Bülent Hacıhamdioğlu

1.0k total citations
54 papers, 564 citations indexed

About

Bülent Hacıhamdioğlu is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Bülent Hacıhamdioğlu has authored 54 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Endocrinology, Diabetes and Metabolism, 15 papers in Molecular Biology and 14 papers in Genetics. Recurrent topics in Bülent Hacıhamdioğlu's work include Vitamin D Research Studies (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Bülent Hacıhamdioğlu is often cited by papers focused on Vitamin D Research Studies (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Growth Hormone and Insulin-like Growth Factors (5 papers). Bülent Hacıhamdioğlu collaborates with scholars based in Türkiye, Serbia and United States. Bülent Hacıhamdioğlu's co-authors include Merih Berberoğlu, Zeynep Şıklar, Şenay Savaş Erdeve, Gönül Öçal, Duygu Övünç Hacıhamdioğlu, Suat Fítöz, Selami Süleymanoğlu, Ferhan Karademır, Nejat Akar and Yonca Eğin and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Medicine.

In The Last Decade

Bülent Hacıhamdioğlu

52 papers receiving 551 citations

Peers

Bülent Hacıhamdioğlu

GENET

EDM

PFM

EPIDE

Vanadin Seifert‐Klauss Germany

Preamrudee Poomthavorn Thailand

Alev Özön Türkiye

I. González Casado Spain

Alisa D. Kjærgaard Denmark

Olcay Evliyaoğlu Türkiye

Amelia Sutton United States

P. Martul Spain

Chan Jong Kim South Korea

Giorgio Zamboni Italy

Vanadin Seifert‐Klauss Germany

Bülent Hacıhamdioğlu

145 ×0.8

131 ×0.9

GENET

155 ×1.1

EDM

94 ×1.0

PFM

105 ×1.2

EPIDE

Citations per year, relative to Bülent Hacıhamdioğlu Bülent Hacıhamdioğlu (= 1×) peers Vanadin Seifert‐Klauss

Countries citing papers authored by Bülent Hacıhamdioğlu

Since Specialization

Citations

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

Fields of papers citing papers by Bülent Hacıhamdioğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bülent Hacıhamdioğlu

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

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.

Hacıhamdioğlu, Bülent, et al.. (2020). Homozygous Mutation in the Insulin Receptor Gene Associated with Mild Type A Insulin Resistance Syndrome: A Case Report. Journal of Clinical Research in Pediatric Endocrinology. 13(1). 100–103. 4 indexed citations

Dursun, Fatma, et al.. (2019). Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A. Journal of Clinical Research in Pediatric Endocrinology. 11(1). 34–40. 18 indexed citations

Hacıhamdioğlu, Bülent, et al.. (2019). A Case of the Perinatal Form Hypophosphatasia Caused by a Novel Large Duplication of the <i>ALPL</i> Gene and Report of One Year Follow-up with Enzyme Replacement Therapy. Journal of Clinical Research in Pediatric Endocrinology. 11(3). 306–310. 1 indexed citations

Hacıhamdioğlu, Bülent, et al.. (2018). Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia. The Turkish Journal of Pediatrics. 60(5). 581–583. 4 indexed citations

Erdeve, Şenay Savaş, et al.. (2016). Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height. Journal of Clinical Research in Pediatric Endocrinology. 8(2). 211–217. 19 indexed citations

Karabulut, Halil Gürhan, et al.. (2016). Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature. Journal of Clinical Research in Pediatric Endocrinology. 8(2). 144–149. 5 indexed citations

Hacıhamdioğlu, Duygu Övünç, Bülent Hacıhamdioğlu, Ferhat Çekmez, et al.. (2016). The Association between Serum 25-Hydroxy Vitamin D Level and Urine Cathelicidin in Children with a Urinary Tract Infection. Journal of Clinical Research in Pediatric Endocrinology. 8(3). 325–329. 39 indexed citations

Vehapoğlu, Aysel, et al.. (2016). Risk assessment of obstructive sleep apnea syndrome in pediatric patients with vitamin D deficiency. Medicine. 95(39). e4632–e4632. 10 indexed citations

10.

Şıklar, Zeynep, et al.. (2015). The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels. Journal of Clinical Research in Pediatric Endocrinology. 7(4). 301–306. 7 indexed citations

11.

Öçal, Gönül, Merih Berberoğlu, Zeynep Şıklar, et al.. (2014). Clinical Review of 95 Patients with 46,XX Disorders of Sex Development Based on the New Chicago Classification. Journal of Pediatric and Adolescent Gynecology. 28(1). 6–11. 15 indexed citations

12.

Şıklar, Zeynep, et al.. (2012). Relationships Between Osteocalcin, Glucose Metabolism and Adiponectin in Obese Children: Is there Crosstalk Between Bone Tissue and Glucose Metabolism?. Journal of Clinical Research in Pediatric Endocrinology. 4(4). 182–188. 18 indexed citations

13.

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

14.

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

15.

Öçal, Gönül, Sarah E. Flanagan, Bülent Hacıhamdioğlu, et al.. (2011). Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell. Journal of Pediatric Endocrinology and Metabolism. 24(11-12). 1019–23. 20 indexed citations

16.

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

17.

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

18.

Erdeve, Şenay Savaş, Zehra Aycan, Merih Berberoğlu, et al.. (2010). A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment. European Journal of Pediatrics. 169(8). 991–995. 8 indexed citations

19.

Gök, Faysal, Yasemin Alanay, Bülent Hacıhamdioğlu, et al.. (2009). Clinical and radiographic findings in two brothers affected with a novel mutation in matrix metalloproteinase 2 gene. European Journal of Pediatrics. 169(3). 363–367. 17 indexed citations

20.

Kendirli, Tanıl, Bülent Ünay, Fuat Tosun, et al.. (2006). Recurrent Streptococcus pneumoniae meningitis in a child with traumatic anterior cranial base defect. Pediatrics International. 48(1). 91–93. 10 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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