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K Kohlmann

Showing results (21-30 of 52) with videos related to

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Journal of Biomedical Informatics|December 11, 2023
Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their ownRichard L Bradshaw, Kensaku Kawamoto, Jemar R Bather, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 4, 2012
Systemic illness moderates the impact of N-acetyl cysteine in bipolar disorderP V Magalhães, O M Dean, A I Bush, et al.
JAMA Network Open|October 28, 2025
Incomplete Family History and Meeting Algorithmic Criteria for Genetic Evaluation of Hereditary CancerAdrian Harris, Jemar R Bather, Richard L Bradshaw, et al.
Molecular Genetics & Genomic Medicine|October 29, 2020
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factorLisa A Cannon-Albright, Craig C Teerlink, Jeffrey Stevens, et al.
African Journal of Psychiatry|September 21, 2013
Deserves a hearing? A case report of remitting tinnitus with N-acetyl cysteineO M Dean, S Jeavons, G S Malhi, et al.
Molecular Ecology|March 17, 2001
Matrilinear phylogeography of Atlantic salmon (Salmo salar L.) in Europe and postglacial colonization of the Baltic Sea areaJ Nilsson, R Gross, T Asplund, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2017
Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair DisordersMichael F Walsh, Vivian Y Chang, Wendy K Kohlmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 17, 2017
Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in ChildhoodSurya P Rednam, Ayelet Erez, Harriet Druker, et al.
Clinical Genetics|May 20, 2020
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposisBryony A Thompson, Angela K Snow, Cathryn Koptiuch, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 4, 2017
Genetic Testing in a Population-Based Sample of Breast and Ovarian Cancer Survivors from the REACH Randomized Trial: Cost Barriers and Moderators of Counseling ModeLaurie E Steffen, Ruofei Du, Amanda Gammon, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Journal of Biomedical Informatics|December 11, 2023
Enhanced family history-based algorithms increase the identification of individuals meeting criteria for genetic testing of hereditary cancer syndromes but would not reduce disparities on their ownRichard L Bradshaw, Kensaku Kawamoto, Jemar R Bather, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry|January 4, 2012
Systemic illness moderates the impact of N-acetyl cysteine in bipolar disorderP V Magalhães, O M Dean, A I Bush, et al.
JAMA Network Open|October 28, 2025
Incomplete Family History and Meeting Algorithmic Criteria for Genetic Evaluation of Hereditary CancerAdrian Harris, Jemar R Bather, Richard L Bradshaw, et al.
Molecular Genetics & Genomic Medicine|October 29, 2020
FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factorLisa A Cannon-Albright, Craig C Teerlink, Jeffrey Stevens, et al.
African Journal of Psychiatry|September 21, 2013
Deserves a hearing? A case report of remitting tinnitus with N-acetyl cysteineO M Dean, S Jeavons, G S Malhi, et al.
Molecular Ecology|March 17, 2001
Matrilinear phylogeography of Atlantic salmon (Salmo salar L.) in Europe and postglacial colonization of the Baltic Sea areaJ Nilsson, R Gross, T Asplund, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 3, 2017
Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair DisordersMichael F Walsh, Vivian Y Chang, Wendy K Kohlmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 17, 2017
Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in ChildhoodSurya P Rednam, Ayelet Erez, Harriet Druker, et al.
Clinical Genetics|May 20, 2020
A novel ribosomal protein S20 variant in a family with unexplained colorectal cancer and polyposisBryony A Thompson, Angela K Snow, Cathryn Koptiuch, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 4, 2017
Genetic Testing in a Population-Based Sample of Breast and Ovarian Cancer Survivors from the REACH Randomized Trial: Cost Barriers and Moderators of Counseling ModeLaurie E Steffen, Ruofei Du, Amanda Gammon, et al.
Pageof 6