Noman Kadhom

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

About

Noman Kadhom is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Noman Kadhom has authored 10 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 2 papers in Biochemistry. Recurrent topics in Noman Kadhom's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (3 papers). Noman Kadhom is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (3 papers). Noman Kadhom collaborates with scholars based in France, Israel and Canada. Noman Kadhom's co-authors include Arnold Münnich, Pierre Rustin, Dominique Chrétien, Agnès Rötig, Vanna Géromel, Gustav Dallner, Lars Ernster, Eeva‐Liisa Appelkvist, Patrick Edery and Laurence Colleaux and has published in prestigious journals such as The Lancet, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Noman Kadhom

10 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.

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

2009 294 citations Sarah Boissel, Orit Reish et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Noman Kadhom

Since Specialization

Citations

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

Fields of papers citing papers by Noman Kadhom

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Noman Kadhom

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations breakdown → 2009 ·The American Journal of Human Genetics ·Sarah Boissel, Orit Reish, Karine Proulx, (unknown), Barbara Sedgwick, Giles S.H. Yeo, Stephen Eyre, Christelle Golzio, Florence Molinari, Noman Kadhom, Heather Etchevers, Vladimı́r Saudek, I. Sadaf Farooqi, Philippe Froguel, Tomas Lindahl, Stephen O’Rahilly, Arnold Münnich, Laurence Colleaux	294
2	A novel mutation of the NDUFS7 gene leads to activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome 2007 ·Molecular Genetics and Metabolism ·Sophie Lebon, Limor Minai, Dominique Chrétien, (unknown), Valérie Serre, Noman Kadhom, Julie Steffann, (unknown), Arnold Münnich, Jean‐Paul Bonnefont, Agnès Rötig	39
3	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy 2005 ·The American Journal of Human Genetics ·Florence Molinari, Annick Raas‐Rothschild, Marlène Rio, Giuseppe Fiermonte, Férechté Encha‐Razavi, Luigi Palmieri, Ferdinando Palmieri, Ziva Ben‐Neriah, Noman Kadhom, Michel Vekemans, Tania Attié‐Bitach, Arnold Münnich, Pierre Rustin, Laurence Colleaux	115
4	A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of α-ketoglutarate dehydrogenase deficiency 2005 ·Human Mutation ·Marie‐Hélène Odièvre, Dominique Chrétien, Arnold Münnich, Brian H. Robinson, (unknown), (unknown), Noman Kadhom, Agnès Rötig, Pierre Rustin, Jean‐Paul Bonnefont	69
5	Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome 2003 ·Human Genetics ·Paule Bénit, Julie Steffann, Sophie Lebon, Dominique Chrétien, Noman Kadhom, Pascale de Lonlay, Alice Goldenberg, Yves Dumez, Marc Dommergues, Pierre Rustin, Arnold Münnich, Agnès Rötig	53
6	Correlation between genotype, metabolic data, and clinical presentation in carnitine palmitoyltransferase 2 (CPT2) deficiency 2003 ·Human Mutation ·Laure Thuillier, Hidayeth Rostane, (unknown), France Demaugre, M. Brivet, Noman Kadhom, Carina Prip‐Buus, Stéphanie Gobin, Jean‐Marie Saudubray, Jean‐Paul Bonnefont	80
7	A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure 2001 ·Nature Genetics ·Pascale de Lonlay, Isabelle Valnot, Antoni Barrientos, Marina S. Gorbatyuk, Alexander Tzagoloff, Jan‐Willem Taanman, Emmanuel Benayoun, Dominique Chrétien, Noman Kadhom, Anne Lombès, Hélène Ogier de Baulny, Patrick Niaudet, Arnold Münnich, Pierre Rustin, Agnès Rötig	232
8	Molecular and Enzymatic Characterization of a Unique Carnitine Palmitoyltransferase 1A Mutation in the Hutterite Community 2001 ·Molecular Genetics and Metabolism ·Carina Prip‐Buus, Laure Thuillier, (unknown), Chitra Prasad, Louise A. Dilling, (unknown), France Demaugre, Cheryl R. Greenberg, James C. Haworth, (unknown), Noman Kadhom, Stéphanie Gobin, P. Kamoun, Jean Girard, Jean‐Paul Bonnefont	47
9	Human cultured skin fibroblasts survive profound inherited ubiquinone depletion 2001 ·Free Radical Research ·Vanna Géromel, Noman Kadhom, Irène Ceballos-Picot, Dominique Chrétien, Arnold Münnich, Agnès Rötig, Pierre Rustin	16
10	Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency 2000 ·The Lancet ·Agnès Rötig, Eeva‐Liisa Appelkvist, Vanna Géromel, Dominique Chrétien, Noman Kadhom, Patrick Edery, (unknown), Gustav Dallner, Arnold Münnich, Lars Ernster, Pierre Rustin	286

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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