Gönül Çatlı - Publications, H-index & Citations

Gönül Çatlı

dokuz eylul university

25H指数

184论文数

2.3K被引数

收录论文 23

发表时间

Could the Use of Pacifiers in Infancy Be Associated with Binge Eating Disorder and Obesity in Adolescents?婴儿期使用安抚奶嘴是否与青少年暴食症和肥胖相关？

JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN

IF0.8

2025-12-01

PREAI

Filibeli, Berna Eroglu; Tuncerler, Gulten; Ozyurt, Gonca; Dundar, Bumin; Catli, Gonul

Androgen receptor CAG repeat polymorphism might be a possible cause of familial constitutional delay of growth and puberty

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

IF3.5

2024-11-21

PREAI

Kagizmanli, Gozde Akin; Sevim, Reyhan Deveci; Manyas, Hayrullah; Paketci, Ahu; Demir, Korcan; Bober, Ece; Catli, Gonul; Anik, Ahmet; Abaci, Ayhan

Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study

CLINICAL ENDOCRINOLOGY

IF2.4

2023-10-10

PREAI

Tarcin, Gurkan; Catli, Gonul; Cetinkaya, Semra; Eren, Erdal; Kardelen, Asli Derya; Akinci, Aysehan; Bober, Ece; Kara, Cengiz; Yildirim, Ruken; Er, Eren; Polat, Recep; Ozhan, Bayram; Yildiz, Melek; Kor, Yilmaz; Evliyaoglu, Olcay; Dundar, Bumin; Ercan, Oya

POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-08-01

OAAI

Cho, Hyun-Ju; Gurbuz, Fatih; Stamou, Maria; Kotan, Leman Damla; Farmer, Stephen Matthew; Can, Sule; Tompkins, Miranda Faith; Mammadova, Jamala; Altincik, S. Ayca; Gokce, Cumali; Catli, Gonul; Bugrul, Fuat; Bartlett, Keenan; Turan, Ihsan; Balasubramanian, Ravikumar; Yuksel, Bilgin; Seminara, Stephanie B.; Wray, Susan; Topaloglu, A. Kemal

Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant

MOLECULAR AND CELLULAR ENDOCRINOLOGY

IF3.6

2023-01-01

OAAI

Catli, Gonul; Gao, Wen; Foley, Corinne; Ozyilmaz, Berk; Edeer, Neslihan; Diniz, Gulden; Losekoot, Monique; van Doorn, Jaap; Dauber, Andrew; Dundar, Bumin N.; Wit, Jan M.; Hwa, Vivian

Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics

DIABETOLOGIA

IF10.2

2021-10-23

OAAI

Patel, Kashyap A.; Ozbek, Mehmet N.; Yildiz, Melek; Guran, Tulay; Kocyigit, Cemil; Acar, Sezer; Siklar, Zeynep; Atar, Muge; Colclough, Kevin; Houghton, Jayne; Johnson, Matthew B.; Ellard, Sian; Flanagan, Sarah E.; Cizmecioglu, Filiz; Berberoglu, Merih; Demir, Korcan; Catli, Gonul; Bas, Serpil; Akcay, Teoman; Demirbilek, Huseyin; Weedon, Michael N.; Hattersley, Andrew T.

Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2021-04-08

OAAI

Yildiz, Melek; Isik, Emregul; Abali, Zehra Yavas; Keskin, Mehmet; Ozbek, Mehmet Nuri; Bas, Firdevs; Ucakturk, Seyit Ahmet; Buyukinan, Muammer; Onal, Hasan; Kara, Cengiz; Storbeck, Karl-Heinz; Darendeliler, Feyza; Cayir, Atilla; Unal, Edip; Anik, Ahmet; Demirbilek, Huseyin; Cetin, Tugba; Dursun, Fatma; Catli, Gonul; Turan, Serap; Falhammar, Henrik; Baris, Tugba; Yaman, Ali; Haklar, Goncagul; Bereket, Abdullah; Guran, Tulay

Comparison of the effectiveness of simple carbohydrates on hypoglycemic episodes in children and adolescents with type 1 diabetes mellitus: A randomized study in a diabetes camp

PEDIATRIC DIABETES

IF5.6

2020-08-09

OAAI

Erbas, Ibrahim Mert; Abaci, Ayhan; Anik, Ahmet; Simsek, Erdem; Tuhan, Hale Unver; Kocyigit, Cemil; Yildiz, Melek; Dundar, Bumin Nuri; Bober, Ece; Catli, Gonul

Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2020-01-17

OAAI

Guran, Tulay; Kara, Cengiz; Yildiz, Melek; Bitkin, Eda C.; Haklar, Goncagul; Lin, Jen-Chieh; Keskin, Mehmet; Barnard, Lise; Anik, Ahmet; Catli, Gonul; Guven, Ayla; Kirel, Birgul; Tutunculer, Filiz; Onal, Hasan; Turan, Serap; Akcay, Teoman; Atay, Zeynep; Yilmaz, Gulay C.; Mamadova, Jamala; Akbarzade, Azad; Sirikci, Onder; Storbeck, Karl-Heinz; Baris, Tugba; Chung, Bon-Chu; Bereket, Abdullah

