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Lawrence H. Uricchio, Ph.D. - Publications

Affiliations: 
2014 Biological and Medical Informatics University of California, San Francisco, San Francisco, CA 
Area:
Genetics, Bioinformatics Biology
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13 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
2022 Ebel ER, Uricchio LH, Petrov DA, Egan ES. Revisiting the malaria hypothesis: accounting for polygenicity and pleiotropy. Trends in Parasitology. PMID 35065882 DOI: 10.1016/j.pt.2021.12.007  0.333
2019 Hernandez RD, Uricchio LH, Hartman K, Ye C, Dahl A, Zaitlen N. Ultrarare variants drive substantial cis heritability of human gene expression. Nature Genetics. 51: 1349-1355. PMID 31477931 DOI: 10.1038/S41588-019-0487-7  0.621
2019 Uricchio LH. Evolutionary perspectives on polygenic selection, missing heritability, and GWAS. Human Genetics. PMID 31201529 DOI: 10.1007/S00439-019-02040-6  0.497
2019 Uricchio LH, Petrov DA, Enard D. Exploiting selection at linked sites to infer the rate and strength of adaptation. Nature Ecology & Evolution. PMID 31061475 DOI: 10.1038/S41559-019-0890-6  0.321
2019 Uricchio LH, Kitano HC, Gusev A, Zaitlen NA. An evolutionary compass for detecting signals of polygenic selection and mutational bias. Evolution Letters. 3: 69-79. PMID 30788143 DOI: 10.1002/evl3.97  0.334
2018 Gignoux CR, Torgerson DG, Pino-Yanes M, Uricchio LH, Galanter J, Roth LA, Eng C, Hu D, Nguyen EA, Huntsman S, Mathias RA, Kumar R, Rodriguez-Santana J, Thakur N, Oh SS, et al. An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos. The Journal of Allergy and Clinical Immunology. PMID 30201514 DOI: 10.1016/J.Jaci.2016.08.057  0.592
2016 Uricchio LH, Zaitlen NA, Ye CJ, Witte JS, Hernandez RD. Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants. Genome Research. PMID 27197206 DOI: 10.1101/Gr.202440.115  0.652
2015 Uricchio LH, Torres R, Witte JS, Hernandez RD. Population genetic simulations of complex phenotypes with implications for rare variant association tests. Genetic Epidemiology. 39: 35-44. PMID 25417809 DOI: 10.1002/Gepi.21866  0.663
2014 Uricchio LH, Hernandez RD. Robust forward simulations of recurrent hitchhiking. Genetics. 197: 221-36. PMID 24561480 DOI: 10.1534/Genetics.113.156935  0.615
2012 Maher MC, Uricchio LH, Torgerson DG, Hernandez RD. Population genetics of rare variants and complex diseases. Human Heredity. 74: 118-28. PMID 23594490 DOI: 10.1159/000346826  0.674
2012 Uricchio LH, Chong JX, Ross KD, Ober C, Nicolae DL. Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals. Genetic Epidemiology. 36: 312-9. PMID 22460724 DOI: 10.1002/Gepi.21623  0.429
2012 Perdry H, Müller-Myhsok B, Clerget-Darpoux F, Génin E, Sahbatou M, Kim W, Londono D, Kazma R, Cardin NJ, Witte JS, Asimit JL, Zeggini E, Jouan L, Gauthier J, Dion PA, ... ... Uricchio LH, et al. Contents Vol. 74, 2012 Human Heredity. 74. DOI: 10.1159/000346894  0.538
2011 Çalışkan M, Chong JX, Uricchio L, Anderson R, Chen P, Sougnez C, Garimella K, Gabriel SB, dePristo MA, Shakir K, Matern D, Das S, Waggoner D, Nicolae DL, Ober C. Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Human Molecular Genetics. 20: 1285-9. PMID 21212097 DOI: 10.1093/Hmg/Ddq569  0.309
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