Comment on

• Beyond Mendel: an evolving view of human genetic disease transmission.

  Badano JL, Katsanis N. Badano JL, et al. Nat Rev Genet. 2002 Oct;3(10):779-89. doi: 10.1038/nrg910. Nat Rev Genet. 2002. PMID: 12360236 Review.
• Mendelian disorders deserve more attention.

  Antonarakis SE, Beckmann JS. Antonarakis SE, et al. Nat Rev Genet. 2006 Apr;7(4):277-82. doi: 10.1038/nrg1826. Nat Rev Genet. 2006. PMID: 16534515 Review.
• The HapMap and genome-wide association studies in diagnosis and therapy.

  Manolio TA, Collins FS. Manolio TA, et al. Annu Rev Med. 2009;60:443-56. doi: 10.1146/annurev.med.60.061907.093117. Annu Rev Med. 2009. PMID: 19630580 Free PMC article. Review.
• Cohort Profile: the 'children of the 90s'--the index offspring of the Avon Longitudinal Study of Parents and Children.

  Boyd A, Golding J, Macleod J, Lawlor DA, Fraser A, Henderson J, Molloy L, Ness A, Ring S, Davey Smith G. Boyd A, et al. Int J Epidemiol. 2013 Feb;42(1):111-27. doi: 10.1093/ije/dys064. Epub 2012 Apr 16. Int J Epidemiol. 2013. PMID: 22507743 Free PMC article.
• Most genetic risk for autism resides with common variation.

  Gaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reichert J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, Hultman CM, Devlin B, Roeder K, Buxbaum JD. Gaugler T, et al. Nat Genet. 2014 Aug;46(8):881-5. doi: 10.1038/ng.3039. Epub 2014 Jul 20. Nat Genet. 2014. PMID: 25038753 Free PMC article.
• The contribution of de novo coding mutations to autism spectrum disorder.

  Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M. Iossifov I, et al. Nature. 2014 Nov 13;515(7526):216-21. doi: 10.1038/nature13908. Epub 2014 Oct 29. Nature. 2014. PMID: 25363768 Free PMC article.
• Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.

  Robinson EB, St Pourcain B, Anttila V, Kosmicki JA, Bulik-Sullivan B, Grove J, Maller J, Samocha KE, Sanders SJ, Ripke S, Martin J, Hollegaard MV, Werge T, Hougaard DM; iPSYCH-SSI-Broad Autism Group; Neale BM, Evans DM, Skuse D, Mortensen PB, Børglum AD, Ronald A, Smith GD, Daly MJ. Robinson EB, et al. Nat Genet. 2016 May;48(5):552-5. doi: 10.1038/ng.3529. Epub 2016 Mar 21. Nat Genet. 2016. PMID: 26998691 Free PMC article.
• Understanding autism and other neurodevelopmental disorders through experimental translational neurobehavioral models.

  Homberg JR, Kyzar EJ, Nguyen M, Norton WH, Pittman J, Poudel MK, Gaikwad S, Nakamura S, Koshiba M, Yamanouchi H, Scattoni ML, Ullman JF, Diamond DM, Kaluyeva AA, Parker MO, Klimenko VM, Apryatin SA, Brown RE, Song C, Gainetdinov RR, Gottesman II, Kalueff AV. Homberg JR, et al. Neurosci Biobehav Rev. 2016 Jun;65:292-312. doi: 10.1016/j.neubiorev.2016.03.013. Epub 2016 Apr 2. Neurosci Biobehav Rev. 2016. PMID: 27048961 Review.
• Advancing the understanding of autism disease mechanisms through genetics.

  de la Torre-Ubieta L, Won H, Stein JL, Geschwind DH. de la Torre-Ubieta L, et al. Nat Med. 2016 Apr;22(4):345-61. doi: 10.1038/nm.4071. Nat Med. 2016. PMID: 27050589 Free PMC article. Review.