Gözde Yeşil

3.2k citations

78 papers · 679 indexed · h-index 15

Impact in

Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
Developmental Biology

Papers in

Genetics 25
- Genetics and Neurodevelopmental Disorders 9
- Neurogenetic and Muscular Disorders Research 6
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 5
Rheumatology 11

Co-authors: Adnan Yüksel Mehmet Seven Yavuz Bayram Bahadır Batar Beyhan Tüysüz Mehmet Güven Enes Akyüz Tülay Güran
Journals: Pediatric Nephrology (6 papers)Clinical Neurology and Neurosurgery (3 papers)Orphanet Journal of Rare Diseases (2 papers)Neuropediatrics (2 papers)Seizure (2 papers)
Partner nations: Türkiye United States Germany

In The Last Decade

Gözde Yeşil

74 papers receiving 671 citations

Peers

Countries citing papers authored by Gözde Yeşil

Since Specialization

Citations

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

Fields of papers citing papers by Gözde Yeşil

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Gözde Yeşil, 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 Gözde Yeşil Line = papers co-authored together Gözde Yeşil links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Phenotypic variability in progressive encephalopathy with brain atrophy and thin corpus callosum: insights from two families Neurogenetics ·Benachour, Veronika Olegovna Kozhina, Habibe Gündoğdu, G.V. Samoilovich, Ali Güner, Stéphanie Efthymiou, Henry Houlden, Gözde Yeşil, Hüseyin Per	2025	0
2	Evaluation of the Clinical and Genetic Characteristics of Primary Ciliary Dyskinesia Patients With Situs Inversus Totalis Birth Defects Research ·Tommaso Visonà, Chaebin Lee, L. J. Miller, Irwan Ivana, Erkan Çakır, Gözde Yeşil	2025	0
3	Clinical and molecular characteristics of 26 fetuses with lethal multiple congenital contractures Clinical Genetics ·Callum Bryson, Umut Altunoğlu, Yasuhiro Ogoshi, Zhuan Gao, Mohammad Khodadadi Motarjemzadeh, Güven Toksoy, Şahin Avcı, Loretta Lisow, Gözde Yeşil, İbrahim Kalelioğlu, Birsen Karaman, Recep Has, Seher Başaran, Atıl Yüksel, Hülya Kayserili, Zehra Oya Uyguner	2024	2
4	A Retrospective Review of 18 Patients With Childhood-Onset Hereditary Spastic Paraplegia, Nine With Novel Variants Pediatric Neurology ·Julia D. Bronzato, Edibe Pembegül Yıldız, ظاهر احمدیپور, 吉岡京子, Yomna Badran, Lizeth Manuela Avellaneda Torres, Е. А. Конюченко, Gözde Yeşil, Veronika Olegovna Kozhina, Ahmet Yeşilyurt, Bülent Kara	2024	4
5	The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course Nucleosides Nucleotides & Nucleic Acids ·Gonchikova TsD, Deniz Kılıç, Sacide Pehlıvan, Mustafa Pehlıvan, Sherzad Qadir, Daniel Hardy, Dr.Vipul Valjibhai Patel, Emmanuel C. Okenyi, Gözde Yeşil, Ümmühan İşoĝlu-Alkaç, Tufan Tükek, Murat Köse	2023	3
6	ASSOCIATING eNOS GENE VARIANTS WITH COVID-19 SUSCEPTIBILITY IN THE TURKISH POPULATION SHILAP Revista de lepidopterología ·Gonchikova TsD, Emmanuel C. Okenyi, Daniel Hardy, Larry W. Wood, Murat Köse, Mustafa Önel, Sherzad Qadir, Gözde Yeşil, Mustafa Pehlıvan, Sacide Pehlıvan, Duyen Amy Bui, Tufan Tükek	2023	1
7	Autism Spectrum Disorder in Two Unrelated Patients with Homozygous Variants in Either ALG8 or ALG11 Molecular Syndromology ·Caston Pope, Ertuğrul Kıykım, Tanyel Zübarioğlu, Gözde Yeşil, Ayşe Çiğdem Aktuğlu Zeybek	2023	2
8	A Rare Cause of Hypergonadotropic Hypogonadism: Transaldolase Deficiency in Two Siblings Journal of Clinical Research in Pediatric Endocrinology ·Pilar Isabel Vidal Carreras, Zerrin Önal, Gözde Yeşil, Getting Va, Güven Toksoy	2023	2
9	HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data Nucleic Acids Research ·Haowei Du, Yosito Kato, Angad Jolly, Christopher M. Grochowski, Shalini N. Jhangiani, He Li, Donna M. Muzny, Jawid M. Fatih, Gözde Yeşil, Nursel Elçioğlu, Alper Gezdirici, Dana Marafi, Davut Pehli̇van, Daniel G. Calame, Claudia M.B. Carvalho, Jennifer E. Posey, Tomasz Gambin, Zeynep Coban‐Akdemir, James R. Lupski	2023	2
