Timeline

Sabine Duchatelet
Post-doc
15 Jul 2017
publication

The Microbiological Landscape of Anaerobic Infections in Hidradenitis Suppurativa: A Prospective Metagenomic Study

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01 Oct 2015
publication

Deciphering the microbiology of hidradenitis suppurativa: a step forward towards understanding an enigmatic inflammatory skin disease

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31 Aug 2015
publication

A. First Nicastrin mutation in PASH syndrome Br

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01 Jun 2015
publication

Erythrokeratodermia variabilis et progressiva allelic to oculo-dento-digital dysplasia

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11 May 2015
team

Functional Genetics of Infectious Diseases

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17 Mar 2015
publication

Olmsted syndrome: clinical, molecular and therapeutic aspects

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02 Nov 2014
publication

Familial pachyonychia congenita with steatocystoma multiplex and multiple abscesses of the scalp due to the p.Asn92Ser mutation in keratin 17

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04 Aug 2014
publication

Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations

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01 Mar 2014
publication

A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia

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01 Mar 2014
publication

Genetics of atopic dermatitis: beyond filaggrin-the role of thymic stromal lymphopoietin in disease persistence

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25 Feb 2014
publication

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

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15 Jul 2013
publication

Identification of a KCNQ1 polymorphism acting as a protective modifier against arrhythmic risk in long-QT syndrome

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17 Oct 2011
publication

Differentiating Alström from Bardet-Biedl syndrome (BBS) using systematic ciliopathy genes sequencing

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17 Sep 2010
publication

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

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08 Oct 2007
publication

FCRL3 -169CT functional polymorphism in type 1 diabetes and autoimmunity traits

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01 Feb 2007
publication

PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits

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21 May 2006
publication

Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism

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03 Nov 2004
publication

Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes

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