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Epigenomics|June 21, 2016
Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbancesSusanne Bens, Julia Kolarova, Jasmin Beygo, et al.Human Genetics|March 11, 2019
The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locusKristina Schlicht, Piotr Nyczka, Amke Caliebe, et al.Forensic Science International|November 8, 2016
A comment on the PCAST report: Skip the "match"/"non-match" stageGeoffrey Stewart Morrison, David H Kaye, David J Balding, et al.Genes|December 24, 2021
Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's DiseaseSebastian Koch, Björn-Hergen Laabs, Meike Kasten, et al.Medrxiv : the Preprint Server for Health Sciences|October 1, 2025
Validation of a Mitochondrial Polygenic Score for Parkinson's DiseaseJoshua Chin Ern Ooi, Yi Wen Tay, Ai Huey Tan, et al.The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|January 25, 2021
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity GenesGuillermo G Torres, Marianne Nygaard, Amke Caliebe, et al.Journal of Medical Genetics|April 12, 2014
A familial disorder of altered DNA-methylationAlmuth Caliebe, Julia Richter, Ole Ammerpohl, et al.Aging Cell|March 24, 2016
Immunochip analysis identifies association of the RAD50/IL13 region with human longevityFriederike Flachsbart, David Ellinghaus, Liljana Gentschew, et al.Nature Communications|May 3, 2018
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval EuropeansBen Krause-Kyora, Marcel Nutsua, Lisa Boehme, et al.Human Genetics|August 10, 2006
Clinical and molecular genetic features of ARC syndromePaul Gissen, Louise Tee, Colin A Johnson, et al.Pageof 28