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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 7, 2024. (Total: 231234Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Multiple Sclerosis and LRP2[original query]
Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis. GWAS Catalog
Journal of neurology, neurosurgery, and psychiatry 2017 Jul .
Zhou Yuan, Graves Jennifer S, Simpson Steve, Charlesworth Jac C, Mei Ingrid van der, Waubant Emmanuelle, Barcellos Lisa F, Belman Anita, Krupp Lauren, Lucas Robyn, Ponsonby Anne-Louise, Taylor Bruce V,
Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.
Multiple sclerosis (Houndmills, Basingstoke, England) 2018 Jan 1352458517749894.
Hilven Kelly, Vandebergh Marijne, Smets Ide, Mallants Klara, Goris An, Dubois Bénédic
Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing.
Brain and behavior 2019 3 9 (4): e01272.
Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor
Smoking, cardiovascular risk factors and LRP2 gene variation: Associations with disease severity, cognitive function and brain structure in primary progressive multiple sclerosis.
Multiple sclerosis and related disorders 2021 10 56 103296.
Chow Helene Højsgaard, Talbot Jacob, Marstrand Lisbet, Lundell Henrik, Roman Siebner Hartwig, Bach Søndergaard Helle, Sellebjerg Fi
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