Samira Ait-El-Mkadem

1.2k citations

14 papers · 374 indexed · h-index 10

Clinical Biochemistry top 10%
- Metabolism and Genetic Disorders 5
Neurology
- Amyotrophic Lateral Sclerosis Research 2
Cell Biology
- Endoplasmic Reticulum Stress and Disease 2
Neurology
- Amyotrophic Lateral Sclerosis Research 2
Molecular Biology
- Mitochondrial Function and Pathology 10
- RNA modifications and cancer 4
- ATP Synthase and ATPases Research 3
- Glycosylation and Glycoproteins Research 1
Genetics
- Genomics and Rare Diseases 1

Co-authors: Véronique Paquis‐Flucklinger Annabelle Chaussenot Sylvie Bannwarth Konstantina Fragaki Cécile Rouzier Valérie Serre Raymond Mengual Jean‐Ehrland Ricci
Cited by: Clinical Biochemistry Neurology Cell Biology
Journals: Human Molecular Genetics (1 paper)Fertility and Sterility (1 paper)Neurobiology of Aging (1 paper)
Partner nations: France United Kingdom Martinique

In The Last Decade

Samira Ait-El-Mkadem

14 papers receiving 370 citations

Peers

Countries citing papers authored by Samira Ait-El-Mkadem

Since Specialization

Citations

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

Fields of papers citing papers by Samira Ait-El-Mkadem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samira Ait-El-Mkadem. 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 Samira Ait-El-Mkadem. The network helps show where Samira Ait-El-Mkadem may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Samira Ait-El-Mkadem, 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 Samira Ait-El-Mkadem Line = papers co-authored together Samira Ait-El-Mkadem links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work
1	Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives Frontiers in Molecular Biosciences ·Justine Labory,Morgane Fierville,Samira Ait-El-Mkadem,Sylvie Bannwarth,Véronique Paquis‐Flucklinger,Silvia Bottini	2020	20
2	Single‐fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases Human Mutation ·Elamine Zereg,Annabelle Chaussenot,Godeliève Morel,Sylvie Bannwarth,Sabrina Sacconi,Marie‐Hélène Soriani,Shahram Attarian,Aline Cano,Jean Pouget,Rémi Bellance,Christine Tranchant,Béatrice Lannes,A. Maues de Paula,Samira Ait-El-Mkadem,B. Chafino,Mathieu Berthet,Konstantina Fragaki,Véronique Paquis‐Flucklinger,Cécile Rouzier	2020	4
3	NDUFS6 related Leigh syndrome: a case report and review of the literature Journal of Human Genetics ·Cécile Rouzier,Annabelle Chaussenot,Konstantina Fragaki,Valérie Serre,Samira Ait-El-Mkadem,Christian Richelme,Véronique Paquis‐Flucklinger,Sylvie Bannwarth	2019	12
4	Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases BMC Medical Genetics ·Morgane Plutino,Annabelle Chaussenot,Cécile Rouzier,Samira Ait-El-Mkadem,Konstantina Fragaki,Véronique Paquis‐Flucklinger,Sylvie Bannwarth	2018	19
5	MT-CYB deletion in an encephalomyopathy with hyperintensity of middle cerebellar peduncles Neurology Genetics ·Annabelle Chaussenot,Cécile Rouzier,Konstantina Fragaki,Sabrina Sacconi,Samira Ait-El-Mkadem,Véronique Paquis‐Flucklinger,Sylvie Bannwarth	2018	5
6	A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions Human Molecular Genetics ·Cécile Rouzier,David Moore,Cécile Delorme,Sandra Lacas‐Gervais,Samira Ait-El-Mkadem,Konstantina Fragaki,Florence Burté,Valérie Serre,Sylvie Bannwarth,Annabelle Chaussenot,Martin Catala,Patrick Yu‐Wai‐Man,Véronique Paquis‐Flucklinger	2017	52
