Gabrielle Rudolf

6PUBLICATIONS
81CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Organic green chemistryPsychology of ageingNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Jan 02, 2024
Molecular and Phenotypic Characterization of the RORB-Related Disorder.

Zeynep Gokce-Samar, Annalisa Vetro, Julitta De Bellescize

|Oct 24, 2020
Reply to "PPP2R5D Genetic Mutations and Early Onset Parkinsonism".

Christine Y Kim, Thomas Wirth, Cécile Hubsch

|Aug 04, 2020
Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation.

Christine Y Kim, Thomas Wirth, Cécile Hubsch

|May 30, 2020
Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia.

Diane Doummar, Christel Dentel, Romane Lyautey

|Oct 31, 2019
Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3.

Rahel T Florian, Florian Kraft, Elsa Leitão

|Oct 31, 2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2.

Mark A Corbett, Thessa Kroes, Liana Veneziano

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Frequent Collaborators

3 joint publications

Thomas Wirth

2 joint publications

Mark A Corbett

2 joint publications

Christel Depienne

2 joint publications

Mark F Bennett