Marissa A. Ehringer - Related publications

University of Colorado, Boulder, Boulder, CO, United States 
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.
50 most relevant papers in past 60 days:
Year Citation  Score
2020 Lathen DR, Merrill CB, Rothenfluh A. Flying Together: as a Tool to Understand the Genetics of Human Alcoholism. International Journal of Molecular Sciences. 21. PMID 32932795 DOI: 10.3390/ijms21186649   
2020 Thapa KS, Chen AB, Lai D, Xuei X, Wetherill L, Tischfield JA, Liu Y, Edenberg HJ. Identification of Functional Genetic Variants Associated with Alcohol Dependence and Related Phenotypes Using a High-Throughput Assay. Alcoholism, Clinical and Experimental Research. PMID 33119910 DOI: 10.1111/acer.14492   
2020 Mullins VA, Bresette W, Johnstone L, Hallmark B, Chilton FH. Genomics in Personalized Nutrition: Can You "Eat for Your Genes"? Nutrients. 12. PMID 33065985 DOI: 10.3390/nu12103118   
2020 Maqsood A, Frome DK, Gibly RF, Larson JE, Patel NM, Sarwark JF. IS (Idiopathic Scoliosis) etiology: Multifactorial genetic research continues. A systematic review 1950 to 2017. Journal of Orthopaedics. 21: 421-426. PMID 32943828 DOI: 10.1016/j.jor.2020.08.005   
2020 Furukawa K, Igarashi M, Jia H, Nogawa S, Kawafune K, Hachiya T, Takahashi S, Saito K, Kato H. A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations. Nutrients. 12. PMID 33080986 DOI: 10.3390/nu12103182   
2020 Sutoh Y, Hachiya T, Suzuki Y, Komaki S, Ohmomo H, Kakisaka K, Wang T, Takikawa Y, Shimizu A. ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G × E interaction analysis. Scientific Reports. 10: 16227. PMID 33004991 DOI: 10.1038/s41598-020-73263-1   
2020 Chatzinakos C, Georgiadis F, Lee D, Cai N, Vladimirov VI, Docherty A, Webb BT, Riley BP, Flint J, Kendler KS, Daskalakis NP, Bacanu SA. TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32954640 DOI: 10.1002/ajmg.b.32823   
2020 Johnson EC, Demontis D, Thorgeirsson TE, Walters RK, Polimanti R, Hatoum AS, Sanchez-Roige S, Paul SE, Wendt FR, Clarke TK, Lai D, Reginsson GW, Zhou H, He J, Baranger DAA, ... , et al. A large-scale genome-wide association study meta-analysis of cannabis use disorder. The Lancet. Psychiatry. PMID 33096046 DOI: 10.1016/S2215-0366(20)30339-4   
2020 Alqudah AM, Haile JK, Alomari DZ, Pozniak CJ, Kobiljski B, Börner A. Genome-wide and SNP network analyses reveal genetic control of spikelet sterility and yield-related traits in wheat. Scientific Reports. 10: 2098. PMID 32034248 DOI: 10.1038/s41598-020-59004-4   
2020 Raymond B, Yengo L, Costilla R, Schrooten C, Bouwman AC, Hayes BJ, Veerkamp RF, Visscher PM. Using prior information from humans to prioritize genes and gene-associated variants for complex traits in livestock. Plos Genetics. 16: e1008780. PMID 32925905 DOI: 10.1371/journal.pgen.1008780   
2020 Ran H, Xiao H, Zhou X, Guo L, Lu S. Single-nucleotide polymorphisms and haplotypes in the interleukin-33 gene are associated with a risk of allergic rhinitis in the Chinese population. Experimental and Therapeutic Medicine. 20: 102. PMID 32973951 DOI: 10.3892/etm.2020.9232   
2020 Zhuo Z, Lu H, Zhu J, Hua RX, Li Y, Yang Z, Zhang J, Cheng J, Zhou H, Li S, Li L, Xia H, He J. METTL14 Gene Polymorphisms Confer Neuroblastoma Susceptibility: An Eight-Center Case-Control Study. Molecular Therapy. Nucleic Acids. 22: 17-26. PMID 32891980 DOI: 10.1016/j.omtn.2020.08.009   
