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Zehra Manav Yiğit

Observed names: Zehra Manav Kabayegit, Zehra Manav Kabayeğit, Zehra Manav Yigit, Zehra Manav-Yiğit
Observed institution: Adnan Menderes University
ORCID: 0000-0002-9505-0371
Observed ORCID: 0000-0002-9505-0371
OpenAlex ID: A5003506908
Clinical, genetic characteristics and treatment outcomes of children and adolescents with osteogenesis imperfecta: a two-center experience
2021 · İbrahim Mert Erbaş, Deniz İlgün Gürel, et al. · Connective Tissue Research · 10
The importance of multiple gene analysis for diagnosis and differential diagnosis in charcot marie tooth disease
2021 · Sinem Yalcintepe, Hakan Gurkan, et al. · Turkish Neurosurgery · 10
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Revisiting Wiedemann-Steiner Syndrome: Novel KMT2A Variants and Broadened Clinical Spectrum
2025 · Zehra Manav Yiğit, Aydan Mengübaş Erbaş, et al. · Balkan Medical Journal · 2
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Charting the genetic landscape of autosomal recessive hereditary spastic paraplegia: A deep dive into 10 exceptionally rare cases
2025 · Zehra Manav Yigit, Osman Semih Dikbas, et al. · Neurogenetics · 2
Expanding the genetic spectrum of achromatopsia: novel CNGA3 and CNGB3 variants
2025 · Zehra Manav Yigit, Nurdamla Sandal Filikci, et al. · International Ophthalmology · 2
Founder Pathogenic Variant in LMNA with Diverse Phenotypic Manifestations in Mandibuloacral Dysplasia: Insights from a Turkish Cohort
2025 · Zehra Manav Yiğit, Mustafa Altan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 2
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A novel homozygous thyroglobulin gene variant presenting with massive congenital goiter and neonatal airway obstruction
2026 · Ayşe Anık, Kübra Şen Küçük, et al. · HORMONES · 1
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Intellectual disability and retinitis pigmentosa due to a homozygous null SCAPER variant: a clinical and genetic insight with review of the literature
2025 · Zehra Manav Yiğit, Osman Semih Dikbaş, et al. · Ophthalmic Genetics · 1
A Case with Autism Spectrum Disorder and Concomitant Arginase Deficiency
2024 · Rabia Eren, Buket Canlan Özaydın, et al. · Journal of Dr Behcet Uz Children s Hospital · 1
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The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · BMC Pediatrics
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Additional file 2 of The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · Figshare
Additional file 1 of The clinical spectrum of MECP2 variants in males: a multicenter Turkish cohort of 22 probands, with implications for diagnosis and variant interpretation
2026 · Çağrı Doğan, Mehmet Burak Mutlu, et al. · Figshare
OPHN1-related neurodevelopmental disorders: clinical and genetic findings with novel variants
2026 · Hilmi Bolat, Hilal Aydın, et al. · Neurological Sciences
BRCA1/2 Pathogenic Variants in a Turkish Cohort: Clinical Spectrum, Novel Truncating Variants, and Non-Canonical Cancers in the Aegean Region
2026 · Zehra Manav Yiğit, Nurdamla Sandal Filikci, et al. · Clinical and Experimental Health Sciences
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A Novel Intracellular Domain Missense Variant in GRM7 Associated with Early-Onset Neurodevelopmental Encephalopathy
2026 · Zehra Manav Yigit, Hulya Kayilioglu, et al. · Molecular Syndromology
CHAMP1-Related Neurodevelopmental Disorder: Two Turkish Cases with Novel Truncating Variants and Literature Review
2026 · Zehra Manav Yigit, Pelin Ozyavuz Cubuk, et al. · Molecular Syndromology
From Methylation to Pluripotency: Epigenetic Programming in Early Embryo Development
2026 · Zehra Manav Yiğit, Lamiya Mardan Hacızade, et al. · Balıkesır Health Sciences Journal
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Biallelic TTBK1 variant causes a severe syndromic neurodevelopmental disorder: clinical and genetic insights from two siblings
2026 · Zehra Manav Yigit, Salih Burak Erarslan, et al. · Journal of Medical Genetics
Genetic Profile of DMD/BMD: MLPA and Sanger Sequencing Results from a Single Center
2025 · Zehra Manav Yiğit, Büşra Sapmaz, et al. · Harran Üniversitesi Tıp Fakültesi Dergisi
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CHEK2 Germline Variants and Their Clinical Implications: Experience from a Turkish Hereditary Cancer Cohort
2025 · Zehra Manav Yigit, Osman Semih Dikbas, et al. · Cancer Investigation
The Opposite Phenotype of Sotos Syndrome: 5q35.2q35.3 Microduplication Syndrome
2025 · Kübra Şen Küçük, Aydan Mengübaş Erbaş, et al. · Journal of Clinical Research in Pediatric Endocrinology
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Two Siblings With Al Kaissi Syndrome: Clinical, Radiological, and Molecular Characterization of Compound Heterozygous CDK10 Variants
2025 · Zehra Manav Yigit, Aydan Mengubas Erbas, et al. · American Journal of Medical Genetics Part A
Spectrum and Prevalence of BRCA1/BRCA2 Variants in Aegean Region Hereditary Breast and Ovarian Cancer Cases
2025 · Zehra Manav Yiğit, Gökay Bozkurt · Muğla Sıtkı Koçman Üniversitesi Tıp Dergisi
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A Case of Sanfilippo Syndrome Type C and Wolfram Syndrome Type 1 and the Role of Next-Generation Sequencing in Diagnosis
2025 · Zehra Manav Yiğit, Rıdvan Savaş, et al. · Journal of Dr Behcet Uz Children s Hospital
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The relationship of pregnancy losses with frequently-used hematologic parameters
2025 · Atakan Turgutkaya, Ayşe Hilal Eroğlu Küçükdiler, et al. · Ege Tıp Dergisi
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Works count: 25
Citation count: 31
H-index: 2
I10-index: 2
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