Alexander E Volk

Germany

Research Interests

Explore related searches

Professors in Germany

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (11)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2022

Collaborators (5)

Dorothee Saur

Professor

University Hospital Leipzig

GERMANY

View details

Nicola Strenzke

University Medical Center Göttingen

GERMANY

View details

Carl Hartmut Göbel

University Hospital Schleswig-Holstein

GERMANY

View details

Christian Kubisch

Full Professor and Chair

University Medical Center Hamburg-Eppendorf (UKE)

GERMANY

View details

Patrick Oeckl

GERMANY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Alexander E Volk

Research Interests

Explore related searches

Contact this professor

Articles (11)

Correction: Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis.

Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis.

Evaluating genome sequencing strategies: trio, singleton, and standard testing in rare disease diagnosis.

Evaluation of Different National Comprehensive Cancer Network Clinical Practice Guidelines in Prostate Cancer for Germline Genetic Testing in Localized and Locally Recurrent Prostate Cancer.

Colonoscopy findings in CDH1 carriers from a multicenter international study.

Serum chitotriosidase-1 (CHIT1) as candidate biomarker for mitochondriopathies.

Neurofilaments and progranulin are related to atrophy in frontotemporal lobar degeneration - A transdiagnostic study cross-validating atrophy and fluid biomarkers.

Complex structural variation and nonsense variant <i>in trans</i> cause <i>VPS50</i>-related disorder.

The heterogeneous cancer phenotype of individuals with biallelic germline pathogenic variants in CHEK2.

A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2.

Collaborators (5)

Dorothee Saur

Nicola Strenzke

Carl Hartmut Göbel

Christian Kubisch

Patrick Oeckl

Make your next move.