Zehra Yavaş Abalı - Concepedia

Author

Zehra Yavaş Abalı

Also Known As

Abali, Z.Y., Z. Y. Abalı, Zehra Abali, Zehra YAVAS ABALI, Zehra Yavas Abali, Zehra Yavas Abalı, Zehra Yavas Abali, Zehra Yavaş Abali, Zehra Yavaş Abalı

101

Publications

904

Citations

H-Index

Concepts

All Affiliations

Istanbul University Marmara University Gazi University Ege University İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi

About

Zehra Yavaş Abalı is an author at Istanbul University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	116
2	Endocrinology	2	2	58
3	Health Sciences	1	1	31
4	Public Health	1	1	27
5	Diabetes	1	1	31

Zehra Yavaş Abalı

Publications

677

Citations

H-Index

Page 1

	Year	Citations
Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort Tülay Güran, Federica Buonocore, Nurçin Saka, The Journal of Clinical Endocrinology & Metabolism	2015	208
Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease Angad Jolly, Yavuz Bayram, Serap Turan, The Journal of Clinical Endocrinology & Metabolism	2019	75
Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency Erdal Kurnaz, Emine Kartal Baykan, Ayberk Türkyılmaz, Hormone Research in Paediatrics	2020	40
Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency Zehra Yavaş Abalı, Mehmet Keskın, Mehmet Nuri Özbek, The Journal of Clinical Endocrinology & Metabolism	2021	40
A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations Aslı Derya Kardelen, Güven Toksoy, Firdevs Baş, Journal of Clinical Research in Pediatric Endocrinology	2018	37
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development Chrysanthi Kouri, Grit Sommer, Idoia Martinez de la Piscina, EBioMedicine	2024	35
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study Zeynep Atay, Ediz Yeşilkaya, Şenay Savaş Erdeve, The Journal of Clinical Endocrinology & Metabolism	2016	33
Prevalence, clinical characteristics and long-term outcomes of classical 11 β-hydroxylase deficiency (11BOHD) in Turkish population and novel mutations in CYP11B1 gene Firdevs Baş, Güven Toksoy, Berrin Ergun-Longmire, The Journal of Steroid Biochemistry and Molecular Biology Cyp11b1 GeneMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2018	32
Body mass index at the presentation of premature adrenarche is associated with components of metabolic syndrome at puberty Gamze Kaya, Zehra Yavaş Abalı, Firdevs Baş, European Journal of Pediatrics ObesityMetabolic SyndromePremature AdrenarcheAdrenal GlandBody Composition	2018	31
International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry Irina Bacila, Nicole Freeman, Eleni Daniel, European Journal of Endocrinology	2021	31

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