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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 17, 2019
Cancer Risks Associated With Germline <i>PALB2</i> Pathogenic Variants: An International Study of 524 Families
Xin Yang, Goska Leslie, Alicja Doroszuk, et al.
Plos Genetics
|
November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Mia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Research Square
|
February 24, 2023
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Anna Morra, Maartje A C Schreurs, Irene L Andrulis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M M Lakeman, Alexandra J van den Broek, Juliën A M Vos, et al.
Human Molecular Genetics
|
March 25, 2016
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
Mitchell J Machiela, Qing Lan, Susan L Slager, et al.
Nature Genetics
|
September 29, 2014
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
James R Cerhan, Sonja I Berndt, Joseph Vijai, et al.
Human Molecular Genetics
|
January 7, 2016
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry
Jonine D Figueroa, Candace D Middlebrooks, A Rouf Banday, et al.
JAMA Oncology
|
July 3, 2020
Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Valentina Silvestri, Goska Leslie, Daniel R Barnes, et al.
Cancer Medicine
|
July 4, 2023
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Anna Morra, Maartje A C Schreurs, Irene L Andrulis, et al.
Plos One
|
July 7, 2012
Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
Tomas Kirchhoff, Mia M Gaudet, Antonis C Antoniou, et al.
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of 43
Search research articles
Search
Showing results (341-350 of 429) with videos related to
Sort By:
Page
of 43
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
December 17, 2019
Cancer Risks Associated With Germline <i>PALB2</i> Pathogenic Variants: An International Study of 524 Families
Xin Yang, Goska Leslie, Alicja Doroszuk, et al.
Plos Genetics
|
November 10, 2010
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Mia M Gaudet, Tomas Kirchhoff, Todd Green, et al.
Research Square
|
February 24, 2023
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Anna Morra, Maartje A C Schreurs, Irene L Andrulis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Inge M M Lakeman, Alexandra J van den Broek, Juliën A M Vos, et al.
Human Molecular Genetics
|
March 25, 2016
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
Mitchell J Machiela, Qing Lan, Susan L Slager, et al.
Nature Genetics
|
September 29, 2014
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
James R Cerhan, Sonja I Berndt, Joseph Vijai, et al.
Human Molecular Genetics
|
January 7, 2016
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry
Jonine D Figueroa, Candace D Middlebrooks, A Rouf Banday, et al.
JAMA Oncology
|
July 3, 2020
Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Valentina Silvestri, Goska Leslie, Daniel R Barnes, et al.
Cancer Medicine
|
July 4, 2023
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
Anna Morra, Maartje A C Schreurs, Irene L Andrulis, et al.
Plos One
|
July 7, 2012
Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
Tomas Kirchhoff, Mia M Gaudet, Antonis C Antoniou, et al.
Page
of 43