Author

Daniela Probst

Observed names: D Probst, Probst D, Probst, Daniela

Institution: Universitätsklinikum Aachen

Observed institutions: Austrian Academy of Sciences, Royal Hallamshire Hospital, University Hospital of Geneva, Universitätsklinikum Aachen, Sheffield Children's Hospital

OpenAlex ID: A5000720832

CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

2012 · J.-M. Lee, E.M. Ramos, et al. · Neurology · 382

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

2017 · Davina J Hensman Moss, Antonio F Pardiñas, et al. · The Lancet Neurology · 310

Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity

2000 · J-L Blouin, M Meeks, et al. · European Journal of Human Genetics · 151

DLK1(PREF1) is a negative regulator of adipogenesis in CD105+/CD90+/CD34+/CD31−/FABP4− adipose-derived stromal cells from subcutaneous abdominal fat pats of adult women

2012 · Maria C Mitterberger, Stefan Lechner, et al. · Stem Cell Research · 94

Clinical manifestations of intermediate allele carriers in Huntington disease

2016 · Esther Cubo, María A. Ramos-Arroyo, et al. · Neurology · 53

Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study

2018 · Paul McNulty, Richard Pilcher, et al. · Journal of Huntington s Disease · 35

Primary Ciliary Dyskinesia: A genome-wide linkage analysis reveals extensive locus heterogeneity.

1999 · JL Blouin, Uppala Radhakrishna, et al. · UCL Discovery (University College London)

Works count: 10

Citation count: 1,025

H-index: 6

I10-index: 6