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Nature Medicine
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June 11, 2025
T and B cell responses against Epstein-Barr virus in primary sclerosing cholangitis
Hesham ElAbd, Mitchell Pesesky, Gabriel Innocenti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Alexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Journal of Hepatology
|
April 24, 2012
Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci
Trine Folseraas, Espen Melum, Philipp Rausch, et al.
Frontiers in Aging Neuroscience
|
April 7, 2022
Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset
Jan Homann, Tim Osburg, Olena Ohlei, et al.
American Journal of Human Genetics
|
December 3, 2014
Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2
Ellen Cottenie, Andrzej Kochanski, Albena Jordanova, et al.
Nutrients
|
May 16, 2017
A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine
Vibeke Andersen, Uffe Holmskov, Signe Bek Sørensen, et al.
Nature Communications
|
May 25, 2017
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
Lam C Tsoi, Philip E Stuart, Chao Tian, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 3, 2018
IKZF1<sup>plus</sup> Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia
Martin Stanulla, Elif Dagdan, Marketa Zaliova, et al.
Human Molecular Genetics
|
April 28, 2017
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis
Matthias Munz, Christina Willenborg, Gesa M Richter, et al.
Nature Communications
|
March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Andreas Keller, Angela Graefen, Markus Ball, et al.
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Search research articles
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Showing results (541-550 of 678) with videos related to
Sort By:
Page
of 68
Nature Medicine
|
June 11, 2025
T and B cell responses against Epstein-Barr virus in primary sclerosing cholangitis
Hesham ElAbd, Mitchell Pesesky, Gabriel Innocenti, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease
Alexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Journal of Hepatology
|
April 24, 2012
Extended analysis of a genome-wide association study in primary sclerosing cholangitis detects multiple novel risk loci
Trine Folseraas, Espen Melum, Philipp Rausch, et al.
Frontiers in Aging Neuroscience
|
April 7, 2022
Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset
Jan Homann, Tim Osburg, Olena Ohlei, et al.
American Journal of Human Genetics
|
December 3, 2014
Truncating and missense mutations in IGHMBP2 cause Charcot-Marie Tooth disease type 2
Ellen Cottenie, Andrzej Kochanski, Albena Jordanova, et al.
Nutrients
|
May 16, 2017
A Proposal for a Study on Treatment Selection and Lifestyle Recommendations in Chronic Inflammatory Diseases: A Danish Multidisciplinary Collaboration on Prognostic Factors and Personalised Medicine
Vibeke Andersen, Uffe Holmskov, Signe Bek Sørensen, et al.
Nature Communications
|
May 25, 2017
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants
Lam C Tsoi, Philip E Stuart, Chao Tian, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 3, 2018
IKZF1<sup>plus</sup> Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia
Martin Stanulla, Elif Dagdan, Marketa Zaliova, et al.
Human Molecular Genetics
|
April 28, 2017
A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis
Matthias Munz, Christina Willenborg, Gesa M Richter, et al.
Nature Communications
|
March 20, 2012
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing
Andreas Keller, Angela Graefen, Markus Ball, et al.
Page
of 68