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

Laurel A. Screven

National Institutes of Health

ORCID: 0009-0007-8630-6754

Also affiliated with Data Tecnica International (United States), National Institute of Neurological Disorders and Stroke, Short and Associates (United States), National Institute on Aging

Biochemistry, Genetics and Molecular BiologyPsychologyMedicineNeuroscience

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
1.2Author DataRank

Indexed papers

4in 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 4 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 15 papers — median percentile 37. Top paper: “Mis-spliced transcripts generate de novo proteins in TDP-43–related ALS/FTD”.

Mis-spliced transcripts generate de novo proteins in TDP-43–related ALS/FTD

Science Translational Medicine(2024)10.1126/scitranslmed.adg7162
N/A
0.769DataRank · unranked
168 citations

Yue Qi, Anna‐Leigh Brown, Oscar G. Wilkins, Colleen Bereda, Cédric Belair +46 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

Mis-spliced transcripts generate de novo proteins in TDP-43-related ALS/FTD

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.23.525149
N/A
0.550DataRank · unranked
38 citations

Yue Qi, Anna‐Leigh Brown, Oscar G. Wilkins, Colleen Bereda, Cédric Belair +41 more

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

Nature Structural & Molecular Biology(2024)10.1038/s41594-024-01423-2
N/A
0.425DataRank · unranked
16 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Andrey Damianov +36 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
0.365DataRank · unranked
6 citations

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

A new AI-assisted data standard accelerates interoperability in biomedical research

medRxiv(2024)10.1101/2024.10.17.24315618
N/A
0.288DataRank · unranked
4 citations

Shannon Ballard, Syed Islamuddin Shah, Owen Bianchi, Lietsel Jones, Mathew J. Koretsky +30 more

Temporal dynamics of proteome and phosphorproteome during neuronal differentiation in the reference KOLF2.1J iPSC line

10.1101/2025.03.25.645331
N/A
0.241DataRank · unranked
4 citations

Ziyi Li, Erika Lara, Daniel M. Ramos, Marianist Santiana, Benjamin Jin +17 more

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

medRxiv(2022)10.1101/2022.11.25.22282764
Top 63%
0.217DataRank
Top 63%3 citations

Madeleine Richer, Simona Jasaityte, Eleanor J. Stafford, Julie Joubert, Tarek Antar +19 more

Harnessing diversity to study Alzheimer’s disease: A new iPSC resource from the NIH CARD and ADNI

Neuron(2024)10.1016/j.neuron.2024.01.026
N/A
0.208DataRank · unranked
3 citations

Caroline B. Pantazis, Katherine M. Andersh, Samantha Hong, Dan Vitale, Erika Lara +12 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

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1

medRxiv(2024)10.1101/2024.02.20.24302827
N/A
0.104DataRank · unranked
1 citations

Peter Wild Crea, Daniel M. Ramos, Emil K. Gustavsson, Mandy Radefeldt, Mary B. Makarious +33 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

Auditory brainstem response audiometry in tauopathy mouse model of human Alzheimer's disease

JASA Express Letters(2024)10.1121/10.0026602
N/A
0DataRank · unranked
3 citations

Laurel A. Screven, Sergio Vicencio-Jiménez, Amanda M. Lauer, Kali Burke

The LRRK2 p.A419V variant associates with risk of Parkinson’s disease in the East Asian population and an evaluation on age of onset

medRxiv(2025)10.1101/2025.08.28.25333987
N/A
0DataRank · unranked
0 citations

María Teresa Periñán, Elaine Guo Yan Chew, Paul Suhwan Lee, Fulya Akçimen, Jia Lun Lim +26 more

Variants in DNAJC13 Are Not Associated with Parkinson’s Disease Across Different Ancestral Backgrounds

medRxiv(2025)10.64898/2025.12.30.25343211
N/A
0DataRank · unranked
0 citations

Mariam Isayan, Yasser Mecheri, Paula Saffie Awad, Maria Milagros Leila, Laurel A. Screven +5 more