Genomics of behavioral diseases

Frontiers in Genetics

Volumn 3, Issue APR, 2012, Pages

  Rogaev, Evgeny I ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84876056016     PISSN: None     EISSN: 16648021     Source Type: Journal    
DOI: 10.3389/fgene.2012.00045     Document Type: Note

References (30)

1. Bassett, A. S., Bury, A., Hodgkinson, K. A., and Honer, W. G. (1996). Reproductive fitness in familial schizophrenia. Schizophr. Res. 21, 151-160.
2. Botstein, D., and Risch, N. (2003). Discovering genotypes underlying human phenotypes: past successes for Mendelian disease, future approaches for complex disease. Nat. Genet. 33(Suppl.), 228-237.
3. Center for Disease Control and Prevention. (2009). Autism and Developmental Disabilities Monitoring (ADDM) Network. Available at: http://www.cdc.gov/ ncbddd/autism/addm.html
4. Donnelly, P. (2008). Progress and challenges in genome-wide association studies in humans. Nature 456, 728-731.
5. Genin, E., Hannequin, D., Wallon, D., Sleegers, K., Hiltunen, M., Combarros, O., Bullido, M. J., Engelborghs, S., De, D. P., Berr, C., Pasquier, F., Dubois, B., Tognoni, G., Fievet, N., Brouwers, N., Bettens, K., Arosio, B., Coto, E., Del, Z. M., Mateo, I., Epelbaum, J., Frank-Garcia, A., Helisalmi, S., Porcellini, E., Pilotto, A., Forti, P., Ferri, R., Scarpini, E., Siciliano, G., Solfrizzi, V., Sorbi, S., Spalletta, G., Valdivieso, F., Vepsalainen, S., Alvarez, V., Bosco, P., Mancuso, M., Panza, F., Nacmias, B., Bossu, P., Hanon, O., Piccardi, P., Annoni, G., Seripa, D., Galimberti, D., Licastro, F., Soininen, H., Dartigues, J. F., Kamboh, M. I., Van, B. C., Lambert, J. C., Amouyel, P., and Campion, D. (2011). APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Mol. Psychiatry 16, 903-907.
6. Girard, S. L., Gauthier, J., Noreau, A., Xiong, L., Zhou, S., Jouan, L., Dionne-Laporte, A., Spiegelman, D., Henrion, E., Diallo, O., Thibodeau, P., Bachand, I., Bao, J. Y., Tong, A. H., Lin, C. H., Millet, B., Jaafari, N., Joober, R., Dion, P. A., Lok, S., Krebs, M. O., and Rouleau, G. A. (2011). Increased exonic de novo mutation rate in individuals with schizophrenia. Nat. Genet. 43, 860-863.
7. Hallmayer, J., Cleveland, S., Torres, A., Phillips, J., Cohen, B., Torigoe, T., Miller, J., Fedele, A., Collins, J., Smith, K., Lotspeich, L., Croen, L. A., Ozonoff, S., Lajonchere, C., Grether, J. K., and Risch, N. (2011). Genetic heritability and shared environmental factors among twin pairs with autism. Arch. Gen. Psychiatry 68,1095-1102.
8. Hubert, A., Szoke, A., Leboyer, M., and Schurhoff, E. (2011). Influence of paternal age in schizophrenia. Encephale 37, 199-206.
9. International Schizophrenia Consortium. (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455, 237-241.
10. Kamnasaran, D., Muir, W. J., Ferguson-Smith, M. A., and Cox, D. W. (2003). Disruption of the neuronal PAS3 gene in a family affected with schizophrenia. J. Med. Genet. 40, 325-332.
11. Karayiorgou, M., Morris, M. A., Morrow, B., Shprintzen, R. J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P. S., and Lasseter, V. K. (1995). Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. U.S.A. 92, 7612-7616.
12. Lam, H. Y., Clark, M. J., Chen, R., Chen, R., Natsoulis, G., O'Huallachain, M., Dewey, E E., Habegger, L., Ashley, E. A., Gerstein, M. B., Butte, A. J., Ji, H. P., and Snyder, M. (2011). Performance comparison of whole-genome sequencing platforms. Nat. Biotechnol. 30, 78-82.
13. Matevossian, A. and Akbarian, S. (2008). Neuronal nuclei isolation from human postmortem brain tissue. J. Vis. Exp. 20, e914.
14. McKusick, V. A. (2007). Mendelian Inheritance in Man and its online version, OMIM. Am. J. Hum. Genet. 80, 588-604.
