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topic_facet:"Research Support, Non-U.S. Gov't"
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PubPharm (57)
1
SLC6A1 variant pathogenicity, molecular function and phenotype : a genetic and clinical analysis
enthalten in:
Brain : a journal of neurology
| 2023
von
Stefanski, A.
|
Pérez-Palma, E.
|
Brünger, T.
| +43
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2
Integrated Nematode Management in a World in Transition : Constraints, Policy, Processes, and Technologies for the Future
enthalten in:
Annual review of phytopathology
| 2023
von
Sikora, R.
|
Helder, J.
|
Molendijk, L.
| +3
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3
Lipids and amyotrophic lateral sclerosis : A two-sample Mendelian randomization study
enthalten in:
European journal of neurology
| 2023
von
Xia, K.
|
Klose, V.
|
Högel, J.
| +5
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4
Cerebellar and subcortical atrophy contribute to psychiatric symptoms in frontotemporal dementia
enthalten in:
Human brain mapping
| 2023
von
Bussy, A.
|
Levy, J.
|
Best, T.
| +141
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5
Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes
enthalten in:
Brain : a journal of neurology
| 2023
von
Brünger, T.
|
Pérez-Palma, E.
|
Montanucci, L.
| +10
CommentIn: Epilepsy Curr. 2023 Jan 18;23(2):118-120. - PMID 37122415
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6
Mutation-specific metabolic profiles in presymptomatic amyotrophic lateral sclerosis
enthalten in:
European journal of neurology
| 2023
von
Xia, K.
|
Witzel, S.
|
Witzel, C.
| +4
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7
Family History for Neurodegeneration in Multiple System Atrophy : Does it Indicate Susceptibility?
enthalten in:
Movement disorders : official journal of the Movement Disorder Society
| 2022
von
Leys, F.
|
Eschlböck, S.
|
Campese, N.
| +12
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8
Compound-heterozygous GRIN2A null variants associated with severe developmental and epileptic encephalopathy
enthalten in:
Epilepsia
| 2022
von
Strehlow, V.
|
Rieubland, C.
|
Gallati, S.
| +7
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9
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
enthalten in:
Brain : a journal of neurology
| 2022
von
Johannesen, K.
|
Liu, Y.
|
Koko, M.
| +98
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10
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder
enthalten in:
EMBO molecular medicine
| 2022
von
Fell, C.
|
Hagelkruys, A.
|
Cicvaric, A.
| +26
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Thema: genetics
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Thema: Research Support, Non-U.S. Gov't
Medienart
57
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57
E-Artikel
57
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Zeitschriftentitel
6
eLife
5
Brain : a journal of neurology
4
Movement disorders : official journal of the Mo...
3
Proceedings of the National Academy of Sciences...
2
American journal of human genetics
2
European journal of neurology
2
Gut
2
Human brain mapping
2
Journal of the American College of Cardiology
1
American journal of hypertension
1
American journal of medical genetics. Part B, N...
1
American journal of respiratory and critical ca...
1
American journal of transplantation : official ...
1
Annual review of phytopathology
1
Biological reviews of the Cambridge Philosophic...
1
Cell
1
Circulation
1
Circulation. Cardiovascular genetics
1
Circulation. Genomic and precision medicine
1
Current Alzheimer research
Alle anzeigen ...
weniger ...
Thema
Research Support, Non-U.S. Gov't
genetics
56
Journal Article
18
Research Support, N.I.H., Extramural
5
Multicenter Study
5
Review
5
epilepsy
5
genomics
4
Biomarkers
4
Meta-Analysis
3
EC 2.7.11.1
3
GWAS
3
Membrane Proteins
3
Parkinson's disease
3
amyotrophic lateral sclerosis
3
epidemiology
3
heart failure
3
kidney
3
neurodevelopmental disorder
2
97C5T2UQ7J
Alle anzeigen ...
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Erscheinungszeitraum
24
2020-
33
2010-2019
Erscheinungsjahr(e)
Von:
Bis:
Sprache
57
Englisch
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