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Javier Gayan, Ph.D. - Publications

Affiliations: 
2000 University of Colorado, Boulder, Boulder, CO, United States 
Area:
Psychobiology Psychology, Psychometrics Psychology, Genetics, Reading Education
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37 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Rice ML, Zubrick SR, Taylor CL, Hoffman L, Gayán J. Longitudinal Study of Language and Speech of Twins at 4 and 6 Years: Twinning Effects Decrease, Zygosity Effects Disappear, and Heritability Increases. Journal of Speech, Language, and Hearing Research : Jslhr. 1-15. PMID 29255901 DOI: 10.1044/2017_Jslhr-L-16-0366  0.337
2014 Real LM, Ruiz A, Gayán J, González-Pérez A, Sáez ME, Ramírez-Lorca R, Morón FJ, Velasco J, Marginet-Flinch R, Musulén E, Carrasco JM, Moreno-Rey C, Vázquez E, Chaves-Conde M, Moreno-Nogueira JA, et al. A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. Plos One. 9: e101178. PMID 24978480 DOI: 10.1371/Journal.Pone.0101178  0.383
2014 Rice ML, Zubrick SR, Taylor CL, Gayán J, Bontempo DE. Late language emergence in 24-month-old twins: heritable and increased risk for late language emergence in twins. Journal of Speech, Language, and Hearing Research : Jslhr. 57: 917-28. PMID 24167238 DOI: 10.1044/1092-4388(2013/12-0350)  0.343
2014 Boada M, Antúnez C, Ramírez-Lorca R, DeStefano AL, González-Pérez A, Gayán J, López-Arrieta J, Ikram MA, Hernández I, Marín J, Galán JJ, Bis JC, Mauleón A, Rosende-Roca M, Moreno-Rey C, et al. ATP5H/KCTD2 locus is associated with Alzheimer's disease risk. Molecular Psychiatry. 19: 682-7. PMID 23857120 DOI: 10.1038/Mp.2013.86  0.349
2013 Martinez-Mir A, González-Pérez A, Gayán J, Antúnez C, Marín J, Boada M, Lopez-Arrieta JM, Fernández E, Ramírez-Lorca R, Sáez ME, Ruiz A, Scholl FG, Real LM. Genetic study of neurexin and neuroligin genes in Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 35: 403-12. PMID 23403532 DOI: 10.3233/Jad-122257  0.397
2013 Ruiz A, Hernández I, Ronsende-Roca M, González-Pérez A, Rodriguez-Noriega E, Ramírez-Lorca R, Mauleón A, Moreno-Rey C, Boswell L, Tune L, Valero S, Alegret M, Gayán J, Becker JT, Real LM, et al. Exploratory analysis of seven Alzheimer's disease genes: disease progression. Neurobiology of Aging. 34: 1310.e1-7. PMID 23036585 DOI: 10.1016/J.Neurobiolaging.2012.08.014  0.452
2012 Matesanz F, González-Pérez A, Lucas M, Sanna S, Gayán J, Urcelay E, Zara I, Pitzalis M, Cavanillas ML, Arroyo R, Zoledziewska M, Marrosu M, Fernández O, Leyva L, Alcina A, et al. Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1. Plos One. 7: e36140. PMID 22570697 DOI: 10.1371/Journal.Pone.0036140  0.398
2012 Alcina A, Abad-Grau Mdel M, Fedetz M, Izquierdo G, Lucas M, Fernández O, Ndagire D, Catalá-Rabasa A, Ruiz A, Gayán J, Delgado C, Arnal C, Matesanz F. Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations. Plos One. 7: e29819. PMID 22253788 DOI: 10.1371/Journal.Pone.0029819  0.319
2012 Boada M, Antunez C, López-Arrieta J, Caruz A, Moreno-Rey C, Ramírez-Lorca R, Morón FJ, Hernández I, Mauleón A, Rosende-Roca M, Martínez-Lage P, Marín J, Tárraga L, Alegret M, Pedrajas JR, et al. Estrogen receptor alpha gene variants are associated with Alzheimer's disease. Neurobiology of Aging. 33: 198.e15-24. PMID 20674091 DOI: 10.1016/J.Neurobiolaging.2010.06.016  0.356
2011 Antúnez C, Boada M, López-Arrieta J, Moreno-Rey C, Hernández I, Marín J, Gayán J, González-Pérez A, Real LM, Alegret M, Tárraga L, Ramírez-Lorca R, Ruiz A. Genetic association of complement receptor 1 polymorphism rs3818361 in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 7: e124-9. PMID 21784344 DOI: 10.1016/J.Jalz.2011.05.2412  0.419
