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

Benjamin M Neale

Showing results (131-140 of 293) with videos related to

Pageof 30
Sort By:
Nature Communications|October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projectsAllison A Regier, Yossi Farjoun, David E Larson, et al.
Nature Communications|February 16, 2021
Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Veera M Rajagopal, et al.
Nature Genetics|May 30, 2012
Exome sequencing and the genetic basis of complex traitsAdam Kiezun, Kiran Garimella, Ron Do, et al.
Nature|May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomesHaley J Abel, David E Larson, Allison A Regier, et al.
Science Translational Medicine|June 26, 2020
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human geneticsJonas Bovijn, Kristi Krebs, Chia-Yen Chen, et al.
Nature Communications|January 26, 2021
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Veera M Rajagopal, et al.
Cell Genomics|May 20, 2022
Genome-wide risk prediction of common diseases across ancestries in one million peopleNina Mars, Sini Kerminen, Yen-Chen A Feng, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Science Translational Medicine|December 1, 2021
Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics"Jonas Bovijn, Kristi Krebs, Chia-Yen Chen, et al.
Pageof 30

Showing results (131-140 of 293) with videos related to

Sort By:
Pageof 30
Nature Communications|October 4, 2018
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projectsAllison A Regier, Yossi Farjoun, David E Larson, et al.
Nature Communications|February 16, 2021
Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Veera M Rajagopal, et al.
Nature Genetics|May 30, 2012
Exome sequencing and the genetic basis of complex traitsAdam Kiezun, Kiran Garimella, Ron Do, et al.
Nature|May 28, 2020
Mapping and characterization of structural variation in 17,795 human genomesHaley J Abel, David E Larson, Allison A Regier, et al.
Science Translational Medicine|June 26, 2020
Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human geneticsJonas Bovijn, Kristi Krebs, Chia-Yen Chen, et al.
Nature Communications|January 26, 2021
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorderDitte Demontis, Raymond K Walters, Veera M Rajagopal, et al.
Cell Genomics|May 20, 2022
Genome-wide risk prediction of common diseases across ancestries in one million peopleNina Mars, Sini Kerminen, Yen-Chen A Feng, et al.
Nature Genetics|April 11, 2018
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell typesHilary K Finucane, Yakir A Reshef, Verneri Anttila, et al.
Molecular Autism|May 27, 2014
Rare deleterious mutations of the gene EFR3A in autism spectrum disordersAbha R Gupta, Michelle Pirruccello, Feng Cheng, et al.
Science Translational Medicine|December 1, 2021
Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics"Jonas Bovijn, Kristi Krebs, Chia-Yen Chen, et al.
Pageof 30