Thomas Haaf

Wuerzburg, BY, Germany

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 151 publications

Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.

Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.

Journal: Clinical epigenetics

Published: June 13, 2026

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

Journal: European journal of human genetics : EJHG

Published: April 17, 2026

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

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

Journal: medRxiv : the preprint server for health sciences

Published: April 10, 2026

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss.

TECTB Variants Reveal Tectorial Membrane Vulnerability in Dominant Non-Syndromic Hearing Loss.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: December 19, 2025

Functional and genomic characterization of LCN2-deficient PC-3 cells reveals insights into prostate cancer progression.

Functional and genomic characterization of LCN2-deficient PC-3 cells reveals insights into prostate cancer progression.

Journal: Frontiers in molecular biosciences

Published: October 23, 2025

Sperm rDNA Copy Number and Methylation Are Associated with Male-Factor Infertility.

Sperm rDNA Copy Number and Methylation Are Associated with Male-Factor Infertility.

Journal: International journal of molecular sciences

Published: September 23, 2025

Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.

Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.

Journal: Clinical epigenetics

Published: August 27, 2025

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

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

Journal: Molecular neurobiology

Published: August 14, 2025

Intraindividual rDNA copy number variation and methylation in humans.

Intraindividual rDNA copy number variation and methylation in humans.

Journal: Experimental cell research

Published: July 22, 2025

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics.

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics.

Journal: Molecular medicine (Cambridge, Mass.)

Published: July 22, 2025

Domain specific phenotypic expansion associated with variants in MACF1.

Domain specific phenotypic expansion associated with variants in MACF1.

Journal: medRxiv : the preprint server for health sciences

Published: July 16, 2025

Promoter hypomethylation drives ABCB1-mediated carfilzomib resistance in multiple myeloma.

Promoter hypomethylation drives ABCB1-mediated carfilzomib resistance in multiple myeloma.

Journal: Clinical epigenetics

Published: July 03, 2025

Showing 1-12 of 151

Last Updated: 09/26/2026