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David E Goldgar

Showing results (1-10 of 201) with videos related to

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Familial Cancer|October 24, 2003
The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testingAlexandre Sibert, David E Goldgar
American Journal of Human Genetics|August 6, 2003
A full-likelihood method for the evaluation of causality of sequence variants from family dataDeborah Thompson, Douglas F Easton, David E Goldgar
BMC Genetics|November 3, 2007
Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellitesBing-Jian Feng, David E Goldgar, Marilys Corbex
The New England Journal of Medicine|August 24, 2017
More on Co-Occurrence of COMT and BRCA1/2 Variants in a PopulationAmanda B Spurdle, David E Goldgar, Douglas F Easton
Human Mutation|October 28, 2008
Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applicationsSean V Tavtigian, Graham B Byrnes, David E Goldgar, et al.
Human Mutation|October 28, 2008
Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working GroupSean V Tavtigian, Marc S Greenblatt, David E Goldgar, et al.
Plos One|August 19, 2011
Design considerations for massively parallel sequencing studies of complex human diseaseBing-Jian Feng, Sean V Tavtigian, Melissa C Southey, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|March 31, 2011
Immunohistochemical staining with Melan-A of uninvolved sun-damaged skin shows features characteristic of lentigo malignaAnneli R Bowen, Betsy N Perry Thacker, David E Goldgar, et al.
International Journal of Cancer|February 22, 2002
Prevalence of the BRCA2 6174 del T mutation in Israeli uveal melanoma patientsJose Iscovich, Mohammed Abdulrazik, Carol Cour, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2020
Considerations in assessing germline variant pathogenicity using cosegregation analysisSophie Belman, Michael T Parsons, Amanda B Spurdle, et al.
Pageof 21

Showing results (1-10 of 201) with videos related to

Sort By:
Pageof 21
Familial Cancer|October 24, 2003
The effect of disease penetrance, family size, and age of onset on family history with application to setting eligibility criteria for genetic testingAlexandre Sibert, David E Goldgar
American Journal of Human Genetics|August 6, 2003
A full-likelihood method for the evaluation of causality of sequence variants from family dataDeborah Thompson, Douglas F Easton, David E Goldgar
BMC Genetics|November 3, 2007
Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellitesBing-Jian Feng, David E Goldgar, Marilys Corbex
The New England Journal of Medicine|August 24, 2017
More on Co-Occurrence of COMT and BRCA1/2 Variants in a PopulationAmanda B Spurdle, David E Goldgar, Douglas F Easton
Human Mutation|October 28, 2008
Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applicationsSean V Tavtigian, Graham B Byrnes, David E Goldgar, et al.
Human Mutation|October 28, 2008
Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working GroupSean V Tavtigian, Marc S Greenblatt, David E Goldgar, et al.
Plos One|August 19, 2011
Design considerations for massively parallel sequencing studies of complex human diseaseBing-Jian Feng, Sean V Tavtigian, Melissa C Southey, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|March 31, 2011
Immunohistochemical staining with Melan-A of uninvolved sun-damaged skin shows features characteristic of lentigo malignaAnneli R Bowen, Betsy N Perry Thacker, David E Goldgar, et al.
International Journal of Cancer|February 22, 2002
Prevalence of the BRCA2 6174 del T mutation in Israeli uveal melanoma patientsJose Iscovich, Mohammed Abdulrazik, Carol Cour, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2020
Considerations in assessing germline variant pathogenicity using cosegregation analysisSophie Belman, Michael T Parsons, Amanda B Spurdle, et al.
Pageof 21