A Barois

2.7k citations

75 papers · 1.5k indexed · h-index 21

Impact in

Genetics top 2%
- Neurogenetic and Muscular Disorders Research
Immunology and Allergy top 5%
- Cell Adhesion Molecules Research

Papers in

Medical Terminology 1
Genetics 18
- Neurogenetic and Muscular Disorders Research 17

Co-authors: B. Estournet A. Leclerc F.M.S. Tomé Teresinha Evangelista M Fardeau Y. Sunada Kevin P. Campbell Emilia Manole
Journals: Neuromuscular Disorders (6 papers)Neurology (4 papers)European Journal of Human Genetics (2 papers)Pediatric Pulmonology (2 papers)CHEST Journal (2 papers)
Partner nations: France Australia United Kingdom

In The Last Decade

A Barois

66 papers receiving 1.4k citations

Peers

Countries citing papers authored by A Barois

Since Specialization

Citations

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

Fields of papers citing papers by A Barois

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Whole-Body muscle MRI in a series of patients with congenital myopathy related to TPM2 gene mutations Neuromuscular Disorders ·Mohamed Jarraya, Susana Quijano-Roy, Nicole Monnier, Anthony Béhin, Daniela Avila‐Smirnow, Norma B. Romero, Valérie Allamand, Pascale Richard, A Barois, Adrien May, B. Estournet, Eugenio Mercuri, Pierre G. Carlier, Robert‐Yves Carlier	2012	33
2	Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation European Journal of Human Genetics ·Rabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, A. Bertrand, Catherine Massart, Annachiara De Sandre‐Giovannoli, Juan Cadiñanos, Kamel Mamchaoui, Gillian Butler‐Browne, B. Estournet, Pascale Richard, A Barois, Nicolas Lévy, Gisèle Bonne	2011	36
3	Riluzole pharmacokinetics in young patients with spinal muscular atrophy British Journal of Clinical Pharmacology ·Chadi Abbara, B. Estournet, Lucette Lacomblez, Bénédicte Lelièvre, Rüştü Güner, Blandine Lehmann, Louis Viollet, A Barois, Bertrand Diquet	2010	20
4	Maladie de Jeune (dystrophie thoracique asphyxiante) et insuffisance respiratoire : intérêt de la ventilation précoce par hyperinsufflations périodiques. Bulletin de l Académie Nationale de Médecine ·Martine POUX, A Barois, Brigitte Estournet-Mathiaud, Qian Xu, Christine Ioos	2007	1
5	Amyotrophie spinale infantile Étude multicentrique prospective et longitudinale de 168 cas suivis 4 ans Bulletin de l Académie Nationale de Médecine ·A Barois, M. Mayer, Isabelle Desguerre, B. Chabrol, C. Bérard, Jean‐Marie Cuisset, F. Liu, Chun Mei Xing, Αννα Π. Καφαντάρη, Brigitte Estournet-Mathiaud	2005	20
6	Respiratory Capacity Course in Patients With Infantile Spinal Muscular Atrophy CHEST Journal ·Christine Ioos, И.В. Чижанькова, Subir Mukhopadhyay, A Barois, Brigitte Estournet-Mathiaud	2004	81
7	Refined genetic mapping of autosomal recessive chronic distal spinal muscular atrophy to chromosome 11q13.3 and evidence of linkage disequilibrium in European families European Journal of Human Genetics ·Louis Viollet, Mohammed Zarhrate, Isabelle Maystadt, Carla Viana Cascarelli, A Barois, Isabelle Desguerre, M. Mayer, B. Chabrol, Bruno Leheup, Véronica Cusin, Thierry Billette de Villemeur, Dominique Bonneau, Pascale Saugier-Véber, Ranya Alsumrani, Anne Delaubier, Jay C. McCutcheon, Marc Jeanpierre, D. W. E. Green, Arnold Münnich	2004	12
8	Severe progressive form of congenital muscular dystrophy with calf pseudohypertrophy, macroglossia and respiratory insufficiency Neuromuscular Disorders ·Susana Quijano‐Roy, Lucía Galán, Ana Ferreiro, F. Chéliout-Héraut, Françoise Gray, Michel Fardeau, A Barois, Pascale Guicheney, Norma B. Romero, B. Estournet	2002	20
