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Eliecer Coto

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Beatriz Tavira; Salvador Tranche; Jorge Arenas; Eliecer Coto; Beatriz Díez; Juan Gómez; Rafael Marín; Kevin Miguélez; Francisco Ortega; Emilio Sánchez; Victoria Alvarez
Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.
Lucía F Cardo; Eliecer Coto; Lorena de Mena; Manuel Menéndez; Germán Moris; Renee Ribacoba; Victoria Alvarez
Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls.
James M Bullock; Onofre Combarros; Mario Cortina Borja; Eliecer Coto; Panos Deloukas; Naomi Hammond; Reinhard Heun; Carla A Ibrahim-Verbaas; Patrick G Kehoe; Heike Kölsch; Donald J Lehmann; Michael G Lehmann; Ignacio Mateo; Christopher Medway; Victoria Alvarez; Rachel Barber; Olivia Belbin; Monique M Breteler; Kristelle Brown; Jonathan A Prince; Maaike Schuur; A David Smith; James C Turton; Cornelia M van Duijn; Donald R Warden; Gordon K Wilcock; Kevin Morgan
Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease.

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2013: Beatriz Tavira; Salvador Tranche; Jorge Arenas; Eliecer Coto; Beatriz Díez; Juan Gómez; Rafael Marín; Kevin Miguélez; Francisco Ortega; Emilio Sánchez; Victoria Alvarez
Association between a MYH9 polymorphism (rs3752462) and renal function in the Spanish RENASTUR cohort.
Gene 2013;520(1):73-6.
2013: Lucía F Cardo; Eliecer Coto; Lorena de Mena; Manuel Menéndez; Germán Moris; Renee Ribacoba; Victoria Alvarez
Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls.
Journal of neurology 2013;260(5):1420-2.
2013: James M Bullock; Onofre Combarros; Mario Cortina Borja; Eliecer Coto; Panos Deloukas; Naomi Hammond; Reinhard Heun; Carla A Ibrahim-Verbaas; Patrick G Kehoe; Heike Kölsch; Donald J Lehmann; Michael G Lehmann; Ignacio Mateo; Christopher Medway; Victoria Alvarez; Rachel Barber; Olivia Belbin; Monique M Breteler; Kristelle Brown; Jonathan A Prince; Maaike Schuur; A David Smith; James C Turton; Cornelia M van Duijn; Donald R Warden; Gordon K Wilcock; Kevin Morgan
Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease.
Neurobiology of aging 2013;34(4):1309.e1-7.
2012: Noemí Eiris; Juan Gómez; Katia López-Corte; Blanca Morales; Rubén Queiro; Jorge Santos-Juanes; Victoria Alvarez; Ana I Corao; Pablo Coto Segura; Marta Díaz; Eliecer Coto
Resequencing of the IL12B gene in psoriasis patients with the rs6887695/rs3212227 risk genotypes.
Cytokine 2012;60(1):27-9.
2012: Eliecer Coto; Marta Díaz; Beatriz Díaz-Molina; Juan Gómez; Sara Iglesias; María Martín; Carlos Morales; César Morís; María Palacín; Julián R Reguero; José L Rodríguez Lambert; Beatriz Tavira; Belén Alonso; Ana I Corao; Victoria Alvarez
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.
The Journal of molecular diagnostics : JMD 2012;14(5):518-24.
2012: Cristina Alonso-Montes; Jorge B Cannata-Andia; Eliecer Coto; Jose Luis Fernandez-Martin; Cesar Moris; Manuel Naves-Diaz; Julian Rodriguez-Reguero; Isabel Rodriguez
New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy.
Molecular biology reports 2012;39(9):8777-85.
2012: Lucía F Cardo; Ana I Corao; Eliecer Coto; Lorena de Mena; Marta Díaz; Oswaldo Lorenzo-Betancor; Ignacio F Mata; Manuel Menéndez; Germán Moris; Pau Pastor; Renee Ribacoba; Lluis Samaranch; Victoria Alvarez
A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.
Journal of molecular neuroscience : MN 2012;47(3):425-30.
2012: Pablo Coto Segura; Marta Díaz; Juan Gómez; Jorge Santos-Juanes; Belén Alonso; Victoria Alvarez; Ana I Corao; Eliecer Coto
Common European mitochondrial haplogroups in the risk for psoriasis and psoriatic arthritis.
Genetic testing and molecular biomarkers 2012;16(6):621-3.
2012: Susana Armesto; Eliecer Coto; Cristina Galache Osuna; Pablo Martinez-Camblor; Jorge Santos-Juanes; Pablo Coto Segura
Psoriasis and type 2 diabetes risk among psoriatic patients in a Spanish population.
The Australasian journal of dermatology 2012;53(2):128-30.
2012: Heike Kölsch; Donald J Lehmann; Michael G Lehmann; Wolfgang Maier; Ignacio Mateo; Kevin Morgan; Maaike Schuur; A David Smith; Cornelia M van Duijn; Donald R Warden; Gordon K Wilcock; Victoria Alvarez; Yurii S Aulchenko; Rachel Barber; Olivia Belbin; Monique Breteler; Kristelle Brown; Onofre Combarros; Mario Cortina Borja; Eliecer Coto; Panos Deloukas; Naomi Hammond; Carla A Ibrahim-Verbaas; Patrick G Kehoe; Reinhard Heun
Interaction of insulin and PPAR-α genes in Alzheimer's disease: the Epistasis Project.
Journal of neural transmission (Vienna, Austria : 1996) 2012;119(4):473-9.
2012: Beatriz Tavira; Armando Torres; Victoria Alvarez; Manuel Arias; Josep M Campistol; Eliecer Coto; Juan M Díaz; Carmen Díaz-Corte; Beatriz Díaz-Molina; Elena González; Carlos López-Larrea; Francisco Ortega; Alberto Ortiz; Marta Ruiz-Ortega; Rafael Selgas
Association between a common KCNJ11 polymorphism (rs5219) and new-onset posttransplant diabetes in patients treated with Tacrolimus.
Molecular genetics and metabolism 2012;105(3):525-7.
2012: Elena Sánchez-Ferrero; Ana I Corao; Eliecer Coto; Adolfo López De Munaín; Emilia Del Castillo; Marta Díaz; Jesús Esteban; Josep Gámez; Juan F Gonzalo; Jon Infante; Celedonio Márquez; Germán Morís; Samuel I Pascual-Pascual; Victoria Alvarez
Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.
Journal of neurology 2012;259(2):246-50.
2012: Reinhard Heun; Carla A Ibrahim-Verbaas; Patrick G Kehoe; Heike Kölsch; Victoria Alvarez; Yurii S Aulchenko; Rachel Barber; Olivia Belbin; Monique Breteler; Kristelle Brown; Onofre Combarros; Mario Cortina Borja; Eliecer Coto; Panos Deloukas; Naomi Hammond; Michael G Lehmann; Ignacio Mateo; Kevin Morgan; Maaike Schuur; A David Smith; Cornelia M van Duijn; Donald R Warden; Gordon K Wilcock; Donald J Lehmann
Interactions between PPAR-α and inflammation-related cytokine genes on the development of Alzheimer's disease, observed by the Epistasis Project.
International journal of molecular epidemiology and genetics 2012;3(1):39-47.
2012: Donald J Lehmann; Michael G Lehmann; Ignacio Mateo; Kevin Morgan; Chris M Morris; Abderrahim Oulhaj; Kathryn Robson; Maaike Schuur; Cornelia M van Duijn; Donald R Warden; Gordon K Wilcock; Victoria Alvarez; Alejandro Arias-Vásquez; Yurii S Aulchenko; Rachel Barker; Olivia Belbin; Monique M Breteler; Kristelle Brown; Onofre Combarros; Mario Cortina Borja; Eliecer Coto; Panos Deloukas; Rhian Gwilliam; Naomi Hammond; Reinhard Heun; M Arfan Ikram; Pat Kehoe; Heike Kölsch; A David Smith
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project.
Neurobiology of aging 2012;33(1):202.e1-13.
