Jean-Francois Prudhomme
Overview
Explore the profile of Jean-Francois Prudhomme including associated specialties, affiliations and a list of published articles.
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16
Citations
499
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Recent Articles
1.
Oudot T, Lesueur F, Guedj M, de Cid R, McGinn S, Heath S, et al.
J Invest Dermatol
. 2009 Jun;
129(11):2637-45.
PMID: 19554025
Psoriasis is a common inflammatory and hyperproliferative skin disease. Recent studies have reported that common genetic factors may underlie both skin and immune-mediated disorders. We hypothesized that such genes may...
2.
Lesueur F, Oudot T, Heath S, Foglio M, Lathrop M, Prudhomme J, et al.
PLoS One
. 2007 Sep;
2(9):e906.
PMID: 17878941
Psoriasis is a chronic skin disorder with multifactorial etiology. In a recent study, we reported results of a genome-wide scan on 46 French extended families presenting with plaque psoriasis. In...
3.
Lesueur F, Lefevre C, Has C, Guilloud-Bataille M, Oudot T, Mahe E, et al.
J Invest Dermatol
. 2007 Mar;
127(6):1403-9.
PMID: 17344932
Plaque psoriasis is a chronic inflammatory disorder of the skin. It is inherited as a multifactorial trait, with a strong genetic component. Linkage studies have identified a large number of...
4.
Hempelmann A, Taylor K, Heils A, Lorenz S, Prudhomme J, Nabbout R, et al.
Epilepsia
. 2006 Oct;
47(10):1682-90.
PMID: 17054691
Purpose: Idiopathic generalized epilepsy (IGE) accounts for approximately 20% of all epilepsies and affects about 0.2% of the general population. The etiology of IGE is genetically determined, but the complex...
5.
Striano P, Lispi M, Gennaro E, Madia F, Traverso M, Bordo L, et al.
Epilepsia
. 2006 Jul;
47(6):1029-34.
PMID: 16822249
Purpose: Benign familial infantile seizures (BFIS) is a genetically heterogeneous condition characterized by partial seizures, onset age from 3 to 9 months, and favorable outcome. BFIS loci were identified on...
6.
Lefevre C, Bouadjar B, Ferrand V, Tadini G, Megarbane A, Lathrop M, et al.
Hum Mol Genet
. 2006 Jan;
15(5):767-76.
PMID: 16436457
We report the identification of mutations in a non-syndromic autosomal recessive congenital ichthyosis (ARCI) in a new gene mapping within a previously identified locus on chromosome 19p12-q12, which has been...
7.
Topcu M, Jobard F, Halliez S, Coskun T, Yalcinkayal C, Ozbas Gerceker F, et al.
Hum Mol Genet
. 2004 Sep;
13(22):2803-11.
PMID: 15385440
l-2-Hydroxyglutaric aciduria (l-2-HGA) is characterized by progressive deterioration of central nervous system function including epilepsy and macrocephaly in 50% of cases, and elevated levels of l-2-hydroxyglutaric acid in urine, blood...
8.
Lefevre C, Bouadjar B, Karaduman A, Jobard F, Saker S, Ozguc M, et al.
Hum Mol Genet
. 2004 Aug;
13(20):2473-82.
PMID: 15317751
We report the genomic localization by homozygosity mapping and the identification of a gene for a new form of non-syndromic autosomal recessive congenital ichthyosis. The phenotype usually presents as non-bullous...
9.
Lefevre C, Audebert S, Jobard F, Bouadjar B, Lakhdar H, Boughdene-Stambouli O, et al.
Hum Mol Genet
. 2003 Aug;
12(18):2369-78.
PMID: 12915478
Lamellar ichthyosis type 2 (LI2) is a rare autosomal recessive skin disorder for which a gene has been localized on chromosome 2q33-35. We report the identification of five missense mutations...
10.
Jobard F, Bouadjar B, Caux F, Hadj-Rabia S, Has C, Matsuda F, et al.
Hum Mol Genet
. 2003 Apr;
12(8):925-35.
PMID: 12668616
Kindler syndrome is a rare autosomal-recessive genodermatosis characterized by bullous poikiloderma with photosensitivity. We report the localization to chromosome 20p12.3 by homozygosity mapping and the identification of a new gene,...