Zehra Yavaş Abalı

920 total citations
48 papers, 243 citations indexed

About

Zehra Yavaş Abalı is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Zehra Yavaş Abalı has authored 48 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Endocrinology, Diabetes and Metabolism, 22 papers in Molecular Biology and 15 papers in Genetics. Recurrent topics in Zehra Yavaş Abalı's work include Sexual Differentiation and Disorders (12 papers), Growth Hormone and Insulin-like Growth Factors (10 papers) and Genetic Syndromes and Imprinting (5 papers). Zehra Yavaş Abalı is often cited by papers focused on Sexual Differentiation and Disorders (12 papers), Growth Hormone and Insulin-like Growth Factors (10 papers) and Genetic Syndromes and Imprinting (5 papers). Zehra Yavaş Abalı collaborates with scholars based in Türkiye, United States and Cyprus. Zehra Yavaş Abalı's co-authors include Feyza Darendelıler, Şükran Poyrazoğlu, Firdevs Baş, Tülay Güran, Abdullah Bereket, Serap Turan, Rüveyde Bundak, Güven Toksoy, Zehra Oya Uyguner and Umut Altunoğlu and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Calcified Tissue International.

In The Last Decade

Zehra Yavaş Abalı

40 papers receiving 243 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zehra Yavaş Abalı Türkiye	9	147	100	82	33	26	48	243
Abdulsalam Abu‐Libdeh Israel	10	187 1.3×	75 0.8×	115 1.4×	24 0.7×	66 2.5×	25	338
Han Hyuk Lim South Korea	10	86 0.6×	61 0.6×	108 1.3×	28 0.8×	45 1.7×	40	283
Erdal Kurnaz Türkiye	10	91 0.6×	48 0.5×	62 0.8×	25 0.8×	38 1.5×	39	242
Jesús Barreiro Spain	10	109 0.7×	133 1.3×	90 1.1×	11 0.3×	71 2.7×	19	303
Nikolaj T. Krarup Denmark	8	177 1.2×	66 0.7×	144 1.8×	20 0.6×	82 3.2×	13	364
Daniela Choukair Germany	10	76 0.5×	72 0.7×	70 0.9×	6 0.2×	34 1.3×	32	217
Athanasia Stoupa France	9	161 1.1×	197 2.0×	92 1.1×	26 0.8×	18 0.7×	23	261
Raymond L. Hintz United States	8	157 1.1×	211 2.1×	95 1.2×	50 1.5×	31 1.2×	8	367
Débora Braslavsky Argentina	12	239 1.6×	168 1.7×	187 2.3×	86 2.6×	73 2.8×	25	454
Joshua C. Randall United Kingdom	4	201 1.4×	30 0.3×	102 1.2×	47 1.4×	51 2.0×	6	405

Countries citing papers authored by Zehra Yavaş Abalı

Since Specialization

Citations

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

Fields of papers citing papers by Zehra Yavaş Abalı

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Zehra Yavaş Abalı. 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 Zehra Yavaş Abalı. The network helps show where Zehra Yavaş Abalı may publish in the future.

Co-authorship network of co-authors of Zehra Yavaş Abalı

This figure shows the co-authorship network connecting the top 25 collaborators of Zehra Yavaş Abalı. A scholar is included among the top collaborators of Zehra Yavaş Abalı 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 Zehra Yavaş Abalı. Zehra Yavaş Abalı 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

Abalı, Saygın, et al.. (2025). Novel IGF1R Variants in Short Stature: Lessons from Two Patients and Outcome of Growth Hormone Therapy. Journal of Clinical Research in Pediatric Endocrinology.