2011: María Palacín; Julián R Reguero; Victoria Alvarez; Beatriz Díaz Molina; María Martín; César Morís; Eliecer Coto
Profile of microRNAs differentially produced in hearts from patients with hypertrophic cardiomyopathy and sarcomeric mutations.
Clinical chemistry 2011;57(11):1614-6.
2011: Eliecer Coto; Marta Díaz; Juan Gómez; Carmen Martínez; Manuel Menéndez; Germán Morís; Belén Alonso; María T Calatayud; Ana I Corao; Victoria Álvarez
Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy.
Neurogenetics 2011;12(4):345-6.
2011: Rebeca Alonso-Arias; Eliecer Coto; Marco A Moro-García; Juan J Solano-Jaurrieta; Francisco M Suárez-García; José R Vidal-Castiñeira; Carlos López-Larrea
IL-15 preferentially enhances functional properties and antigen-specific responses of CD4+CD28(null) compared to CD4+CD28+ T cells.
Aging cell 2011;10(5):844-52.
2011: Ana Miar; Germán Morís; Marta Díaz; Carmen Martínez; Manuel Menéndez; Belén Alonso; Victoria Alvarez; María T Calatayud; Ana I Corao; Eliecer Coto
Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.
Journal of molecular neuroscience : MN 2011;45(1):5-9.
2011: Pilar Alejandra Saiz; Emilio Sotomayor; Victoria Alvarez; Celso Arango; Maria-Teresa Bascaran; Manuel Bousoño; Paul Corcoran; Eliecer Coto; Gerardo Flórez; Paz García-Portilla; Blanca Morales; Begoña Paredes; Julio Bobes
Role of serotonergic-related systems in suicidal behavior: Data from a case-control association study.
Progress in neuro-psychopharmacology & biological psychiatry 2011;35(6):1518-24.
2011: Pablo Coto Segura; Marta Díaz; Albert Mas-Vidal; Blanca Morales; Belén Alonso; Victoria Alvarez; Eliecer Coto; Jorge Santos-Juanes
Influence of endothelial nitric oxide synthase polymorphisms in psoriasis risk.
Archives of dermatological research 2011;303(6):445-9.
2011: Eliecer Coto; Jorge Santos-Juanes; Pablo Coto Segura; Victoria Alvarez
New psoriasis susceptibility genes: momentum for skin-barrier disruption.
The Journal of investigative dermatology 2011;131(5):1003-5.
2011: Beatriz Tavira; Armando Torres; Victoria Alvarez; Manuel Arias; Jose M Campistol; Eliecer Coto; Juan M Díaz; Carmen Díaz-Corte; Carlos López-Larrea; Francisco Ortega; Marta Ruiz-Ortega; Rafael Selgas
KCNQ1 gene variants and risk of new-onset diabetes in tacrolimus-treated renal-transplanted patients.
Clinical transplantation 2011;25(3):E284-91.
2011: Ana Miar; Victoria Alvarez; Ana I Corao; Belén Alonso; Marta Díaz; Manuel Menéndez; Carmen Martínez; Maite Calatayud; Germán Morís; Eliecer Coto
Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.
Brain research 2011;1383():252-6.
2011: Ignacio Mata; Dora Yearout; Victoria Alvarez; Eliecer Coto; Lorena de Mena; Renee Ribacoba; Oswaldo Lorenzo-Betancor; Lluis Samaranch; Pau Pastor; Sebastian Cervantes; Jon Infante; Ines Garcia-Gorostiaga; Maria Sierra; Onofre Combarros; Katherine W Snapinn; Karen L Edwards; Cyrus P Zabetian
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2011;26(5):819-23.
2011: María Martín; Isabel Rodríguez; María Palacín; Enrique Ríos-Gómez; Eliecer Coto
TGFBR2 gene mutational spectrum in aortic pathology.
Journal of the American College of Cardiology 2011;57(4):518-9; author reply 519.
2011: María Palacín; Victoria Alvarez; María Martín; Marta Díaz; Ana I Corao; Belén Alonso; Beatriz Díaz-Molina; Iñigo Lozano; Pablo Avanzas; César Morís; Julián R Reguero; Isabel Rodríguez; Carlos López-Larrea; Jorge Cannata-Andía; Alberto Batalla; Marta Ruiz-Ortega; Pablo Martínez-Camblor; Eliecer Coto
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.
Mitochondrion 2011;11(1):176-81.
2011: José David Herrero-Morín; Julián Rodríguez; Eliecer Coto; Helena Gil-Peña; Victoria Alvarez; Laura Espinosa; César Loris; Marta Gil-Calvo; Fernando Santos
Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2011;26(1):151-5.
2010: María Martín; Isabel Rodríguez; María Palacín; Eliecer Coto
Metalloproteinase polymorphisms and bicuspid aortic valves.
Revista española de cardiología 2010;63(11):1383-4.
2010: Michelle Liu; Sally Shi; Sean Senthilnathan; Julie Yu; Elliot Wu; Carsten Bergmann; Klaus Zerres; Nadja Bogdanova; Eliecer Coto; Constantinos Deltas; Alkis Pierides; Kyproula Demetriou; Olivier Devuyst; Berenice Gitomer; Marku Laakso; Anne Lumiaho; Klea Lamnissou; Riccardo Magistroni; Patrick Parfrey; Martijn Breuning; Dorien J M Peters; Roser Torra; Christopher G Winearls; Vicente E Torres; Peter C Harris; Andrew D Paterson; York Pei
Genetic variation of DKK3 may modify renal disease severity in ADPKD.
Journal of the American Society of Nephrology : JASN 2010;21(9):1510-20.
2010: Lorena de Mena; Eliecer Coto; Lucía F Cardo; Marta Díaz; Marta Blázquez; René Ribacoba; Carlos Salvador; Pau Pastor; Lluis Samaranch; Germán Moris; Manuel Menéndez; Ana I Corao; Victoria Alvarez
Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(6):1234-9.
2010: Miguel Angel Blanco-Gelaz; Beatriz Suarez-Alvarez; Gertrudis Ligero; Laura Sanchez; Jose Ramon Vidal-Castiñeira; Eliecer Coto; Harry Moore; Pablo Menendez; Carlos Lopez-Larrea
Endoplasmic reticulum stress signals in defined human embryonic stem cell lines and culture conditions.
Stem cell reviews 2010;6(3):462-72.
2010: Taofeng Zhou; Yuxia Zhang; Antonio Macchiarulo; Zhihong Yang; Marco Cellanetti; Eliecer Coto; Pingyi Xu; Roberto Pellicciari; L Wang
Novel polymorphisms of nuclear receptor SHP associated with functional and structural changes.
The Journal of biological chemistry 2010;285(32):24871-81.
2010: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Rocío Herrero; Celso Arango; Paul Corcoran; Blanca Morales; María Teresa Bascarán; Victoria Alvarez; Eliecer Coto; Begoña Paredes; Juan M Fernández; Julio Bobes
Interactions between functional serotonergic polymorphisms and demographic factors influence personality traits in healthy Spanish Caucasians.
Psychiatric genetics 2010;20(4):171-8.
2010: Lorena de Mena; Lucía F Cardo; Eliecer Coto; Ana Miar; Marta Díaz; Ana I Corao; Belén Alonso; René Ribacoba; Carlos Salvador; Manuel Menéndez; Germán Morís; Victoria Alvarez
FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.
Neuroscience letters 2010;479(1):22-5.
2010: Eliecer Coto; Beatriz Tavira; Rafael Marín; Francisco Ortega; Carlos López-Larrea; Marta Ruiz-Ortega; Alberto Ortiz; Marta Díaz; Ana I Corao; Belén Alonso; Victoria Alvarez
Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy.
Biochemical and biophysical research communications 2010;397(3):576-9.
2010: Mónica García-Castro; Cristina García; Julián R Reguero; Ana Miar; José M Rubín; Victoria Alvarez; César Morís; Eliecer Coto
The spectrum of SCN5A gene mutations in Spanish Brugada syndrome patients.
Revista española de cardiología 2010;63(7):856-9.
