Zehra Manav Yiğit

10PUBLICATIONS
38CO-AUTHORS
NeonatologyNeurology and neuromuscular diseasesCancer geneticsGene mappingCell and nuclear division
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Publications (10)

|Jul 16, 2026
A novel homozygous thyroglobulin gene variant presenting with massive congenital goiter and neonatal airway obstruction.

|Jan 16, 2026
Biallelic TTBK1 variant causes a severe syndromic neurodevelopmental disorder: clinical and genetic insights from two siblings.

Zehra Manav Yigit, Salih Burak Erarslan, Ayse Tosun

|Dec 19, 2025
CHEK2 Germline Variants and Their Clinical Implications: Experience from a Turkish Hereditary Cancer Cohort.

Zehra Manav Yigit, Osman Semih Dikbas, Fatih Mergen

|Dec 01, 2025
Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum.

Zehra Manav Yiğit, Aydan Mengübaş Erbaş, Ayberk Türkyılmaz

|Sep 17, 2025
Two Siblings With Al Kaissi Syndrome: Clinical, Radiological, and Molecular Characterization of Compound Heterozygous CDK10 Variants.

Zehra Manav Yigit, Aydan Mengubas Erbas, Ridvan Savas

|Aug 09, 2025
Charting the genetic landscape of autosomal recessive hereditary spastic paraplegia: A deep dive into 10 exceptionally rare cases.

Zehra Manav Yigit, Osman Semih Dikbas, Ayse Tosun

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Frequent Collaborators

4 joint publications

Ahmet Anık

4 joint publications

Gökay Bozkurt

2 joint publications

Göksel Tuzcu

2 joint publications

Aydan Mengubas Erbas