Nature Search

Insulin-like growth factor-1 (IGF1) genotype predicts breast volume after pregnancy and hormonal contraception and is associated with circulating IGF-1 levels: implications for risk of early-onset breast cancer in young women from hereditary breast cancer families

H Jernström
T Sandberg
H Olsson
ResearchOpen Access01 Mar 2005
British Journal of Cancer

Volume: 92, P: 857-866
Absence of the common Insulin-like growth factor-1 19-repeat allele is associated with early age at breast cancer diagnosis in multiparous women

E Bågeman
C Ingvar
H Jernström
ResearchOpen Access20 Feb 2007
British Journal of Cancer

Volume: 96, P: 712-717
Coffee intake and CYP1A2*1F genotype predict breast volume in young women: implications for breast cancer

H Jernström
M Henningson
H Olsson
ResearchOpen Access23 Sept 2008
British Journal of Cancer

Volume: 99, P: 1534-1538
Hormone replacement therapy before breast cancer diagnosis significantly reduces the overall death rate compared with never-use among 984 breast cancer patients

H Jernström
J Frenander
H Olsson
ResearchOpen Access11 Jun 1999
British Journal of Cancer

Volume: 80, P: 1453-1458
A population-based cohort study of HRT use and breast cancer in southern Sweden

H Olsson
A Bladström
T R Möller
ResearchOpen Access28 Aug 2001
British Journal of Cancer

Volume: 85, P: 674-677
Understanding the genetic complexity of puberty timing across the allele frequency spectrum

A multi-ancestry genome-wide association study for age at menarche followed by fine mapping and downstream analysis implicates 665 pubertal timing genes, such as the G-protein-coupled receptor 83 (GPR83) and other genes expressed in the ovaries involved in the DNA damage response.

Katherine A. Kentistou
Lena R. Kaisinger
Ken K. Ong
ResearchOpen Access01 Jul 2024
Nature Genetics

Volume: 56, P: 1397-1411
Genetic drivers and cellular selection of female mosaic X chromosome loss

A large-scale meta-analysis across eight biobank datasets identifies common genetic variants associated with mosaic loss of the X chromosome in female participants.

Aoxing Liu
Giulio Genovese
Mitchell J. Machiela
Research12 Jun 2024
Nature

Volume: 631, P: 134-141
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

A region on chromosome 19p13 is associated with the risk of developing ovarian and breast cancer. Here, the authors genotyped SNPs in this region in thousands of breast and ovarian cancer patients and identified SNPs associated with three genes, which were analysed with functional studies.

Kate Lawrenson
Siddhartha Kar
Simon A. Gayther
ResearchOpen Access07 Sept 2016
Nature Communications

Volume: 7, P: 1-22
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Katherine A. Kentistou
Lena R. Kaisinger
Ken K. Ong
Amendments and CorrectionsOpen Access09 Jul 2024
Nature Genetics

Volume: 56, P: 1763-1764
Follow-up of patients with Hodgkin's disease following curative treatment: the routine CT scan is of little value

E T Dryver
H Jernström
K R Imrie
ResearchOpen Access29 Jul 2003
British Journal of Cancer

Volume: 89, P: 482-486
Author Correction: Genetic drivers and cellular selection of female mosaic X chromosome loss

Aoxing Liu
Giulio Genovese
Mitchell J. Machiela
Amendments and Corrections03 Dec 2024
Nature

Volume: 636, P: E7
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

The risk of germline copy number variants (CNVs) in BRCA1 and BRCA2 pathogenic variant carriers in breast cancer is assessed, with CNVs overlapping SULT1A1 decreasing breast cancer risk in BRCA1 carriers.

Christopher Hakkaart
John F. Pearson
Logan C. Walker
ResearchOpen Access06 Oct 2022
Communications Biology

Volume: 5, P: 1-15
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

A Osorio
R L Milne
J Benítez
ResearchOpen Access22 Mar 2011
British Journal of Cancer

Volume: 104, P: 1356-1361
CYP2C8 and CYP2C9 polymorphisms in relation to tumour characteristics and early breast cancer related events among 652 breast cancer patients

H Jernström
E Bågeman
C Ingvar
ResearchOpen Access24 Nov 2009
British Journal of Cancer

Volume: 101, P: 1817-1823
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Gisella Figlioli
Massimo Bogliolo
Paolo Peterlongo
ResearchOpen Access01 Nov 2019
npj Breast Cancer

Volume: 5, P: 1-14
Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

Frank Qian
Matti A. Rookus
Dezheng Huo
ResearchOpen Access19 Jun 2019
British Journal of Cancer

Volume: 121, P: 180-192
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

A Osorio
R L Milne
J Benítez
ResearchOpen Access17 Nov 2009
British Journal of Cancer

Volume: 101, P: 2048-2054
Androgen receptor genotypes predict response to endocrine treatment in breast cancer patients

K B Lundin
M Henningson
H Jernström
ResearchOpen Access27 Oct 2011
British Journal of Cancer

Volume: 105, P: 1676-1683
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

A Jakubowska
D Rozkrut
J Lubinski
ResearchOpen Access15 May 2012
British Journal of Cancer

Volume: 106, P: 2016-2024

Search

Insulin-like growth factor-1 (IGF1) genotype predicts breast volume after pregnancy and hormonal contraception and is associated with circulating IGF-1 levels: implications for risk of early-onset breast cancer in young women from hereditary breast cancer families

Absence of the common Insulin-like growth factor-1 19-repeat allele is associated with early age at breast cancer diagnosis in multiparous women

Coffee intake and CYP1A21F* genotype predict breast volume in young women: implications for breast cancer

Hormone replacement therapy before breast cancer diagnosis significantly reduces the overall death rate compared with never-use among 984 breast cancer patients

A population-based cohort study of HRT use and breast cancer in southern Sweden

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Genetic drivers and cellular selection of female mosaic X chromosome loss

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum

Follow-up of patients with Hodgkin's disease following curative treatment: the routine CT scan is of little value

Author Correction: Genetic drivers and cellular selection of female mosaic X chromosome loss

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2

CYP2C8 and CYP2C9 polymorphisms in relation to tumour characteristics and early breast cancer related events among 652 breast cancer patients

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

Androgen receptor genotypes predict response to endocrine treatment in breast cancer patients

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

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