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Ingo Kurth

30PUBLICATIONS

450CO-AUTHORS

Neurology and neuromuscular diseasesHaematological tumoursGene mappingSensory systemsNeurogenetics

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Publications (30)

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|Mar 30, 2026

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

|Feb 27, 2026

MDM4 haploinsufficiency leads to p53-mediated bone marrow failure.

Richa Sharma, Senthil Velan Bhoopalan, Robert Meyer

|Feb 14, 2026

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.

Benita Menden, Rana D Incebacak Eltemur, German Demidov

|Jan 06, 2026

Frequent and clinically relevant germline DNA repair gene variants in young and familial myeloproliferative neoplasms.

Robert Meyer, Maria Jimena Rodriguez, Madeline Caduc

|Oct 24, 2025

Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction.

Noortje W M van den Braak, Samuel Kuehs, Greta Z Peschke

|Sep 15, 2025

Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

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Frequent Collaborators

12 joint publications

Miriam Elbracht

9 joint publications

Florian Kraft

8 joint publications

Miriam Elbracht

6 joint publications

Robert Meyer

6 joint publications

Tobias Haack

4 joint publications

Hannah Klinkhammer

4 joint publications

Thomas Eggermann

4 joint publications

Tim H Brümmendorf

4 joint publications

Axel Schmidt

4 joint publications

Malte Spielmann

Frequent Collaborators

12 joint publications

Miriam Elbracht

9 joint publications

Florian Kraft

8 joint publications

Miriam Elbracht

6 joint publications

Robert Meyer

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