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Karin A W Wadt

Showing results (1-10 of 35) with videos related to

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Journal of Medical Genetics|September 5, 2015
Melanoma geneticsJazlyn Read, Karin A W Wadt, Nicholas K Hayward
Familial Cancer|June 22, 2015
High accuracy of family history of melanoma in Danish melanoma casesKarin A W Wadt, Krzysztof T Drzewiecki, Anne-Marie Gerdes
Cancers|April 27, 2024
National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families-The Danish ModelLars Joachim Lindberg, Karin A W Wadt, Christina Therkildsen, et al.
Pigment Cell & Melanoma Research|November 29, 2014
Genetics of familial melanoma: 20 years after CDKN2ALauren G Aoude, Karin A W Wadt, Antonia L Pritchard, et al.
Genes, Chromosomes & Cancer|August 26, 2018
Putative new childhood leukemia cancer predisposition syndrome caused by germline bi-allelic missense mutations in DDX41Birgitte R Diness, Lotte Risom, Thomas L Frandsen, et al.
Familial Cancer|June 22, 2012
Novel germline c-MET mutation in a family with hereditary papillary renal carcinomaKarin A W Wadt, Anne-Marie Gerdes, Thomas V O Hansen, et al.
Journal of Medical Genetics|June 9, 2026
Interpreting <i>TP53</i> variants: somatic mosaicism and <i>ERCC6L2</i>-driven clonal evolutionAmalie Noergaard Andersson, Anna Byrjalsen, Ida Elisabeth Viller Tuxen, et al.
Nature Communications|February 29, 2024
The evolutionary impact of childhood cancer on the human gene poolUlrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.
Familial Cancer|March 27, 2026
Re-evaluating hereditary breast and ovarian cancer risk: clinical impact of updated multigene panel sequencing and genetic counselingJulie Isabelle Plougmann Gislinge, Anna Byrjalsen, Klara Vinsand Naver, et al.
Familial Cancer|January 21, 2015
Germline RAD51B truncating mutation in a family with cutaneous melanomaKarin A W Wadt, Lauren G Aoude, Lisa Golmard, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|September 5, 2015
Melanoma geneticsJazlyn Read, Karin A W Wadt, Nicholas K Hayward
Familial Cancer|June 22, 2015
High accuracy of family history of melanoma in Danish melanoma casesKarin A W Wadt, Krzysztof T Drzewiecki, Anne-Marie Gerdes
Cancers|April 27, 2024
National Experiences from 30 Years of Provider-Mediated Cascade Testing in Lynch Syndrome Families-The Danish ModelLars Joachim Lindberg, Karin A W Wadt, Christina Therkildsen, et al.
Pigment Cell & Melanoma Research|November 29, 2014
Genetics of familial melanoma: 20 years after CDKN2ALauren G Aoude, Karin A W Wadt, Antonia L Pritchard, et al.
Genes, Chromosomes & Cancer|August 26, 2018
Putative new childhood leukemia cancer predisposition syndrome caused by germline bi-allelic missense mutations in DDX41Birgitte R Diness, Lotte Risom, Thomas L Frandsen, et al.
Familial Cancer|June 22, 2012
Novel germline c-MET mutation in a family with hereditary papillary renal carcinomaKarin A W Wadt, Anne-Marie Gerdes, Thomas V O Hansen, et al.
Journal of Medical Genetics|June 9, 2026
Interpreting <i>TP53</i> variants: somatic mosaicism and <i>ERCC6L2</i>-driven clonal evolutionAmalie Noergaard Andersson, Anna Byrjalsen, Ida Elisabeth Viller Tuxen, et al.
Nature Communications|February 29, 2024
The evolutionary impact of childhood cancer on the human gene poolUlrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.
Familial Cancer|March 27, 2026
Re-evaluating hereditary breast and ovarian cancer risk: clinical impact of updated multigene panel sequencing and genetic counselingJulie Isabelle Plougmann Gislinge, Anna Byrjalsen, Klara Vinsand Naver, et al.
Familial Cancer|January 21, 2015
Germline RAD51B truncating mutation in a family with cutaneous melanomaKarin A W Wadt, Lauren G Aoude, Lisa Golmard, et al.
Pageof 4