Ilham Ratbi

1.5k citations

45 papers · 629 · h-index 15

Impact in

Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders
Cardiology and Cardiovascular Medicine top 10%
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies

Papers in

Molecular Biology 21
- RNA modifications and cancer 5
- Muscle Physiology and Disorders 3
- Mitochondrial Function and Pathology 3
Genetics 12
- Neurogenetic and Muscular Disorders Research 6
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 3
- Genetic Syndromes and Imprinting 3

Co-authors: Abdelaziz Sefiani (41 shared papers)Jaber Lyahyai (12 shared papers)Siham Chafai Elalaoui (11 shared papers)Amina Barkat (4 shared papers)Connie R. Bezzina (3 shared papers)Mariëlle Alders (2 shared papers)Arthur van den Wijngaard (1 shared paper)Arthur A.M. Wilde (1 shared paper)
Journals: European Journal of Medical Genetics (2 papers)Clinica Chimica Acta (1 paper)Gene (1 paper)BMC Genetics (1 paper)International Journal of Pediatric Otorhinolaryngology (1 paper)
Partner nations: Morocco France Netherlands

In The Last Decade

Ilham Ratbi

44 papers receiving 620 citations

Peers

Countries citing papers authored by Ilham Ratbi

Since Specialization

Citations

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

Fields of papers citing papers by Ilham Ratbi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Ilham Ratbi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Ilham Ratbi Line = papers co-authored together Ilham Ratbi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 45 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence Journal of the American College of Cardiology ·Roos F. Marsman, Julien Barc, Leander Beekman, Mariëlle Alders, Dennis Dooijes, Arthur van den Wijngaard, Ilham Ratbi, Abdelaziz Sefiani, Zahurul A. Bhuiyan, Arthur A.M. Wilde, Connie R. Bezzina	2013	114
2	Exome sequencing reveals a novel Moroccan founder mutation inSLC19A3as a new cause of early-childhood fatal Leigh syndrome Brain ·Mike Gerards, Rick Kamps, Jo van Oevelen, Iris Boesten, Eveline Jongen, Bart de Koning, H.R. Scholte, Isabel de Angst, Kees Schoonderwoerd, Abdelaziz Sefiani, Ilham Ratbi, Wouter Coppieters, Latifa Karim, I.F.M. de Coo, Bianca van den Bosch, Hubert J.M. Smeets	2013	69
3	Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling Human Reproduction ·Ilham Ratbi, Marie Legendre, Florence Niel, Josiane Martin, Jean-Claude Soufir, Vincent Izard, Bruno Costes, Cathérine Costa, Michel Goossens, Emmanuelle Girodon	2007	50
4	Non lethal Raine syndrome and differential diagnosis European Journal of Medical Genetics ·Siham Chafai Elalaoui, Nada Al-Sheqaih, Ilham Ratbi, Jill Urquhart, James O’Sullivan, Sanjeev S. Bhaskar, (unknown), Mustapha Elalloussi, Jaber Lyahyai, L. Sbihi, Imane Cherkaoui Jaouad, Abdelhafid Sbihi, William G. Newman, Abdelaziz Sefiani	2016	35
5	Rarely occurring mutation of ACVR1 gene in Moroccan patient with fibrodysplasia ossificans progressiva Clinical Rheumatology ·Ilham Ratbi, Renata Borcciadi, Asmâa Regragui, Roberto Ravazzolo, Abdelaziz Sefiani	2009	29
6	Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1variants in Moroccan population BMC Genetics ·Soukaina Guaoua, Ilham Ratbi, Fatima Zahra Laarabi, Siham Chafai Elalaoui, Imane Cherkaoui Jaouad, Amina Barkat, Abdelaziz Sefiani	2014	28
7	Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene European Journal of Medical Genetics ·Ilham Ratbi, Imane Cherkaoui Jaouad, Hamza ELORCH, Nada Al-Sheqaih, Mustapha Elalloussi, Jaber Lyahyai, A. Berraho, William G. Newman, Abdelaziz Sefiani	2016	22
8	Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns Genetic Testing and Molecular Biomarkers ·Jaber Lyahyai, Aziza Sbiti, Amina Barkat, Ilham Ratbi, Abdelaziz Sefiani	2011	21
9	Carrier Frequency of the c.525delT Mutation in the SGCG Gene and Estimated Prevalence of Limb Girdle Muscular Dystrophy Type 2C Among the Moroccan Population Genetic Testing and Molecular Biomarkers ·F. El Kerch, Ilham Ratbi, Aziza Sbiti, Fatima Zahra Laarabi, Amina Barkat, Abdelaziz Sefiani	2014	20
