Mahmut Şamil Sağıroğlu

1.0k total citations
31 papers, 492 citations indexed

About

Mahmut Şamil Sağıroğlu is a scholar working on Molecular Biology, Genetics and Artificial Intelligence. According to data from OpenAlex, Mahmut Şamil Sağıroğlu has authored 31 papers receiving a total of 492 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Artificial Intelligence. Recurrent topics in Mahmut Şamil Sağıroğlu's work include Genomics and Rare Diseases (5 papers), Genomics and Phylogenetic Studies (5 papers) and Cancer Genomics and Diagnostics (4 papers). Mahmut Şamil Sağıroğlu is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomics and Phylogenetic Studies (5 papers) and Cancer Genomics and Diagnostics (4 papers). Mahmut Şamil Sağıroğlu collaborates with scholars based in Türkiye, United States and Colombia. Mahmut Şamil Sağıroğlu's co-authors include Aytül Erçi̇l, Mete Akgün, Bayram Yüksel, Bekir Ergüner, Burcu Bakır-Güngör, Buğra Özer, Zehra Ölçer, Yıldız Uludağ, Orçun Haçarız and Can Alkan and has published in prestigious journals such as Bioinformatics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Mahmut Şamil Sağıroğlu

30 papers receiving 477 citations

Peers

Countries citing papers authored by Mahmut Şamil Sağıroğlu

Since Specialization

Citations

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

Fields of papers citing papers by Mahmut Şamil Sağıroğlu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mahmut Şamil Sağıroğlu. 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 Mahmut Şamil Sağıroğlu. The network helps show where Mahmut Şamil Sağıroğlu may publish in the future.

