Skip to results
Modify your search
NARROW
1-20 of 20
Authors: Robert Winqvist
Journal Article
BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells Open Access
Human Molecular Genetics, Volume 28, Issue 24, 15 December 2019, Pages 4148–4160, https://doi.org/10.1093/hmg/ddz252
Published: 20 October 2019
Journal Article
Body mass index and breast cancer survival: a Mendelian randomization analysis Open Access
International Journal of Epidemiology, Volume 46, Issue 6, December 2017, Pages 1814–1822, https://doi.org/10.1093/ije/dyx131
Published: 09 October 2017
Journal Article
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression Free
Human Molecular Genetics, Volume 25, Issue 17, 1 September 2016, Pages 3863–3876, https://doi.org/10.1093/hmg/ddw223
Published: 11 July 2016
Journal Article
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers Free
JNCI: Journal of the National Cancer Institute, Volume 108, Issue 2, February 2016, djv315, https://doi.org/10.1093/jnci/djv315
Published: 19 November 2015
Journal Article
Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization Free
JNCI: Journal of the National Cancer Institute, Volume 107, Issue 11, November 2015, djv219, https://doi.org/10.1093/jnci/djv219
Published: 20 August 2015
Journal Article
Identification of Novel Genetic Markers of Breast Cancer Survival Open Access
JNCI: Journal of the National Cancer Institute, Volume 107, Issue 5, May 2015, djv081, https://doi.org/10.1093/jnci/djv081
Published: 18 April 2015
Journal Article
Prediction of Breast Cancer Risk Based on Profiling With Common Genetic Variants Open Access
JNCI: Journal of the National Cancer Institute, Volume 107, Issue 5, May 2015, djv036, https://doi.org/10.1093/jnci/djv036
Published: 02 April 2015
Journal Article
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 Open Access
Human Molecular Genetics, Volume 24, Issue 10, 15 May 2015, Pages 2966–2984, https://doi.org/10.1093/hmg/ddv035
Published: 04 February 2015
Journal Article
Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer Get access
Carcinogenesis, Volume 36, Issue 2, February 2015, Pages 256–271, https://doi.org/10.1093/carcin/bgu326
Published: 13 January 2015
Journal Article
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk Get access
Human Molecular Genetics, Volume 24, Issue 1, 1 January 2015, Pages 285–298, https://doi.org/10.1093/hmg/ddu431
Published: 28 August 2014
Journal Article
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium Open Access
Human Molecular Genetics, Volume 23, Issue 22, 15 November 2014, Pages 6096–6111, https://doi.org/10.1093/hmg/ddu311
Published: 18 June 2014
Journal Article
Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade Get access
Human Molecular Genetics, Volume 23, Issue 22, 15 November 2014, Pages 6034–6046, https://doi.org/10.1093/hmg/ddu300
Published: 13 June 2014
Journal Article
A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium Get access
Human Molecular Genetics, Volume 23, Issue 7, 1 April 2014, Pages 1934–1946, https://doi.org/10.1093/hmg/ddt581
Published: 15 November 2013
Journal Article
The role of genetic breast cancer susceptibility variants as prognostic factors Get access
Human Molecular Genetics, Volume 21, Issue 17, 1 September 2012, Pages 3926–3939, https://doi.org/10.1093/hmg/dds159
Published: 24 April 2012
Journal Article
Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium Get access
Human Molecular Genetics, Volume 20, Issue 23, 1 December 2011, Pages 4693–4706, https://doi.org/10.1093/hmg/ddr368
Published: 18 August 2011
Journal Article
Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies Get access
JNCI: Journal of the National Cancer Institute, Volume 103, Issue 3, 2 February 2011, Pages 250–263, https://doi.org/10.1093/jnci/djq526
Published: 29 December 2010
Journal Article
Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice Get access
Human Molecular Genetics, Volume 19, Issue 15, 1 August 2010, Pages 3021–3029, https://doi.org/10.1093/hmg/ddq207
Published: 18 May 2010
Journal Article
Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer Get access
Carcinogenesis, Volume 28, Issue 5, May 2007, Pages 1040–1045, https://doi.org/10.1093/carcin/bgl237
Published: 13 December 2006
Journal Article
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability Get access
Carcinogenesis, Volume 27, Issue 8, August 2006, Pages 1593–1599, https://doi.org/10.1093/carcin/bgi360
Published: 12 February 2006
Journal Article
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype Get access
Human Molecular Genetics, Volume 1, Issue 7, October 1992, Pages 467–473, https://doi.org/10.1093/hmg/1.7.467
Published: 01 October 1992
