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J Camp

Showing results (471-480 of 555) with videos related to

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HGG Advances|November 13, 2025
Inherited genetic risk in stillbirth: A shared genomic segments analysis of high-risk pedigreesTsegaselassie Workalemahu, Michael J Madsen, Sarah Lopez, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
International Journal of Cancer|September 16, 2011
A comprehensive study of polymorphisms in the ABCB1, ABCC2, ABCG2, NR1I2 genes and lymphoma riskDaniele Campa, Katja Butterbach, Susan L Slager, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 15, 2015
A Pooled Analysis of Reproductive Factors, Exogenous Hormone Use, and Risk of Multiple Myeloma among Women in the International Multiple Myeloma ConsortiumLaura Costas, Brice H Lambert, Brenda M Birmann, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 25, 2010
Genetic susceptibility variants for chronic lymphocytic leukemiaSusan L Slager, Lynn R Goldin, Sara S Strom, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2021
Rare protein-coding variants implicate genes involved in risk of suicide deathEmily DiBlasi, Andrey A Shabalin, Eric T Monson, et al.
Molecular Psychiatry|October 25, 2018
Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicideHilary Coon, Todd M Darlington, Emily DiBlasi, et al.
Cancer Research|May 12, 2011
National Cancer Institute Prostate Cancer Genetics WorkshopWilliam J Catalona, Joan E Bailey-Wilson, Nicola J Camp, et al.
British Journal of Haematology|June 23, 2016
Multiple myeloma and family history of lymphohaematopoietic cancers: Results from the International Multiple Myeloma ConsortiumLeah H Schinasi, Elizabeth E Brown, Nicola J Camp, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 12, 2013
Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypesSusan L Slager, Sara J Achenbach, Yan W Asmann, et al.
Pageof 56

Showing results (471-480 of 555) with videos related to

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Pageof 56
HGG Advances|November 13, 2025
Inherited genetic risk in stillbirth: A shared genomic segments analysis of high-risk pedigreesTsegaselassie Workalemahu, Michael J Madsen, Sarah Lopez, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic herniaCammon B Arrington, Steven B Bleyl, Nori Matsunami, et al.
International Journal of Cancer|September 16, 2011
A comprehensive study of polymorphisms in the ABCB1, ABCC2, ABCG2, NR1I2 genes and lymphoma riskDaniele Campa, Katja Butterbach, Susan L Slager, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 15, 2015
A Pooled Analysis of Reproductive Factors, Exogenous Hormone Use, and Risk of Multiple Myeloma among Women in the International Multiple Myeloma ConsortiumLaura Costas, Brice H Lambert, Brenda M Birmann, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 25, 2010
Genetic susceptibility variants for chronic lymphocytic leukemiaSusan L Slager, Lynn R Goldin, Sara S Strom, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 27, 2021
Rare protein-coding variants implicate genes involved in risk of suicide deathEmily DiBlasi, Andrey A Shabalin, Eric T Monson, et al.
Molecular Psychiatry|October 25, 2018
Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicideHilary Coon, Todd M Darlington, Emily DiBlasi, et al.
Cancer Research|May 12, 2011
National Cancer Institute Prostate Cancer Genetics WorkshopWilliam J Catalona, Joan E Bailey-Wilson, Nicola J Camp, et al.
British Journal of Haematology|June 23, 2016
Multiple myeloma and family history of lymphohaematopoietic cancers: Results from the International Multiple Myeloma ConsortiumLeah H Schinasi, Elizabeth E Brown, Nicola J Camp, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 12, 2013
Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypesSusan L Slager, Sara J Achenbach, Yan W Asmann, et al.
Pageof 56