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Publications

Population genetic differentiation of height and body mass index across Europe.

Robinson MR, Hemani G, Medina-Gomez C, et al. Population genetic differentiation of height and body mass index across Europe. Nat Genet. 2015;47(11):1357-62. doi:10.1038/ng.3401

Predicting facial characteristics from complex polygenic variations.

Fagertun J, Wolffhechel K, Pers TH, et al. Predicting facial characteristics from complex polygenic variations. Forensic Sci Int Genet. 2015;19:263-8. doi:10.1016/j.fsigen.2015.08.004

Cas9 gRNA engineering for genome editing, activation and repression.

Kiani S, Chavez A, Tuttle M, et al. Cas9 gRNA engineering for genome editing, activation and repression. Nat Methods. 2015;12(11):1051-4. doi:10.1038/nmeth.3580

APOE and cerebral amyloid angiopathy in community-dwelling older persons.

Yu L, Boyle PA, Nag S, et al. APOE and cerebral amyloid angiopathy in community-dwelling older persons. Neurobiol Aging. 2015;36(11):2946-53. doi:10.1016/j.neurobiolaging.2015.08.008

Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans.

Hsu YH, Liu Y, Hannan MT, et al. Genome-wide association meta-analyses to identify common genetic variants associated with hallux valgus in Caucasian and African Americans. J Med Genet. 2015;52(11):762-9. doi:10.1136/jmedgenet-2015-103142

Gender Disparity and Mutation Burden in Metastatic Melanoma.

Gupta S, Artomov M, Goggins W, Daly M, Tsao H. Gender Disparity and Mutation Burden in Metastatic Melanoma. J Natl Cancer Inst. 2015;107(11). doi:10.1093/jnci/djv221

Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies.

Ilkovski B, Pagnamenta AT, O’Grady GL, et al. Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol deficiencies. Hum Mol Genet. 2015;24(21):6146-59. doi:10.1093/hmg/ddv331

Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome.

Karaca E, Yuregir OO, Bozdogan ST, et al. Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome. Am J Med Genet A. 2015;167A(11):2795-9. doi:10.1002/ajmg.a.37263

Genotype-specific variation in West Nile virus dispersal in California.

Duggal NK, Reisen WK, Fang Y, et al. Genotype-specific variation in West Nile virus dispersal in California. Virology. 2015;485:79-85. doi:10.1016/j.virol.2015.07.004

Biomarkers in multiple sclerosis.

Housley WJ, Pitt D, Hafler DA. Biomarkers in multiple sclerosis. Clin Immunol. 2015;161(1):51-8. doi:10.1016/j.clim.2015.06.015