Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Autor: Szatmari, P, Paterson, AD, Zwaigenbaum, L, Roberts, W, Brian, J, Liu, XQ, Vincent, JB, Skaug, JL, Thompson, AP, Senman, L, Feuk, L, Qian, C, Bryson, SE, Jones, MB, Marshall, CR, Scherer, SW, Vieland, VJ, Bartlett, C, Mangin, LV, Goedken, R, Segre, A, Pericak-Vance, MA, Cuccaro, ML, Gilbert, JR, Wright, HH, Abramson, RK, Betancur, C, Bourgeron, T, Gillberg, C, Leboyer, M, Buxbaum, JD, Davis, KL, Hollander, E, Silverman, JM, Hallmayer, J, Lotspeich, L, Sutcliffe, JS, Haines, JL, Folstein, SE, Piven, J, Wassink, TH, Sheffield, V, Geschwind, DH, Bucan, M, Brown, WT, Cantor, RM, Constantino, JN, Gilliam, TC, Herbert, M, LaJonchere, C, Ledbetter, DH, Lese-Martin, C, Miller, J, Nelson, S, Samango-Sprouse, CA, Spence, S, State, M, Tanzi, RE, Coon, H, Dawson, G, Devlin, B, Estes, A, Flodman, P, Klei, L, McMahon, WM, Minshew, N, Munson, J, Korvatska, E, Rodier, PM, Schellenberg, GD, Smith, M, Spence, MA, Stodgell, C, Tepper, PG, Wijsman, EM, Yu, CE, Rogé, B, Mantoulan, C, Wittemeyer, K, Poustka, A, Felder, B, Klauck, SM, Schuster, C, Poustka, F, Bölte, S, Feineis-Matthews, S, Herbrecht, E, Schmötzer, G, Tsiantis, J, Papanikolaou, K, Maestrini, E, Bacchelli, E

Publikováno v: Szatmari, P; Paterson, AD; Zwaigenbaum, L; Roberts, W; Brian, J; Liu, XQ; et al.(2007). Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics, 39(3), 319-328. doi: 10.1038/ng1985. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/9s05v2sn

Autism spectrum disorders (ASDs) are common, heritable neurodevelopmental conditions. The genetic architecture of ASDs is complex, requiring large samples to overcome heterogeneity. Here we broaden coverage and sample size relative to other studies o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::3f75a1c477e040f4db908e554c2b8e8e
http://www.escholarship.org/uc/item/9s05v2sn

Autism and the serotonin transporter: The long and short of it

Autor: Devlin, B, Cook, EH, Coon, H, Dawson, G, Grigorenko, EL, McMahon, W, Minshew, N, Pauls, D, Smith, M, Spence, MA, Rodier, PM, Stodgell, C, Schellenberg, GD, Bennett, P, Lainart, J, Escamilla, J, Abbott, R, Estes, A, Munson, J, Yu, CE

Publikováno v: Devlin, B; Cook, EH; Coon, H; Dawson, G; Grigorenko, EL; McMahon, W; et al.(2005). Autism and the serotonin transporter: The long and short of it. Molecular Psychiatry, 10(12), 1110-1116. doi: 10.1038/sj.mp.4001724. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/2v85m3hw

Autism is a neurodevelopmental disorder manifesting early in childhood. Some symptoms of autism are alleviated by treatment with selective serotonin reuptake inhibitors, which are known to interact with the serotonin transporter. Moreover, variation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::8094bfaf310fc054ac39a062e97143c9
http://www.escholarship.org/uc/item/2v85m3hw

Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific

Autor: Grady, DL, Harxhi, A, Smith, M, Flodman, P, Spence, MA, Swanson, JM, Moyzis, RK

Publikováno v: Grady, DL; Harxhi, A; Smith, M; Flodman, P; Spence, MA; Swanson, JM; et al.(2005). Sequence variants of the DRD4 gene in autism: Further evidence that rare DRD4 7R haplotypes are ADHD specific. American Journal of Medical Genetics-Neuropsychiatric Genetics, 136 B(1), 33-35. doi: 10.1002/ajmg.b.30182. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/1br2s92x

A high prevalence of rare dopamine receptor D4 (DRD4) alleles in children diagnosed with attention-deficit hyperactivity disorder (ADHD) has been reported [Grady et al., 2003]. In this prior study, extensive resequencing/haplotype data of the DRD4 lo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::e160cb54a93a8fc86787640eb70abe10
http://www.escholarship.org/uc/item/1br2s92x

Dopamine genes and ADHD

Autor: Swanson, JM, Flodman, P, Kennedy, S, Spence, MA, Moyzis, R, Schuck, S, Murias, M, Moriarity, J, Barr, C, Smith, M, Posner, M

Publikováno v: Swanson, JM; Flodman, P; Kennedy, S; Spence, MA; Moyzis, R; Schuck, S; et al.(2000). Dopamine genes and ADHD. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 24(1), 21-25. doi: 10.1016/S0149-7634(99)00062-7. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/57942574

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::dc719168ee0dbd13f57d5cb08a18f671
http://www.escholarship.org/uc/item/57942574

CHROMOSOME MAPPING OF BLOOD-PRESSURE REGULATORY LOCI IN THE SHR BY TOTAL GENOME SCANNING OF RECOMBINANT INBRED STRAINS

Autor: Michal Pravenec, Gauguier, D., Schott, J., Buard, G., Kren, V., Wong, A., Szpirer, C., Szpirer, J., Wang, Jm, Stlezin, E., Spence, Ma, Flodman, P., Lathrop, M., Vergnaud, G., Kurtz, Tw

Publikováno v: ResearcherID
Publons

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http://ora.ox.ac.uk/objects/uuid:2a492e29-98a6-48a2-9e45-a7318bcfb7bc