Schwalb MN - Search Results

1

Copy number variations in three children with sudden infant death.

Toruner GA, Kurvathi R, Sugalski R, Shulman L, Twersky S, Pearson PG, Tozzi R, Schwalb MN, Wallerstein R. Toruner GA, et al. Among authors: schwalb mn. Clin Genet. 2009 Jul;76(1):63-8. doi: 10.1111/j.1399-0004.2009.01161.x. Clin Genet. 2009. PMID: 19659761

2

An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.

Toruner GA, Streck DL, Schwalb MN, Dermody JJ. Toruner GA, et al. Among authors: schwalb mn. Am J Med Genet A. 2007 Apr 15;143A(8):824-9. doi: 10.1002/ajmg.a.31656. Am J Med Genet A. 2007. PMID: 17366576

3

Comprehensive genome-wide comparison of DNA and RNA level scan using microarray technology for identification of candidate cancer-related genes in the HL-60 cell line.

Ulger C, Toruner GA, Alkan M, Mohammed M, Damani S, Kang J, Galante A, Aviv H, Soteropoulos P, Tolias PP, Schwalb MN, Dermody JJ. Ulger C, et al. Among authors: schwalb mn. Cancer Genet Cytogenet. 2003 Nov;147(1):28-35. doi: 10.1016/s0165-4608(03)00155-9. Cancer Genet Cytogenet. 2003. PMID: 14580768

4

Association between gene expression profile and tumor invasion in oral squamous cell carcinoma.

Toruner GA, Ulger C, Alkan M, Galante AT, Rinaggio J, Wilk R, Tian B, Soteropoulos P, Hameed MR, Schwalb MN, Dermody JJ. Toruner GA, et al. Among authors: schwalb mn. Cancer Genet Cytogenet. 2004 Oct 1;154(1):27-35. doi: 10.1016/j.cancergencyto.2004.01.026. Cancer Genet Cytogenet. 2004. PMID: 15381369

5

Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells.

Malfitano AM, Toruner GA, Gazzerro P, Laezza C, Husain S, Eletto D, Orlando P, De Petrocellis L, Terskiy A, Schwalb M, Vitale E, Bifulco M. Malfitano AM, et al. Immunol Lett. 2007 Apr 15;109(2):145-54. doi: 10.1016/j.imlet.2007.02.004. Epub 2007 Mar 5. Immunol Lett. 2007. PMID: 17360047

6

Novel X-linked mental retardation syndrome with short stature maps to Xq24.

Vitale E, Specchia C, Devoto M, Angius A, Rong S, Rocchi M, Schwalb M, Demelas L, Paglietti D, Manca S, Mastropaolo C, Serra G. Vitale E, et al. Am J Med Genet. 2001 Sep 15;103(1):1-8. doi: 10.1002/ajmg.1495. Am J Med Genet. 2001. PMID: 11562927

7

Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.

Vitale E, Cook S, Sun R, Specchia C, Subramanian K, Rocchi M, Nathanson D, Schwalb M, Devoto M, Rohowsky-Kochan C. Vitale E, et al. Hum Mol Genet. 2002 Feb 1;11(3):295-300. doi: 10.1093/hmg/11.3.295. Hum Mol Genet. 2002. PMID: 11823448

8

High incidence of two methylenetetrahydrofolate reductase mutations (C677T and A1298C) in Hispanics.

Chowdary D, Streck D, Schwalb MN, Dermody JJ. Chowdary D, et al. Among authors: schwalb mn. Genet Test. 2003 Fall;7(3):255-7. doi: 10.1089/109065703322537296. Genet Test. 2003. PMID: 14642003

9

Gene expression after crush injury of human saphenous vein: using microarrays to define the transcriptional profile.

Price RM, Tulsyan N, Dermody JJ, Schwalb M, Soteropoulos P, Castronuovo JJ Jr. Price RM, et al. J Am Coll Surg. 2004 Sep;199(3):411-8. doi: 10.1016/j.jamcollsurg.2004.04.023. J Am Coll Surg. 2004. PMID: 15325611

10

Subjective and objective risk of breast cancer in Ashkenazi Jewish individuals at risk for BRCA1/2 mutations.

Kelly K, Leventhal H, Marvin M, Toppmeyer D, Much J, Dermody J, Baran J, Schwalb M. Kelly K, et al. Genet Test. 2004 Summer;8(2):139-47. doi: 10.1089/gte.2004.8.139. Genet Test. 2004. PMID: 15345111

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