2020 Manshaei R, Merico D, Reuter MS, Engchuan W, Mojarad BA, Chaturvedi R, Heung T, Pellecchia G, Zarrei M, Nalpathamkalam T, Khan R, Okello JBA, Liston E, Curtis M, Yuen RKC, et al. Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences. Frontiers in Genetics. 11: 957. PMID 33110418 DOI: 10.3389/fgene.2020.00957   
2020 Yadav T, Magotra A, Kumar R, Bangar Y, Rani Garg A, Kumar S, Jeet V, Malik BS. Evaluation of candidate genotype of Leptin gene associated with fertility and production traits in Hardhenu (Bos taurus x Bos indicus) cattle. Reproduction in Domestic Animals = Zuchthygiene. PMID 32965761 DOI: 10.1111/rda.13826   
2020 Roberson-Nay R, Lapato DM, Wolen AR, Lancaster EE, Webb BT, Verhulst B, Hettema JM, York TP. An epigenome-wide association study of early-onset major depression in monozygotic twins. Translational Psychiatry. 10: 301. PMID 32843619 DOI: 10.1038/s41398-020-00984-2   
2020 Shinohara T, Urayama KY, Watanabe A, Akahane K, Goi K, Huang M, Kagami K, Abe M, Sugita K, Okada Y, Goto H, Minegishi M, Iwamoto S, Inukai T. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Journal of Cellular and Molecular Medicine. PMID 33002292 DOI: 10.1111/jcmm.15882   
2020 Shinohara T, Urayama KY, Watanabe A, Akahane K, Goi K, Huang M, Kagami K, Abe M, Sugita K, Okada Y, Goto H, Minegishi M, Iwamoto S, Inukai T. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Journal of Cellular and Molecular Medicine. PMID 33002292 DOI: 10.1111/jcmm.15882   
2020 Owen KA, Price A, Ainsworth H, Aidukaitis BN, Bachali P, Catalina MD, Dittman JM, Howard TD, Kingsmore KM, Labonte AC, Marion MC, Robl RD, Zimmerman KD, Langefeld CD, Grammer AC, et al. Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries. American Journal of Human Genetics. PMID 33031749 DOI: 10.1016/j.ajhg.2020.09.007   
2020 Satturu V, Vattikuti JL, J DS, Kumar A, Singh RK, M SP, Zaw H, Jubay ML, Satish L, Rathore A, Mulinti S, Lakshmi Vg I, Chakraborty A, Thirunavukkarasu N. Multiple Genome Wide Association Mapping Models Identify Quantitative Trait Nucleotides for Brown Planthopper () Resistance in MAGIC Population of Rice. Vaccines. 8. PMID 33066559 DOI: 10.3390/vaccines8040608   
2020 Hebbar P, Abubaker JA, Abu-Farha M, Alsmadi O, Elkum N, Alkayal F, John SE, Channanath A, Iqbal R, Pitkaniemi J, Tuomilehto J, Sladek R, Al-Mulla F, Thanaraj TA. Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Human Genetics. PMID 32902719 DOI: 10.1007/s00439-020-02222-7   
2020 Trajanoska K, Seppala LJ, Medina-Gomez C, Hsu YH, Zhou S, van Schoor NM, de Groot LCPGM, Karasik D, Richards JB, Kiel DP, Uitterlinden AG, Perry JRB, van der Velde N, Day FR, Rivadeneira F. Genetic basis of falling risk susceptibility in the UK Biobank Study. Communications Biology. 3: 543. PMID 32999390 DOI: 10.1038/s42003-020-01256-x   
2020 Cohen C, Figueiredo EA, Belangero PS, Andreoli CV, Leal MF, Ejnisman B. Genetic Aspects in Shoulder Disorders. Revista Brasileira De Ortopedia. 55: 537-542. PMID 33093716 DOI: 10.1055/s-0040-1702955   
2020 Teng J, Huang S, Chen Z, Gao N, Ye S, Diao S, Ding X, Yuan X, Zhang H, Li J, Zhang Z. Optimizing genomic prediction model given causal genes in a dairy cattle population. Journal of Dairy Science. PMID 32952023 DOI: 10.3168/jds.2020-18233   
2020 Teng J, Huang S, Chen Z, Gao N, Ye S, Diao S, Ding X, Yuan X, Zhang H, Li J, Zhang Z. Optimizing genomic prediction model given causal genes in a dairy cattle population. Journal of Dairy Science. PMID 32952023 DOI: 10.3168/jds.2020-18233   
