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Sare Betül Kaygusuz

Observed names: Betul Sare Kaygusuz, KAYGUSUZ, SARE BETÜL, Kaygusuz SB, Kaygusuz Sare Betul, Kaygusuz, Sare Betul, Kaygusuz, Sare Betül, S.B., Kaygusuz, Sare Betul Kaygusuz, Sare Betul Kaygusuz, Sare Kaygusuz, Sare Betul Kaygusuz
ORCID: 0000-0001-8457-8042
Observed ORCID: 0000-0001-8457-8042
OpenAlex ID: A5013656817
Does Genotype–Phenotype Correlation Exist in Vitamin D-Dependent Rickets Type IA: Report of 13 New Cases and Review of the Literature
2021 · Sare Betul Kaygusuz, Ceren Alavanda, et al. · Calcified Tissue International · 34
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
2024 · Zeynep Siklar, Emine Camtosun, et al. · Endocrine · 26
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A Rare Cause of Hypophosphatemia: Raine Syndrome Changing Clinical Features with Age
2020 · Mehmet Eltan, Ceren Alavanda, et al. · Calcified Tissue International · 19
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Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects
2021 · Sare Betul Kaygusuz, Esra Arslan Ates, et al. · The Journal of Clinical Endocrinology & Metabolism · 15
Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency
2021 · Busra Gurpinar Tosun, Yasemin Kendir Demirkol, et al. · The Journal of Clinical Endocrinology & Metabolism · 12
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Low DHEAS Concentration in a Girl Presenting with Short Stature and Premature Pubarche: A Novel PAPSS2 Gene Mutation
2019 · Mehmet Eltan, Zehra Yavas Abali, et al. · Hormone Research in Paediatrics · 12
Adrenocortical carcinoma in atypical Beckwith‐Wiedemann syndrome due to loss of methylation at imprinting control region 2
2019 · Mehmet Eltan, Esra Arslan Ates, et al. · Pediatric Blood & Cancer · 11
Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity
2022 · Serap Turan, Steven Mumm, et al. · JBMR Plus · 10
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Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature
2019 · Zehra Yavas Abali, Gozde Yesil, et al. · HORMONES · 10
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
2023 · Tarık Kırkgöz, Sare Betül Kaygusuz, et al. · Journal of Pediatric Endocrinology and Metabolism · 7
Efficacy of the Novel Degludec/Aspart Insulin Co-formulation in Children and Adolescents with Type 1 Diabetes: A Real-life Experience with One Year of IDegAsp Therapy in Poorly Controlled and Non-compliant Patients
2021 · Tarık Kırkgöz, Mehmet Eltan, et al. · Journal of Clinical Research in Pediatric Endocrinology · 7
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Total oxidant and antioxidant status and paraoxonase 1 levels of children with noncystic fibrosis bronchiectasis
2019 · GEDİK, AHMET HAKAN, ÇAKIR, ERKAN, et al. · TURKISH JOURNAL OF MEDICAL SCIENCES · 5
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Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia
2024 · Mehmet Eltan, Ceren Alavanda, et al. · The Journal of Clinical Endocrinology & Metabolism · 4
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature
2023 · Tarik Kirkgoz, Saygin Abali, et al. · Hormone Research in Paediatrics · 3
Adrenal androgens as predictors of growth characteristics in premature pubarche
2026 · Mehmet Eltan, Zehra Yavas Abali, et al. · European Journal of Endocrinology · 2
Genotype, phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type IA (VDDR1A): A nationwide multi-centre retrospective cross-sectional study
2025 · Atilla Cayir, Huseyin Demirbilek, et al. · Hormone Research in Paediatrics · 2
Dysgenesis and Dysfunction of the Pancreas and Pituitary Due to FOXA2 Gene Defects
2022 · Kaygusuz SB, E Arslan Ates, et al. · Yearbook of pediatric endocrinology · 1
An 18 Month Old Boy with Hypoglycemic Convulsion and Obesity Due to POMC Deficiency
2018 · Kaygusuz Sare Betul, Gözde Yeşil, et al. · Dspace Repository (Marmara Üniversitesi) · 1
Rare SERPINH1 and SERPINF1 variants in autosomal recessive osteogenesis imperfecta type X and type VI
2026 · Fan Wang, Alice Costantini, et al. · European Journal of Medical Genetics
Anti-Müllerian hormone levels in girls with precocious puberty
2026 · Merve Nur Hepokur, Aşan Önder Çamaş, et al. · Journal of Pediatric Endocrinology and Metabolism
Off-Label Use of Teriparatide for Osteotomy Healing in an Adolescent with Osteogenesis Imperfecta Type VIII: A Case Report
2026 · Aylin Günay, Sare Betül Kaygusuz, et al. · Journal of Clinical Research in Pediatric Endocrinology
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A diagnosis of MODY 2 following MIS-C
2025 · Sare Kaygusuz, Fuat Bugrul, et al. · Endocrine Abstracts
Supplementary Material for: Challenges in the management of a 7 years old child with thyrotropin-secreting pituitary adenoma and the review of the literature
2023 · T., Kirkgöz, S., Abali, et al. · Figshare
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C
2022 · Cicek D, Warr N, et al. · Yearbook of pediatric endocrinology
Genotype, phenotype characteristics and long-term follow-up of patients with Vitamin D Dependent Rickets Type IA (VDDR1a): A nationwide multicentre retrospective cross-sectional study
2022 · EREN, ERDAL, ŞAHİN, KADRİYE CANSU, et al. · Bursa Uludag University - AVESIS
Works count: 54
Citation count: 181
H-index: 9
I10-index: 9
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