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List of works by Isabelle Bailleul-Forestier

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

scientific article published on 26 October 2015

Caries experience in a severely obese adolescent population

scientific article published on 01 September 2007

Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations

scientific article published in July 2010

Direct Microscopy: A Useful Tool to Diagnose Oral Candidiasis in Children and Adolescents

scientific article published on 02 September 2015

Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome

scientific article published in January 2010

Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta

scientific article

Generalized periodontitis associated with Chédiak-Higashi syndrome

scientific article published in July 2008

Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome

scientific article published on 16 June 2015

Gingival Biopsy to Detect Mosaicism in Overgrowth Syndromes: Report of Two Cases of Megalencephaly-Capillary Malformation Syndrome with Periodontal Anomalies

scientific article published on 12 September 2020

High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosis.

scientific article

LEF1 haploinsufficiency causes ectodermal dysplasia

scientific article published on 17 February 2020

Mesiodens

scientific article published on 04 January 2008

Morbidity and Mortality Review in a University Dental Hospital: A Necessary Tool to Improve Quality of Care

scientific article published on 07 January 2021

Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia

article

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.

scientific article published on 10 February 2015

Necrotizing Periodontal Diseases in Children: A Literature Review and Adjustment of Treatment

scientific article published on 10 March 2016

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations ⬇️

scientific article

Oral manifestations of patients with Kenny-Caffey Syndrome

scientific article published on 30 March 2012

Orofacial manifestations of SAPHO syndrome: a systematic review of case reports

scientific article published on 09 May 2020

Proteus syndrome: Report of a case with AKT1 mutation in a dental cyst.

scientific article published on 14 March 2015

Recurrent Aphthous Stomatitis As a Marker of Celiac Disease in Children

scientific article published on 01 March 2016

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

scientific article (publication date: 2014)

The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders

scientific article published on 26 March 2008

The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement

scientific article published on 23 May 2008

The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patients

scientific article published in January 2008

[Orthodontic treatment of children suffering from attention deficit disorder with hyperactivity (ADHD)]

scientific article published on 04 September 2009

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