Gönül Öçal

2.1k total citations
102 papers, 1.2k citations indexed

About

Gönül Öçal is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Gönül Öçal has authored 102 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Endocrinology, Diabetes and Metabolism, 34 papers in Molecular Biology and 30 papers in Genetics. Recurrent topics in Gönül Öçal's work include Sexual Differentiation and Disorders (25 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Gönül Öçal is often cited by papers focused on Sexual Differentiation and Disorders (25 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (13 papers). Gönül Öçal collaborates with scholars based in Türkiye, France and United States. Gönül Öçal's co-authors include Merih Berberoğlu, Zeynep Şıklar, Pelin Adıyaman, Zehra Aycan, Olcay Evliyaoğlu, Şenay Savaş Erdeve, Bülent Hacıhamdioğlu, Ayça Törel Ergür, Ergün Çetinkaya and Nejat Akar and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Fertility and Sterility and Archives of Disease in Childhood.

In The Last Decade

Gönül Öçal

99 papers receiving 1.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Gönül Öçal	483	468	397	158	153	102	1.2k
Zeynep Şıklar	432 0.9×	404 0.9×	389 1.0×	163 1.0×	218 1.4×	140	1.4k
Teoman Akçay	383 0.8×	417 0.9×	315 0.8×	77 0.5×	228 1.5×	42	1.1k
Merih Berberoğlu	717 1.5×	726 1.6×	579 1.5×	211 1.3×	347 2.3×	173	2.0k
Maria G. Vogiatzi	500 1.0×	648 1.4×	220 0.6×	321 2.0×	178 1.2×	54	2.1k
Norbert Albers	217 0.4×	468 1.0×	251 0.6×	133 0.8×	145 0.9×	38	1.1k
B Boscherini	779 1.6×	659 1.4×	460 1.2×	193 1.2×	266 1.7×	87	1.6k
Chunxiu Gong	408 0.8×	269 0.6×	353 0.9×	107 0.7×	240 1.6×	123	961
Laura Audí	412 0.9×	702 1.5×	533 1.3×	117 0.7×	78 0.5×	54	1.2k
Gi Baroncelli	506 1.0×	351 0.8×	299 0.8×	149 0.9×	110 0.7×	53	1.2k
Kathleen Laborde	868 1.8×	590 1.3×	186 0.5×	203 1.3×	416 2.7×	55	1.8k

Countries citing papers authored by Gönül Öçal

Since Specialization

Citations

This map shows the geographic impact of Gönül Öçal'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 Gönül Öçal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gönül Öçal more than expected).

Fields of papers citing papers by Gönül Öçal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gönül Öçal. 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 Gönül Öçal. The network helps show where Gönül Öçal may publish in the future.

Co-authorship network of co-authors of Gönül Öçal

This figure shows the co-authorship network connecting the top 25 collaborators of Gönül Öçal. A scholar is included among the top collaborators of Gönül Öçal 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 Gönül Öçal. Gönül Öçal 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

Öçal, Gönül, Merih Berberoğlu, Zeynep Şıklar, et al.. (2012). The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromosome DSD?. European Journal of Pediatrics. 171(10). 1497–1502. 18 indexed citations

Şıklar, Zeynep, Merih Berberoğlu, Şenay Savaş Erdeve, et al.. (2011). Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents. Journal of Pediatric Endocrinology and Metabolism. 24(1-2). 21–4. 10 indexed citations

Erdeve, Şenay Savaş, Gönül Öçal, Merih Berberoğlu, et al.. (2011). The endocrine spectrum of intracranial cysts in childhood and review of the literature. Journal of Pediatric Endocrinology and Metabolism. 24(11-12). 867–75. 13 indexed citations

Erdeve, Şenay Savaş, Merih Berberoğlu, Zeynep Şıklar, et al.. (2011). Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation. Journal of Pediatric Endocrinology and Metabolism. 24(9-10). 853–5. 8 indexed citations

Berberoğlu, Merih, Begüm Atasay, Zeynep Şıklar, et al.. (2009). Vitamin D Deficiency in Turkish Mothers and Their Neonates and in Women of Reproductive Age. Journal of Clinical Research in Pediatric Endocrinology. 1(6). 266–269. 62 indexed citations

Şıklar, Zeynep, et al.. (2008). Cytokines as a Common Components of Two Different Disorders: Metabolic Syndrome and Hemophagocytic Lymphohystiositosis. Experimental and Clinical Endocrinology & Diabetes. 117(2). 57–59. 2 indexed citations