2010: Javier Soto-Sánchez; Jorge Santos-Juanes; Pablo Coto Segura; Eliecer Coto; Marta Díaz; Isabel Rodríguez; Victoria Alvarez
Genetic variation at the CCR5/CCR2 gene cluster and risk of psoriasis and psoriatic arthritis.
Cytokine 2010;50(2):114-6.
2010: Pablo Coto Segura; Eliecer Coto; Victoria Alvarez; Jorge Santos-Juanes
Apolipoprotein epsilon4 allele is associated with psoriasis severity: reply.
Archives of dermatological research 2010;302(3):237-8.
2010: Daniel Alvarez-Hernández; Ignacio González-Suárez; José L Fernández-Martín; Isabel Rodríguez; I Santamaría; Eliecer Coto; Jorge B Cannata-Andía
Residue 826 in the calcium-sensing receptor is implicated in the response to calcium and to R-568 calcimimetic compound.
Calcified tissue international 2010;86(3):227-33.
2010: Pablo Coto Segura; Eliecer Coto; Victoria Alvarez; Blanca Morales; Javier Soto-Sánchez; A I Corao; Jorge Santos-Juanes
Apolipoprotein epsilon4 allele is associated with psoriasis severity.
Archives of dermatological research 2010;302(2):145-9.
2010: Pilar A Sáiz; Maria P García-Portilla; Celso Arango; Blanca Morales; Bárbara Arias; Paul Corcoran; Juan M Fernández; Victoria Alvarez; Eliecer Coto; María Teresa Bascarán; Manuel Bousoño; Lourdes Fañanas; Julio Bobes
Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association study.
Progress in neuro-psychopharmacology & biological psychiatry 2010;34(1):26-31.
2010: Onofre Combarros; Donald R Warden; Naomi Hammond; Mario Cortina Borja; Olivia Belbin; Michael G Lehmann; Gordon K Wilcock; Kristelle Brown; Patrick G Kehoe; Rachel Barber; Eliecer Coto; Victoria Alvarez; Panos Deloukas; Rhian Gwilliam; Reinhard Heun; Heike Kölsch; Ignacio Mateo; Abderrahim Oulhaj; Alejandro Arias-Vásquez; Maaike Schuur; Yurii Aulchenko; M Arfan Ikram; Monique Breteler; Cornelia M van Duijn; Kevin Morgan; A David Smith; Donald J Lehmann
The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project.
BMC medical genetics 2010;11():162.
2010: Victoria Alvarez; Elena Sánchez-Ferrero; Christian Beetz; Marta Díaz; Belén Alonso; Ana I Corao; Josep Gámez; Jesús Esteban; Juan F Gonzalo; Samuel I Pascual-Pascual; Adolfo López de Munain; Germán Moris; Renne Ribacoba; Celedonio Márquez; Jordi Rosell; Rosario Marín; Maria J García-Barcina; Emilia Del Castillo; Carmen Benito; Eliecer Coto
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia.
BMC neurology 2010;10():89.
2010: Eliecer Coto; María Palacín; María Martín; Mónica G Castro; Julián R Reguero; Cristina García; José R Berrazueta; César Morís; Blanca Morales; Francisco Ortega; Ana I Corao; Marta Díaz; Beatriz Tavira; Victoria Alvarez
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.
Journal of translational medicine 2010;8():64.
2010: Eliecer Coto; Jorge Santos-Juanes; Pablo Coto Segura; Marta Díaz; Javier Soto; Rubén Queiro; Victoria Alvarez
Mutation analysis of the LCE3B/LCE3C genes in Psoriasis.
BMC medical genetics 2010;11():45.
2010: Natalia Mejia-Gaviria; Helena Gil-Peña; Eliecer Coto; Teresa M Pérez-Menéndez; Fernando Santos
Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report.
Orphanet journal of rare diseases 2010;5():1.
2009: Pablo Coto Segura; Victoria Alvarez; Javier Soto-Sánchez; Blanca Morales; Eliecer Coto; Jorge Santos-Juanes
Lack of association between angiotensin I-converting enzyme insertion/deletion polymorphism and psoriasis or psoriatic arthritis in Spain.
International journal of dermatology 2009;48(12):1320-3.
2009: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Gerardo Florez; Paul Corcoran; Celso Arango; Blanca Morales; Juan C Leza; Sandra Alvarez; Eva M Díaz; Victoria Alvarez; Eliecer Coto; Luis Nogueiras; Julio Bobes
Polymorphisms of the IL-1 gene complex are associated with alcohol dependence in Spanish Caucasians: data from an association study.
Alcoholism, clinical and experimental research 2009;33(12):2147-53.
2009: Lorena De Mena; Eliecer Coto; Elena Sánchez-Ferrero; René Ribacoba; Luis M Guisasola; Carlos Salvador; Marta Blázquez; Victoria Alvarez
Mutational screening of the mortalin gene (HSPA9) in Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2009;116(10):1289-93.
2009: Pablo Román-García; Eliecer Coto; Julián R Reguero; Jorge B Cannata-Andía; Iñigo Lozano; Pablo Avanzas; César Morís; Isabel Rodríguez
Matrix metalloproteinase 1 promoter polymorphisms and risk of myocardial infarction: a case-control study in a Spanish population.
Coronary artery disease 2009;20(6):383-6.
2009: Beatriz Suárez-Alvarez; Rebeca Alonso-Arias; Cristina Bravo-Mendoza; Antonio López-Vázquez; Teresa Ortega; Jose Maria Baltar; Eliecer Coto; Francisco Ortega; Carlos López-Larrea
Identification of epitopes and immunodominant regions on the MICA protein defined by alloantibodies from kidney transplant patients.
Transplantation 2009;88(3 Suppl):S68-77.
2009: Eliecer Coto; Beatriz Tavira
Pharmacogenetics of calcineurin inhibitors in renal transplantation.
Transplantation 2009;88(3 Suppl):S62-7.
2009: María Palacín; Fernando Rodriguez-Pascual; Julián R Reguero; Isabel Rodríguez; Pablo Avanzas; Iñigo Lozano; Cesar Morís; Victoria Alvarez; Jorge B Cannata-Andía; Santiago Lamas; Monica García-Castro; Eliecer Coto
Lack of association between endothelin-1 gene variants and myocardial infarction.
Journal of atherosclerosis and thrombosis 2009;16(4):388-95.
2009: Elena Sánchez-Ferrero; Eliecer Coto; Marta Blázquez; René Ribacoba; Luis M Guisasola; Carlos Salvador; Victoria Alvarez
Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease.
Parkinsonism & related disorders 2009;15(6):468-70.
2009: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Gerardo Florez; Celso Arango; Paul Corcoran; Blanca Morales; Maria-Teresa Bascaran; Cesar Alvarez; Gema San Narciso; Eduardo Carreño; Victoria Alvarez; Eliecer Coto; Julio Bobes
Differential role of serotonergic polymorphisms in alcohol and heroin dependence.
Progress in neuro-psychopharmacology & biological psychiatry 2009;33(4):695-700.
2009: Eliecer Coto; Mónica G Castro; Ana I Corao; Cristina Alonso-Montes; Julián R Reguero; César Morís; Victoria Alvarez
Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy.
American journal of medical genetics. Part A 2009;149A(2):286-9.
2009: Onofre Combarros; Cornelia M van Duijn; Naomi Hammond; Olivia Belbin; Alejandro Arias-Vásquez; Mario Cortina Borja; Michael G Lehmann; Yurii S Aulchenko; Maaike Schuur; Heike Kölsch; Reinhard Heun; Gordon K Wilcock; Kristelle Brown; Patrick G Kehoe; Rachel Harrison; Eliecer Coto; Victoria Alvarez; Panos Deloukas; Ignacio Mateo; Rhian Gwilliam; Kevin Morgan; Donald R Warden; A David Smith; Donald J Lehmann
Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease.
Journal of neuroinflammation 2009;6():22.
