Hayat Erdem‐Yurter

724 citations

38 papers · 553 indexed · h-index 13

Genetics top 10%
- Neurogenetic and Muscular Disorders Research 18
Molecular Medicine top 10%
Clinical Biochemistry top 10%
Molecular Biology
- RNA modifications and cancer 16
- RNA Research and Splicing 6
- Histone Deacetylase Inhibitors Research 5
- Mitochondrial Function and Pathology 3
Geriatrics and Gerontology
Surgery
- Congenital Anomalies and Fetal Surgery 5
Pulmonary and Respiratory Medicine
- Cystic Fibrosis Research Advances 5
Pathology and Forensic Medicine
- Vitamin D Research Studies 4

Co-authors: Gamze Bora Didem Dayangaç Erden Sevim Dalkara Ayhan S. Demir Kemal Yelekçi Meral Özgüç Engin Yılmaz Ayşen Karaduman
Cited by: Genetics Molecular Medicine Clinical Biochemistry
Journals: SHILAP Revista de lepidopterología (1 paper)Human Molecular Genetics (1 paper)Human Reproduction (1 paper)
Partner nations: Türkiye Germany United Kingdom

In The Last Decade

Hayat Erdem‐Yurter

36 papers receiving 535 citations

Peers

Countries citing papers authored by Hayat Erdem‐Yurter

Since Specialization

Citations

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

Fields of papers citing papers by Hayat Erdem‐Yurter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hayat Erdem‐Yurter. 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 Hayat Erdem‐Yurter. The network helps show where Hayat Erdem‐Yurter may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hayat Erdem‐Yurter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hayat Erdem‐Yurter Line = papers co-authored together Hayat Erdem‐Yurter links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Alterations in insulin‐like growth factor system in spinal muscular atrophy Muscle & Nerve ·Ayşe Yeşbek Kaymaz,Sevgi Köstel Bal,Gamze Bora,Beril Talim,Alev Özön,Ayfer Alikaşifoğlu,Haluk Topaloğlu,Hayat Erdem‐Yurter	2022	6
2	SMN loss dysregulates microtubule-associated proteins in spinal muscular atrophy model Molecular and Cellular Neuroscience ·Pelin Zobaroğlu Özer,Dila Koyunoğlu,Çağdaş Devrim Son,Hayat Erdem‐Yurter,Gamze Bora	2022	4
3	Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy Human Molecular Genetics ·Gamze Bora,Niko Hensel,Sebastian Rademacher,Dila Koyunoğlu,Merve Sunguroğlu,Evrim Aksu‐Menges,Burcu Balcı-Hayta,Peter Claus,Hayat Erdem‐Yurter	2020	16
4	Class I histone deacetylase inhibition by aryl butenoic acid derivatives: In silico and in vitro studies Journal of Research in Pharmacy ·Gamze Bora,Suat Sarı,Gülce Taşkor Önel,Sevim Dalkara,Hayat Erdem‐Yurter	2019	1
5	Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients European Journal of Medical Genetics ·Gamze Bora,Ayşe Yeşbek-Kaymaz,Can Ebru Bekircan‐Kurt,Sevim Erdem‐Özdamar,Hayat Erdem‐Yurter	2015	5
6	Investigations of Curcumin and Resveratrol on Neurite Outgrowth: Perspectives on Spinal Muscular Atrophy BioMed Research International ·Gamze Bora,Hayat Erdem‐Yurter	2014	15
7	Carboxylic acid derivatives of histone deacetylase inhibitors induce full length SMN2 transcripts: a promising target for spinal muscular atrophy therapeutics Archives of Medical Science ·Didem Dayangaç Erden,Gamze Bora,Sevim Dalkara,Ayhan S. Demir,Hayat Erdem‐Yurter	2011	12
8	Evaluation of the effects of vitamin D receptor and estrogen receptor 1 gene polymorphisms on bone mineral density in postmenopausal women Clinical Rheumatology ·Mine Durusu Tanrıöver,Gamze Bora,Tenzile Deniz Uluturk,Didem Dayangaç Erden,Altug Tanriover,Alpaslan Kılıçarslan,S. Gul Oz,Hayat Erdem‐Yurter,Tümay Sözen,Gülay Sain Güven	2010	26