Berberoğlu, Merih, Zeynep Şıklar, Feyza Darendelıler, et al.. (2008). Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study. Journal of Clinical Research in Pediatric Endocrinology. 1(1). 30–37. 11 indexed citations

Sadeghi, Fatemeh, Merih Berberoğlu, Zehra Aycan, et al.. (2008). Identification of Frequency and Distribution of the Nine Most Frequent Mutations among Patients with 21-Hydroxylase Deficiency in Turkey. Journal of Pediatric Endocrinology and Metabolism. 21(8). 781–7. 25 indexed citations

Şıklar, Zeynep, Gönül Öçal, Pelin Adıyaman, Ayça Törel Ergür, & Merih Berberoğlu. (2007). Functional Ovarian Hyperandrogenism and Polycystic Ovary Syndrome in Prepubertal Girls with Obesity and/or Premature Pubarche. Journal of Pediatric Endocrinology and Metabolism. 20(4). 475–81. 12 indexed citations

10.

Kuloğlu, Zarife, Aydan Kansu, Merih Berberoğlu, et al.. (2007). The Incidence and Evolution of Thyroid Dysfunction During Interferon-α Therapy in Children with Chronic Hepatitis Β Infection. Journal of Pediatric Endocrinology and Metabolism. 20(2). 237–45. 7 indexed citations

11.

Öçal, Gönül, et al.. (2007). Efficacy of levamisole on experimental endometriosis. International Journal of Gynecology & Obstetrics. 99(1). 38–42. 12 indexed citations

12.

Uslu, Runa, Didem Behice Öztop, Özlem Özcan, et al.. (2007). Factors Contributing to Sex Assignment and Reassignment Decisions in Turkish Children with 46,XY Disorders of Sex Development. Journal of Pediatric Endocrinology and Metabolism. 20(9). 1001–15. 10 indexed citations

13.

Evliyaoğlu, Olcay, Merih Berberoğlu, Pelin Adıyaman, et al.. (2006). Incidence of Iodine Deficiency in Patients Presenting with Goitre - Discrepancy Between Clinical and Ultrasonographic Evaluation of the Thyroid: Comparison of Patients With and Without Autoimmune Thyroiditis - Clinical, Hormonal and Urinary Iodine Excretion Studies. Journal of Pediatric Endocrinology and Metabolism. 19(1). 39–44. 4 indexed citations

14.

Berberoğlu, Merih, Olcay Evliyaoğlu, Pelin Adıyaman, et al.. (2006). Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphism (-675 4G/SG) Associated with Obesity and Vascular Risk in Children. Journal of Pediatric Endocrinology and Metabolism. 19(5). 741–8. 27 indexed citations

15.

Fítöz, Suat, Çetin Atasoy, Pelin Adıyaman, et al.. (2006). Testicular adrenal rests in a patient with congenital adrenal hyperplasia: US and MRI features. Computerized Medical Imaging and Graphics. 30(8). 465–468. 13 indexed citations

16.

Adıyaman, Pelin, Merih Berberoğlu, Zehra Aycan, Olcay Evliyaoğlu, & Gönül Öçal. (2004). Seckel-like Syndrome: A Patient with Precocious Puberty Associated with Nonclassical Congenital Adrenal Hyperplasia. Journal of Pediatric Endocrinology and Metabolism. 17(1). 105–10. 8 indexed citations

17.

Öçal, Gönül, Pelin Adıyaman, Merih Berberoğlu, et al.. (2002). Mutations of the 5α-Steroid Reductase Type 2 Gene in Six Turkish Patients from Unrelated Families and a Large Pedigree of an Isolated Turkish Village. Journal of Pediatric Endocrinology and Metabolism. 15(4). 411–21. 28 indexed citations

18.

Çetinkaya, Şerife Esra, Gönül Öçal, Merih Berberoğlu, et al.. (2001). Association of Partial Gonadal Dysgenesis, Nephropathy and WT1 Gene Mutation Without Wilms' Tumor: Incomplete Denys-Drash Syndrome. Journal of Pediatric Endocrinology and Metabolism. 14(5). 561–4. 3 indexed citations

19.

Arcasoy, Ayten, Gönül Öçal, Sabri Kemahlı, et al.. (1999). Recombinant human growth hormone treatment in children with thalassemia major. Pediatrics International. 41(6). 655–661. 12 indexed citations

20.

Gözdaşoğlu, Sevgi, et al.. (1995). Late Effects of Chemoradiotherapy in Pediatric Hodgkin’s Disease. Journal of Chemotherapy. 7(5). 463–466. 8 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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