Prof. Dr. Esra Deniz PAPATYA ÇAKIR

1. Clinical Significance of Carotid Artery Intima-Media Thickness in Childhood Obesity Obezite Hastalığı ile Takipli Olan Hastalardaki İnternal Karotis Arterin İntima Kalınlığının Takip Açısından Önemi

Menentoğlu M. E., Akyol B., PALABIYIK F., Menentoğlu B., HATİPOĞLU S. S., PAPATYA ÇAKIR E. D., et al.

Medical Journal of Bakirkoy , cilt.22, sa.2, ss.142-146, 2026 (ESCI, Scopus, TRDizin)

2. Rare in Rare: Overlapping Clinical Features in a Patient With Both Gaucher Disease Type 1 and B4GALT-CDG: Expanding the Clinical Spectrum With a Novel Pathogenic Variant

Ersoy M., Bitkin E. Ç., PAPATYA ÇAKIR E. D., Erdin S., Onay H.

Clinical Genetics , cilt.109, sa.4, ss.811-812, 2026 (SCI-Expanded, Scopus)

3. Dual molecular genetic diagnosis with combined malonic and methylmalonic aciduria (CMAMMA): implications of coexisting genetic disorders on clinical presentation

Ersoy M., Abali Z. Y., PAPATYA ÇAKIR E. D., Erdin S., Yararbas K., ABALI S.

Journal of Pediatric Endocrinology and Metabolism , cilt.38, sa.12, ss.1340-1349, 2025 (SCI-Expanded, Scopus)

4. Endocrine Disorders in Children with Primary Mitochondrial Diseases: Single Center Experience

PAPATYA ÇAKIR E. D., Ersoy M., Çakır Biçer N., GEDİKBAŞI A.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.17, sa.1, ss.34-45, 2025 (SCI-Expanded, Scopus, TRDizin)

5. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

ŞIKLAR Z., ÇAMTOSUN E., Bolu S., Yildiz M., Akinci A., BAŞ F., et al.

Endocrine , cilt.85, sa.3, ss.1407-1416, 2024 (SCI-Expanded, Scopus)

6. In Response to: “Involvement of the Endocrine System is Common in Mitochondrial Disorders and Requires Long-term Comprehensive Investigations”

PAPATYA ÇAKIR E. D., Ersoy M., Çakır Biçer N., GEDİKBAŞI A.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.16, sa.4, ss.516-518, 2024 (SCI-Expanded, Scopus, TRDizin)

7. Evaluation of the impact of childhood obesity on retrobulbar hemodynamics and retinal microvasculature

ÇELİK G., GÜNAY M., Ozcabi B., Gulturk U., KIZILAY O., VURAL A., et al.

European Journal of Ophthalmology , cilt.32, sa.6, ss.3556-3563, 2022 (SCI-Expanded, Scopus)

8. The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

Borman P., Balcan A., Eyigör S., COŞKUN E., Ayhan F., DUYUR ÇAKIT B., et al.

Turkish Journal of Medical Sciences , cilt.52, sa.4, ss.1139-1147, 2022 (SCI-Expanded, Scopus, TRDizin)

9. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

KOTAN L. D., Ternier G., Cakir A. D., Emeksiz H. C., TURAN İ., Delpouve G., et al.

Genetics in Medicine , cilt.23, sa.6, ss.1008-1016, 2021 (SCI-Expanded, Scopus)

10. Evaluation of normal thyroid tissue and autoimmune thyroiditis in children using shear wave elastography

PALABIYIK F., İnci E., PAPATYA ÇAKIR E. D., HOCAOĞLU E.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.11, sa.2, ss.132-139, 2019 (SCI-Expanded, Scopus, TRDizin)

11. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

Sari E., BEREKET A., Yeşilkaya E., BAŞ F., Bundak R., Aydin B. K., et al.

American Journal of Medical Genetics, Part A , cilt.170, sa.4, ss.942-948, 2016 (SCI-Expanded, Scopus)

12. Growth curves for Turkish girls with turner syndrome: Results of the Turkish turner syndrome study group

Darendeliler F., Yeşilkaya E., BEREKET A., BAŞ F., Bundak R., Sarı E., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.3, ss.183-191, 2015 (SCI-Expanded, Scopus, TRDizin)

13. Turner syndrome and associated problems in turkish children: A multicenter study

Yeşilkaya E., BEREKET A., Darendeliler F., BAŞ F., POYRAZOĞLU Ş., Aydın B. K., et al.

JCRPE Journal of Clinical Research in Pediatric Endocrinology , cilt.7, sa.1, ss.27-36, 2015 (SCI-Expanded, Scopus, TRDizin)

Prof. Dr. Esra Deniz PAPATYA ÇAKIR

Yayınlar & Eserler

1. Clinical Significance of Carotid Artery Intima-Media Thickness in Childhood Obesity Obezite Hastalığı ile Takipli Olan Hastalardaki İnternal Karotis Arterin İntima Kalınlığının Takip Açısından Önemi

2. Rare in Rare: Overlapping Clinical Features in a Patient With Both Gaucher Disease Type 1 and B4GALT-CDG: Expanding the Clinical Spectrum With a Novel Pathogenic Variant

3. Dual molecular genetic diagnosis with combined malonic and methylmalonic aciduria (CMAMMA): implications of coexisting genetic disorders on clinical presentation

4. Endocrine Disorders in Children with Primary Mitochondrial Diseases: Single Center Experience

5. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

6. In Response to: “Involvement of the Endocrine System is Common in Mitochondrial Disorders and Requires Long-term Comprehensive Investigations”

7. Evaluation of the impact of childhood obesity on retrobulbar hemodynamics and retinal microvasculature

8. The clinical and demographical characteristics of Turkish pediatric lymphedema patients: a multicenter study

9. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism

10. Evaluation of normal thyroid tissue and autoimmune thyroiditis in children using shear wave elastography

11. Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

12. Growth curves for Turkish girls with turner syndrome: Results of the Turkish turner syndrome study group

13. Turner syndrome and associated problems in turkish children: A multicenter study

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

Tez Danışmanlığı

Açık Erişim