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Authors: Robert Winqvist
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Journal Article
BRCA1 mislocalization leads to aberrant DNA damage response in heterozygous ABRAXAS1 mutation carrier cells Open Access
Muthiah Bose and others
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
An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression Free
Asaf Wyszynski and others
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
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 Open Access
Nick Orr and others
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
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
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Wei-Yu Lin and others
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
Roger L. Milne and others
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
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Kristen S. Purrington and others
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
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Roger L. Milne and others
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
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Peter A. Fasching and others
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
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Jonine D. Figueroa and others
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
Inactivation of Palb2 gene leads to mesoderm differentiation defect and early embryonic lethality in mice
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Pia Rantakari and others
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
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype
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Peggy Shelbourne and others
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
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