Fatih Gürbüz

1.8k total citations · 1 hit paper
62 papers, 1.1k citations indexed

About

Fatih Gürbüz is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Fatih Gürbüz has authored 62 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 19 papers in Genetics and 18 papers in Reproductive Medicine. Recurrent topics in Fatih Gürbüz's work include Hypothalamic control of reproductive hormones (16 papers), Sexual Differentiation and Disorders (11 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Fatih Gürbüz is often cited by papers focused on Hypothalamic control of reproductive hormones (16 papers), Sexual Differentiation and Disorders (11 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). Fatih Gürbüz collaborates with scholars based in Türkiye, United States and United Kingdom. Fatih Gürbüz's co-authors include Bilgin Yüksel, A. Kemal Topaloğlu, Leman Damla Kotan, Fatih Temiz, Mehmet Nuri Özbek, Javier A. Tello, Mehmet Bertan Yılmaz, Şeref Erdoğan, Robert P. Millar and Eda Mengen and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Fatih Gürbüz

58 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

InactivatingKISS1Mutation and Hypogonadotropic Hypogonadism

2012 349 citations A. Kemal Topaloğlu, Javier A. Tello et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Fatih Gürbüz Türkiye	16	552	530	433	194	130	62	1.1k
Bruno Francou France	15	711 1.3×	498 0.9×	459 1.1×	155 0.8×	113 0.9×	37	1.1k
Ericka Barbosa Trarbach Brazil	20	883 1.6×	678 1.3×	524 1.2×	429 2.2×	68 0.5×	56	1.5k
Pierre-Marc Bouloux United Kingdom	15	484 0.9×	364 0.7×	242 0.6×	192 1.0×	65 0.5×	27	866
Margaret Au United States	14	478 0.9×	404 0.8×	348 0.8×	141 0.7×	37 0.3×	23	840
Haruhiko Kanasaki Japan	22	997 1.8×	550 1.0×	389 0.9×	315 1.6×	248 1.9×	122	1.7k
Kirsi Vaaralahti Finland	16	438 0.8×	332 0.6×	283 0.7×	198 1.0×	61 0.5×	35	719
Guillermina M. Luque Argentina	20	479 0.9×	284 0.5×	108 0.2×	287 1.5×	380 2.9×	42	1.1k
Aki Oride Japan	16	498 0.9×	243 0.5×	118 0.3×	137 0.7×	100 0.8×	85	781
Lacey Plummer United States	24	1.6k 2.9×	1.1k 2.0×	1.0k 2.3×	405 2.1×	157 1.2×	54	2.3k
Lawrence C. Layman United States	26	1.2k 2.2×	762 1.4×	778 1.8×	370 1.9×	466 3.6×	76	2.0k

Countries citing papers authored by Fatih Gürbüz

Since Specialization

Citations

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

Fields of papers citing papers by Fatih Gürbüz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatih Gürbüz

This figure shows the co-authorship network connecting the top 25 collaborators of Fatih Gürbüz. A scholar is included among the top collaborators of Fatih Gürbüz 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 Fatih Gürbüz. Fatih Gürbüz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ekinci, Rabia Miray Kışla, Sibel Balcı, Fatih Gürbüz, et al.. (2025). When it’s not juvenile idiopathic arthritis: unmasking monogenic mimickers in children. European Journal of Pediatrics. 184(12). 791–791.

Topaloğlu, A. Kemal, Enver Şimşek, Matthew Adam Kocher, et al.. (2022). Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humans. Human Genetics. 141(2). 295–304. 7 indexed citations

Doğruel, Dilek, et al.. (2022). The utility of annual growth velocity standard deviation scores and measurements of biochemical parameters in long-term treatment monitoring of children with 21-hydroxylase deficiency. HORMONES. 21(3). 391–397. 2 indexed citations

Cho, Hyun-Ju, Seyit Ahmet Uçaktürk, Semra Çeti̇nkaya, et al.. (2022). PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism. Journal of Neuroendocrinology. 34(4). e13103–e13103. 4 indexed citations

Doğruel, Dilek, et al.. (2021). Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey. Journal of Pediatric Endocrinology and Metabolism. 34(10). 1303–1309. 29 indexed citations

Turan, İhsan, Sevcan Erdem, Leman Damla Kotan, et al.. (2021). Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets. Journal of Pediatric Endocrinology and Metabolism. 34(5). 639–648. 4 indexed citations

Erdeve, Şenay Savaş, Zehra Aycan, Semra Çeti̇nkaya, et al.. (2020). Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia. Journal of Clinical Research in Pediatric Endocrinology. 13(2). 180–186. 2 indexed citations

Güran, Tülay, Başak Tezel, Ayşehan Akıncı, et al.. (2020). Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants. Journal of Clinical Research in Pediatric Endocrinology. 12(3). 287–294. 13 indexed citations

Ekinci, Rabia Miray Kışla, Fatih Gürbüz, Sibel Balcı, et al.. (2019). Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in <i>GALNT3</i> Gene: Experience from Southern Turkey. Journal of Clinical Research in Pediatric Endocrinology. 11(1). 94–99. 9 indexed citations

10.

Gürbüz, Fatih, et al.. (2019). Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma. Journal of Clinical Research in Pediatric Endocrinology. 11(2). 202–206. 9 indexed citations

11.

Güran, Tülay, Başak Tezel, Fatih Gürbüz, et al.. (2019). Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. Journal of Clinical Research in Pediatric Endocrinology. 11(1). 13–23. 16 indexed citations

12.

Turan, İhsan, et al.. (2018). Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistance. Clinical Endocrinology. 88(6). 799–805. 13 indexed citations

13.

Güran, Tülay, Başak Tezel, Fatih Gürbüz, et al.. (2018). Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants. Journal of Clinical Research in Pediatric Endocrinology. 1 indexed citations

14.

Kılınç, Yurdanur, et al.. (2017). Endocrine Complications in Thalassemia Major. Blood. 130. 4759–4759. 1 indexed citations

15.

Gürbüz, Fatih, et al.. (2017). Kronik karaciğer hastalığı olan çocukların D vitamini düzeyleri. SHILAP Revista de lepidopterología. 43(4). 1–1. 1 indexed citations

16.

Uçaktürk, Seyit Ahmet, et al.. (2017). Prevalence of ZnT8 Antibody in Turkish Children and Adolescents with New Onset Type 1 Diabetes. Journal of Clinical Research in Pediatric Endocrinology. 10(2). 108–112. 15 indexed citations

17.

Kotan, Leman Damla, Charlton Cooper, Şükran Darcan, et al.. (2016). Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1. 86. 1 indexed citations

18.

Dimitri, Paul, Elisa De Franco, Abdelhadi Habeb, et al.. (2016). An emerging, recognizable facial phenotype in association with mutations in GLI‐similar 3 (GLIS3). American Journal of Medical Genetics Part A. 170(7). 1918–1923. 16 indexed citations

19.

Mungan, Neslihan Önenli, et al.. (2014). Evaluation of Two Different Pamidronate Treatment Protocols in Children with Osteogenesis Imperfecta. SHILAP Revista de lepidopterología. 1 indexed citations

20.

Tello, Javier A., Leman Damla Kotan, Mehmet Nuri Özbek, et al.. (2012). Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism. Obstetrical & Gynecological Survey. 67(6). 352–353. 21 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.

Explore authors with similar magnitude of impact