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Christian Fuchsberger

Showing results (41-50 of 151) with videos related to

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Plos One|June 24, 2025
Systematic mediation and interaction analyses of kidney function genetic loci in a general population studyDariush Ghasemi-Semeskandeh, David Emmert, Eva König, et al.
Frontiers in Neurology|August 26, 2021
Frequency of Heterozygous Parkin (<i>PRKN</i>) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS CohortMaria Paulina Castelo Rueda, Athina Raftopoulou, Martin Gögele, et al.
Metabolites|July 27, 2022
Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS CohortEva König, Johannes Rainer, Vinicius Verri Hernandes, et al.
Nature Genetics|October 4, 2016
Reference-based phasing using the Haplotype Reference Consortium panelPo-Ru Loh, Petr Danecek, Pier Francesco Palamara, et al.
Journal of Translational Medicine|December 6, 2019
Microbiota, type 2 diabetes and non-alcoholic fatty liver disease: protocol of an observational studyBenedetta M Motta, Christoph Grander, Martin Gögele, et al.
G3 (Bethesda, Md.)|August 23, 2018
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association StudiesGenevieve L Wojcik, Christian Fuchsberger, Daniel Taliun, et al.
Journal of Molecular Neuroscience : MN|October 12, 2012
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genesIrene Pichler, Christine Schwienbacher, Alessandra Zanon, et al.
HGG Advances|February 9, 2026
A reference panel for linkage disequilibrium and genotype imputation using whole-genome sequencing data from 2,680 participants across IndiaZheng Li, Wei Zhao, Xiang Zhou, et al.
BMC Genomic Data|September 17, 2025
Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunctionMohammed Aslam Imtiaz, Konstantinos Melas, Adrienne Tin, et al.
BMC Proceedings|December 19, 2014
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigreesLaura Almasy, Thomas D Dyer, Juan M Peralta, et al.
Pageof 16

Showing results (41-50 of 151) with videos related to

Sort By:
Pageof 16
Plos One|June 24, 2025
Systematic mediation and interaction analyses of kidney function genetic loci in a general population studyDariush Ghasemi-Semeskandeh, David Emmert, Eva König, et al.
Frontiers in Neurology|August 26, 2021
Frequency of Heterozygous Parkin (<i>PRKN</i>) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS CohortMaria Paulina Castelo Rueda, Athina Raftopoulou, Martin Gögele, et al.
Metabolites|July 27, 2022
Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS CohortEva König, Johannes Rainer, Vinicius Verri Hernandes, et al.
Nature Genetics|October 4, 2016
Reference-based phasing using the Haplotype Reference Consortium panelPo-Ru Loh, Petr Danecek, Pier Francesco Palamara, et al.
Journal of Translational Medicine|December 6, 2019
Microbiota, type 2 diabetes and non-alcoholic fatty liver disease: protocol of an observational studyBenedetta M Motta, Christoph Grander, Martin Gögele, et al.
G3 (Bethesda, Md.)|August 23, 2018
Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association StudiesGenevieve L Wojcik, Christian Fuchsberger, Daniel Taliun, et al.
Journal of Molecular Neuroscience : MN|October 12, 2012
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genesIrene Pichler, Christine Schwienbacher, Alessandra Zanon, et al.
HGG Advances|February 9, 2026
A reference panel for linkage disequilibrium and genotype imputation using whole-genome sequencing data from 2,680 participants across IndiaZheng Li, Wei Zhao, Xiang Zhou, et al.
BMC Genomic Data|September 17, 2025
Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunctionMohammed Aslam Imtiaz, Konstantinos Melas, Adrienne Tin, et al.
BMC Proceedings|December 19, 2014
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigreesLaura Almasy, Thomas D Dyer, Juan M Peralta, et al.
Pageof 16