Rare Inherited Variation in Autism: Beginning to See the Forest and a Few Trees

Neuron

Volumn 77, Issue 2, 2013, Pages 209-211

  Stein, Jason L ^a   Parikshak, Neelroop N ^a   Geschwind, Daniel H ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMT GENE; AUTISM; AUTOSOME; COPY NUMBER VARIATION; EXOME; GENE; GENE DELETION; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC DISORDER; GENETIC RISK; GENETIC VARIABILITY; GERM LINE; HEMIZYGOTE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INHERITANCE; PATHOPHYSIOLOGY; PENETRANCE; PEX7 GENE; POPULATION GENETICS; PRIORITY JOURNAL; RARE DISEASE; SHORT SURVEY; SYMPTOM; SYNE1 GENE; X CHROMOSOME;

EID: 84872714472     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2013.01.010     Document Type: Short Survey

References (16)

1. Anney R., Klei L., Pinto D., Almeida J., Bacchelli E., Baird G., Bolshakova N., Bölte S., Bolton P.F., Bourgeron T., et al. Hum. Mol. Genet. 2012, 21:4781-4792.
2. Berg J.M., Geschwind D.H. Genome Biol. 2012, 13:247.
3. Devlin B., Scherer S.W. Curr. Opin. Genet. Dev. 2012, 22:229-237.
4. Hallmayer J., Cleveland S., Torres A., Phillips J., Cohen B., Torigoe T., Miller J., Fedele A., Collins J., Smith K., et al. Arch. Gen. Psychiatry 2011, 68:1095-1102.
5. Hosmer D., Lemeshow S. Applied Logic Regression 2000, John Wiley & Sons, Inc., New York, pp. 164-167. Second Edition.
6. Iossifov I., Ronemus M., Levy D., Wang Z., Hakker I., Rosenbaum J., Yamrom B., Lee Y.H., Narzisi G., Leotta A., et al. Neuron 2012, 74:285-299.
7. Klei L., Sanders S.J., Murtha M.T., Hus V., Lowe J.K., Willsey A.J., Moreno-De-Luca D., Yu T.W., Fombonne E., Geschwind D., et al. Mol. Autism 2012, 3:9.
8. Lim E.T., Raychaudhuri S., Sanders S.J., Stevens C., Sabo A., MacArthur D.G., Neale B.M., Kirby A., Ruderfer D.M., Fromer M., et al. Neuron 2013, 77:235-242. this issue.
9. Luo R., Sanders S.J., Tian Y., Voineagu I., Huang N., Chu S.H., Klei L., Cai C., Ou J., Lowe J.K., et al. Am. J. Hum. Genet. 2012, 91:38-55.
10. MacArthur D.G., Balasubramanian S., Frankish A., Huang N., Morris J., Walter K., Jostins L., Habegger L., Pickrell J.K., Montgomery S.B., et al. Science 2012, 335:823-828. 1000 Genomes Project Consortium.
11. Michaelson J.J., Shi Y., Gujral M., Zheng H., Malhotra D., Jin X., Jian M., Liu G., Greer D., Bhandari A., et al. Cell 2012, 151:1431-1442.
12. Neale B.M., Kou Y., Liu L., Ma'ayan A., Samocha K.E., Sabo A., Lin C.F., Stevens C., Wang L.S., Makarov V., et al. Nature 2012, 485:242-245.
13. Novarino G., El-Fishawy P., Kayserili H., Meguid N.A., Scott E.M., Schroth J., Silhavy J.L., Kara M., Khalil R.O., Ben-Omran T., et al. Science 2012, 338:394-397.
14. O'Roak B.J., Vives L., Girirajan S., Karakoc E., Krumm N., Coe B.P., Levy R., Ko A., Lee C., Smith J.D., et al. Nature 2012, 485:246-250.
15. Sanders S.J., Murtha M.T., Gupta A.R., Murdoch J.D., Raubeson M.J., Willsey A.J., Ercan-Sencicek A.G., DiLullo N.M., Parikshak N.N., Stein J.L., et al. Nature 2012, 485:237-241.
16. Yu T.W., Chahrour M.H., Coulter M.E., Jiralerspong S., Okamura-Ikeda K., Ataman B., Schmitz-Abe K., Harmin D.A., Adli M., Malik A.N., et al. Neuron 2013, 77:259-273. this issue.