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Esin Karakılıç Özturan

Observed names: E Karakilic-Ozturan, E. Karakilic-Ozturan, ESİN KARAKILIÇ ÖZTURAN, Esin Karakilic, Esin Karakilic Ozturan, Esin Karakilic-Ozturan, Esin Karakilic‐Ozturan, Esin Karakılıc, Esin Karakılıc Ozturan, Esin Karakılıç Özturhan, Esin Karakılıç-Özturan, KARAKILIÇ ÖZTURAN, ESİN, KARAKILIÇ ÖZTURHAN, ESİN, KarakilicOzturan, E., Karakılıc Ozturan E, Karakılıç Özturan, Esin, Ozturan Esin Karakilic, Özturan Esin Karakiliç
ORCID: 0000-0002-8842-1752
Observed ORCID: 0000-0002-8842-1752
OpenAlex ID: A5074293095
Cranial MRI Abnormalities and Long-term Follow-up of the Lesions in 770 Girls With Central Precocious Puberty
2021 · Didem Helvacıoğlu, Serap Demircioğlu Turan, et al. · The Journal of Clinical Endocrinology & Metabolism · 28
Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience
2019 · İhsan Esen, Elvan Bayramoğlu, et al. · Journal of Clinical Research in Pediatric Endocrinology · 17
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LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency
2020 · Aslı Derya Kardelen, Manolya Kara, et al. · HORMONES · 12
Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey
2023 · Esin Karakılıç Özturan, Ayşe Pınar Öztürk, et al. · Journal of Clinical Research in Pediatric Endocrinology · 11
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Bone Health and Growth in Spinal Muscular Atrophy Type 2 and 3
2022 · Osman Kipoğlu, Esin Karakılıç Özturan, et al. · Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi · 9
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Novel variants ensued genomic imprinting in familial central precocious puberty
2024 · V. Karaman, E. Karakilic-Ozturan, et al. · Journal of Endocrinological Investigation · 7
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Growth and Pubertal Features in a Cohort of 83 Patients with Osteogenesis Imperfecta
2022 · Ayşe Pınar Öztürk, Aslı Dudaklı, et al. · Klinische Pädiatrie · 7
The Role of Anti-Neutrophil Antibodies in the Etiologic Classification of Childhood Neutropenia: A Cross-Sectional Study in a Tertiary Center
2019 · Esin Karakilic-Ozturan, Serap Karaman, et al. · Journal of Pediatric Hematology/Oncology · 6
Body proportions in patients with Turner syndrome on growth hormone treatment
2023 · ASLI DERYA KARDELEN AL, NUR MİNE ŞÜKÜR, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 5
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Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience
2020 · Zehra Yavas Abali, Elisa De Franco, et al. · Hormone Research in Paediatrics · 5
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Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinism
2025 · Zehra Yavas Abali, Firdevs Bas, et al. · Endocrine · 4
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
2023 · Aslı Derya Kardelen, Adam Najaflı, et al. · Journal of Clinical Research in Pediatric Endocrinology · 4
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Evaluation of Growth Characteristics and Final Heights of Cases Diagnosed with Noonan Syndrome on GH Treatment
2024 · Zeynep Şıklar, Merih Berberoğlu, et al. · Journal of Clinical Research in Pediatric Endocrinology · 3
A Novel RNPC3 Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy
2023 · Zehra Yavas Abali, Ezgi Gokpinar Ili, et al. · Hormone Research in Paediatrics · 3
Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome
2022 · Esin Karakilic‐Ozturan, Umut Altunoglu, et al. · American Journal of Medical Genetics Part A · 3
SLC34A3 Gene Mutation as a Rare Cause of Hypophosphatemia in Two Siblings
2022 · E Karakilic-Ozturan · Acta Endocrinologica (Bucharest) · 3
A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care
2022 · Aslı Derya Kardelen, Esin Karakılıç Özturan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 2
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Long-term Follow-up of a Toddler with Papillary Thyroid Carcinoma: A Case Report with a Literature Review of Patients Under 5 Years of Age
2021 · Ayşe Pınar Öztürk, Esin Karakılıç Özturan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 2
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Expanding the Clinical and Mutational Spectrum of Biallelic POC1A Variants: Characterization of Four Patients and a Comprehensive Review of POC1A ‐Related Phenotypes
2024 · Umut Altunoglu, Gozde Tutku Turgut, et al. · Clinical Genetics · 1
Gonadoblastoma with Dysgerminoma in a Virilized Adolescent with Karyotype 46,XX: A Case Report and Review of the Literature
2024 · Tuğçe Kandemir, Esin Karakilic Ozturan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 1
In response to: “Letter to: Endocrinological Approach to Adolescents with Gender Dysphoria: Experience of a Pediatric Endocrinology Department in a Tertiary Center in Turkey”
2023 · Esin Karakılıç Özturan, Ayşe Pınar Öztürk, et al. · Journal of Clinical Research in Pediatric Endocrinology · 1
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COMPARISON OF SINGLE DOSE AND MULTI-DOSE hCG STIMULATION TESTS
2022 · Aslı Kardelen Al, Esin Karakılıç Özturan, et al. · Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi · 1
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Cranial MRI abnormalities and long-term follow-up of the lesions in 770 girls with central precocious puberty
2021 · Helvacıoğlu D, Demircioğlu Turan S, et al. · Yearbook of pediatric endocrinology · 1
Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype
2018 · Aslı Derya Kardelen, Feyza Darendelıler, et al. · 57th Annual ESPE · 1
Thyroid
2026 · Trotsenburg Paul van, Esin Karakılıc, et al. · Yearbook of pediatric endocrinology
Works count: 60
Citation count: 137
H-index: 7
I10-index: 4
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