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

Marcelo Kauffman

Austral University

ORCID: 0000-0003-1680-5092

Also affiliated with Hospital Ramos Mejía

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

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 4%percentile
0.769Author 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 →

Top data-sharing exemplar

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 11 papers — median percentile 74. Top paper: “Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease”.

Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Nature Genetics(2023)10.1038/s41588-023-01584-8
N/A
0.839DataRank · unranked
268 citations

Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella Aslibekyan +95 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

Disease modification and biomarker development in Parkinson disease

Neurology(2020)10.1212/wnl.0000000000009107
N/A
0.738DataRank · unranked
136 citations

Lorraine V. Kalia, Ziv Gan‐Or, Caroline H. Williams‐Gray, Philippe L. Bédard, Steven M. Rowe +21 more

Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy

European Journal of Medical Genetics(2019)10.1016/j.ejmg.2018.11.005
N/A
0.529DataRank · unranked
33 citations

Patricia Vega, María Victoria Piccirilli, Carla Chicco, Carlos Ciraolo, Silvia Christiansen +11 more

Social concepts and the cerebellum: behavioural and functional connectivity signatures in cerebellar ataxic patients

Philosophical Transactions of the Royal Society B Biological Sciences(2022)10.1098/rstb.2021.0364
N/A
0.462DataRank · unranked
11 citations

Sol Fittipaldi, Cecilia González Campo, Marcelo Kauffman, Sergio Rodríguez Quiroga, Darío Andrés Yacovino +4 more

Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

npj Parkinson s Disease(2025)10.1038/s41531-025-00967-4
N/A
0.269DataRank · unranked
5 citations

Spencer Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea +95 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

Resolving ‘vascular parkinsonism’ –COL22A1 as a genetic adult-onset leukoencephalopathy

Parkinsonism & Related Disorders(2023)10.1016/j.parkreldis.2023.105898
N/A
0DataRank · unranked
2 citations

Marcelo Kauffman, Diandra Rufin Florat, Amir Zaidi, Vanesa Botsford, Jennifer Sharma +5 more

“Mini Molar Tooth” Sign in POLR3B ‐Associated Cerebellar Ataxia with Hypomyelinating Leukodystrophy

Movement Disorders Clinical Practice(2025)10.1002/mdc3.70176
N/A
0DataRank · unranked
0 citations

Marcelo Kauffman, Blanca Talavera de la Esperanza, Zhuanzhuan Yu, Donald L. Gilbert, Alberto J. Espay +1 more

EPIDEMIOLOGY OF LEVODOPA-INDUCED DYSKINESIA: PREVALENCE AND ASSOCIATED CLINICAL FACTORS IN LATIN AMERICA

medRxiv(2025)10.1101/2025.08.25.25334104
N/A
0DataRank · unranked
0 citations

Daniel Teixeira dos Santos, Emily Waldo, Thiago Peixoto Leal, Miguel Inca‐Martinez, Sarael Alcauter +44 more

How have advances in genetic technology modified movement disorder nosology?

European Journal of Neurology(2020)10.1111/ene.14294
N/A
0DataRank · unranked
10 citations

Luca Marsili, Abhimanyu Mahajan, Maria Barbara Grimberg, Marcelo Kauffman, Alberto J. Espay +1 more