Redman J - Search Results

1

A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma.

Nemesure B, Jiao X, He Q, Leske MC, Wu SY, Hennis A, Mendell N, Redman J, Garchon HJ, Agarwala R, Schäffer AA, Hejtmancik F; Barbados Family Study Group. Nemesure B, et al. Among authors: redman j. Hum Genet. 2003 May;112(5-6):600-9. doi: 10.1007/s00439-003-0910-z. Epub 2003 Mar 4. Hum Genet. 2003. PMID: 12616399

2

Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screening.

Hantash FM, Redman JB, Starn K, Anderson B, Buller A, McGinniss MJ, Quan F, Peng M, Sun W, Strom CM. Hantash FM, et al. Among authors: redman jb. Hum Genet. 2006 Mar;119(1-2):126-36. doi: 10.1007/s00439-005-0082-0. Epub 2005 Dec 17. Hum Genet. 2006. PMID: 16362824

3

Extensive sequencing of the CFTR gene: lessons learned from the first 157 patient samples.

McGinniss MJ, Chen C, Redman JB, Buller A, Quan F, Peng M, Giusti R, Hantash FM, Huang D, Sun W, Strom CM. McGinniss MJ, et al. Among authors: redman jb. Hum Genet. 2005 Dec;118(3-4):331-8. doi: 10.1007/s00439-005-0065-1. Epub 2005 Sep 28. Hum Genet. 2005. PMID: 16189704

4

Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descent.

Strom CM, Janeczko RA, Anderson B, Redman J, Quan F, Buller A, McGinniss MJ, Sun WM. Strom CM, et al. Among authors: redman j. Genet Med. 2005 Nov-Dec;7(9):633-9. doi: 10.1097/01.gim.0000187120.93597.16. Genet Med. 2005. PMID: 16301865 Free article.

5

Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T.

Buller A, Olson S, Redman JB, Hantash F, Chen R, Strom CM. Buller A, et al. Genet Med. 2004 Mar-Apr;6(2):108-9. doi: 10.1097/01.gim.0000117332.18002.ff. Genet Med. 2004. PMID: 15017334 Free article.

6

Cystic fibrosis screening: lessons learned from the first 320,000 patients.

Strom CM, Crossley B, Redman JB, Buller A, Quan F, Peng M, McGinnis M, Sun W. Strom CM, et al. Genet Med. 2004 May-Jun;6(3):136-40. doi: 10.1097/01.gim.0000127268.65149.69. Genet Med. 2004. PMID: 15354331

7

Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratory.

Strom CM, Crossley B, Redman JB, Quan F, Buller A, McGinniss MJ, Sun W. Strom CM, et al. Among authors: redman jb. Genet Med. 2004 May-Jun;6(3):145-52. doi: 10.1097/01.gim.0000127267.57526.d1. Genet Med. 2004. PMID: 15354333

8

Detection of 677CT/1298AC "double variant" chromosomes: implications for interpretation of MTHFR genotyping results.

Brown NM, Pratt VM, Buller A, Pike-Buchanan L, Redman JB, Sun W, Chen R, Crossley B, McGinniss MJ, Quan F, Strom CM. Brown NM, et al. Among authors: redman jb. Genet Med. 2005 Apr;7(4):278-82. doi: 10.1097/01.gim.0000159904.92850.d5. Genet Med. 2005. PMID: 15834246 Free article.

9

Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.

Strom CM, Crossley B, Redman JB, Buller A, Quan F, Peng M, McGinnis M, Fenwick RG Jr, Sun W. Strom CM, et al. Genet Med. 2007 Jan;9(1):46-51. doi: 10.1097/gim.0b013e31802d833c. Genet Med. 2007. PMID: 17224689 Free article.

10

Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator gene.

Hantash FM, Redman JB, Goos D, Kammesheidt A, McGinniss MJ, Sun W, Strom CM. Hantash FM, et al. Among authors: redman jb. J Mol Diagn. 2007 Sep;9(4):556-60. doi: 10.2353/jmoldx.2007.060141. Epub 2007 Aug 9. J Mol Diagn. 2007. PMID: 17690208 Free PMC article.

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