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Rolf Sijmons

Showing results (1-10 of 21) with videos related to

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The New England Journal of Medicine|October 1, 2015
ClinGen and Genetic TestingMaartje Nielsen, Sanne ten Broeke, Rolf Sijmons
Journal of Breast Cancer|April 18, 2013
Prevalence of BRCA1 and BRCA2 Germline Mutations in Breast Cancer Women of Multiple Ethnic Region in Northwest ChinaJianghua Ou, Tao Wu, Rolf Sijmons, et al.
Oncotarget|May 19, 2016
SETD2: an epigenetic modifier with tumor suppressor functionalityJun Li, Gerben Duns, Helga Westers, et al.
Cancers|September 30, 2020
Cancer Predisposition Genes in Cancer-Free FamiliesGuoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
A rare large duplication of MLH1 identified in Lynch syndromeAbhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, et al.
Cells|January 8, 2023
Investigation of Rare Non-Coding Variants in Familial Multiple MyelomaYasmeen Niazi, Nagarajan Paramasivam, Joanna Blocka, et al.
Communications Medicine|November 19, 2025
Systemic barriers and opportunities for equity in early implementation of genetic testing and counseling for cardiomyopathies in TanzaniaMohamed Zahir Alimohamed, Abdilahi Kiula, Lulu Fundikira, et al.
Familial Cancer|July 31, 2009
Attitude towards pre-implantation genetic diagnosis for hereditary cancerChantal Lammens, Eveline Bleiker, Neil Aaronson, et al.
Database : the Journal of Biological Databases and Curation|September 20, 2015
SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype dataChao Pang, Annet Sollie, Anna Sijtsma, et al.
Blood Cancer Journal|February 15, 2021
Characterization of rare germline variants in familial multiple myelomaCalogerina Catalano, Nagarajan Paramasivam, Joanna Blocka, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The New England Journal of Medicine|October 1, 2015
ClinGen and Genetic TestingMaartje Nielsen, Sanne ten Broeke, Rolf Sijmons
Journal of Breast Cancer|April 18, 2013
Prevalence of BRCA1 and BRCA2 Germline Mutations in Breast Cancer Women of Multiple Ethnic Region in Northwest ChinaJianghua Ou, Tao Wu, Rolf Sijmons, et al.
Oncotarget|May 19, 2016
SETD2: an epigenetic modifier with tumor suppressor functionalityJun Li, Gerben Duns, Helga Westers, et al.
Cancers|September 30, 2020
Cancer Predisposition Genes in Cancer-Free FamiliesGuoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
A rare large duplication of MLH1 identified in Lynch syndromeAbhishek Kumar, Nagarajan Paramasivam, Obul Reddy Bandapalli, et al.
Cells|January 8, 2023
Investigation of Rare Non-Coding Variants in Familial Multiple MyelomaYasmeen Niazi, Nagarajan Paramasivam, Joanna Blocka, et al.
Communications Medicine|November 19, 2025
Systemic barriers and opportunities for equity in early implementation of genetic testing and counseling for cardiomyopathies in TanzaniaMohamed Zahir Alimohamed, Abdilahi Kiula, Lulu Fundikira, et al.
Familial Cancer|July 31, 2009
Attitude towards pre-implantation genetic diagnosis for hereditary cancerChantal Lammens, Eveline Bleiker, Neil Aaronson, et al.
Database : the Journal of Biological Databases and Curation|September 20, 2015
SORTA: a system for ontology-based re-coding and technical annotation of biomedical phenotype dataChao Pang, Annet Sollie, Anna Sijtsma, et al.
Blood Cancer Journal|February 15, 2021
Characterization of rare germline variants in familial multiple myelomaCalogerina Catalano, Nagarajan Paramasivam, Joanna Blocka, et al.
Pageof 3