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

Ralitza H. Gavrilova

Mayo Clinic

ORCID: 0000-0002-4942-6358

Also affiliated with Mayo Clinic in Florida

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
4.7Author 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 →

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.

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

Alzheimer s & Dementia(2020)10.1002/alz.12033
Top 8%
2.6DataRank
Top 8%169 citations

Danielle Brushaber, Jeremy A. Syrjanen, Walter K. Kremers, Julie A. Fields, Leah K. Forsberg +80 more

Papers

Driven by 14 papers — median percentile 89. Top paper: “Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium”.

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

Alzheimer s & Dementia(2020)10.1002/alz.12033
Top 8%
2.6DataRank
Top 8%169 citations

Danielle Brushaber, Jeremy A. Syrjanen, Walter K. Kremers, Julie A. Fields, Leah K. Forsberg +80 more

Mitochondrial diseases in North America

Neurology Genetics(2020)10.1212/nxg.0000000000000402
Top 11%
2.0DataRank
Top 11%77 citations

Yuelin Long, Victoria Cooley, Robert Schoenaker, Valentina Emmanuele, Salvatore DiMauro +30 more

Comprehensive cross-sectional and longitudinal analyses of plasma neurofilament light across FTD spectrum disorders

Cell Reports Medicine(2022)10.1016/j.xcrm.2022.100607
N/A
0.641DataRank · unranked
71 citations

Michael G. Heckman, Launia J. White, Austin M. Veire, Otto Pedraza, Alexander R. Burch +77 more

ASLPrep: a platform for processing of arterial spin labeled MRI and quantification of regional brain perfusion

Nature Methods(2022)10.1038/s41592-022-01458-7
N/A
0.590DataRank · unranked
50 citations

Maxwell A. Bertolero, Sudipto Dolui, Matthew Cieslak, Kristin Murtha, Erica B. Baller +94 more

Assessing network degeneration and phenotypic heterogeneity in genetic frontotemporal lobar degeneration by decoding FDG-PET

NeuroImage Clinical(2023)10.1016/j.nicl.2023.103559
Top 73%
0.106DataRank
Top 73%1 citations

Leland R Barnard, Scott A. Przybelski, Venkatsampath Gogineni, Hugo Botha, Jonathan Graff‐Radford +15 more

Temporal order of clinical and biomarker changes in familial frontotemporal dementia

Nature Medicine(2022)10.1038/s41591-022-01942-9
N/A
0DataRank · unranked
138 citations

Melanie Quintana, Barbara Wendelberger, Hilary W. Heuer, Lucy L. Russell, Yann Cobigo +95 more

Brain volumetric deficits in MAPT mutation carriers: a multisite study

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51249
N/A
0DataRank · unranked
35 citations

Taru Flagan, Adam M. Staffaroni, Lize C. Jiskoot, Jersey Deng, Salvatore Spina +54 more

Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome

Acta Neuropathologica(2020)10.1007/s00401-020-02223-w
N/A
0DataRank · unranked
46 citations

Edgard Verdura, Natalia Juliá‐Palacios, Eric N. Anderson, Leire Goicoechea, Laura Planas‐Serra +33 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012
N/A
0DataRank · unranked
38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

Reliability and Validity of Smartphone Cognitive Testing for Frontotemporal Lobar Degeneration

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.4266
N/A
0DataRank · unranked
21 citations

Annie L Clark, Jack C. Taylor, Hilary W. Heuer, Mark Sanderson‐Cimino, Amy B. Wise +72 more

Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders

European Journal of Human Genetics(2024)10.1038/s41431-024-01576-0
N/A
0DataRank · unranked
5 citations

Kim Lee Ng, Filippo Pinto e Vairo, James Collins, Ronald D. Cohn, Kacie Riley +6 more

Multiple sclerosis in Somali Americans: Nature or nurture?

Multiple Sclerosis and Related Disorders(2024)10.1016/j.msard.2024.105842
N/A
0DataRank · unranked
2 citations

Nur Neyal, Elizabeth J. Atkinson, Brian G. Weinshenker, Jan-Mendelt Tillema, B. Mark Keegan +11 more

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.019
N/A
0DataRank · unranked
25 citations

Philipp Kirchner, Antje Wiesener, Irma van de Beek, Quinten Waisfisz, Mieke M. van Haelst +43 more

Clinical Practice Guidelines for the Diagnosis, Management, and Surveillance of LMNB1 -Related Autosomal Dominant Leukodystrophy

Neurology Genetics(2025)10.1212/nxg.0000000000200287
N/A
0DataRank · unranked
0 citations

W. Oliver Tobin, Pietro Cortelli, Quasar Saleem Padiath, Karthik Muthusamy, Ujjal Didar Singh Sekhon +12 more