Concepedia

Manuela Wiessner

MW

Statistics

Publications

6

Citations

218

H-Index

6

Active since

2017

Affiliations

Ludwig-Maximilians-Universität München(Current)

Friedrich Baur Stiftung

German Center for Neurodegenerative Diseases

Newcastle University

Medical University of Vienna

Manuela Wiessner is an author at Ludwig-Maximilians-Universität München specializing in genetics, neurogenetics, and medical genetics.

Publications per year

2017–2023

6

Publications

6

Mutations in INPP5K , Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment

Manuela Wiessner, Andreas Roos, Christopher J. Munn et al. · The American Journal of Human Genetics · 2017 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Biallelic variants in <i>HPDL</i> cause pure and complicated hereditary spastic paraplegia

Manuela Wiessner, Reza Maroofian, Meng-Yuan Ni et al. · Brain · 2021 · 51 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

The genetic landscape of axonal neuropathies in the middle-aged and elderly

Jan Senderek, Petra Laššuthová, Dagmara Kabzińska et al. · Neurology · 2020 · 31 citations · Full text

Medicine, Genetics, Neurology +17

SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy

Katharina Vill, Wolfgang Müller‐Felber, Dieter Gläser et al. · Human Genetics · 2018 · 28 citations · Full text

Medicine, Genetics, Neurology +12

Association of A Novel Splice Site Mutation in P/Q-Type Calcium Channels with Childhood Epilepsy and Late-Onset Slowly Progressive Non-Episodic Cerebellar Ataxia

Claudia Stendel, Maria Cristina D’Adamo, Manuela Wiessner et al. · International Journal of Molecular Sciences · 2020 · 20 citations · Full text

Life Sciences, Genetics, Neurology +17

1–5 of 6