Mehmet Seven

1.9k total citations
59 papers, 765 citations indexed

About

Mehmet Seven is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mehmet Seven has authored 59 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 17 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mehmet Seven's work include Pharmacological Effects and Toxicity Studies (9 papers), Epilepsy research and treatment (8 papers) and Genetic and rare skin diseases. (4 papers). Mehmet Seven is often cited by papers focused on Pharmacological Effects and Toxicity Studies (9 papers), Epilepsy research and treatment (8 papers) and Genetic and rare skin diseases. (4 papers). Mehmet Seven collaborates with scholars based in Türkiye, United States and United Kingdom. Mehmet Seven's co-authors include Adnan Yüksel, Müjgan Cengiz, Turgut Ulutin, Aslıhan Tolun, Mehmet Buğrahan Düz, Mustafa Özen, Ömer Faruk Karataş, Çiğdem Köroğlu, Gözde Yeşil and Mehmet Güven and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Investigative Ophthalmology & Visual Science.

In The Last Decade

Mehmet Seven

56 papers receiving 740 citations

Peers

Countries citing papers authored by Mehmet Seven

Since Specialization

Citations

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

Fields of papers citing papers by Mehmet Seven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mehmet Seven

This figure shows the co-authorship network connecting the top 25 collaborators of Mehmet Seven. A scholar is included among the top collaborators of Mehmet Seven 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 Mehmet Seven. Mehmet Seven 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	HMGA2 associated ceRNA-HOTAIR pathway in breast cancer patients from clinicopathological perspective 2025 ·TURKISH JOURNAL OF MEDICAL SCIENCES ·(unknown), (unknown), Mehmet Velidedeoğlu, Mehmet Seven, (unknown)	0
2	An Evaluation of DNA Methylation Levels and Sleep in Relation to Hot Flashes: A Cross-Sectional Study 2024 ·Journal of Clinical Medicine ·(unknown), (unknown), Gülçin Benbir Şenel, Derya Karadeniz, (unknown), (unknown), Mehmet Seven, (unknown)	2
3	A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature 2024 ·CEN Case Reports ·(unknown), (unknown), Ahmet Murt, (unknown), Mehmet Seven, (unknown)	1
4	Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene 2022 ·Ophthalmic Genetics ·(unknown), (unknown), (unknown), Gökhan Çelik, (unknown), Mehmet Seven, Hüseyin Yetik	1
5	Evaluation of IL1B rs1143634 and IL6 rs1800796 Polymorphisms with Autism Spectrum Disorder in the Turkish Children 2021 ·Immunological Investigations ·(unknown), (unknown), Burak Doğangün, Mehmet Seven	3
6	A rare case of an NLRP12-associated autoinflammatory disease 2021 ·European Journal of Medical Genetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Mehmet Seven, Serdal Uğurlu	8
7	Assessment of Fetal Rhesus D and Gender with Cell-Free DNA and Exosomes from Maternal Blood 2020 ·Reproductive Sciences ·(unknown), Orhan Şahin, (unknown), Mehmet Seven, Selçuk Sözer	14
8	Calculation of Embryo/Fetus Dose in Pregnant Thyroid Patients Who Have Accidentally Received Radioiodine 2018 ·(unknown), (unknown), Nami Yeyin, Mohammad Abuqbeitah, Lebriz Uslu, (unknown), Mehmet Buğrahan Düz, Mehmet Seven	0
9	Three novel mutations in 20 patients with hereditary spastic paraparesis 2018 ·Neurological Sciences ·Mehmet Buğrahan Düz, Selçuk Daşdemir, (unknown), (unknown), Mehmet Seven	1
10	The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome 2018 ·American Journal of Men s Health ·(unknown), (unknown), Şükrü Palanduz, Selçuk Daşdemir, Mehmet Seven	7
11	DNA repair gene XPD Asp312Asn and XRCC4 G-1394T polymorphisms and the risk of autism spectrum disorder. 2016 ·PubMed ·Selçuk Daşdemir, Mehmet Güven, (unknown), (unknown), Burak Doğangün, (unknown), Muhammed Tayyib Kadak, (unknown), Mehmet Seven	12
12	Whole-exome sequencing revealed two novel mutations in Usher syndrome 2015 ·Gene ·Asuman Koparır, Ömer Faruk Karataş, (unknown), Bayram Yüksel, Mahmut Şamil Sağıroğlu, Mehmet Seven, Hakan Ulucan, Adnan Yüksel, Mustafa Özen	4
13	Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome 2015 ·Gene ·Byeonghyeon Lee, Mehmet Buğrahan Düz, (unknown), Asuman Koparır, Kyu-Yup Lee, Jae Young Choi, Mehmet Seven, Adnan Yüksel, Un‐Kyung Kim, Mustafa Özen	5
14	A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication 2013 ·Gene ·Mehmet Seven, Alper Gezdirici, Hakan Ulucan, Ömer Faruk Karataş, (unknown), Adnan Yüksel, Mustafa Özen	5
15	The Effect of Genetic Polymorphisms of Cytochrome P450 CYP2C9, CYP2C19, and CYP2D6 on Drug-Resistant Epilepsy in Turkish Children 2013 ·Molecular Diagnosis & Therapy ·Mehmet Seven, Bahadır Batar, (unknown), Gözde Yeşil, Adnan Yüksel, Mehmet Güven	20
16	The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children 2013 ·Molecular Biology Reports ·Mehmet Seven, Bahadır Batar, (unknown), Gözde Yeşil, Adnan Yüksel, Mehmet Güven	34
17	A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve–Melchior–Clausen syndrome 2013 ·Clinical Dysmorphology ·Mehmet Seven, Erkan Koparir, Alper Gezdirici, Hatip Aydın, Heyko Skladny, (unknown), (unknown), Ömer Faruk Karataş, Asuman Koparır, Mustafa Özen, Hakan Ulucan	7
18	The Effects of Vigabatrin on Rat Liver Antioxidant Status 2005 ·Drug metabolism and drug interactions ·Müjgan Cengiz, Adnan Yüksel, (unknown), (unknown), (unknown), Mehmet Seven	6
19	A case of acampomelic campomelic dysplasia. 2002 ·PubMed ·(unknown), Mehmet Seven, Adnan Yüksel	3
20	Erythrocyte Glutathione, Glutathione Peroxidase, Superoxide Dismutase and Serum Lipid Peroxidation in Epileptic Children With Valproate and Carbamazepine Monotherapy 2000 ·Journal of Basic and Clinical Physiology and Pharmacology ·Adnan Yüksel, Müjgan Cengiz, Mehmet Seven, Turgut Ulutin	69

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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