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Author

Ayça Kocaağa

Observed names: A. Kocaaga, AYÇA KOCAAĞA, Ayca Kocaaga, Ayça KOCAAĞA, Ayça Kocaaga, Kocaaga, Ayca, Kocaağa, Ayça
ORCID: 0000-0003-0434-8445
Observed ORCID: 0000-0003-0434-8445
OpenAlex ID: A5015308031
Psoriasis: An Immunogenetic Perspective
2022 · Ayca Kocaaga, Mustafa Kocaaga · Global Medical Genetics · 21
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Identification of Novel Gene Variants in Children With Drug-Resistant Epilepsy: Expanding the Genetic Spectrum
2022 · Ayca Kocaaga, Sevgi Yimenicioglu · Pediatric Neurology · 11
The pattern of chromosomal abnormalities in recurrent miscarriages: a single center retrospective study
2022 · Ayca Kocaaga, Halime Kilic, et al. · Annals of Saudi Medicine · 11
Evaluation of Molecular and Clinical Findings in Children With Neurofibromatosis Type 1: Identification of 15 Novel Variants
2023 · Yasar Bildirici, Ayca Kocaaga, et al. · Pediatric Neurology · 6
Identification of novel variants in retinitis pigmentosa genes by whole-exome sequencing
2023 · Ayca Kocaaga, İrem Öztürk Aköz, et al. · Revista da Associação Médica Brasileira · 6
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First report of tethered cord syndrome in a patient with Verheij syndrome
2022 · A. Kocaaga, S. Yimenicioglu, et al. · Ophthalmic Genetics · 5
Association of NOD1, NOD2, PYDC1 and PYDC2 genes with Behcet’s disease susceptibility and clinical manifestations
2021 · Ayca Kocaaga, Gunes Cakmak Genc, et al. · Ophthalmic Genetics · 5
Expanding the spectrum of white matter abnormalities in Wolfram syndrome: a retrospective review
2025 · Justin Simo, Heather M. Lugar, et al. · Frontiers in Neurology · 4
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Koolen-de Vries syndrome: A de novo missense KANSL1 variant
2022 · S. Yimenicioglu, A. Kocaaga · Clinical Neurology and Neurosurgery · 4
Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutation
2022 · Hatice Mine Cakmak, Omer Kartal, et al. · Pediatrics & Neonatology · 4
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Association Between IL28B, IL29 Gene Polymorphisms and Clinical Manifestations of Behçet’s Disease
2020 · G. Cakmak Genc, S. Karakas Celık, et al. · Immunological Investigations · 4
A review of the immunogenetics of Stevens-Johnson syndrome and toxic epidermal necrolysis
2025 · Ayca Kocaaga, Mustafa Kocaaga · Global Medical Genetics · 3
Incidence and Spectrum of Thrombophilia in Women With Recurrent Pregnancy Loss: a Retrospective Study
2023 · AYÇA KOCAAĞA, HALİME KILIÇ, et al. · Eskisehir Medical Journal Eskisehir City Hospital · 3
Novel NR2F1 variant identified by whole-exome sequencing in a patient with Bosch–Boonstra–Schaaf optic atrophy syndrome
2022 · Ayca Kocaaga, Sevgi Yimenicioglu, et al. · Indian Journal of Ophthalmology · 3
The immunogenetics of subacute sclerosing panencephalitis: A comprehensive review
2022 · Ayça Kocaağa · Karnataka Pediatric Journal · 3
Presentation of an Infant with Chromosome 18p Deletion Syndrome and Asymmetric Septal Hypertrophy
2022 · Ayca Kocaaga, Sevgi Yimenicioglu · Global Medical Genetics · 3
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Chromosomal abnormalities of embryos from sporadic and recurrent miscarriages: a tertiary center experience
2025 · A. Kocaaga, E. Akca Salik · Molecular Biology Reports · 2
A rare case of Coffin–Lowry syndrome accompanied by a copper-beaten skull appearance
2023 · Ayca Kocaaga, Sevgi Yimenicioglu · Neurology Asia · 2
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A p.Val412Serfs pathogenic variant associated with Wolfram-like syndrome and leukodystrophy
2023 · Ayca Kocaaga, Sevgi Yimenicioglu, et al. · The Egyptian Journal of Neurology Psychiatry and Neurosurgery · 2
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The genetic spectrum of polycystic kidney disease in children
2023 · Ayca Kocaaga, Yesim Özdemir Atikel, et al. · Revista da Associação Médica Brasileira · 2
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An immunogenetic perspective of ANCA-associated vasculitides
2022 · A. Kocaaga, M. Kocaaga · Egyptian Rheumatology and Rehabilitation · 2
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De novo STXBP1 mutation in a child with hypotonia, intellectual disability, tremor and without epilepsy
2023 · Sevgi Yimenicioglu, Ayca Kocaaga · Neurology Asia · 1
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Identification of Novel Mutations in Children with Hereditary Spherocytosis by Targeted Exome Sequencing: A Single Center Experience
2022 · Ayça KOCAAĞA, Hatice Mine ÇAKMAK · Medical Journal of Western Black Sea · 1
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Association of NOD1 and NOD2 Polymorphisms With Susceptibility to Subacute Sclerosing Panencephalitis
2022 · Ayça Kocaaga, Gunes Cakmak Genc, et al. · Journal of Child Neurology · 1
A novel p.Ala34Val variant in C19orf12 is associated with neurodegeneration with brain iron accumulation
2022 · Ayca Kocaaga, Pınar Uzun Uslu · Neurology Asia · 1
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Works count: 45
Citation count: 113
H-index: 5
I10-index: 3
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