Lindsay C Burrage

22PUBLICATIONS
167CO-AUTHORS
Metabolic medicineCell and nuclear divisionNeurogeneticsDevelopmental genetics (incl. sex determination)Gene mapping
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Publications (22)

|Feb 25, 2026
Metabolic masqueraders of paediatric and adult rheumatic diseases.

Steven H Lang, Cher Sha, Chelsi M Rose

|Sep 10, 2025
LONP1 Variants Are Associated With Clinically Diverse Phenotypes.

Randee E Young, Lu Qiao, Rebecca Hernan

|Jul 28, 2025
Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia.

Harsha Murthy, Ny Hoang, Jamie C Stark

|Aug 21, 2024
Recessive loss-of-function variants in DPH1 identified as the molecular cause in a sibling pair previously diagnosed with Fine-Lubinsky syndrome.

Emily R Waskow, Lisa T Emrick, Jill A Rosenfeld

|Jul 06, 2024
Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing.

Hongzheng Dai, Shamika Ketkar, Taotao Tan

|Jul 04, 2024
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders.

Dongxue Mao, Chaozhong Liu, Linhua Wang

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