2009: Eliecer Coto; Gabriel Arriba; Mónica García-Castro; Fernando Santos; Ana I Corao; Marta Díaz; Marta Sánchez Heras; María A Basterrechea; Serafín Tallón; Victoria Alvarez
Clinical and analytical findings in Gitelman's syndrome associated with homozygosity for the c.1925 G>A SLC12A3 mutation.
American journal of nephrology 2009;30(3):218-21.
2009: Mónica García-Castro; Eliecer Coto; Julián R Reguero; José R Berrazueta; Victoria Alvarez; Belén Alonso; Rocío Sainz; María Martín; Cesar Morís
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].
Revista española de cardiología 2009;62(1):48-56.
2009: York Pei; James Obaji; Annie Dupuis; Andrew D Paterson; riccardo magistroni; Elizabeth Dicks; Patrick Parfrey; Benvon Cramer; Eliecer Coto; Roser Torra; Jose L San Millan; Robert Gibson; Martijn H Breuning; Dorien Peters; David Ravine
Unified criteria for ultrasonographic diagnosis of ADPKD.
Journal of the American Society of Nephrology : JASN 2009;20(1):205-12.
2008: Daniel Alvarez-Hernandez; Manuel Naves-Diaz; Carlos Gomez-Alonso; Eliecer Coto; Jorge B Cannata-Andia
Tissue-specific effect of VDR gene polymorphisms on the response to calcitriol.
Journal of nephrology 2008;21(6):843-9.
2008: Grace Tamara Moscoso-Solorzano; Francisco Ortega; Isabel Rodríguez; Mónica García-Castro; Ernesto Gómez; Carmen Díaz-Corte; José M Baltar; Victoria Alvarez; alberto ortiz; Eliecer Coto
A search for cyclophilin-A gene variants in cyclosporine A-treated renal transplanted patients.
Clinical transplantation 2008;22(6):722-9.
2008: Pilar Alejandra Saiz; Maria P García-Portilla; Begoña Paredes; Celso Arango; Blanca Morales; Victoria Alvarez; Eliecer Coto; Maria-Teresa Bascaran; Manuel Bousoño; Julio Bobes
Association between the A-1438G polymorphism of the serotonin 2A receptor gene and nonimpulsive suicide attempts.
Psychiatric genetics 2008;18(5):213-8.
2008: Gerardo Florez; Pilar Alejandra Saiz; Paz Garcia-Portilla; Sandra Alvarez; Luis Nogueíras; Blanca Morales; Victoria Alvarez; Eliecer Coto; Julio Bobes
Association between the Stin2 VNTR polymorphism of the serotonin transporter gene and treatment outcome in alcohol-dependent patients.
Alcohol and alcoholism (Oxford, Oxfordshire) 2008;43(5):516-22.
2008: Maximilian Posch; Laura Thiemann; Pavol Tomasov; Josef Veselka; nuno cardim; Monica Garcia-Castro; Eliecer Coto; Andreas Perrot; Christian Geier; Rainer Dietz; Wilhelm Haverkamp; Cemil Ozcelik
Sequence analysis of myozenin 2 in 438 European patients with familial hypertrophic cardiomyopathy.
Medical science monitor : international medical journal of experimental and clinical research 2008;14(7):CR372-4.
2008: Victoria Alvarez; Pelayo González; Ana I Corao; Manuel Menéndez; Carlos H Lahoz; Carmen Martínez; Maite Calatayud; Blanca Morales; Eliecer Coto
The Sp1/Egr1-tandem repeat polymorphism in the 5-lipoxygenase gene promoter is not associated with late onset Alzheimer disease.
Alzheimer disease and associated disorders 2008;22(2):177-80.
2008: Victoria Alvarez; Ana I Corao; Cristina Alonso-Montes; Elena Sánchez-Ferrero; Lorena De Mena; Blanca Morales; Mónica García-Castro; Eliecer Coto
Mitochondrial transcription factor A (TFAM) gene variation and risk of late-onset Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2008;13(3):275-80.
2008: M Palacín; I Rodríguez; Mónica García-Castro; F Ortega; J R Reguero; C López-Larrea; C Morís; Victoria Alvarez; Eliecer Coto
A search for cyclophilin-A gene (PPIA) variation and its contribution to the risk of atherosclerosis and myocardial infarction.
International journal of immunogenetics 2008;35(2):159-64.
2008: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Celso Arango; Blanca Morales; Maria-Teresa Bascaran; Sara Martinez-Barrondo; Gerardo Florez; Emilio Sotomayor; Begoña Paredes; Cesar Alvarez; Gema San Narciso; Eduardo Carreño; Igor Bombin; Victoria Alvarez; Eliecer Coto; Juan M Fernandez; Manuel Bousoño; Julio Bobes
Association study between obsessive-compulsive disorder and serotonergic candidate genes.
Progress in neuro-psychopharmacology & biological psychiatry 2008;32(3):765-70.
2008: Victoria Alvarez; Ana I Corao; Elena Sánchez-Ferrero; Lorena De Mena; Cristina Alonso-Montes; Cecilia Huerta; Marta Blázquez; René Ribacoba; Luis M Guisasola; Carlos Salvador; Mónica García-Castro; Eliecer Coto
Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.
Neuroscience letters 2008;432(1):79-82.
2008: Pilar A Sáiz; Maria P García-Portilla; Celso Arango; Blanca Morales; S Martínez-Barrondo; C Alvarez; G San Narciso; E Carreño; Victoria Alvarez; Eliecer Coto; Julio Bobes
Association between heroin dependence and 5-HT2A receptor gene polymorphisms.
European addiction research 2008;14(1):47-52.
2008: Esther Mancebo; Miguel A Moreno-Pelayo; Angeles Mencía; Oscar de la Calle-Martín; Luis M Allende; Padma Sivadorai; Luba Kalaydjieva; Jaume Bertranpetit; Eliecer Coto; Sara Calleja-Antolín; Jesús Ruiz Contreras; Estela Paz-Artal
Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.
Molecular immunology 2008;45(2):479-84.
2007: Mónica García-Castro; Julián R Reguero; César Morís; Cristina Alonso-Montes; José R Berrazueta; Rocío Sainz; Victoria Alvarez; Eliecer Coto
Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients.
International journal of cardiology 2007;121(1):115-6.
2007: Mónica G Castro; Nicolás Terrados; Julián R Reguero; Victoria Alvarez; Eliecer Coto
Mitochondrial haplogroup T is negatively associated with the status of elite endurance athlete.
Mitochondrion 2007;7(5):354-7.
2007: Helena Gil; Fernando Santos; Enrique García; María Victoria Alvarez; Flor A Ordóñez; Serafín Málaga; Eliecer Coto
Distal RTA with nerve deafness: clinical spectrum and mutational analysis in five children.
Pediatric nephrology (Berlin, Germany) 2007;22(6):825-8.
2007: Pilar A Sáiz; Maria P García-Portilla; Celso Arango; Blanca Morales; Victoria Alvarez; Eliecer Coto; Juan M Fernández; María Teresa Bascarán; Manuel Bousoño; Julio Bobes
Association study of serotonin 2A receptor (5-HT2A) and serotonin transporter (5-HTT) gene polymorphisms with schizophrenia.
Progress in neuro-psychopharmacology & biological psychiatry 2007;31(3):741-5.
2007: Isabel Rodríguez; Eliecer Coto; Julián R Reguero; Pelayo González; Vicente Andrés; Iñigo Lozano; María Martín; Victoria Alvarez; César Morís
Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 genes in the risk of atherosclerosis and myocardial infarction.
Cell cycle (Georgetown, Tex.) 2007;6(5):620-5.
2007: Cecilia Huerta; Elena Sánchez-Ferrero; Eliecer Coto; Marta Blázquez; Renee Ribacoba; Luis M Guisasola; Carlos Salvador; Victoria Alvarez
No association between Parkinson's disease and three polymorphisms in the eNOS, nNOS, and iNOS genes.
Neuroscience letters 2007;413(3):202-5.
2007: Rafael Pardo De La Vega; Serafín Málaga; Victoria Alvarez; Eliecer Coto
Vesicoureteric reflux and tumor necrosis factor-alpha gene polymorphism.
