Christine Klein

Also affiliated with University of Lübeck

MedicineNeuroscience

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 1%percentile

9.0Author DataRank

Indexed papers

11in 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 11 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.

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

PLoS Genetics(2012)10.1371/journal.pgen.1002548

Top 3%

6.9DataRank

Top 3%543 citations

Johannes T. Roehr, Matthew B. McQueen, Fotini K. Kavvoura, Sachin Bagade, Brit-Maren M. Schjeide +61 more

Papers

Driven by 65 papers — median percentile 45. Top paper: “Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database”.

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

PLoS Genetics(2012)10.1371/journal.pgen.1002548

Top 3%

6.9DataRank

Top 3%543 citations

Johannes T. Roehr, Matthew B. McQueen, Fotini K. Kavvoura, Sachin Bagade, Brit-Maren M. Schjeide +61 more

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

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Neurobiology of Aging(2011)10.1016/j.neurobiolaging.2011.05.024

N/A

1.8DataRank · unranked

33 citations

Demetrius M. Maraganore, Peter Nuernberg, Grazia Annesi, Nadine Abahuni, Anna Rita Bentivoglio +42 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

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

The Lancet Neurology(2008)10.1016/s1474-4422(08)70117-0

N/A

1.1DataRank · unranked

1574 citations

Mario Falchi, Sean S O'Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman +20 more

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

The Lancet Neurology(2011)10.1016/s1474-4422(11)70175-2

N/A

0.876DataRank · unranked

343 citations

Michael G. Heckman, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +60 more

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

Brain(2020)10.1093/brain/awaa246

N/A

0.789DataRank · unranked

192 citations

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

LifeTime and improving European healthcare through cell-based interceptive medicine

Nature(2020)10.1038/s41586-020-2715-9

N/A

0.747DataRank · unranked

144 citations

Geneviève Almouzni, Stanislaw A. Gorski, Stein Aerts, Ido Amit, Michela G. Bertero +178 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

Genotype–phenotype correlation in PRKN-associated Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00677-3

N/A

0.612DataRank · unranked

58 citations

Sara Sambin, Baptiste Crinière‐Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse +49 more

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

Movement Disorders(2024)10.1002/mds.29902

N/A

0.550DataRank · unranked

38 citations

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

Population‐specific frequencies for LRRK2 susceptibility variants in the genetic epidemiology of Parkinson's disease (GEO‐PD) consortium

Movement Disorders(2013)10.1002/mds.25600

N/A

0.538DataRank · unranked

35 citations

Alexandra I. Soto‐Ortolaza, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien +65 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

Genome-wide association studies of LRRK2 modifiers of Parkinson's disease

medRxiv(2020)10.1101/2020.12.14.20224378

N/A

0.360DataRank · unranked

10 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +55 more

Genome-wide case-only analysis of gene-gene interactions with known Parkinson’s disease risk variants reveals link between LRRK2 and SYT10

npj Parkinson s Disease(2023)10.1038/s41531-023-00550-9

N/A

0.360DataRank · unranked

8 citations

Joanne Trinh, Hampton L. Leonard, Sylvie Delcambre, Elsa Leitão, Dongbing Lai +19 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

Large-scale genetic characterization of Parkinson’s disease in the African and African admixed populations

medRxiv(2025)10.1101/2025.01.14.25320205

Top 55%

0.301DataRank

Top 55%4 citations

Kimberly Paquette, Peter Wild Crea, Paula Saffie Awad, Charles Achoru, Funmilola Taiwo +95 more

Large-scale genetic characterization of Parkinson’s disease in the African and African admixed populations

Brain(2025)10.1093/brain/awaf379

Top 56%

0.288DataRank

Top 56%3 citations

Kimberly Paquette, Peter Wild Crea, Kathryn Step, Emily Waldo, Mathew J. Koretsky +95 more

Segmental and Multifocal Isolated Dystonias: Similarities and Differences

Movement Disorders Clinical Practice(2025)10.1002/mdc3.70390

Top 61%

0.241DataRank

Top 61%4 citations

Vittorio Velucci, Daniele Belvisi, Gamze Kilic‐Berkmen, Joel S. Perlmutter, Laura Wright +34 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

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

Movement Disorders(2024)10.1002/mds.29968

N/A

0.241DataRank · unranked

4 citations

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

Impact of Y chromosome loss on the risk of Parkinson's disease and progression

EBioMedicine(2025)10.1016/j.ebiom.2025.105769

N/A

0.241DataRank · unranked

4 citations

Xinyi Chen, Wenxuan Du, Cha Lin, Liao Yu, Jean‐Christophe Corvol +43 more

PPM1M, an LRRK2-counteracting, phosphoRab12-preferring phosphatase with a potential link to Parkinson’s disease

