Thomas Klopstock

German Center for Neurodegenerative Diseases

Also affiliated with Friedrich Baur Stiftung, Ludwig-Maximilians-Universität München

NeuroscienceMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 3%percentile

1.2Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Mammalian Genome(2020)10.1007/s00335-020-09827-3

Top 17%

1.2DataRank

Top 17%33 citations

Heike Kollmus, Helmut Fuchs, Christoph Lengger, Hamed Haselimashhadi, Molly A. Bogue +36 more

Papers

Driven by 18 papers — median percentile 83. Top paper: “Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset”.

Efficacy and Safety of Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy Treated within 6 Months of Disease Onset

Ophthalmology(2021)10.1016/j.ophtha.2020.12.012

N/A

3.6DataRank · unranked

166 citations

Patrick Yu‐Wai‐Man, Valério Carelli, Mark L. Moster, Valérie Biousse, Catherine Vignal +55 more

Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy

Neurology(2023)10.1212/wnl.0000000000207402

N/A

1.5DataRank · unranked

72 citations

Enrico Bertini, Valério Carelli, Bruce H. Cohen, Gregory M. Enns, Marni J. Falk +59 more

A comprehensive and comparative phenotypic analysis of the collaborative founder strains identifies new and known phenotypes

Mammalian Genome(2020)10.1007/s00335-020-09827-3

Top 17%

1.2DataRank

Top 17%33 citations

Heike Kollmus, Helmut Fuchs, Christoph Lengger, Hamed Haselimashhadi, Molly A. Bogue +36 more

Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation

Ophthalmology and Therapy(2022)10.1007/s40123-022-00611-x

N/A

0.755DataRank · unranked

30 citations

Nancy J. Newman, Patrick Yu‐Wai‐Man, Valérie Biousse, Mark L. Moster, Prem S. Subramanian +79 more

Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic Neuropathy

JAMA Ophthalmology(2024)10.1001/jamaophthalmol.2024.5375

N/A

0.743DataRank · unranked

24 citations

Nancy J. Newman, Valérie Biousse, Valério Carelli, Mark L. Moster, Catherine Vignal‐Clermont +59 more

Interactions of dopamine, iron, and alpha-synuclein linked to dopaminergic neuron vulnerability in Parkinson's disease and Neurodegeneration with Brain Iron Accumulation disorders

Neurobiology of Disease(2022)10.1016/j.nbd.2022.105920

N/A

0.701DataRank · unranked

106 citations

Annika Wagener, Urban M. Fietzek, Thomas Klopstock, Eugene V. Mosharov, Fabio A. Zucca +4 more

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207

N/A

0.691DataRank · unranked

99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Clinico‐Genetic, Imaging and Molecular Delineation of COQ8A‐Ataxia: A Multicenter Study of 59 Patients

Annals of Neurology(2020)10.1002/ana.25751

N/A

0.654DataRank · unranked

77 citations

Tommaso Schirinzi, Lucia Laugwitz, Nathan H. Murray, C.A. Bingman, Selina Reich +37 more

Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.015

N/A

0.604DataRank · unranked

55 citations

Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger +41 more

Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice

Nature Communications(2022)10.1038/s41467-022-34515-y

N/A

0.568DataRank · unranked

43 citations

Helmut Fuchs, Enzo Scifo, Dan Liu, Ahmad Aziz, Juan Antonio Aguilar‐Pimentel +44 more

De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia

Movement Disorders(2022)10.1002/mds.28959

N/A

0.494DataRank · unranked

26 citations

Jonathan De Winter, Danique Beijer, Giulia Coarelli, Melanie Wayand, Robin Palvadeau +33 more

Towards the international interoperability of clinical research networks for rare diseases: recommendations from the IRDiRC Task Force

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-023-02650-4

N/A

0.373DataRank · unranked

11 citations

Galliano Zanello, Dixie B. Baker, Lora Black, Isabella Brambilla, Orion J. Buske +14 more

Deep Phenotyping and Lifetime Trajectories Reveal Limited Effects of Longevity Regulators on the Aging Process in C57BL/6J Mice

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.25.485824

N/A

0.292DataRank · unranked

6 citations

Helmut Fuchs, Enzo Scifo, Dan Liu, Ahmad Aziz, Juan Antonio Aguilar-Pimentel +44 more

Community Consensus Guidelines to Support FAIR Data Standards in Clinical Research Studies in Primary Mitochondrial Disease

Advanced Genetics(2021)10.1002/ggn2.202100047

N/A

0.208DataRank · unranked

3 citations

Laura E. MacMullen, John C. Campbell, John Christodoulou, Bruce H. Cohen, Thomas Klopstock +11 more

Adult‐Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERDND): Time to Move Beyond the Skin

Movement Disorders(2022)10.1002/mds.29071

N/A

0DataRank · unranked

22 citations

Demet Önder, Andreas Traschütz, Xenia Kobeleva, Ivan Karin, Martina Minnerop +25 more

Cross-Sectional Analysis of Baseline Visual Parameters in Subjects Recruited Into the RESCUE and REVERSE ND4-LHON Gene Therapy Studies

Journal of Neuro-Ophthalmology(2021)10.1097/wno.0000000000001316

N/A

0DataRank · unranked

7 citations

Robert C. Sergott, Nancy J. Newman, Patrick Yu‐Wai‐Man, Valério Carelli, Molly Scannell Bryan +16 more

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

medRxiv(2021)10.1101/2021.04.01.21254633

N/A

0DataRank · unranked

33 citations

Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston +48 more

Longitudinal changes of SARA scale in Friedreich ataxia: Strong influence of baseline score and age at onset

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51886

N/A

0DataRank · unranked

7 citations

Mario Fichera, Lorenzo Nanetti, Eliana Rulli, Paola Giunti, Michael Parkinson +21 more

Thomas Klopstock

Indexed papers

Top data-sharing exemplar

Papers