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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Neurological Disorders
Last data update: May 03, 2024
. (Total: 63770 Documents since 2012)
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The familial risk and heritability of multiple sclerosis and its onset phenotypes: A case-control study.
Graysen Steele Boles et al. Mult Scler 2023 13524585231185258
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Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry.
Joshua R Breedon et al. Brain communications 2023 5(2) fcad041
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A Cross-Trait, Mendelian Randomization Study to Investigate Whether Migraine Is a Risk Factor for Multiple Sclerosis.
Horton Mary K et al. Neurology 2023
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Familial autoimmunity in patients with idiopathic inflammatory myopathies.
Che Weng Ian et al. Journal of internal medicine 2022
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The White Matter Rounds experience: The importance of a multidisciplinary network to accelerate the diagnostic process for adult patients with rare white matter disorders.
Huang Yu Tong et al. Frontiers in neurology 2022 13928493
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Joint Genetic Inhibition of PCSK9 and CETP and the Association With Coronary Artery Disease: A Factorial Mendelian Randomization Study.
Cupido Arjen J et al. JAMA cardiology 2022
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Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans.
Shams Hengameh et al. Brain : a journal of neurology 2022
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Epidemiology of familial multiple sclerosis in Iran: a national registry-based study.
Salehi Zahra et al. BMC neurology 2022 22(1) 76
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Genetics and familial distribution of multiple sclerosis: A review.
Balcerac A et al. Revue neurologique 2022
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Persistently reduced humoral and cellular immune response following third SARS-CoV-2 mRNA vaccination in anti-CD20-treated multiple sclerosis patients
HM Bajwa et al, MEDRXIV, January 28, 2022
Developing a clinical-environmental-genotypic prognostic index for relapsing-onset multiple sclerosis and clinically isolated syndrome.
Fuh-Ngwa Valery et al. Brain communications 2021 3(4) fcab288
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Cellular and humoral immune responses following SARS-CoV-2 mRNA vaccination in patients with multiple sclerosis on anti-CD20 therapy
SA Apostolides et al, Nature Medicine, September 14, 2021
Familial History of Autoimmune Disorders Among Patients With Pediatric Multiple Sclerosis.
Greenberg Benjamin M et al. Neurology(R) neuroimmunology & neuroinflammation 2021 8(5)
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Identification of differential DNA methylation associated with multiple sclerosis: A family-based study.
Garcia-Manteiga J M et al. Journal of neuroimmunology 2021 356577600
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Aggregation of autoimmunity in extended families of people with autoimmune Addison's disease.
Fichna Marta et al. Internal medicine journal 2021
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Next-Generation Sequencing Technologies and Neurogenetic Diseases.
Sun Hui et al. Life (Basel, Switzerland) 2021 11(4)
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Genome-wide genetic links between amyotrophic lateral sclerosis and autoimmune diseases.
Li Chun Yu et al. BMC medicine 2021 Feb 19(1) 27
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Familial aggregation of multiple sclerosis: Results from the national registry of the disease in Saudi Arabia.
AlJumah Mohammed et al. Multiple sclerosis journal - experimental, translational and clinical 6(4) 2055217320960499
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Variants of genes encoding TNF receptors and ligands and proteins regulating TNF activation in familial multiple sclerosis.
Torre-Fuentes Laura et al. CNS neuroscience & therapeutics 2020 Sep
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The PNPLA3 rs738409 variant can increase the risk of liver toxicity in multiple sclerosis patients treated with beta-interferon.
Capone Fioravante et al. Clinical neurology and neurosurgery 2020 Aug 197106166
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[The analysis of association between multiple sclerosis and genetic markers identified in genome-wide association studies].
Timasheva Y R et al. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2020 120(7. Vyp. 2) 54-60
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Predicting self-reported depression after the onset of multiple sclerosis using genetic and non-genetic factors.
Wang Frances M et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2020 May 1352458520921073
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Elucidation of the genetic background in familial multiple sclerosis requires genetic work-up.
Finsterer Josef et al. Clinical neurology and neurosurgery 2019 184105425
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Predicting onset of secondary-progressive multiple sclerosis using genetic and non-genetic factors.
Misicka Elina et al. Journal of neurology 2020 Apr
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Understanding Participation in Genetic Research Among Patients With Multiple Sclerosis: The Influences of Ethnicity, Gender, Education, and Age.
Cuccaro Michael L et al. Frontiers in genetics 2020 11120
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Summary-data-based mendelian randomization reveals druggable targets for multiple sclerosis
BM Jacobs et al, BioRXIV preprints, January 25, 2020
Familial multiple sclerosis in Greece: Distinct clinical and imaging characteristics in comparison with the sporadic disease.
Katsavos Serafeim et al. Clinical neurology and neurosurgery 2018 173144-149
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Unraveling susceptibility to multiple sclerosis.
Briggs Farren, et al. Science (New York, N.Y.) 2019 0 0. (6460) 1383-1384
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Are Personalized Diets Ready for Prime Time?
D Koenig, WebMD, September 19, 2019
Study Tests Immunotherapy in People with Cancer and Autoimmune Diseases
NCI, August 26, 2019
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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