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8 May 2013
A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient
- May Sanyoura
- , Cédric Woudstra
- , George Halaby
- , Patrick Baz
- , Valérie Senée
- , Pierre-Jean Guillausseau
- , Pierre Zalloua
- & Cécile Julier
European Journal of Human Genetics 22 , 140–143

Rights & permissionsfor article A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient . Opens in a new window.
Research | 1 July 1993
Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR
Nature Genetics 4 , 305–310

Rights & permissionsfor article Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR . Opens in a new window.
Research | 17 April 2005
A variant in the CD209 promoter is associated with severity of dengue disease
Nature Genetics 37 , 507–513

Rights & permissionsfor article A variant in the CD209 promoter is associated with severity of dengue disease . Opens in a new window.
Research | 1 August 2000
EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome
Nature Genetics 25 , 406–409

Rights & permissionsfor article EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome . Opens in a new window.
Research | 21 May 2006
Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism
- Valérie Senée
- , Claude Chelala
- , Sabine Duchatelet
- , Daorong Feng
- , Hervé Blanc
- , Jack-Christophe Cossec
- , Céline Charon
- , Marc Nicolino
- , Pascal Boileau
- , Douglas R Cavener
- , Pierre Bougnères
- , Doris Taha
- & Cécile Julier
Nature Genetics 38 , 682–687

Rights & permissionsfor article Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism . Opens in a new window.
News and Views | 1 December 2001
Lost in translation
- Cécile Julier
Nature Genetics 29 , 358–359

Rights & permissionsfor article Lost in translation . Opens in a new window.
Research | 10 May 2009
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
- Jeffrey C Barrett
- , David G Clayton
- , Patrick Concannon
- , Beena Akolkar
- , Jason D Cooper
- , Henry A Erlich
- , Cécile Julier
- , Grant Morahan
- , Jørn Nerup
- , Concepcion Nierras
- , Vincent Plagnol
- , Flemming Pociot
- , Helen Schuilenburg
- , Deborah J Smyth
- , Helen Stevens
- , John A Todd
- , Neil M Walker
- & Stephen S Rich
Nature Genetics 41 , 703–707

Rights & permissionsfor article Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes . Opens in a new window.

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A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient

Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR

A variant in the CD209 promoter is associated with severity of dengue disease

EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

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

Lost in translation

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

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