Journal of pediatric urology 2007;3(1):24-7.
2007: Victor Asensi; A Hugo Montes; Eulalia Valle; Marcos G Ocaña; AURORA ASTUDILLO; Victoria Alvarez; Esteban López-Anglada; Angeles Solís; Eliecer Coto; Alvaro Meana; Pelayo Gonzalez; José Antonio Carton; José Paz; Joshua Fierer; Antonio Celada
The NOS3 (27-bp repeat, intron 4) polymorphism is associated with susceptibility to osteomyelitis.
Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2007;16(1):44-53.
2007: Pelayo González; Victoria Alvarez; Manuel Menendez; Carlos H Lahoz; Carmen Martínez; Ana I Corao; María T Calatayud; Joaquín Peña; Mónica García-Castro; Eliecer Coto
Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms.
Neuroscience letters 2007;411(1):47-51.
2007: Pilar A Sáiz; Maria P García-Portilla; Begoña Paredes; Celso Arango; Blanca Morales; Victoria Alvarez; Eliecer Coto; Teresa Bascarán; Manuel Bousoño; Julio Bobes
Lack of association between endothelial nitric oxide synthase (NOS3) gene polymorphisms and suicide attempts.
Behavioral and brain functions : BBF 2007;3():32.
2006: Mónica G Castro; Cecilia Huerta; Julián R Reguero; María Isabel Soto; Enric Doménech; Victoria Alvarez; Montserrat Gómez-Zaera; Virginia Nunes; Pelayo González; Ana Corao; Eliecer Coto
Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy.
International journal of cardiology 2006;112(2):202-6.
2006: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Celso Arango; Blanca Morales; Sara Martinez-Barrondo; Victoria Alvarez; Eliecer Coto; Juan Fernandez; Manuel Bousono; Julio Bobes
Interleukin-1 gene complex in schizophrenia: an association study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(6):678-80.
2006: Pilar Alejandra Saiz; Maria P Garcia-Portilla; Celso Arango; Blanca Morales; Victoria Alvarez; Eliecer Coto; Juan M Fernandez; Manuel Bousono; Julio Bobes
N-acetyltransferase-2 polymorphisms and schizophrenia.
European psychiatry : the journal of the Association of European Psychiatrists 2006;21(5):333-7.
2006: María Martín; Pelayo González; J J R Reguero; Alberto Batalla; Mónica García-Castro; Eliecer Coto; César Morís
ABCA1 polymorphisms and prognosis after myocardial infarction in young patients.
International journal of cardiology 2006;110(2):267-8.
2006: Eliecer Coto; Manuel Menendez; R Navarro; Mónica García-Castro; Victoria Alvarez
A new de novo Notch3 mutation causing CADASIL.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2006;13(6):628-31.
2006: Africa Fernandez-L; Francisco Sanz-Rodriguez; Roberto Zarrabeitia; Alfonso Perez-Molino; Carmelo Morales; Carlos M Restrepo; Jose R Ramirez; Eliecer Coto; Gennaro M Lenato; Carmelo Bernabeu; Luisa M Botella
Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1.
Human mutation 2006;27(3):295.
2006: Pelayo González; Mónica García-Castro; Julián R Reguero; A Batalla; A G Ordóñez; R L Palop; Ramon Lopez Palop; M Montes; Victoria Alvarez; Eliecer Coto
The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction.
Journal of medical genetics 2006;43(2):167-9.
2006: S Martínez-Barrondo; Pilar A Sáiz; Blanca Morales; Maria P García-Portilla; Eliecer Coto; Victoria Alvarez; María Teresa Bascarán; Manuel Bousoño; Julio Bobes
Negative evidences in association between apolipoprotein E polymorphism and panic disorder.
European psychiatry : the journal of the Association of European Psychiatrists 2006;21(1):59-61.
2005: Eliecer Coto; Daniel Armenta; Raúl Espinosa; Joaquín Argente; Mónica G Castro; Victoria Alvarez
Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene.
Movement disorders : official journal of the Movement Disorder Society 2005;20(12):1626-9.
2005: Cecilia Huerta; Mónica G Castro; Eliecer Coto; Marta Blázquez; Renee Ribacoba; Luis M Guisasola; Carlos Salvador; Carmen Martínez; Carlos H Lahoz; Victoria Alvarez
Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
Journal of the neurological sciences 2005;236(1-2):49-54.
2005: Mónica García-Castro; Julián R Reguero; Victoria Alvarez; Alberto Batalla; María Isabel Soto; Vicente Albaladejo; Eliecer Coto
Hypertrophic cardiomyopathy linked to homozygosity for a new mutation in the myosin-binding protein C gene (A627V) suggests a dosage effect.
International journal of cardiology 2005;102(3):501-7.
2005: S Martínez-Barrondo; Pilar Alejandra Saiz; Blanca Morales; Maria P García-Portilla; Eliecer Coto; Victoria Alvarez; Julio Bobes
Serotonin gene polymorphisms in patients with panic disorder.
Actas españolas de psiquiatría 2005;33(4):210-5.
2005: Ignacio Mata; Victoria Alvarez; Eliecer Coto; Marta Blazquez; Luis M Guisasola; Carlos Salvador; Jennifer Kachergus; Sarah J Lincoln; Matthew J Farrer
Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.
Neuroscience letters 2005;380(3):257-9.
2005: Eliecer Coto; Rafael Marín; V Alvarez; Manuel Praga; C Fernández Andrade; M Arias; Rafael Poveda; M Vallés; J M Galcerán; José Luño; F Rivera; J M Campistol
[Pharmacogenetics of angiotensin system in non diabetic nephropathy].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2005;25(4):381-6.
2005: Mark B Consugar; Sarah A Anderson; Sandro Rossetti; V Shane Pankratz; Christopher J Ward; Roser Torra; Eliecer Coto; Mounif El-Youssef; Sibel Kantarci; Boris Utsch; Friedhelm Hildebrandt; William E Sweeney; Ellis D Avner; Vicente E Torres; Julie M Cunningham; Peter C Harris
Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2005;45(1):77-87.
2004: Cecilia Huerta; Victoria Alvarez; Ignacio Mata; Eliecer Coto; Renee Ribacoba; Carmen Martínez; Marta Blázquez; Luis M Guisasola; Carlos Salvador; Carlos H Lahoz; Joaquín Peña
Chemokines (RANTES and MCP-1) and chemokine-receptors (CCR2 and CCR5) gene polymorphisms in Alzheimer's and Parkinson's disease.
Neuroscience letters 2004;370(2-3):151-4.
2004: Francisco Sanz-Rodriguez; Africa Fernandez-L; Roberto Zarrabeitia; Alfonso Perez-Molino; Jose R Ramírez; Eliecer Coto; Carmelo Bernabeu; Luisa M Botella
Mutation analysis in Spanish patients with hereditary hemorrhagic telangiectasia: deficient endoglin up-regulation in activated monocytes.
Clinical chemistry 2004;50(11):2003-11.
2004: Victor Asensi; Eulalia Valle; Alvaro Meana; Joshua Fierer; Antonio Celada; Victoria Alvarez; José Paz; Eliecer Coto; José Antonio Carton; José A Maradona; Angeles Dieguez; Julián Sarasúa; Marcos G Ocaña; José Manuel Arribas
In vivo interleukin-6 protects neutrophils from apoptosis in osteomyelitis.
Infection and immunity 2004;72(7):3823-8.
2004: Rafael Pardo De La Vega; Serafín Málaga; Eliecer Coto
[NOS3 polymorphism and reflux nephropathy].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2004;24(4):390-1.
2004: Pelayo González; Antonio Díez-Juan; Eliecer Coto; Victoria Alvarez; Julián R Reguero; Alberto Batalla; Vicente Andrés
A single-nucleotide polymorphism in the human p27kip1 gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction.
BMC biology 2004;2():5.
2004: Eliecer Coto; Julian Rodriguez; Nikola Jeck; Victoria Alvarez; Rosario Stone; Cesar Loris; Luis M Rodriguez; Michel Fischbach; Hannsjörg W Seyberth; Fernando Santos
A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies.
