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Plos One|August 26, 2020
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran programMarina Serper, Marijana Vujkovic, David E Kaplan, et al.
Medrxiv : the Preprint Server for Health Sciences|November 14, 2023
CXCL12 drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Daniela Zanetti, Jiayan Zhou, et al.
Cell|March 6, 2025
CXCL12 drives natural variation in coronary artery anatomy across diverse populationsPamela E Rios Coronado, Jiayan Zhou, Xiaochen Fan, et al.
Medrxiv : the Preprint Server for Health Sciences|October 13, 2021
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran ProgramAnurag Verma, Noah Tsao, Lauren Thomann, et al.
Nature Communications|May 3, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucomaJoel T Rämö, Bryan R Gorman, Lu-Chen Weng, et al.
Medrxiv : the Preprint Server for Health Sciences|March 22, 2023
Correlates of suicidal behaviors and genetic risk among United States veterans with schizophrenia or bipolar I disorderTim B Bigdeli, Peter B Barr, Nallakkandi Rajeevan, et al.
Molecular Psychiatry|March 16, 2024
Correlates of suicidal behaviors and genetic risk among United States veterans with schizophrenia or bipolar I disorderTim B Bigdeli, Peter B Barr, Nallakkandi Rajeevan, et al.
Nature|October 15, 2020
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cellsErik L Bao, Satish K Nandakumar, Xiaotian Liao, et al.
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