Corinna Berghoff

Statistics

Publications

Citations

179

H-Index

Active since

2003

Affiliations

Friedrich-Alexander-Universität Erlangen-Nürnberg(Current)

Universidad de Costa Rica

Justus-Liebig-Universität Gießen

Universidad Nacional

Corinna Berghoff is an author at Friedrich-Alexander-Universität Erlangen-Nürnberg specializing in human genetics, genetic disorders, and charcot-marie-tooth disease.

Publications per year

2003–2018

Publications

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models

Alejandro Leal, Kathrin Huehne, Finn Bauer et al. · Neurogenetics · 2009 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

The polynucleotide kinase 3′-phosphatase gene (PNKP) is involved in Charcot-Marie-Tooth disease (CMT2B2) previously related to MED25

Alejandro Leal, Sixto Bogantes-Ledezma, Arif B. Ekici et al. · Neurogenetics · 2018 · 37 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Clinical and electrophysiological characteristics of autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2B) that maps to chromosome 19q13.3

Corinna Berghoff, Martin Berghoff, Alejandro Leal et al. · Neuromuscular Disorders · 2004 · 23 citations · Full text

Life Sciences, Genetics, Neurology +13

Annexin expression in inflammatory myopathies

Stefan Probst‐Cousin, Corinna Berghoff, B. Neundörfer · Muscle & Nerve · 2004 · 21 citations

Medicine, Pathobiology, Pathology +17

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero ( MPZ , P0 ) gene causes different phenotypes in homozygous and heterozygous carriers within one family

Alejandro Leal, Corinna Berghoff, Martin Berghoff et al. · Neurogenetics · 2003 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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