Matthew T. Whitehead

Also affiliated with SUNY Upstate Medical University, University of Pennsylvania Health System, University of Pennsylvania

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 4%percentile

0.669Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Networks Underlie Temporal Onset of Dysplasia‐Related Epilepsy: A MELD Study

Annals of Neurology(2022)10.1002/ana.26442

Top 30%

0.669DataRank

Top 30%24 citations

Xiaozhen You, Manu Krishnamurthy, Leigh Sepeta, Anqing Zhang, Chima Oluigbo +7 more

Papers

Driven by 17 papers — median percentile 70. Top paper: “Integrating neuroimaging biomarkers into the multicentre, high-dose erythropoietin for asphyxia and encephalopathy (HEAL) trial: rationale, protocol and harmonisation”.

Integrating neuroimaging biomarkers into the multicentre, high-dose erythropoietin for asphyxia and encephalopathy (HEAL) trial: rationale, protocol and harmonisation

BMJ Open(2021)10.1136/bmjopen-2020-043852

N/A

0.678DataRank · unranked

21 citations

Stefan Blüml, Ashok Panigrahy, Amit Mathur, Jeffrey Berman, Ping-Sun Keven Chen +28 more

Networks Underlie Temporal Onset of Dysplasia‐Related Epilepsy: A MELD Study

Annals of Neurology(2022)10.1002/ana.26442

Top 30%

0.669DataRank

Top 30%24 citations

Xiaozhen You, Manu Krishnamurthy, Leigh Sepeta, Anqing Zhang, Chima Oluigbo +7 more

Review of Multi-Modal Imaging in Urea Cycle Disorders: The Old, the New, the Borrowed, and the Blue

Frontiers in Neurology(2021)10.3389/fneur.2021.632307

N/A

0DataRank · unranked

31 citations

Afrouz Anderson, Matthew T. Whitehead, Andrea Gropman, Kuntal Sen

Imaging of pediatric head and neck tumors: A COG Diagnostic Imaging Committee/SPR Oncology Committee/ASPNR White Paper

Pediatric Blood & Cancer(2022)10.1002/pbc.30151

N/A

0DataRank · unranked

5 citations

Usha D. Nagaraj, Lillian M. Lai, Christopher Liu, Jason W. Schroeder, Paritosh C. Khanna +8 more

Neonatal Botulism: A Case Series Suggesting Varied Presentations

Pediatric Neurology(2023)10.1016/j.pediatrneurol.2023.06.004

N/A

0DataRank · unranked

4 citations

Philip Eye, Matthew T. Whitehead, Diana Bharucha‐Goebel, Emmeline Roth, Tayyba Anwar +3 more

Dysfunctional Postnatal Mitochondrial Energy Metabolism in a Patient with Neurodevelopmental Defects Caused by Intrauterine Growth Restriction Due to Idiopathic Placental Insufficiency

Preprints.org(2023)10.20944/preprints202312.1253.v1

N/A

0DataRank · unranked

1 citations

Andrea Gropman, Matthew T. Whitehead, Christine A. Brantner, Eliana Gropman, Anne Chiaramello +1 more

Machine-learning based prediction of future outcome using multimodal MRI during early childhood

Seminars in Fetal and Neonatal Medicine(2024)10.1016/j.siny.2024.101561

N/A

0DataRank · unranked

10 citations

Matthew T. Whitehead, Sovesh Mohapatra, Tianjia Zhu, Hao Huang, Minhui Ouyang

Ophthalmic manifestations of NAA10 ‐related and NAA15 ‐related neurodevelopmental syndromes: Analysis of cortical visual impairment and refractive errors

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63821

N/A

0DataRank · unranked

6 citations

Agnes Park, Elaine Marchi, Andrea Gropman, Matthew T. Whitehead, Gholson J. Lyon +1 more

Ophthalmic Manifestations of NAA10-Related and NAA15-Related Neurodevelopmental Syndrome: Analysis of Cortical Visual Impairment and Refractive Errors

medRxiv(2024)10.1101/2024.02.01.24302161

N/A

0DataRank · unranked

6 citations

Agnes Park, Elaine Marchi, Andrea Gropman, Matthew T. Whitehead, Gholson J. Lyon +1 more

Neuroanatomical Features of NAA10- and NAA15-Related Neurodevelopmental Syndromes

medRxiv(2024)10.1101/2024.06.24.24309433

N/A

0DataRank · unranked

4 citations

Rikhil Makwana, Carolina Christ, Elaine Marchi, Nathaniel Ung, Randie Harpell +5 more

A Diagnostic Blind Spot: Deep intronic SVA_E Insertion identified as the most Common Pathogenic Variant Associated with Canavan Disease

medRxiv(2024)10.1101/2024.12.18.24318806

N/A

0DataRank · unranked

1 citations

Katrina M. Bell, Ramakrishnan Rajagopalan, M. De Silva, Aída Lemes, Cristina Zoco Zabala +24 more

Fetal malformations of cortical development: review and clinical guidance

Brain(2025)10.1093/brain/awaf094

N/A

0DataRank · unranked

22 citations

Sonika Agarwal, Charu Venkatesan, Barbara Scelsa, Brigitte Vollmer, Tomo Tarui +13 more

Deep Intronic SVA_E Insertion Identified as the Most Common Pathogenic Variant Associated With Canavan Disease

Neurology Genetics(2025)10.1212/nxg.0000000000200291

N/A

0DataRank · unranked

3 citations

Katrina M. Bell, Ramakrishnan Rajagopalan, M. De Silva, Aída Lemes, Cristina Zoco Zabala +24 more

Bi-allelic variants in BCAT1 impair mitochondrial function and are associated with a candidate neurometabolic disorder

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100525

N/A

0DataRank · unranked

1 citations

Giulia S. Porcari, Lívia Sertori Finoti, Leonardo Ramos-Rodriguez, Devin M Burris, Justin A. McDonough +15 more

Age and Sex Influences Gamma-aminobutyric Acid Concentrations in the Developing Brain of Very Premature Infants

Scientific Reports(2020)10.1038/s41598-020-67188-y

N/A

0DataRank · unranked

25 citations

Subechhya Pradhan, Marni Jacobs, Mariam Said, Kushal Kapse, Jonathan Murnick +5 more

BLOC1S1 variants cause lysosomal and autophagic defects resulting in a hypomyelinating leukodystrophy with epileptic encephalopathy

medRxiv(2025)10.1101/2025.07.17.25331211

N/A

0DataRank · unranked

0 citations

Carlos González, Chad D. Williamson, Guy Helman, Leslie E. Sanderson, Brianna Disanza +34 more

Fifteen years of urea cycle disorders brain research: Looking back, looking forward

Analytical Biochemistry(2021)10.1016/j.ab.2021.114343

N/A

0DataRank · unranked

38 citations

Matthew T. Whitehead, Carlos Castillo, Ljubica Caldovic, Andrea Gropman, Kuntal Sen

Matthew T. Whitehead

Indexed papers

Top data-sharing exemplar

Papers