Co-authorship network of co-authors of Mahmut Şamil Sağıroğlu

This figure shows the co-authorship network connecting the top 25 collaborators of Mahmut Şamil Sağıroğlu. A scholar is included among the top collaborators of Mahmut Şamil Sağıroğlu 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 Mahmut Şamil Sağıroğlu. Mahmut Şamil Sağıroğlu 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	Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span 2018 ·Brain and Development ·(unknown), Emrah Yücesan, Dilek Yalnızoğlu, Kader Karlı Oğuz, Mahmut Şamil Sağıroğlu, Uğur Özbek, (unknown), Başar Bılgıç, Sevim Erdem‐Özdamar, Sı̇bel Aylı̇n Uğur İşerı̇, Haşmet Hanağası, Hakan Gürvıt, Rıza Köksal Özgül, Ali Dursun	9
2	A further family of Stromme syndrome carrying CENPF mutation 2017 ·American Journal of Medical Genetics Part A ·Ferda Özkınay, Tahir Atık, (unknown), (unknown), Mahmut Şamil Sağıroğlu, (unknown), (unknown), Hüseyin Önay	10
3	SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from Turkey 2017 ·Neurological Sciences ·Emrah Yücesan, Sı̇bel Aylı̇n Uğur İşerı̇, Başar Bılgıç, (unknown), Burcu Bakır-Güngör, (unknown), Özkan Özdemir, Mahmut Şamil Sağıroğlu, Hakan Gürvıt, Haşmet Hanağası, Uğur Özbek	6
4	Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease 2017 ·Neuromuscular Disorders ·(unknown), (unknown), (unknown), (unknown), Hacer Durmuş, Bekir Ergüner, Hüseyin Demirci, Mahmut Şamil Sağıroğlu, Yeşim Parman, Feza Deymeer, Hülya Yılmaz, Sadrettin Pençe, Can Ebru Bekircan‐Kurt, Ersin Tan, Sevim Erdem‐Özdamar, Duran Üstek, Urs Giger, Oğuz Öztürk, Piraye Oflazer	10
5	A patient with mitochondrial disorder due to a novel mutation in MRPS22 2017 ·Metabolic Brain Disease ·Mustafa Kılıç, (unknown), Esra KAYA KILIÇ, Deniz Yüksel, Hüseyin Demirci, Mahmut Şamil Sağıroğlu, (unknown), Rıza Köksal Özgül	10
6	A System Architecture for Efficient Transmission of Massive DNA Sequencing Data 2017 ·Journal of Computational Biology ·Mahmut Şamil Sağıroğlu, (unknown)	1
7	A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family 2015 ·Epilepsy Research ·(unknown), (unknown), Mustafa Çalık, (unknown), Mahmut Şamil Sağıroğlu, (unknown), Bayram Yüksel, Betül Baykan, Nerses Bebek, Akın İşcan, Sı̇bel Aylı̇n Uğur İşerı̇, Uğur Özbek	9
8	Privacy preserving processing of genomic data: A survey 2015 ·Journal of Biomedical Informatics ·Mete Akgün, (unknown), Buğra Özer, Mahmut Şamil Sağıroğlu	46
9	Comparative transcriptome profiling approach to glean virulence and immunomodulation-related genes of Fasciola hepatica 2015 ·BMC Genomics ·Orçun Haçarız, Mete Akgün, (unknown), Bayram Yüksel, Mahmut Şamil Sağıroğlu	15
10	NovelPOC1Amutation in primordial dwarfism reveals new insights for centriole biogenesis 2015 ·Human Molecular Genetics ·Asuman Koparır, Ömer Faruk Karataş, (unknown), Bayram Yüksel, (unknown), (unknown), Mahmut Şamil Sağıroğlu, Alper Gezdirici, (unknown), (unknown), Arzu Karabay, Chad J. Creighton, Adnan Yüksel, Mustafa Özen	26
11	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
12	Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene 2015 ·Journal of Human Genetics ·Fatih Bayraklı, Hatice Gamze Poyrazoğlu, (unknown), Cengiz Yakıcıer, Bekir Ergüner, Mahmut Şamil Sağıroğlu, (unknown), Buğra Özer, Selim Doğanay, Bahattin Tanrıkulu, Aşkın Şeker, (unknown), Ali Çağlar Özen, Hüseyin Per, Sefer Kumandaş, Yasemin Altuner Torun, Yaşar Bayri, (unknown), Adnan Dağçınar, Ibrahim M. Ziyal	17
13	GeneCOST: a novel scoring-based prioritization framework for identifying disease causing genes 2015 ·Bioinformatics ·Buğra Özer, Mahmut Şamil Sağıroğlu, Hüseyin Demirci	2
14	Robustness of Massively Parallel Sequencing Platforms 2015 ·PLoS ONE ·(unknown), Bayram Yüksel, (unknown), (unknown), Tunga Güngör, Faraz Hach, S. Cenk Şahinalp, (unknown), Can Alkan, Mahmut Şamil Sağıroğlu	2
15	Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair 2014 ·Journal of Medical Genetics ·(unknown), Bekir Ergüner, Mahmut Şamil Sağıroğlu, Bayram Yüksel, Onur Emre Onat, Can Alkan, Tayfun Özçelık	38
16	Design and characterisation of a thin-film electrode array with shared reference/counter electrodes for electrochemical detection 2014 ·Biosensors and Bioelectronics ·Yıldız Uludağ, Zehra Ölçer, Mahmut Şamil Sağıroğlu	31
17	Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype 2013 ·BMC Genetics ·Fatih Bayraklı, Bülent Güçlü, Cengiz Yakıcıer, Hatice Balaban, (unknown), Bekir Ergüner, Mahmut Şamil Sağıroğlu, (unknown), (unknown), (unknown), (unknown), (unknown)	42
18	Automated Assembly Problem Using an FFT Based Matching Approach 2006 ·Mahmut Şamil Sağıroğlu, Aytül Erçi̇l	1
19	A Texture Based Matching Approach for Automated Assembly of Puzzles 2006 ·Mahmut Şamil Sağıroğlu, Aytül Erçi̇l	56
20	A texture based approach to reconstruction of archaeological finds 2005 ·Mahmut Şamil Sağıroğlu, Aytül Erçi̇l	21

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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