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Kasmintan Schrader

Showing results (1-10 of 17) with videos related to

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Cancer Treatment and Research|June 3, 2010
Hereditary diffuse gastric cancerKasmintan Schrader, David Huntsman
Oncology (Williston Park, N.Y.)|June 27, 2012
Genetic testing in gastrointestinal cancers: a case-based approachKasmintan Schrader, Kenneth Offit, Zsofia K Stadler
Familial Cancer|March 12, 2013
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancerShaheen Alanee, Sohela Shah, Joseph Vijai, et al.
European Journal of Human Genetics : EJHG|April 29, 2018
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing resultsYvonne Bombard, Marc Clausen, Chloe Mighton, et al.
Briefings in Bioinformatics|September 12, 2015
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genesSteven N Hart, Kara N Maxwell, Tinu Thomas, et al.
European Journal of Human Genetics : EJHG|May 20, 2020
Quality of life drives patients' preferences for secondary findings from genomic sequencingChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
European Journal of Human Genetics : EJHG|February 6, 2019
Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genesMykyta Artomov, Vijai Joseph, Grace Tiao, et al.
Public Health Genomics|October 24, 2024
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer SyndromesRidhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, et al.
European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Cancer Treatment and Research|June 3, 2010
Hereditary diffuse gastric cancerKasmintan Schrader, David Huntsman
Oncology (Williston Park, N.Y.)|June 27, 2012
Genetic testing in gastrointestinal cancers: a case-based approachKasmintan Schrader, Kenneth Offit, Zsofia K Stadler
Familial Cancer|March 12, 2013
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancerShaheen Alanee, Sohela Shah, Joseph Vijai, et al.
European Journal of Human Genetics : EJHG|April 29, 2018
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing resultsYvonne Bombard, Marc Clausen, Chloe Mighton, et al.
Briefings in Bioinformatics|September 12, 2015
Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genesSteven N Hart, Kara N Maxwell, Tinu Thomas, et al.
European Journal of Human Genetics : EJHG|May 20, 2020
Quality of life drives patients' preferences for secondary findings from genomic sequencingChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
European Journal of Human Genetics : EJHG|February 6, 2019
Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genesMykyta Artomov, Vijai Joseph, Grace Tiao, et al.
Public Health Genomics|October 24, 2024
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer SyndromesRidhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, et al.
European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.
American Journal of Human Genetics|August 7, 2012
Rare de novo germline copy-number variation in testicular cancerZsofia K Stadler, Diane Esposito, Sohela Shah, et al.
Pageof 2