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Author Details
Full Name
Xiaoqing Chen
Affiliation
QIMR Berghofer Medical Research Institute
ORCID
Career Start Year
1999
Papers
113
H Index
41
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35263119
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
J Clin Oncol
2022
35263119
TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
J Clin Oncol
2022
34093841
Mutational Landscape of PI3K-AKT-mTOR Pathway in Breast Cancer: Implications for Targeted Therapeutics.
J Cancer
2021
33968723
Characterization of Frequently Mutated Cancer Genes and Tumor Mutation Burden in Chinese Breast Cancer.
Front Oncol
2021
34093841
Mutational Landscape of PI3K-AKT-mTOR Pathway in Breast Cancer: Implications for Targeted Therapeutics.
J Cancer
2021
34454403
Genetic and immune characteristics of sentinel lymph node metastases and multiple lymph node metastases compared to their matched primary breast tumours.
EBioMedicine
2021
34454403
Genetic and immune characteristics of sentinel lymph node metastases and multiple lymph node metastases compared to their matched primary breast tumours.
EBioMedicine
2021
33968723
Characterization of Frequently Mutated Cancer Genes and Tumor Mutation Burden in Chinese Breast Cancer.
Front Oncol
2021
32638235
Genetic mutation profile of Chinese HER2-positive breast cancers and genetic predictors of responses to Neoadjuvant anti-HER2 therapy.
Breast Cancer Res Treat
2020
32638235
Genetic mutation profile of Chinese HER2-positive breast cancers and genetic predictors of responses to Neoadjuvant anti-HER2 therapy.
Breast Cancer Res Treat
2020
31168460
Characterization of frequently mutated cancer genes in Chinese breast tumors: a comparison of Chinese and TCGA cohorts.
Ann Transl Med
2019
30135485
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.
Eur J Hum Genet
2019
31168460
Characterization of frequently mutated cancer genes in Chinese breast tumors: a comparison of Chinese and TCGA cohorts.
Ann Transl Med
2019
30135485
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.
Eur J Hum Genet
2019
29344954
Mixed ductal-lobular carcinomas: evidence for progression from ductal to lobular morphology.
J Pathol
2018
29915430
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Nat Genet
2018
29344954
Mixed ductal-lobular carcinomas: evidence for progression from ductal to lobular morphology.
J Pathol
2018
29915430
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Nat Genet
2018
27171545
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
Genet Med
2017
28346442
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Nat Genet
2017
29059683
Association analysis identifies 65 new breast cancer risk loci.
Nature
2017
29058716
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nat Genet
2017
27171545
Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab.
Genet Med
2017
28145423
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.
Eur J Hum Genet
2017
28346442
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
Nat Genet
2017
28145423
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.
Eur J Hum Genet
2017
29059683
Association analysis identifies 65 new breast cancer risk loci.
Nature
2017
29058716
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Nat Genet
2017
26840454
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer.
Oncotarget
2016
26840454
Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer.
Oncotarget
2016
27087319
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Am J Hum Genet
2016
26711112
Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.
Nat Genet
2016
26711112
Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.
Nat Genet
2016
27087319
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
Am J Hum Genet
2016
26075790
Genome-wide significant risk associations for mucinous ovarian carcinoma.
Nat Genet
2015
26075790
Genome-wide significant risk associations for mucinous ovarian carcinoma.
Nat Genet
2015
24957074
ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.
J Natl Cancer Inst
2014
24810093
Paclitaxel sensitivity in relation to ABCB1 expression, efflux and single nucleotide polymorphisms in ovarian cancer.
Sci Rep
2014
24957074
ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.
J Natl Cancer Inst
2014
24810093
Paclitaxel sensitivity in relation to ABCB1 expression, efflux and single nucleotide polymorphisms in ovarian cancer.
Sci Rep
2014
23535649
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
Nat Commun
2013
23756864
Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer.
Br J Cancer
2013
23917080
ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas.
Gynecol Oncol
2013
23535649
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
Nat Commun
2013
23535731
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Nat Genet
2013
23917080
ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: a comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas.
Gynecol Oncol
2013
23756864
Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer.
Br J Cancer
2013
23535731
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Nat Genet
2013
22348646
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.
Breast Cancer Res
2012
22351618
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
Cancer Epidemiol Biomarkers Prev
2012
1 - 50 of 226
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Jenny Chang-Claude
German Cancer Research Center (DKFZ)
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Siranoush Manoukian
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Sue Healey
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Hoda Anton-Culver
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Jan Lubinski
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