Kidney international 2004;65(1):25-9.
2003: Mónica García-Castro; Julián R Reguero; Alberto Batalla; Felicitas Catalán; Juan Mayordomo; Eliecer Coto
[Direct detection of malignant mutations in patients with hypertrophic cardiomyopathy].
Revista española de cardiología 2003;56(10):1022-5.
2003: Alberto Batalla; Julián R Reguero; Eliecer Coto
The T-786C endothelial nitric oxide synthase genotype and coronary artery disease.
Journal of the American College of Cardiology 2003;42(6):1140; author reply 1140-1.
2003: Mónica García-Castro; Julián R Reguero; Alberto Batalla; Beatriz Díaz-Molina; Pelayo González; Victoria Alvarez; Arturo Cortina; Gustavo I Cubero; Eliecer Coto
Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients.
Clinical chemistry 2003;49(8):1279-85.
2003: Sandro Rossetti; Roser Torra; Eliecer Coto; Mark B Consugar; Vickie Kubly; Serafín Málaga; Mercedes Navarro; Mounif El-Youssef; Vicente E Torres; Peter C Harris
A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees.
Kidney international 2003;64(2):391-403.
2003: Victor Asensi; Victoria Alvarez; Eulalia Valle; Alvaro Meana; Joshua Fierer; Eliecer Coto; José Antonio Carton; José A Maradona; José Paz; Maria Angeles Dieguez; Belén de la Fuente; Alfonso Moreno; Silvino Rubio; Maria José Tuya; Julián Sarasúa; Sara Llames; José Manuel Arribas
IL-1 alpha (-889) promoter polymorphism is a risk factor for osteomyelitis.
American journal of medical genetics. Part A 2003;119A(2):132-6.
2003: riccardo magistroni; Ning He; Kairong Wang; Robin Andrew; Ann Johnson; Patricia Gabow; Elizabeth Dicks; Patrick Parfrey; Roser Torra; Jose L San-Millan; Eliecer Coto; Marjan Van Dijk; Martijn H Breuning; Dorien Peters; Nadja Bogdanova; Guido Ligabue; Alberto Albertazzi; Nick Hateboer; Kyproula Demetriou; Alkis Pierides; C Constantinou Deltas; Peter St George-Hyslop; David Ravine; York Pei
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease.
Journal of the American Society of Nephrology : JASN 2003;14(5):1164-74.
2003: Eliecer Coto; Julián R Reguero; Victoria Alvarez; Blanca Morales; Alberto Batalla; Pelayo González; María Martín; Mónica García-Castro; Gustavo Iglesias-Cubero; Arturo Cortina
5-Hydroxytryptamine 5-HT2A receptor and 5-hydroxytryptamine transporter polymorphisms in acute myocardial infarction.
Clinical science (London, England : 1979) 2003;104(3):241-5.
2003: Rafael Pardo De La Vega; Serafín Málaga; Eliecer Coto; Mercedes Navarro; Victoria Alvarez; Laura Espinosa; Ruth Alvarez; Alfredo Vallo; Cesar Loris; Socorro Braga
Renin-angiotensin system polymorphisms and renal scarring.
Pediatric nephrology (Berlin, Germany) 2003;18(2):110-4.
2003: P González; R Alvarez; V Alvarez; Eliecer Coto
[Genetic variation and progression of renal failure].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2003;23 Suppl 4():36-41.
2003: V Alvarez Martínez; Eliecer Coto
[Nephronophthisis and medullar cystic disease: genetic aspects].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2003;23 Suppl 1():46-51.
2002: Pelayo González; Ruth Alvarez; Julián R Reguero; Alberto Batalla; Victoria Alvarez; Arturo Cortina; Gustavo I Cubero; Mónica García-Castro; Eliecer Coto
Variation in the lipoprotein receptor-related protein, alpha2-macroglobulin and lipoprotein receptor-associated protein genes in relation to plasma lipid levels and risk of early myocardial infarction.
Coronary artery disease 2002;13(5):251-4.
2002: Victoria Alvarez; Ignacio Mata; Pelayo González; Carlos H Lahoz; Carmen Martínez; Joaquín Peña; Luis M Guisasola; Eliecer Coto
Association between the TNFalpha-308 A/G polymorphism and the onset-age of Alzheimer disease.
American journal of medical genetics 2002;114(5):574-7.
2002: Juan P. Rodrigo; María V González; Pedro S Lazo; Sofía Ramos; Eliecer Coto; Ignacio Alvarez; Luis A García; Carlos Suárez
Genetic alterations in squamous cell carcinomas of the hypopharynx with correlations to clinicopathological features.
Oral oncology 2002;38(4):357-63.
2002: Pilar A Sáiz; Blanca Morales; M P G-Portilla; Victoria Alvarez; Eliecer Coto; Juan M Fernández; Manuel Bousoño; Julio Bobes
Apolipoprotein E genotype and schizophrenia: further negative evidence.
Acta psychiatrica Scandinavica 2002;105(1):71-5.
2001: Victoria Alvarez; Luis M Guisasola; V G Moreira; Carlos H Lahoz; Eliecer Coto
Early-onset Parkinson's disease associated with a new parkin mutation in a Spanish family.
Neuroscience letters 2001;313(1-2):108-10.
2001: Alberto Batalla; R Alvarez; Julián R Reguero; Pelayo González; Victoria Alvarez; Gustavo I Cubero; Arturo Cortina; Eliecer Coto
Lack of association between polymorphisms of the coagulation factor VII and myocardial infarction in middle-aged Spanish men.
International journal of cardiology 2001;80(2-3):209-12.
2001: Ruth Alvarez; Pelayo González; Alberto Batalla; Julián R Reguero; Gustavo Iglesias-Cubero; Sergio Hevia; Arturo Cortina; E Merino; I González; Victoria Alvarez; Eliecer Coto
Association between the NOS3 (-786 T/C) and the ACE (I/D) DNA genotypes and early coronary artery disease.
Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2001;5(4):343-8.
2001: Juan P. Rodrigo; Carlos Suárez; María V González; Pedro S Lazo; Sofía Ramos; Eliecer Coto; I Alvarez; Luis A García; J A Martínez
Variability of genetic alterations in different sites of head and neck cancer.
The Laryngoscope 2001;111(7):1297-301.
2001: Juan P. Rodrigo; Eliecer Coto; María V González; Miguel Maldonado Fernandez; Carlos Suárez
P53 allelic loss and outcome in patients with squamous cell carcinoma of the head and neck.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2001;258(5):255-8.
2001: P González; R Alvarez; A Batalla; Julián R Reguero; Victoria Alvarez; AURORA ASTUDILLO; Gustavo I Cubero; Arturo Cortina; Eliecer Coto
Genetic variation at the chemokine receptors CCR5/CCR2 in myocardial infarction.
Genes and immunity 2001;2(4):191-5.
2001: Eliecer Coto
[Polymorphisms of the ACE gene and cardiovascular disease].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2001;21 Suppl 1():67-9.
2001: Alberto Batalla; R Alvarez; Sergio Hevia; Julián R Reguero; Eliecer Coto
Apolipoprotein E genotype and coronary heart disease.
Journal of the American College of Cardiology 2001;37(1):329-31.
2000: Alberto Batalla; Ruth Alvarez; Julián R Reguero; Sergio Hevia; Gustavo Iglesias-Cubero; Victoria Alvarez; Arturo Cortina; Pelayo González; M M Celada; A Medina; Eliecer Coto
Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction.
Clinical chemistry 2000;46(12):1910-5.
2000: Angel José González-Ordóñez; José-Manuel Fernández-Carreira; Carmen Rosa Fernández-Alvarez; L Martin; J Sánchez Garcia; JM Medina Rodríguez; María Victoria Alvarez; Eliecer Coto
Normal frequencies of the C677T genotypes on the methylenetetrahydrofolate reductase (MTHFR) gene among lymphoproliferative disorders but not in multiple myeloma.
Leukemia & lymphoma 2000;39(5-6):607-12.
