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Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Gut
|
July 5, 2022
Genetic variation in <i>TERT</i> modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study
Stephan Buch, Hamish Innes, Philipp Ludwig Lutz, et al.
The Lancet. Neurology
|
October 15, 2017
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Barbara Schormair, Chen Zhao, Steven Bell, et al.
Annals of Clinical and Translational Neurology
|
June 19, 2025
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Human Molecular Genetics
|
February 8, 2021
Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations
Frauke Degenhardt, Gabriele Mayr, Mareike Wendorff, et al.
Human Mutation
|
June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Roxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 10, 2019
Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay
Liu Shi, Sarah Westwood, Alison L Baird, et al.
Human Molecular Genetics
|
October 4, 2017
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling
Nick Dand, Sören Mucha, Lam C Tsoi, et al.
Inflammatory Bowel Diseases
|
September 21, 2017
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea
Britt-Sabina Petersen, Dietrich August, Renate Abt, et al.
Plos Genetics
|
May 31, 2019
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Manuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
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of 68
Search research articles
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Showing results (581-590 of 678) with videos related to
Sort By:
Page
of 68
Medrxiv : the Preprint Server for Health Sciences
|
March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality
Tomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Gut
|
July 5, 2022
Genetic variation in <i>TERT</i> modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study
Stephan Buch, Hamish Innes, Philipp Ludwig Lutz, et al.
The Lancet. Neurology
|
October 15, 2017
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
Barbara Schormair, Chen Zhao, Steven Bell, et al.
Annals of Clinical and Translational Neurology
|
June 19, 2025
Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large-Scale Exome Sequencing
Mirja Thomsen, Fabian Ott, Sebastian Loens, et al.
Human Molecular Genetics
|
February 8, 2021
Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations
Frauke Degenhardt, Gabriele Mayr, Mareike Wendorff, et al.
Human Mutation
|
June 22, 2017
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges
Roxana Daneshjou, Yanran Wang, Yana Bromberg, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 10, 2019
Discovery and validation of plasma proteomic biomarkers relating to brain amyloid burden by SOMAscan assay
Liu Shi, Sarah Westwood, Alison L Baird, et al.
Human Molecular Genetics
|
October 4, 2017
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling
Nick Dand, Sören Mucha, Lam C Tsoi, et al.
Inflammatory Bowel Diseases
|
September 21, 2017
Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea
Britt-Sabina Petersen, Dietrich August, Renate Abt, et al.
Plos Genetics
|
May 31, 2019
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Manuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Page
of 68