Mohammed Selloum

4.1k total citations
22 papers, 724 citations indexed

About

Mohammed Selloum is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Mohammed Selloum has authored 22 papers receiving a total of 724 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Physiology. Recurrent topics in Mohammed Selloum's work include Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (6 papers) and Adipose Tissue and Metabolism (4 papers). Mohammed Selloum is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (6 papers) and Adipose Tissue and Metabolism (4 papers). Mohammed Selloum collaborates with scholars based in France, United States and Netherlands. Mohammed Selloum's co-authors include Johan Auwerx, Marie‐France Champy, Manuel Serrano, Jorge Moscat, Ángeles Durán, Juana M. Flores, Angelina Rodríguez, F. Javier Dı́ez-Guerra, María T. Díaz‐Meco and Claudia Caradec and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Cell Metabolism.

In The Last Decade

Mohammed Selloum

22 papers receiving 716 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammed Selloum France 12 362 189 147 140 93 22 724
Hyang Mi Moon United States 8 448 1.2× 179 0.9× 167 1.1× 89 0.6× 121 1.3× 10 821
Charlotte Lee United States 9 261 0.7× 198 1.0× 178 1.2× 62 0.4× 152 1.6× 13 914
Romina Ficarella Italy 16 345 1.0× 115 0.6× 271 1.8× 80 0.6× 73 0.8× 33 800
Alberto Blázquez Spain 18 750 2.1× 146 0.8× 129 0.9× 141 1.0× 45 0.5× 50 1.1k
Suvi T. Ruohonen Finland 16 245 0.7× 98 0.5× 156 1.1× 74 0.5× 78 0.8× 32 741
Zahra Tanfin France 17 365 1.0× 99 0.5× 143 1.0× 81 0.6× 67 0.7× 36 746
Enrica Torretta Italy 17 440 1.2× 72 0.4× 192 1.3× 57 0.4× 103 1.1× 43 717
Ingrid Masse France 18 355 1.0× 104 0.6× 181 1.2× 46 0.3× 130 1.4× 27 923
Joanne Doran United Kingdom 9 372 1.0× 150 0.8× 98 0.7× 108 0.8× 18 0.2× 11 866
Ohad Shaham Israel 10 638 1.8× 60 0.3× 226 1.5× 110 0.8× 112 1.2× 11 880

Countries citing papers authored by Mohammed Selloum

Since Specialization
Citations

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

Fields of papers citing papers by Mohammed Selloum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammed Selloum

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammed Selloum. A scholar is included among the top collaborators of Mohammed Selloum 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 Mohammed Selloum. Mohammed Selloum 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
1.
Kharouf, Naji, Yvan de Féraudy, Gergő Gógl, et al.. (2024). The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome. Scientific Reports. 14(1). 445–445. 2 indexed citations
2.
Cifuentes-Díaz, Carmen, et al.. (2023). A human dynein heavy chain mutation impacts cortical progenitor cells causing developmental defects, reduced brain size and altered brain architecture. Neurobiology of Disease. 180. 106085–106085. 6 indexed citations
3.
Wagner, Christel, Sylvain Hugel, Ilaria Morella, et al.. (2023). Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein. Genome biology. 24(1). 261–261. 7 indexed citations
4.
Riet, Fabrice, et al.. (2022). Behavioral Testing Design for Evaluation of Cognitive Disabilities. Current Protocols. 2(2). e382–e382. 2 indexed citations
5.
Brault, Véronique, Giovanni Iacono, Marie‐Christine Birling, et al.. (2021). Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome. PLoS Genetics. 17(9). e1009777–e1009777. 25 indexed citations
6.
Lebrun, Nicolas, Chloé Delépine, Mohammed Selloum, et al.. (2021). HDAC inhibitor ameliorates behavioral deficits in Mecp2308/y mouse model of Rett syndrome. Brain Research. 1772. 147670–147670. 11 indexed citations
7.
Naudon, Laurent, Hamid Méziane, Goran Lakisic, et al.. (2020). BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice. PLoS ONE. 15(5). e0232789–e0232789. 6 indexed citations
8.
Collins, Stephan C., Ana Uzquiano, Mohammed Selloum, et al.. (2019). The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia. Journal of Anatomy. 235(3). 637–650. 11 indexed citations
9.
Collins, Stephan C., Ana Uzquiano, Mohammed Selloum, et al.. (2018). The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia. HAL (Le Centre pour la Communication Scientifique Directe). 2 indexed citations
10.
Dubos, Aline, Hamid Méziane, Giovanni Iacono, et al.. (2018). A new mouse model of ARX dup24 recapitulates the patients’ behavioral and fine motor alterations. Human Molecular Genetics. 27(12). 2138–2153. 14 indexed citations
11.
Arbogast, Thomas, Giovanni Iacono, Claire Chevalier, et al.. (2017). Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition. PLoS Genetics. 13(7). e1006886–e1006886. 20 indexed citations
12.
Méziane, Hamid, Malik Khelfaoui, Noemi Morello, et al.. (2016). Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability. Human Molecular Genetics. 25(11). 2314–2323. 29 indexed citations
13.
Méziane, Hamid, Valérie Fraulob, Fabrice Riet, et al.. (2013). The homeodomain factor Gbx1 is required for locomotion and cell specification in the dorsal spinal cord. PeerJ. 1. e142–e142. 6 indexed citations
14.
Blom, Daniël, Ting-Ting Yamin, Marie‐France Champy, et al.. (2010). Altered lipoprotein metabolism in P2Y13 knockout mice. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1801(12). 1349–1360. 38 indexed citations
15.
Derry, Jonathan M.J., Judy Zhong, Cliona Molony, et al.. (2010). Identification of Genes and Networks Driving Cardiovascular and Metabolic Phenotypes in a Mouse F2 Intercross. PLoS ONE. 5(12). e14319–e14319. 36 indexed citations
16.
Selloum, Mohammed, et al.. (2010). Reduced body weight in male Tspan8-deficient mice. International Journal of Obesity. 35(4). 605–617. 23 indexed citations
17.
Champy, Marie‐France, Mohammed Selloum, Claudia Caradec, et al.. (2008). Genetic background determines metabolic phenotypes in the mouse. Mammalian Genome. 19(5). 318–331. 82 indexed citations
18.
Guimond, Alain, Marius Teletin, Erwan Garo, et al.. (2007). Quantitative ultrasonic tissue characterization as a new tool for continuous monitoring of chronic liver remodelling in mice. Liver International. 27(6). 854–864. 25 indexed citations
19.
Rodríguez, Angelina, Ángeles Durán, Mohammed Selloum, et al.. (2006). Mature-onset obesity and insulin resistance in mice deficient in the signaling adapter p62. Cell Metabolism. 3(3). 211–222. 250 indexed citations
20.
Selloum, Mohammed, et al.. (2004). Mouse functional genomics requires standardization of mouse handling and housing conditions. Mammalian Genome. 15(10). 768–783. 97 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Hyang Mi Moon Breakdown of academic impact, for papers by Charlotte Lee Breakdown of academic impact, for papers by Romina Ficarella Breakdown of academic impact, for papers by Alberto Blázquez Breakdown of academic impact, for papers by Suvi T. Ruohonen Breakdown of academic impact, for papers by Zahra Tanfin Breakdown of academic impact, for papers by Enrica Torretta Breakdown of academic impact, for papers by Ingrid Masse Breakdown of academic impact, for papers by Joanne Doran Breakdown of academic impact, for papers by Ohad Shaham
Rankless by CCL
2026