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Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.Nature Medicine|August 25, 2015
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesYun R Li, Jin Li, Sihai D Zhao, et al.Plos One|December 14, 2012
Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populationsClara C Elbers, Yiran Guo, Vinicius Tragante, et al.The Review of Scientific Instruments|October 17, 2024
Overview of the early campaign diagnostics for the SPARC tokamak (invited)M L Reinke, I Abramovic, A Albert, et al.The Pharmacogenomics Journal|July 19, 2017
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiologyA A Seyerle, C M Sitlani, R Noordam, et al.Biorxiv : the Preprint Server for Biology|March 18, 2026
Disrupted Higher-Order Topology in OCD Brain Networks Revealed by Hodge Laplacian - an ENIGMA StudyHanyang Ruan, Moo K Chung, Willem B Bruin, et al.Physical Review Letters|December 23, 2022
Observation of a Strongly Isospin-Mixed Doublet in ^{26}Si via β-Delayed Two-Proton Decay of ^{26}PJ J Liu, X X Xu, L J Sun, et al.Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Toward trustworthy clinical AI for obsessive-compulsive disorder: reliability, generalizability, and interpretability of a transformer model across the ENIGMA-OCD consortiumMaria Pak, Youngchan Ryu, Sangyoon Bae, et al.Molecular Psychiatry|May 2, 2023
The functional connectome in obsessive-compulsive disorder: resting-state mega-analysis and machine learning classification for the ENIGMA-OCD consortiumWillem B Bruin, Yoshinari Abe, Pino Alonso, et al.Translational Psychiatry|February 22, 2022
The thalamus and its subnuclei-a gateway to obsessive-compulsive disorderCees J Weeland, Selina Kasprzak, Niels T de Joode, et al.Pageof 283