9	Molecular modifications on carboxylic acid derivatives as potent histone deacetylase inhibitors: Activity and docking studies Bioorganic & Medicinal Chemistry ·Gamze Bora,Didem Dayangaç Erden,Ayhan S. Demir,Sevim Dalkara,Kemal Yelekçi,Hayat Erdem‐Yurter	2009	138
10	Histone Deacetylase Inhibition Activity and Molecular Docking of (E )‐Resveratrol: Its Therapeutic Potential in Spinal Muscular Atrophy Chemical Biology & Drug Design ·Didem Dayangaç Erden,Gamze Bora,Peruze Ayhan,Çetin Kocaefe,Sevim Dalkara,Kemal Yelekçi,Ayhan S. Demir,Hayat Erdem‐Yurter	2009	38
11	A preliminary report on spinal muscular atrophy lymphoblastoid cell lines: Are they an appropriate tool for drug screening? Advances in Therapy ·Didem Dayangaç Erden,Haluk Topaloğlu,Hayat Erdem‐Yurter	2008	4
12	Polymorphisms of vitamin D receptor gene in Turkish familial psoriasis patients Archives of Dermatological Research ·Didem Dayangaç Erden,Ayşen Karaduman,Hayat Erdem‐Yurter	2007	50
13	Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens Human Reproduction ·D Dayangaç,Hayat Erdem‐Yurter,Engin Yılmaz,Ahmet Şahin,Christof Sohn,Meral Özgüç,Thilo Dörk	2004	41
14	Analysis of the modifying effects of TAP 1/2 genes on cystic fibrosis phenotype. PubMed ·Filiz Özbas‐Gerçeker,Uğur Özçelik,Nural Ki̇per,Deniz Anadol,Ayhan Göçmen,Engin Yılmaz,Hayat Erdem‐Yurter,Meral Özgüç	2002	3
15	Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Unrelated Turkish Families Neuropediatrics ·K. Gücüyener,Rıza Köksal Özgül,Caroline Paternotte,Hayat Erdem‐Yurter,J Prudhomme,Meral Özgüç,Haluk Topaloğlu	2001	24
16	Deletion analysis in Turkish patients with spinal muscular atrophy Brain and Development ·Hayat Erdem‐Yurter,Sacide Pehlıvan,Haluk Topaloğlu,Meral Özgüç	1999	21
17	Clinical Observations in Autosomal Recessive Spastic Paraplegia in Childhood and Further Evidence for Genetic Heterogeneity Neuropediatrics ·Haluk Topaloğlu,Faruk Güçlü Pınarlı,Hayat Erdem‐Yurter,K. Gücüyener,Aynur Ayşe Karaduman,Merve Torun Topçu,Nurten Akarsu,Meral Özgüç	1998	4
18	Study of 12 Mutations in Turkish Cystic Fibrosis Patients Human Heredity ·Engin Yılmaz,Hayat Erdem‐Yurter,M. Ouml zg uuml ccedil,Tülin Coşkun,U. Ouml z ccedil elik,A. G ouml ccedil men,Idot . Ouml zalp	1995	23
19	Allele frequencies of Mp6D‐9 and GATT markers in 32 Turkish cystic fibrosis families Clinical Genetics ·Meral Özgüç,Engin Yılmaz,Hayat Erdem‐Yurter,Teoman Coşkun,Uğur Özçelik,İnci̇ Togan,Ayhan Göçmen,S Ayter,İ Özalp	1994	0
20	Analysis of ΔF508 Mutation in Cystic Fibrosis Pathology Specimens Pediatric Pathology ·Meral Özgüç,Ali Tekin,Hayat Erdem‐Yurter,Engin Yılmaz,S Ayter,Turgay Coşkun,Alp Can,S Göğüş,M Cağlar,G. Kale,Zühal Akçören	1994	1

About Hayat Erdem‐Yurter

Hayat Erdem‐Yurter is a scholar working on Genetics, Clinical Biochemistry and Molecular Biology, having authored 38 papers that have together received 553 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (18 papers), RNA modifications and cancer (16 papers), RNA Research and Splicing (6 papers), Congenital Anomalies and Fetal Surgery (5 papers), Histone Deacetylase Inhibitors Research (5 papers), Cystic Fibrosis Research Advances (5 papers), Vitamin D Research Studies (4 papers) and Mitochondrial Function and Pathology (3 papers). The work is most often cited by research in Genetics (111 citations), Molecular Medicine (36 citations) and Clinical Biochemistry (44 citations). Hayat Erdem‐Yurter has collaborated with scholars based in Türkiye, Germany and United Kingdom. Frequent co-authors include Gamze Bora, Didem Dayangaç Erden, Sevim Dalkara, Ayhan S. Demir, Kemal Yelekçi, Meral Özgüç, Engin Yılmaz, Ayşen Karaduman, Haluk Topaloğlu and Turgay Coşkun. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Human Reproduction.

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