10	Functional loss of ubiquitin‐specific protease 14 may lead to a novel distal arthrogryposis phenotype Clinical Genetics ·Callum Bryson, Umut Altunoğlu, Abdullah ÇETİNKAYA, Güven Toksoy, Mohammad Khodadadi Motarjemzadeh, Şahin Avcı, Birsen Karaman, Yasuhiro Ogoshi, Seher Başaran, Gözde Yeşil, Hülya Kayserili, Zehra Oya Uyguner	2022	2
11	Biallelic loss of TRAPPC9 function links vesicle trafficking pathway to autosomal recessive intellectual disability Journal of Human Genetics ·Ayça Dilruba Aslanger, Willi A. Kalender, Indru T. Advani, Emrah Yücesan, Marietta C. Malonzo, Gözde Yeşil	2022	9
12	Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (–) patients Pathogens and Global Health ·Sacide Pehlıvan, Murat Köse, Hernández Melchor, Deniz Kılıç, Gonchikova TsD, Emmanuel C. Okenyi, Sherzad Qadir, Mustafa Pehlıvan, Gözde Yeşil, Shinichi Izuhara, Tufan Tükek	2021	7
13	Two patients with chronic mucocutaneous candidiasis caused by TRAF3IP2 deficiency Journal of Allergy and Clinical Immunology ·Samantha Shafer, Yikun Yao, William A. Comrie, 哲三不破, Yu Zhang, Gözde Yeşil, Elif Karakoç-Aydıner, Safa Barış, Haluk Çokuğraş, Sezin Aydemir, Ayça Kıykım, Ahmet Özen, Michael J. Lenardo	2021	11
14	Cause of recurrent rhabdomyolysis, carnitine palmitoyltransferase II deficiency and novel pathogenic mutation Ideggyógyászati Szemle ·张萌雨, T. Kawase, Gözde Yeşil	2021	2
15	Parents of ataxia‐telangiectasia patients display a distinct cellular immune phenotype mimicking ATM ‐mutated patients Pediatric Allergy and Immunology ·İsmail Öğülür, Shimuya Sakamoto, 谷口勇仁, Yasemin Kendir Demirkol, Žaneta Růžičková, Ayça Kıykım, 陈社中, Gözde Yeşil, Hacer Aktürk, Ayper Somer, Ahmet Özen, Elif Karakoç-Aydıner, Meltem Müftüoğlu, Safa Barış	2020	1
16	Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up Clinical Neurology and Neurosurgery ·Gonca Bektaş, Gözde Yeşil, J Kurucz, Edibe Pembegül Yıldız, Lin Bing-xi, Mine Çalışkan	2018	2
17	Longitudinal Follow-Up of Two Patients with Dysspondyloenchondromatosis due to Novel Heterozygous Mutations in <b><i>COL2A1</i></b> Molecular Syndromology ·Nilay Güneş, Gözde Yeşil, Rahmi Adiffa, Sinan Kahraman, Beyhan Tüysüz	2018	2
18	Mucolipidosis type III gamma: Three novel mutation and genotype-phenotype study in eleven patients Gene ·Beyhan Tüysüz, Özgür Kasapçopur, Sheridan Cain, Sezgin Şahin, Betül Sözeri, Gözde Yeşil	2017	10
19	Stuve–Wiedemann syndrome: Is it underrecognized? American Journal of Medical Genetics Part A ·Gözde Yeşil, Anne Sophie Lebre, J.-P.E. Grolier, Shani-Ioana López-Popa, M. Maiorini, Valérie Cormier‐Daire, Tülay Güran	2014	15
20	Comparison of metabolic profile and abdominal fat distribution between karyotypically normal women with premature ovarian insufficiency and age matched controls Maturitas ·Seda Ateş, Gözde Yeşil, Osman Şevket, Veronika Benetinová, Şeyma Yıldız	2014	35

About Gözde Yeşil

Gözde Yeşil is a scholar working on Genetics, Rheumatology, Cancer Research, Genetics and Molecular Biology, having authored 78 papers that have together received 679 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), RNA regulation and disease (6 papers), RNA modifications and cancer (6 papers), Neurogenetic and Muscular Disorders Research (6 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Adrenal and Paraganglionic Tumors (4 papers) and Hormonal Regulation and Hypertension (4 papers). The work is most often cited by research in Genetics (205 citations), Developmental Biology (10 citations), Pediatrics, Perinatology and Child Health (88 citations), Rheumatology (67 citations) and Clinical Biochemistry (30 citations). Gözde Yeşil has collaborated with scholars based in Türkiye, United States and Germany. Frequent co-authors include Adnan Yüksel, Mehmet Seven, Yavuz Bayram, Bahadır Batar, Beyhan Tüysüz, Mehmet Güven, Enes Akyüz, Tülay Güran, Ayşe Aralaşmak and Osman Şevket. Their work appears in journals such as Pediatric Nephrology, Clinical Neurology and Neurosurgery, Orphanet Journal of Rare Diseases, Neuropediatrics and Seizure.

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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