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Results: 1 to 20 of 77

1.

Mitochondrial dysfunction in autism.

Giulivi C, Zhang YF, Omanska-Klusek A, Ross-Inta C, Wong S, Hertz-Picciotto I, Tassone F, Pessah IN.

JAMA. 2010 Dec 1;304(21):2389-96. doi: 10.1001/jama.2010.1706.

PMID:
21119085
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Bioenergetics and the epigenome: interface between the environment and genes in common diseases.

Wallace DC.

Dev Disabil Res Rev. 2010 Jun;16(2):114-9. doi: 10.1002/ddrr.113. Review.

PMID:
20818725
[PubMed - indexed for MEDLINE]
3.

Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes.

Li M, Schönberg A, Schaefer M, Schroeder R, Nasidze I, Stoneking M.

Am J Hum Genet. 2010 Aug 13;87(2):237-49. doi: 10.1016/j.ajhg.2010.07.014.

PMID:
20696290
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Autism spectrum disorders and epigenetics.

Grafodatskaya D, Chung B, Szatmari P, Weksberg R.

J Am Acad Child Adolesc Psychiatry. 2010 Aug;49(8):794-809. doi: 10.1016/j.jaac.2010.05.005. Epub 2010 Jul 3. Review.

PMID:
20643313
[PubMed - indexed for MEDLINE]
5.

Clinical genetic testing for patients with autism spectrum disorders.

Shen Y, Dies KA, Holm IA, Bridgemohan C, Sobeih MM, Caronna EB, Miller KJ, Frazier JA, Silverstein I, Picker J, Weissman L, Raffalli P, Jeste S, Demmer LA, Peters HK, Brewster SJ, Kowalczyk SJ, Rosen-Sheidley B, McGowan C, Duda AW 3rd, Lincoln SA, Lowe KR, Schonwald A, Robbins M, Hisama F, Wolff R, Becker R, Nasir R, Urion DK, Milunsky JM, Rappaport L, Gusella JF, Walsh CA, Wu BL, Miller DT; Autism Consortium Clinical Genetics/DNA Diagnostics Collaboration.

Pediatrics. 2010 Apr;125(4):e727-35. doi: 10.1542/peds.2009-1684. Epub 2010 Mar 15.

PMID:
20231187
[PubMed - indexed for MEDLINE]
Free Article
6.

5q14.3 deletion manifesting as mitochondrial disease and autism: case report.

Ezugha H, Goldenthal M, Valencia I, Anderson CE, Legido A, Marks H.

J Child Neurol. 2010 Oct;25(10):1232-5. doi: 10.1177/0883073809361165. Epub 2010 Feb 22.

PMID:
20179003
[PubMed - indexed for MEDLINE]
7.

The genetics of autism: key issues, recent findings, and clinical implications.

El-Fishawy P, State MW.

Psychiatr Clin North Am. 2010 Mar;33(1):83-105. doi: 10.1016/j.psc.2009.12.002. Review.

PMID:
20159341
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Functional organization of mammalian mitochondrial DNA in nucleoids: history, recent developments, and future challenges.

Spelbrink JN.

IUBMB Life. 2010 Jan;62(1):19-32. doi: 10.1002/iub.282. Review.

PMID:
20014006
[PubMed - indexed for MEDLINE]
9.

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan.

Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Feb 1;34(1):189-92. doi: 10.1016/j.pnpbp.2009.11.004. Epub 2009 Nov 10.

PMID:
19913066
[PubMed - indexed for MEDLINE]
10.

Fever plus mitochondrial disease could be risk factors for autistic regression.

Shoffner J, Hyams L, Langley GN, Cossette S, Mylacraine L, Dale J, Ollis L, Kuoch S, Bennett K, Aliberti A, Hyland K.

J Child Neurol. 2010 Apr;25(4):429-34. doi: 10.1177/0883073809342128. Epub 2009 Sep 22.

PMID:
19773461
[PubMed - indexed for MEDLINE]
11.

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.

Fernandez BA, Roberts W, Chung B, Weksberg R, Meyn S, Szatmari P, Joseph-George AM, Mackay S, Whitten K, Noble B, Vardy C, Crosbie V, Luscombe S, Tucker E, Turner L, Marshall CR, Scherer SW.

J Med Genet. 2010 Mar;47(3):195-203. doi: 10.1136/jmg.2009.069369. Epub 2009 Sep 15.

PMID:
19755429
[PubMed - indexed for MEDLINE]
12.

Syndromic autism: causes and pathogenetic pathways.

Benvenuto A, Moavero R, Alessandrelli R, Manzi B, Curatolo P.

World J Pediatr. 2009 Aug;5(3):169-76. doi: 10.1007/s12519-009-0033-2. Epub 2009 Aug 20. Review.

PMID:
19693459
[PubMed - indexed for MEDLINE]
13.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):569-73. doi: 10.1038/nature07953. Epub 2009 Apr 28.

PMID:
19404257
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H.

Nature. 2009 May 28;459(7246):528-33. doi: 10.1038/nature07999. Epub 2009 Apr 28.

PMID:
19404256
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Nuclear and mitochondrial genome defects in autisms.

Smith M, Spence MA, Flodman P.

Ann N Y Acad Sci. 2009 Jan;1151:102-32. doi: 10.1111/j.1749-6632.2008.03571.x. Review.

PMID:
19154520
[PubMed - indexed for MEDLINE]
16.

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.

Loat CS, Curran S, Lewis CM, Duvall J, Geschwind D, Bolton P, Craig IW.

Genes Brain Behav. 2008 Oct;7(7):754-60. doi: 10.1111/j.1601-183X.2008.00414.x.

PMID:
19125863
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Mitochondrial disease in autism spectrum disorder patients: a cohort analysis.

Weissman JR, Kelley RI, Bauman ML, Cohen BH, Murray KF, Mitchell RL, Kern RL, Natowicz MR.

PLoS One. 2008;3(11):e3815. doi: 10.1371/journal.pone.0003815. Epub 2008 Nov 26.

PMID:
19043581
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.

Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL.

J Med Genet. 2009 Apr;46(4):242-8. doi: 10.1136/jmg.2008.059907. Epub 2008 Sep 19.

PMID:
18805830
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Mitochondrial control of epigenetics.

Naviaux RK.

Cancer Biol Ther. 2008 Aug;7(8):1191-3. Epub 2008 Aug 4. No abstract available.

PMID:
18719362
[PubMed - indexed for MEDLINE]
Free Article
20.

Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism.

Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, Hattori E, Toyota T, Suda S, Takei N, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya KJ, Sugihara G, Ouchi Y, Sugiyama T, Yoshikawa T, Mori N.

Int J Neuropsychopharmacol. 2008 Dec;11(8):1073-84. doi: 10.1017/S1461145708009036. Epub 2008 Jul 2.

PMID:
18593506
[PubMed - indexed for MEDLINE]

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