B. Crossley

发表

Testing for variants in CYP2C19: population frequencies and testing experience in a clinical laboratory

Weimin Sun, C. Strom, Mei Peng, 2011, Genetics in Medicine.

Cystic fibrosis screening using the College panel: Platform comparison and lessons learned from the first 20,000 samples

Weimin Sun, C. Strom, Ben Anderson, 2002, Genetics in Medicine.

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

Weimin Sun, C. Strom, Mei Peng, 2004, Genetics in Medicine.

Cystic fibrosis testing 8 years on: Lessons learned from carrier screening and sequencing analysis

Weimin Sun, C. Strom, Mei Peng, 2011, Genetics in Medicine.

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

Weimin Sun, C. Strom, M. Mcginniss, 2004, Genetics in Medicine.

Tay-Sachs carrier screening in the genomics age: Gene sequencing versus enzyme analysis in non-Jewish individuals

N. Park, C. Strom, B. Crossley, 2013 .

The sensitivity and specificity of hyperglycosylated hCG (hhCG) levels to reliably diagnose clinical IVF pregnancies at 6 days following embryo transfer

C. Strom, R. Alvero, M. Cedars, 2012, Journal of Assisted Reproduction and Genetics.

Mutation Yield of a 34-Gene Solid Tumor Panel in Community-Based Tumor Samples

F. Waldman, J. Catanese, J. Sninsky, 2016, Molecular Diagnosis & Therapy.

Immunoglobulin somatic hypermutation has clinical impact in DLBCL and potential implications for immune checkpoint blockade and neoantigen-based immunotherapies

J. Winter, M. Piris, W. Tam, 2019, Journal of Immunotherapy for Cancer.

Measurable residual disease detection by high-throughput sequencing improves risk stratification for pediatric B-ALL.

M. Loh, B. Wood, H. Robins, 2018, Blood.

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

Weimin Sun, C. Strom, F. Hantash, 2011, Genetics in Medicine.

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

Weimin Sun, C. Strom, Mei Peng, 2007, Genetics in Medicine.

Characterisation of T cell receptor repertoires in coeliac disease

R. Emerson, G. Bhagat, D. Williamson, 2022, Journal of clinical pathology.

Detection of 677CT/1298AC “double variant” chromosomes: Implications for interpretation of MTHFR genotyping results

Weimin Sun, C. Strom, M. Mcginniss, 2005, Genetics in Medicine.

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

David D. Clark, Weimin Sun, Charles M Strom, 2004, Clinical chemistry.