Fuli:Publications

Publications 2010 1. The International HapMap 3 Consortium. Integrating common and rare genetic variation in diverse human populations. Nature 467, 52-58 (2 September 2010) 2. The 1000 Genomes consortium. A map of human genome variation from population scale sequencing. Nature 2010 In press. 3. Jinchuan Xing, W. Scott Watkins, Ya Hu, Chad D. Huff, Aniko Sabo, Donna M. Muzny, Michael J. Bamshad, Richard A. Gibbs, Lynn B. Jorde, and Fuli Yu*. Inference of human expansion in Eurasia and genetic diversity in India. Genome Biology 2010. *Corresponding Author Submitted. 4. Cristian Coarfa, Fuli Yu, Zuozhou Chen, Christopher A. Miller, R. Alan Harris, Aleksandar Milosavljevic. Pash 3.0: A versatile software package for read mapping, sequence comparison and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing. In submission 5. Marco Campos, Wei Sun, Fuli Yu (co-first author), Maja Barbalic, Weihong Tang, Woody Chambless, Christie Ballantyne, Aaron Folsom, Eric Boerwinkle, Jing-fei Dong. Genetic Determinants of Plasma von Willebrand Factor Antigen Levels: A Target Gene SNP and Haplotype Analysis of ARIC Cohort. 2010 Submitted. 2009 1. Yufeng Shen, Zhengzheng Wan, Cristian Coarfa, Rafal Drabek, Lei Chen, Elizabeth A. Ostrowski, Yue Liu, George M. Weinstock, David A. Wheeler, Richard A. Gibbs and Fuli Yu*. A SNP discovery method to assess variant allele probability in next generation resequencing data. Genome Research In press. 2009 *Corresponding Author PDF Supplemental Materials 2. Fuli Yu*, Alon Keinan, Hua Chen, Russell J. Ferland, Robert S. Hill, Andre A. Mignault, Christopher A. Walsh and David Reich. Detecting natural selection by empirical comparison to random regions of the genome. Human Molecular Genetics, 2009, Vol. 18, No. 24 4853–4867 *Corresponding Author PDF [Supplemental Materials] 3. Florez JC, Price AL, Campbell D, Riba L, Parra MV, Fuli Yu, Duque C, Saxena R, Gallego N, Tello-Ruiz M, Franco L, Rodríguez-Torres M, Villegas A, Bedoya G, Aguilar-Salinas CA, Tusié-Luna MT, Ruiz-Linares A, Reich D. Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes. Diabetologia'52(8):1528-36, 2009 Before 2009 1. The International HapMap Consortium. Genome-wide detection and characterization of positive selection in human populations. Nature, 449(7164):913-8. 2007 2. The International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature, 449(7164):851-61. 2007 3. Alkes L. Price, Nick Patterson, Fuli Yu, David R. Cox … and David Reich. A genomewide admixture map for Latino populations. American Journal of Human Genetics, 80(6):1024-1036. 2007. 4. Fuli Yu, R. Sean Hill, Eric T. Wang, Andre A. Mignault … and David Reich. Comment on “Ongoing Adaptive Evolution of ASPM, a Brain Size Determinant in Homo sapiens”. Science, 316(5823):370. 2007. 5. The International HapMap Consortium. A haplotype map of the human genome. Nature 437, 1299-1320. 2005. 6. Fuli Yu, Pardis C. Sabeti, Paul Hardenbol, Qing Fu … and Richard A. Gibbs. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. PLoS Genetics 1(3):e41. 2005. 7. Paul Hardenbol, Fuli Yu, John Belmont, Jennifer Barrett … and Richard Gibbs. Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay. Genome Research 15:269-275. 2005. 8. The International HapMap Consortium. Integrating ethics and science in the International HapMap Project. Nature Reviews Genetics 5:465-475. 2004. 9. The International HapMap Consortium. The International HapMap Project. Nature 426:789-796. 2003. 10. M. Maheshwari, J. Belmont, S. Fernbach, T. Ho, L. Molinari, I. Yakub, Fuli Yu … and Richard Gibbs. PTPN11 mutations in Noonan syndrome type I: detection of recurrent mutations in exon 3 and 13. Human Mutation 20:298-304. 2002. Talks September, 2010—Fuli Yu. Detecting Rare Genetic Variants in the Large-Scale 1000 Genomes Exome Resequencing Project. INVITED TALK Cambridge Healthtech Institute's Fourth Annual NGx: Evolution of Next-Generation Sequencing meeting, Providence, RI April, 2009—Fuli Yu. A SNP discovery method to assess variant allele probability in 2nd generation resequencing data, and examples for follow-up studies. INVITED TALK Fudan University, Shanghai, China. November, 2008—Fuli Yu. Empirical detection of recent selection at two brain-related genes: FOXP2 and AHI1. INVITED TALK Health science center at Houston, School of public health, The University of Texas. October, 2006—Fuli Yu. Empirical detection of natural selection at two brain-related genes (FOXP2 and AHI1) but failure to confirm evidence at ASPM. The American Society of Human Genetics 56th Annual Meeting, New Orleans, Louisiana. April, 2005—Fuli Yu. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. The Annual Symposium of Society of Chinese Bioscientists in America (SCBA), Texas Chapter, Houston, Texas. January, 2005—Fuli Yu. The status of the BCM-HGSC HapMap Project, and positive selection of a pre-expansion CAG repeat of human Spinocerebellar Ataxia Type 2 gene. INVITED TALK. Beijing Genomics Institute, Chinese Academy of Sciences, Beijing, China. December, 2004—Fuli Yu. The status of the BCM-HGSC HapMap Project. The Sixth Strategy Meeting of the International HapMap Project. Tokyo, Japan. February, 2004—Fuli Yu. The haplotype structure and linkage disequilibrium of human Chromosome 12. The 5th Annual Advances in Genome Biology and Technology (AGBT) and Automation in Mapping and DNA Sequencing (AMS) Meeting. Marco Island, Florida. [home page]