Robert Winqvist


Ontology type: schema:Person     


Person Info

NAME

Robert

SURNAME

Winqvist

Publications in SciGraph latest 50 shown

  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2018-12 Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls in SCIENTIFIC REPORTS
  • 2018-07 A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer in NATURE GENETICS
  • 2017-12 Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study in BREAST CANCER RESEARCH
  • 2017-12 Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility in SCIENTIFIC REPORTS
  • 2017-12 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer in NATURE GENETICS
  • 2017-11 FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-11 Association analysis identifies 65 new breast cancer risk loci in NATURE
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk in NATURE GENETICS
  • 2016-12 Patient survival and tumor characteristics associated with CHEK2:p.I157T – findings from the Breast Cancer Association Consortium in BREAST CANCER RESEARCH
  • 2016-12 Genetic predisposition to ductal carcinoma in situ of the breast in BREAST CANCER RESEARCH
  • 2016-12 Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus in BREAST CANCER RESEARCH
  • 2016-10 Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs) in SCIENTIFIC REPORTS
  • 2016-07 Heterozygous PALB2 c.1592delT mutation channels DNA double-strand break repair into error-prone pathways in breast cancer patients in ONCOGENE
  • 2016-05 Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry in CANCER CAUSES & CONTROL
  • 2016-04-27 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer in NATURE COMMUNICATIONS
  • 2016-04 Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 in NATURE GENETICS
  • 2016-01 Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium in HUMAN GENETICS
  • 2015-12 Common germline polymorphisms associated with breast cancer-specific survival in BREAST CANCER RESEARCH
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-04 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer in NATURE GENETICS
  • 2014-12 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy in NATURE COMMUNICATIONS
  • 2014-12 Refined histopathological predictors of BRCA1 and BRCA2mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia in BREAST CANCER RESEARCH
  • 2014-12 Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation in NATURE COMMUNICATIONS
  • 2014-12 Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer in BMC CANCER
  • 2014-10 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche in NATURE
  • 2014-06 Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study in BREAST CANCER RESEARCH
  • 2014-02 FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium in BRITISH JOURNAL OF CANCER
  • 2013-12 Heterozygous mutations in PALB2 cause DNA replication and damage response defects in NATURE COMMUNICATIONS
  • 2013-12 Evaluation of the need for routine clinical testing of PALB2 c.1592delT mutation in BRCA negative Northern Finnish breast cancer families in BMC MEDICAL GENETICS
  • 2013-04 Large-scale genotyping identifies 41 new loci associated with breast cancer risk in NATURE GENETICS
  • 2013-04 Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer in NATURE GENETICS
  • 2012-08 PREDICT Plus: development and validation of a prognostic model for early breast cancer that includes HER2 in BRITISH JOURNAL OF CANCER
  • 2012-03 Genome-wide association analysis identifies three new breast cancer susceptibility loci in NATURE GENETICS
  • 2011-12 Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility in BREAST CANCER RESEARCH AND TREATMENT
  • 2011-12 Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk in BRITISH JOURNAL OF CANCER
  • 2011-12 Mutation screening of the RNF8, UBC13 and MMS2 genes in Northern Finnish breast cancer families in BMC MEDICAL GENETICS
  • 2011-12 A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer in NATURE GENETICS
  • 2010-12 Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families in JOURNAL OF HUMAN GENETICS
  • 2010-12 Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families in FAMILIAL CANCER
  • 2010-10 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 population in NATURE GENETICS
  • 2010-08 Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families in BREAST CANCER RESEARCH
  • 2010-02 Mutation screening of the MERIT40 gene encoding a novel BRCA1 and RAP80 interacting protein in breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2009-12 Mutation analysis of the AATF gene in breast cancer families in BMC CANCER
  • 2009-12 Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations in FAMILIAL CANCER
  • 2009-04 Familial breast cancer screening reveals an alteration in the RAP80 UIM domain that impairs DNA damage response function in ONCOGENE
  • 2008-12 Somatic mutation analysis of MYH11in breast and prostate cancer in BMC CANCER
  • 2008-12 Analysis of large deletions in BRCA1, BRCA2 and PALB2 genes in Finnish breast and ovarian cancer families in BMC CANCER
  • 2007-01 Mutation analysis of aryl hydrocarbon receptor interacting protein (AIP) gene in colorectal, breast, and prostate cancers in BRITISH JOURNAL OF CANCER
  • 2005-08 Mutation analysis of the ATRgene in breast and ovarian cancer families in BREAST CANCER RESEARCH
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