GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profiles

por Antanaviciute, Agne, Daly, Catherine, Crinnion, Laura A., Markham, Alexander F., Watson, Christopher M., Bonthron, David T., Carr, Ian M.
Publicado en Bioinformatics (2015)

Towards a Next-Generation Sequencing Diagnostic Service for Tumour Genotyping: A Comparison of Panels and Platforms

por Burghel, George J., Hurst, Carolyn D., Watson, Christopher M., Chambers, Phillip A., Dickinson, Helen, Roberts, Paul, Knowles, Margaret A.
Publicado en Biomed Res Int (2015)

OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization

por Antanaviciute, Agne, Watson, Christopher M., Harrison, Sally M., Lascelles, Carolina, Crinnion, Laura, Markham, Alexander F., Bonthron, David T., Carr, Ian M.
Publicado en Bioinformatics (2015)

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome

por Watson, Christopher M., Crinnion, Laura A., Harrison, Sally M., Lascelles, Carolina, Antanaviciute, Agne, Carr, Ian M., Bonthron, David T., Sheridan, Eamonn
Publicado en PLoS One (2016)

Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplications

por Watson, Christopher M., Crinnion, Laura A., Hewitt, Sarah, Bates, Jennifer, Robinson, Rachel, Carr, Ian M., Sheridan, Eamonn, Adlard, Julian, Bonthron, David T.
Publicado en Lab Invest (2019)

Simulated Pediatric Resuscitation Use for Personal Protective Equipment Adherence Measurement and Training During the 2009 Influenza (H1N1) Pandemic

por Watson, Christopher M., Duval-Arnould, Jordan M., McCrory, Michael C., Froz, Stephan, Connors, Cheryl, Perl, Trish M., Hunt, Elizabeth A.
Publicado en Jt Comm J Qual Patient Saf (2011)

Reducing Accidental Dislodgement of the Percutaneous Endoscopic Gastrostomy: A Prospective Trial of the “SafetyBreak” Device

por Rosenberger, Laura H., Guidry, Christopher A., Davis, John P., Hranjec, Tjasa, Johnston, Vonda K., Wages, Nolan A., Watson, Christopher M., Sawyer, Robert G.
Publicado en Surg Innov (2015)

Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping

por Watson, Christopher M., Crinnion, Laura A., Berry, Ian R., Harrison, Sally M., Lascelles, Carolina, Antanaviciute, Agne, Charlton, Ruth S., Dobbie, Angus, Carr, Ian M., Bonthron, David T.
Publicado en BMC Med Genet (2016)

m6aViewer: software for the detection, analysis, and visualization of N(6)-methyladenosine peaks from m(6)A-seq/ME-RIP sequencing data

por Antanaviciute, Agne, Baquero-Perez, Belinda, Watson, Christopher M., Harrison, Sally M., Lascelles, Carolina, Crinnion, Laura, Markham, Alexander F., Bonthron, David T., Whitehouse, Adrian, Carr, Ian M.
Publicado en RNA (2017)

Characterizing hospital workers' willingness to report to duty in an influenza pandemic through threat- and efficacy-based assessment

por Catlett Christina L, Hsu Edbert B, Thompson Carol B, Barnett Daniel J, Balicer Ran D, Watson Christopher M, Semon Natalie L, Gwon Howard S, Links Jonathan M
Publicado 2010-07-01

Characterizing hospital workers' willingness to report to duty in an influenza pandemic through threat- and efficacy-based assessment

por Balicer, Ran D, Barnett, Daniel J, Thompson, Carol B, Hsu, Edbert B, Catlett, Christina L, Watson, Christopher M, Semon, Natalie L, Gwon, Howard S, Links, Jonathan M
Publicado 2010

Deficiency of the myogenic factor MyoD causes a perinatally lethal fetal akinesia

por Watson, Christopher M, Crinnion, Laura A, Murphy, Helen, Newbould, Melanie, Harrison, Sally M, Lascelles, Carolina, Antanaviciute, Agne, Carr, Ian M, Sheridan, Eamonn, Bonthron, David T, Smith, Audrey
Publicado en J Med Genet (2016)

Structure of Ubiquitin-fold Modifier 1-specific Protease UfSP2

por Ha, Byung Hak, Jeon, Young Joo, Shin, Sang Chul, Tatsumi, Kanako, Komatsu, Masaaki, Tanaka, Keiji, Watson, Christopher M., Wallis, Gillian, Chung, Chin Ha, Kim, Eunice EunKyeong
Publicado 2011

Characterizing Hospital Workers' Willingness to Respond to a Radiological Event

por Balicer, Ran D., Catlett, Christina L., Barnett, Daniel J., Thompson, Carol B., Hsu, Edbert B., Morton, Melinda J., Semon, Natalie L., Watson, Christopher M., Gwon, Howard S., Links, Jonathan M.
Publicado 2011

Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data

por Watson, Christopher M., Crinnion, Laura A., Gurgel‐Gianetti, Juliana, Harrison, Sally M., Daly, Catherine, Antanavicuite, Agne, Lascelles, Carolina, Markham, Alexander F., Pena, Sergio D. J., Bonthron, David T., Carr, Ian M.
Publicado en Hum Mutat (2015)

A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing

por Poulter, James A., Smith, Claire E. L., Murrillo, Gina, Silva, Sandra, Feather, Sally, Howell, Marianella, Crinnion, Laura, Bonthron, David T., Carr, Ian M., Watson, Christopher M., Inglehearn, Chris F., Mighell, Alan J.
Publicado en Mol Genet Genomic Med (2015)

Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface

por Watson, Christopher M, Crinnion, Laura A, Morgan, Joanne E, Harrison, Sally M, Diggle, Christine P, Adlard, Julian, Lindsay, Helen A, Camm, Nick, Charlton, Ruth, Sheridan, Eamonn, Bonthron, David T, Taylor, Graham R, Carr, Ian M
Publicado en Hum Mutat (2014)

Mutation Screening of Retinal Dystrophy Patients by Targeted Capture from Tagged Pooled DNAs and Next Generation Sequencing

por Watson, Christopher M., El-Asrag, Mohammed, Parry, David A., Morgan, Joanne E., Logan, Clare V., Carr, Ian M., Sheridan, Eamonn, Charlton, Ruth, Johnson, Colin A., Taylor, Graham, Toomes, Carmel, McKibbin, Martin, Inglehearn, Chris F., Ali, Manir
Publicado 2014

Obesity Is Not Associated with Antimicrobial Treatment Failure for Intra-Abdominal Infection

por Dietch, Zachary C., Duane, Therese M., Cook, Charles H., O'Neill, Patrick J., Askari, Reza, Napolitano, Lena M., Namias, Nicholas, Watson, Christopher M., Dent, Daniel L., Edwards, Brandy L., Shah, Puja M., Guidry, Christopher A., Davies, Stephen W., Willis, Rhett N., Sawyer, Robert G.
Publicado en Surg Infect (Larchmt) (2016)

A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development

por Diggle, Christine P., Martinez-Garay, Isabel, Molnar, Zoltan, Brinkworth, Martin H., White, Ed, Fowler, Ewan, Hughes, Ruth, Hayward, Bruce E., Carr, Ian M., Watson, Christopher M., Crinnion, Laura, Asipu, Aruna, Woodman, Ben, Coletta, P. Louise, Markham, Alexander F., Dear, T. Neil, Bonthron, David T., Peckham, Michelle, Morrison, Ewan E., Sheridan, Eamonn
Publicado en PLoS One (2017)