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Current Opinion in Pulmonary Medicine|July 12, 2012
Familial forms of nonspecific interstitial pneumonia/idiopathic pulmonary fibrosis: clinical course and genetic backgroundRaphael Borie, Caroline Kannengiesser, Bruno CrestaniNature Reviews. Genetics|June 13, 2019
Somatic genetic rescue in Mendelian haematopoietic diseasesPatrick Revy, Caroline Kannengiesser, Alain FischerNature Reviews. Genetics|September 23, 2022
Genetics of human telomere biology disordersPatrick Revy, Caroline Kannengiesser, Alison A BertuchFEBS Letters|May 20, 2003
Signal-induced ubiquitination of p57(Kip2) is independent of the C-terminal consensus Cdk phosphorylation siteMarie Pierre Leibovitch, Caroline Kannengiesser, Serge Alexandre LeibovitchBlood Cells, Molecules & Diseases|June 26, 2009
Not all DMT1 mutations lead to iron overloadEsther Blanco, Caroline Kannengiesser, Bernard Grandchamp, et al.Current Opinion in Pulmonary Medicine|June 19, 2024
Syndromic genetic causes of pulmonary fibrosisRaphaël Borie, Ibrahima Ba, Marie-Pierre Debray, et al.Seminars in Hematology|April 25, 2026
Genetic aspects of telomere biology disordersSophie de Tocqueville, Helene Morel, Ibrahima Ba, et al.Blood|July 4, 2008
Two nonsense mutations in the TMPRSS6 gene in a patient with microcytic anemia and iron deficiencyFlavia Guillem, Sarah Lawson, Caroline Kannengiesser, et al.Presse Medicale (Paris, France : 1983)|May 22, 2020
Impact of genetic factors on fibrosing interstitial lung diseases. Incidence and clinical presentation in adultsRaphael Borie, Caroline Kannengiesser, Clairelyne Dupin, et al.European Respiratory Review : an Official Journal of the European Respiratory Society|April 28, 2017
Management of suspected monogenic lung fibrosis in a specialised centreRaphael Borie, Caroline Kannengiesser, Flore Sicre de Fontbrune, et al.Pageof 12