Mark P. Fitzgerald

Also affiliated with University of Pennsylvania

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care system”.

Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care system

Epilepsia(2020)10.1111/epi.16733

N/A

0DataRank · unranked

64 citations

Anup D. Patel, Renée A. Shellhaas, Anne T. Berg, Erika Axeen, Jeffrey Bolton +20 more

Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID ‐19 pandemic

Developmental Medicine & Child Neurology(2022)10.1111/dmcn.15406

N/A

0DataRank · unranked

7 citations

Julie Xian, Peter D. Galer, Shridhar Parthasarathy, Alexander K. Gonzalez, Jillian L. McKee +4 more

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01485-w

N/A

0DataRank · unranked

217 citations

Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi +95 more

Periodic Discharges in Critically Ill Children: Predictors and Outcome

Journal of Clinical Neurophysiology(2023)10.1097/wnp.0000000000000986

N/A

0DataRank · unranked

2 citations

Darshana Parikh, Shavonne L. Massey, Mark P. Fitzgerald, Lisa Vala, Maureen Donnelly +6 more

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8

N/A

0DataRank · unranked

58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more

Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function

Nature Genetics(2025)10.1038/s41588-025-02361-5

N/A

0DataRank · unranked

3 citations

Aisha Ahmad, Paranchai Boonsawat, Jasmine Shahanoor Hinzen, Mareike Lohse, Boris Bouazza‐Arostegui +95 more

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010

N/A

0DataRank · unranked

1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406

N/A

0DataRank · unranked

1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more