Abalı, Zehra Yavaş & Tülay Güran. (2024). Diagnosis and management of non-CAH 46,XX disorders/differences in sex development. Frontiers in Endocrinology. 15. 1354759–1354759. 1 indexed citations

Abalı, Zehra Yavaş, Firdevs Baş, Güven Toksoy, et al.. (2023). A <i>Novel RNPC3</i> Gene Variant Expands the Phenotype in Patients with Congenital Hypopituitarism and Neuropathy. Hormone Research in Paediatrics. 97(2). 157–164. 3 indexed citations

Abalı, Zehra Yavaş, et al.. (2023). Two new cases with novel pathogenic variants reflecting the clinical diversity of Schaaf‐Yang syndrome. Clinical Genetics. 104(1). 127–132. 1 indexed citations

Abalı, Saygın, Aşkın Şeker, Belma Haliloğlu, et al.. (2023). Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature. Hormone Research in Paediatrics. 96(5). 527–537.

Abalı, Zehra Yavaş, Firdevs Baş, Şükran Poyrazoğlu, et al.. (2023). Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A SingleCenter Experience. Turkish Archives of Pediatrics. 58(3). 308–313. 5 indexed citations

Abalı, Zehra Yavaş, Belma Haliloğlu, Serap Turan, et al.. (2023). Development of external genitalia during mini-puberty: is it related to somatic growth or reproductive hormones?. European Journal of Pediatrics. 183(3). 1325–1332.

Abalı, Zehra Yavaş, Ayça Dilruba Aslanger, Firdevs Baş, et al.. (2023). Phenotype-Genotype Correlations of <i>GH1</i> Gene Variants in Patients with Isolated Growth Hormone Deficiency or Multiple Pituitary Hormone Deficiency. Hormone Research in Paediatrics. 97(2). 126–133. 2 indexed citations

Baş, Firdevs, Birsen Karaman, Güven Toksoy, et al.. (2023). PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency. Journal of Clinical Research in Pediatric Endocrinology. 15(4). 338–347. 2 indexed citations

10.

Altunoğlu, Umut, Zehra Yavaş Abalı, Şahin Avcı, et al.. (2022). Evaluation of growth, puberty, osteoporosis, and the response to long‐term bisphosphonate therapy in four patients with osteoporosis‐pseudoglioma syndrome. American Journal of Medical Genetics Part A. 188(7). 2061–2070. 2 indexed citations

11.

Uyguner, Zehra Oya, Firdevs Baş, Umut Altunoğlu, et al.. (2022). Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD. Journal of Clinical Research in Pediatric Endocrinology. 14(2). 153–171. 3 indexed citations

12.

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

13.

Kara, Manolya, Zehra Yavaş Abalı, Serdar Ceylaner, et al.. (2020). LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency. HORMONES. 20(2). 389–394. 5 indexed citations

14.

Abalı, Zehra Yavaş, Elisa De Franco, Şükran Poyrazoğlu, et al.. (2020). Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience. Hormone Research in Paediatrics. 93(7-8). 423–432. 3 indexed citations

15.

Abalı, Zehra Yavaş, Serap Turan, Halil Tuğtepe, et al.. (2019). Persistent Müllerian Duct Syndrome: A Rare But Important Etiology of Inguinal Hernia and Cryptorchidism. Sexual Development. 13(5-6). 264–270. 4 indexed citations

16.

Abalı, Zehra Yavaş, Gözde Yeşil, Harika Alpay, et al.. (2019). Rare cause of severe hypertension in an adolescent boy presenting with short stature: Questions. Pediatric Nephrology. 35(3). 403–404. 4 indexed citations

17.

Abalı, Zehra Yavaş, Gözde Yeşil, Harika Alpay, et al.. (2019). Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers. Pediatric Nephrology. 35(3). 405–407. 5 indexed citations

18.

Darendelıler, Feyza, et al.. (2018). Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype. 1 indexed citations

19.

Baş, Firdevs, Zehra Yavaş Abalı, Güven Toksoy, et al.. (2018). Precocious or early puberty in patients with combined pituitary hormone deficiency due to POU1F1 gene mutation: case report and review of possible mechanisms. HORMONES. 17(4). 581–588. 8 indexed citations

20.

Abalı, Zehra Yavaş, et al.. (2018). Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty. European Journal of Pediatrics. 177(11). 1593–1601. 23 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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