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M. Roussey · SciRah

Researcher profile · Semantic Scholar

M. Roussey

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M. Roussey — researcher profile on SciRah

h-index: 29
Works: 199
Citations: 2,422

Most-cited papers

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening
C. Thauvin-Robinet, A. Munck, F. Huet, E. Genin +41 more
2009Journal of Medical Genetics121 citations Open access
Semantic Scholar
Influence of interleukin-10 on Aspergillus fumigatus infection in patients with cystic fibrosis.
J. Brouard, N. Knauer, P. Boelle, H. Corvol +14 more
2005Journal of Infectious Diseases119 citations
Semantic Scholar
Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: A 10‐year retrospective study in a French region (Brittany)
D. Siret, G. Bretaudeau, B. Branger, A. Dabadie +8 more
2003Pediatric Pulmonology104 citations
Semantic Scholar
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.
V. Scotet, M. de Braekeleer, M. Roussey, G. Rault +14 more
2000The Lancet103 citations
Semantic Scholar
Subtle health impairment and socioeducational attainment in young adult patients with congenital hypothyroidism diagnosed by neonatal screening: a longitudinal population-based cohort study.
J. Léger, E. Écosse, M. Roussey, J. Lanöe +1 more
2011Journal of Clinical Endocrinology and Metabolism88 citations
Semantic Scholar
Combining immunoreactive trypsinogen and pancreatitis-associated protein assays, a method of newborn screening for cystic fibrosis that avoids DNA analysis.
J. Sarles, P. Berthézène, C. Le Louarn, C. Somma +8 more
2005Jornal de Pediatria87 citations
Semantic Scholar
Whole-body post-mortem computed tomography compared with autopsy in the investigation of unexpected death in infants and children
M. Proisy, A. Marchand, P. Loget, R. Bouvet +6 more
2013European Radiology86 citations
Semantic Scholar
Efficiency of neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency in children born in mainland France between 1996 and 2003.
B. Coulm, J. Coste, V. Tardy, E. Écosse +3 more
2012Archives of Pediatrics & Adolescent Medicine78 citations Open access
Semantic Scholar
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
I. Sermet-Gaudelus, E. Girodon, D. Sands, Nathalie Stremmler +18 more
2010American Journal of Respiratory and Critical Care Medicine77 citations
Semantic Scholar
Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis.
Y. Barry, C. Bonaldi, V. Goulet, R. Coutant +5 more
2016Annals of Epidemiology74 citations
Semantic Scholar
Microbiologic contamination study of nebulizers after aerosol therapy in patients with cystic fibrosis.
S. Vassal, R. Taamma, N. Marty, A. Sardet +13 more
2000American Journal of Infection Control72 citations
Semantic Scholar
Liver disease in pediatric patients with cystic fibrosis is associated with glutathione S‐transferase P1 polymorphism
A. Henrion-Caude, C. Flamant, M. Roussey, C. Housset +5 more
2002Hepatology69 citations Open access
Semantic Scholar
Implementation of the French nationwide cystic fibrosis newborn screening program.
A. Munck, J. Dhondt, C. Sahler, M. Roussey
2008Jornal de Pediatria66 citations
Semantic Scholar
Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France
V. Scotet, I. Duguépéroux, P. Saliou, G. Rault +3 more
2012Orphanet Journal of Rare Diseases64 citations Open access
Semantic Scholar
Psychological effects of false-positive results in cystic fibrosis newborn screening: a two-year follow-up.
J. Beucher, E. Leray, E. Deneuville, M. Roblin +12 more
2010Jornal de Pediatria59 citations
Semantic Scholar
Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis
I. Sermet-Gaudelus, E. Girodon, Delphine Roussel, E. Deneuville +13 more
2010Thorax50 citations
Semantic Scholar
