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Auflistung nach Autor "Huttenlocher-Moser, Johanna"

Anzeige der Dokumente 1-8 von 8

A mutation in APP protects against Alzheimer's disease and age-related cognitive decline

Huttenlocher-Moser, Johanna (2012)
Common variant at 16p11.2 conferring risk of psychosis

Huttenlocher-Moser, Johanna (2014)
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts

Huttenlocher-Moser, Johanna; Brockmann, Kathrin; Berg, Daniela; Gasser, Thomas; Bonin, Michael; Bauer, Peter; Krüger, Rejko; Rieß, Olaf (2015)
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease

Huttenlocher-Moser, Johanna; Rieß, Olaf; Bauer, Peter (2015)
Identifikation und Charakterisierung genetischer Risikofaktoren der Parkinson Erkrankung in der isländischen Bevölkerung

Huttenlocher-Moser, Johanna (2016)
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

Synofzik, Matthis; Huttenlocher-Moser, Johanna; Schöls, Ludger (2015)
Truncating mutations in RBM12 are associated with psychosis

Huttenlocher-Moser, Johanna (2017)
Variant of TREM2 Associated with the Risk of Alzheimer's Disease

Huttenlocher-Moser, Johanna (2013)

Anzeige der Dokumente 1-8 von 8

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