15. Millar, J. K., Wilson-Annan, J. C., Anderson, S., Christie, S., Taylor, M. S., Semple, C. A., Devon, R. S., St Clair, D. M., Muir, W. J., Blackwood, D. H., and Porteous, D. J. (2000). Disruption of two novel genes by a translo-cation co-segregating with schizophrenia. Hum. Mol. Genet. 9, 1415-1423.
16. Mulle, J. G., Dodd, A. F., McGrath, J. A., Wolyniec, P. S., Mitchell, A. A., Shetty, A. C., Sobreira, N. L., Valle, D., Rudd, M. K., Satten, G., Cutler, D. J., Pulver, A. E., and Warren, S. T. (2010). Microdeletions of 3q29 confer high risk for schizophrenia. Am. J. Hum. Genet. 87, 229-236.
17. O'Roak, B. J., Deriziotis, P., Lee, C., Vives, L., Schwartz, J. J., Girirajan, S., Karakoc, E., Mackenzie, A. P., Ng, S. B., Baker, C., Rieder, M. J., Nickerson, D. A., Bernier, R., Fisher, S. E., Shendure, J., and Eichler, E. E. (2011). Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nat. Genet. 43, 585-589.
18. Park, P. J. (2008). Epigenetics meets next-generation sequencing. Epigenetics3, 318-321.
19. Parker, H. G., Shearin, A. L., and Ostrander, E. A. (2010). Man's best friend becomes biology's best in show: genome analyses in the domestic dog. Annu. Rev. Genet. 44, 309-336.
20. Pearson, T. A., and Manolio, T. A. (2008). How to interpret a genome-wide association study. JAMA 299, 1335-1344.
21. Roach, J. C., Glusman, G., Smit, A. F., Huff, C. D., Hubley, R., Shannon, P. T., Rowen, L., Pant, K. P., Goodman, N., Bamshad, M., Shendure, J., Drmanac, R., Jorde, L. B., Hood, L., and Galas, D. J. (2010). Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science 328, 636-639.
22. Rogaev, E. I., Sherrington, R., Rogaeva, E. A., Levesque, G., Ikeda, M., Liang, Y., Chi, H., Lin, C., Holman, K., Tsuda, T., Mar, L., Sorbi, S., Nacmias, B., Piacentini, S., Amaducci, L., Chumakov, I., Cohen, D., Lannfelt, L., Fraser, P. E., Rommens, J. M., and St George-Hyslop, P. H. (1995). Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 376, 775-778.
23. Saha, S., Chant, D., Welham, J., and McGrath, J. (2005). A systematic review of the prevalence of schizophrenia. PLoS Med. 2, e141. doi: 10.1371/journal. pmed.0020141
24. Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Li, G., Holman, K., Tsuda, T., Mar, L., Foncin, J. F., Bruni, A. C., Montesi, M. P., Sorbi, S., Rainero, I., Pinessi, L., Nee, L., Chumakov, I., Pollen, D., Brookes, A., Sanseau, P., Polinsky, R. J., Wasco, W., Da Silva, H. A., Haines, J. L., Perkicak-Vance, M. A., Tanzi, R. E., Roses, A. D., Fraser, P. E., Rommens, J. M., and St George-Hyslop, P. H. (1995). Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature 375, 754-760.
25. Spady, T. C., and Ostrander, E. A. (2008). Canine behavioral genetics: pointing out the phenotypes and herding up the genes. Am. J. Hum. Genet. 82, 10-18.
26. Tolstorukov, M. Y., Volfovsky, N., Stephens, R. M., and Park, P. J. (2011). Impact of chromatin structure on sequence variability in the human genome. Nat. Struct. Mol. Biol. 18, 510-515.
27. Trut, L., Oskina, I., Kharlamova, A. (2009). Animal evolution during domestication: the domesticated fox as a model. Bioessays 31, 349-360.
28. Vacic, V., McCarthy, S., Malhotra, D., Murray, F., Chou, H. H., Peoples, A., Makarov, V., Yoon, S., Bhandari, A., Corominas, R., Iakoucheva, L. M., Krastoshevsky, O., Krause, V., Larach-Walters, V., Welsh, D. K., Craig, D., Kelsoe, J. R., Gershon, E. S., Leal, S. M., Dell, A. M., Morris, D. W., Gill, M., Corvin, A., Insel, P. A., McClellan, J., King, M. C., Karayiorgou, M., Levy, D. L., Delisi, L. E., and Sebat, J. (2011). Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. Nature 471, 499-503.
29. Wellcome Trust Case Control Consortium. (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661-678.
30. Xu, B., Roos, J. L., Dexheimer, P., Boone, B., Plummer, B., Levy, S., Gogos, J. A., and Karayiorgou, M. (2011). Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat. Genet. 43, 864-868.