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Genotype phasing in pedigrees using whole-genome sequence data.
Blackburn AN, Blondell L, Kos MZ, Blackburn NB, Peralta JM, Stevens PT, Lehman DM, Blangero J, Göring HHH. Blackburn AN, et al. Among authors: blondell l. Eur J Hum Genet. 2020 Jun;28(6):790-803. doi: 10.1038/s41431-020-0574-3. Epub 2020 Jan 29. Eur J Hum Genet. 2020. PMID: 31996801 Free PMC article.
Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performance.
Kos MZ, Carless MA, Peralta J, Curran JE, Quillen EE, Almeida M, Blackburn A, Blondell L, Roalf DR, Pogue-Geile MF, Gur RC, Göring HHH, Nimgaonkar VL, Gur RE, Almasy L. Kos MZ, et al. Among authors: blondell l. Am J Med Genet B Neuropsychiatr Genet. 2017 Dec;174(8):817-827. doi: 10.1002/ajmg.b.32597. Epub 2017 Sep 13. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28902459 Free PMC article.
Independent test assessment using the extreme value distribution theory.
Almeida M, Blondell L, Peralta JM, Kent JW Jr, Jun G, Teslovich TM, Fuchsberger C, Wood AR, Manning AK, Frayling TM, Cingolani PE, Sladek R, Dyer TD, Abecasis G, Duggirala R, Blangero J. Almeida M, et al. Among authors: blondell l. BMC Proc. 2016 Oct 18;10(Suppl 7):245-249. doi: 10.1186/s12919-016-0038-5. eCollection 2016. BMC Proc. 2016. PMID: 27980644 Free PMC article.