Personal information

Websites & social links

CLIRINX - Clinical Research IT
CRID - Clinical Research ID (unique patient ID)
RDDR - The Rare Disease Data Repository

Other IDs

Scopus Author ID: 57218372360

Countries

Ireland

Activities

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Employment (1)

CLIRINX: Dublin, IE

CEO
Employment
Source: Self-asserted source
Gerard Nesbitt

Works (11)

Assessing Communication Impairments in a Rare Neurodevelopmental Disorder

Neurology Clinical Practice
2025-02 | Journal article
DOI: 10.1212/CPJ.0000000000200391
Contributors: Anne T. Berg; Amanda N. Nili; Lindsey Evans; Katherine C. Paltell; Ariela J.E. Kaiser; Erica L. Anderson; Shawn M. Egan; Aaron J. Kaat; Gerry Nesbitt; Leah S. Myers
Source: check_circle
Crossref

Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders

Brain
2024-04-23 | Journal article
DOI: 10.1093/brain/awae125
Part of ISSN: 0006-8950
Part of ISSN: 1460-2156
Contributors: Anne Berg; Christopher H Thompson; Leah Schust Myers; Erica Anderson; Lindsey Evans; Ariela J E Kaiser; Katherine Paltell; Amanda N Nili; Jean-Marc DeKeyser; Tatiana V Abramova et al.
Source: Self-asserted source
Gerard Nesbitt

CRID - A unique, universal, patient-generated identifier to facilitate collaborative rare disease clinical research

Informatics in Medicine Unlocked
2022 | Journal article
DOI: 10.1016/j.imu.2022.100973
Contributors: Gerry C. Nesbitt; Patricia A. Murphy
Source: check_circle
Crossref
grade
Preferred source (of 2)‎

Nonseizure consequences of Dravet syndrome, KCNQ2-DEE, KCNB1-DEE, Lennox–Gastaut syndrome, ESES: A functional framework

Epilepsy & Behavior
2020-10 | Journal article
DOI: 10.1016/j.yebeh.2020.107287
Part of ISSN: 1525-5050
Source: Self-asserted source
Gerard Nesbitt
grade
Preferred source (of 2)‎

Early Life Epilepsy Natural History Project – Advancing Knowledge of Ultra-Rare Diseases with The CLIRINX Informatics Platform

Americal Epilepsy Society
2019 | Conference poster
Source: Self-asserted source
Gerard Nesbitt

ERGENT: Early Recognition of Genetic Epilepsy in Neonates

American Epilepsy Society
2019 | Conference poster
Source: Self-asserted source
Gerard Nesbitt

Functional Impairments in Young People with Early Life Epilepsies: Influences of Seizures, Medications and Sleep

American Epilepsy Society
2019 | Conference poster
Source: Self-asserted source
Gerard Nesbitt

An informatics infrastructure for KCNQ2 Encephalopathy research including a patient registry, database, curation platform, and website

Americal Epilepsy Society
2016 | Conference poster
Source: Self-asserted source
Gerard Nesbitt

The Epilepsy Phenome/Genome Project

Clinical Trials
2013-08 | Journal article
DOI: 10.1177/1740774513484392
Part of ISSN: 1740-7745
Part of ISSN: 1740-7753
Source: Self-asserted source
Gerard Nesbitt

The Epilepsy Phenome/Genome Project (EPGP) informatics platform

International Journal of Medical Informatics
2013-04 | Journal article
DOI: 10.1016/j.ijmedinf.2012.03.004
Part of ISSN: 1386-5056
Source: Self-asserted source
Gerard Nesbitt
grade
Preferred source (of 2)‎

The Epilepsy Phenome/Genome Project (EPGP): Informatics Tools and Workflow for Processing Electroencephalogram (EEG) Data

American Epilepsy Society
2010 | Conference poster
Source: Self-asserted source
Gerard Nesbitt
How many people are using ORCID?