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

H Ledbetter

Showing results (371-380 of 388) with videos related to

Pageof 39
Sort By:
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Frontiers in Genetics|September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass indexRobert M Cronin, Julie R Field, Yuki Bradford, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Science (New York, N.Y.)|April 30, 2020
Feasibility of blood testing combined with PET-CT to screen for cancer and guide interventionAnne Marie Lennon, Adam H Buchanan, Isaac Kinde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Expert Review of Molecular Diagnostics|January 27, 2016
Toward clinical genomics in everyday medicine: perspectives and recommendationsSusan K Delaney, Michael L Hultner, Howard J Jacob, et al.
Nature|October 22, 2020
Exome sequencing and characterization of 49,960 individuals in the UK BiobankCristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Pageof 39

Showing results (371-380 of 388) with videos related to

Sort By:
Pageof 39
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2011
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilitiesErin B Kaminsky, Vineith Kaul, Justin Paschall, et al.
Frontiers in Genetics|September 2, 2014
Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass indexRobert M Cronin, Julie R Field, Yuki Bradford, et al.
American Journal of Human Genetics|November 9, 2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophreniaDaniel Moreno-De-Luca, , Jennifer G Mulle, et al.
Science (New York, N.Y.)|April 30, 2020
Feasibility of blood testing combined with PET-CT to screen for cancer and guide interventionAnne Marie Lennon, Adam H Buchanan, Isaac Kinde, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Recommendations for the integration of genomics into clinical practiceSarah Bowdin, Adel Gilbert, Emma Bedoukian, et al.
Expert Review of Molecular Diagnostics|January 27, 2016
Toward clinical genomics in everyday medicine: perspectives and recommendationsSusan K Delaney, Michael L Hultner, Howard J Jacob, et al.
Nature|October 22, 2020
Exome sequencing and characterization of 49,960 individuals in the UK BiobankCristopher V Van Hout, Ioanna Tachmazidou, Joshua D Backman, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Pageof 39