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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Taru A Muranen, Dario Greco, Carl Blomqvist, et al.
Cancers
|
July 27, 2022
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Martine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
American Journal of Human Genetics
|
February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survival
Anna Morra, Nasim Mavaddat, Taru A Muranen, et al.
Breast Cancer Research : BCR
|
January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study
Roger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
The Journal of Pathology
|
December 13, 2021
Validated biomarker assays confirm that ARID1A loss is confounded with MMR deficiency, CD8<sup>+</sup> TIL infiltration, and provides no independent prognostic value in endometriosis-associated ovarian carcinomas
Karolin Heinze, Tayyebeh M Nazeran, Sandra Lee, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
June 27, 2019
A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases
Nicola S Meagher, Linyuan Wang, Peter F Rambau, et al.
Human Genetics
|
December 2, 2015
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
Jieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Endocrine-Related Cancer
|
November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer
Deborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
Human Genetics
|
December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk
Luis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Nature Genetics
|
May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysis
Timothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
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Search research articles
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Showing results (51-60 of 142) with videos related to
Sort By:
Page
of 15
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2016
Genetic modifiers of CHEK2*1100delC-associated breast cancer risk
Taru A Muranen, Dario Greco, Carl Blomqvist, et al.
Cancers
|
July 27, 2022
Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
Martine Dumont, Nana Weber-Lassalle, Charles Joly-Beauparlant, et al.
American Journal of Human Genetics
|
February 24, 2023
The impact of coding germline variants on contralateral breast cancer risk and survival
Anna Morra, Nasim Mavaddat, Taru A Muranen, et al.
Breast Cancer Research : BCR
|
January 4, 2011
Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study
Roger L Milne, Mia M Gaudet, Amanda B Spurdle, et al.
The Journal of Pathology
|
December 13, 2021
Validated biomarker assays confirm that ARID1A loss is confounded with MMR deficiency, CD8<sup>+</sup> TIL infiltration, and provides no independent prognostic value in endometriosis-associated ovarian carcinomas
Karolin Heinze, Tayyebeh M Nazeran, Sandra Lee, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
June 27, 2019
A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases
Nicola S Meagher, Linyuan Wang, Peter F Rambau, et al.
Human Genetics
|
December 2, 2015
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
Jieping Lei, Anja Rudolph, Kirsten B Moysich, et al.
Endocrine-Related Cancer
|
November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer
Deborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
Human Genetics
|
December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk
Luis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Nature Genetics
|
May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysis
Timothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
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of 15