Maher BS - Search Results

1

Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.

Weese-Mayer DE, Berry-Kravis EM, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Among authors: maher bs. Am J Med Genet A. 2003 Mar 15;117A(3):268-74. doi: 10.1002/ajmg.a.20005. Am J Med Genet A. 2003. PMID: 12599191

2

Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.

Weese-Mayer DE, Zhou L, Berry-Kravis EM, Maher BS, Silvestri JM, Marazita ML. Weese-Mayer DE, et al. Among authors: maher bs. Am J Med Genet A. 2003 Oct 15;122A(3):238-45. doi: 10.1002/ajmg.a.20427. Am J Med Genet A. 2003. PMID: 12966525

3

Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b.

Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Silvestri JM, Curran ME, Marazita ML. Weese-Mayer DE, et al. Among authors: maher bs. Am J Med Genet A. 2003 Dec 15;123A(3):267-78. doi: 10.1002/ajmg.a.20527. Am J Med Genet A. 2003. PMID: 14608649

4

Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.

Weese-Mayer DE, Berry-Kravis EM, Zhou L, Maher BS, Curran ME, Silvestri JM, Marazita ML. Weese-Mayer DE, et al. Among authors: maher bs. Pediatr Res. 2004 Sep;56(3):391-5. doi: 10.1203/01.PDR.0000136285.91048.4A. Epub 2004 Jul 7. Pediatr Res. 2004. PMID: 15240857

5

3' UTR polymorphism of the serotonin transporter gene and sudden infant death syndrome: haplotype analysis.

Maher BS, Marazita ML, Rand C, Zhou L, Berry-Kravis EM, Weese-Mayer DE. Maher BS, et al. Am J Med Genet A. 2006 Jul 1;140(13):1453-7. doi: 10.1002/ajmg.a.31261. Am J Med Genet A. 2006. PMID: 16691588 No abstract available.

6

Nicotine metabolizing genes GSTT1 and CYP1A1 in sudden infant death syndrome.

Rand CM, Weese-Mayer DE, Maher BS, Zhou L, Marazita ML, Berry-Kravis EM. Rand CM, et al. Among authors: maher bs. Am J Med Genet A. 2006 Jul 1;140(13):1447-52. doi: 10.1002/ajmg.a.31306. Am J Med Genet A. 2006. PMID: 16763966

7

Sudden infant death syndrome: Case-control frequency differences in paired like homeobox (PHOX) 2B gene.

Rand CM, Weese-Mayer DE, Zhou L, Maher BS, Cooper ME, Marazita ML, Berry-Kravis EM. Rand CM, et al. Among authors: maher bs. Am J Med Genet A. 2006 Aug 1;140(15):1687-91. doi: 10.1002/ajmg.a.31336. Am J Med Genet A. 2006. PMID: 16830328 No abstract available.

8

Case/control family study of autonomic nervous system dysfunction in idiopathic congenital central hypoventilation syndrome.

Weese-Mayer DE, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Maher BS, Cooper ME, Marazita ML. Weese-Mayer DE, et al. Among authors: maher bs. Am J Med Genet. 2001 May 1;100(3):237-45. doi: 10.1002/ajmg.1249. Am J Med Genet. 2001. PMID: 11343310

9

Facial phenotype in children and young adults with PHOX2B-determined congenital central hypoventilation syndrome: quantitative pattern of dysmorphology.

Todd ES, Weinberg SM, Berry-Kravis EM, Silvestri JM, Kenny AS, Rand CM, Zhou L, Maher BS, Marazita ML, Weese-Mayer DE. Todd ES, et al. Among authors: maher bs. Pediatr Res. 2006 Jan;59(1):39-45. doi: 10.1203/01.pdr.0000191814.73340.1d. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16327002

10

Genetic segregation analysis of autonomic nervous system dysfunction in families of probands with idiopathic congenital central hypoventilation syndrome.

Marazita ML, Maher BS, Cooper ME, Silvestri JM, Huffman AD, Smok-Pearsall SM, Kowal MH, Weese-Mayer DE. Marazita ML, et al. Among authors: maher bs. Am J Med Genet. 2001 May 1;100(3):229-36. doi: 10.1002/ajmg.1284. Am J Med Genet. 2001. PMID: 11343309

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