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Ebiomedicine|March 15, 2026
Testing the performance of polygenic scores for multiple traits to explain cerebral palsy in two independent cohortsJodi T Thomas, Alexander S F Berry, Matthew T Oetjens, et al.
International Journal of Radiation Oncology, Biology, Physics|March 31, 2009
Preliminary study of oxygen-enhanced longitudinal relaxation in MRI: a potential novel biomarker of oxygenation changes in solid tumorsJames P B O'Connor, Josephine H Naish, Geoff J M Parker, et al.
European Journal of Human Genetics : EJHG|July 12, 2020
Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of EnglandNicola Flaum, Robert D Morgan, George J Burghel, et al.
The Journal of Emergency Medicine|March 30, 2023
Timing and Outcomes After Coronary Angiography Following Out-of-Hospital Cardiac Arrest Without Signs of ST-Segment Elevation Myocardial InfarctionAndrew R Helber, David R Helfer, Aarika R Ferko, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
Clinical and genetic correlates of a circadian subtype of depression in the Australian Genetics of Depression StudyEmiliana Tonini, Jacob J Crouse, Mirim Shin, et al.
Nature Communications|August 17, 2022
GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elementsPeter H Dixon, Adam P Levine, Inês Cebola, et al.
Orphanet Journal of Rare Diseases|April 22, 2017
Graves' orbitopathy as a rare disease in Europe: a European Group on Graves' Orbitopathy (EUGOGO) position statementP Perros, L Hegedüs, L Bartalena, et al.
Molecular Biology Reports|March 20, 2021
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial diseaseAlejandro Horga, Andreea Manole, Alice L Mitchell, et al.
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