Ani W. Manichaikul

Affiliations: 
2008 Biostatistics Johns Hopkins University, Baltimore, MD 
 2008-2009 Biomedical Engineering University of Virginia, Charlottesville, VA 
 2009- Public Health Sciences University of Virginia, Charlottesville, VA 
Website:
http://people.virginia.edu/~am3xa/
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"Ani Manichaikul"

Parents

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Karl W. Broman grad student 2008 Johns Hopkins (MathTree)
 (Statistical methods for mapping quantitative trait loci in experimental crosses)
Jason A. Papin post-doc 2008-2009 UVA
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Publications

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Yengo L, Vedantam S, Marouli E, et al. (2022) A saturated map of common genetic variants associated with human height. Nature
Graham SE, Clarke SL, Wu KH, et al. (2021) The power of genetic diversity in genome-wide association studies of lipids. Nature
Katz DH, Tahir UA, Bick AG, et al. (2021) Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights into Cardiovascular Disease. Circulation
Mikhaylova AV, McHugh CP, Polfus LM, et al. (2021) Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. American Journal of Human Genetics
Yang C, Hallmark B, Chai JC, et al. (2021) Impact of Amerind ancestry and FADS genetic variation on omega-3 deficiency and cardiometabolic traits in Hispanic populations. Communications Biology. 4: 918
Aherrahrou R, Guo L, Nagraj VP, et al. (2020) Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Circulation Research
Bootpetch TC, Hafrén L, Elling CL, et al. (2020) Multi-omic studies on missense PLG variants in families with otitis media. Scientific Reports. 10: 15035
Vuckovic D, Bao EL, Akbari P, et al. (2020) The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 182: 1214-1231.e11
Chen MH, Raffield LM, Mousas A, et al. (2020) Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 182: 1198-1213.e14
Li X, Li Z, Zhou H, et al. (2020) Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale. Nature Genetics
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