Publications by authors named "Beryl Crossley"

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Characterisation of T cell receptor repertoires in coeliac disease.
Lik Wee Lee, Shahin Shafiani, Beryl Crossley, Ryan O Emerson, David Williamson

J Clin Pathol· January 2024

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Immunoglobulin somatic hypermutation has clinical impact in DLBCL and potential implications for immune checkpoint blockade and neoantigen-based immunotherapies.
Zijun Y Xu-Monette, Jianyong Li, Yi Xia, Beryl Crossley, Robert D Bremel

J Immunother Cancer· October 2019

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Measurable residual disease detection by high-throughput sequencing improves risk stratification for pediatric B-ALL.
Brent Wood, David Wu, Beryl Crossley, Yunfeng Dai, David Williamson

Blood· March 2018

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Mutation Yield of a 34-Gene Solid Tumor Panel in Community-Based Tumor Samples.
Heather Sanders, Kevin Qu, Hairong Li, Lin Ma, Cindy Barlan, Beryl Crossley

Mol Diagn Ther· June 2016

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The sensitivity and specificity of hyperglycosylated hCG (hhCG) levels to reliably diagnose clinical IVF pregnancies at 6 days following embryo transfer.
Charles M Strom, Ruben Bonilla-Guererro, Ke Zhang, Kevin J Doody, David Tourgeman, Beryl Crossley

J Assist Reprod Genet· July 2012

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Testing for variants in CYP2C19: population frequencies and testing experience in a clinical laboratory.
Charles M Strom, Dana Goos, Beryl Crossley, Ke Zhang, Arlene Buller-Burkle

Genet Med· January 2012

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Cystic fibrosis testing 8 years on: lessons learned from carrier screening and sequencing analysis.
Charles M Strom, Beryl Crossley, Arlene Buller-Buerkle, Michael Jarvis, Franklin Quan

Genet Med· February 2011

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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.
Feras M Hantash, Dana M Goos, Beryl Crossley, Ben Anderson, Ke Zhang

Genet Med· January 2011

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Development of a web-based query tool for quality assurance of clinical molecular genetic test results.
Matthew J McGinniss, Rebecca Chen, Victoria M Pratt, Arlene Buller, Franklin Quan, Beryl Crossley

J Mol Diagn· February 2007

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Molecular testing for Fragile X Syndrome: lessons learned from 119,232 tests performed in a clinical laboratory.
Charles M Strom, Beryl Crossley, Joy B Redman, Arlene Buller, Franklin Quan

Genet Med· January 2007

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Detection of 677CT/1298AC "double variant" chromosomes: implications for interpretation of MTHFR genotyping results.
Nicholas M Brown, Victoria M Pratt, Arlene Buller, Lisa Pike-Buchanan, Joy B Redman, Beryl Crossley

Genet Med· April 2005

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Cystic fibrosis screening: lessons learned from the first 320,000 patients.
Charles M Strom, Beryl Crossley, Joy B Redman, Arlene Buller, Franklin Quan

Genet Med· February 2005

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Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratory.
Charles M Strom, Beryl Crossley, Joy B Redman, Franklin Quan, Arlene Buller

Genet Med· February 2005

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Direct visualization of cystic fibrosis transmembrane regulator mutations in the clinical laboratory setting.
Charles M Strom, David D Clark, Feras M Hantash, Larry Rea, Ben Anderson, Beryl Crossley

Clin Chem· May 2004

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Cystic fibrosis screening using the College panel: platform comparison and lessons learned from the first 20,000 samples.
Charles M Strom, Donghui Huang, Arlene Buller, Joy Redman, Beryl Crossley

Genet Med· November 2002

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