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

Jill V. Hunter

Baylor College of Medicine

ORCID: 0000-0003-3522-578X

Also affiliated with Texas Children's Hospital

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 100%percentile
0Author 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 →

Papers

Driven by 11 papers. Top paper: “Acute White Matter Differences in the Fornix Following Mild Traumatic Brain Injury Using Diffusion Tensor Imaging”.

Acute White Matter Differences in the Fornix Following Mild Traumatic Brain Injury Using Diffusion Tensor Imaging

Journal of Neuroimaging(2013)10.1111/j.1552-6569.2010.00537.x
N/A
0.657DataRank · unranked
79 citations

Elisabeth A. Wilde, Erin D. Bigler, Stephen R. McCauley, Gerri Hanten, Maya Troyanskaya +5 more

TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.10.007
N/A
0.500DataRank · unranked
27 citations

Linda M. Reis, Davut Pehli̇van, Jonathan A. Bernstein, Michael Muriello, Erin Syverson +33 more

A novel de novo intronic variant in ITPR1 causes Gillespie syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62232
N/A
0.434DataRank · unranked
17 citations

Ming‐Ming Jiang, Xiaohui Li, Ronit Marom, Hongzheng Dai, David R. Murdock +16 more

Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51003
N/A
0DataRank · unranked
30 citations

Tadahiro Mitani, Sedat Işıkay, Jozef Hertecant, Mohammed Almannai, Kandamurugu Manickam +19 more

Dopamine neuron stimulation induces context-dependent abnormal involuntary movements in healthy rats.

Deep Blue (University of Michigan)(2022)10.7302/7981
N/A
0DataRank · unranked
0 citations

Antonio Bova, Andrew Stevens, DK Leventhal, Jill V. Hunter

Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.013
N/A
0DataRank · unranked
43 citations

Tianyu Guo, Chen Wang, Lillian Garrett, Angad Jolly, Moez Dawood +63 more

Argininosuccinate lyase deficiency causes blood-brain barrier disruption via nitric oxide–mediated dysregulation of claudin expression

JCI Insight(2023)10.1172/jci.insight.168475
N/A
0DataRank · unranked
12 citations

Urszula Polak, Ming‐Ming Jiang, John D. Odom, Jill V. Hunter, Saima Ali +8 more

Clinical exome sequencing uncovers genetic disorders in neonates with suspected hypoxic–ischemic encephalopathy: A retrospective analysis

Clinical Genetics(2024)10.1111/cge.14522
N/A
0DataRank · unranked
8 citations

Roni Zemet, Matthew A. Shanahan, Brian Burnett, Elizabeth Mizerik, Jill A. Rosenfeld +5 more

Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia

Annals of Neurology(2022)10.1002/ana.26381
N/A
0DataRank · unranked
9 citations

Isabella Herman, Reza Maroofian, Aren E. Marshall, Karina Carvalho Donis, Jawid M. Fatih +60 more

Two novel bi‐allelic KDELR2 missense variants cause osteogenesis imperfecta with neurodevelopmental features

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62221
N/A
0DataRank · unranked
18 citations

Isabella Herman, Fatima Rahman, Najwa Anwar, Reza Maroofian, Janice Yip +17 more

NAXE deficiency: A neurometabolic disorder of NAD(P)HX repair amenable for metabolic correction

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.04.003
N/A
0DataRank · unranked
31 citations

Daniel G. Calame, Charul Gijavanekar, Kristen Fisher, Jill V. Hunter, Elizabeth Mizerik +4 more