Associated Papers
Genome sequencing enhances the diagnostic yield and expands the genetic landscape of male breast cancer.
Wen W et al.
Genetics in Medicine Open, 2025
39981113 (PubMed )
Supplement: mmc4.xlsx › Sheet1
MCM8 interacts with DDX5 to promote R-loop resolution.
Wen C et al.
The Embo Journal, 2024
Molecular functions of MCM8 and MCM9 and their associated pathologies.
Helderman NC et al.
Iscience, 2023
Meiosis interrupted: the genetics of female infertility via meiotic failure.
Biswas L et al.
Reproduction (cambridge, England), 2021
MCM8IP activates the MCM8-9 helicase to promote DNA synthesis and homologous recombination upon DNA damage.
Huang JW et al.
Nature Communications, 2020
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.
Fachal L et al.
Nature Genetics, 2020
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
Gallagher CS et al.
Nature Communications, 2019
Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan.
Ruth KS et al.
Human Molecular Genetics, 2019
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
Rafnar T et al.
Nature Communications, 2018
Association analysis identifies 65 new breast cancer risk loci.
Michailidou K et al.
Nature, 2017
MCM8-9 complex promotes resection of double-strand break ends by MRE11-RAD50-NBS1 complex.
Lee KY et al.
Nature Communications, 2015
XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.
Talukder AK et al.
Plos One, 2015
25905921 (PubMed )
Supplement: pone.0123569.s008.xls › BC4_ERR166308
Loci at chromosomes 13, 19 and 20 influence age at natural menopause.
Stolk L et al.
Nature Genetics, 2009
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