Stephen Erickson, Ph.D. - Related publications

Affiliations: 
2006 University of California, Los Angeles, Los Angeles, CA 
Area:
Mathematics, Biostatistics Biology
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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Escott-Price V, Schmidt KM. Challenges of Adjusting Single-Nucleotide Polymorphism Effect Sizes for Linkage Disequilibrium. Human Heredity. 1-11. PMID 33582669 DOI: 10.1159/000513303   
2021 Selvarajan I, Toropainen A, Garske KM, López Rodríguez M, Ko A, Miao Z, Kaminska D, Õunap K, Örd T, Ravindran A, Liu OH, Moreau PR, Jawahar Deen A, Männistö V, Pan C, et al. Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease. American Journal of Human Genetics. PMID 33626337 DOI: 10.1016/j.ajhg.2021.02.006   
2021 Li Y, Wang W, Gao R, Xu X, Zhang Y. Genome-wide prioritization reveals novel gene signatures associated with cardiotoxic effects of tyrosine kinase inhibitors. Oncology Letters. 21: 94. PMID 33376527 DOI: 10.3892/ol.2020.12355   
2021 Schwartzentruber J, Cooper S, Liu JZ, Barrio-Hernandez I, Bello E, Kumasaka N, Young AMH, Franklin RJM, Johnson T, Estrada K, Gaffney DJ, Beltrao P, Bassett A. Genome-wide meta-analysis, fine-mapping and integrative prioritization implicate new Alzheimer's disease risk genes. Nature Genetics. PMID 33589840 DOI: 10.1038/s41588-020-00776-w   
2021 Zhu R, Tian D, Zhao Y, Zhang C, Liu X. Genome-Wide Detection of mA-Associated Genetic Polymorphisms Associated with Ischemic Stroke. Journal of Molecular Neuroscience : Mn. PMID 33580473 DOI: 10.1007/s12031-021-01805-x   
2021 Yuan Y, Bao J, Chen Z, Villanueva AD, Wen W, Wang F, Zhao D, Fu X, Cai Q, Long J, Shu XO, Zheng D, Moreno V, Zheng W, Lin W, et al. Multi-omics analysis to identify susceptibility genes for colorectal cancer. Human Molecular Genetics. PMID 33481017 DOI: 10.1093/hmg/ddab021   
2021 Yao Q, Ferragina P, Reshef Y, Lettre G, Bauer DE, Pinello L. Motif-Raptor: A Cell Type-Specific and Transcription Factor Centric Approach for Post-GWAS Prioritization of Causal Regulators. Bioinformatics (Oxford, England). PMID 33532840 DOI: 10.1093/bioinformatics/btab072   
2021 Padula AM, Yang W, Schultz K, Lee C, Lurmann F, Hammond SK, Shaw GM. Gene-environment interactions between air pollution and biotransformation enzymes and risk of birth defects. Birth Defects Research. PMID 33569925 DOI: 10.1002/bdr2.1880   
2021 Liu CX, Yin RX, Shi ZH, Zheng PF, Deng GX, Guan YZ, Wei BL. Associations between SNPs, their haplotypes, gene-gene, and gene-environment interactions and dyslipidemia. Aging. 13. PMID 33612478 DOI: 10.18632/aging.202514   
2021 Peng W, Zhao ZZ, Jiao L, Wu T, Chen H, Zhang CY, Song JJ, Liu TY, Wu LJ, Wang MJ, Chen J, Zhou Y, Ying BW. Prospective study of ALDH1A1 gene polymorphisms associated with antituberculosis drug-induced liver injury in Western Chinese Han population. Microbiology and Immunology. PMID 33527427 DOI: 10.1111/1348-0421.12877   
2021 Langmyhr M, Henriksen SP, Cappelletti C, van de Berg WDJ, Pihlstrøm L, Toft M. Allele-specific expression of Parkinson's disease susceptibility genes in human brain. Scientific Reports. 11: 504. PMID 33436766 DOI: 10.1038/s41598-020-79990-9   
2021 Zhang L, Sun Y, Zhang X, Shan X, Li J, Yao Y, Shu Y, Lin K, Huang X, Yang Z, Chu J, Huang L, Sun H. Three novel genetic variants in the FAM110D, CACNA1A and NLRP12 genes are associated with susceptibility to hypertension among Dai people. American Journal of Hypertension. PMID 33621312 DOI: 10.1093/ajh/hpab040   
