Kharrazi M - Search Results

1

Novel CFTR variants identified during the first 3 years of cystic fibrosis newborn screening in California.

Prach L, Koepke R, Kharrazi M, Keiles S, Salinas DB, Reyes MC, Pian M, Opsimos H, Otsuka KN, Hardy KA, Milla CE, Zirbes JM, Chipps B, O'Bra S, Saeed MM, Sudhakar R, Lehto S, Nielson D, Shay GF, Seastrand M, Jhawar S, Nickerson B, Landon C, Thompson A, Nussbaum E, Chin T, Wojtczak H; California Cystic Fibrosis Newborn Screening Consortium. Prach L, et al. Among authors: kharrazi m. J Mol Diagn. 2013 Sep;15(5):710-22. doi: 10.1016/j.jmoldx.2013.05.006. Epub 2013 Jun 28. J Mol Diagn. 2013. PMID: 23810505 Free PMC article.

2

Identification of novel and rare mutations in California Hispanic and African American cystic fibrosis patients.

Alper OM, Wong LJ, Young S, Pearl M, Graham S, Sherwin J, Nussbaum E, Nielson D, Platzker A, Davies Z, Lieberthal A, Chin T, Shay G, Hardy K, Kharrazi M. Alper OM, et al. Among authors: kharrazi m. Hum Mutat. 2004 Oct;24(4):353. doi: 10.1002/humu.9281. Hum Mutat. 2004. PMID: 15365999

3

Delayed diagnosis of cystic fibrosis and the family perspective.

Kharrazi M, Kharrazi LD. Kharrazi M, et al. Among authors: kharrazi ld. J Pediatr. 2005 Sep;147(3 Suppl):S21-5. doi: 10.1016/j.jpeds.2005.08.011. J Pediatr. 2005. PMID: 16202777

4

Comprehensive genetic analysis of the cystic fibrosis transmembrane conductance regulator from dried blood specimens--implications for newborn screening.

Kammesheidt A, Kharrazi M, Graham S, Young S, Pearl M, Dunlop C, Keiles S. Kammesheidt A, et al. Among authors: kharrazi m. Genet Med. 2006 Sep;8(9):557-62. doi: 10.1097/01.gim.0000237793.19868.97. Genet Med. 2006. PMID: 16980811 Free article.

5

Multiplex ligation-dependent probe amplification identification of whole exon and single nucleotide deletions in the CFTR gene of Hispanic individuals with cystic fibrosis.

Schrijver I, Rappahahn K, Pique L, Kharrazi M, Wong LJ. Schrijver I, et al. Among authors: kharrazi m. J Mol Diagn. 2008 Jul;10(4):368-75. doi: 10.2353/jmoldx.2008.080004. Epub 2008 Jun 13. J Mol Diagn. 2008. PMID: 18556774 Free PMC article.

6

Impact of IVS8-(TG)m(T)n on IRT and sweat chloride levels in newborns identified by California CF newborn screening.

Keiles S, Koepke R, Parad R, Kharrazi M; California Cystic Fibrosis Newborn Screening Consortium. Keiles S, et al. Among authors: kharrazi m. J Cyst Fibros. 2012 May;11(3):257-60. doi: 10.1016/j.jcf.2011.11.010. Epub 2011 Dec 30. J Cyst Fibros. 2012. PMID: 22209734 Free article.

7

Benign outcome among positive cystic fibrosis newborn screen children with non-CF-causing variants.

Salinas DB, Sosnay PR, Azen C, Young S, Raraigh KS, Keens TG, Kharrazi M. Salinas DB, et al. Among authors: kharrazi m. J Cyst Fibros. 2015 Nov;14(6):714-9. doi: 10.1016/j.jcf.2015.03.006. Epub 2015 Mar 29. J Cyst Fibros. 2015. PMID: 25824995 Free PMC article.

8

Newborn Screening for Cystic Fibrosis in California.

Kharrazi M, Yang J, Bishop T, Lessing S, Young S, Graham S, Pearl M, Chow H, Ho T, Currier R, Gaffney L, Feuchtbaum L; California Cystic Fibrosis Newborn Screening Consortium. Kharrazi M, et al. Pediatrics. 2015 Dec;136(6):1062-72. doi: 10.1542/peds.2015-0811. Epub 2015 Nov 16. Pediatrics. 2015. PMID: 26574590

9

The Spectrum of CFTR Variants in Nonwhite Cystic Fibrosis Patients: Implications for Molecular Diagnostic Testing.

Schrijver I, Pique L, Graham S, Pearl M, Cherry A, Kharrazi M. Schrijver I, et al. Among authors: kharrazi m. J Mol Diagn. 2016 Jan;18(1):39-50. doi: 10.1016/j.jmoldx.2015.07.005. J Mol Diagn. 2016. PMID: 26708955 Free article.

10

Next-Generation Molecular Testing of Newborn Dried Blood Spots for Cystic Fibrosis.

Lefterova MI, Shen P, Odegaard JI, Fung E, Chiang T, Peng G, Davis RW, Wang W, Kharrazi M, Schrijver I, Scharfe C. Lefterova MI, et al. Among authors: kharrazi m. J Mol Diagn. 2016 Mar;18(2):267-82. doi: 10.1016/j.jmoldx.2015.11.005. Epub 2016 Feb 1. J Mol Diagn. 2016. PMID: 26847993 Free PMC article.

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