Erika L. Nurmi, Ph.D. - Related publications

Affiliations: 
2003 Vanderbilt University, Nashville, TN 
Area:
Genetics, Neuroscience Biology, Molecular Biology, Pathology
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.
18 most relevant papers in past 60 days:
Year Citation  Score
2021 Xie X, Li L, Wu H, Hou F, Chen Y, Xue Q, Zhou Y, Zhang J, Gong J, Song R. Comprehensive Integrative Analyses Identify TIGD5 rs75547282 as a Risk Variant for Autism Spectrum Disorder. Autism Research : Official Journal of the International Society For Autism Research. PMID 33393181 DOI: 10.1002/aur.2466   
2021 Chawner SJRA, Doherty JL, Anney RJL, Antshel KM, Bearden CE, Bernier R, Chung WK, Clements CC, Curran SR, Cuturilo G, Fiksinski AM, Gallagher L, Goin-Kochel RP, Gur RE, Hanson E, ... , et al. A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants. The American Journal of Psychiatry. 178: 77-86. PMID 33384013 DOI: 10.1176/appi.ajp.2020.20010015   
2021 Manoli DS, State MW. Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms. The American Journal of Psychiatry. 178: 30-38. PMID 33384012 DOI: 10.1176/appi.ajp.2020.20111608   
2021 Liu Z, Mao X, Dan Z, Pei Y, Xu R, Guo M, Liu K, Zhang F, Chen J, Su C, Zhuang Y, Tang J, Xia Y, Qin L, Hu Z, et al. Gene variations in autism spectrum disorder are associated with alteration of gut microbiota, metabolites and cytokines. Gut Microbes. 13: 1-16. PMID 33412999 DOI: 10.1080/19490976.2020.1854967   
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 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 Qaiser F, Yin Y, Mervis CB, Morris CA, Klein-Tasman BP, Tam E, Osborne LR, Yuen RKC. Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype. Orphanet Journal of Rare Diseases. 16: 6. PMID 33407644 DOI: 10.1186/s13023-020-01648-6   
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 Li F, Liu J, Liu W, Gao J, Lei Q, Han H, Yang J, Li H, Cao D, Zhou Y. Genome-wide association study of body size traits in Wenshang Barred chickens based on the specific-locus amplified fragment sequencing technology. Animal Science Journal = Nihon Chikusan Gakkaiho. 92: e13506. PMID 33398896 DOI: 10.1111/asj.13506   
2021 Zhang P, Liu J, Li X, Gao M, Feng F, Wang W, Zhang Q, Yao W. NF1 and PTEN gene polymorphisms and the susceptibility to soft tissue sarcomas in a Chinese population: A case-control study. Experimental and Molecular Pathology. 104603. PMID 33422488 DOI: 10.1016/j.yexmp.2021.104603   
2021 Garrido N, Cruz F, Egea RR, Simon C, Sadler-Riggleman I, Beck D, Nilsson E, Ben Maamar M, Skinner MK. Sperm DNA methylation epimutation biomarker for paternal offspring autism susceptibility. Clinical Epigenetics. 13: 6. PMID 33413568 DOI: 10.1186/s13148-020-00995-2   
2021 Ayaad M, Han Z, Zheng K, Hu G, Abo-Yousef M, Sobeih SES, Xing Y. Bin-based genome-wide association studies reveal superior alleles for improvement of appearance quality using a 4-way MAGIC population in rice. Journal of Advanced Research. 28: 183-194. PMID 33364055 DOI: 10.1016/j.jare.2020.08.001   
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 Efthymiou S, Dutra-Clarke M, Maroofian R, Kaiyrzhanov R, Scala M, Reza Alvi J, Sultan T, Christoforou M, Tuyet Mai Nguyen T, Mankad K, Vona B, Rad A, Striano P, Salpietro V, Guillen Sacoto MJ, et al. Expanding the phenotype of PIGS-associated early onset epileptic developmental encephalopathy. Epilepsia. PMID 33410539 DOI: 10.1111/epi.16801   
2021 Zheng Q, Bi R, Xu M, Zhang DF, Tan LW, Lu YP, Yao YG. Exploring the Genetic Association of the ABAT Gene with Alzheimer's Disease. Molecular Neurobiology. PMID 33404980 DOI: 10.1007/s12035-020-02271-z   
2021 Borg R, Farrugia Wismayer M, Bonavia K, Farrugia Wismayer A, Vella M, van Vugt JJFA, Kenna BJ, Kenna KP, Vassallo N, Veldink JH, Cauchi RJ. Genetic analysis of ALS cases in the isolated island population of Malta. European Journal of Human Genetics : Ejhg. PMID 33414559 DOI: 10.1038/s41431-020-00767-9   
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 Zhang C, Fang X, Zhang H, Gao W, Hsu HJ, Roman RJ, Fan F. Genetic susceptibility of hypertension-induced kidney disease. Physiological Reports. 9: e14688. PMID 33377622 DOI: 10.14814/phy2.14688