Atilla Çayır

909 total citations
64 papers, 408 citations indexed

About

Atilla Çayır is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Atilla Çayır has authored 64 papers receiving a total of 408 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Pediatrics, Perinatology and Child Health and 11 papers in Surgery. Recurrent topics in Atilla Çayır's work include Thyroid Disorders and Treatments (6 papers), Sexual Differentiation and Disorders (4 papers) and Pharmacological Effects and Toxicity Studies (4 papers). Atilla Çayır is often cited by papers focused on Thyroid Disorders and Treatments (6 papers), Sexual Differentiation and Disorders (4 papers) and Pharmacological Effects and Toxicity Studies (4 papers). Atilla Çayır collaborates with scholars based in Türkiye, United Kingdom and United States. Atilla Çayır's co-authors include Mehmet İbrahim Turan, Behzat Özkan, Yasemin Çayır, Nezahat Kurt, Hüseyin Tan, Avni Kaya, Abdülkadir Yıldırım, Zerrin Orbak, Hakan Döneray and Erdal Kurnaz and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and PEDIATRICS.

In The Last Decade

Atilla Çayır

55 papers receiving 394 citations

Peers

Atilla Çayır

PFM

PPCH

EDM

Ramis Çolak Türkiye

Jovana Kaludjerovic Canada

Rebecca D. Murray United States

Matilde Calanchini Italy

Anna Capozzi Italy

James Woods United States

Kanako Ogura Japan

Lara K Park United States

E Kauf Germany

Kyung Hoon Paik South Korea

Ramis Çolak Türkiye

Atilla Çayır

61 ×0.6

89 ×1.2

56 ×0.8

PFM

37 ×0.6

PPCH

156 ×2.7

EDM

Citations per year, relative to Atilla Çayır Atilla Çayır (= 1×) peers Ramis Çolak

Countries citing papers authored by Atilla Çayır

Since Specialization

Citations

This map shows the geographic impact of Atilla Çayır's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Atilla Çayır with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Atilla Çayır more than expected).

Fields of papers citing papers by Atilla Çayır

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Atilla Çayır. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Atilla Çayır. The network helps show where Atilla Çayır may publish in the future.

Co-authorship network of co-authors of Atilla Çayır

This figure shows the co-authorship network connecting the top 25 collaborators of Atilla Çayır. A scholar is included among the top collaborators of Atilla Çayır based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Atilla Çayır. Atilla Çayır is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ünal, Edip, Atilla Çayır, Esra Deniz Papatya Çakır, et al.. (2025). Phenotypes Linked to Duplication Upstream of SOX9: New Insights Into Presentation and Diagnosis. The Journal of Clinical Endocrinology & Metabolism. 110(10). e3482–e3488. 1 indexed citations

Kurnaz, Erdal, et al.. (2024). Genetic Analyses in a Cohort of Pediatric Patients with Congenital Hypothyroidism Based on Congenital Hypothyroidism Consensus Guideline. Hormone Research in Paediatrics. 99(1). 23–37.

Çelik, Nurullah, Korcan Demir, Bumin Nuri Dündar, et al.. (2024). Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre retrospective study. European Journal of Pediatrics. 184(1). 92–92.

Dursun, Fatma, İhsan Turan, Elvan Bayramoğlu, et al.. (2024). Natural history of ENPP1 deficiency: Nationwide Turkish Cohort Study of autosomal‐recessive hypophosphataemic rickets type 2. Clinical Endocrinology. 101(5). 475–484. 3 indexed citations

Şimşek, Enver, et al.. (2024). Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2. Molecular Syndromology. 16(1). 1–10. 1 indexed citations

Yıldırım, Ruken, et al.. (2022). The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey. Endocrine. 79(2). 376–383.

Gürbüz, Taşkın, et al.. (2022). Relationship between the TAS2R38 and TAS1R2 polymorphisms and the dental status in obese children. Dental and Medical Problems. 59(2). 233–240. 4 indexed citations

Çayır, Atilla, et al.. (2022). BİR BÖLGE EĞİTİM VE ARAŞTIRMA HASTANESİ’NE BAŞVURAN ÇOCUKLARDA AŞIYLA ÖNLENEBİLİR HASTALIKLARIN SEROPREVALANSLARININ DEĞERLENDİRİLMESİ. Kırıkkale Üniversitesi Tıp Fakültesi Dergisi. 24(2). 218–224.

Çayır, Atilla, et al.. (2022). A rare cause of primary amenorrhea: LHCGR gene mutations. European Journal of Obstetrics & Gynecology and Reproductive Biology. 272. 193–197. 3 indexed citations

10.

Mutlu, Gül Yeşiltepe, Belma Haliloğlu, Heves Kırmızıbekmez, et al.. (2022). The effects of the covid-19 pandemic on puberty: a cross-sectional, multicenter study from Turkey. The Italian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 144–144. 17 indexed citations

11.

Çayır, Atilla, et al.. (2021). The Relationship between Psychopathology, Self-esteem, Body Perception and Serum Sex Steroids in Pubertal Gynecomastia. Clinical Psychopharmacology and Neuroscience. 19(3). 498–506. 5 indexed citations

12.

Kurnaz, Erdal, et al.. (2021). First Report of a de novo 10q23.31q23.33 Microdeletion: Obesity, Intellectual Disability and Microcephaly. Molecular Syndromology. 12(4). 258–262. 1 indexed citations

13.

Kurnaz, Erdal, Zehra Yavaş Abalı, Serap Turan, et al.. (2020). Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency. Hormone Research in Paediatrics. 93(9-10). 558–566. 11 indexed citations

14.

Demirbilek, Hüseyin, Atilla Çayır, Doğuş Vurallı, et al.. (2020). Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis. Journal of Clinical Research in Pediatric Endocrinology. 13(1). 34–43. 2 indexed citations

15.

Akıncı, Ayşehan, Doğa Türkkahraman, İbrahim Tekedereli, et al.. (2019). Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study. Journal of Clinical Research in Pediatric Endocrinology. 11(4). 341–349. 22 indexed citations

16.

Demir, Korcan, Hakan Döneray, Cengiz Kara, et al.. (2019). Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children. Journal of Clinical Research in Pediatric Endocrinology. 11(2). 140–148. 9 indexed citations

17.

Çayır, Atilla, et al.. (2019). Systemic Pseudohypoaldosteronism Type 1 due to 3 Novel Mutations in SCNN1Aand SCNN1BGenes. Hormone Research in Paediatrics. 91(3). 175–185. 8 indexed citations

18.

Çayır, Atilla, et al.. (2018). Is growth hormone deficiency associated with anxiety disorder and depressive symptoms in children and adolescents?: A case-control study. Growth Hormone & IGF Research. 41. 23–27. 12 indexed citations

19.

Kara, Soner Sertan, et al.. (2016). An Unusual Congenital Anomaly in Fanconi Aplastic Anemia: Congenital Lobar Emphysema. Turkish Journal of Hematology. 33(3). 263–264. 2 indexed citations

20.

Çayır, Yasemin, et al.. (2012). Çocukluk Çağı Karın Ağrıları: Prospektif Bir Çalışma. Çocuk Dergisi / Journal of Child. 12(2). 78–82.

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