2000: Ruth Alvarez; Nicolás Terrados; R Ortolano; Gustavo Iglesias-Cubero; Julián R Reguero; Alberto Batalla; Arturo Cortina; Benjamin Fernández-García; C Rodríguez; S Braga; Victoria Alvarez; Eliecer Coto
Genetic variation in the renin-angiotensin system and athletic performance.
European journal of applied physiology 2000;82(1-2):117-20.
2000: Nick Hateboer; Barbara Veldhuisen; D Peters; Martijn H Breuning; José L San Millán; Nadja Bogdanova; Eliecer Coto; Meindert A van Dijk; Ali R Afzal; Steve Jeffery; Anand K Saggar-Malik; Roser Torra; D Dimitrakov; I Martinez; S S de Castro; M Krawczak; David Ravine
Location of mutations within the PKD2 gene influences clinical outcome.
Kidney international 2000;57(4):1444-51.
2000: Victoria Alvarez; Serafín Málaga; Mercedes Navarro; L Espinosa; E Hidalgo; J Badía; R Alvarez; Eliecer Coto
Analysis of chromosome 6p in Spanish families with recessive polycystic kidney disease.
Pediatric nephrology (Berlin, Germany) 2000;14(3):205-7.
2000: A J Ordóñez; J M Carreira; C R Alvarez; J M Rodríguez; María Victoria Alvarez; Eliecer Coto
Comparison of the risk of pulmonary embolism and deep vein thrombosis in the presence of factor V Leiden or prothrombin G20210A.
Thrombosis and haemostasis 2000;83(2):352-4.
2000: Alberto Batalla; Julián R Reguero; Gustavo I Cubero; Eliecer Coto
[Hyperlipemia and glycoprotein IIIa polymorphism].
Medicina clínica 2000;114(2):77.
1999: Alberto Batalla; Julián R Reguero; Gustavo I Cubero; Eliecer Coto
Prothrombotic genetic risk factors and myocardial infarction at young age.
Blood 1999;94(11):3959.
1999: Ruth Alvarez; Victoria Alvarez; Carlos H Lahoz; Carmen Martínez; Joaquín Peña; J M Sánchez; Luis M Guisasola; J Salas-Puig; Germán Morís; JA Vidal; Renee Ribacoba; Bernardino B Menes; DF Uría; Eliecer Coto
Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 1999;67(6):733-6.
1999: David Reynolds; T Hayashi; Y Cai; Barbara Veldhuisen; Terry Watnick; Xose M Lens; T Mochizuki; Feng Qian; Y Maeda; L Li; R Fossdal; Eliecer Coto; G Wu; Martijn H Breuning; Gregory G Germino; Dorien J M Peters; Stefan Somlo
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease.
Journal of the American Society of Nephrology : JASN 1999;10(11):2342-51.
1999: V Alvarez; R Alvarez; J Peña; C H Lahoz; C Martínez; L Menéndez-Guisasola; J Salas-Puig; Germán Morís; DF Uría; Bernardino B Menes; Renee Ribacoba; JA Vidal; Eliecer Coto
[Frequency of the APOE-4 allele in Alzheimer's disease and its variation with age in Asturias (Spain)].
Medicina clínica 1999;113(12):441-3.
1999: Victoria Alvarez; Ruth Alvarez; Carlos H Lahoz; Carmen Martínez; Joaquín Peña; Luis M Guisasola; J Salas-Puig; Germán Morís; DF Uría; Bernardino B Menes; Renee Ribacoba; JA Vidal; J M Sánchez; Eliecer Coto
Association between an alpha(2) macroglobulin DNA polymorphism and late-onset Alzheimer's disease.
Biochemical and biophysical research communications 1999;264(1):48-50.
1999: Angel José González-Ordóñez; J M Medina Rodriguez; L Martín; V Alvarez; Eliecer Coto
The O blood group protects against venous thromboembolism in individuals with the factor V Leiden but not the prothrombin (factor II G20210A) mutation.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1999;10(5):303-7.
1999: Nick Hateboer; M A v Dijk; Nadja Bogdanova; Eliecer Coto; Anand K Saggar-Malik; J L San Millan; Roser Torra; Martijn H Breuning; David Ravine
Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group.
Lancet 1999;353(9147):103-7.
1999: M Vargas; Inmaculada Soto; Carmen R Pinto; MF Urgelles; Alberto Batalla; JJ Rodriguez Reguero; Arturo Cortina; Victoria Alvarez; Eliecer Coto
The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1999;10(1):39-41.
1998: Julián R Reguero; Gustavo I Cubero; Alberto Batalla; Victoria Alvarez; Sergio Hevia; Arturo Cortina; Eliecer Coto
Apolipoprotein A1 gene polymorphisms and risk of early coronary disease.
Cardiology 1998;90(3):231-5.
1998: Ruth Alvarez; Julián R Reguero; Alberto Batalla; Gustavo Iglesias-Cubero; Arturo Cortina; Victoria Alvarez; Eliecer Coto
Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: association with early coronary disease.
Cardiovascular research 1998;40(2):375-9.
1998: M Vargas; Inmaculada Soto; Carmen R Pinto; MF Urgelles; Eliecer Coto
Mild hyperhomocysteinemia and MTHFR C677T do not increase the risk for venous thrombosis in a Spanish population.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 1998;9(6):555-6.
1998: María V González; MF Pello; P Ablanedo; Carlos Suárez; Victoria Alvarez; Eliecer Coto
Chromosome 3p loss of heterozygosity and mutation analysis of the FHIT and beta-cat genes in squamous cell carcinoma of the head and neck.
Journal of clinical pathology 1998;51(7):520-4.
1998: María V González; Victoria Alvarez; MF Pello; MJ Menéndez; Carlos Suárez; Eliecer Coto
Genetic polymorphism of N-acetyltransferase-2, glutathione S-transferase-M1, and cytochromes P450IIE1 and P450IID6 in the susceptibility to head and neck cancer.
Journal of clinical pathology 1998;51(4):294-8.
1998: V Alvarez; C López-Larrea; Eliecer Coto
Mutational analysis of the CCR5 and CXCR4 genes (HIV-1 co-receptors) in resistance to HIV-1 infection and AIDS development among intravenous drug users.
Human genetics 1998;102(4):483-6.
1997: J M García-Gala; Victoria Alvarez; Carmen R Pinto; Inmaculada Soto; Manuel F Urgellés; MJ Menéndez; C Carracedo; C López-Larrea; Eliecer Coto
Factor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based on the Spanish population.
Clinical genetics 1997;52(4):206-10.
1997: Barbara Veldhuisen; Jasper J Saris; Simone de Haij; T Hayashi; David Reynolds; T Mochizuki; Rob Elles; R Fossdal; Nadja Bogdanova; Meindert A van Dijk; Eliecer Coto; David Ravine; S Nørby; C Verellen-Dumoulin; Martijn H Breuning; Stefan Somlo; Dorien J M Peters
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).
American journal of human genetics 1997;61(3):547-55.
1997: M Ariza; Victoria Alvarez; R Marín; S Aguado; C López-Larrea; J Alvarez; MJ Menéndez; Eliecer Coto
A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes.
Journal of medical genetics 1997;34(7):587-9.
1997: María V González; MF Pello; C López-Larrea; Carlos Suárez; MJ Menéndez; Eliecer Coto
Deletion and methylation of the tumour suppressor gene p16/CDKN2 in primary head and neck squamous cell carcinoma.
Journal of clinical pathology 1997;50(6):509-12.
1997: María V González; M L Artímez; L Rodrigo; C López-Larrea; MJ Menéndez; Victoria Alvarez; R Pérez; M F Fresno; M J Pérez; A Sampedro; Eliecer Coto
Mutation analysis of the p53, APC, and p16 genes in the Barrett's oesophagus, dysplasia, and adenocarcinoma.
Journal of clinical pathology 1997;50(3):212-7.
1997: S Gonzalez-Roces; María Victoria Alvarez; Segundo Gonzalez; A Dieye; H Makni; D G Woodfield; L Housan; VI Konenkov; M C Abbadi; N Grunnet; Eliecer Coto; Carlos López-Larrea
HLA-B27 polymorphism and worldwide susceptibility to ankylosing spondylitis.
