Mahmoud Mansouri

1.0k total citations
21 papers, 522 citations indexed

About

Mahmoud Mansouri is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Mahmoud Mansouri has authored 21 papers receiving a total of 522 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Pathology and Forensic Medicine and 7 papers in Molecular Biology. Recurrent topics in Mahmoud Mansouri's work include Chronic Lymphocytic Leukemia Research (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Mahmoud Mansouri is often cited by papers focused on Chronic Lymphocytic Leukemia Research (10 papers), Lymphoma Diagnosis and Treatment (8 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Mahmoud Mansouri collaborates with scholars based in Sweden, Denmark and Iran. Mahmoud Mansouri's co-authors include Niklas Dahl, Richard Rosenquist, Birgit Carlsson, Jesper Jurlander, Anders Isaksson, Edward J. Davey, Catharina Larsson, Peter Gustavsson, Karl‐Henrik Gustavson and I. White and has published in prestigious journals such as Blood, Human Molecular Genetics and British Journal of Haematology.

In The Last Decade

Mahmoud Mansouri

20 papers receiving 517 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mahmoud Mansouri Sweden 12 211 174 159 116 106 21 522
Maurizio Trubia Italy 16 303 1.4× 80 0.5× 79 0.5× 52 0.4× 104 1.0× 18 615
Timothy M. Chlon United States 17 532 2.5× 106 0.6× 137 0.9× 202 1.7× 42 0.4× 32 936
Adrienne L. Watson United States 14 310 1.5× 70 0.4× 38 0.2× 48 0.4× 59 0.6× 22 663
Silvia De Matteis Italy 8 884 4.2× 174 1.0× 130 0.8× 73 0.6× 40 0.4× 10 1.2k
Sean Young Canada 13 261 1.2× 201 1.2× 55 0.3× 50 0.4× 155 1.5× 27 736
Xingjiang Yu China 14 479 2.3× 63 0.4× 144 0.9× 229 2.0× 24 0.2× 29 801
Stef van Lieshout Netherlands 7 243 1.2× 208 1.2× 34 0.2× 76 0.7× 72 0.7× 11 519
Francesco Acquadro Spain 13 241 1.1× 118 0.7× 60 0.4× 43 0.4× 70 0.7× 19 536
Martine Guillier France 15 388 1.8× 82 0.5× 123 0.8× 60 0.5× 34 0.3× 27 628
Sergei Vatolin United States 11 783 3.7× 228 1.3× 37 0.2× 133 1.1× 39 0.4× 18 901

Countries citing papers authored by Mahmoud Mansouri

Since Specialization
Citations

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

Fields of papers citing papers by Mahmoud Mansouri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mahmoud Mansouri

