genetic variants
N Mavaddat, PDP Pharoah, K Michailidou, J Tyrer, MN Brook, MK Bolla, ...
Journal of the National Cancer Institute 107 (5), djv036, 2015
6702015
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
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
SE Bojesen, KA Pooley, SE Johnatty, J Beesley, K Michailidou, JP Tyrer, ...
Nature genetics 45 (4), 371-384, 2013
6462013
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
JRB Perry, F Day, CE Elks, P Sulem, DJ Thompson, T Ferreira, C He, ...
Nature 514 (7520), 92-97, 2014
5992014
A recurrent mutation in PALB2 in Finnish cancer families
H Erkko, B Xia, J Nikkilä, J Schleutker, K Syrjäkoski, A Mannermaa, ...
Nature 446 (7133), 316-319, 2007
5602007
Genome-wide association studies identify four ER negative–specific breast cancer risk loci
M Garcia-Closas, FJ Couch, S Lindstrom, K Michailidou, MK Schmidt, ...
Nature genetics 45 (4), 392-398, 2013
4712013
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general …
AC Antoniou, X Wang, ZS Fredericksen, L McGuffog, R Tarrell, ...
Nature genetics 42 (10), 885-892, 2010
4062010
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
FR Day, KS Ruth, DJ Thompson, KL Lunetta, N Pervjakova, DI Chasman, ...
Nature genetics 47 (11), 1294-1303, 2015
3972015
Genome-wide association analysis identifies three new breast cancer susceptibility loci
M Ghoussaini, O Fletcher, K Michailidou, C Turnbull, MK Schmidt, E Dicks, ...
Nature genetics 44 (3), 312-318, 2012
3632012
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
3542017
Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families
X Yang, G Leslie, A Doroszuk, S Schneider, J Allen, B Decker, ...
Journal of clinical oncology 38 (7), 674-685, 2020
3512020
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer
CA Haiman, GK Chen, CM Vachon, F Canzian, A Dunning, RC Millikan, ...
Nature genetics 43 (12), 1210-1214, 2011
3482011
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
JD French, M Ghoussaini, SL Edwards, KB Meyer, K Michailidou, ...
The American Journal of Human Genetics 92 (4), 489-503, 2013
2532013
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS
MC Southey, DE Goldgar, R Winqvist, K Pylkäs, F Couch, M Tischkowitz, ...
Journal of medical genetics 53 (12), 800-811, 2016
2382016
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
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