Murat Sincan

2.4k total citations
28 papers, 574 citations indexed

About

Murat Sincan is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Murat Sincan has authored 28 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Cancer Research. Recurrent topics in Murat Sincan's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). Murat Sincan is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (5 papers) and Cancer Genomics and Diagnostics (4 papers). Murat Sincan collaborates with scholars based in United States, Türkiye and United Kingdom. Murat Sincan's co-authors include Cornelius F. Boerkoel, William A. Gahl, David R. Adams, Thomas C. Markello, Camilo Toro, Payal Verma, Cynthia J. Tifft, Ulaş Bağcı, Denise K. Liberton and Janice S. Lee and has published in prestigious journals such as Circulation, Neurology and IEEE Transactions on Medical Imaging.

In The Last Decade

Murat Sincan

25 papers receiving 565 citations

Peers

Countries citing papers authored by Murat Sincan

Since Specialization

Citations

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

Fields of papers citing papers by Murat Sincan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Murat Sincan

This figure shows the co-authorship network connecting the top 25 collaborators of Murat Sincan. A scholar is included among the top collaborators of Murat Sincan 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 Murat Sincan. Murat Sincan 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	Racial and Ethnic Inequities at the Practice and Physician Levels in Timely Next-Generation Sequencing for Patients With Advanced Non–Small-Cell Lung Cancer Treated in the US Community Setting 2024 ·JCO Oncology Practice ·Gregory A. Vidal, Neha Jain, Aaron Fisher, Daniel Sheinson, Katherine T Lofgren, Esprit Ma, Elaine Yu, Leah A. Comment, Rebecca A. Miksad, Murat Sincan, (unknown), Richard Zuniga, Davey B. Daniel	3
2	Enabling the clinical application of artificial intelligence in genomics: a perspective of the AMIA Genomics and Translational Bioinformatics Workgroup 2023 ·Journal of the American Medical Informatics Association ·Nephi Walton, (unknown), Chen Wang, Murat Sincan, Robert R. Freimuth, David B. Everman, (unknown), (unknown), Dominick J. Lemas, Panayiotis V. Benos, Alexander V. Alekseyenko, Qianqian Song, Ece D. Gamsiz Uzun, Casey Overby Taylor, Alper Uzun, Thomas N. Person, Nadav Rappoport, Zhongming Zhao, Marc S. Williams	7
3	Abstract 12277: Concordance of High Polygenic CAD Risk Score With High Coronary Artery Calcium Score & Low Polygenic CAD Risk Score With Low Coronary Artery Calcium Score: A Real World Experience 2021 ·Circulation ·(unknown), (unknown), (unknown), Catherine Hajek, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Kevin Coy, Michael Herman, Murat Sincan, Adam Styŝ, (unknown), Tomasz Styŝ	1
4	Deep Geodesic Learning for Segmentation and Anatomical Landmarking 2018 ·IEEE Transactions on Medical Imaging ·(unknown), Denise K. Liberton, Payal Verma, Murat Sincan, Janice S. Lee, Ulaş Bağcı	97
5	Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience 2016 ·Genetics in Medicine ·(unknown), Karen Xu, (unknown), Amanda E. Links, (unknown), David R. Adams, Elise D. Flynn, Elise Valkanas, (unknown), Cynthia J. Tifft, Cornelius F. Boerkoel, William A. Gahl, Murat Sincan	12
6	The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience 2014 ·Genetics in Medicine ·(unknown), Murat Sincan, Thomas C. Markello, David R. Adams, Fred A. Gill, Rena A. Godfrey, Gretchen Golas, Catherine Groden, Dennis M.D. Landis, Michele Nehrebecky, Grace Park, Ariane Soldatos, Cynthia J. Tifft, Camilo Toro, Colleen E. Wahl, Lynne A. Wolfe, William A. Gahl, Cornelius F. Boerkoel	49
7	Developing genomic knowledge bases and databases to support clinical management: current perspectives 2014 ·Pharmacogenomics and Personalized Medicine ·Vojtech Huser, Murat Sincan, James J. Cimino	14
