Author

Alexis R. Karlin

Children's Hospital of PhiladelphiaORCID 0009-0007-4254-4267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1

Frequent Co-Authors

Ingo HelbigiD· 2 shared Alex Gonzalez· 1 shared Danielle deCampoiD· 1 shared Donna SchaareiD· 1 shared Jan H. MagielskiiD· 1 shared Julie XianiD· 1 shared Katie Rose SullivaniD· 1 shared Kendra AllisoniD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Ingo HelbigORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 14, 2024

A Longitudinal Exploration of CACNA1A-related Hemiplegic Migraine in Children

Donna Schaare, Laina G. Lusk, Alexis R. Karlin…·Ingo Helbig

This study examines the longitudinal course of CACNA1A-related hemiplegic migraine in children, finding unpredictable severity and timing of events with no clear correlation with epilepsy.

1 citation

humanstatistical model

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Genetic & Genomic MedicinemedRxivPreprintFeb 12, 2023

The genetic spectrum of febrile infection-related epilepsy syndrome (FIRES) and refractory status epilepticus

Danielle deCampo, Julie Xian, Alexis R. Karlin…·Ingo Helbig

This paper analyzes the clinical and genetic landscape of FIRES and RSE, finding 36% of RSE patients have genetic causes, while FIRES remains largely undiagnosed.

DOI 10.1101/2023.02.12.23285754

humanelectronic health records

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