Frazer, Kelly A.

Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21

Patil, N., Berno, A. J., Hinds, D. A., Barrett, W. A., Doshi, J. M., Hacker, C. R., Kautzer, C. R., Lee, D. H., Marjoribanks, C., McDonough, D. P., et al. (2001) · Science

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 1,145

Human genetic variation and its contribution to complex traits

Frazer, K. A., Murray, S. S., Schork, N. J., & Topol, E. J. (2009) · Nature Reviews Genetics

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 1,073

Common vs. rare allele hypotheses for complex diseases

Schork, N. J., Murray, S. S., Frazer, K. A., & Topol, E. J. (2009) · Current Opinion in Genetics & Development

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 649

Evaluation of next generation sequencing platforms for population targeted sequencing studies

Harismendy, O., Ng, P. C., Strausberg, R. L., Wang, X., Stockwell, T. B., Beeson, K. Y., Schork, N. J., Murray, S. S., Topol, E. J., Levy, S., et al. (2009) · Genome Biology

Genomics and Phylogenetic StudiesGenomics and Rare Diseases

Cited by 614

Microdroplet-based PCR enrichment for large-scale targeted sequencing

Tewhey, R., Warner, J. B., Nakano, M., Libby, B., Medkova, M., David, P. H., Kotsopoulos, S. K., Samuels, M. L., Hutchison, J. B., Larson, J. W., et al. (2009) · Nature Biotechnology

Innovative Microfluidic and Catalytic Techniques InnovationGenomics and Phylogenetic Studies

Cited by 454

Common deletions and SNPs are in linkage disequilibrium in the human genome

Hinds, D. A., Kloek, A. P., Jen, M., Chen, X., & Frazer, K. A. (2006) · Nature Genetics

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 372

Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

Lindström, S., Wang, L., Smith, E. N., Gordon, W., van Hylckama Vlieg, A., de Andrade, M., Brody, J. A., Pattee, J. W., Haessler, J., Brumpton, B. M., et al. (2019) · Blood

Genetic Associations and EpidemiologyBlood Coagulation and Thrombosis Mechanisms

Cited by 223

Enhancer release and retargeting activates disease-susceptibility genes

Oh, S., Shao, J., Mitra, J., Xiong, F., D’Antonio, M., Wang, R., Garcia-Bassets, I., Ma, Q., Zhu, X., Lee, J.-H., et al. (2021) · Nature

Genomics and Chromatin DynamicsChromatin Remodeling and Cancer

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Fine mapping in 94 inbred mouse strains using a high-density haplotype resource

Kirby, A., Kang, H. M., Wade, C. M., Cotsapas, C., Kostem, E., Han, B., Furlotte, N., Kang, E. Y., Rivas, M., Bogue, M. A., et al. (2010) · Genetics

Genetic Mapping and Diversity in Plants and AnimalsGenetic Associations and Epidemiology

Cited by 102

Identification of Common and Rare Genetic Variation Associated With Plasma Protein Levels Using Whole-Exome Sequencing and Mass Spectrometry

Solomon, T., Lapek, J. D., Jensen, S. B., Greenwald, W. W., Hindberg, K., Matsui, H., Latysheva, N., Braekken, S. K., Gonzalez, D. J., Frazer, K. A., et al. (2018) · Circulation: Genomic and Precision Medicine

Genetic Associations and EpidemiologyGenomics and Rare Diseases

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