Published Data Registry

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TitleAuthorsJournalPublication year
DOI
PMID
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.(Open Access) Xiao X, Wang L, (...), Li MTranslational psychiatry2017
Every-other-day feeding extends lifespan but fails to delay many symptoms of aging in mice.(Open Access) Xie K, Neff F, (...), Ehninger DNature communications2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.(Open Access) Yokoyama JS, Karch CM, (...), Desikan RSActa neuropathologica2017
Inflammatory CNS disease caused by immune checkpoint inhibitors: status and perspectives.Yshii LM, Hohlfeld R, Liblau RSNature reviews. Neurology2017
KMT2B rare missense variants in generalized dystonia.Zech M, Jech R, (...), Winkelmann JMovement disorders : official journal of the Movement Disorder Society2017
Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing.Zech M, Jech R, (...), Winkelmann JNeurogenetics2017
Role of the ribosomal quality control machinery in nucleocytoplasmic translocation of polyQ-expanded huntingtin exon-1.(Open Access) Zheng J, Yang J, (...), Liu BBiochemical and biophysical research communications2017
Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalities.(Open Access) Herebian D, Alhaddad B, (...), Distelmaier FEuropean journal of human genetics : EJHG2017
Antibodies inhibit transmission and aggregation of C9orf72 poly-GA dipeptide repeat proteins.(Open Access) Zhou Q, Lehmer C, (...), Edbauer DEMBO molecular medicine2017
Genetic diagnosis of Mendelian disorders via RNA sequencing.(Open Access) Kremer LS, Bader DM, (...), Prokisch HNature communications2017