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Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Individuals whose phenotype deviates from genetic expectation defined by common variation are enriched for rare damaging variants in genes that cause rare diseaseNikolas A Baya, Frederik H Lassen, Barney Hill, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Family-based association study of DYX1C1 variants in autismTero Ylisaukko-Oja, Myriam Peyrard-Janvid, Cecilia M Lindgren, et al.
Medical & Biological Engineering & Computing|January 29, 2010
A technique based on laser Doppler flowmetry and photoplethysmography for simultaneously monitoring blood flow at different tissue depthsJ Hagblad, L-G Lindberg, A Kaisdotter Andersson, et al.
Biochimica Et Biophysica Acta|August 10, 2000
Deletion analogues of transportanU Soomets, M Lindgren, X Gallet, et al.
Diabetes|March 12, 2008
Common variants in maturity-onset diabetes of the young genes and future risk of type 2 diabetesJohan Holmkvist, Peter Almgren, Valeriya Lyssenko, et al.
Genetic Epidemiology|December 30, 2009
A powerful approach to sub-phenotype analysis in population-based genetic association studiesAndrew P Morris, Cecilia M Lindgren, Eleftheria Zeggini, et al.
Journal of Medical Genetics|May 10, 2005
Global analysis of uniparental disomy using high density genotyping arraysS Bruce, R Leinonen, C M Lindgren, et al.
Schizophrenia Research|May 3, 2017
Anti-neuronal anti-bodies in patients with early psychosisO Mantere, M Saarela, T Kieseppä, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 22, 2007
Large-scale zygosity testing using single nucleotide polymorphismsUlf Hannelius, Loreana Gherman, Ville-Veikko Mäkelä, et al.
The Journal of Clinical Endocrinology and Metabolism|December 30, 2021
Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary SyndromeJia Zhu, Natàlia Pujol-Gualdo, Laura B L Wittemans, et al.
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