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

Angela Morgan

ORCID: 0000-0003-1147-7405

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
0.503Author 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.

Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals

Journal of Medical Genetics(2024)10.1136/jmg-2023-109702
Top 38%
0.503DataRank
Top 38%16 citations

Milou G. P. Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth E. Palmer +12 more

Papers

Driven by 11 papers — median percentile 62. Top paper: “Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people”.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2202764119
N/A
0.738DataRank · unranked
136 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +90 more

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002
N/A
0.568DataRank · unranked
43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +95 more

Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals

Journal of Medical Genetics(2024)10.1136/jmg-2023-109702
Top 38%
0.503DataRank
Top 38%16 citations

Milou G. P. Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth E. Palmer +12 more

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Translational Psychiatry(2022)10.1038/s41398-022-02250-z
N/A
0.406DataRank · unranked
14 citations

Karen Wigg, Else Eising, Yu Feng, Kirsten Blokland, Margaret Wilkinson +85 more

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40

Brain(2023)10.1093/brain/awad314
N/A
0.406DataRank · unranked
14 citations

Thomas Scerri, Adam P. Vogel, Christopher A. Reid, Mara Quach, Victoria E. Jackson +28 more

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.04.466897
N/A
0.406DataRank · unranked
14 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +85 more

Speech and language classification in the human phenotype ontology

European Journal of Human Genetics(2024)10.1038/s41431-024-01635-6
N/A
0.312DataRank · unranked
7 citations

Ben D Coleman, Adam P. Vogel, Alisdair McNeill, Peter N. Robinson, Angela Morgan

Atypical development of Broca’s area in a large family with inherited stuttering

Brain(2021)10.1093/brain/awab364
N/A
0DataRank · unranked
20 citations

Thomas Scerri, Susan Block, Samantha J. Turner, Sheena Reilly, Elaina Kefalianos +8 more

Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy

JAMA Pediatrics(2021)10.1001/jamapediatrics.2021.0878
N/A
0DataRank · unranked
449 citations

Linda Fetters, Lars Adde, Nadia Badawi, Ada Bancale, Roslyn N. Boyd +37 more

De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63559
N/A
0DataRank · unranked
7 citations

Angela Morgan, Meghan N. Bartos, Katelyn Beatty, Benjamin Cogné, Dominique Braun +27 more

Factor analysis of signs of childhood apraxia of speech

Journal of Communication Disorders(2020)10.1016/j.jcomdis.2020.106033
N/A
0DataRank · unranked
33 citations

Amanda Brignell, Angela Morgan, Danielle Gagné, Andrea Norton, Helen Tager‐Flusberg +4 more