Immunoreactive Trypsin/DNA Newborn Screening for Cystic Fibrosis: Should the R117H Variant Be Included in CFTR Mutation Panels?
V. Scotet, M. Audrézet, M. Roussey, G. Rault +5 more
2006Pediatrics47 citations
Semantic Scholar
Glutathione-S-transferase M1, M3, P1 and T1 polymorphisms and severity of lung disease in children with cystic fibrosis.
C. Flamant, A. Henrion-Caude, P. Böelle, F. Brémont +9 more
2004Pharmacogenetics (London)46 citations
Semantic Scholar
Neonatal screening for cystic fibrosis: comparing the performances of IRT/DNA and IRT/PAP.
J. Sarles, R. Giorgi, P. Berthézène, A. Munck +3 more
2014Journal of Cystic Fibrosis45 citations Open access
Semantic Scholar
Non‐classic cystic fibrosis associated with D1152H CFTR mutation
P. Burgel, Isabelle Fajac, Dominique Hubert, Dominique Grenet +16 more
2010Clinical Genetics44 citations Open access
Semantic Scholar
Blood concentrations of pancreatitis associated protein in neonates: relevance to neonatal screening for cystic fibrosis
J. Sarles, S. Barthellémy, C. Férec, J. Iovanna +8 more
1999Archives of Disease in Childhood: Fetal and Neonatal Edition44 citations Open access
Semantic Scholar
Clinical and economic aspects of newborn screening for severe combined immunodeficiency: DEPISTREC study results.
C. Thomas, I. Durand-zaleski, J. Frenkiel, S. Mirallié +11 more
2019Clinical Immunology42 citations
Semantic Scholar
Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France
V. Scotet, M. Audrézet, M. Roussey, G. Rault +3 more
2003Human Genetics42 citations
Semantic Scholar
Pancreatic enzyme replacement therapy for young cystic fibrosis patients.
A. Munck, J. Duhamel, T. Lamireau, B. Le Luyer +12 more
2009Journal of Cystic Fibrosis38 citations Open access
Semantic Scholar
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
A.-M. Jouanolle, Patricia Fergelot, M. Raoul, G. Gandon +5 more
1998Annales de Genetique38 citations
Semantic Scholar
Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960
V. Scotet, D. Gillet, I. Duguépéroux, M. Audrézet +8 more
2002Human Genetics35 citations
Semantic Scholar
CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders
C. Thauvin-Robinet, A. Munck, F. Huet, A. de Becdelièvre +49 more
2013Journal of Medical Genetics28 citations
Semantic Scholar
Guidelines for the clinical management and follow-up of infants with inconclusive cystic fibrosis diagnosis through newborn screening.
I. Sermet-Gaudelus, J. Brouard, M. Audrézet, L. Kohen +11 more
2017Archives de pédiatrie26 citations
Semantic Scholar
Optimization of the French cystic fibrosis newborn screening programme by a centralized tracking process
A. Munck, D. Delmas, M. Audrézet, L. Lemonnier +2 more
2017Journal of Medical Screening23 citations Open access
Semantic Scholar
Screening to detect permanent childhood hearing impairment in neonates transferred from the newborn nursery.
R. Dauman, M. Roussey, V. Belot, F. Denoyelle +8 more
2009International Journal of Pediatric Otorhinolaryngology23 citations
Semantic Scholar
Neonatal Screening for Cystic Fibrosis in Brittany, France: Assessment of 10 Years’ Experience and Impact on Prenatal Diagnosis
V. Scotet, M. de Braekeleer, M. Roussey, G. Rault +14 more
200122 citations
Semantic Scholar
Formative evaluation to improve prevention of sudden infant death syndrome (SIDS): a prospective study
Amélie Ryckewaert D'Halluin, M. Roussey, B. Branger, A. Venisse +1 more
2011Acta paediatrica16 citations
Semantic Scholar
Role of congenital long-QT syndrome in unexplained sudden infant death: proposal for an electrocardiographic screening in relatives
A. Baruteau, J. Baruteau, Ryad Joomye, R. Martins +5 more
2009European Journal of Pediatrics16 citations
Semantic Scholar
PAP assays in newborn screening for cystic fibrosis: a population-based cost-effectiveness study