9	[Respiratory problems in severe scoliosis]. PubMed ·A Barois	1999	24
10	Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency. Radiology ·А. В. Изатулин, Robert Carlier, Jean-Marc Pinard, D. Mompoint, N. A. Estrada-Alfaro, Emmanuel Burdairon, B. Estournet, A Barois, C. Vallée	1998	28
11	ENERGY EXPENDITURE(EE) AND BODY COMPOSITION OF CHILDREN WITH INHERITED NEUROMUSCULAR DISEASE. Journal of Pediatric Gastroenterology and Nutrition ·V. Varille, A Barois, ARLENE DUNN, Muhammad Achail Darwis, Patricia Katz, A Boulier, M. Stiévenard, И В Грибов, J Navarro	1997	1
12	Respiratory problems in spinal muscular atrophies Pediatric Pulmonology ·A Barois, Brigitte Estournet-Mathiaud	1997	19
13	Thoracoabdominal Pattern of Breathing in Neuromuscular Disorders CHEST Journal ·Angela Cristina Calvo, Davi Schilling, ZeleznikSkousen J. D.J. G., A Barois, Jorge Gallego	1996	63
14	Autopsies of sudden infant death syndrome—classification and epidemiology Acta Paediatrica ·F Hatton, M‐H Bouvier‐Colle, A Barois, MC Imbert, Ariane Leroyer, Frédéric Landry, Éric Jougla	1995	15
15	Diaphragmatic paralysis in children: A review of 11 cases Pediatric Pulmonology ·M. Noel, Steef Kurstjens, A Barois	1994	42
16	Ondine's Curse: A Discussion of Five Cases Neuropediatrics ·Ghulam Maulana Ilman, A Randaline, B. Estournet, A Barois	1993	22
17	Ostéoarthrite mycosique du genou avec destruction articulaire traitée par kétoconazole. F. Hervé, E. Drouhet, Benoît Dupont, A Barois, Min-Shin Cho	1983	3
18	[Trial treatment of severe viral hepatitis with hyperbaric oxygenation (apropos of 16 cases)]. PubMed ·M Goulon, M Rapin, A Barois, 捷晃金森, P. H. Boyle, P Gajdos, Paymon Azizi	1971	2
19	Embolies gazeuses probables en cours d'insufflation pour coelioscopie. La Presse Médicale ·M Goulon, Nam Van Le, M Rapin, A Barois, Er Henderson, S Kernbaum	1969	1
20	N'EPHROPATHIE INTERSTITIELLE AIGUUE ET TROUBLES NEUROLOGIQUES AU COURS D'UN TRAITEMENT MASSIF ET PROLONG'E PAR LE M'ETHANE-SULFONATE DE COLISTINE. La Presse Médicale ·M Rapin, P Bagros, Dash Sthitaprajna, A Barois, M Goulon	1965	0

About A Barois

A Barois is a scholar working on Medical Terminology, Genetics, Surgery, Cardiology and Cardiovascular Medicine and Molecular Biology, having authored 75 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (17 papers), Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (8 papers), RNA Research and Splicing (6 papers), Congenital Diaphragmatic Hernia Studies (5 papers), RNA modifications and cancer (5 papers), Respiratory Support and Mechanisms (4 papers) and Nuclear Structure and Function (4 papers). The work is most often cited by research in Genetics (393 citations), Immunology and Allergy (107 citations), Molecular Biology (850 citations), Cardiology and Cardiovascular Medicine (267 citations) and Cellular and Molecular Neuroscience (200 citations). A Barois has collaborated with scholars based in France, Australia and United Kingdom. Frequent co-authors include B. Estournet, A. Leclerc, F.M.S. Tomé, Teresinha Evangelista, M Fardeau, Y. Sunada, Kevin P. Campbell, Emilia Manole, Brigitte Estournet-Mathiaud and Martine Papiernik. Their work appears in journals such as Neuromuscular Disorders, Neurology, European Journal of Human Genetics, Pediatric Pulmonology and CHEST Journal.

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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