Anderson B - Search Results

1

Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory.

Rosenthal SH, Gerasimova A, Ruiz-Vega R, Livingston K, Kagan RM, Liu Y, Anderson B, Owen R, Bernstein L, Smolgovsky A, Xu D, Chen R, Grupe A, Tanpaiboon P, Lacbawan F. Rosenthal SH, et al. Among authors: anderson b. Sci Rep. 2022 Feb 8;12(1):2054. doi: 10.1038/s41598-022-06091-0. Sci Rep. 2022. PMID: 35136154 Free PMC article.

2

Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory.

Guy C, Haji-Sheikhi F, Rowland CM, Anderson B, Owen R, Lacbawan FL, Alagia DP. Guy C, et al. Among authors: anderson b. Mol Genet Genomic Med. 2019 Mar;7(3):e545. doi: 10.1002/mgg3.545. Epub 2019 Jan 31. Mol Genet Genomic Med. 2019. PMID: 30706702 Free PMC article.

3

Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS).

Strom CM, Anderson B, Tsao D, Zhang K, Liu Y, Livingston K, Elzinga C, Evans M, Nguyen Q, Wolfson D, Rowland C, Kolacki P, Maxwell M, Wang JC, Rabin D, Catanese J, Owen R, Braastad C, Sun W. Strom CM, et al. Among authors: anderson b. PLoS One. 2017 Mar 1;12(3):e0167130. doi: 10.1371/journal.pone.0167130. eCollection 2017. PLoS One. 2017. PMID: 28248967 Free PMC article.

4

Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish population.

Hantash FM, Olson SC, Anderson B, Buller A, Chen R, Crossly B, Sun W, Strom CM. Hantash FM, et al. Among authors: anderson b. J Mol Diagn. 2006 May;8(2):282-7. doi: 10.2353/jmoldx.2006.050026. J Mol Diagn. 2006. PMID: 16645217 Free PMC article.

5

Maternal chromosome Xp deletion identified by prenatal cell-free DNA screening.

Ilagan BJ, Maxwell MD, Fisher BM, Milanovich J, Owen R, Anderson B, Zhang K, Strom CM. Ilagan BJ, et al. Among authors: anderson b. Prenat Diagn. 2017 Sep;37(9):935-937. doi: 10.1002/pd.5103. Epub 2017 Jul 25. Prenat Diagn. 2017. PMID: 28654736 No abstract available.

6

Direct visualization of cystic fibrosis transmembrane regulator mutations in the clinical laboratory setting.

Strom CM, Clark DD, Hantash FM, Rea L, Anderson B, Maul D, Huang D, Traul D, Chen Tubman C, Garcia R, Hess PP, Wang H, Crossley B, Woodruff E, Chen R, Killeen M, Sun W, Beer J, Avens H, Polisky B, Jenison RD. Strom CM, et al. Among authors: anderson b. Clin Chem. 2004 May;50(5):836-45. doi: 10.1373/clinchem.2003.026088. Epub 2004 Mar 9. Clin Chem. 2004. PMID: 15010427

7

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: anderson b. 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

8

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States.

Hantash FM, Goos DM, Crossley B, Anderson B, Zhang K, Sun W, Strom CM. Hantash FM, et al. Among authors: anderson b. Genet Med. 2011 Jan;13(1):39-45. doi: 10.1097/GIM.0b013e3181fa9fad. Genet Med. 2011. PMID: 21116185 Free article.

9

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: anderson b. Genet Med. 2005 Nov-Dec;7(9):633-9. doi: 10.1097/01.gim.0000187120.93597.16. Genet Med. 2005. PMID: 16301865 Free article.

10

CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype.

Sun W, Anderson B, Redman J, Milunsky A, Buller A, McGinniss MJ, Quan F, Anguiano A, Huang S, Hantash F, Strom C. Sun W, et al. Among authors: anderson b. Genet Med. 2006 Jun;8(6):339-45. doi: 10.1097/01.gim.0000223549.57443.16. Genet Med. 2006. PMID: 16778595 Free article.

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