2011 Antúnez C, Boada M, González-Pérez A, Gayán J, Ramírez-Lorca R, Marín J, Hernández I, Moreno-Rey C, Morón FJ, López-Arrieta J, Mauleón A, Rosende-Roca M, Noguera-Perea F, Legaz-García A, Vivancos-Moreau L, et al. The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease. Genome Medicine. 3: 33. PMID 21627779 DOI: 10.1186/Gm249  0.391
2011 Ramírez-Lorca R, Boada M, Antúnez C, López-Arrieta J, Moreno-Rey C, Hernández I, Marín J, Gayán J, González-Pérez A, Alegret M, Tárraga L, Real LM, Ruiz A. The MTHFD1L gene rs11754661 marker is not associated with Alzheimer's disease in a sample of the Spanish population. Journal of Alzheimer's Disease : Jad. 25: 47-50. PMID 21383495 DOI: 10.3233/Jad-2011-101983  0.409
2010 Sáez ME, González-Pérez A, Martínez-Larrad MT, Gayán J, Real LM, Serrano-Ríos M, Ruiz A. WWOX gene is associated with HDL cholesterol and triglyceride levels. Bmc Medical Genetics. 11: 148. PMID 20942981 DOI: 10.1186/1471-2350-11-148  0.341
2010 Gayán J, González-Pérez A, Ruiz A. "Does replication groups scoring reduce false positive rate in SNP interaction discovery? Response". Bmc Genomics. 11: 403. PMID 20576100 DOI: 10.1186/1471-2164-11-403  0.334
2010 Gayán J, Galan JJ, González-Pérez A, Sáez ME, Martínez-Larrad MT, Zabena C, Rivero MC, Salinas A, Ramírez-Lorca R, Morón FJ, Royo JL, Moreno-Rey C, Velasco J, Carrasco JM, Molero E, et al. Genetic structure of the Spanish population. Bmc Genomics. 11: 326. PMID 20500880 DOI: 10.1186/1471-2164-11-326  0.401
2010 Ruiz-Marín M, Matilla-García M, Cordoba JA, Susillo-González JL, Romo-Astorga A, González-Pérez A, Ruiz A, Gayán J. An entropy test for single-locus genetic association analysis. Bmc Genetics. 11: 19. PMID 20331859 DOI: 10.1186/1471-2156-11-19  0.428
2009 Rice ML, Smith SD, Gayán J. Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment. Journal of Neurodevelopmental Disorders. 1: 264-82. PMID 19997522 DOI: 10.1007/S11689-009-9031-X  0.501
2009 Antúnez C, Boada M, López-Arrieta J, Ramirez-Lorca R, Hernández I, Marín J, Martínez-Lage P, González-Pérez A, Jorge Galan J, Gayán J, Real LM, Ruiz A. GOLPH2 gene markers are not associated with Alzheimer's disease in a sample of the Spanish population. Journal of Alzheimer's Disease : Jad. 18: 751-4. PMID 19749441 DOI: 10.3233/Jad-2009-1200  0.408
2009 Ramirez-Lorca R, Boada M, Saez ME, Hernandez I, Mauleon A, Rosende-Roca M, Martinez-Lage P, Gutierrez M, Real LM, Lopez-Arrieta J, Gayan J, Antunez C, Gonzalez-Perez A, Tarraga L, Ruiz A. GAB2 gene does not modify the risk of Alzheimer's disease in Spanish APOE 4 carriers. The Journal of Nutrition, Health & Aging. 13: 214-9. PMID 19262956 DOI: 10.1007/S12603-009-0061-6  0.375
2009 González-Pérez A, Gayán J, Marín J, Galán JJ, Sáez ME, Real LM, Antúnez C, Ruiz A. Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson's disease. Neurogenetics. 10: 173-81. PMID 19156451 DOI: 10.1007/S10048-009-0170-8  0.332
2009 Brocklebank D, Gayán J, Andresen JM, Roberts SA, Young AB, Snodgrass SR, Penney JB, Ramos-Arroyo MA, Cha JJ, Rosas HD, Hersch SM, Feigin A, Cherny SS, Wexler NS, Housman DE, et al. Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 425-9. PMID 18712713 DOI: 10.1002/Ajmg.B.30826  0.391
2008 Gayán J, González-Pérez A, Bermudo F, Sáez ME, Royo JL, Quintas A, Galan JJ, Morón FJ, Ramirez-Lorca R, Real LM, Ruiz A. A method for detecting epistasis in genome-wide studies using case-control multi-locus association analysis. Bmc Genomics. 9: 360. PMID 18667089 DOI: 10.1186/1471-2164-9-360  0.41
