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Karol Estrada

Showing results (21-30 of 92) with videos related to

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Plos Genetics|August 15, 2009
Tissue effect on genetic control of transcript isoform variationTony Kwan, Elin Grundberg, Vonda Koka, et al.
Clinical Epigenetics|June 17, 2020
Harnessing peripheral DNA methylation differences in the Alzheimer's Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of diseaseAparna Vasanthakumar, Justin W Davis, Kenneth Idler, et al.
American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
European Journal of Human Genetics : EJHG|March 17, 2011
Genomic inflation factors under polygenic inheritanceJian Yang, Michael N Weedon, Shaun Purcell, et al.
Genome Research|August 6, 2009
Population genomics in a disease targeted primary cell modelElin Grundberg, Tony Kwan, Bing Ge, et al.
Human Molecular Genetics|September 13, 2016
Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing studyYi-Hsiang Hsu, Guo Li, Ching-Ti Liu, et al.
Plos Genetics|January 8, 2021
Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptomeDenis A Baird, Jimmy Z Liu, Jie Zheng, et al.
Diabetes Care|January 15, 2013
High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam StudyLing Oei, M Carola Zillikens, Abbas Dehghan, et al.
Nature Genetics|January 2, 2025
Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traitsNora Scherer, Daniel Fässler, Oleg Borisov, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Pageof 10

Showing results (21-30 of 92) with videos related to

Sort By:
Pageof 10
Plos Genetics|August 15, 2009
Tissue effect on genetic control of transcript isoform variationTony Kwan, Elin Grundberg, Vonda Koka, et al.
Clinical Epigenetics|June 17, 2020
Harnessing peripheral DNA methylation differences in the Alzheimer's Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of diseaseAparna Vasanthakumar, Justin W Davis, Kenneth Idler, et al.
American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
European Journal of Human Genetics : EJHG|March 17, 2011
Genomic inflation factors under polygenic inheritanceJian Yang, Michael N Weedon, Shaun Purcell, et al.
Genome Research|August 6, 2009
Population genomics in a disease targeted primary cell modelElin Grundberg, Tony Kwan, Bing Ge, et al.
Human Molecular Genetics|September 13, 2016
Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing studyYi-Hsiang Hsu, Guo Li, Ching-Ti Liu, et al.
Plos Genetics|January 8, 2021
Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptomeDenis A Baird, Jimmy Z Liu, Jie Zheng, et al.
Diabetes Care|January 15, 2013
High bone mineral density and fracture risk in type 2 diabetes as skeletal complications of inadequate glucose control: the Rotterdam StudyLing Oei, M Carola Zillikens, Abbas Dehghan, et al.
Nature Genetics|January 2, 2025
Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traitsNora Scherer, Daniel Fässler, Oleg Borisov, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Pageof 10