Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

David W Craig

Showing results (21-30 of 161) with videos related to

Pageof 17
Sort By:
Nature Reviews. Genetics|March 22, 2016
Translating RNA sequencing into clinical diagnostics: opportunities and challengesSara A Byron, Kendall R Van Keuren-Jensen, David M Engelthaler, et al.
F1000Research|November 13, 2023
Multiomic sequencing of paired primary and metastatic small bowel carcinoidsMackenzie D Postel, Sourat Darabi, James R Howe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2016
Dystonia in ATP2B3-associated X-linked spinocerebellar ataxiaTimothy Feyma, Keri Ramsey, , et al.
Archives of Neurology|August 12, 2009
Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosisManuel Comabella, David W Craig, Carlos Morcillo-Suárez, et al.
BMC Genomics|May 7, 2013
Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairsAlexis Christoforides, John D Carpten, Glen J Weiss, et al.
Neurology. Genetics|February 10, 2017
A gain-of-function mutation in the <i>GRIK2</i> gene causes neurodevelopmental deficitsYomayra F Guzmán, Keri Ramsey, Jacob R Stolz, et al.
Plos One|October 23, 2008
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphismsManuel Comabella, David W Craig, Montse Camiña-Tato, et al.
Nature Reviews. Genetics|September 17, 2011
Assessing and managing risk when sharing aggregate genetic variant dataDavid W Craig, Robert M Goor, Zhenyuan Wang, et al.
Neuroscience Letters|August 16, 2011
Induction of pluripotent stem cells from autopsy donor-derived somatic cellsBrooke E Hjelm, Jon B Rosenberg, Szabolcs Szelinger, et al.
Translational Psychiatry|November 25, 2020
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in miceKazuo Nakajima, Alannah Miranda, David W Craig, et al.
Pageof 17

Showing results (21-30 of 161) with videos related to

Sort By:
Pageof 17
Nature Reviews. Genetics|March 22, 2016
Translating RNA sequencing into clinical diagnostics: opportunities and challengesSara A Byron, Kendall R Van Keuren-Jensen, David M Engelthaler, et al.
F1000Research|November 13, 2023
Multiomic sequencing of paired primary and metastatic small bowel carcinoidsMackenzie D Postel, Sourat Darabi, James R Howe, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2016
Dystonia in ATP2B3-associated X-linked spinocerebellar ataxiaTimothy Feyma, Keri Ramsey, , et al.
Archives of Neurology|August 12, 2009
Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosisManuel Comabella, David W Craig, Carlos Morcillo-Suárez, et al.
BMC Genomics|May 7, 2013
Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairsAlexis Christoforides, John D Carpten, Glen J Weiss, et al.
Neurology. Genetics|February 10, 2017
A gain-of-function mutation in the <i>GRIK2</i> gene causes neurodevelopmental deficitsYomayra F Guzmán, Keri Ramsey, Jacob R Stolz, et al.
Plos One|October 23, 2008
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphismsManuel Comabella, David W Craig, Montse Camiña-Tato, et al.
Nature Reviews. Genetics|September 17, 2011
Assessing and managing risk when sharing aggregate genetic variant dataDavid W Craig, Robert M Goor, Zhenyuan Wang, et al.
Neuroscience Letters|August 16, 2011
Induction of pluripotent stem cells from autopsy donor-derived somatic cellsBrooke E Hjelm, Jon B Rosenberg, Szabolcs Szelinger, et al.
Translational Psychiatry|November 25, 2020
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in miceKazuo Nakajima, Alannah Miranda, David W Craig, et al.
Pageof 17