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

Kristin Barañano

Johns Hopkins University

ORCID: 0000-0002-4157-2019

Also affiliated with Johns Hopkins Medicine

Biochemistry, 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 5%percentile
0.535Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series

Prenatal Diagnosis(2022)10.1002/pd.6269
Top 36%
0.535DataRank
Top 36%11 citations

Marisa Gilstrop Thompson, Neeta L. Vora, Kelly L. Gilmore, Karin J. Blakemore, Kristen A. Miller +16 more

Papers

Driven by 11 papers — median percentile 64. Top paper: “Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series”.

Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series

Prenatal Diagnosis(2022)10.1002/pd.6269
Top 36%
0.535DataRank
Top 36%11 citations

Marisa Gilstrop Thompson, Neeta L. Vora, Kelly L. Gilmore, Karin J. Blakemore, Kristen A. Miller +16 more

Regulation of human development by ubiquitin chain editing of chromatin remodelers

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.23.917450
N/A
0DataRank · unranked
3 citations

Mohammed A. Basar, Anthony J. Asmar, Joyce J. Thompson, Hirotsugu Oda, Daniela Tiaki Uehara +24 more

Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variation

Science Advances(2021)10.1126/sciadv.abe2116
N/A
0DataRank · unranked
50 citations

Mohammed A. Basar, Anthony J. Asmar, Joyce J. Thompson, Hirotsugu Oda, Daniela Tiaki Uehara +28 more

De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus

Brain(2021)10.1093/brain/awab299
N/A
0DataRank · unranked
42 citations

Ban H. Edani, Simone Martinelli, Hana Hansíková, Erik A. Eklund, Caterina Caputi +45 more

Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms

Molecular Genetics & Genomic Medicine(2021)10.1002/mgg3.1809
N/A
0DataRank · unranked
14 citations

Jessica Kianmahd, Meghna Singh, Maria F. Palafox, Angela Wei, Kathryn Elliott +40 more

The association between educational attainment and SCA 3 age of onset and disease course

Parkinsonism & Related Disorders(2022)10.1016/j.parkreldis.2022.02.025
N/A
0DataRank · unranked
6 citations

Rosa Shi, Reece Carter, Rachel Huynh, Owen P. Morgan, Sheng‐Han Kuo +13 more

A neurodevelopmental disorder caused by a dysfunctional CACNA1A allele

eNeurologicalSci(2023)10.1016/j.ensci.2023.100456
N/A
0DataRank · unranked
10 citations

Daniel F. Bennett, Kristin Barañano, Roger A. Bannister, Audra A. Kramer

MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.001
N/A
0DataRank · unranked
13 citations

Maria Carla Borroto, Sadegheh Haghshenas, A Namasivayam, Jack Reilly, Michael A. Levy +61 more

Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors

Nature Communications(2024)10.1038/s41467-024-52095-x
N/A
0DataRank · unranked
9 citations

Daniel Woike, Daniel Greene, Sarada Das, Kevin Pfeifer, Weimin Yuan +53 more

Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5

Neuron(2020)10.1016/j.neuron.2020.01.030
N/A
0DataRank · unranked
27 citations

Connor Kenny, Abbe Lai, Dilenny M. Gonzalez, Edward Stronge, Gabrielle Séjourné +18 more

An expansion of the phenotype in individuals with SYNCRIP-Related Neurodevelopmental Disorder

Rare(2024)10.1016/j.rare.2024.100052
N/A
0DataRank · unranked
4 citations

Joanna L. Feng, Lindsay A. Phillips, Kara Murias, Marcia Ferguson, Kristin Barañano +26 more