Mustafa Doğan

453 total citations
45 papers, 266 citations indexed

About

Mustafa Doğan is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mustafa Doğan has authored 45 papers receiving a total of 266 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Surgery. Recurrent topics in Mustafa Doğan's work include Forensic and Genetic Research (4 papers), Adipokines, Inflammation, and Metabolic Diseases (4 papers) and Hereditary Neurological Disorders (3 papers). Mustafa Doğan is often cited by papers focused on Forensic and Genetic Research (4 papers), Adipokines, Inflammation, and Metabolic Diseases (4 papers) and Hereditary Neurological Disorders (3 papers). Mustafa Doğan collaborates with scholars based in Türkiye, Cyprus and Bosnia and Herzegovina. Mustafa Doğan's co-authors include Recep Eröz, Bülent Oran, Fatih Kara, Harun Peru, Alper Gezdirici, Bülent Altun, Pembegül Güneş, İzzet Titiz, Ethem Ünal and Osman Gökalp and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Immunology and PLoS ONE.

In The Last Decade

Mustafa Doğan

39 papers receiving 265 citations

Peers

Countries citing papers authored by Mustafa Doğan

Since Specialization

Citations

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

Fields of papers citing papers by Mustafa Doğan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mustafa Doğan

This figure shows the co-authorship network connecting the top 25 collaborators of Mustafa Doğan. A scholar is included among the top collaborators of Mustafa Doğan 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 Mustafa Doğan. Mustafa Doğan 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	Genotype, Phenotype, and Clinical Characteristics of Maturity-onset Diabetes of the Young (MODY): Predominance of GCK-MODY 2025 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Ayşehan Akıncı, (unknown), (unknown), (unknown), (unknown), İbrahim Tekedereli, Mustafa Doğan	0
2	Variant Spectrum of Renal Ciliopathies in Turkish Cohort and Genotype–Phenotype Association Specifically in Autosomal Dominant Polycystic Kidney Disease 2024 ·Clinical Genetics ·(unknown), (unknown), (unknown), (unknown), Mustafa Doğan, Sevgi Yavuz, (unknown), Alper Gezdirici	0
3	Discovery of a novel homozygous SOD1 truncating variant bolsters infantile SOD1 deficiency syndrome 2024 ·Molecular Biology Reports ·Mustafa Doğan, Kerem Teralı, Recep Eröz, Hüseyin Kılıç, Alper Gezdirici, (unknown)	5
4	Novel biallelic nonsense mutation in IGHMBP2 gene linked to neuropathy (CMT2S): A comprehensive clinical, genetic and bioinformatic analysis of a Turkish patient with literature review 2024 ·Brain and Development ·(unknown), Mustafa Doğan, (unknown), (unknown), Recep Eröz	2
5	A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del) 2024 ·Genes & Genomics ·(unknown), Mustafa Doğan, Recep Eröz, (unknown)	3
6	Batı Ege Bölgesinde α-Talasemi Genotipleri ve α-Talasemi Genotip Frekansı 2023 ·DergiPark (Istanbul University) ·(unknown), (unknown), (unknown), (unknown), Mustafa Doğan, Recep Eröz	4
7	Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism 2023 ·Journal of Clinical Research in Pediatric Endocrinology ·(unknown), Ayşehan Akıncı, (unknown), (unknown), (unknown), Mustafa Doğan, (unknown)	5
8	A Deeper Insight into <i>COL4A3</i>, <i>COL4A4</i>, and <i>COL4A5 </i>Variants and Genotype-Phenotype Correlation of a Turkish Cohort with Alport Syndrome 2023 ·Molecular Syndromology ·(unknown), (unknown), Mustafa Doğan, Alper Gezdirici, (unknown), (unknown), (unknown), (unknown), Onur Bender, Cemal Ün	3
9	Evaluation of Y Chromosome Microdeletion and Chromosome Analysis Results in Infertile Male Patients 2023 ·Konuralp Tıp Dergisi ·(unknown), Mustafa Doğan, Recep Eröz, Halil Lütfi Canat	0
10	Ailesel Akdeniz Ateşi Hastalarının MEFV Gen Mutasyon Tiplerinin Sıklığı ve Hastalarda Gen Mutasyonu ile Klinik Bulgular Arasındaki ilişkilerin Değerlendirilmesi 2023 ·Dicle Medical Journal / Dicle Tip Dergisi ·(unknown), (unknown), (unknown), Recep Eröz, (unknown), Mustafa Doğan	0
11	Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel 2022 ·Molecular Biology Reports ·Mustafa Doğan, Recep Eröz, Semih Bolu, (unknown), Alper Gezdirici, İlknur Arslanoğlu, Kerem Teralı	6
12	Biallelic Novel USP53 Splicing Variant Disrupting the Gene Function that Causes Cholestasis Phenotype and Review of the Literature 2022 ·Molecular Syndromology ·Alper Gezdirici, (unknown), Mustafa Doğan, (unknown), (unknown)	6
13	Clinical, radiological and computational studies on two novel GNPTG variants causing mucolipidosis III gamma phenotypes with varying severity 2021 ·Molecular Biology Reports ·Mustafa Doğan, Recep Eröz, Kerem Teralı, Alper Gezdirici, Semih Bolu	2
14	Clinical and molecular findings in a Turkish family with an ultra-rare condition, ELP2-related neurodevelopmental disorder 2021 ·Molecular Biology Reports ·Mustafa Doğan, Kerem Teralı, Recep Eröz, Hüseyin Demirci, Kenan Kocabay	5
15	An integrated clinical and molecular study of a cohort of Turkish patients with Marfan syndrome harboring known and novel FBN1 variants 2021 ·Journal of Human Genetics ·Alper Gezdirici, Kerem Teralı, Elif Yılmaz Güleç, (unknown), Mustafa Doğan, Recep Eröz	4
16	Genetic relationships of Southwest Asian and Mediterranean populations 2021 ·Forensic Science International Genetics ·Kenneth K. Kídd, Özlem Bülbül, Cemal Gürkan, Mustafa Doğan, (unknown), Pavlos I. Neophytou, Lotfi Cherni, David Gurwitz, William C. Speed, Michael T. Murtha, Judith R. Kidd, A.J. Pakstis	8
17	Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature 2020 ·The Turkish Journal of Pediatrics ·Semih Bolu, Recep Eröz, Mehmet Tekin, Mustafa Doğan	4
18	A glimpse at the intricate mosaic of ethnicities from Mesopotamia: Paternal lineages of the Northern Iraqi Arabs, Kurds, Syriacs, Turkmens and Yazidis 2017 ·PLoS ONE ·(unknown), Cemal Gürkan, Mustafa Doğan, (unknown), (unknown), (unknown), (unknown), Damir Marjanović	16
19	Spontaneous pneumomediastinum in childhood: report of an adolescent case diagnose with asthma 2014 ·Tuberkuloz ve Toraks ·Fatih Fırıncı, (unknown), Mustafa Doğan, Ali Koçyiğit, (unknown)	2
20	Serum Paraoxonase (a High-density Lipoprotein-associated Lipophilic Antioxidant) Activity and Lipid Profile in Experimental Acute Pancreatitis 2005 ·Pancreas ·Ethem Ünal, Hafize Uzun, (unknown), Mustafa Doğan, Habibe Genç, Pembegül Güneş, İzzet Titiz	22

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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