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Ingo Helbig

74PUBLICATIONS
604CO-AUTHORS
Neurology and neuromuscular diseasesCancer geneticsNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
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Journal

Publications (74)

Sort by Publication Date:
|Jul 14, 2026
A prospective natural history study protocol for clinical trial readiness in synaptic disorders.

|Jul 10, 2026
Monogenic epilepsies exhibit distinct sleep endophenotypes.

|May 23, 2026
White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy.

|May 18, 2026
Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

|Apr 20, 2026
DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneity.

|Apr 15, 2026
Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretation.

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Frequent Collaborators

17 joint publications

Michael C Kaufman

16 joint publications

Sarah Ruggiero

13 joint publications

Jillian L McKee

9 joint publications

Julie Xian

8 joint publications

Katherine L Helbig

8 joint publications

Jan Magielski

7 joint publications

Ethan M Goldberg

6 joint publications

David Lewis-Smith

5 joint publications

Shiva Ganesan

5 joint publications

Holger Lerche

Frequent Collaborators

17 joint publications

Michael C Kaufman

16 joint publications

Sarah Ruggiero

13 joint publications

Jillian L McKee

9 joint publications

Julie Xian