Miriam Elbracht

19PUBLICATIONS

232CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesHaematological tumoursPharmacogenomicsGenetic immunology

Get your video featured.

Publish with JoVE

Get your video featured.

Publish with JoVE

Publications (19)

Sort by Publication Date:

|Jun 25, 2026

Prenatal Genetic Testing for Beckwith-Wiedemann Syndrome: Considerations, Challenges and Observations (A Real-World Study).

|Apr 10, 2026

Neurodevelopmental Disorder with Dystonia and Chorea Linked to De Novo Variants in the Splicing Regulator SRRM4.

Philip Harrer, Volker Kittke, Alice Saparov

|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 04, 2026

The potential of whole genome sequencing in pharmacogenetics: a retrospective health record study in rare disease patients.

Madeline Gorny, Katja S Just, Tim Krüger

|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

Pageof 4

Frequent Collaborators

11 joint publications

Kraft Florian

10 joint publications

Miriam Elbracht

Ingo Kurth

Thomas Eggermann

Robert Meyer

Jeremias Krause

Tobias Haack

Marc Sturm

Alexej Knaus

Cordula Knopp

Frequent Collaborators

11 joint publications

Kraft Florian

10 joint publications

Miriam Elbracht

8 joint publications

Ingo Kurth

7 joint publications

Thomas Eggermann