Lance Rodan

10PUBLICATIONS
41CO-AUTHORS
Circuits and systemsForensic epidemiologyBiomechanical engineeringMedical biochemistry - amino acids and metabolitesMedical infection agents (incl. prions)
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Publications (10)

|Feb 04, 2026
Epilepsy Phenotype and EEG Finding of Rhythmic High-Amplitude Delta With Superimposed Spikes (RHADS) in Succinate Dehydrogenase Deficiency.

Aaron B Bowen, Chiadika Nwanze, Cesar Alves

|Dec 04, 2024
Telehealth Is Effective in the Evaluation of Individuals With Undiagnosed Rare Disorders: An Undiagnosed Diseases Network Study.

Queenie K-G Tan, Allyn McConkie-Rosell, Rachel M Brown

|Nov 06, 2024
Basic helix-loop-helix transcription factor BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, tone and movement abnormalities.

Carolyn Le, Emanuela Argilli, Elizabeth George

|Sep 26, 2024
Case Report of Friedreich's Ataxia and ALG1 -Related Biochemical Abnormalities in a Patient With Progressive Spastic Paraplegia.

Aisling Quinlan, Lance Rodan, Elizabeth Barkoudah

|May 11, 2022
Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders.

Lauren O'Grady, Samantha A Schrier Vergano, Trevor L Hoffman

|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.

Caroline Dias, Rolph Pfundt, Tjitske Kleefstra

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Frequent Collaborators

2 joint publications

Francois Lecoquierre

1 joint publications

Philip M Boone

1 joint publications

Weimin Bi

1 joint publications

Clara Hildebrandt