V. Séror, C. Cao, M. Roussey, R. Giorgi
2016Journal of Medical Screening15 citations
Semantic Scholar
The importance of sweat testing for older siblings of patients with cystic fibrosis identified by newborn screening.
A. Munck, E. Houssin, M. Roussey
2009Jornal de Pediatria14 citations
Semantic Scholar
[Child protection system: Knowledge and role of the general practitioners in Ille-et-Vilaine].
M. Balençon, A. Arrieta, C.-A. You, J. Brun +2 more
2016Archives de pédiatrie11 citations
Semantic Scholar
Whole-body MR imaging in suspected physical child abuse: comparison with skeletal survey and bone scintigraphy findings from the PEDIMA prospective multicentre study
M. Proisy, P. Vivier, B. Morel, B. Bruneau +125 more
2021European Radiology10 citations
Semantic Scholar
[Indoor fungal exposure: What impact on clinical and biological status regarding Aspergillus during cystic fibrosis].
D. Pricope, E. Deneuville, S. Frain, S. Chevrier +3 more
2015Journal de Mycologie Médicale9 citations
Semantic Scholar
Non-specific post-mortem modifications on whole-body post-mortem computed tomography in sudden unexpected death in infancy
M. Proisy, P. Loget, R. Bouvet, M. Roussey +5 more
20158 citations
Semantic Scholar
[Glomerular nephropathy with IgA mesangium deposits and Crohn disease].
A. Dabadie, S. Gié, S. Taque, J. Babut +1 more
1996Archives de pédiatrie8 citations
Semantic Scholar
[National French guidelines for management of infants with cystic fibrosis].
I. Sermet-Gaudelus, L. Couderc, S. Vrielynck, J. Brouard +11 more
2014Archives de pédiatrie7 citations
Semantic Scholar
[Infants living with their mothers in the Rennes, France, prison for women between 1998 and 2013. Facts and perspectives].
A. Blanchard, L. Bébin, S. Leroux, M. Roussey +5 more
2018Archives de pédiatrie6 citations
Semantic Scholar
Magnetic resonance imaging in Pelizaeus-Merzbacher disease
H. Journel, M. Roussey, Y. Gandon, C. Allaire +2 more
2004Neuroradiology6 citations
Semantic Scholar
[Anemia and limping in a vegetarian adolescent].
R. Chiron, A. Dabadie, V. Gandemer-Delignieres, M. Balençon +2 more
2001Archives de pédiatrie6 citations
Semantic Scholar
Pulmonary Outcome Differences in U.S. and French Cystic Fibrosis Cohorts Diagnosed through Newborn Screening
A. Walsh, G. Rault, Z. Li, V. Scotet +5 more
2009Journal of Cystic Fibrosis5 citations Open access
Semantic Scholar
[Kangaroo mother care: bibliographical review on the current attitudes, their interests and their limits].
T. Dzukou, A. Delapintiere, P. Bétrémieux, G. Vittu +2 more
2004Archives de pédiatrie5 citations
Semantic Scholar
[Adult care centers for patients with cystic fibrosis: prerequisites and practical organization. Cystic Fibrosis Care Centers of Rennes and Lille].
M. Roussey, B. Desrues, D. Turck, T. Pérez +1 more
2000Revue des maladies respiratoires5 citations
Semantic Scholar
Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy
M. Audrézet, A. Munck, V. Scotet, M. Claustres +4 more
2014Genetics in Medicine4 citations Open access
Semantic Scholar
[Can we explain the sudden infant death syndrome? About a series of 80 cases with an autopsy in Rennes University Hospital, France in the period 1994-2007].
C. Saint-Stéban, E. Leray, H. Jouan, P. Loget +2 more
2010Archives de pédiatrie4 citations
Semantic Scholar
[Questions raised and answers provided since the French nationwide cystic fibrosis newborn screening program was initiated].
M. Roussey, A. Munck
2009Archives de pédiatrie3 citations
Semantic Scholar

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M. Audrézet×11
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V. Scotet — researcher profile on SciRah

M. de Braekeleer×5

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