2021 Mone F, McMullan DJ, Williams D, Chitty LS, Maher ER, Kilby MD, , . Evidence to Support the Clinical Utility of Prenatal Exome Sequencing in Evaluation of the Fetus with Congenital Anomalies: Scientific Impact Paper No. 64 [February] 2021. Bjog : An International Journal of Obstetrics and Gynaecology. PMID 33590639 DOI: 10.1111/1471-0528.16616   
2021 Zhang W, Reeves GR, Tautz D. Testing Implications of the Omnigenic Model for the Genetic Analysis of Loci Identified through Genome-wide Association. Current Biology : Cb. PMID 33417882 DOI: 10.1016/j.cub.2020.12.023   
2021 Wang J, Luo X, Pan J, Dong X, Tian X, Tu Z, Ju W, Zhang M, Zhong M, De Chen C, Flory M, Wang Y, Ted Brown W, Zhong N. (Epi)genetic variants of the sarcomere-desmosome are associated with premature utero-contraction in spontaneous preterm labor. Environment International. 148: 106382. PMID 33472089 DOI: 10.1016/j.envint.2021.106382   
2021 Shi C, Ray-Jones H, Ding J, Duffus K, Fu Y, Gaddi VP, Gough O, Hankinson J, Martin P, McGovern A, Yarwood A, Gaffney P, Eyre S, Rattray M, Warren RB, et al. Chromatin looping links target genes with genetic risk loci for dermatological traits. The Journal of Investigative Dermatology. PMID 33607115 DOI: 10.1016/j.jid.2021.01.015   
2021 Ruan D, Zhuang Z, Ding R, Qiu Y, Zhou S, Wu J, Xu C, Hong L, Huang S, Zheng E, Cai G, Wu Z, Yang J. Weighted Single-Step GWAS Identified Candidate Genes Associated with Growth Traits in a Duroc Pig Population. Genes. 12. PMID 33477978 DOI: 10.3390/genes12010117   
2021 Barbeira AN, Bonazzola R, Gamazon ER, Liang Y, Park Y, Kim-Hellmuth S, Wang G, Jiang Z, Zhou D, Hormozdiari F, Liu B, Rao A, Hamel AR, Pividori MD, Aguet F, , ... , et al. Exploiting the GTEx resources to decipher the mechanisms at GWAS loci. Genome Biology. 22: 49. PMID 33499903 DOI: 10.1186/s13059-020-02252-4   
2021 Hu S, Uniken Venema WT, Westra HJ, Vich Vila A, Barbieri R, Voskuil MD, Blokzijl T, Jansen BH, Li Y, Daly MJ, Xavier RJ, Dijkstra G, Festen EA, Weersma RK. Inflammation status modulates the effect of host genetic variation on intestinal gene expression in inflammatory bowel disease. Nature Communications. 12: 1122. PMID 33602935 DOI: 10.1038/s41467-021-21458-z   
2021 Cheng Y, Schlosser P, Hertel J, Sekula P, Oefner PJ, Spiekerkoetter U, Mielke J, Freitag DF, Schmidts M, , Kronenberg F, Eckardt KU, Thiele I, Li Y, Köttgen A. Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism. Nature Communications. 12: 964. PMID 33574263 DOI: 10.1038/s41467-020-20877-8   
2021 Cheng Y, Schlosser P, Hertel J, Sekula P, Oefner PJ, Spiekerkoetter U, Mielke J, Freitag DF, Schmidts M, , Kronenberg F, Eckardt KU, Thiele I, Li Y, Köttgen A. Rare genetic variants affecting urine metabolite levels link population variation to inborn errors of metabolism. Nature Communications. 12: 964. PMID 33574263 DOI: 10.1038/s41467-020-20877-8   
2021 Au KS, Hebert L, Hillman P, Baker C, Brown MR, Kim DK, Soldano K, Garrett M, Ashley-Koch A, Lee S, Gleeson J, Hixson JE, Morrison AC, Northrup H. Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration. Scientific Reports. 11: 3639. PMID 33574475 DOI: 10.1038/s41598-021-83058-7   
2021 Xue H, Yu A, Chen X, Lin N, Lin M, Huang H, Xu L. Prenatal diagnosis of duplication by single nucleotide polymorphism array in a family with Pelizaeus-Merzbacher disease. Aging. 13. PMID 33429367 DOI: 10.18632/aging.202477   
2021 Corradi C, Gentiluomo M, Gajdán L, Cavestro GM, Kreivenaite E, Di Franco G, Sperti C, Giaccherini M, Petrone MC, Tavano F, Gioffreda D, Morelli L, Soucek P, Andriulli A, Izbicki JR, et al. Genome-wide scan of long noncoding RNA single nucleotide polymorphisms and pancreatic cancer susceptibility. International Journal of Cancer. PMID 33534179 DOI: 10.1002/ijc.33475   
