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Items: 1 to 20 of 34

1.

Genetic architectures of psychiatric disorders: the emerging picture and its implications.

Sullivan PF, Daly MJ, O'Donovan M.

Nat Rev Genet. 2012 Jul 10;13(8):537-51. doi: 10.1038/nrg3240. Review.

2.

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.

Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, Biernacka JM, Brice A, DeStefano AL, Do CB, Eriksson N, Factor SA, Farrer MJ, Foroud T, Gasser T, Hamza T, Hardy JA, Heutink P, Hill-Burns EM, Klein C, Latourelle JC, Maraganore DM, Martin ER, Martinez M, Myers RH, Nalls MA, Pankratz N, Payami H, Satake W, Scott WK, Sharma M, Singleton AB, Stefansson K, Toda T, Tung JY, Vance J, Wood NW, Zabetian CP; 23andMe Genetic Epidemiology of Parkinson's Disease Consortium.; International Parkinson's Disease Genomics Consortium.; Parkinson's Disease GWAS Consortium.; Wellcome Trust Case Control Consortium 2)., Young P, Tanzi RE, Khoury MJ, Zipp F, Lehrach H, Ioannidis JP, Bertram L.

PLoS Genet. 2012;8(3):e1002548. doi: 10.1371/journal.pgen.1002548. Epub 2012 Mar 15.

3.

CNVs: harbingers of a rare variant revolution in psychiatric genetics.

Malhotra D, Sebat J.

Cell. 2012 Mar 16;148(6):1223-41. doi: 10.1016/j.cell.2012.02.039. Review.

4.

Genomics, intellectual disability, and autism.

Mefford HC, Batshaw ML, Hoffman EP.

N Engl J Med. 2012 Feb 23;366(8):733-43. doi: 10.1056/NEJMra1114194. Review. No abstract available.

5.

In-silico human genomics with GeneCards.

Stelzer G, Dalah I, Stein TI, Satanower Y, Rosen N, Nativ N, Oz-Levi D, Olender T, Belinky F, Bahir I, Krug H, Perco P, Mayer B, Kolker E, Safran M, Lancet D.

Hum Genomics. 2011 Oct;5(6):709-17.

6.

AutismKB: an evidence-based knowledgebase of autism genetics.

Xu LM, Li JR, Huang Y, Zhao M, Tang X, Wei L.

Nucleic Acids Res. 2012 Jan;40(Database issue):D1016-22. doi: 10.1093/nar/gkr1145. Epub 2011 Dec 1.

7.

Ensembl 2012.

Flicek P, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P, Coates G, Fairley S, Fitzgerald S, Gil L, Gordon L, Hendrix M, Hourlier T, Johnson N, Kähäri AK, Keefe D, Keenan S, Kinsella R, Komorowska M, Koscielny G, Kulesha E, Larsson P, Longden I, McLaren W, Muffato M, Overduin B, Pignatelli M, Pritchard B, Riat HS, Ritchie GR, Ruffier M, Schuster M, Sobral D, Tang YA, Taylor K, Trevanion S, Vandrovcova J, White S, Wilson M, Wilder SP, Aken BL, Birney E, Cunningham F, Dunham I, Durbin R, Fernández-Suarez XM, Harrow J, Herrero J, Hubbard TJ, Parker A, Proctor G, Spudich G, Vogel J, Yates A, Zadissa A, Searle SM.

Nucleic Acids Res. 2012 Jan;40(Database issue):D84-90. doi: 10.1093/nar/gkr991. Epub 2011 Nov 15.

8.

The conundrums of understanding genetic risks for autism spectrum disorders.

State MW, Levitt P.

Nat Neurosci. 2011 Oct 30;14(12):1499-506. doi: 10.1038/nn.2924. Review.

9.

Mouse model of Timothy syndrome recapitulates triad of autistic traits.

Bader PL, Faizi M, Kim LH, Owen SF, Tadross MR, Alfa RW, Bett GC, Tsien RW, Rasmusson RL, Shamloo M.

Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15432-7. doi: 10.1073/pnas.1112667108. Epub 2011 Aug 30.

10.

Genetics of autism spectrum disorders.

Geschwind DH.

Trends Cogn Sci. 2011 Sep;15(9):409-16. doi: 10.1016/j.tics.2011.07.003. Epub 2011 Aug 18.

11.

Rett syndrome: exploring the autism link.

Percy AK.

Arch Neurol. 2011 Aug;68(8):985-9. doi: 10.1001/archneurol.2011.149. Review.

12.

Systems biology of JAK-STAT signalling in human malignancies.

Vera J, Rateitschak K, Lange F, Kossow C, Wolkenhauer O, Jaster R.

Prog Biophys Mol Biol. 2011 Aug;106(2):426-34. doi: 10.1016/j.pbiomolbio.2011.06.013. Epub 2011 Jul 6. Review.

PMID:
21762720
13.

Genetic heritability and shared environmental factors among twin pairs with autism.

Hallmayer J, Cleveland S, Torres A, Phillips J, Cohen B, Torigoe T, Miller J, Fedele A, Collins J, Smith K, Lotspeich L, Croen LA, Ozonoff S, Lajonchere C, Grether JK, Risch N.

Arch Gen Psychiatry. 2011 Nov;68(11):1095-102. doi: 10.1001/archgenpsychiatry.2011.76. Epub 2011 Jul 4.

14.

Activation and function of the MAPKs and their substrates, the MAPK-activated protein kinases.

Cargnello M, Roux PP.

Microbiol Mol Biol Rev. 2011 Mar;75(1):50-83. doi: 10.1128/MMBR.00031-10. Review. Erratum in: Microbiol Mol Biol Rev. 2012 Jun;76(2):496.

15.

Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.

Betancur C.

Brain Res. 2011 Mar 22;1380:42-77. doi: 10.1016/j.brainres.2010.11.078. Epub 2010 Dec 1. Review.

PMID:
21129364
16.

The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored.

Szklarczyk D, Franceschini A, Kuhn M, Simonovic M, Roth A, Minguez P, Doerks T, Stark M, Muller J, Bork P, Jensen LJ, von Mering C.

Nucleic Acids Res. 2011 Jan;39(Database issue):D561-8. doi: 10.1093/nar/gkq973. Epub 2010 Nov 2.

17.

genenames.org: the HGNC resources in 2011.

Seal RL, Gordon SM, Lush MJ, Wright MW, Bruford EA.

Nucleic Acids Res. 2011 Jan;39(Database issue):D514-9. doi: 10.1093/nar/gkq892. Epub 2010 Oct 6.

18.

Fragile X: leading the way for targeted treatments in autism.

Wang LW, Berry-Kravis E, Hagerman RJ.

Neurotherapeutics. 2010 Jul;7(3):264-74. doi: 10.1016/j.nurt.2010.05.005. Review.

19.

SFARI Gene: an evolving database for the autism research community.

Banerjee-Basu S, Packer A.

Dis Model Mech. 2010 Mar-Apr;3(3-4):133-5. doi: 10.1242/dmm.005439. No abstract available.

20.

Socio-behavioral characteristics of children with Rubinstein-Taybi syndrome.

Galéra C, Taupiac E, Fraisse S, Naudion S, Toussaint E, Rooryck-Thambo C, Delrue MA, Arveiler B, Lacombe D, Bouvard MP.

J Autism Dev Disord. 2009 Sep;39(9):1252-60. doi: 10.1007/s10803-009-0733-4. Epub 2009 Apr 7.

PMID:
19350377

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