Kamran Moradkhani

1.6k total citations
29 papers, 934 citations indexed

About

Kamran Moradkhani is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Kamran Moradkhani has authored 29 papers receiving a total of 934 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 10 papers in Molecular Biology. Recurrent topics in Kamran Moradkhani's work include Hemoglobinopathies and Related Disorders (10 papers), Prenatal Screening and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Kamran Moradkhani is often cited by papers focused on Hemoglobinopathies and Related Disorders (10 papers), Prenatal Screening and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (8 papers). Kamran Moradkhani collaborates with scholars based in France, United States and Netherlands. Kamran Moradkhani's co-authors include Henri Wajcman, Ettore Capoluongo, Bruno Giardina, Cecilia Zuppi, Angelo Minucci, George P. Patrinos, Ross C. Hardison, Marina Bartsakoulia, Belinda Giardine and Webb Miller and has published in prestigious journals such as Nucleic Acids Research, Blood and Human Reproduction.

In The Last Decade

Kamran Moradkhani

29 papers receiving 917 citations

Peers

Countries citing papers authored by Kamran Moradkhani

Since Specialization

Citations

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

Fields of papers citing papers by Kamran Moradkhani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kamran Moradkhani

This figure shows the co-authorship network connecting the top 25 collaborators of Kamran Moradkhani. A scholar is included among the top collaborators of Kamran Moradkhani 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 Kamran Moradkhani. Kamran Moradkhani 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	Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder 2021 ·Clinical Genetics ·Jonathan Lévy, (unknown), Anna Maruani, (unknown), Céline Dupont, Séverine Drunat, (unknown), (unknown), Richard Delorme, (unknown), Bertrand Isidor, Olivier Pichon, Kamran Moradkhani, Alain Verloès, Anne‐Claude Tabet	8
2	Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome 2020 ·European Journal of Medical Genetics ·(unknown), (unknown), Kamran Moradkhani, Olivier Pichon, Sébastien Richard, Madeleine Joubert, Stéphane Bezieau	1
3	Morphokinetic parameters in chromosomal translocation carriers undergoing preimplantation genetic testing 2018 ·Reproductive BioMedicine Online ·Jenna Lammers, Arnaud Reignier, Carole Splingart, Kamran Moradkhani, P. Barrière, Thomas Fréour	5
4	Updates of the HbVar database of human hemoglobin variants and thalassemia mutations 2013 ·Nucleic Acids Research ·Belinda Giardine, Joseph Borg, Emmanouil Viennas, Cristiana Pavlidis, Kamran Moradkhani, Philippe Joly, Marina Bartsakoulia, Cathy Riemer, Webb Miller, Giannis Tzimas, Henri Wajcman, Ross C. Hardison, George P. Patrinos	326
5	Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis 2013 ·Cytogenetic and Genome Research ·Samarth Bhatt, Marina Manvelyan, Kamran Moradkhani, (unknown), Kristin Mrasek, Jacques Puechberty, G. Lefort, P. Sardá, Anja Weise, Thomas Liehr, Franck Pellestor	6
6	Pitfalls in the genetic diagnosis of Hb S 2012 ·Clinical Biochemistry ·Kamran Moradkhani, J. Riou, Henri Wajcman	8
7	Estimation of the difference in HbF expression due to loss of the 5' -globin BCL11A binding region 2012 ·Haematologica ·(unknown), Laure Lecerf, (unknown), Bruno Costes, Kamran Moradkhani, D. Bachir, Frederic Galactéros, Serge Pissard	10
8	Glucose-6-phosphate dehydrogenase (G6PD) mutations database: Review of the “old” and update of the new mutations 2012 ·Blood Cells Molecules and Diseases ·Angelo Minucci, Kamran Moradkhani, (unknown), Cecilia Zuppi, Bruno Giardina, Ettore Capoluongo	207
9	Two new class III G6PD variants [G6PD Tunis (c.920A > C: p.307Gln > Pro) and G6PD Nefza (c.968T > C: p.323 Leu > Pro)] and overview of the spectrum of mutations in Tunisia 2012 ·Blood Cells Molecules and Diseases ·(unknown), Kamran Moradkhani, (unknown), Henri Wajcman, (unknown), (unknown), Salem Abbès, Claude Préhu	14
10	Practical approach for characterization of glucose 6‐phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: Description of seven new G6PD mutants 2011 ·American Journal of Hematology ·Kamran Moradkhani, (unknown), Michel Bahuau, (unknown), Muriel Holder, Serge Pissard, Claude Préhu, Christian Rosé, Henri Wajcman, Frédéric Galactéros	8
11	Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia 2011 ·BMC Research Notes ·Soad K. Al Jaouni, (unknown), Esam I. Azhar, Kamran Moradkhani	18
12	Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants 2008 ·Annals of Hematology ·Kamran Moradkhani, Claude Préhu, John Old, Shirley Henderson, (unknown), Hongyuan Luo, Man‐Chiu Poon, David H.K. Chui, Henri Wajcman, George P. Patrinos	31
13	Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions 2008 ·European Journal of Human Genetics ·Samarth Bhatt, Kamran Moradkhani, Kristin Mrasek, Jacques Puechberty, Marina Manvelyan, (unknown), Geneviève Lefort, Anja Weise, James Lespinasse, Pierre Sarda, Thomas Liehr, S. Hamamah, Franck Pellestor	14
14	An α⁰-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α^3.7Gene 2008 ·Hemoglobin ·Kamran Moradkhani, (unknown), Piero C. Giordano, Henri Wajcman, Claude Préhu	3
15	Disturbance in the HIF-1α pathway associated with erythrocytosis: Further evidences brought by frameshift and nonsense mutations in the prolyl hydroxylase domain protein 2 (PHD2) gene 2007 ·Blood Cells Molecules and Diseases ·(unknown), Kamran Moradkhani, Marc Lopez, Henri Wajcman, Claude Préhu	41
16	Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm 2007 ·Molecular Human Reproduction ·Samarth Bhatt, Kamran Moradkhani, Kristin Mrasek, Jacques Puechberty, G. Lefort, J. Lespinasse, P. Sardá, Thomas Liehr, S. Hamamah, Franck Pellestor	15
17	Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases 2006 ·Human Reproduction ·Kamran Moradkhani, Jacques Puechberty, Samarth Bhatt, Philippe Vago, L. Janny, G. Lefort, S. Hamamah, P. Sardá, Franck Pellestor	19
18	Mosaic trisomy 16 in a fetus: the complex relationship between phenotype and genetic mechanisms 2006 ·Prenatal Diagnosis ·Kamran Moradkhani, Jacques Puechberty, Patricia Blanchet, Christine Coubes, (unknown), (unknown), Geneviève Lefort, Pierre Sarda	9
19	Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report 2006 ·Human Reproduction ·Kamran Moradkhani, Jacques Puechberty, Samarth Bhatt, J. Lespinasse, Philippe Vago, G. Lefort, P. Sardá, S. Hamamah, Franck Pellestor	26
20	Mosaic maternal uniparental isodisomy for chromosome 7q21‐qter 2006 ·Clinical Genetics ·(unknown), (unknown), Nicolas Biteau, (unknown), Laurent Rebouissoux, Kamran Moradkhani, (unknown), Robert Saura, Benoı̂t Arveiler, Didier Lacombe, Laurence Taine, A. Iron	19

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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