2021 Tibbs Cortes L, Zhang Z, Yu J. Status and prospects of genome-wide association studies in plants. The Plant Genome. e20077. PMID 33442955 DOI: 10.1002/tpg2.20077   
2021 Hernández Cordero AI, Li X, Milne S, Yang CX, Bossé Y, Joubert P, Timens W, van den Berge M, Nickle D, Hao K, Sin DD. Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19. Human Genetics. PMID 33604698 DOI: 10.1007/s00439-021-02264-5   
2021 Parker LE, Landstrom AP. Genetic Etiology of Left-Sided Obstructive Heart Lesions: A Story in Development. Journal of the American Heart Association. e019006. PMID 33432820 DOI: 10.1161/JAHA.120.019006   
2021 Chen H, Wang T, Huang S, Zeng P. New novel non-MHC genes were identified for cervical cancer with an integrative analysis approach of transcriptome-wide association study. Journal of Cancer. 12: 840-848. PMID 33403041 DOI: 10.7150/jca.47918   
2021 Valenzuela CE, Ballesta P, Ahmar S, Fiaz S, Heidari P, Maldonado C, Mora-Poblete F. Haplotype- and SNP-Based GWAS for Growth and Wood Quality Traits in Trees under Arid Conditions. Plants (Basel, Switzerland). 10. PMID 33450896 DOI: 10.3390/plants10010148   
2021 Lv J, Tu S, Xu L. Detection of Phenotype-related Mutations of COVID-19 via the Whole Genomic Data. Ieee/Acm Transactions On Computational Biology and Bioinformatics. PMID 33417561 DOI: 10.1109/TCBB.2021.3049836   
2021 Wei CY, Yang JH, Yeh EC, Tsai MF, Kao HJ, Lo CZ, Chang LP, Lin WJ, Hsieh FJ, Belsare S, Bhaskar A, Su MW, Lee TC, Lin YL, Liu FT, et al. Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese. Npj Genomic Medicine. 6: 10. PMID 33574314 DOI: 10.1038/s41525-021-00178-9   
2021 Chia R, Sabir MS, Bandres-Ciga S, Saez-Atienzar S, Reynolds RH, Gustavsson E, Walton RL, Ahmed S, Viollet C, Ding J, Makarious MB, Diez-Fairen M, Portley MK, Shah Z, Abramzon Y, ... , et al. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature Genetics. PMID 33589841 DOI: 10.1038/s41588-021-00785-3   
2021 Zhu J, Liu YH, He XL, Kohlmeier M, Zhou LL, Shen LW, Yi XX, Tang QY, Cai W, Wang B. Dietary Choline Intake during Pregnancy and PEMT rs7946 Polymorphism on Risk of Preterm Birth: A Case-Control Study. Annals of Nutrition & Metabolism. 1-10. PMID 33503637 DOI: 10.1159/000507472   
2021 Jayaseelan VP, Ramesh A, Arumugam P. Breast cancer and DDT: putative interactions, associated gene alterations, and molecular pathways. Environmental Science and Pollution Research International. PMID 33506412 DOI: 10.1007/s11356-021-12489-6   
2021 Scelsi MA, Napolioni V, Greicius MD, Altmann A, . Network propagation of rare variants in Alzheimer's disease reveals tissue-specific hub genes and communities. Plos Computational Biology. 17: e1008517. PMID 33411734 DOI: 10.1371/journal.pcbi.1008517   
2021 Gao S, Xu T, Mao C, Cheng J, Xun C, Liang W, Sheng W. Lack of Associations between Gene Polymorphisms and Ankylosing Spondylitis: A Meta-analysis with Trial Sequential Analysis. Immunological Investigations. 1-12. PMID 33401999 DOI: 10.1080/08820139.2020.1869253   
2021 Dai Y, Wang J, Jeong HH, Chen W, Jia P, Zhao Z. Association of with COVID-19 severity: Delineating the host genetic factors in transcriptomic regulation. Biorxiv : the Preprint Server For Biology. PMID 33619490 DOI: 10.1101/2021.02.17.431554   
