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Genome Biology
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January 18, 2017
GAVIN: Gene-Aware Variant INterpretation for medical sequencing
K Joeri van der Velde, Eddy N de Boer, Cleo C van Diemen, et al.
Nature Communications
|
July 1, 2018
Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'
Nicola Pirastu, Peter K Joshi, Paul S de Vries, et al.
Nature Genetics
|
June 30, 2019
High-throughput identification of human SNPs affecting regulatory element activity
Joris van Arensbergen, Ludo Pagie, Vincent D FitzPatrick, et al.
BMC Biology
|
June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting
Bharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Plos Genetics
|
January 24, 2013
Human disease-associated genetic variation impacts large intergenic non-coding RNA expression
Vinod Kumar, Harm-Jan Westra, Juha Karjalainen, et al.
Genome Biology
|
January 15, 2022
Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression
Thomas H Jonkman, Koen F Dekkers, Roderick C Slieker, et al.
The Lancet. Neurology
|
March 4, 2008
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen
Hylke M Blauw, Jan H Veldink, Michael A van Es, et al.
NAR Genomics and Bioinformatics
|
February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflow
Willem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
BMJ Open
|
August 31, 2015
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics
Ettje F Tigchelaar, Alexandra Zhernakova, Jackie A M Dekens, et al.
Nature
|
August 12, 2021
Phantom epistasis between unlinked loci
Gibran Hemani, Joseph E Powell, Huanwei Wang, et al.
Page
of 27
Search research articles
Search
Showing results (81-90 of 265) with videos related to
Sort By:
Page
of 27
Genome Biology
|
January 18, 2017
GAVIN: Gene-Aware Variant INterpretation for medical sequencing
K Joeri van der Velde, Eddy N de Boer, Cleo C van Diemen, et al.
Nature Communications
|
July 1, 2018
Reply to 'Misestimation of heritability and prediction accuracy of male-pattern baldness'
Nicola Pirastu, Peter K Joshi, Paul S de Vries, et al.
Nature Genetics
|
June 30, 2019
High-throughput identification of human SNPs affecting regulatory element activity
Joris van Arensbergen, Ludo Pagie, Vincent D FitzPatrick, et al.
BMC Biology
|
June 26, 2019
RNA-Seq in 296 phased trios provides a high-resolution map of genomic imprinting
Bharati Jadhav, Ramin Monajemi, Kristina K Gagalova, et al.
Plos Genetics
|
January 24, 2013
Human disease-associated genetic variation impacts large intergenic non-coding RNA expression
Vinod Kumar, Harm-Jan Westra, Juha Karjalainen, et al.
Genome Biology
|
January 15, 2022
Functional genomics analysis identifies T and NK cell activation as a driver of epigenetic clock progression
Thomas H Jonkman, Koen F Dekkers, Roderick C Slieker, et al.
The Lancet. Neurology
|
March 4, 2008
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen
Hylke M Blauw, Jan H Veldink, Michael A van Es, et al.
NAR Genomics and Bioinformatics
|
February 13, 2026
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflow
Willem T K Maassen, Charlotte C E T Pape, Carlos G Urzua-Traslavina, et al.
BMJ Open
|
August 31, 2015
Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics
Ettje F Tigchelaar, Alexandra Zhernakova, Jackie A M Dekens, et al.
Nature
|
August 12, 2021
Phantom epistasis between unlinked loci
Gibran Hemani, Joseph E Powell, Huanwei Wang, et al.
Page
of 27