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I. Sermet · SciRah

Researcher profile · Semantic Scholar

I. Sermet

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I. Sermet — researcher profile on SciRah

h-index: 18
Works: 52
Citations: 1,853

Most-cited papers

Recommendations for the classification of diseases as CFTR-related disorders.
C. Bombieri, M. Claustres, K. De Boeck, N. Derichs +29 more
2011Journal of Cystic Fibrosis409 citations Open access
Semantic Scholar
Defining DIOS and Constipation in Cystic Fibrosis With a Multicentre Study on the Incidence, Characteristics, and Treatment of DIOS
R. Houwen, H. V. D. van der Doef, I. Sermet, A. Munck +6 more
2010Journal of Pediatric Gastroenterology and Nutrition - JPGN179 citations
Semantic Scholar
Lung clearance index: evidence for use in clinical trials in cystic fibrosis.
L. Kent, P. Reix, J. Innes, S. Zielen +14 more
2014Journal of Cystic Fibrosis175 citations Open access
Semantic Scholar
Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis.
E. Bismuth, K. Laborde, P. Taupin, G. Velho +7 more
2008Jornal de Pediatria151 citations
Semantic Scholar
New clinical diagnostic procedures for cystic fibrosis in Europe.
K. De Boeck, N. Derichs, Isabelle Fajac, H. D. de Jonge +9 more
2011Journal of Cystic Fibrosis112 citations Open access
Semantic Scholar
A European consensus for the evaluation and management of infants with an equivocal diagnosis following newborn screening for cystic fibrosis.
S. Mayell, A. Munck, J. Craig, I. Sermet +4 more
2009Journal of Cystic Fibrosis112 citations Open access
Semantic Scholar
Comparing Mycobacterium massiliense and Mycobacterium abscessus lung infections in cystic fibrosis patients.
A. Roux, É. Catherinot, Nathalie Soismier, B. Heym +15 more
2015Journal of Cystic Fibrosis90 citations Open access
Semantic Scholar
Follow-up of 452 totally implantable vascular devices in cystic fibrosis patients
A. Munck, S. Malbezin, J. Bloch, M. Gerardin +6 more
2004European Respiratory Journal80 citations Open access
Semantic Scholar
Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis
C. Goubau, M. Wilschanski, V. Skalická, P. Lebecque +9 more
2009Thorax77 citations Open access
Semantic Scholar
Effectiveness of bacteriophages in the sputum of cystic fibrosis patients.
E. Saussereau, I. Vachier, R. Chiron, B. Godbert +7 more
2014Clinical Microbiology and Infection65 citations Open access
Semantic Scholar
Standards of care for CFTR variant-specific therapy (including modulators) for people with cystic fibrosis.
K. Southern, C. Castellani, E. Lammertyn, A. Smyth +38 more
2022Journal of Cystic Fibrosis63 citations Open access
Semantic Scholar
Therapeutic Approaches for Patients with Cystic Fibrosis Not Eligible for Current CFTR Modulators
I. Fajac, I. Sermet
2021Cells56 citations Open access
Semantic Scholar
Nasal polyposis and cystic fibrosis(CF): review of the literature.
M. Feuillet-Fieux, G. Lenoir, I. Sermet, C. Elie +7 more
2011Rhinology38 citations Open access
Semantic Scholar
A new large CFTR rearrangement illustrates the importance of searching for complex alleles
Florence Niel, M. Legendre, Thierry Bienvenu, E. Bieth +11 more
2006Human Mutation34 citations Open access
Semantic Scholar
Clinimetric properties of bronchoalveolar lavage inflammatory markers in cystic fibrosis
M. Fayon, L. Kent, S. Bui, L. Dupont +1 more
2013European Respiratory Journal28 citations Open access
Semantic Scholar
Guideline on the design and conduct of cystic fibrosis clinical trials: the European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN).
K. De Boeck, V. Bulteel, H. Tiddens, Thomas O. F. Wagner +8 more
2011Journal of Cystic Fibrosis28 citations Open access
Semantic Scholar
Exhaled nitric oxide in cystic fibrosis: relationships with airway and lung vascular impairments
