Publications by authors named "Jessica Booker"

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The challenges and opportunities of offering and integrating training in clinical molecular genetics and clinical cytogenetics: A survey of LGG Fellowship Program Directors.
Joshua L Deignan, Vimla Aggarwal, Allen E Bale, Daniel B Bellissimo, Jessica K Booker

Genet Med Open· February 2024

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Correction: Common-variant associations with fragile X syndrome.
James J Crowley, Jin Szatkiewicz, Anna K Kähler, Paola Giusti-Rodriguez, NaEshia Ancalade, Jessica K Booker

Mol Psychiatry· December 2020

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Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
Tamara S Roman, Stephanie B Crowley, Myra I Roche, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker

Am J Hum Genet· October 2020

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Common-variant associations with fragile X syndrome.
James J Crowley, Jin Szatkiewicz, Anna K Kähler, Paola Giusti-Rodriguez, NaEshia Ancalade, Jessica K Booker

Mol Psychiatry· March 2019

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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Lisa R Susswein, Megan L Marshall, Rachel Nusbaum, Kristen J Vogel Postula, Scott M Weissman, Jessica K Booker

Genet Med· August 2016

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FNA smears as a potential source of DNA for targeted next-generation sequencing of lung adenocarcinomas.
Amanda L Treece, Nathan D Montgomery, Nirali M Patel, Chris J Civalier, Leslie G Dodd, Jessica K Booker

Cancer Cytopathol· June 2016

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CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids.
Florian S Eichler, Jiankang Li, Yiran Guo, Paul A Caruso, Andrew C Bjonnes, Jessica K Booker

Brain· June 2016

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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe

Genet Med· May 2016

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The Prothrombin 20209C>T Sequence Variant: To Test or Not to Test.
Denise I Quigley, Jessica K Booker, Daynna J Wolff

J Assoc Genet Technol· July 2011

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Sensorineural hearing loss in a pediatric population: association of congenital cytomegalovirus infection with intracranial abnormalities.
Jane W Kimani, Craig A Buchman, Jessica K Booker, Benjamin Y Huang, Mauricio Castillo

Arch Otolaryngol Head Neck Surg· October 2010

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Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing.
Shannon D Barker, Sherri Bale, Jessica Booker, Arlene Buller, Soma Das

J Mol Diagn· November 2009

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Validation of clinical testing for warfarin sensitivity: comparison of CYP2C9-VKORC1 genotyping assays and warfarin-dosing algorithms.
Michael R Langley, Jessica K Booker, James P Evans, Howard L McLeod, Karen E Weck

J Mol Diagn· May 2009

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Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10).
Karen Fritchie, Eija Siintola, Diane Armao, Anna-Elina Lehesjoki, Thomas Marino, Jessica M Booker

Acta Neuropathol· February 2009

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High levels of Epstein-Barr virus DNA in latently infected gastric adenocarcinoma.
Julie L Ryan, Douglas R Morgan, Ricardo L Dominguez, Leigh B Thorne, Sandra H Elmore, Jessica K Booker

Lab Invest· January 2009

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Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.
Lisa R Susswein, Cécile Skrzynia, Leslie A Lange, Jessica K Booker, Mark L Graham

J Clin Oncol· January 2008

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A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.
Girish V Putcha, Bassem A Bejjani, Stacey Bleoo, Jessica K Booker, John C Carey

Genet Med· July 2007

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Analytic validation of a quantitative real-time PCR assay to measure CMV viral load in whole blood.
Leigh B Thorne, Chris Civalier, Jessica Booker, Hongxin Fan, Margaret L Gulley

Diagn Mol Pathol· June 2007

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Glutaric acidemia type 1 in patients of Lumbee heritage from North Carolina.
Alice A Basinger, Jessica K Booker, Dianne M Frazier, Dwight D Koeberl, Jennifer A Sullivan

Mol Genet Metab· May 2006

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Diagnosis of human congenital cytomegalovirus infection by amplification of viral DNA from dried blood spots on perinatal cards.
Lori Scanga, Shu Chaing, Cynthia Powell, Arthur S Aylsworth, Lizzie J Harrell, Jessica Booker

J Mol Diagn· May 2006

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Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.
Hongxin Fan, Chris Civalier, Jessica K Booker, Margaret L Gulley, Thomas W Prior

J Mol Diagn· May 2006

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False-negative factor V Leiden genetic testing in a patient with recurrent deep venous thrombosis.
Edward N Libby, Jessica K Booker, Margaret L Gulley, David Garcia, Stephan Moll

Am J Hematol· April 2006

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Mosaicism for an FMR1 gene deletion in a fragile X female.
Hongxin Fan, Jessica K Booker, Shawn E McCandless, Vandana Shashi, Alison Fleming

Am J Med Genet A· July 2005

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