Alper Han Çebi

548 total citations
35 papers, 143 citations indexed

About

Alper Han Çebi is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Alper Han Çebi has authored 35 papers receiving a total of 143 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 13 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in Alper Han Çebi's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Metabolism and Genetic Disorders (3 papers). Alper Han Çebi is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Metabolism and Genetic Disorders (3 papers). Alper Han Çebi collaborates with scholars based in Türkiye, Cyprus and Antigua and Barbuda. Alper Han Çebi's co-authors include Mevlit Íkbal, Murat Çakır, Mukaddes Kalyoncu, Ferhat Demir, Gülay Karagüzel, Hamdi Cihan Emeksiz, Ali Cansu, Gürdal Yılmaz, Ahmet Arman and Bilgen Bilge Geçkinli and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Clinical Genetics.

In The Last Decade

Alper Han Çebi

32 papers receiving 138 citations

Peers

Countries citing papers authored by Alper Han Çebi

Since Specialization

Citations

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

Fields of papers citing papers by Alper Han Çebi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alper Han Çebi. 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 Alper Han Çebi. The network helps show where Alper Han Çebi may publish in the future.

Co-authorship network of co-authors of Alper Han Çebi

This figure shows the co-authorship network connecting the top 25 collaborators of Alper Han Çebi. A scholar is included among the top collaborators of Alper Han Çebi 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 Alper Han Çebi. Alper Han Çebi 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	Comparison of Clinical and Genetic Characteristics of Familial Mediterranean Fever Patients Among Adult Age Groups 2024 ·The Turkish Journal of Gastroenterology ·(unknown), (unknown), (unknown), (unknown), (unknown), Alper Han Çebi, (unknown), Arif Coşar	0
2	The first Turkish family with a novel biallelic missense variant of the ALKBH8 gene: A study on the clinical and variant spectrum of ALKBH8‐related intellectual developmental disorders 2024 ·American Journal of Medical Genetics Part A ·Mustafa Yılmaz, (unknown), Kerem Teralı, Alper Han Çebi, (unknown)	4
3	Primary Immunodeficiencies in Children Initially Admitted with Gastrointestinal/Liver Manifestations 2023 ·Pediatric Gastroenterology Hepatology & Nutrition ·Murat Çakır, (unknown), (unknown), (unknown), (unknown), Alper Han Çebi, Fazıl Orhan	2
4	Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome 2023 ·Clinical and Translational Science ·Kerem Teralı, (unknown), (unknown), Alper Han Çebi	1
5	Genotype/Phenotype Correlation of Cases with <i>PTPN11</i> Gene Mutation: Eastern Black Sea Experience 2022 ·(unknown), Alper Han Çebi, (unknown), (unknown)	0
6	Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency 2022 ·Journal of Assisted Reproduction and Genetics ·(unknown), (unknown), (unknown), Bilgen Bilge Geçkinli, (unknown), (unknown), (unknown), Alper Han Çebi, (unknown), (unknown), Pınar Ata, Ahmet Arman	12
7	Genetic Landscape of <b><i>SCN1A</i></b> Variants in a Turkish Cohort with GEFS+ Spectrum and Dravet Syndrome 2022 ·Molecular Syndromology ·(unknown), (unknown), (unknown), Alper Han Çebi	2
8	Molecular characterization of Turkish patients with demyelinating Charcot-Marie-Tooth disease 2022 ·Neurogenetics ·(unknown), (unknown), (unknown), (unknown), (unknown), Alper Han Çebi, Yasemin Akın	1
9	De novo Pure Partial Trisomy 6p Associated with Facial Dysmorphism, Developmental Delay, Brain Anomalies, and Primary Congenital Hypothyroidism 2022 ·Molecular Syndromology ·(unknown), (unknown), Alper Han Çebi, Elif Acar Arslan, Gülay Karagüzel	2
10	Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in <b><i>ASPM</i></b> and <b><i>WDR62</i></b> Genes 2022 ·Molecular Syndromology ·Hilmi Bolat, (unknown), (unknown), Alper Han Çebi, Yasemin Akın, Hüseyin Önay, Ferda Özkınay, Gül Ünsel‐Bolat	2
11	Early onset congenital diarrheas; single center experience 2021 ·Pediatrics & Neonatology ·Murat Çakır, (unknown), (unknown), (unknown), (unknown), Alper Han Çebi, Thomas Müller, (unknown), Andreas Janecke	2
12	Structural Characteristics in the γ Chain Variants Associated with Fibrinogen Storage Disease Suggest the Underlying Pathogenic Mechanism 2020 ·International Journal of Molecular Sciences ·(unknown), Emanuele Bellacchio, (unknown), Alper Han Çebi, (unknown), (unknown), Güldal Yılmaz, (unknown), Murat Çakır, Francesco Callea	13
13	MicroRNA Expression Levels in Patients with Hashimoto Thyroiditis: A Single Centre Study 2020 ·Endocrine Metabolic & Immune Disorders - Drug Targets ·(unknown), Alper Han Çebi, Mustafa Koçak, Halil Önder Ersöz, Mevlit Íkbal	3
14	Plasma microRNA levels in childhood IgA vasculitis 2020 ·Clinical Rheumatology ·Alper Han Çebi, Ferhat Demir, Mevlit Íkbal, Mukaddes Kalyoncu	2
15	Extending the Phenotypic Spectrum of Huntington Disease: Hypothermia 2020 ·Molecular Syndromology ·(unknown), (unknown), Alper Han Çebi	2
16	Application of Chromosome Microarray Analysis in the Investigation of Developmental Disabilities and Congenital Anomalies: Single Center Experience and Review of <b><i>NRXN3</i></b> and <b><i>NEDD4L</i></b> Deletions 2020 ·Molecular Syndromology ·Alper Han Çebi, (unknown)	5
17	IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease 2019 ·SHILAP Revista de lepidopterología ·(unknown), Hamdi Cihan Emeksiz, (unknown), Alper Han Çebi, (unknown), (unknown)	2
18	Evaluation of plasma microRNA expressions in patients with juvenile idiopathic arthritis 2018 ·Clinical Rheumatology ·Ferhat Demir, Alper Han Çebi, Mukaddes Kalyoncu	14
19	IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease 2018 ·Jornal de Pediatria ·(unknown), Hamdi Cihan Emeksiz, (unknown), Alper Han Çebi, (unknown), (unknown)	9
20	The evaluation of genotoxic potential of ornidazole, nitroimidazole, in lymphocyte culture of patients with amebiasis 2011 ·Drug and Chemical Toxicology ·Mevlit Íkbal, Gürdal Yılmaz, (unknown), (unknown), Alper Han Çebi	10

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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