D. Hubert, F. Aubourg, B. Fauroux, L. Trinquart +7 more
2009European Respiratory Journal25 citations Open access
Semantic Scholar
Suboptimal Ciprofloxacin Dosing as a Potential Cause of Decreased Pseudomonas aeruginosa Susceptibility in Children with Cystic Fibrosis
Emmanuelle Guillot, I. Sermet, A. Ferroni, S. Chhun +3 more
2010Pharmacotherapy20 citations
Semantic Scholar
Novel CFTR mutations in black cystic fibrosis patients
M. N. Feuillet-Fieux, M. Ferrec, N. Gigarel, Laure Thuillier +4 more
2004Clinical Genetics18 citations
Semantic Scholar
Isolation, cultivation, and application of primary respiratory epithelial cells obtained by nasal brushing, polyp samples, or lung explants
A. Golec, I. Pranke, P. Scudieri, K. Hayes +6 more
2022STAR Protocols16 citations Open access
Semantic Scholar
Glutathione S-transferases related to P. aeruginosa lung infection in cystic fibrosis children: preliminary study.
M. Feuillet-Fieux, T. Nguyen-Khoa, M. Loriot, M. Kelly +7 more
2009Clinical Biochemistry16 citations
Semantic Scholar
Is the raised volume rapid thoracic compression technique ready for use in clinical trials in infants with cystic fibrosis?
S. Matecki, L. Kent, K. De Boeck, M. Le Bourgeois +7 more
2016Journal of Cystic Fibrosis14 citations Open access
Semantic Scholar
Lung transplantation in childhood and adolescence: unicentric 14-year experience with sex matching as the main prognosticator.
Giuseppe Mangiameli, A. Arame, V. Boussaud, T. Petitti +10 more
2016European Journal of Cardio-Thoracic Surgery13 citations Open access
Semantic Scholar
Defining DIOS and constipation in cystic fibrosis: a multicenter study on the incidence characteristics and treatment of DIOS
H. van der Doer, R. Houwen, I. Sermet, A. Munck +6 more
200810 citations Open access
Semantic Scholar
Urgent lung transplantation in cystic fibrosis patients: experience of a French center.
M. Saueressig, S. Pelluau, I. Sermet, R. Souilamas
2011European Journal of Cardio-Thoracic Surgery9 citations Open access
Semantic Scholar
Influence of perfusate temperature on nasal potential difference
I. Bronsveld, F. Vermeulen, Dorotha Sands, T. Leal +8 more
2012European Respiratory Journal7 citations Open access
Semantic Scholar
Pharmacokinetics and Diffusion into Sputum of Oseltamivir and Oseltamivir Carboxylate in Adults with Cystic Fibrosis
V. Jullien, D. Hubert, O. Launay, G. Babany +2 more
2011Antimicrobial Agents and Chemotherapy6 citations Open access
Semantic Scholar
Nasal polyposis and cystic fibrosis: review of literature and case report
M. Feuillet-Fieux, Gérard Lenoir, I. Sermet, C. Elie +7 more
20101 citations Open access
Semantic Scholar
S1334 Defining Distal Intestinal Obstruction Syndrome (DIOS) and Constipation in Cystic Fibrosis: A Multicenter Study On the Incidence, Characteristics and Treatment of DIOS
R. Houwen, H. V. D. van der Doef, I. Sermet, A. Munck +6 more
20081 citations
Semantic Scholar
A French collaborative study indicative of a very low classical-CF penetrance of R117H; implications for genetic counselling
C. Thauvin-Robinet, A. Munck, F. Huet, G. Bellis +20 more
20081 citations Open access
Semantic Scholar
Identification of a novel mutation, 1087delT, in exon 7 of the CFTR gene in a patient with cystic fibrosis
M. Feuillet-Fieux, I. Sermet, A. Edelman, Tania Torossi +5 more
2000Human Mutation1 citations Open access
Semantic Scholar
EPS2.01 Hear my voice: research by and with children with cystic fibrosis
S. Caldani, E. Devouche, É. Cappe, I. Sermet +1 more
2023Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
689 Pharmacological chaperones improve intradomain stability and interdomain assembly via distinct binding sites to rescue misfolded cystic fibrosis transmembrane conductance regulator
