Murat Karaoglan | Endocrinology | Best Researcher Award

Murat Karaoglan | Endocrinology | Best Researcher Award

Associate Professor at Gaziantep University, Faculty of medicine, Turkey

Dr. Murat Karaoğlan is a distinguished faculty member at Gaziantep University, specializing in Pediatric Endocrinology. With a career dedicated to advancing pediatric health, he has made significant contributions to the field through research and education. His expertise encompasses various aspects of pediatric endocrinology, including hormonal disorders and metabolic diseases. Dr. Karaoğlan is recognized for his impactful publications and active engagement in clinical practice, making him a respected figure in the medical community. His work not only enhances understanding in his specialty but also directly informs patient care and treatment strategies for children.

Publication Profile

Scopus

Educational Background

Dr. Karaoğlan completed his Bachelor’s degree in Medicine at Ege University in 1993, laying a strong foundation for his medical career. He pursued specialization in Pediatric Health and Diseases at Gaziantep University, earning his degree in 2000. Furthering his expertise, he completed a subspecialty in Pediatric Endocrinology at the same institution in 2014. This comprehensive educational journey equipped him with in-depth knowledge and skills, enabling him to excel in his field. His academic achievements reflect a commitment to lifelong learning and a passion for improving pediatric health outcomes.

Experience

Dr. Karaoğlan has extensive academic experience in the field of Pediatric Endocrinology. He served as an Assistant Professor at Gaziantep University from 2017 to 2020 and was subsequently promoted to Associate Professor in 2020. His roles have included teaching, mentoring students, and conducting research. Throughout his career, he has contributed to developing educational programs and clinical practices in pediatric endocrinology. His dedication to academic excellence and commitment to advancing the field make him a valuable asset to Gaziantep University and the broader medical community.

Research Focus

Dr. Karaoğlan’s research focuses on critical areas within Pediatric Endocrinology, including precocious puberty, hormonal deficiencies, and maturity-onset diabetes of the young (MODY). His work investigates the intrafamilial genotype-phenotype relationships associated with 21-hydroxylase deficiency, contributing to genetic understanding and management of endocrine disorders. Additionally, he explores the role of the olfactory bulb in relation to obesity and puberty, bridging neurobiology and endocrinology. Dr. Karaoğlan’s research aims to enhance clinical outcomes for children with endocrine disorders, making significant contributions to both academia and clinical practice.

Awards and honors

Dr. Karaoğlan has received recognition for his contributions to Pediatric Endocrinology through various awards and honors throughout his career. His research has been published in prestigious journals, showcasing his commitment to advancing medical knowledge and practice. He is respected for his active involvement in academic conferences and workshops, where he shares insights and collaborates with fellow researchers. His dedication to improving pediatric healthcare and his impact on the field have garnered him respect from colleagues and recognition as a leading figure in Pediatric Endocrinology.

Conclusion

Dr. Murat Karaoğlan is a highly qualified candidate for the Best Researcher Award, showcasing a robust academic background, significant contributions to pediatric endocrinology, and a strong publication record. His ongoing research addresses critical issues in child health, making a meaningful impact in his field. By fostering collaborations, seeking funding opportunities, and enhancing his presence at conferences, he can further elevate his research profile. Given his accomplishments and potential, Dr. Karaoğlan is a commendable choice for this recognition.

Publication Top Notes

Title: Genotype-biochemical phenotype analysis in newborns with biotinidase deficiency in Southeastern Anatolia
Authors: Karaoglan, M., Nacarkahya, G., Aytac, E.H., Keskin, M.
Year: 2024
Citation: Egyptian Journal of Medical Human Genetics, 25(1), 28.

Title: Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management
Authors: Arik, E., Keskin, Ö., Albayrak, S., Yildirim, A., Kucukosmanoglu, E.
Year: 2024
Citation: Journal of Pediatric Endocrinology and Metabolism, 37(10), pp. 866–874.

Title: 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
Authors: Siklar, Z., Camtosun, E., Bolu, S., Seymen, G., Berberoglu, M.
Year: 2024
Citation: Endocrine, 85(3), pp. 1407–1416.

Title: Genotype and clinical phenotype of children with Marfan syndrome in Southeastern Anatolia
Authors: Karaoglan, M., Nacarkahya, G., Aytac, E.H., Keskin, M.
Year: 2024
Citation: European Journal of Pediatrics, 183(8), pp. 3219–3232.

Title: Effect of Bisphenol-A on Thyroid Hormones and Some Biochemical Parameters in Children with Juvenile Diabetes
Authors: Diril, H., Karaoglan, M., Çimenci, İ.G., Ulusal, H.
Year: 2024
Citation: Eastern Journal of Medicine, 29(1), pp. 99–107.

Title: Short Stature due to Bioinactive Growth Hormone (Kowarski Syndrome)
Authors: Karaoglan, M.
Year: 2023
Citation: Endocrine Practice, 29(11), pp. 902–911.

Title: Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in Turkey
Authors: Kiral, E., Kirel, B., Havan, M., Simsek, E., Dinleyici, E.C.
Year: 2022
Citation: Frontiers in Pediatrics, 10, 926013.

Title: Challenges of CYP21A2 genotyping in children with 21-hydroxylase deficiency: determination of genotype–phenotype correlation using next generation sequencing in Southeastern Anatolia
Authors: Karaoğlan, M., Nacarkahya, G., Aytaç, E.H., Keskin, M.
Year: 2021
Citation: Journal of Endocrinological Investigation, 44(11), pp. 2395–2405.

Title: The role of placental iodine storage in the neonatal thyroid stimulating hormone surge: iodine as a driving force to adapt the terrestrial life
Authors: Karaoglan, M., İşbilen, E.
Year: 2021
Citation: Journal of Endocrinological Investigation, 44(5), pp. 1041–1052.

Title: Immunological interpretation of minipuberty: Minipuberty as the driving force of sexual dimorphism in the immune response
Authors: Karaoglan, M., Nacarkahya, G.
Year: 2021
Citation: Clinical Endocrinology, 94(4), pp. 575–582