State MW - Search Results

1

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.

State MW, Greally JM, Cuker A, Bowers PN, Henegariu O, Morgan TM, Gunel M, DiLuna M, King RA, Nelson C, Donovan A, Anderson GM, Leckman JF, Hawkins T, Pauls DL, Lifton RP, Ward DC. State MW, et al. Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4684-9. doi: 10.1073/pnas.0730775100. Epub 2003 Apr 7. Proc Natl Acad Sci U S A. 2003. PMID: 12682296 Free PMC article.

2

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Fernandez T, Morgan T, Davis N, Klin A, Morris A, Farhi A, Lifton RP, State MW. Fernandez T, et al. Among authors: state mw. Am J Hum Genet. 2004 Jun;74(6):1286-93. doi: 10.1086/421474. Epub 2004 Apr 21. Am J Hum Genet. 2004. PMID: 15106122 Free PMC article.

3

Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22.

Cuker A, State MW, King RA, Davis N, Ward DC. Cuker A, et al. Among authors: state mw. Am J Med Genet A. 2004 Sep 15;130A(1):37-9. doi: 10.1002/ajmg.a.30066. Am J Med Genet A. 2004. PMID: 15368493

4

Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13.

Nahed BV, Seker A, Guclu B, Ozturk AK, Finberg K, Hawkins AA, DiLuna ML, State M, Lifton RP, Gunel M. Nahed BV, et al. Am J Hum Genet. 2005 Jan;76(1):172-9. doi: 10.1086/426953. Epub 2004 Nov 11. Am J Hum Genet. 2005. PMID: 15540160 Free PMC article.

5

Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.

Mani A, Radhakrishnan J, Farhi A, Carew KS, Warnes CA, Nelson-Williams C, Day RW, Pober B, State MW, Lifton RP. Mani A, et al. Among authors: state mw. Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2975-9. doi: 10.1073/pnas.0409852102. Epub 2005 Jan 31. Proc Natl Acad Sci U S A. 2005. PMID: 15684060 Free PMC article.

6

Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23).

Drazinic CM, Ercan-Sencicek AG, Gault LM, Hisama FM, Qumsiyeh MB, Nowak NJ, Cubells JF, State MW. Drazinic CM, et al. Among authors: state mw. Am J Med Genet A. 2005 Apr 30;134(3):282-9. doi: 10.1002/ajmg.a.30616. Am J Med Genet A. 2005. PMID: 15754353

7

Sequence variants in SLITRK1 are associated with Tourette's syndrome.

Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS 4th, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW. Abelson JF, et al. Among authors: state mw. Science. 2005 Oct 14;310(5746):317-20. doi: 10.1126/science.1116502. Science. 2005. PMID: 16224024

8

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.

Plant LD, Bowers PN, Liu Q, Morgan T, Zhang T, State MW, Chen W, Kittles RA, Goldstein SA. Plant LD, et al. Among authors: state mw. J Clin Invest. 2006 Feb;116(2):430-5. doi: 10.1172/JCI25618. J Clin Invest. 2006. PMID: 16453024 Free PMC article.

9

A surprising METamorphosis: autism genetics finds a common functional variant.

State MW. State MW. Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16621-2. doi: 10.1073/pnas.0608027103. Epub 2006 Oct 30. Proc Natl Acad Sci U S A. 2006. PMID: 17075042 Free PMC article. No abstract available.

10

Rapid identification of disease-causing mutations using copy number analysis within linkage intervals.

Bayrakli F, Bilguvar K, Mason CE, DiLuna ML, Bayri Y, Gungor L, Terzi M, Mane SM, Lifton RP, State MW, Gunel M. Bayrakli F, et al. Among authors: state mw. Hum Mutat. 2007 Dec;28(12):1236-40. doi: 10.1002/humu.20592. Hum Mutat. 2007. PMID: 17676595

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