N. Baatallah, A. Elbahnsi, J. Mornon, B. Chevalier +8 more
2022Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
673 Elexacaftor/tezacaftor/ivacaftor corrects function of H1085R-, N1303K-, and R334W-cystic fibrosis transmembrane conductance regulator and improves clinical status of patients
I. Pranke, E. Dréano, A. Hatton, A. Lepissier +8 more
2022Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
P205 Patient-reported outcome measures in the current context of new generation modulator therapies in cystic fibrosis
K. Hayes, E. Lammertyn, H. de Keyser, T. Havermans +2 more
20210 citations Open access
Semantic Scholar
ePS5.08 “Il faut continuer à poser des questions/We must continue to ask questions.” Patient-reported outcomes in cystic fibrosis: a qualitative study of patients with cystic fibrosis and their caregivers
K. Hayes, I. Sermet, V. Bontemps, P. de Carli +4 more
20200 citations Open access
Semantic Scholar
ePS5.01 Patient reported outcome measures used in clinical practice: an ECFS CTN and CF Europe survey
K. Hayes, E. Lammertyn, H. de Keyser, P. de Carli +1 more
2020Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
WS09.5 Penetrance is a critical parameter for assessing the disease liability of CFTR variants
A. Boussaroque, M. Audrézet, C. Raynal, I. Sermet +7 more
2020Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
WS04.4 Guidance on the use of sputum biomarkers to monitor treatment response and act as trial outcomes in cystic fibrosis
A. Lepissier, C. Addy, D. Downey, K. Hayes +1 more
20200 citations Open access
Semantic Scholar
P012 CFTR-NGS, an expanded version of the CFTR-France database for the interpretation of whole CFTR next generation sequencing data
C. Bareil, S. Sasorith, C. Lemattre, J. Ducharlet +13 more
2019Journal of Cystic Fibrosis0 citations Open access
Semantic Scholar
138 Sampling and processing for Pseudomonas aeruginosa identification across ECFS-CTN sites: Standardisation of clinical practice is important for patient selection for research studies
M. Denton, L. Kent, I. Sermet, G. Taccetti
20130 citations Open access
Semantic Scholar
184 Determinants of nontuberculous mycobacteria eradication in cystic fibrosis
L. Coupet, A. Prevotat, S. Dominique, G. Rault +8 more
20130 citations Open access
Semantic Scholar
Reply to Anile et al.
M. Saueressig, S. Pelluau, I. Sermet, R. Souilamas
20120 citations
Semantic Scholar
Universal Protocol for Nasal Potential Difference Studies: Results of An International Multi-center Clinical Trial
G. Solomon, M. Konstan, M. Wilschanski, J. Billings +10 more
20090 citations
Semantic Scholar
CF pediatric lung transplantation single center experience
R. Souilamas, R. Guillemain, V. Boussaud, C. Amrein +6 more
20080 citations Open access
Semantic Scholar
Chronic sinusitis in CF child carrying two missense mutations S519G and G576A in the NBF1 domain of CFTR
M. Feuillet-Fieux, J. Bonnefont, M. Ferrec, I. Sermet +2 more
20080 citations Open access
Semantic Scholar
[Cervical tumefaction in a teenager with cystic fibrosis].
S. Vrielynck, C. Roques, I. Sermet, S. Emond +1 more
2007Archives de pédiatrie0 citations
Semantic Scholar
168* Combined lung and liver transplantation in cystic fibrosis
R. Souilamas, Gérard Lenoir, I. Sermet, D. Dusser +6 more
20070 citations Open access
Semantic Scholar
067 - The presence of proteinase 3 at the plasma membrane after apoptosis decreased the rate of phagocytosis by macrophages: a new pro-inflammatory role of membrane proteinase 3 in CF neutrophils
C. Kantari, M. Pederzoli, S. Moriceau, I. Sermet +2 more
20060 citations
Semantic Scholar
Mucoviscidose : y a-t-il des alternatives aux thérapies géniques ?
J. Lallemand, B. Leclaire, I. Sermet, G. Lenoir
20050 citations Open access
Semantic Scholar

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