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Human Genomics|June 6, 2025
Parents' perspectives on expanded newborn genomic screening in Abu Dhabi, United Arab EmiratesYasir Ahmed Mohammed Elhadi, Marwa Alkatheeri, Maryam Alktifan, et al.Human Genomics|July 21, 2026
ExposoGenomics: integrating genome and exposome as jointly dynamic systems for causal discovery and precision healthVasilis Vasiliou, Nicholas Katsanis, Giuseppe Novelli, et al.Human Genomics|July 21, 2026
Association of APOC2 upstream variant rs10425530 with BMI predicted to overlap with NR2C2, GCM2 and NR2C1 binding sitesSuzanne A Al-Bustan, Babitha G Annice, Hasan AlhaddadHuman Genomics|June 13, 2022
From COVID to fibrosis: lessons from single-cell analyses of the human lungAurelien Justet, Amy Y Zhao, Naftali KaminskiHuman Genomics|February 8, 2011
A short survey of computational analysis methods in analysing ChIP-seq dataHyunmin Kim, Jihye Kim, Heather Selby, et al.Human Genomics|July 24, 2010
ETHNOS : A versatile electronic tool for the development and curation of national genetic databasesSjozef van Baal, Joël Zlotogora, George Lagoumintzis, et al.Human Genomics|June 1, 2010
The clinical application of UGT1A1 pharmacogenetic testing: gene-environment interactionsSara Correia Marques, Ogechi N IkediobiHuman Genomics|June 1, 2010
Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorderGunda Millonig, Martina U Muckenthaler, Sebastian MuellerHuman Genomics|September 18, 2010
An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) geneDavid S Millar, Carolyn Tysoe, Lazarus P Lazarou, et al.Human Genomics|September 18, 2010
KinSNP software for homozygosity mapping of disease genes using SNP microarraysEl-Ad David Amir, Ofer Bartal, Efrat Morad, et al.Pageof 112