Julia Doll

6PUBLICATIONS
29CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Cellular nervous systemGene mapping
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Publications (6)

|Apr 10, 2026
FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss.

Daniel Liedtke, Kristen Rak, Katrina M Schrode

|Jan 09, 2026
Expansion of Molecular and Clinical Aspects of EPS8L2 (DFNB106)-Associated Hearing Loss Emphasizes a Potential Therapeutic Window.

Daniel Owrang, Aboulfazl Rad, Masoome Alerasool

|Sep 28, 2023
mRNA Abundance of Neurogenic Factors Correlates with Hearing Capacity in Auditory Brainstem Nuclei of the Rat.

Jonas Engert, Julia Doll, Barbara Vona

|Nov 14, 2020
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.

Julia Doll, Barbara Vona, Linda Schnapp

|Jun 11, 2020
A novel missense variant in MYO3A is associated with autosomal dominant high-frequency hearing loss in a German family.

Julia Doll, Michaela A H Hofrichter, Paulina Bahena

|Jan 08, 2020
Novel Loss-of-Function Variants in CDC14A are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients.

Julia Doll, Susanne Kolb, Linda Schnapp

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Frequent Collaborators

6 joint publications

Barbara Vona

3 joint publications

Thomas Haaf

2 joint publications

Linda Schnapp

2 joint publications

Aboulfazl Rad