Mohsen Karbasiyan

921 total citations
9 papers, 445 citations indexed

About

Mohsen Karbasiyan is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Mohsen Karbasiyan has authored 9 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Mohsen Karbasiyan's work include Congenital gastrointestinal and neural anomalies (2 papers), Genomics and Rare Diseases (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Mohsen Karbasiyan is often cited by papers focused on Congenital gastrointestinal and neural anomalies (2 papers), Genomics and Rare Diseases (1 paper) and Hearing, Cochlea, Tinnitus, Genetics (1 paper). Mohsen Karbasiyan collaborates with scholars based in Germany, Oman and Austria. Mohsen Karbasiyan's co-authors include André Reis, Joachim Köchling, Anna Rajab, Raymonda Varon, Liza McCann, Simone Spuler, Susanne Lützkendorf, Rita Barresi, Volker Straub and Markus Schuelke and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Mohsen Karbasiyan

9 papers receiving 435 citations

Peers

Countries citing papers authored by Mohsen Karbasiyan

Since Specialization

Citations

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

Fields of papers citing papers by Mohsen Karbasiyan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohsen Karbasiyan

This figure shows the co-authorship network connecting the top 25 collaborators of Mohsen Karbasiyan. A scholar is included among the top collaborators of Mohsen Karbasiyan 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 Mohsen Karbasiyan. Mohsen Karbasiyan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Epigenetic Clock and Relative Telomere Length Represent Largely Different Aspects of Aging in the Berlin Aging Study II (BASE-II) 2018 ·The Journals of Gerontology Series A ·Valentin Max Vetter, Antje Meyer, Mohsen Karbasiyan, Elisabeth Steinhagen‐Thiessen, Werner Hopfenmüller, Ilja Demuth	57
2	Fcγ-Receptor IIIA Polymorphism p.158F Has No Negative Predictive Impact on Rituximab Therapy with and without Sequential Chemotherapy in CD20-Positive Posttransplant Lymphoproliferative Disorder 2014 ·Journal of Immunology Research ·Heiner Zimmermann, (unknown), Jamie P. Nourse, Maher K. Gandhi, Petra Reinke, R. Neuhaus, Mohsen Karbasiyan, Barbara C. Gärtner, Ioannis Anagnostopoulos, Hanno Riess, Ralf Ulrich Trappe, Stephan Oertel	2
3	QF-PCR as a molecular-based method for autosomal aneuploidies detection 2013 ·(unknown), (unknown), (unknown), Raymonda Varon, Christiane Bommer, Mohsen Karbasiyan, Heidemarie Neitzel	1
4	Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP 2011 ·Human Molecular Genetics ·(unknown), Emmanuel Derivery, Hongbo Hu, Masoud Garshasbi, Mohsen Karbasiyan, Marco J. Herold, Gudrun Nürnberg, Reinhard Ullmann, Alexis Gautreau, Karl Sperling, Raymonda Varon, Anna Rajab	62
5	Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations 2010 ·PLoS Genetics ·Anna Rajab, Volker Straub, Liza McCann, Dominik Seelow, Raymonda Varon, Rita Barresi, (unknown), Barbara Lucke, Susanne Lützkendorf, Mohsen Karbasiyan, Sebastian Bachmann, Simone Spuler, Markus Schuelke	181
6	Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia 2006 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Alexander E. Volk, Mohsen Karbasiyan, Alexander Semmler, Unda Todt, Horst Urbach, Thomas Klockgether, Michael Linnebank	10
7	Genetic deafness in a preterm infant with a critical postnatal course 2006 ·Pediatric Critical Care Medicine ·Petra Koehne, (unknown), Elisabeth Walch, Markus Schuelke, Raymonda Varon, Mohsen Karbasiyan, (unknown), Michael Obladen	2
8	Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome 2004 ·The American Journal of Human Genetics ·Hans Christian Hennies, Anita Rauch, Wenke Seifert, (unknown), Elisabeth Moser, (unknown), Gholamali Tariverdian, Krystyńa Chrzańowska, Małgorzata Krajewska‐Walasek, Anna Rajab, Roberto Giugliani, Thomas Neumann, Katja‐Martina Eckl, Mohsen Karbasiyan, André Reis, Denise Horn	55
9	Spectrum of mutations and genotype–phenotype analysis in Currarino syndrome 2001 ·European Journal of Human Genetics ·Joachim Köchling, Mohsen Karbasiyan, André Reis	75

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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