Get started
Author

Hamide Betül Gerik Çelebi

Observed names: Celebi, Hamide Betul Gerik, H. Betül Gerik Çelebi, H.B., Gerik-Celebi, Hamide Betul Gerik Celebi, Hamide Betul Gerik Çelebi, Hamide Betul Gerik-Celebi, Hamide Betul Gerik‐Celebi, Hamide Betül GERİK ÇELEBİ, Hamide Betül Gerik-Celebi, Hamide Betül Gerik-Çelebi, Hamide Betul Gerik‐Celebi, Hamide Betül Gerik Çelebi, Hamıde Betul GERİK CELEBİ, Hamıde Betul Gerik Celebi
ORCID: 0000-0001-5218-7880
Observed ORCID: 0000-0001-5218-7880
OpenAlex ID: A5005468563
Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders
2024 · Hamide Betul Gerik‐Celebi, Hilmi Bolat, et al. · Developmental Neurobiology · 13
Clinical and Genetic Characteristics of Patients with Unexplained Intellectual Disability/Developmental Delay without Epilepsy
2023 · Hamide Betul Gerik-Celebi, Hilal Aydin, et al. · Molecular Syndromology · 13
PDF
Molecular analyses of ADAMTS-1, -4, -5, and IL-17 a cytokine relationship in patients with ulcerative colitis
2023 · Tahir Buran, Muhammet Burak Batır, et al. · BMC Gastroenterology · 10
PDF
Genetic and clinical spectrum of PIEZO2-related disorders: insights from a multicenter study of 26 patients
2025 · Gulcin Akinci, Berk Ozyilmaz, et al. · Neuromuscular Disorders · 6
Utility of Optical Genome Mapping in Repeat Disorders
2024 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Clinical Genetics · 6
Coincidental occurance of episodic ataxia and multiple sclerosis: a case report and review of the literature
2020 · Melike Batum, Ayşın Kısabay Ak, et al. · International Journal of Neuroscience · 4
Investigation of patients with childhood epilepsy in single center: Comprehensive genetic testing experience
2024 · Hamide Betul Gerik‐Celebi, İpek Dokurel Çetin, et al. · International Journal of Developmental Neuroscience · 3
Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders
2023 · Hamide Betul Gerik-Celebi, Gul Unsel-Bolat, et al. · Molecular Syndromology · 3
PDF
Investigation of Genetic Changes in Three Families with Bipolar Disease
2024 · Esra Çolak-Geniş, Müjdan Özdemir Erdoğan, et al. · Molecular Syndromology · 2
PDF
BRCA and non-BRCA Variants Detected by Next Generation Sequencing in Patients with Hereditary Breast and/or Ovarian Cancer Syndrome
2022 · Hamide Betül Gerik-Çelebi, Hilmi Bolat · Acta Oncologica Turcica · 2
PDF
Two Opposite Phenotypes of Glucose Disorders in a Family with Heterozygous P.SER453LEU (C.1358C> T) Mutation in the Glucokinase (GCK) Gene: Maturity Onset Diabetes in Young and Insulinoma
2022 · M Demiral, H B G Çelebi, et al. · Acta Endocrinologica (Bucharest) · 2
PDF
Coinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family
2020 · Dilek Gun Bilgic, Hamide Betul Gerik Celebi, et al. · Journal of Clinical Neuroscience · 2
The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications
2026 · Sanem Yilmaz, Esra Serdaroglu, et al. · European Journal of Paediatric Neurology · 1
First Reported Co-Occurrence of Bardet-Biedl Syndrome Type 10 and Autism Spectrum Disorder: A Case Report and Clinical Review
2025 · Ahmet Güleç, Hamide Betul Gerik-Celebi · Molecular Syndromology · 1
PDF
Effects of the Missense Variants on Complete Phenotype and Splicing Variant on Severe Growth Retardation in the BPTF Gene
2025 · Gül Ünsel‐Bolat, Hamide Betul Gerik‐Celebi, et al. · Developmental Neurobiology · 1
PDF
Hereditary hypomagnesemia with secondary hypocalcemia caused by a novel mutation in TRPM6 gene
2023 · İpek Dokurel Çetin, Hamide Betül Gerik-Çelebi, et al. · Journal of Pediatric Endocrinology and Metabolism · 1
A novel CACNA1A mutation in a neonate with severe encephalopathy at birth
2023 · Mine Ozdil, Arzu Eroglu, et al. · Acta Neurologica Belgica · 1
Evaluation of variants in maturity onset of diabetes young related genes in Balıkesir region
2023 · Hamide Betül GERİK ÇELEBİ, Meliha DEMİRAL · Anatolian Current Medical Journal · 1
PDF
A new clinical entity in T704M mutation in periodic paralysis
2020 · Dilek Gun Bilgic, Aydeniz Aydin Gumus, et al. · Journal of Clinical Neuroscience · 1
The Impact of 8p23 Copy Number Variations on Neurodevelopmental Aetiology: A Focus on Rare Deletions
2026 · Ahmet Güleç, Hamide Betul Gerik‐Celebi · International Journal of Developmental Neuroscience
A Girl with Imerslund Grasbeck Syndrome: Presentıng with Hypocalcemia
2026 · Yeşim Yiğit, Meliha Demiral, et al. · Güncel Pediatri
PDF
A novel compound heterozygous YY1AP1 variant in Grange syndrome: importance of early signs in preventing life-threatening vascular complications
2026 · Gul Unsel-Bolat, Neslihan Tezcan, et al. · Journal of Human Genetics
Multimodal Imaging and Electrophysiological Features of Genetically Confirmed Inherited Retinal Dystrophies
2026 · Gozde Sahın Vural, Hamıde Betul Gerik Celebi, et al. · Balıkesır Health Sciences Journal
PDF
Keipert syndrome beyond classical features: novel GPC4 variant associated with epilepsy but preserved cognition
2026 · Hilmi Bolat, Hilal Aydın, et al. · Neurological Sciences
Hereditary Hyperferritinemia Cataract Syndrome Mimicking Iron Overload in a Pediatric Patient With Coexisting HFE H63D Homozygosity
2026 · Yeşim Yiğit, Hamide Betül Gerik Çelebi · Case Reports in Pediatrics
Works count: 49
Citation count: 71
H-index: 5
I10-index: 3
Year
Topic
Type