Cell Reports(2025)10.1016/j.celrep.2025.116031

N/A

0.208DataRank · unranked

3 citations

Neringa Pratuseviciute, Yu‐En Lin, Ayan Adhikari, Wondwossen M Yeshaw, Chloe Flitton +19 more

Two lysosomal genes ATP13A2 and GBA1 interact to drive neurodegeneration

Molecular Neurodegeneration(2026)10.1186/s13024-025-00923-z

N/A

0.208DataRank · unranked

3 citations

Jinghan Zhao, Mingxi Deng, Guang Lin, Xueyang Pan, Wenwen Lin +13 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

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

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

Evaluation of a Mitochondrial Polygenic Score for Parkinson's Disease Across Ancestries

Movement Disorders(2025)10.1002/mds.30285

N/A

0.165DataRank · unranked

2 citations

Yi Wen Tay, Ai Huey Tan, Chin‐Hsien Lin, Kajsa Brolin, Björn‐Hergen Laabs +14 more

The R1441C-LRRK2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.12.562063

N/A

0.165DataRank · unranked

2 citations

Karen N. McFarland, Hannah A. Staley, Noelle Neighbarger, Susen Schaake, Norbert Brüggemann +6 more

PPM1M, a LRRK2-counteracting, phosphoRab12-preferring phosphatase with potential link to Parkinson’s disease

10.1101/2025.03.19.644182

N/A

0.165DataRank · unranked

2 citations

Neringa Pratuseviciute, Yu‐En Lin, Ayan Adhikari, Wondwossen M Yeshaw, Chloe Flitton +18 more

Alternative Translation Initiation in PRKN Delays the Onset of Parkinson's Disease and Offers a Therapeutic Target

Annals of Neurology(2026)10.1002/ana.78180

N/A

0.104DataRank · unranked

1 citations

Katja Lohmann, Manabu Funayama, Poornima J. Menon, Eva‐Juliane Vollstedt, Teresa Kleinz +10 more

RAB32 -linked Parkinson’s disease: Deep phenotyping, MDSGene literature review, and application of SynNeurGe criteria

medRxiv(2025)10.1101/2025.06.03.25328628

N/A

0.104DataRank · unranked

1 citations

Francesco Cavallieri, Max Borsche, Giulia Toschi, Franco Valzania, Valentina Fioravanti +22 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 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

Definition and Classification of Dystonia

Movement Disorders(2025)10.1002/mds.30220

N/A

0DataRank · unranked

100 citations

Kailash P. Bhatia, Victor S.C. Fung, Mark Hallett, Joseph Jankovic, Christine Klein +9 more

Parkinson’s Disease Subtypes: Critical Appraisal and Recommendations

Journal of Parkinson s Disease(2021)10.3233/jpd-202472

N/A

0DataRank · unranked

136 citations

Seyed-Mohammad Fereshtehnejad, Daniela Berg, Nicolaas I. Bohnen, Kathy Dujardin, Roberto Erro +19 more

Genetic Diversity and Expanded Phenotypes in Dystonia: Insights From Large‐Scale Exome Sequencing

Annals of Clinical and Translational Neurology(2025)10.1002/acn3.70100

N/A

0DataRank · unranked

13 citations

Fabian Ott, Sebastian Loens, Gamze Kilic‐Berkmen, Ai Huey Tan, Shen‐Yang Lim +43 more

Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: A new generation of opportunities

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.07.014

N/A

0DataRank · unranked

6 citations

Alastair J. Noyce, Ignácio F. Mata, Laurel A. Screven, J Solle, Sonya B. Dumanis +7 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

Translating the Transcriptome: A Connectomics Approach for Gene-Network Mapping and Clinical Application

medRxiv(2025)10.1101/2025.08.08.25333301

N/A

0DataRank · unranked

1 citations

Bassam Al‐Fatly, Barbara Hollunder, Ningfei Li, Garance M. Meyer, Nanditha Rajamani +40 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

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

Mitochondrial haplogroups and cognitive progression in Parkinson’s disease

Brain(2022)10.1093/brain/awac327

N/A

0DataRank · unranked

24 citations

Chunming Ni, Jiamin Zhan, Weimin Li, Junfeng Luo, Zhixiang Liao +42 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

Diagnosis and classification of blepharospasm: Recommendations based on empirical evidence

Journal of the Neurological Sciences(2022)10.1016/j.jns.2022.120319

N/A

0DataRank · unranked

16 citations

Giovanni Defazio, Mark Hallett, Alfredo Berardelli, Gina Ferrazzano, Daniele Belvisi +7 more

