Isam Naom

1.7k total citations · 1 hit paper
18 papers, 1.2k citations indexed

About

Isam Naom is a scholar working on Molecular Biology, Cell Biology and Immunology and Allergy. According to data from OpenAlex, Isam Naom has authored 18 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 5 papers in Cell Biology and 5 papers in Immunology and Allergy. Recurrent topics in Isam Naom's work include Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (5 papers) and Adipose Tissue and Metabolism (4 papers). Isam Naom is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Cell Adhesion Molecules Research (5 papers) and Adipose Tissue and Metabolism (4 papers). Isam Naom collaborates with scholars based in United Kingdom, Türkiye and France. Isam Naom's co-authors include Christopher G. Mathew, Caroline A. Sewry, Gilles Thomas, Victor Dubowitz, Jane M. Olson, Marianne Orholm, Jean‐Pierre Hugot, Jean‐Frédéric Colombel, Corinne Gower‐Rousseau and Jean Weissenbach and has published in prestigious journals such as Nature, The Lancet and Nucleic Acids Research.

In The Last Decade

Isam Naom

18 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

1996 727 citations Jean‐Pierre Hugot, Pierre Laurent‐Puig et al. Nature profile →

Peers

Countries citing papers authored by Isam Naom

Since Specialization

Citations

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

Fields of papers citing papers by Isam Naom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isam Naom

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiency 2002 ·Neuromuscular Disorders ·Federica Deodato, Mario Sabatelli, Enzo Ricci, Eugenio Mercuri, Francesco Muntoni, Caroline A. Sewry, Isam Naom, P. Tonali, F Guzzetta	35
2	Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42 2000 ·The American Journal of Human Genetics ·Martin Brockington, Caroline A. Sewry, R. Herrmann, Isam Naom, Andrew Dearlove, Michael D. Rhodes, Haluk Topaloğlu, Victor Dubowitz, (unknown), Francesco Muntoni	56
3	Mutations in the laminin α2-chain gene in two children with early-onset muscular dystrophy 2000 ·Brain ·Isam Naom, Mariella D’Alessandro, Caroline A. Sewry, Philip Jardine, Alessandra Ferlini, Timothy J. M. Moss, Victor Dubowitz, Francesco Muntoni	22
4	Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status 1999 ·Neuromuscular Disorders ·Eugenio Mercuri, (unknown), J. Philpot, (unknown), Serena J. Counsell, Sheila Henderson, (unknown), Isam Naom, Graeme M. Bydder, Victor Dubowitz, Francesco Muntoni	27
5	Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndrome 1999 ·Neuromuscular Disorders ·Behzad Moghadaszadeh, Haluk Topaloğlu, Luciano Merlini, Francesco Muntoni, B. Estournet, Caroline A. Sewry, Isam Naom, A Barois, Michel Fardeau, F.M.S. Tomé, Pascale Guicheney	21
6	Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy? 1999 ·Human Genetics ·Mariella D’Alessandro, Isam Naom, Alessandra Ferlini, Caroline A. Sewry, Victor Dubowitz, Francesco Muntoni	3
7	Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy 1998 ·Neuromuscular Disorders ·Isam Naom, Mariella D’Alessandro, Caroline A. Sewry, J. Philpot, A. Manzur, Victor Dubowitz, Francesco Muntoni	43
8	An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary α2 laminin deficiency unlinked to the LAMA2 locus on 6q22 1998 ·European Journal of Paediatric Neurology ·Francesco Muntoni, Jacqueline Taylor, Caroline A. Sewry, Isam Naom, Victor Dubowitz	19
9	The role of immunocytochemistry and linkage analysis in the prenatal diagnosis of merosin-deficient congenital muscular dystrophy 1997 ·Human Genetics ·Isam Naom, Mariella D’Alessandro, Caroline A. Sewry, Alessandra Ferlini, Haluk Topaloğlu, A. Leclerc, Pascale Guicheney, Ketty Schwartz, Zühal Akçören, Victor Dubowitz, Francesco Muntoni	11
10	Prenatal diagnosis in merosin-deficient congenital muscular dystrophy 1997 ·Neuromuscular Disorders ·Isam Naom, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	14
11	Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency 1997 ·Neuromuscular Disorders ·Ersin Tan, Haluk Topaloğlu, Caroline A. Sewry, Yaşar Zorlu, Isam Naom, Sevim Erdem‐Özdamar, Mariella D’Alessandro, Francesco Muntoni, Victor Dubowitz	59
12	Expression of Laminin Chains in Skin in Merosin-Deficient Congenital Muscular Dystrophy 1997 ·Neuropediatrics ·(unknown), Mariella D’Alessandro, Leslie Wilson, Lydia Sorokin, Isam Naom, Savino Bruno, Alessandra Ferlini, Victor Dubowitz, Francesco Muntoni	25
13	Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy. 1997 ·Journal of Medical Genetics ·Isam Naom, Mariella D’Alessandro, Haluk Topaloğlu, Caroline A. Sewry, Alessandra Ferlini, A. Leclerc, Pascale Guicheney, J. Weissenbach, K Schwartz, Kate Bushby, J. Philpot, Victor Dubowitz, Francesco Muntoni	33
14	Mapping of a susceptibility locus for Crohn's disease on chromosome 16 breakdown → 1996 ·Nature ·Jean‐Pierre Hugot, Pierre Laurent‐Puig, Corinne Gower‐Rousseau, Jane M. Olson, John C. Lee, Laurent Beaugerie, Isam Naom, Jean‐Louis Dupas, A. Van Gossum, (unknown), Marianne Orholm, Catherine Bonaïti‐Pellié, Jean Weissenbach, Christopher G. Mathew, John Edward Lennard-Jones, Antoine Cortot, Jean‐Frédéric Colombel, Gilles Thomas	727
15	Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy 1996 ·The Lancet ·Caroline A. Sewry, J. Philpot, (unknown), Isam Naom, (unknown), Mariella D’Alessandro, Victor Dubowitz, Francesco Muntoni, Lydia Sorokin	52
16	Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel disease. 1996 ·PubMed ·Isam Naom, (unknown), (unknown), Simon Bowman, Jerry S. Lanchbury, (unknown), S V Hodgson, Douglas F. Easton, J E Lennard‐Jones, Christopher G. Mathew	30
17	Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2. 1995 ·PubMed ·A. Leclerc, Haluk Topaloğlu, (unknown), C. Sewry, Gàbor Gyapay, Isam Naom, Francesco Muntoni, (unknown), A Barois, B. Estournet	30
18	Molecular organization ofsbcC, a gene that affects genetic recombination and the viability of DNA palindromes inEscherichia coliK-12 1989 ·Nucleic Acids Research ·Isam Naom, (unknown), David R. F. Leach, Robert G. Lloyd	35

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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