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

All Works

20 of 20 papers shown
2.
Hosseini, Arezoo, Navid Shomali, Mahmoud Mansouri, et al.. (2021). miR-193a-5p as a promising therapeutic candidate in colorectal cancer by reducing 5-FU and Oxaliplatin chemoresistance by targeting CXCR4. International Immunopharmacology. 92. 107355–107355. 42 indexed citations
3.
Mansouri, Mahmoud, et al.. (2020). Frequency of Hepatitis C Virus Genotypes in Patients Who Had Hepatocellular Carcinoma in Gastroenterological Hospitals of Tabriz. Journal of Gastrointestinal Cancer. 52(1). 145–149. 1 indexed citations
4.
Shanehbandi, Dariush, et al.. (2020). Altered expression levels of miR-212, miR-133b and miR-27a in tongue squamous cell carcinoma (TSCC) with clinicopathological considerations. Gene Reports. 19. 100622–100622. 3 indexed citations
5.
Halldórsdóttir, Anna Margrét, Birgitta Sander, Hanna Göransson, et al.. (2010). High‐resolution genomic screening in mantle cell lymphoma—specific changes correlate with genomic complexity, the proliferation signature and survival. Genes Chromosomes and Cancer. 50(2). 113–121. 19 indexed citations
6.
Marincevic, Millaray, Mahmoud Mansouri, Meena Kanduri, et al.. (2010). Distinct gene expression profiles in subsets of chronic lymphocytic leukemia expressing stereotyped IGHV4-34 B-cell receptors. Haematologica. 95(12). 2072–2079. 25 indexed citations
7.
Marincevic, Millaray, Nicola Cahill, Rebeqa Gunnarsson, et al.. (2010). High-density screening reveals a different spectrum of genomic aberrations in chronic lymphocytic leukemia patients with 'stereotyped' IGHV3-21 and IGHV4-34 B-cell receptors. Haematologica. 95(9). 1519–1525. 28 indexed citations
8.
Crowther-Swanepoel, Dalemari, Mahmoud Mansouri, Anna Enjuanes, et al.. (2010). Verification that common variation at 2q37.1, 6p25.3, 11q24.1, 15q23, and 19q13.32 influences chronic lymphocytic leukaemia risk. British Journal of Haematology. 150(4). 473–479. 30 indexed citations
9.
Mansouri, Mahmoud, et al.. (2010). Recurrent Genomic Aberrations in Chronic Lymphocytic Leukaemia – Implications for Disease Pathogenesis and Prognosis. European Oncology & Haematology. 0(4). 80–80. 2 indexed citations
10.
Gunnarsson, Rebeqa, Anders Isaksson, Mahmoud Mansouri, et al.. (2009). Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: A high-resolution genomic screening in newly diagnosed patients. Lund University Publications (Lund University). 94. 354–354. 1 indexed citations
11.
Mansouri, Mahmoud, Anna Åleskog, Mikael Jondal, et al.. (2009). IGHV3‐21 gene usage is associated with high TCL1 expression in chronic lymphocytic leukemia. European Journal Of Haematology. 84(2). 109–116. 9 indexed citations
12.
Mansouri, Mahmoud, Gerard Tobin, Mikael Jondal, et al.. (2009). Lipoprotein lipase is differentially expressed in prognostic subsets of chronic lymphocytic leukemia but displays invariably low catalytical activity. Leukemia Research. 34(3). 301–306. 30 indexed citations
13.
Kanduri, Meena, Mahmoud Mansouri, Anne Mette Buhl, et al.. (2009). LPL Is the Strongest Prognostic Factor in a Comparative Study of RNA-Based Markers in Chronic Lymphocytic Leukemia.. Blood. 114(22). 1254–1254. 2 indexed citations
14.
Entesarian, Miriam, Birgit Carlsson, Mahmoud Mansouri, et al.. (2009). A chromosome 10 variant with a 12 Mb inversion [inv(10)(q11.22q21.1)] identical by descent and frequent in the Swedish population. American Journal of Medical Genetics Part A. 149A(3). 380–386. 11 indexed citations
15.
Bremer, Anna, MaiBritt Giacobini, Magnus Nordenskjöld, et al.. (2009). Screening for copy number alterations in loci associated with autism spectrum disorders by two‐color multiplex ligation‐dependent probe amplification. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 280–285. 11 indexed citations
16.
Mansouri, Mahmoud, Nicola Cahill, Rebeqa Gunnarsson, et al.. (2009). Lack of association between the MDM2 promoter polymorphism SNP309 and clinical outcome in chronic lymphocytic leukemia. Leukemia Research. 34(3). 335–339. 10 indexed citations
17.
Mansouri, Mahmoud, Jens Schuster, Jitendra Badhai, et al.. (2008). Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Human Molecular Genetics. 17(23). 3776–3783. 99 indexed citations
18.
Gunnarsson, Rebeqa, Johan Staaf, Mattias Jansson, et al.. (2008). Screening for copy‐number alterations and loss of heterozygosity in chronic lymphocytic leukemia—A comparative study of four differently designed, high resolution microarray platforms. Genes Chromosomes and Cancer. 47(8). 697–711. 90 indexed citations
19.
Mansouri, Mahmoud, Birgit Carlsson, Edward J. Davey, et al.. (2006). Molecular genetic analysis of a de novo balanced translocation t(6;17)(p21.31;q11.2) associated with hypospadias and anorectal malformation. Human Genetics. 119(1-2). 162–168. 14 indexed citations
20.
Mansouri, Mahmoud, Lena Marklund, Peter Gustavsson, et al.. (2005). Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation. European Journal of Human Genetics. 13(8). 970–977. 94 indexed citations

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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