Janet Hoenicka

12PUBLICATIONS
35CO-AUTHORS
PharmacogenomicsGene and molecular therapyCancer geneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (12)

|Oct 16, 2025
Lysosomal Network Defects in Early-Onset Parkinson's Disease Patients Carrying Rare Variants in Lysosomal Hydrolytic Enzyme Genes.

Alba Pascual, Thaleia Moulka, Oriol de Fàbregues

|Aug 15, 2025
Biallelic Variants in the DARS2 Gene as a Novel Cause of Axonal Charcot-Marie-Tooth Disease.

Berta Estévez-Arias, Siiri Sarv, Nathalie Bonello-Palot

|Mar 13, 2023
Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites.

Lara Cantarero, Gisela García-Vargas, Janet Hoenicka

|Jan 18, 2023
Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants.

Daniel Natera-de Benito, Jonathan Olival, Carla Garcia-Cabau

|Mar 25, 2022
Non-Motor Symptoms in PLA2G6-Associated Dystonia-Parkinsonism: A Case Report and Literature Review.

Lydia Vela-Desojo, Daniele Urso, Mireia Osuna-López

|Sep 13, 2021
Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin.

Charlotte von der Lippe, Kristian Tveten, Trine E Prescott

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Frequent Collaborators

8 joint publications

Francesc Palau

4 joint publications

Jordi Pijuan

2 joint publications

Lydia Vela-Desojo

2 joint publications

Juan Darío Ortigoza-Escobar