ChristianMoyaMD

PubMed

• 29 citations
  Association study of 69 genes in the ret pathway identifies low-penetrance loci in sporadic medullary thyroid carcinoma.
  Sergio Ruiz-Llorente, Cristina Montero-Conde, Roger L. Milne, Christian M. Moya, Arancha Cebrián, Rocío Letón, Alberto Cascón, Fátima Mercadillo, Iñigo Landa, Salud Bo...> ;Cancer Research. 2007 Oct 1
• 60 citations
  Functional Study of a Novel Single Deletion in the TITF1/NKX2.1 Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress
  Christian M. Moya, Guiomar Perez de Nanclares, Luis Castaño, Neus Potau, J. Ramón Bilbao, Antonio Carrascosa, María Bargadá, Raquel Coya, P. Martul, Enric Vicens-Calve...> ;The Journal of Clinical Endocrinology and Metabolism. 2006 May 1
• 24 citations
  A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: a mutational hot spot could explai...
  Carina M. Rivolta, Christian M. Moya, Viviana J. Gutnisky, Viviana Varela, José M. Miralles-García, Rogelio González-Sarmiento, Héctor M. Targovnik> ;The Journal of Clinical Endocrinology and Metabolism. 2005 Jun 1
• 9 citations
  La tiroides como modelo de mecanismos moleculares en enfermedades genéticas
  Carina M. Rivolta, Christian M. Moya, Sebastián A. Esperante, Viviana J. Gutnisky, Viviana Varela, Héctor M. Targovnik> ;Medicina. 2005 Jan 1
• 49 citations
  Two Distinct Compound Heterozygous Constellations (R277X/IVS34–1G>C and R277X/R1511X) in the Thyroglobulin (TG) Gene in Affected Individuals of a Brazilian Kindred wit...
  Viviana J. Gutnisky, Christian M. Moya, Carina M. Rivolta, Sabina Domené, Viviana Varela, Jussara V. Toniolo, Geraldo Medeiros-Neto, Héctor M. Targovnik> ;The Journal of Clinical Endocrinology and Metabolism. 2004 Feb 1
• 39 citations
  Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect
  Carina M. Rivolta, Sebastián A. Esperante, Laura Gruñeiro-Papendieck, Ana Chiesa, Christian M. Moya, Sabina Domené, Viviana Varela, Héctor M. Targovnik> ;Human Mutation. 2003 Sep 1
• 55 citations
  Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-->A [R2223H]) resulting in fetal goitrous hypothyroidism.
  Philippe Caron, Christian M. Moya, D Malet, Viviana J. Gutnisky, Bernard Chabardes, Carina M. Rivolta, Héctor M. Targovnik> ;The Journal of Clinical Endocrinology and Metabolism. 2003 Aug 1
• 12 citations
  Identification and characterization of a novel large insertion/deletion polymorphism of 1464 base pair in the human thyroglobulin gene.
  Christian M. Moya, Viviana Varela, Carina M. Rivolta, Fernando Mendive, Héctor M. Targovnik> ;Thyroid. 2003 Apr 1
• 12 citations
  Genotyping and characterization of two polymorphic microsatellite markers located within introns 29 and 30 of the human thyroglobulin gene.
  Carina M. Rivolta, Christian M. Moya, Fernando Mendive, Héctor M. Targovnik> ;Thyroid. 2002 Sep 1
• 41 citations
  Genomic organization of the human thyroglobulin gene: the complete intron-exon structure
  Fernando Mendive, Carina M. Rivolta, Christian M. Moya, Gilbert Vassart, Héctor M. Targovnik> ;European Journal of Endocrinology. 2001 Oct 1
• 45 citations
  Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene
  Héctor M. Targovnik, Carina M. Rivolta, Fernando Mendive, Christian M. Moya, Jussara Vono, Geraldo Medeiros-Neto> ;Thyroid. 2001 Jul 1
• 21 citations
  Genomic organization of the 5' region of the human thyroglobulin gene.
  Christian M. Moya, Fernando Mendive, Carina M. Rivolta, Gilbert Vassart, Héctor M. Targovnik> ;European Journal of Endocrinology. 2000 Dec 1
• WNT/beta-catenin increases the production of incretins by entero-endocrine cells.
  García-Martínez, J. M., Chocarro-Calvo, A., Moya, C. M., García-Jiménez, C.> ;Diabetologia. 2009 Sep 01
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