2008 Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE. Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32: 445-53. PMID 18481795 DOI: 10.1002/Gepi.20317  0.427
2007 Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Annals of Human Genetics. 71: 295-301. PMID 17181545 DOI: 10.1111/J.1469-1809.2006.00335.X  0.336
2005 Gayán J, Willcutt EG, Fisher SE, Francks C, Cardon LR, Olson RK, Pennington BF, Smith SD, Monaco AP, DeFries JC. Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 46: 1045-56. PMID 16178928 DOI: 10.1111/J.1469-7610.2005.01447.X  0.606
2004 Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/Pnas.0308679101  0.43
2003 Gayán J, Olson RK. Genetic and environmental influences on individual differences in printed word recognition. Journal of Experimental Child Psychology. 84: 97-123. PMID 12609495 DOI: 10.1016/S0022-0965(02)00181-9  0.636
2002 Knopik VS, Smith SD, Cardon L, Pennington B, Gayan J, Olson RK, DeFries JC. Differential genetic etiology of reading component processes as a function of IQ. Behavior Genetics. 32: 181-98. PMID 12141780 DOI: 10.1023/A:1016069012111  0.671
2002 Kaplan DE, Gayán J, Ahn J, Won TW, Pauls D, Olson RK, DeFries JC, Wood F, Pennington BF, Page GP, Smith SD, Gruen JR. Evidence for linkage and association with reading disability on 6p21.3-22. American Journal of Human Genetics. 70: 1287-98. PMID 11951179 DOI: 10.1086/340449  0.652
2002 Willcutt EG, Pennington BF, Smith SD, Cardon LR, Gayán J, Knopik VS, Olson RK, DeFries JC. Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder. American Journal of Medical Genetics. 114: 260-8. PMID 11920845 DOI: 10.1002/Ajmg.10205  0.596
2002 Gayán J, Olson RK. Genetic and environmental influences on orthographic and phonological skills in children with reading disabilities. Developmental Neuropsychology. 20: 483-507. PMID 11892949 DOI: 10.1207/S15326942Dn2002_3  0.627
2002 Fisher SE, Francks C, Marlow AJ, MacPhie IL, Newbury DF, Cardon LR, Ishikawa-Brush Y, Richardson AJ, Talcott JB, Gayán J, Olson RK, Pennington BF, Smith SD, DeFries JC, Stein JF, et al. Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature Genetics. 30: 86-91. PMID 11743577 DOI: 10.1038/Ng792  0.649
2001 Smith SD, Kelley PM, Askew JW, Hoover DM, Deffenbacher KE, Gayán J, Brower AM, Olson RK. Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate gene. Journal of Learning Disabilities. 34: 512-9. PMID 15503566 DOI: 10.1177/002221940103400604  0.559
2001 Davis CJ, Gayán J, Knopik VS, Smith SD, Cardon LR, Pennington BF, Olson RK, DeFries JC. Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability. Behavior Genetics. 31: 625-35. PMID 11838539 DOI: 10.1023/A:1013305730430  0.646
2000 Gayán J, Olson RK. Reading disability: evidence for a genetic etiology. European Child & Adolescent Psychiatry. 52-5. PMID 10638371 DOI: 10.1007/Pl00010695  0.649
1999 Castles A, Datta H, Gayan J, Olson RK. Varieties of developmental reading disorder: genetic and environmental influences. Journal of Experimental Child Psychology. 72: 73-94. PMID 9927524 DOI: 10.1006/Jecp.1998.2482  0.615
1999 Gayán J, Smith SD, Cherny SS, Cardon LR, Fulker DW, Brower AM, Olson RK, Pennington BF, DeFries JC. Quantitative-trait locus for specific language and reading deficits on chromosome 6p. American Journal of Human Genetics. 64: 157-64. PMID 9915954 DOI: 10.1086/302191  0.632
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