8	Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation 2013 ·European Journal of Human Genetics ·Cristina Dias, (unknown), Murat Sincan, Rosemarie Rupps, Thomas C. Markello, Ramona Salvarinova, (unknown), Kamal Menghrajani, (unknown), Darren Sutherland, Edgardo S. Fortuno, Tobias R. Kollmann, Michelle Demos, Jan M. Friedman, David P. Speert, William A. Gahl, Cornelius F. Boerkoel	11
9	VAR-MD: A tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance 2012 ·Human Mutation ·Murat Sincan, Dimitre R. Simeonov, David R. Adams, Thomas C. Markello, Tyler Mark Pierson, Camilo Toro, William A. Gahl, Cornelius F. Boerkoel	25
10	An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia 2012 ·Human Mutation ·Cristina Dias, Murat Sincan, Praveen F. Cherukuri, Rosemarie Rupps, Yan Huang, Hannah Briemberg, Kathryn Selby, James C. Mullikin, Thomas C. Markello, David R. Adams, William A. Gahl, Cornelius F. Boerkoel	22
11	Detecting false-positive signals in exome sequencing 2012 ·Human Mutation ·(unknown), David R. Adams, (unknown), Christopher E. Mason, Murat Sincan, Cynthia J. Tifft, Camilo Toro, Cornelius F. Boerkoel, William A. Gahl, Thomas C. Markello	100
12	Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM ₁ -gangliosidosis 2012 ·Neurology ·Tyler Mark Pierson, David A. Adams, Thomas C. Markello, Gretchen Golas, Sandra Yang, Murat Sincan, Dimitre R. Simeonov, Karin Fuentes Fajardo, Nancy F. Hansen, Praveen F. Cherukuri, Pedro Cruz, Jamie K. Teer, James C. Mullikin, (unknown), Cornelius F. Boerkoel, William A. Gahl, Cynthia J. Tifft	23
13	Analysis of DNA sequence variants detected by high-throughput sequencing 2012 ·Human Mutation ·David R. Adams, Murat Sincan, Karin Fuentes Fajardo, James C. Mullikin, Tyler Mark Pierson, Camilo Toro, Cornelius F. Boerkoel, Cynthia J. Tifft, William A. Gahl, Tom Markello	25
14	Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration 2011 ·European Journal of Human Genetics ·(unknown), Tyler Mark Pierson, Dimitre R. Simeonov, Murat Sincan, David A. Adams, Thomas C. Markello, Gretchen Golas, (unknown), Nancy F. Hansen, Praveen F. Cherukuri, Pedro Cruz, (unknown), Cynthia J. Tifft, Cornelius F. Boerkoel, William A. Gahl	44
15	Personalized genomic medicine: Lessons from the exome 2011 ·Molecular Genetics and Metabolism ·Benjamin D. Solomon, Daniel Pineda‐Alvarez, Donald W. Hadley, NISC Comparative Sequencing Program, Jamie K. Teer, Praveen F. Cherukuri, Nancy F. Hansen, Pedro Cruz, Alice Young, Robert W. Blakesley, Brendan C. Lanpher, (unknown), Murat Sincan, Settara C. Chandrasekharappa, James C. Mullikin	11
16	Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution function 2011 ·Molecular Genetics and Metabolism ·Thomas C. Markello, Hannah Carlson-Donohoe, Murat Sincan, David R. Adams, David M. Bodine, Jason E. Farrar, Adrianna Vlachos, Jeffrey M. Lipton, Arleen D. Auerbach, Elaine A. Ostrander, Settara C. Chandrasekharappa, Cornelius F. Boerkoel, William A. Gahl	17
17	Assessing hospital information systems processes: A validation of prise information systems success model in healthcare 2008 ·Journal of the Association for Information Systems ·Sevgi Özkan, (unknown), Murat Sincan	2
18	TIP FAKÜLTELERİNDE KLİNİK ÖNCESİ DÖNEMDE ARAŞTIRMA EĞİTİM 2007 ·DergiPark (Istanbul University) ·Sevgi Turan, Murat Sincan, Melih Elçin, (unknown), İskender Sayek	1
19	Statement on Reporting of Evaluation Studies in Health Informatics 2007 ·Jan Talmon, Elske Ammenwerth, Jytte Brender, Nicolette F. de Keizer, Pirkko Nykänen, Michael Rigby, Jos Aarts, Petra Knaup, Zahra Niazkhani, Christian Nøhr, (unknown), Rainer Röhrig, Murat Sincan, (unknown), Johanna Westbrook, Jeremy C Wyatt	15
20	Kanıta Dayalı Tıp ve Tıp Kütüphaneciliği 2003 ·Bilgi Dünyası ·Murat Sincan	0

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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