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Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discoveryJack Humphrey, Ali Oku, Marta Byrska-Bishop, et al.Plos Genetics|February 6, 2014
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysmsMitja I Kurki, Emília Ilona Gaál, Johannes Kettunen, et al.Plos One|December 31, 2020
Impact of COVID-19 pandemic on mental health: An international studyAndrew T Gloster, Demetris Lamnisos, Jelena Lubenko, et al.Cell Genomics|October 23, 2023
The functional impact of rare variation across the regulatory cascadeTaibo Li, Nicole Ferraro, Benjamin J Strober, et al.Science (New York, N.Y.)|May 9, 2015
Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptomeManuel A Rivas, Matti Pirinen, Donald F Conrad, et al.Medrxiv : the Preprint Server for Health Sciences|December 16, 2024
Epigenome-wide Association Analysis of Mitochondrial Heteroplasmy Provides Insight into Molecular Mechanisms of DiseaseMeng Lai, Kyeezu Kim, Yinan Zheng, et al.Science (New York, N.Y.)|September 11, 2020
The impact of sex on gene expression across human tissuesMeritxell Oliva, Manuel Muñoz-Aguirre, Sarah Kim-Hellmuth, et al.Cancers|December 24, 2021
Mental Health and Adherence to COVID-19 Protective Behaviors among Cancer Patients during the COVID-19 Pandemic: An International, Multinational Cross-Sectional StudyAngelos P Kassianos, Alexandros Georgiou, Maria Kyprianidou, et al.Science (New York, N.Y.)|October 5, 2013
Integrative annotation of variants from 1092 humans: application to cancer genomicsEkta Khurana, Yao Fu, Vincenza Colonna, et al.European Journal of Human Genetics : EJHG|August 3, 2018
Registered access: authorizing data accessStephanie O M Dyke, Mikael Linden, Ilkka Lappalainen, et al.Pageof 115