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

Kelly L. Gilmore

University of North Carolina Health Care

ORCID: 0000-0002-9125-8714
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 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 14 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

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in Medicine(2022)10.1016/j.gim.2022.04.010
N/A
0DataRank · unranked
21 citations

Marieke Joosten, Caroline Alby, Tania Attié‐Bitach, Kelly L. Gilmore, Christèle Dubourg +50 more

Parental motivations for and adaptation to trio‐exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosis

Prenatal Diagnosis(2022)10.1002/pd.6112
N/A
0DataRank · unranked
18 citations

Kelly L. Gilmore, Emily E. Hardisty, Anne Drapkin Lyerly, Christine Rini, Neeta L. Vora +1 more

How can prenatal exome sequencing inform future pregnancies?

American Journal of Obstetrics and Gynecology(2022)10.1016/j.ajog.2022.02.008
N/A
0DataRank · unranked
2 citations

Kelly L. Gilmore, Emily Hardisty, Neeta L. Vora, Asha N. Talati

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010
N/A
0DataRank · unranked
54 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis

Prenatal Diagnosis(2023)10.1002/pd.6466
N/A
0DataRank · unranked
23 citations

Eoghan Laffan, Preethi A. Jacob, Caitlin Baptiste, Heinz Gabriel, Teresa N. Sparks +21 more

Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63150
N/A
0DataRank · unranked
7 citations

Karen Chong, David Chitayat, Kelly L. Gilmore, Alexander A.L. Jorge, Bruna Lucheze Freire +10 more

Two unrelated fetuses with ITPR1 missense variants and fetal hydrops

Prenatal Diagnosis(2023)10.1002/pd.6439
N/A
0DataRank · unranked
1 citations

Manesha Putra, Kelly L. Gilmore, Neeta L. Vora, Sarah Harris

The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease

Prenatal Diagnosis(2024)10.1002/pd.6527
N/A
0DataRank · unranked
10 citations

Miles Bomback, Atlas Khan, Sarath Krishna Murthy, David E. Solowiejczyk, Neeta L. Vora +9 more

Evolving Features of RASopathies Among Pregnancies With Abnormal Fetal Fluid Collections

Prenatal Diagnosis(2025)10.1002/pd.70039
N/A
0DataRank · unranked
2 citations

W. John Boscardin, Billie R. Lianoglou, Katie Tick, Carmen M. Avram, Kristen A. Miller +13 more

Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene

Prenatal Diagnosis(2025)10.1002/pd.6736
N/A
0DataRank · unranked
1 citations

Kelly L. Gilmore, Smriti Singh, Neeta L. Vora, Cordelia Muir

Prenatal Detection of TGFBR1 Variant Associated With Severe Ventriculomegaly and Loeys–Dietz Syndrome

Prenatal Diagnosis(2025)10.1002/pd.6811
N/A
0DataRank · unranked
0 citations

Sarah Harris, Brianna Murphy, Kelly L. Gilmore, Neeta L. Vora, Morrison Hodges

Neural Cell Adhesion Molecule-Secreting Transgenic Mice Display Abnormalities in GABAergic Interneurons and Alterations in Behavior

UNC Libraries(2021)10.17615/q602-n019
N/A
0DataRank · unranked
1 citations

Galina P. Demyanenko, Kelly L. Gilmore, Z. Josh Huang, Patricia F. Maness, Anitha K. Panicker +3 more

Bi-allelic deleterious variants in SNAPIN, which encodes a retrograde dynein adaptor, cause a prenatal-onset neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.015
N/A
0DataRank · unranked
0 citations

Maayke A. de Koning, Kamal Khan, Kelly L. Gilmore, Mariëtte J.V. Hoffer, Georgios Kellaris +21 more