10	Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European Journal of Human Genetics ·Najim Lahrouchi, Elisabeth M. Lodder, Maria Mansouri, Rafik Tadros, Layla Zniber, Najlae Adadi, Sally‐Ann B. Clur, Karin Y. van Spaendonck‐Zwarts, Alex V. Postma, Abdelaziz Sefiani, Ilham Ratbi, Connie R. Bezzina	2017	20
11	High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast–ovarian cancer prevention and control BMC Research Notes ·Fatima Zahra Laarabi, Ilham Ratbi, Siham Chafai Elalaoui, Loubna Mezzouar, Yassamine Doubaj, Laila Bouguenouch, Karim Ouldim, Noureddine Benjaafar, Abdelaziz Sefiani	2017	18
12	Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies Nucleic Acids Research ·Petros Papadopoulos, Emmanouil Viennas, Vassiliki Gkantouna, Cristiana Pavlidis, Marina Bartsakoulia, Zafeiria-Marina Ioannou, Ilham Ratbi, Abdelaziz Sefiani, John Tsaknakis, Konstantinos Poulas, Giannis Tzimas, George P. Patrinos	2013	18
13	First application of next-generation sequencing in Moroccan breast/ovarian cancer families and report of a novel frameshift mutation of the BRCA1 gene Oncology Letters ·Farah Jouali, Fatima Zahra Laarabi, Nabila Marchoudi, Ilham Ratbi, Siham Chafai Elalaoui, Houria Rhaissi, Jamal Fekkak, Abdelaziz Sefiani	2016	17
14	Cystic fibrosis carrier frequency and estimated prevalence of the disease in Morocco Journal of Cystic Fibrosis ·Ilham Ratbi, Emmanuelle Génin, Marie Legendre, Annick Le Floch, Cathérine Costa, Souad Cherkaoui-Deqqaqi, Michel Goossens, Abdelaziz Sefiani, Emmanuelle Girodon	2008	15
15	A Novel Mutation in the Endothelin B Receptor Gene in a Moroccan Family with Shah-Waardenburg Syndrome Molecular Syndromology ·Yassamine Doubaj, Véronique Pingault, Siham Chafai Elalaoui, Ilham Ratbi, M.M. Azouz, Hicham Zerhouni, Fouad Ettayebi, Abdelaziz Sefiani	2015	14
16	Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene Current Research in Translational Medicine ·Lamia Boualla, Wafaa Jdioui, Kenza Soulami, Ilham Ratbi, Abdelaziz Sefiani	2016	13
17	Marfanoid habitus is a nonspecific feature of Perrault syndrome Clinical Dysmorphology ·Maria Zerkaoui, Leigh Demain, Imane Cherkaoui Jaouad, Ilham Ratbi, K. Amjoud, Jill Urquhart, James O’Sullivan, William G. Newman, Abdelaziz Sefiani	2017	10
18	Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients Gene ·Iman Hama, Ilham Ratbi, S. Reggoug, Fatiha Elkerch, G Kharrasse, I. Errabih, H. Ouazzani, Abdelaziz Sefiani	2012	10
19	Novel nonsense mutation of BRCA2 gene in a Moroccan man with familial breast cancer African Health Sciences ·Soukaina Guaoua, Ilham Ratbi, Jaber Lyahyai, SC El Alaoui, Fatima Zahra Laarabi, Abdelaziz Sefiani	2014	9
20	NAT2 Genotypes in Moroccan Patients with Hepatotoxicity Due to Antituberculosis Drugs Genetic Testing and Molecular Biomarkers ·Soukaina Guaoua, Ilham Ratbi, Omaima El Bouazzi, Sanaa Hammi, Amina Tebaa, Jamal Eddine Bourkadi, Rachida Soulaymani Bencheikh, Abdelaziz Sefiani	2016	9

About Ilham Ratbi

Ilham Ratbi is a scholar working on Molecular Biology, Genetics, Genetics, Pulmonary and Respiratory Medicine and Cardiology and Cardiovascular Medicine, having authored 45 papers that have together received 629 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (6 papers), RNA modifications and cancer (5 papers), Muscle Physiology and Disorders (3 papers), BRCA gene mutations in cancer (3 papers), Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers), Mitochondrial Function and Pathology (3 papers) and Cystic Fibrosis Research Advances (3 papers). The work is most often cited by research in Clinical Biochemistry (59 citations), Cardiology and Cardiovascular Medicine (115 citations), Rheumatology (73 citations), Genetics (49 citations) and Genetics (135 citations). Ilham Ratbi has collaborated with scholars based in Morocco, France and Netherlands. Frequent co-authors include Abdelaziz Sefiani, Jaber Lyahyai, Siham Chafai Elalaoui, Amina Barkat, Connie R. Bezzina, Mariëlle Alders, Arthur van den Wijngaard, Arthur A.M. Wilde, Imane Cherkaoui Jaouad and Leander Beekman. Their work appears in journals such as European Journal of Medical Genetics, Clinica Chimica Acta, Gene, BMC Genetics and International Journal of Pediatric Otorhinolaryngology.

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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