Jose Ramon Bilbao
Jose Ramon Bilbao
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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
G Trynka, KA Hunt, NA Bockett, J Romanos, V Mistry, A Szperl, SF Bakker, ...
Nature genetics 43 (12), 1193-1201, 2011
Epigenetic Defects of GNAS in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy
GP de Nanclares, E Fernández-Rebollo, I Santin, B Garcia-Cuartero, ...
The Journal of Clinical Endocrinology & Metabolism 92 (6), 2370-2373, 2007
A long noncoding RNA associated with susceptibility to celiac disease
A Castellanos-Rubio, N Fernandez-Jimenez, R Kratchmarov, X Luo, ...
Science 352 (6281), 91-95, 2016
TH17 (and TH1) signatures of intestinal biopsies of CD patients in response to gliadin
A Castellanos-Rubio, I Santin, I Irastorza, L Castaño, J Carlos Vitoria, ...
Autoimmunity 42 (1), 69-73, 2009
Prospective population screening for celiac disease: high prevalence in the first 3 years of life
L Castaño, E Blarduni, L Ortiz, J Núñez, JR Bilbao, I Rica, P Martul, ...
Journal of pediatric gastroenterology and nutrition 39 (1), 80-84, 2004
Association of insulin-dependent diabetes mellitus and celiac disease: a study based on serologic markers
JC Vitoria, L Castaño, R Itxaso, JR Bilbao, A Arrieta, ...
Journal of pediatric gastroenterology and nutrition 27 (1), 47-52, 1998
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants
J Romanos, A Rosén, V Kumar, G Trynka, L Franke, A Szperl, ...
Gut 63 (3), 415-422, 2014
Mutations in GCK and HNF‐1α explain the majority of cases with clinical diagnosis of MODY in Spain
I Estalella, I Rica, GP De Nanclares, JR Bilbao, JA Vazquez, JI San Pedro, ...
Clinical endocrinology 67 (4), 538-546, 2007
DNA methylation in childhood asthma: an epigenome-wide meta-analysis
CJ Xu, C Söderhäll, M Bustamante, N Baïz, O Gruzieva, U Gehring, ...
The lancet Respiratory medicine 6 (5), 379-388, 2018
Functional Study of a Novel Single Deletion in the TITF1/NKX2.1 Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not …
CM Moya, G Perez de Nanclares, L Castaño, N Potau, JR Bilbao, ...
The Journal of Clinical Endocrinology & Metabolism 91 (5), 1832-1841, 2006
MICA response to gliadin in intestinal mucosa from celiac patients
A Martín-Pagola, G Pérez-Nanclares, L Ortiz, JC Vitoria, I Hualde, ...
Immunogenetics 56 (8), 549-554, 2004
Coregulation and modulation of NFκB-related genes in celiac disease: uncovered aspects of gut mucosal inflammation
N Fernandez-Jimenez, A Castellanos-Rubio, L Plaza-Izurieta, I Irastorza, ...
Human molecular genetics 23 (5), 1298-1310, 2014
Revisiting genome wide association studies (GWAS) in coeliac disease: replication study in Spanish population and expression analysis of candidate genes
L Plaza-Izurieta, A Castellanos-Rubio, I Irastorza, N Fernández-Jimenez, ...
Journal of medical genetics 48 (7), 493-496, 2011
Killer cell immunoglobulin-like receptor (KIR) genes in the Basque population: association study of KIR gene contents with type 1 diabetes mellitus
I Santin, GP de Nanclares, B Calvo, A Gaafar, L Castaño, JR Bilbao, ...
Human immunology 67 (1-2), 118-124, 2006
Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus
JIS Pedro, JR Bilbao, G Perez de Nanclares, JC Vitoria, P Martul, ...
Autoimmunity 38 (6), 439-444, 2005
HLA‐DRB1 and MHC class 1 chain‐related A haplotypes in Basque families with celiac disease
JR Bilbao, A Martín‐Pagola, JC Vitoria, P Zubillaga, L Ortiz, L Castano
Tissue antigens 60 (1), 71-76, 2002
HLA‐DRB1 and MICA in Autoimmunity: Common Associated Alleles in Autoimmune Disorders
Annals of the New York Academy of Sciences 1005 (1), 314-318, 2003
Conserved extended haplotypes discriminate HLA-DR3-homozygous Basque patients with type 1 diabetes mellitus and celiac disease
JR Bilbao, B Calvo, AM Aransay, A Martin-Pagola, GP de Nanclares, ...
Genes & Immunity 7 (7), 550-554, 2006
Identification of a novel nonsense mutation and a missense substitution in the vasopressin-neurophysin II gene in two Spanish kindreds with familial neurohypophyseal diabetes …
B Calvo, JR Bilbao, I Urrutia, J Eizaguirre, S Gaztambide, L Castano
The Journal of Clinical Endocrinology & Metabolism 83 (3), 995-997, 1998
A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain
J Rodríguez-Soriano, A Vallo, GP de Nanclares, JR Bilbao, L Castaño
Pediatric Nephrology 20 (7), 891-896, 2005
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