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

Madelyn A. Gillentine

Seattle Children's Hospital

ORCID: 0000-0002-8989-2214

Also affiliated with Baylor Genetics

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 2%percentile
2.1Author 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.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Papers

Driven by 11 papers — median percentile 77. Top paper: “Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders”.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Integrated gene analyses of de novo mutations from 46,612 trios with autism and developmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.15.460398
Top 33%
0.594DataRank
Top 33%13 citations

Chang H. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +4 more

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786
N/A
0.241DataRank · unranked
4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 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

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

Rare(2024)10.1016/j.rare.2024.100040
N/A
0DataRank · unranked
3 citations

Samuel J. Huang, Alyna Khan, Katie Golden‐Grant, Brenna Boyd, Elisabeth A. Rosenthal +37 more

Concordance of whole-genome long-read sequencing with standard clinical testing for Prader-Willi and Angelman syndromes

medRxiv(2024)10.1101/2024.04.02.24305233
N/A
0DataRank · unranked
1 citations

Miranda Galey, Anita E. Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju +4 more

Concordance of Whole-Genome Long-Read Sequencing with Standard Clinical Testing for Prader-Willi and Angelman Syndromes

Journal of Molecular Diagnostics(2025)10.1016/j.jmoldx.2024.12.003
N/A
0DataRank · unranked
6 citations

Miranda P.G. Zalusky, Anita E. Beck, Madelyn A. Gillentine, Jaya Narayanan, Nikhita Damaraju +4 more

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y
N/A
0DataRank · unranked
217 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Androgens mediate sexual dimorphism in Pilarowski-Bjornsson Syndrome

medRxiv(2025)10.1101/2025.05.06.25326635
N/A
0DataRank · unranked
2 citations

Eirny Tholl Thorolfsdottir, Ilana M. Nodelman, Sara Tholl Halldorsdottir, Stefania Benónísdóttir, Malak Alghamdi +64 more

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6
N/A
0DataRank · unranked
117 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency

Human Mutation(2022)10.1002/humu.24332
N/A
0DataRank · unranked
16 citations

Tianyun Wang, Madelyn A. Gillentine, Tiana M. Scott, Aliska M. Berry, Mahshid S. Azamian +19 more