Katja Lohmann

Also affiliated with University of Lübeck

MedicineNeuroscienceBiochemistry, Genetics and Molecular Biology

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

1.3Author DataRank

Indexed papers

3in 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 3 indexed papers 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.

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w

Top 26%

0.769DataRank

Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Papers

Driven by 27 papers — median percentile 48. Top paper: “Large-scale replication and heterogeneity in Parkinson disease genetic loci”.

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Neurology(2012)10.1212/wnl.0b013e318264e353

N/A

6.6DataRank · unranked

132 citations

Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Muin J. Khoury, Maria Bozi +160 more

The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants

Neurobiology of Aging(2014)10.1016/j.neurobiolaging.2013.07.013

N/A

1.6DataRank · unranked

41 citations

Alexis Elbaz, Daniel J. Serie, Grazia Annesi, Georg Auburger, Justin A. Bacon +55 more

Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

npj Parkinson s Disease(2023)10.1038/s41531-023-00533-w

Top 26%

0.769DataRank

Top 26%39 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +95 more

Independent and joint effects of the MAPT and SNCA genes in Parkinson disease

Annals of Neurology(2011)10.1002/ana.22321

N/A

0.663DataRank · unranked

82 citations

Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto‐Ortolaza, Frédéric Moisan, Jan Aasly +40 more

NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

medRxiv(2023)10.1101/2023.11.06.23298176

N/A

0.658DataRank · unranked

23 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort

Movement Disorders(2023)10.1002/mds.29288

N/A

0.590DataRank · unranked

50 citations

Susen Schaake, Katja Lohmann, Shalini Padmanabhan, Alexis Brice, Suzanne Lesage +95 more

Classification and Genotype–Phenotype Relationships of GBA1 Variants: MDSGene Systematic Review

Movement Disorders(2025)10.1002/mds.30141

N/A

0.500DataRank · unranked

27 citations

Susen Schaake, Tatiana Usnich, Johann Boehm, Nina Steffen, Nathalie Schell +11 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

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson’s Disease Project

PLoS ONE(2023)10.1371/journal.pone.0292180

Top 52%

0.332DataRank

Top 52%7 citations

Harutyun Madoev, Anna Aasly, Azlina Ahmad‐Annuar, Bashayer Al‐Mubarak, Roy N. Alcalay +78 more

The Global Landscape of Genetic Variation in Parkinson’s disease: Multi-Ancestry Insights into Established Disease Genes and their Translational Relevance

medRxiv(2025)10.1101/2025.07.08.25330815

N/A

0.312DataRank · unranked

7 citations

Zih‐Hua Fang, Mary B. Makarious, Nicole Kuznetsov, Kajsa Brolin, Shannon Ballard +41 more

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population

npj Parkinson s Disease(2025)10.1038/s41531-025-00896-2

N/A

0.241DataRank · unranked

4 citations

Kristin Levine, Susan H. Fox, Connie Marras, Nazish Ahmed, Nicole Kuznetsov +95 more

Understanding monogenic Parkinson's disease at a global scale

medRxiv(2024)10.1101/2024.03.12.24304154

N/A

0.208DataRank · unranked

3 citations

Lara M. Lange, Eva‐Juliane Vollstedt, Karisha Roopnarain, Maria Leila M. Doquenia, Azlina Ahmad +29 more

Phosphorylated Ubiquitin as a Clinical Biomarker for Mitochondrial Damage in Neurodegenerative Diseases

Aging and Disease(2025)10.14336/ad.2025.1220

N/A

0.165DataRank · unranked

2 citations

Jens O. Watzlawik, Michael G. Heckman, Sophia G. Blumenfeld, Michael J. Rigby, Mohammed Kehili +10 more

Rare but Relevant? Assessing Variants in Dystonia‐Linked Genes in Parkinson's Disease

Movement Disorders(2025)10.1002/mds.70073

Top 70%

0.165DataRank

Top 70%2 citations

Zih‐Hua Fang, Laurel A. Screven, Ai Huey Tan, Roy N. Alcalay, Rim Amouri +33 more

