Naj AC, Jun G, Reitz C, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. JAMA Neurol. 2014;71(11):1394-404. doi:10.1001/jamaneurol.2014.1491
Tonomura N, Elvers I, Thomas R, et al. Genome-wide association study identifies shared risk loci common to two malignancies in golden retrievers. PLoS Genet. 2015;11(2):e1004922. doi:10.1371/journal.pgen.1004922
Smith CJ, Saftlas AF, Spracklen CN, et al. Genetic Risk Score for Essential Hypertension and Risk of Preeclampsia. Am J Hypertens. 2016;29(1):17-24. doi:10.1093/ajh/hpv069
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
Yuan C, Clish CB, Wu C, et al. Circulating Metabolites and Survival Among Patients With Pancreatic Cancer. J Natl Cancer Inst. 2016;108(6):djv409. doi:10.1093/jnci/djv409
Gschwend M, Levran O, Kruglyak L, et al. A locus for Fanconi anemia on 16q determined by homozygosity mapping. Am J Hum Genet. 1996;59(2):377-84.
Lehto M, Tuomi T, Mahtani MM, et al. Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect. J Clin Invest. 1997;99(4):582-91. doi:10.1172/JCI119199
Francioli LC, Cretu-Stancu M, Garimella KV, et al. A framework for the detection of de novo mutations in family-based sequencing data. Eur J Hum Genet. 2017;25(2):227-233. doi:10.1038/ejhg.2016.147
Gabriel S, Ziaugra L. SNP genotyping using Sequenom MassARRAY 7K platform. Curr Protoc Hum Genet. 2004;Chapter 2:Unit 2.12. doi:10.1002/0471142905.hg0212s42
Balczerski B, Matsutani M, Castillo P, Osborne N, Stainier DYR, Crump G. Analysis of sphingosine-1-phosphate signaling mutants reveals endodermal requirements for the growth but not dorsoventral patterning of jaw skeletal precursors. Dev Biol. 2012;362(2):230-41. doi:10.1016/j.ydbio.2011.12.010