Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing
Susswein, Lisa R., Marshall, Megan L., Nusbaum, Rachel, Vogel Postula, Kristen J., Weissman, Scott M., Yackowski, Lauren, Vaccari, Erica M., Bissonnette, Jeffrey, Booker, Jessica K., Cremona, M. Laura, Gibellini, Federica, Murphy, Patricia D., Pineda-Alvarez, Daniel E., Pollevick, Guido D., Xu, Zhixiong, Richard, Gabi, Bale, Sherri, Klein, Rachel T., Hruska, Kathleen S., Chung, Wendy K.
Published in Genetics in medicine (01.08.2016)
Published in Genetics in medicine (01.08.2016)
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FNA smears as a potential source of DNA for targeted next-generation sequencing of lung adenocarcinomas
Treece, Amanda L, Montgomery, Nathan D, Patel, Nirali M, Civalier, Chris J, Dodd, Leslie G, Gulley, Margaret L, Booker, Jessica K, Weck, Karen E
Published in Cancer cytopathology (01.06.2016)
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Increased Uptake of BRCA1/2 Genetic Testing Among African American Women With a Recent Diagnosis of Breast Cancer
SUSSWEIN, Lisa R, SKRZYNIA, Cécile, LANGE, Leslie A, BOOKER, Jessica K, GRAHAM, Mark L, EVANS, James P
Published in Journal of clinical oncology (01.01.2008)
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CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids
Eichler, Florian S, Li, Jiankang, Guo, Yiran, Caruso, Paul A, Bjonnes, Andrew C, Pan, Jessica, Booker, Jessica K, Lane, Jacqueline M, Tare, Archana, Vlasac, Irma, Hakonarson, Hakon, Gusella, James F, Zhang, Jianguo, Keating, Brendan J, Saxena, Richa
Published in Brain (London, England : 1878) (01.06.2016)
Published in Brain (London, England : 1878) (01.06.2016)
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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing
Berg, Jonathan S., Foreman, Ann Katherine M., O'Daniel, Julianne M., Booker, Jessica K., Boshe, Lacey, Carey, Timothy, Crooks, Kristy R., Jensen, Brian C., Juengst, Eric T., Lee, Kristy, Nelson, Daniel K., Powell, Bradford C., Powell, Cynthia M., Roche, Myra I., Skrzynia, Cecile, Strande, Natasha T., Weck, Karen E., Wilhelmsen, Kirk C., Evans, James P.
Published in Genetics in medicine (01.05.2016)
Published in Genetics in medicine (01.05.2016)
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Correction: Common-variant associations with fragile X syndrome
Crowley, James J, Szatkiewicz, Jin, Kähler, Anna K, Giusti-Rodriguez, Paola, Ancalade, NaEshia, Booker, Jessica K, Carr, Jennifer L
Published in Molecular psychiatry (01.12.2020)
Published in Molecular psychiatry (01.12.2020)
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Common-variant associations with fragile X syndrome
Crowley, James J, Szatkiewicz, Jin, Kähler, Anna K, Giusti-Rodriguez, Paola, Ancalade, NaEshia, Booker, Jessica K, Carr, Jennifer L, Crawford, Greg E, Losh, Molly, Stockmeier, Craig A, Taylor, Annette K, Piven, Joseph, Sullivan, Patrick F
Published in Molecular psychiatry (01.03.2019)
Published in Molecular psychiatry (01.03.2019)
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High levels of Epstein-Barr virus DNA in latently infected gastric adenocarcinoma
RYAN, Julie L, MORGAN, Douglas R, DOMINGUEZ, Ricardo L, THORNE, Leigh B, ELMORE, Sandra H, MINO-KENUDSON, Mari, LAUWERS, Gregory Y, BOOKER, Jessica K, GULLEY, Margaret L
Published in Laboratory investigation (01.01.2009)
Published in Laboratory investigation (01.01.2009)
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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
Deignan, Joshua L., Aggarwal, Vimla, Bale, Allen E., Bellissimo, Daniel B., Booker, Jessica K., Cao, Yang, Crooks, Kristy R., Deak, Kristen L., Del Gaudio, Daniela, Funke, Birgit, Hoppman, Nicole L., Horner, Vanessa, Hufnagel, Robert B., Jackson-Cook, Colleen, Koduru, Prasad, Leung, Marco L., Li, Shibo, Liu, Pengfei, Luo, Minjie, Mao, Rong, Mason-Suares, Heather, Mikhail, Fady M., Moore, Stephen R., Naeem, Rizwan C., Pollard, Laura M., Repnikova, Elena A., Shao, Lina, Shaw, Brandon M., Shetty, Shashirekha, Smolarek, Teresa A., Spiteri, Elizabeth, Van Ziffle, Jessica, Vance, Gail H., Vnencak-Jones, Cindy L., Williams, Eli S.
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Validation of Clinical Testing for Warfarin Sensitivity: Comparison of CYP2C9-VKORC1 Genotyping Assays and Warfarin-Dosing Algorithms
Langley, Michael R, Booker, Jessica K, Evans, James P, McLeod, Howard L, Weck, Karen E
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
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A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort
Putcha, Girish V, Bejjani, Bassem A, Bleoo, Stacey, Booker, Jessica K, Carey, John C, Carson, Nancy, Das, Soma, Dempsey, Melissa A, Gastier-Foster, Julie M, Greinwald, Jr, John H, Hoffmann, Marcy L, Jeng, Linda Jo Bone, Kenna, Margaret A, Khababa, Ishrag, Lilley, Margaret, Mao, Rong, Muralidharan, Kasinathan, Otani, Iris M, Rehm, Heidi L, Schaefer, Fred, Seltzer, William K, Spector, Elaine B, Springer, Michelle A, Weck, Karen E, Wenstrup, Richard J, Withrow, Stacey, Wu, Bai-Lin, Zariwala, Maimoona A, Schrijver, Iris
Published in Genetics in medicine (01.07.2007)
Published in Genetics in medicine (01.07.2007)
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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
Fan, Hongxin, Civalier, Chris, Booker, Jessica K., Gulley, Margaret L., Prior, Thomas W., Farber, Rosann A.
Published in The Journal of molecular diagnostics : JMD (01.05.2006)
Published in The Journal of molecular diagnostics : JMD (01.05.2006)
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Mosaicism for an FMR1 gene deletion in a fragile X female
Fan, Hongxin, Booker, Jessica K., McCandless, Shawn E., Shashi, Vandana, Fleming, Alison, Farber, Rosann A.
Published in American journal of medical genetics. Part A (15.07.2005)
Published in American journal of medical genetics. Part A (15.07.2005)
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Sensorineural Hearing Loss in a Pediatric Population: Association of Congenital Cytomegalovirus Infection With Intracranial Abnormalities
Kimani, Jane W, Buchman, Craig A, Booker, Jessica K, Huang, Benjamin Y, Castillo, Mauricio, Powell, Cynthia M, Weck, Karen E
Published in Archives of otolaryngology--head & neck surgery (01.10.2010)
Published in Archives of otolaryngology--head & neck surgery (01.10.2010)
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Validation of Clinical Testing for Warfarin Sensitivity: Comparison of
Langley, Michael R., Booker, Jessica K., Evans, James P., McLeod, Howard L., Weck, Karen E.
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
Published in The Journal of molecular diagnostics : JMD (01.05.2009)
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