Warren ST - Search Results

1

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.

Moreno-De-Luca D; SGENE Consortium; Mulle JG; Simons Simplex Collection Genetics Consortium; Kaminsky EB, Sanders SJ; GeneSTAR; Myers SM, Adam MP, Pakula AT, Eisenhauer NJ, Uhas K, Weik L, Guy L, Care ME, Morel CF, Boni C, Salbert BA, Chandrareddy A, Demmer LA, Chow EW, Surti U, Aradhya S, Pickering DL, Golden DM, Sanger WG, Aston E, Brothman AR, Gliem TJ, Thorland EC, Ackley T, Iyer R, Huang S, Barber JC, Crolla JA, Warren ST, Martin CL, Ledbetter DH. Moreno-De-Luca D, et al. Among authors: warren st. Am J Hum Genet. 2010 Nov 12;87(5):618-30. doi: 10.1016/j.ajhg.2010.10.004. Epub 2010 Nov 4. Am J Hum Genet. 2010. PMID: 21055719 Free PMC article.

2

Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction.

Ledbetter SA, Nelson DL, Warren ST, Ledbetter DH. Ledbetter SA, et al. Among authors: warren st. Genomics. 1990 Mar;6(3):475-81. doi: 10.1016/0888-7543(90)90477-c. Genomics. 1990. PMID: 2328990

3

Molecular evidence for true isochromosome 21q.

Priest JH, Blackston RD, Pearse LA, Warren ST. Priest JH, et al. Among authors: warren st. Hum Genet. 1988 Dec;81(1):1-3. doi: 10.1007/BF00283718. Hum Genet. 1988. PMID: 2974012

4

Emerin deletions occurring on both Xq28 inversion backgrounds.

Small K, Warren ST. Small K, et al. Among authors: warren st. Hum Mol Genet. 1998 Jan;7(1):135-9. doi: 10.1093/hmg/7.1.135. Hum Mol Genet. 1998. PMID: 9384614

5

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

Kenneson A, Zhang F, Hagedorn CH, Warren ST. Kenneson A, et al. Among authors: warren st. Hum Mol Genet. 2001 Jul 1;10(14):1449-54. doi: 10.1093/hmg/10.14.1449. Hum Mol Genet. 2001. PMID: 11448936

6

Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome.

Coffee B, Zhang F, Ceman S, Warren ST, Reines D. Coffee B, et al. Among authors: warren st. Am J Hum Genet. 2002 Oct;71(4):923-32. doi: 10.1086/342931. Epub 2002 Sep 13. Am J Hum Genet. 2002. PMID: 12232854 Free PMC article.

7

The pathophysiology of fragile x syndrome.

Penagarikano O, Mulle JG, Warren ST. Penagarikano O, et al. Among authors: warren st. Annu Rev Genomics Hum Genet. 2007;8:109-29. doi: 10.1146/annurev.genom.8.080706.092249. Annu Rev Genomics Hum Genet. 2007. PMID: 17477822 Review.

8

Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways.

Nishimura Y, Martin CL, Vazquez-Lopez A, Spence SJ, Alvarez-Retuerto AI, Sigman M, Steindler C, Pellegrini S, Schanen NC, Warren ST, Geschwind DH. Nishimura Y, et al. Among authors: warren st. Hum Mol Genet. 2007 Jul 15;16(14):1682-98. doi: 10.1093/hmg/ddm116. Epub 2007 May 21. Hum Mol Genet. 2007. PMID: 17519220

9

Replication stress induces tumor-like microdeletions in FHIT/FRA3B.

Durkin SG, Ragland RL, Arlt MF, Mulle JG, Warren ST, Glover TW. Durkin SG, et al. Among authors: warren st. Proc Natl Acad Sci U S A. 2008 Jan 8;105(1):246-51. doi: 10.1073/pnas.0708097105. Epub 2007 Dec 27. Proc Natl Acad Sci U S A. 2008. PMID: 18162546 Free PMC article.

10

Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature.

Coffee B, Ikeda M, Budimirovic DB, Hjelm LN, Kaufmann WE, Warren ST. Coffee B, et al. Among authors: warren st. Am J Med Genet A. 2008 May 15;146A(10):1358-67. doi: 10.1002/ajmg.a.32261. Am J Med Genet A. 2008. PMID: 18412117 Free PMC article. Review.

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