Javier Gayan, Ph.D. - Related publications

Affiliations: 
2000 University of Colorado, Boulder, Boulder, CO, United States 
Area:
Psychobiology Psychology, Psychometrics Psychology, Genetics, Reading Education
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
21 most relevant papers in past 60 days:
Year Citation  Score
2022 Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, ... , et al. The genetic architecture of pediatric cardiomyopathy. American Journal of Human Genetics. PMID 35026164 DOI: 10.1016/j.ajhg.2021.12.006   
2022 Ng JW, Chong ETJ, Lee PC. An Updated Review on the Role of Single Nucleotide Polymorphisms in COVID-19 Disease Severity: A Global Aspect. Current Pharmaceutical Biotechnology. PMID 35034591 DOI: 10.2174/1389201023666220114162347   
2022 Restuadi R, Steyn FJ, Kabashi E, Ngo ST, Cheng FF, Nabais MF, Thompson MJ, Qi T, Wu Y, Henders AK, Wallace L, Bye CR, Turner BJ, Ziser L, Mathers S, et al. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Medicine. 14: 7. PMID 35042540 DOI: 10.1186/s13073-021-01006-6   
2022 Null M, Yilmaz F, Astling D, Yu HC, Cole JB, Hallgrímsson B, Santorico SA, Spritz RA, Shaikh TH, Hendricks AE. Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. Hgg Advances. 3: 100082. PMID 35047866 DOI: 10.1016/j.xhgg.2021.100082   
2022 Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y. From GWAS variant to function: A study of ∼148,000 variants for blood cell traits. Hgg Advances. 3: 100063. PMID 35047852 DOI: 10.1016/j.xhgg.2021.100063   
2022 Zhao Y, Pu Y, Liang B, Bai T, Liu Y, Jiang L, Ma Y. A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep. Animal Genetics. PMID 35040155 DOI: 10.1111/age.13169   
2022 Bao J, Wen Z, Kim M, Saykin AJ, Thompson PM, Zhao Y, Shen L, . Identifying imaging genetic associations via regional morphometricity estimation. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 27: 97-108. PMID 34890140   
2022 Kim C, Kim YJ, Choi W, Jang HM, Hwang MY, Jung S, Lim H, Hong SB, Yoon K, Kim BJ, Park HY, Han B. Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals. Human Molecular Genetics. PMID 35043955 DOI: 10.1093/hmg/ddac016   
2022 Nam Y, Jung SH, Verma A, Sriram V, Won HH, Yun JS, , Kim D. netCRS: Network-based comorbidity risk score for prediction of myocardial infarction using biobank-scaled PheWAS data. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 27: 325-336. PMID 34890160   
2022 Qi G, Dutta D, Leroux A, Ray D, Muschelli J, Crainiceanu C, Chatterjee N. Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Genetic Epidemiology. PMID 35043453 DOI: 10.1002/gepi.22441   
2022 Dharmadasa T, Scaber J, Edmond E, Marsden R, Thompson A, Talbot K, Turner MR. Genetic testing in motor neurone disease. Practical Neurology. PMID 35027459 DOI: 10.1136/practneurol-2021-002989   
2022 Burton AR, Gravem SA, Barreto FS. Little evidence for genetic variation associated with susceptibility to sea star wasting syndrome in the keystone species Pisaster ochraceus. Molecular Ecology. 31: 197-205. PMID 34626020 DOI: 10.1111/mec.16212   
2022 Jiao B, Xiao X, Yuan Z, Guo L, Liao X, Zhou Y, Zhou L, Wang X, Liu X, Liu H, Jiang Y, Lin Z, Zhu Y, Yang Q, Zhang W, et al. Associations of risk genes with onset age and plasma biomarkers of Alzheimer's disease: a large case-control study in mainland China. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 35001095 DOI: 10.1038/s41386-021-01258-1   
2022 Chen X, Huang X, Zheng C, Wang X, Zhang W. Using the optimal method-explained variance weighted genetic risk score to predict the efficacy of folic acid therapy to hyperhomocysteinemia. European Journal of Clinical Nutrition. PMID 35001080 DOI: 10.1038/s41430-021-01055-5   
2022 Li C, Duan D, Xue Y, Han X, Wang K, Qiao R, Li XL, Li XJ. An association study on imputed whole-genome resequencing from high-throughput sequencing data for body traits in crossbred pigs. Animal Genetics. PMID 35026054 DOI: 10.1111/age.13170   
2022 Lopes KP, Snijders GJL, Humphrey J, Allan A, Sneeboer MAM, Navarro E, Schilder BM, Vialle RA, Parks M, Missall R, van Zuiden W, Gigase FAJ, Kübler R, van Berlekom AB, Hicks EM, et al. Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies. Nature Genetics. 54: 4-17. PMID 34992268 DOI: 10.1038/s41588-021-00976-y   
2022 Xia G, Li Y, Pan W, Qian C, Ma L, Zhou J, Xu H, Cheng C. SLAMF6 is associated with the susceptibility and severity of rheumatoid arthritis in the Chinese population. Journal of Orthopaedic Surgery and Research. 17: 13. PMID 35016729 DOI: 10.1186/s13018-021-02901-9   
2022 Chen B, Li Y, Tian M, Su H, Sun W, Li Y. Linkage mapping and QTL analysis of growth traits in Rhopilema esculentum. Scientific Reports. 12: 471. PMID 35013486 DOI: 10.1038/s41598-021-04431-0   
2022 Wong HS, Tsai SY, Chu HW, Lin MR, Lin GH, Tai YT, Shen CY, Chang WC. Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Plos Genetics. 18: e1009952. PMID 35051171 DOI: 10.1371/journal.pgen.1009952   
2022 Abou-Khater L, Maalouf F, Jighly A, Alsamman AM, Rubiales D, Rispail N, Hu J, Ma Y, Balech R, Hamwieh A, Baum M, Kumar S. Genomic regions associated with herbicide tolerance in a worldwide faba bean (Vicia faba L.) collection. Scientific Reports. 12: 158. PMID 34996977 DOI: 10.1038/s41598-021-03861-0   
2022 Wang Z, Zhou L, Lan Y, Li X, Wang J, Dong J, Guo W, Jing D, Liu Q, Zhang S, Liu Z, Shi W, Yang W, Yang T, Sun F, et al. An aspartic protease 47 causes quantitative recessive resistance to rice black-streaked dwarf virus disease and southern rice black-streaked dwarf virus disease. The New Phytologist. PMID 35015901 DOI: 10.1111/nph.17961