NOVEL VDR MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATION

ENDOCRINE PRACTICE

IF4.6

2020-01-01

OAAI

Demir, Korcan; Zou, Minjing; Al-Rijjal, Roua A.; BinEssa, Huda; Acar, Sezer; Durmaz, Erdem; Catl, Gonul; Al-Enezi, Anwar F.; Alzahrani, Ali S.; Meyer, Brian F.; Shi, Yufei

Social cognition and emotion regulation may be impaired in adolescents with obesity independent of the presence of binge eating disorder: a two-center study

PSYCHIATRY AND CLINICAL PSYCHOPHARMACOLOGY

IF0.6

2019-11-28

OAAI

Turan, Serkan; Ozyurt, Gonca; Catli, Gonul; Ozturk, Yesim; Abaci, Ayhan; Akay, Aynur Pekcanlar

A Novel Homozygous Selenocysteine Insertion Sequence Binding Protein 2 (SECISBP2, SBP2) Gene Mutation in a Turkish Boy

THYROID

IF6.7

2018-09-01

OAAI

Catli, Goenuel; Fujisawa, Haruki; Kirbiyik, Ozgur; Mimoto, Mizuho S.; Gencpinar, Pinar; Ozdemir, Taha Resid; Dundar, Bumin Nuri; Dumitrescu, Alexandra M.

Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from Turkey

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

IF3.5

2018-08-21

PREAI

Abaci, A.; Catli, G.; Kirbiyik, O.; Sahin, N. M.; Abali, Z. Y.; Unal, E.; Siklar, Z.; Mengen, E.; Ozen, S.; Guran, T.; Kara, C.; Yildiz, M.; Eren, E.; Nalbantoglu, O.; Guven, A.; Cayir, A.; Akbas, E. D.; Kor, Y.; Curek, Y.; Aycan, Z.; Bas, F.; Darcan, S.; Berberoglu, M.

Brain injury markers: S100 calcium-binding protein B, neuron-specific enolase and glial fibrillary acidic protein in children with diabetic ketoacidosis 脑损伤标志物: 糖尿病酮症酸中毒患儿的S100钙结合蛋白B，神经元特异性烯醇化酶和神经胶质纤维酸性蛋白

PEDIATRIC DIABETES

IF5.6

2018-03-13

OAAI

Catli, Goenuel; Anik, Ahmet; Acar, Sezer; Kume, Tuncay; Karabulut, Melike; Calan, Ozlem Gursoy; Dundar, Bumin Nuri; Abaci, Ayhan

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2016-08-01

OAAI

Demir, Korcan; van Gucht, Anja L. M.; Buyukinan, Muammer; Catli, Goenuel; Ayhan, Yavuz; Bas, Veysel Nijat; Dundar, Bumin; Ozkan, Behzat; Meima, Marcel E.; Visser, W. Edward; Peeters, Robin P.; Visser, Theo J.

Circulating betatrophin concentration is negatively correlated with insulin resistance in obese children and adolescents 肥胖儿童和青少年的循环betatrophin浓度与胰岛素抵抗呈负相关

DIABETES RESEARCH AND CLINICAL PRACTICE

IF7.4

2016-04-01

PREAI

Tuhan, Hale; Abaci, Ayhan; Anik, Ahmet; Catli, Gonul; Kume, Tuncay; Calan, Ozlem Gursoy; Acar, Sezer; Bober, Ece

Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

IF5.1

2016-01-01

128

OAAI

Guran, Tulay; Buonocore, Federica; Saka, Nurcin; Ozbek, Mehmet Nuri; Aycan, Zehra; Bereket, Abdullah; Bas, Firdevs; Darcan, Sukran; Bideci, Aysun; Guven, Ayla; Demir, Korcan; Akinci, Aysehan; Buyukinan, Muammer; Aydin, Banu Kucukemre; Turan, Serap; Agladioglu, Sebahat Yilmaz; Atay, Zeynep; Abali, Zehra Yavas; Tarim, Omer; Catli, Gonul; Yuksel, Bilgin; Akcay, Teoman; Yildiz, Metin; Ozen, Samim; Doger, Esra; Demirbilek, Huseyin; Ucar, Ahmet; Isik, Emregul; Ozhan, Bayram; Bolu, Semih; Ozgen, Ilker Tolga; Suntharalingham, Jenifer P.; Achermann, John C.

Serum nesfatin-1 and leptin levels in non-obese girls with premature thelarche

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

IF3.5

2015-04-02

PREAI

Catli, G.; Anik, A.; Kume, T.; Calan, O. G.; Dundar, B. N.; Bober, E.; Abaci, A.

A novel missense mutation in HSD17B3 gene in a 46, XY adolescent presenting with primary amenorrhea and virilization at puberty

CLINICA CHIMICA ACTA

IF2.9

2015-01-01

PREAI

Tuhan, Hale Unver; Anik, Ahmet; Catli, Gonul; Ceylaner, Serdar; Dundar, Bumin; Bober, Ece; Abaci, Ayhan