2020 Teng J, Huang S, Chen Z, Gao N, Ye S, Diao S, Ding X, Yuan X, Zhang H, Li J, Zhang Z. Optimizing genomic prediction model given causal genes in a dairy cattle population. Journal of Dairy Science. PMID 32952023 DOI: 10.3168/jds.2020-18233   
2020 Olvany JM, Sausville LN, White MJ, Tacconelli A, Tavera G, Sobota RS, Ciccacci C, Bohlbro AS, Wejse C, Williams SM, Sirugo G. CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa). Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 104560. PMID 32971250 DOI: 10.1016/j.meegid.2020.104560   
2020 Sui M, Wang Y, Bao Y, Wang X, Li R, Lv Y, Yan M, Quan C, Li C, Teng W, Li W, Zhao X, Han Y. Genome-wide association analysis of sucrose concentration in soybean (Glycine max L.) seed based on high-throughput sequencing. The Plant Genome. e20059. PMID 33058418 DOI: 10.1002/tpg2.20059   
2020 Xu C, Zhang R, Xia Y, Xiong L, Yang W, Wang P. Annotation of susceptibility SNPs associated with atrial fibrillation. Aging. 12. PMID 32902410 DOI: 10.18632/aging.103615   
2020 Zrzavy T, Leutmezer F, Kristoferitsch W, Kornek B, Schneider C, Rommer P, Berger T, Zimprich A. Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families. Genes. 11. PMID 32854198 DOI: 10.3390/genes11090988   
2020 Xu ZM, Burgess S. Polygenic modelling of treatment effect heterogeneity. Genetic Epidemiology. PMID 32779269 DOI: 10.1002/gepi.22347   
2020 Pividori M, Rajagopal PS, Barbeira A, Liang Y, Melia O, Bastarache L, Park Y, Consortium G, Wen X, Im HK. PhenomeXcan: Mapping the genome to the phenome through the transcriptome. Science Advances. 6. PMID 32917697 DOI: 10.1126/sciadv.aba2083   
2020 Ghoussaini M, Mountjoy E, Carmona M, Peat G, Schmidt EM, Hercules A, Fumis L, Miranda A, Carvalho-Silva D, Buniello A, Burdett T, Hayhurst J, Baker J, Ferrer J, Gonzalez-Uriarte A, et al. Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics. Nucleic Acids Research. PMID 33045747 DOI: 10.1093/nar/gkaa840   
2020 Wright GEB, Caron NS, Ng B, Casal L, Casazza W, Xu X, Ooi J, Pouladi MA, Mostafavi S, Ross CJD, Hayden MR. Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington disease. Human Molecular Genetics. PMID 32898862 DOI: 10.1093/hmg/ddaa184   
2020 Crouch DJM, Bodmer WF. Polygenic inheritance, GWAS, polygenic risk scores, and the search for functional variants. Proceedings of the National Academy of Sciences of the United States of America. 117: 18924-18933. PMID 32753378 DOI: 10.1073/pnas.2005634117   
2020 Liu X, Mefford JA, Dahl A, He Y, Subramaniam M, Battle A, Price AL, Zaitlen N. GBAT: a gene-based association test for robust detection of trans-gene regulation. Genome Biology. 21: 211. PMID 32831138 DOI: 10.1186/s13059-020-02120-1   
2020 León-Reyes G, Rivera-Paredez B, López JCF, Ramírez-Salazar EG, Aquino-Gálvez A, Gallegos-Carrillo K, Denova-Gutiérrez E, Salmerón J, Velázquez-Cruz R. The Variant rs1784042 of the Gene is Associated with Metabolic Syndrome through Low HDL-c Levels in a Mexican Population. Genes. 11. PMID 33066450 DOI: 10.3390/genes11101192   
2020 Langer T, Clemens E, Broer L, Maier L, Uitterlinden AG, de Vries ACH, van Grotel M, Pluijm SFM, Binder H, Mayer B, von dem Knesebeck A, Byrne J, van Dulmen-den Broeder E, Crocco M, Grabow D, ... , et al. Association of candidate pharmacogenetic markers with platinum-induced ototoxicity: PanCareLIFE dataset. Data in Brief. 32: 106227. PMID 32939381 DOI: 10.1016/j.dib.2020.106227   
