Natalia N Antonenkova
Overview
Explore the profile of Natalia N Antonenkova including associated specialties, affiliations and a list of published articles.
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42
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4731
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Recent Articles
11.
Park H, Neumeyer S, Michailidou K, Bolla M, Wang Q, Dennis J, et al.
Br J Cancer
. 2021 Aug;
125(8):1135-1145.
PMID: 34341517
Background: Despite a modest association between tobacco smoking and breast cancer risk reported by recent epidemiological studies, it is still equivocal whether smoking is causally related to breast cancer risk....
12.
Baxter J, Johnson N, Tomczyk K, Gillespie A, Maguire S, Brough R, et al.
Am J Hum Genet
. 2021 Jun;
108(7):1190-1203.
PMID: 34146516
A combination of genetic and functional approaches has identified three independent breast cancer risk loci at 2q35. A recent fine-scale mapping analysis to refine these associations resulted in 1 (signal...
13.
Johnson N, Maguire S, Morra A, Middha Kapoor P, Tomczyk K, Jones M, et al.
Br J Cancer
. 2021 Jan;
124(4):842-854.
PMID: 33495599
Background: Epidemiological studies provide strong evidence for a role of endogenous sex hormones in the aetiology of breast cancer. The aim of this analysis was to identify genetic variants that...
14.
Dorling L, Carvalho S, Allen J, Gonzalez-Neira A, Luccarini C, Wahlstrom C, et al.
N Engl J Med
. 2021 Jan;
384(5):428-439.
PMID: 33471991
Background: Genetic testing for breast cancer susceptibility is widely used, but for many genes, evidence of an association with breast cancer is weak, underlying risk estimates are imprecise, and reliable...
15.
Liu J, Prager-van der Smissen W, Collee J, Bolla M, Wang Q, Michailidou K, et al.
Sci Rep
. 2020 Jun;
10(1):9688.
PMID: 32546843
In breast cancer, high levels of homeobox protein Hox-B13 (HOXB13) have been associated with disease progression of ER-positive breast cancer patients and resistance to tamoxifen treatment. Since HOXB13 p.G84E is...
16.
Fachal L, Aschard H, Beesley J, Barnes D, Allen J, Kar S, et al.
Nat Genet
. 2020 Jan;
52(1):56-73.
PMID: 31911677
Genome-wide association studies have identified breast cancer risk variants in over 150 genomic regions, but the mechanisms underlying risk remain largely unknown. These regions were explored by combining association analysis...
17.
Figlioli G, Bogliolo M, Catucci I, Caleca L, Lasheras S, Pujol R, et al.
NPJ Breast Cancer
. 2019 Nov;
5:38.
PMID: 31700994
Breast cancer is a common disease partially caused by genetic risk factors. Germline pathogenic variants in DNA repair genes , , , , and are associated with breast cancer risk....
18.
Jiang X, Finucane H, Schumacher F, Schmit S, Tyrer J, Han Y, et al.
Nat Commun
. 2019 Sep;
10(1):4386.
PMID: 31548585
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
19.
Jiang X, Finucane H, Schumacher F, Schmit S, Tyrer J, Han Y, et al.
Nat Commun
. 2019 Jan;
10(1):431.
PMID: 30683880
Quantifying the genetic correlation between cancers can provide important insights into the mechanisms driving cancer etiology. Using genome-wide association study summary statistics across six cancer types based on a total...
20.
Mavaddat N, Michailidou K, Dennis J, Lush M, Fachal L, Lee A, et al.
Am J Hum Genet
. 2018 Dec;
104(1):21-34.
PMID: 30554720
Stratification of women according to their risk of breast cancer based on polygenic risk scores (PRSs) could improve screening and prevention strategies. Our aim was to develop PRSs, optimized for...