7	Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes Biological Research ·Konstantina Fragaki,Annabelle Chaussenot,Jean‐François Benoist,Samira Ait-El-Mkadem,Sylvie Bannwarth,Cécile Rouzier,Charlotte Cochaud,Véronique Paquis‐Flucklinger	2016	16
8	A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibers Neuromuscular Disorders ·Godeliève Morel,Sylvie Bannwarth,Annabelle Chaussenot,Aline Cano,Konstantina Fragaki,Samira Ait-El-Mkadem,Cécile Rouzier,A. Maues de Paula,B. Chabrol,Véronique Paquis‐Flucklinger	2016	4
9	CHCHD10-Related Disorders Samira Ait-El-Mkadem,Annabelle Chaussenot,Sylvie Bannwarth,Cécile Rouzier,Véronique Paquis‐Flucklinger	2015	2
10	Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients Neurobiology of Aging ·Annabelle Chaussenot,Isabelle Le Ber,Samira Ait-El-Mkadem,Agnès Camuzat,Anne de Septenville,Sylvie Bannwarth,Emmanuelle C. Genin,Valérie Serre,Gaëlle Augé,Alexis Brice,Jean Pouget,Véronique Paquis‐Flucklinger	2014	68
11	Mutation update and uncommon phenotypes in a French cohort of 96 patients with WFS1‐related disorders Clinical Genetics ·Annabelle Chaussenot,Cécile Rouzier,M.P. Quéré,Morgane Plutino,Samira Ait-El-Mkadem,Sylvie Bannwarth,M. Barth,Hélène Dollfus,Perrine Charles,Marc Nicolino,B. Chabrol,B. Vialettes,Véronique Paquis‐Flucklinger	2014	35
12	Quantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort European Journal of Human Genetics ·Cécile Rouzier,Annabelle Chaussenot,Valérie Serre,Konstantina Fragaki,Sylvie Bannwarth,Samira Ait-El-Mkadem,Shahram Attarian,Elsa Kaphan,Aline Cano,Émilien Delmont,Sabrina Sacconi,Bénédicte Mousson de Camaret,Marlène Rio,Anne-Sophie Lèbre,Claude Jardel,Romain Deschamps,Christian Richelme,Jean Pouget,B. Chabrol,Véronique Paquis‐Flucklinger	2013	28
13	Refractory epilepsy and mitochondrial dysfunction due to GM3 synthase deficiency European Journal of Human Genetics ·Konstantina Fragaki,Samira Ait-El-Mkadem,Annabelle Chaussenot,Catherine Gire,Raymond Mengual,Laurent Bonesso,Marie Bénéteau,Jean‐Ehrland Ricci,Valérie Desquiret‐Dumas,Vincent Procaccio,Agnès Rötig,Véronique Paquis‐Flucklinger	2012	98
14	Association of insulin receptor genetic variants with polycystic ovary syndrome in a population of women from Central Europe Fertility and Sterility ·Felicia A. Hanzu,Serban Radian,Redha Attaoua,Samira Ait-El-Mkadem,Simona Fica,Monica Livia Gheorghiu,M. Coculescu,Florin Grigorescu	2010	11

About Samira Ait-El-Mkadem

Samira Ait-El-Mkadem is a scholar working on Clinical Biochemistry, Molecular Biology and Neurology, having authored 14 papers that have together received 374 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (5 papers), RNA modifications and cancer (4 papers), ATP Synthase and ATPases Research (3 papers), Endoplasmic Reticulum Stress and Disease (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Glycosylation and Glycoproteins Research (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Clinical Biochemistry (66 citations), Neurology (40 citations) and Cell Biology (75 citations). Samira Ait-El-Mkadem has collaborated with scholars based in France, United Kingdom and Martinique. Frequent co-authors include Véronique Paquis‐Flucklinger, Annabelle Chaussenot, Sylvie Bannwarth, Konstantina Fragaki, Cécile Rouzier, Valérie Serre, Raymond Mengual, Jean‐Ehrland Ricci, Vincent Procaccio and Valérie Desquiret‐Dumas. Their work appears in journals such as Human Molecular Genetics, Fertility and Sterility and Neurobiology of Aging.

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