Gabriel C Dworschak

7PUBLICATIONS
31CO-AUTHORS
Predictive and prognostic markersEpigenetics (incl. genome methylation and epigenomics)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Cancer genetics
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Publications (7)

|Dec 23, 2024
TFAP2E is implicated in central nervous system, orofacial and maxillofacial anomalies.

Jeshurun C Kalanithy, Enrico Mingardo, Jil D Stegmann

|Jul 29, 2023
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation.

Ricarda Köllges, Jil Stegmann, Sophia Schneider

|Nov 15, 2022
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems.

Caroline M Kolvenbach, Tim Felger, Luca Schierbaum

|Nov 09, 2022
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy.

Enrico Mingardo, Glenda Beaman, Philip Grote

|Nov 02, 2022
Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations.

Julia Fabian, Gabriel C Dworschak, Lea Waffenschmidt

|May 31, 2021
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies.

Gabriel C Dworschak, Jaya Punetha, Jeshurun C Kalanithy

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Frequent Collaborators

5 joint publications

Heiko Reutter

3 joint publications

Ekkehart Jenetzky

2 joint publications

Stefanie Heilmann-Heimbach

2 joint publications

Philip Grote