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M Neale

Showing results (371-380 of 551) with videos related to

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The American Journal of Psychiatry|March 2, 2019
Genetic Markers of ADHD-Related Variations in Intracranial VolumeMarieke Klein, Raymond K Walters, Ditte Demontis, et al.
Nature Human Behaviour|July 4, 2024
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variationCaitlin E Carey, Rebecca Shafee, Robbee Wedow, et al.
Bioinformatics (Oxford, England)|September 25, 2016
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysisJie Zheng, A Mesut Erzurumluoglu, Benjamin L Elsworth, et al.
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.
Pageof 56

Showing results (371-380 of 551) with videos related to

Sort By:
Pageof 56
The American Journal of Psychiatry|March 2, 2019
Genetic Markers of ADHD-Related Variations in Intracranial VolumeMarieke Klein, Raymond K Walters, Ditte Demontis, et al.
Nature Human Behaviour|July 4, 2024
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variationCaitlin E Carey, Rebecca Shafee, Robbee Wedow, et al.
Bioinformatics (Oxford, England)|September 25, 2016
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysisJie Zheng, A Mesut Erzurumluoglu, Benjamin L Elsworth, et al.
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.
Pageof 56