Şükran Poyrazoğlu

1.7k total citations
84 papers, 794 citations indexed

About

Şükran Poyrazoğlu is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Şükran Poyrazoğlu has authored 84 papers receiving a total of 794 indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Endocrinology, Diabetes and Metabolism, 35 papers in Molecular Biology and 29 papers in Genetics. Recurrent topics in Şükran Poyrazoğlu's work include Sexual Differentiation and Disorders (24 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Birth, Development, and Health (13 papers). Şükran Poyrazoğlu is often cited by papers focused on Sexual Differentiation and Disorders (24 papers), Growth Hormone and Insulin-like Growth Factors (21 papers) and Birth, Development, and Health (13 papers). Şükran Poyrazoğlu collaborates with scholars based in Türkiye, United States and Cyprus. Şükran Poyrazoğlu's co-authors include Feyza Darendelıler, Firdevs Baş, Rüveyde Bundak, Nurçin Saka, Hülya Günöz, Zehra Yavaş Abalı, Ahmet Uçar, Zehra Oya Uyguner, Güven Toksoy and Ensar Yekeler and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Clinical Endocrinology.

In The Last Decade

Şükran Poyrazoğlu

75 papers receiving 778 citations

Peers

Countries citing papers authored by Şükran Poyrazoğlu

Since Specialization

Citations

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

Fields of papers citing papers by Şükran Poyrazoğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Şükran Poyrazoğlu

