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1 . Academic Journal
A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study
저자
by
Adams, Lisa
;
Adlard, Julian
;
Alfonso, Rosa
;
Ali, Saira
;
Andrew, Angela
, et al.
소스
In
The Lancet Oncology
November 2021 22(11):1618-1631
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7 . Academic Journal
10-year performance of four models of breast cancer risk: a validation study
저자
by
Terry, Mary Beth
;
Liao, Yuyan
;
Whittemore, Alice S
;
Leoce, Nicole
;
Buchsbaum, Richard
, et al.
소스
In
The Lancet Oncology
April 2019 20(4):504-517
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7 . Academic Journal
P721: Computational tool performance across BRCA1: A case-control informed analysis
저자
by
Pew, Scott
;
Wiffler, Madison
;
Boyle, Julie
;
Tavtigian, Sean
;
Goldgar, David
.
소스
In
Genetics in Medicine Open
2024 2 Supplement 1
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7 . Academic Journal
Challenges and approaches to calibrating patient phenotype as evidence for cancer gene variant classification under ACMG/AMP guidelines.
저자
by
Fortuno, Cristina
;
Michailidou, Kyriaki
;
Parsons, Michael
;
Dolinsky, Jill S
;
Pesaran, Tina
, et al.
소스
Human Molecular Genetics; 4/15/2024, Vol. 33 Issue 8, p724-732, 9p
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7 . Academic Journal
P534: Investigating independence of PS3 and PM1 evidence categories using case-control data in BRCA1
저자
by
Pew, Scott
;
Baugh, Madison
;
Boyle, Julie
;
Goldgar, David
;
Tavtigian, Sean
.
소스
In
Genetics in Medicine Open
2023 1(1) Supplement
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7 . Academic Journal
P076: The ClinGen ENIGMA BRCA1/2 expert panel: A dynamic framework for evidence-based recommendations to improve classification criteria for variants in BRCA1/2*
저자
by
Parsons, Michael
;
Anderson, Michael
;
Berkofsky-Fessler, Windy
;
Caputo, Sandrine
;
Chan, Raymond
, et al.
소스
In
Genetics in Medicine Open
2023 1(1) Supplement
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7 . Academic Journal
Haplotype analysis and ancient origin of the BRCA1 c.4035delA Baltic founder mutation
저자
by
Janavičius, Ramūnas
;
Rudaitis, Vilius
;
Feng, Bing-Jian
;
Ozolina, Silvija
;
Griškevičius, Laimonas
, et al.
소스
In
European Journal of Medical Genetics
March 2013 56(3):125-130
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7 . Academic Journal
Likelihood ratios to assess genetic evidence for clinical significance of uncertain variants: Hereditary hemorrhagic telangiectasia as a model
저자
by
Bayrak-Toydemir, Pınar
;
McDonald, Jamie
;
Mao, Rong
;
Phansalkar, Amit
;
Gedge, Friederike
, et al.
소스
In
Experimental and Molecular Pathology
2008 85(1):45-49
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7 . Academic Journal
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2: the BRCA1 and BRCA2 Cohort Consortium
저자
by
Kast, Karin
;
John, Esther M.
;
Hopper, John L.
;
Andrieu, Nadine
;
Noguès, Catherine
, et al.
소스
Breast Cancer Research
. 25(1)
Open Access (BioMed Central)
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7 . Academic Journal
Oral Contraceptive Use in BRCA1 and BRCA2 Mutation Carriers: Absolute Cancer Risks and Benefits.
저자
by
Schrijver, Lieske H
;
Mooij, Thea M
;
Pijpe, Anouk
;
Sonke, Gabe S
;
Mourits, Marian J E
, et al.
소스
JNCI: Journal of the National Cancer Institute
. Apr2022, Vol. 114 Issue 4, p540-552. 13p.
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