Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis-Reference-Cited by-同舟云学术

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Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis

Published:2019-03-01 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Nel Melissa,Mulder Nicola,Europa Tarin A.,Heckmann Jeannine M.

Funder

Association Française contre les Myopathies

Rare Disease Foundation

National Research Foundation

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

Reference55 articles.

1. An integrated map of genetic variation from 1,092 human genomes.;Abecasis;Nature,2012

2. Genetic effects on gene expression across human tissues.;Aguet;Nature,2017

3. Differences in gene expression between strabismic and normal human extraocular muscles.;Altick;Investig. Ophthalmol. Vis. Sci.,2012

4. Data quality control in genetic case-control association studies.;Anderson;Nat. Protoc.,2010

5. A global reference for human genetic variation.;Auton;Nature,2015

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2. Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans;Neurology Genetics;2023-08

3. Mitochondrial bioenergetics in ocular fibroblasts of two myasthenia gravis cases;IBRO Neuroscience Reports;2022-06

4. DCAF12 and HSPA1A May Serve as Potential Diagnostic Biomarkers for Myasthenia Gravis;BioMed Research International;2022-05-24

5. Post-Infectious Autoimmunity in the Central (CNS) and Peripheral (PNS) Nervous Systems: An African Perspective;Frontiers in Immunology;2022-03-09

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