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

#	Work	Indexed citations
1	Target gene variations of PPAR isoforms may contribute to MODY heterogeneity: A preliminary comparative study with type 2 diabetes 2024 ·Diabetes Research and Clinical Practice ·Hülya Yılmaz, (unknown), Nurdan Gül, (unknown), Şükran Poyrazoğlu, Yıldız Tütüncü, (unknown), Oğuz Öztürk, İlhan Satman	0
2	Novel variants ensued genomic imprinting in familial central precocious puberty 2024 ·Journal of Endocrinological Investigation ·(unknown), (unknown), Şükran Poyrazoğlu, Metin Yusuf Gelmez, Firdevs Baş, Feyza Darendelıler, Zehra Oya Uyguner	1
3	A National Multicenter Study of Leptin and Leptin Receptor Deficiency and Systematic Review 2023 ·The Journal of Clinical Endocrinology & Metabolism ·(unknown), (unknown), Samim Özen, Semra Çeti̇nkaya, Leyla Akın, (unknown), Zafer Pekkolay, (unknown), Elif Özsu, Şenay Savaş Erdeve, Şükran Poyrazoğlu, Merih Berberoğlu, Murat Aydın, (unknown), Barış Akıncı, Korcan Demir, Elif A Oral	7
4	Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls 2023 ·Sexual Development ·Guilherme Guaragna‐Filho, Gil Guerra‐Júnior, Rieko Tadokoro‐Cuccaro, Ieuan A. Hughes, (unknown), Olaf Hiort, Antonio Balsamo, Tülay Güran, Paul Martin Holterhus, Sabine E Hannema, Şükran Poyrazoğlu, Feyza Darendelıler, Jillian Bryce, S. Faisal Ahmed, Charmian A. Quigley	1
5	Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience 2023 ·Turkish Archives of Pediatrics ·Zehra Yavaş Abalı, (unknown), Firdevs Baş, Şükran Poyrazoğlu, (unknown), Rejin Kebudi, (unknown), Rüveyde Bundak, Feyza Darendelıler	5
6	Phenotype-Genotype Correlations of <i>GH1</i> Gene Variants in Patients with Isolated Growth Hormone Deficiency or Multiple Pituitary Hormone Deficiency 2023 ·Hormone Research in Paediatrics ·(unknown), Zehra Yavaş Abalı, Ayça Dilruba Aslanger, Firdevs Baş, Güven Toksoy, (unknown), (unknown), Şükran Poyrazoğlu, Zehra Oya Uyguner, Feyza Darendelıler	2
7	Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome 2022 ·American Journal of Medical Genetics Part A ·(unknown), Umut Altunoğlu, (unknown), (unknown), Zehra Yavaş Abalı, Şahin Avcı, Bernd Wollnik, Şükran Poyrazoğlu, Firdevs Baş, Zehra Oya Uyguner, Hülya Kayserili, Feyza Darendelıler	2
8	Genotype of congenital adrenal hyperplasia patients with testicular adrenal rest tumor 2022 ·European Journal of Medical Genetics ·Zehra Aycan, (unknown), (unknown), Şenay Savaş Erdeve, Firdevs Baş, Şükran Poyrazoğlu, Pınar Öztürk, (unknown), Oya Ercan, Tülay Güran, Nihal Hatipoğlu, Seyit Ahmet Uçaktürk, Gönül Çatlı, Nesibe Akyürek, (unknown), (unknown), Semra Çeti̇nkaya	6
9	Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD 2022 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Zehra Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, (unknown), (unknown), Rüveyde Bundak, Seher Başaran, Feyza Darendelıler	3
10	Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome 2021 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Firdevs Baş, (unknown), Zeynep Şıklar, (unknown), Merih Berberoğlu, (unknown), Elvan Bayramoğlu, Şükran Poyrazoğlu, Murat Aydın, Ayça Törel Ergür, Damla Gökşen, Semih Bolu, Zehra Aycan, Beyhan Tüysüz, Oya Ercan, Olcay Evliyaoğlu	8
11	LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency 2020 ·HORMONES ·(unknown), Manolya Kara, (unknown), (unknown), Zehra Yavaş Abalı, Serdar Ceylaner, Ayça Kıykım, (unknown), Selda Hançerlı Törün, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendelıler	5
12	Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience 2020 ·Hormone Research in Paediatrics ·Zehra Yavaş Abalı, Elisa De Franco, (unknown), Şükran Poyrazoğlu, Rüveyde Bundak, Firdevs Baş, Sarah E. Flanagan, Feyza Darendelıler	3
13	Etiologic Evaluation of Severe Short Stature in Children at a Tertiary Pediatric Endocrinology Centre 2019 ·Çocuk Dergisi / Journal of Child ·(unknown), Firdevs Baş, Şükran Poyrazoğlu, (unknown), Feyza Darendelıler, Rüveyde Bundak	0
14	Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome 2019 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·(unknown), Firdevs Baş, (unknown), Ahmet Uçar, Şükran Poyrazoğlu, Rüveyde Bundak, Feyza Darendelıler	9
15	A Novel Homozygous Mutation of the Acid-Labile Subunit <i>(IGFALS)</i> Gene in a Male Adolescent 2019 ·Journal of Clinical Research in Pediatric Endocrinology ·Şükran Poyrazoğlu, Vivian Hwa, Firdevs Baş, Andrew Dauber, Ron G. Rosenfeld, Feyza Darendelıler	9
16	Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype 2018 ·(unknown), Feyza Darendelıler, (unknown), (unknown), (unknown), (unknown), Zehra Yavaş Abalı, Şükran Poyrazoğlu, Kemal Nişli, Firdevs Baş	1
17	Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty 2018 ·European Journal of Pediatrics ·(unknown), Zehra Yavaş Abalı, Firdevs Baş, Şükran Poyrazoğlu, Feyza Darendelıler	23
18	Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 families 2016 ·European Journal of Medical Genetics ·(unknown), (unknown), Yeliz Güven, Firdevs Baş, Umut Altunoğlu, (unknown), Şükran Poyrazoğlu, Güven Toksoy, Hülya Kayserili, Zehra Oya Uyguner	30
19	Adiponectin is an indicator of insulin resistance in non‐obese prepubertal children born large for gestational age (LGA) and is affected by birth weight 2008 ·Clinical Endocrinology ·Feyza Darendelıler, Şükran Poyrazoğlu, (unknown), Firdevs Baş, Gülbin Gökçay, (unknown), Nurten Eskiyurt	27
20	Serum leptin levels in patients with 21-hydroxylase deficiency before and after treatment. 2003 ·SHILAP Revista de lepidopterología ·Şükran Poyrazoğlu, Hülya Günöz, Feyza Darendelıler	8

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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