Özge Besci
Biochemistry, Genetics and Molecular Biology · University of Michigan
Publications
38
Citations
220
Est. group size
~7
Recurring co-author estimate
Active years
6
Publishing since 2020
Typically publishes in teams of ~8 · 3% small-team papers (≤3 authors) · across 18 venues
- Advances of pharmacological therapies in lipodystrophy syndromes: current evidence and future directions
Expert Review of Endocrinology & Metabolism · 2025
- Potential Impact of Parental Origin of Inheritance on the Clinical Presentation of Familial Partial Lipodystrophy Type 2 Syndrome
Clinical Endocrinology · 2025
- No Regression With Imatinib Treatment for Craniofacial Fibrous Dysplasia Associated With McCune-Albright Syndrome
Journal of Pediatric Hematology/Oncology · 2025
- Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppression
Journal of Pediatric Endocrinology and Metabolism · 2025
- SUN-202 Nerve Conduction Studies May Predict the Natural Course of Mild Subclinical Hypothyroidism in Children
Journal of the Endocrine Society · 2025
- SUN-646 Immune Landscape and Clinical Characteristics of Patients with Acquired Partial and Generalized Lipodystrophy Syndromes
Journal of the Endocrine Society · 2025
- SUN-642 Mortality Outcomes in Patients with Lipodystrophy: Key Insights from the LD-Lync Study
Journal of the Endocrine Society · 2025
- MON-571 Unusual presentation of mitochondrial disease with diabetes, lipomatosis, and metabolic dyslipidemia: clinical lessons to recognize phenotype for the endocrinologist
Journal of the Endocrine Society · 2025
- SUN-645 Leptin- And Incretin-based Combination Therapy In Lipodystrophy: A Promising Metabolic Strategy?
Journal of the Endocrine Society · 2025
- High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transients
Journal of Endocrinological Investigation · 2024
- Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach
Journal of Clinical Research in Pediatric Endocrinology · 2024
- 6889 Potential Impact of Parental Origin of Inheritance in Presentation of Familial Partial Lipodystrophy
Journal of the Endocrine Society · 2024
- Deciphering the Clinical Presentations in LMNA-related Lipodystrophy: Report of 115 Cases and a Systematic Review
The Journal of Clinical Endocrinology & Metabolism · 2023
- A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review
The Journal of Clinical Endocrinology & Metabolism · 2023
- A Very-Low-Calorie Diet Can Cause Remission of Diabetes Mellitus and Hypertriglyceridemia in Familial Partial Lipodystrophy
Obesity Facts · 2023
- Journal of Clinical Research in Pediatric Endocrinology×6
- Journal of the Endocrine Society×6
- Journal of Pediatric Endocrinology and Metabolism×5
- The Journal of Clinical Endocrinology & Metabolism×2
- Journal of Endocrinological Investigation×2
- Ümit Çavdar
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Barış Akıncı
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Donatella Gilio
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Elif A Oral
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Maria Cristina Foss‐Freitas
Biochemistry, Genetics and Molecular Biology · University of Michigan
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 25, 2026.
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