Andrea E. Byrnes, Ph.D. - Publications

Affiliations: 
2013 Biostatistics University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Biostatistics Biology, Bioinformatics Biology

10 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
2019 Farhan SMK, Howrigan DP, Abbott LE, Klim JR, Topp SD, Byrnes AE, Churchhouse C, Phatnani H, Smith BN, Rampersaud E, Wu G, Wuu J, Shatunov A, Iacoangeli A, Al Khleifat A, et al. Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience. PMID 31768050 DOI: 10.1038/S41593-019-0530-0  0.316
2018 Ganna A, Satterstrom FK, Zekavat SM, Das I, Kurki MI, Churchhouse C, Alfoldi J, Martin AR, Havulinna AS, Byrnes A, Thompson WK, Nielsen PR, Karczewski KJ, Saarentaus E, Rivas MA, et al. Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. American Journal of Human Genetics. PMID 29861106 DOI: 10.1016/J.Ajhg.2018.05.002  0.384
2018 Finucane HK, Reshef YA, Anttila V, Slowikowski K, Gusev A, Byrnes A, Gazal S, Loh PR, Lareau C, Shoresh N, Genovese G, Saunders A, Macosko E, Pollack S, et al. Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. Nature Genetics. 50: 621-629. PMID 29632380 DOI: 10.1038/S41588-018-0081-4  0.378
2017 Tukiainen T, Villani AC, Yen A, Rivas MA, Marshall JL, Satija R, Aguirre M, Gauthier L, Fleharty M, Kirby A, Cummings BB, Castel SE, Karczewski KJ, Aguet F, Byrnes A, et al. Landscape of X chromosome inactivation across human tissues. Nature. 550: 244-248. PMID 29022598 DOI: 10.1038/Nature24265  0.319
2016 Ganna A, Genovese G, Howrigan DP, Byrnes A, Kurki MI, Zekavat SM, Whelan CW, Kals M, Nivard MG, Bloemendal A, Bloom JM, Goldstein JI, Poterba T, Seed C, Handsaker RE, et al. Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nature Neuroscience. PMID 27694993 DOI: 10.1038/Nn.4404  0.343
2016 Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Byrnes AE, et al. Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. 48: 1296. PMID 27681292 DOI: 10.1038/Ng1016-1296C  0.318
2016 Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, ... ... Byrnes AE, et al. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nature Genetics. PMID 27322543 DOI: 10.1038/Ng.3598  0.384
2015 Yan S, Yuan S, Xu Z, Zhang B, Zhang B, Kang G, Byrnes A, Li Y. Likelihood-based complex trait association testing for arbitrary depth sequencing data. Bioinformatics (Oxford, England). PMID 25979475 DOI: 10.1093/Bioinformatics/Btv307  0.405
2013 Byrnes AE, Wu MC, Wright FA, Li M, Li Y. The value of statistical or bioinformatics annotation for rare variant association with quantitative trait. Genetic Epidemiology. 37: 666-74. PMID 23836599 DOI: 10.1002/Gepi.21747  0.422
2010 Li Y, Byrnes AE, Li M. To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests. American Journal of Human Genetics. 87: 728-35. PMID 21055717 DOI: 10.1016/J.Ajhg.2010.10.014  0.444
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