2020 Ma C, Li X, Chen J, Li Z, Guan J, Li Y, Yin S, Shi Y. Association Analysis Between Common Variants of the Gene and Three Mental Disorders in the Han Chinese Population. Genetic Testing and Molecular Biomarkers. PMID 33001715 DOI: 10.1089/gtmb.2019.0096   
2020 Crawford H, Scerif G, Wilde L, Beggs A, Stockton J, Sandhu P, Shelley L, Oliver C, McCleery J. Genetic modifiers in rare disorders: the case of fragile X syndrome. European Journal of Human Genetics : Ejhg. PMID 32862204 DOI: 10.1038/s41431-020-00711-x   
2020 Shi X, Chai X, Yang Y, Cheng Q, Jiao Y, Chen H, Huang J, Yang C, Liu J. A tissue-specific collaborative mixed model for jointly analyzing multiple tissues in transcriptome-wide association studies. Nucleic Acids Research. PMID 32978944 DOI: 10.1093/nar/gkaa767   
2020 Chen SY, Oliveira HR, Schenkel FS, Pedrosa VB, Melka MG, Brito LF. Using imputed whole-genome sequence variants to uncover candidate mutations and genes affecting milking speed and temperament in Holstein cattle. Journal of Dairy Science. PMID 32952011 DOI: 10.3168/jds.2020-18897   
2020 Chhetri HB, Furches A, Macaya-Sanz D, Walker AR, Kainer D, Jones P, Harman-Ware AE, Tschaplinski TJ, Jacobson D, Tuskan GA, DiFazio SP. Genome-Wide Association Study of Wood Anatomical and Morphological Traits in . Frontiers in Plant Science. 11: 545748. PMID 33013968 DOI: 10.3389/fpls.2020.545748   
2020 Miller AK, Chen A, Bartlett J, Wang L, Williams SM, Buchner DA. A Novel Mapping Strategy Utilizing Mouse Chromosome Substitution Strains Identifies Multiple Epistatic Interactions That Regulate Complex Traits. G3 (Bethesda, Md.). PMID 33023974 DOI: 10.1534/g3.120.401824   
2020 Akhatar J, Singh MP, Sharma A, Kaur H, Kaur N, Sharma S, Bharti B, Sardana VK, Banga SS. Association Mapping of Seed Quality Traits Under Varying Conditions of Nitrogen Application in L. Czern & Coss. Frontiers in Genetics. 11: 744. PMID 33088279 DOI: 10.3389/fgene.2020.00744   
2020 Qin N, Li Y, Wang C, Zhu M, Dai J, Hong T, Albanes D, Lam S, Tardon A, Chen C, Goodman G, Bojesen SE, Landi MT, Johansson M, Risch A, et al. Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma. Frontiers of Medicine. PMID 32889700 DOI: 10.1007/s11684-020-0779-4   
2020 Benedek I, Altbӓcker V, Zsolnai A, Molnár T. Exploring the Genetic Background of the Differences in Nest-Building Behavior in European Rabbit. Animals : An Open Access Journal From Mdpi. 10. PMID 32899658 DOI: 10.3390/ani10091579   
2020 Wang M, Ma SJ, Wu XY, Zhang X, Abesig J, Xiao ZH, Huang X, Yan HP, Wang J, Chen MS, Tan HZ. Impact of gene polymorphisms and gene-tea interaction on susceptibility to tuberculosis. World Journal of Clinical Cases. 8: 4320-4330. PMID 33083391 DOI: 10.12998/wjcc.v8.i19.4320   
2020 Sun R, Lin X. Genetic Variant Set-Based Tests Using the Generalized Berk-Jones Statistic with Application to a Genome-Wide Association Study of Breast Cancer. Journal of the American Statistical Association. 115: 1079-1091. PMID 33041403 DOI: 10.1080/01621459.2019.1660170   
2020 Nakamura R, Misawa K, Tohnai G, Nakatochi M, Furuhashi S, Atsuta N, Hayashi N, Yokoi D, Watanabe H, Watanabe H, Katsuno M, Izumi Y, Kanai K, Hattori N, Morita M, et al. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. Communications Biology. 3: 526. PMID 32968195 DOI: 10.1038/s42003-020-01251-2   
2020 Xu M, Li J, Xiao Z, Lou J, Pan X, Ma Y. Integrative genomics analysis identifies promising SNPs and genes implicated in tuberculosis risk based on multiple omics datasets. Aging. 12. PMID 33051402 DOI: 10.18632/aging.103744