Emilio G de la Concha
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Explore the profile of Emilio G de la Concha including associated specialties, affiliations and a list of published articles.
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68
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1650
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Recent Articles
1.
Santiago J, de la Concha E, de la Serna J, Sevilla C, Urcelay E, Ruiz de Leon A
Hum Immunol
. 2012 Aug;
73(11):1207-9.
PMID: 22917541
A functional polymorphism (rs6554199) located in the c-kit gene was associated with achalasia in a Turkish cohort. Our aim was to replicate this result in a large cohort of Spanish...
2.
de la Concha E, Cavanillas M, Cenit M, Urcelay E, Arroyo R, Fernandez O, et al.
PLoS One
. 2012 Feb;
7(2):e31018.
PMID: 22363536
Background: Multiple sclerosis (MS) is a multifactorial disease with a genetic basis. The strongest associations with the disease lie in the Human Leukocyte Antigen (HLA) region. However, except for the...
3.
Trynka G, Hunt K, Bockett N, Romanos J, Mistry V, Szperl A, et al.
Nat Genet
. 2011 Nov;
43(12):1193-201.
PMID: 22057235
Using variants from the 1000 Genomes Project pilot European CEU dataset and data from additional resequencing studies, we densely genotyped 183 non-HLA risk loci previously associated with immune-mediated diseases in...
4.
Espino-Paisan L, De La Calle H, Fernandez-Arquero M, Figueredo M, de la Concha E, Urcelay E, et al.
Autoimmunity
. 2011 Aug;
44(8):624-30.
PMID: 21875375
Type 1 diabetes (T1D) is a multifactorial disease mainly associated with the human leukocyte antigen region. Previous studies suggested the association of interleukin-2 (IL2) gene polymorphisms and its alpha- and...
5.
Nunez C, Garcia-Gonzalez M, Santiago J, Benito M, Mearin F, de la Concha E, et al.
Hum Immunol
. 2011 Jun;
72(9):749-52.
PMID: 21641950
Idiopathic achalasia is an esophageal motor disorder of unknown etiology. A wealth of evidence supports the concept that achalasia is an immune-mediated disease. According to this evidence, achalasia has been...
6.
Espino-Paisan L, De La Calle H, Fernandez-Arquero M, Figueredo M, de la Concha E, Urcelay E, et al.
Immunogenetics
. 2011 Jan;
63(4):255-8.
PMID: 21246196
The Wellcome Trust Case Control Consortium (WTCCC) genome-wide study found association of PTPN2 with three autoimmune diseases, among them is type 1 diabetes (T1D). This result was confirmed by a...
7.
Blanco-Kelly F, Matesanz F, Alcina A, Teruel M, Diaz-Gallo L, Gomez-Garcia M, et al.
PLoS One
. 2010 Jul;
5(7):e11520.
PMID: 20634952
Background: A functional polymorphism located at -1 from the start codon of the CD40 gene, rs1883832, was previously reported to disrupt a Kozak sequence essential for translation. It has been...
8.
Villar L, Espino M, Cavanillas M, Roldan E, Urcelay E, de la Concha E, et al.
Clin Immunol
. 2010 Jul;
137(1):51-9.
PMID: 20621566
We described previously that multiple sclerosis (MS) patients with oligoclonal IgM against myelin lipids (M+) develop an aggressive disease. Our aim was to assess possible mechanisms regulating the production of...
9.
Perdigones N, Martin E, Robledo G, Lamas J, Taxonera C, Diaz-Rubio M, et al.
Hum Immunol
. 2010 Jun;
71(8):826-8.
PMID: 20561984
Chromosomal region 5p13 includes regulatory elements of the prostaglandin receptor EP4 (PTGER4) gene and is associated with inflammatory bowel disease (IBD) susceptibility. We aimed at corroborating the association of the...
10.
del Pozo N, Medrano L, Cenit M, Fernandez-Arquero M, Ferreira A, Garcia-Rodriguez M, et al.
Hum Immunol
. 2010 Jun;
71(9):861-4.
PMID: 20542071
The etiology of selective IgA deficiency (IgAD) is clearly influenced by human leukocyte antigen (HLA) genetic composition, although the susceptibility observed has not been ascribed to any specific gene/s. A...