2021 Abegaz F, Van Lishout F, Mahachie John JM, Chiachoompu K, Bhardwaj A, Duroux D, Gusareva ES, Wei Z, Hakonarson H, Van Steen K. Performance of model-based multifactor dimensionality reduction methods for epistasis detection by controlling population structure. Biodata Mining. 14: 16. PMID 33608043 DOI: 10.1186/s13040-021-00247-w   
2021 Shareef S, Ebrahimi SO, Reiisi S. Contribution of hsa-miR-146a and hsa-miR-223 gene variations in patients with multiple sclerosis reveals association of rs2910164 and rs1044165 with risk of multiple sclerosis susceptibility. Journal of Investigative Medicine : the Official Publication of the American Federation For Clinical Research. PMID 33478974 DOI: 10.1136/jim-2020-001539   
2021 Korologou-Linden R, Leyden GM, Relton CL, Richmond RC, Richardson TG. Multi-omics analyses of cognitive traits and psychiatric disorders highlights brain-dependent mechanisms. Human Molecular Genetics. PMID 33481009 DOI: 10.1093/hmg/ddab016   
2021 Chernus JM, Sherman SL, Feingold E. Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21. Prenatal Diagnosis. PMID 33596328 DOI: 10.1002/pd.5919   
2021 Boix CA, James BT, Park YP, Meuleman W, Kellis M. Regulatory genomic circuitry of human disease loci by integrative epigenomics. Nature. PMID 33536621 DOI: 10.1038/s41586-020-03145-z   
2021 Wu C, Tan S, Liu L, Cheng S, Li P, Li W, Liu H, Zhang F, Wang S, Ning Y, Wen Y, Zhang F. Transcriptome-wide association study identifies susceptibility genes for rheumatoid arthritis. Arthritis Research & Therapy. 23: 38. PMID 33482886 DOI: 10.1186/s13075-021-02419-9   
2021 Díez-Obrero V, Dampier CH, Moratalla-Navarro F, Devall M, Plummer SJ, Díez-Villanueva A, Peters U, Bien S, Huyghe JR, Kundaje A, Ibáñez-Sanz G, Guinó E, Obón-Santacana M, Carreras-Torres R, Casey G, et al. Genetic effects on transcriptome profiles in colon epithelium provide functional insights for genetic risk loci. Cellular and Molecular Gastroenterology and Hepatology. PMID 33601062 DOI: 10.1016/j.jcmgh.2021.02.003   
2021 Zhang Y, Yang H, Li S, Li WD, Wang J, Wang Y. Association analysis framework of genetic and exposure risks for COVID-19 in middle-aged and elderly adults. Mechanisms of Ageing and Development. 111433. PMID 33444631 DOI: 10.1016/j.mad.2021.111433   
2021 Curtis D. Multiple Linear Regression Allows Weighted Burden Analysis of Rare Coding Variants in an Ethnically Heterogeneous Population. Human Heredity. 1-10. PMID 33412546 DOI: 10.1159/000512576   
2021 Horowitz JE, Kosmicki JA, Damask A, Sharma D, Roberts GHL, Justice AE, Banerjee N, Coignet MV, Yadav A, Leader JB, Marcketta A, Park DS, Lanche R, Maxwell E, Knight SC, et al. Common genetic variants identify targets for COVID-19 and individuals at high risk of severe disease. Medrxiv : the Preprint Server For Health Sciences. PMID 33619501 DOI: 10.1101/2020.12.14.20248176   
2021 Liu YC, Peng XX, Lu YB, Wu XX, Chen LW, Feng H. Genome-wide association study reveals the genes associated with the leaf inclusion contents in Chinese medical tree Eucommia ulmoides. Bioscience, Biotechnology, and Biochemistry. 85: 233-241. PMID 33604631 DOI: 10.1093/bbb/zbaa005   
2021 Zhu J, Liu X, Yin H, Gao Y, Yu H. Convergent lines of evidence support BIN1 as a risk gene of Alzheimer's disease. Human Genomics. 15: 9. PMID 33516273 DOI: 10.1186/s40246-021-00307-6   
2021 Kajiya-Kanegae H, Nagasaki H, Kaga A, Hirano K, Ogiso-Tanaka E, Matsuoka M, Ishimori M, Ishimoto M, Hashiguchi M, Tanaka H, Akashi R, Isobe S, Iwata H. Whole-genome sequence diversity and association analysis of 198 soybean accessions in mini-core collections. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. PMID 33492369 DOI: 10.1093/dnares/dsaa032