Effect Modification between Genes and Environment and Parkinson's Disease Risk

Annals of Neurology(2022)10.1002/ana.26467

N/A

0DataRank · unranked

40 citations

Kajsa Brolin, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Christine Klein, Ziv Gan‐Or +6 more

NEMO reshapes the α-Synuclein aggregate interface and acts as an autophagy adapter by co-condensation with p62

Nature Communications(2023)10.1038/s41467-023-44033-0

N/A

0DataRank · unranked

38 citations

Verian Bader, Lena Angersbach, Alina Blusch, Simran Goel, Ana Sánchez‐Vicente +26 more

Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser Parkinsonism

Movement Disorders(2023)10.1002/mds.29563

N/A

0DataRank · unranked

23 citations

Carolin Gabbert, Sebastian Koch, Inke R. König, Amke Caliebe, Björn‐Hergen Laabs +9 more

International Genetic Testing and Counseling Practices for Parkinson's Disease

Movement Disorders(2023)10.1002/mds.29442

N/A

0DataRank · unranked

16 citations

Deborah Raymond, Roberto A. Ortega, Ali Shalash, Emilia Gatto, Mehri Salari +24 more

An Empirical Comparison of Commonly Used Universal Rating Scales for Dystonia

Movement Disorders Clinical Practice(2023)10.1002/mdc3.13909

N/A

0DataRank · unranked

9 citations

Gamze Kilic‐Berkmen, Joel S. Perlmutter, Scott A. Norris, Laura J. Wright, Christine Klein +13 more

Clinical Features and Evolution of Blepharospasm: A Multicenter International Cohort and Systematic Literature Review

Dystonia(2022)10.3389/dyst.2022.10359

N/A

0DataRank · unranked

40 citations

Hyun Joo Cho, Gamze Kilic‐Berkmen, J. Lucas McKay, Mark Hallett, Christine Klein +24 more

COVID-19 vaccine-associated cerebral venous thrombosis in Germany

medRxiv(2021)10.1101/2021.04.30.21256383

N/A

0DataRank · unranked

29 citations

Peter Berlit, Hans‐Christoph Diener, Christian Gerloff, Andreas Greinacher, Christine Klein +9 more

Interaction of mitochondrial polygenic score and environmental factors in LRRK2 p.Gly2019Ser parkinsonism

medRxiv(2023)10.1101/2023.01.02.23284113

N/A

0DataRank · unranked

2 citations

Carolin Gabbert, Inke R. König, Amke Caliebe, Sebastian Koch, Björn‐Hergen Laabs +9 more

The combined effect of lifestyle factors and polygenic scores on age at onset in Parkinson’s disease

medRxiv(2023)10.1101/2023.08.25.23294466

N/A

0DataRank · unranked

2 citations

Leonie Blöbaum, Theresa Lüth, Inke R. König, Amke Caliebe, Sebastian Koch +4 more

A biological classification of Parkinson's disease: the SynNeurGe research diagnostic criteria

The Lancet Neurology(2024)10.1016/s1474-4422(23)00404-0

N/A

0DataRank · unranked

502 citations

Charles H. Adler, Daniela Berg, Christine Klein, Tiago F. Outeiro, Werner Poewe +4 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

Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and Recommendations

Movement Disorders Clinical Practice(2021)10.1002/mdc3.13376

N/A

0DataRank · unranked

30 citations

Sarah Pirio Richardson, Joel S. Perlmutter, Mark Hallett, Christine Klein, Aparna Wagle Shukla +21 more

Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease

Annals of Neurology(2021)10.1002/ana.26094

N/A

0DataRank · unranked

50 citations

Babak Alipanahi, Pierre Fontanillas, Tae‐Hwi Schwantes‐An, Jan Aasly, Roy N. Alcalay +56 more

The combined effect of lifestyle factors and polygenic scores on age at onset in Parkinson’s disease

Scientific Reports(2024)10.1038/s41598-024-65640-x

N/A

0DataRank · unranked

16 citations

Leonie Blöbaum, Theresa Lüth, Inke R. König, Amke Caliebe, Sebastian Sendel +4 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

The R1441C-Lrrk2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner in mice

Science Translational Medicine(2024)10.1126/scitranslmed.adl1535

N/A

0DataRank · unranked

14 citations

Karen N. McFarland, Hannah A. Staley, Noelle Neighbarger, Susen Schaake, Norbert Brüggemann +6 more

Christine Klein

Indexed papers

Top data-sharing exemplar

Papers