How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson’s disease

medRxiv(2025)10.1101/2025.11.15.25339249

N/A

0DataRank · unranked

0 citations

Eva‐Juliane Vollstedt, Ana Westenberger, Lara M. Lange, Joanne Trinh, Meike Kasten +12 more

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

Annals of Clinical and Translational Neurology(2026)10.1002/acn3.70332

N/A

0DataRank · unranked

0 citations

Theresa Lüth, Susen Schaake, Carolin Gabbert, Marius Möller, Hauke Busch +14 more

Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism

Brain(2020)10.1093/brain/awaa246

N/A

0DataRank · unranked

191 citations

Inke R. König, Sylvie Delcambre, Simona Petrucci, Alexander Balck, Norbert Brüggemann +17 more

Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study

Brain(2024)10.1093/brain/awae142

N/A

0DataRank · unranked

93 citations

Jennifer Verbrugge, Tae‐Hwi Schwantes‐An, Jeanine Schulze, Tatiana Foroud, Anne Hall +31 more

Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinic

The Lancet Neurology(2024)10.1016/s1474-4422(24)00378-8

N/A

0DataRank · unranked

73 citations

Ai Huey Tan, Azlina Ahmad, Njideka Ulunma Okubadejo, Katja Lohmann, Huw R. Morris +16 more

NeuroBooster Array: A Genome‐Wide Genotyping Platform to Study Neurological Disorders Across Diverse Populations

Movement Disorders(2024)10.1002/mds.29902

N/A

0DataRank · unranked

38 citations

Faraz Faghri, Elisa Majounie, Mathew J. Koretsky, Jeffrey Kim, Kristin Levine +29 more

Sex Differences in Dystonia

Movement Disorders Clinical Practice(2024)10.1002/mdc3.14059

N/A

0DataRank · unranked

15 citations

Laura Scorr, Lucas McKay, Mehreen Thayani, Yuping Donsante, Joel S. Perlmutter +18 more

Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale

Movement Disorders(2024)10.1002/mds.29925

N/A

0DataRank · unranked

10 citations

Lara M. Lange, Eva‐Juliane Vollstedt, Karisha Roopnarain, Maria Leila M. Doquenia, Azlina Ahmad Annuar +29 more

Genetic Risk Factors in Isolated Dystonia Escape Genome‐Wide Association Studies

Movement Disorders(2024)10.1002/mds.29968

N/A

0DataRank · unranked

4 citations

Katja Lohmann, Eva‐Juliane Vollstedt, Tobias Reinberger, Lisa‐Marie Nuxoll, Gamze Kilic‐Berkmen +53 more

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights from Large-Scale Exome Sequencing

medRxiv(2024)10.1101/2024.12.02.24316741

N/A

0DataRank · unranked

5 citations

Fabian Ott, Sebastian Loens, Gamze Kilic‐Berkmen, Ai Huey Tan, Shen‐Yang Lim +42 more

RAB32 ‐Linked Parkinson's Disease: Deep Phenotyping, MDSGene Literature Review, and Application of SynNeurGe Criteria

Movement Disorders(2025)10.1002/mds.70037

N/A

0DataRank · unranked

5 citations

Francesco Cavallieri, Max Borsche, Giulia Toschi, Franco Valzania, Valentina Fioravanti +23 more

Screening of Hidden Pathogenic Structural Variants in PRKN

Movement Disorders(2025)10.1002/mds.30267

N/A

0DataRank · unranked

0 citations

Guillaume Cogan, Christelle Tesson, Suzanne Lesage, Susen Schaake, Alexander Balck +15 more

Rare but Relevant: Assessing Variants in Dystonia-linked Genes in Parkinson’s Disease

medRxiv(2025)10.1101/2025.07.10.25330831

N/A

0DataRank · unranked

0 citations

Zih‐Hua Fang, Laurel A. Screven, Ai Huey Tan, Roy N. Alcalay, Rim Amouri +33 more

Katja Lohmann

Indexed papers

Top data-sharing exemplar

Papers