🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Nicholas Wood

Queen Mary University of London

ORCID: 0000-0002-9500-3348

Also affiliated with University College London

MedicineBiochemistry, 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 1%percentile

6.9Author DataRank

Indexed papers

2in 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 2 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 17 papers — median percentile 97. 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

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

JAMA Neurology(2021)10.1001/jamaneurol.2020.5257

N/A

4.5DataRank · unranked

205 citations

David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina Hertfelder Reynolds +85 more

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Nature(2011)10.1038/nature10251

N/A

1.2DataRank · unranked

2729 citations

Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos +241 more

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Nature Genetics(2014)10.1038/ng.3043

N/A

1.1DataRank · unranked

1956 citations

NeuroGenetics Research Consortium (NGRC), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), Alzheimer Genetic Analysis Group, Nathan Pankratz +49 more

Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

Nature Communications(2021)10.1038/s41467-021-26280-1

N/A

0.808DataRank · unranked

217 citations

Demis A. Kia, Mona M. Almramhi, Sara Bandres-Ciga, Chris Finan, Alastair J. Noyce +170 more

Genome-wide determinants of mortality and motor progression in Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00729-8

N/A

0.565DataRank · unranked

15 citations

Michael Lawton, Miriam I. Pollard, Emmeline Brown, Raquel Real, Alejandro Martínez-Carrasco +35 more

Identification of an age-related Parkinson's disease risk factor that regulates sulfur metabolism

Research Square(2021)10.21203/rs.3.rs-1168396/v1

N/A

0.208DataRank · unranked

3 citations

Shani Stern, Sara B. Linker, Diogo H. Da Silva, Nako Nakatsuka, Juliane Tampé +12 more

Dissecting the Phenotype and Genotype of PLA2G6‐Related Parkinsonism

Movement Disorders(2021)10.1002/mds.28807

N/A

0DataRank · unranked

59 citations

Sahil Mehta, Giulia Di Lazzaro, Anna Latorre, Mark J. Edwards, Bettina Balint +20 more

RFC1-related ataxia is a mimic of early multiple system atrophy

Journal of Neurology Neurosurgery & Psychiatry(2021)10.1136/jnnp-2020-325092

N/A

0DataRank · unranked

43 citations

Wai Yan Yau, Viorica Chelban, Salvatore Rossi, Natalia Dominik, Emer O’Connor +5 more

Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia

Journal of Clinical Investigation(2021)10.1172/jci140625

N/A

0DataRank · unranked

39 citations

Marisa M. Brockmann, Jinye Dai, Sander Pajusalu, Burcu Atasu, Joaquín Campos +30 more

Exploring the Role of Plasma Lipids and Statins Interventions on Multiple Sclerosis Risk and Severity: A Mendelian Randomization Study

medRxiv(2022)10.1101/2022.08.01.22277781

N/A

0DataRank · unranked

2 citations

Chris Finan, Catherine S. Storm, Amand F. Schmidt, Demis A. Kia, Rachel Coneys +4 more

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Nature Communications(2024)10.1038/s41467-024-46354-0

N/A

0DataRank · unranked

43 citations

Henriette Aksnes, Reza Maroofian, Lauren C. LaMonica, Luís Seabra, Anette Siggervåg +55 more

Repeat expansion disorders

Practical Neurology(2024)10.1136/pn-2023-003938

N/A

0DataRank · unranked

22 citations

Huw R. Morris, James Polke, Nicholas Wood, Sonia Gandhi, Mina Ryten +3 more

Ancestry-specific gene expression in peripheral monocytes mediates risk of neurodegenerative disease

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.20.624489

N/A

0DataRank · unranked

0 citations

Regina Hertfelder Reynolds, Jia Nee Foo, Aine Fairbrother-Browne, Emil K. Gustavsson, Sarah Galgiano-Turin +4 more

Genome-wide association studies of cognitive and motor progression in Parkinson's disease

medRxiv(2020)10.1101/2020.05.07.20084343

N/A

0DataRank · unranked

21 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 more

Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease

Movement Disorders(2020)10.1002/mds.28342

N/A

0DataRank · unranked

173 citations

Michael Lawton, Edwin Jabbari, Regina Hertfelder Reynolds, Hirotaka Iwaki, Cornelis Blauwendraat +23 more

Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R

Neurobiology of Disease(2020)10.1016/j.nbd.2020.105079

N/A

0DataRank · unranked

8 citations

Helen Ling, Marla Gearing, Beth A. Dombroski, Laura B. Cantwell, Lea R’Bibo +12 more