Tissue antigens 1997;49(2):116-23.
1996: Segundo Gonzalez; F Setién; Eliecer Coto; C López-Larrea
Genetic structure and organization of the membrane attack complement components.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1996;23(3):181-97.
1996: V Alvarez; Eliecer Coto; F Setién; Segundo Gonzalez; S Gonzalez-Roces; C López-Larrea
Characterization of interleukin-8 receptors in non-human primates.
Immunogenetics 1996;43(5):261-7.
1996: V Alvarez; Eliecer Coto; F Setién; S González-Roces; C López-Larrea
Molecular evolution of the N-formyl peptide and C5a receptors in non-human primates.
Immunogenetics 1996;44(6):446-52.
1995: María V González; M F Pello; C López-Larrea; Carlos Suárez; MJ Menéndez; Eliecer Coto
Loss of heterozygosity and mutation analysis of the p16 (9p21) and p53 (17p13) genes in squamous cell carcinoma of the head and neck.
Clinical cancer research : an official journal of the American Association for Cancer Research 1995;1(9):1043-9.
1995: Eliecer Coto; J F Toral; MJ Menéndez; I Hernando; A Plasencia; A Benavides; C López-Larrea
PCR-based study of the presence of Y-chromosome sequences in patients with Ullrich-Turner syndrome.
American journal of medical genetics 1995;57(3):393-6.
1995: C López-Larrea; S Gonzalez-Roces; M Peña; O Dominguez; Eliecer Coto; V Alvarez; M Moreno; O Hernandez; R Burgos-Vargas; Clara Gorodezky
Characterization of B27 haplotypes by oligotyping and genomic sequencing in the Mexican Mestizo population with ankylosing spondylitis: juvenile and adult onset.
Human immunology 1995;43(3):174-80.
1995: Eliecer Coto; S Sanz de Castro; S Aguado; J Alvarez; M Arias; MJ Menéndez; C López-Larrea
DNA microsatellite analysis of families with autosomal dominant polycystic kidney disease types 1 and 2: evaluation of clinical heterogeneity between both forms of the disease.
Journal of medical genetics 1995;32(6):442-5.
1995: C López-Larrea; K Sujirachato; Narinder K Mehra; P Chiewsilp; D Isarangkura; Uma Kanga; O Dominguez; Eliecer Coto; M Penã; F Setién
HLA-B27 subtypes in Asian patients with ankylosing spondylitis. Evidence for new associations.
Tissue antigens 1995;45(3):169-76.
1995: V Alvarez; Eliecer Coto; F Setién; P J Spath; C López-Larrea
Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.
American journal of medical genetics 1995;55(4):408-13.
1994: Eliecer Coto; C Bousoño; MJ Menéndez; R Cue; J F Toral; A Benavides; I Hernando; A Plasencia; C López-Larrea
[Cystic fibrosis in Asturias: an elevated frequency of the delta F508 mutation].
Medicina clínica 1994;103(18):681-3.
1994: S González-Roces; C Brautbar; M Peña; O Dominguez; Eliecer Coto; V Alvarez; R Segal; C López-Larrea
Molecular analysis of HLA-B27 haplotypes in Caucasoids. Frequencies of B27-Cw in Jewish and Spanish populations.
Human immunology 1994;41(2):127-34.
1994: F Setién Baranda; Eliecer Coto; J Menéndez Díaz; E Martínez-Naves; V Alvarez Martínez; C López-Larrea
HLA class II and susceptibility and resistance to insulin-dependent diabetes mellitus in a population from the northwest of Spain.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1994;21(4):219-29.
1994: V Alvarez; Eliecer Coto; F Setién; C López-Larrea
A physical map of two clusters containing the genes for six proinflammatory receptors.
Immunogenetics 1994;40(2):100-3.
1993: F Setién; V Alvarez; Eliecer Coto; R G DiScipio; C López-Larrea
A physical map of the human complement component C6, C7, and C9 genes.
Immunogenetics 1993;38(5):341-4.
1992: F Núñez; O Domínguez; Eliecer Coto; Carlos Suárez Nieto; P Pérez; C López-Larrea
Analysis of ras oncogene mutations in human squamous cell carcinoma of the head and neck.
Surgical oncology 1992;1(6):405-11.
1992: Eliecer Coto; S Aguado; J Alvarez; M J Menéndez Díaz; C López-Larrea
Genetic and clinical studies in autosomal dominant polycystic kidney disease type 1 (ADPKD1).
Journal of medical genetics 1992;29(4):243-6.
1992: Eliecer Coto; S Aguado; J Alvarez; S Sanz de Castro; M Arias; J Fernández Toral; A Benavides; I Hernando; A Plasencia; J Herrera
[Diagnosis of dominant renal polycystosis in adults by analysis of DNA polymorphism].
Medicina clínica 1992;98(11):409-12.
1992: O Dominguez; Eliecer Coto; E Martinez-Naves; S Y Choo; C López-Larrea
Molecular typing of HLA-B27 alleles.
Immunogenetics 1992;36(5):277-82.
1991: Peter C Harris; S Thomas; Peter J Ratcliffe; M H Breuning; Eliecer Coto; C Lopez-Larrea
Rapid genetic analysis of families with polycystic kidney disease 1 by means of a microsatellite marker.
Lancet 1991;338(8781):1484-7.
1991: M Victoria-Gutierrez; E Martinez-Naves; Eliecer Coto; O Dominguez; F Uría; JM Urra; C López-Larrea
DNA analysis of HLA-DR4B1 subtypes in multiple sclerosis by specific oligonucleotide probes.
Journal of neuroimmunology 1991;32(3):279-83.
1991: E Martínez-Naves; Eliecer Coto; V Gutiérrez; JM Urra; F Setién; O Domínguez; L E Hood; C López-Larrea
Germline repertoire of T-cell receptor beta-chain genes in patients with insulin-dependent diabetes mellitus.
Human immunology 1991;31(2):77-80.
1991: E Martínez-Naves; Eliecer Coto; JM Urra; F Setién; C Lopez-Larrea
SacI polymorphism at the human TCR delta chain constant region (TCRD).
Nucleic acids research 1991;19(3):685.
1991: Eliecer Coto; O Domínguez; E Martínez-Naves; F Setién; V Gutiérrez; C López-Larrea
MspI polymorphism at the human complement component C6 gene (C6).
Nucleic acids research 1991;19(1):194.
1991: Eliecer Coto; E Martínez-Naves; O Domínguez; R G DiScipio; JM Urra; C López-Larrea
DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes.
Immunogenetics 1991;33(3):184-7.
1990: Eliecer Coto; O Domínguez; E Martínez-Naves; JM Urra; V Gutiérrez; C López-Larrea
TaqI polymorphism at the human complement component C9 gene.
Nucleic acids research 1990;18(18):5581.
1990: Eliecer Coto; E Martínez-Naves; O Domínguez; C López-Larrea
DNA polymorphism of the human complement component C7 gene in familial deficiencies.
Human genetics 1990;85(2):251-2.
1990: C López-Larrea; DF Uría; Eliecer Coto
HLA antigens in multiple sclerosis of northern Spanish population.
Journal of neurology, neurosurgery, and psychiatry 1990;53(5):434-5.
1990: C López-Larrea; J C Torre Alonso; A Rodriguez Perez; Eliecer Coto
HLA antigens in psoriatic arthritis subtypes of a Spanish population.
Annals of the rheumatic diseases 1990;49(5):318-9.
1990: Eliecer Coto; E Martinez-Naves; O Dominguez; JM Urra; V Rodriguez; C López-Larrea
TaqI polymorphism in the complement component C7 gene.
Nucleic acids research 1990;18(7):1929.
1990: C López-Larrea; O Dominguez; E Martinez-Naves; Eliecer Coto
Study of genetic polymorphism of seventh complement component in two families with hereditary deficit.
Complement and inflammation 1990;7(2):90-4.