Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders
O'Brien, Heath E, Hannon, Eilis, Hill, Matthew J, Toste, Carolina C, Robertson, Matthew J, Morgan, Joanne E, McLaughlin, Gemma, Lewis, Cathryn M, Schalkwyk, Leonard C, Hall, Lynsey S, Pardiñas, Antonio F, Owen, Michael J, O'Donovan, Michael C, Mill, Jonathan, Bray, Nicholas J
Published in Genome Biology (12.11.2018)
Published in Genome Biology (12.11.2018)
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Journal Article
Young Offenders’ Emotion Recognition Dysfunction Across Emotion Intensities: Explaining Variation Using Psychopathic Traits, Conduct Disorder and Offense Severity
Bowen, Katharine L., Morgan, Joanne E., Moore, Simon C., van Goozen, Stephanie H. M.
Published in Journal of psychopathology and behavioral assessment (01.03.2014)
Published in Journal of psychopathology and behavioral assessment (01.03.2014)
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Journal Article
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Logan, Clare V, Lucke, Barbara, Pottinger, Caroline, Abdelhamed, Zakia A, Parry, David A, Szymanska, Katarzyna, Diggle, Christine P, van Riesen, Anne, Morgan, Joanne E, Markham, Grace, Ellis, Ian, Manzur, Adnan Y, Markham, Alexander F, Shires, Mike, Helliwell, Tim, Scoto, Mariacristina, Hübner, Christoph, Bonthron, David T, Taylor, Graham R, Sheridan, Eamonn, Muntoni, Francesco, Carr, Ian M, Schuelke, Markus, Johnson, Colin A
Published in Nature genetics (01.12.2011)
Published in Nature genetics (01.12.2011)
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Journal Article
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
Parry, David A., Brookes, Steven J., Logan, Clare V., Poulter, James A., El-Sayed, Walid, Al-Bahlani, Suhaila, Al Harasi, Sharifa, Sayed, Jihad, Raïf, El Mostafa, Shore, Roger C., Dashash, Mayssoon, Barron, Martin, Morgan, Joanne E., Carr, Ian M., Taylor, Graham R., Johnson, Colin A., Aldred, Michael J., Dixon, Michael J., Wright, J. Tim, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Published in American journal of human genetics (07.09.2012)
Published in American journal of human genetics (07.09.2012)
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Journal Article
Cardiac malformations and midline skeletal defects in mice lacking filamin A
Hart, Alan W., Morgan, Joanne E., Schneider, Jürgen, West, Katrine, McKie, Lisa, Bhattacharya, Shoumo, Jackson, Ian J., Cross, Sally H.
Published in Human molecular genetics (15.08.2006)
Published in Human molecular genetics (15.08.2006)
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Journal Article
Mutation screening of retinal dystrophy patients by targeted capture from tagged pooled DNAs and next generation sequencing
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
Published in PloS one (18.08.2014)
Published in PloS one (18.08.2014)
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Journal Article
Robust Diagnostic Genetic Testing Using Solution Capture Enrichment and a Novel Variant-Filtering Interface
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.
Published in Human mutation (01.04.2014)
Published in Human mutation (01.04.2014)
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Journal Article
Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma
Khan, Kamron, Rudkin, Adam, Parry, David A., Burdon, Kathryn P., McKibbin, Martin, Logan, Clare V., Abdelhamed, Zakia I.A., Muecke, James S., Fernandez-Fuentes, Narcis, Laurie, Kate J., Shires, Mike, Fogarty, Rhys, Carr, Ian M., Poulter, James A., Morgan, Joanne E., Mohamed, Moin D., Jafri, Hussain, Raashid, Yasmin, Meng, Ngy, Piseth, Horm, Toomes, Carmel, Casson, Robert J., Taylor, Graham R., Hammerton, Michael, Sheridan, Eamonn, Johnson, Colin A., Inglehearn, Chris F., Craig, Jamie E., Ali, Manir
Published in American journal of human genetics (09.09.2011)
Published in American journal of human genetics (09.09.2011)
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Journal Article
Genetic diagnosis of familial breast cancer using clonal sequencing
Morgan, Joanne E, Carr, Ian M, Sheridan, Eamonn, Chu, Carol E, Hayward, Bruce, Camm, Nick, Lindsay, Helen A, Mattocks, Chris J, Markham, Alexander F, Bonthron, David T, Taylor, Graham R
Published in Human mutation (01.04.2010)
Published in Human mutation (01.04.2010)
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Journal Article
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects
Khan, Kamron, Logan, Clare V., McKibbin, Martin, Sheridan, Eamonn, Elçioglu, Nursel H., Yenice, Ozlem, Parry, David A., Fernandez-Fuentes, Narcis, Abdelhamed, Zakia I.A., Al-Maskari, Ahmed, Poulter, James A., Mohamed, Moin D., Carr, Ian M., Morgan, Joanne E., Jafri, Hussain, Raashid, Yasmin, Taylor, Graham R., Johnson, Colin A., Inglehearn, Chris F., Toomes, Carmel, Ali, Manir
Published in Human molecular genetics (15.02.2012)
Published in Human molecular genetics (15.02.2012)
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Journal Article
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis
Diggle, Christine P., Parry, David A., Logan, Clare V., Laissue, Paul, Rivera, Carolina, Restrepo, Carlos Martín, Fonseca, Dora J., Morgan, Joanne E., Allanore, Yannick, Fontenay, Michaela, Wipff, Julien, Varret, Mathilde, Gibault, Laure, Dalantaeva, Nadezhda, Korbonits, Márta, Zhou, Bowen, Yuan, Gang, Harifi, Ghita, Cefle, Kivanc, Palanduz, Sukru, Akoglu, Hadim, Zwijnenburg, Petra J., Lichtenbelt, Klaske D., Aubry-Rozier, Bérengère, Superti-Furga, Andrea, Dallapiccola, Bruno, Accadia, Maria, Brancati, Francesco, Sheridan, Eamonn G., Taylor, Graham R., Carr, Ian M., Johnson, Colin A., Markham, Alexander F., Bonthron, David T.
Published in Human mutation (01.08.2012)
Published in Human mutation (01.08.2012)
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Journal Article
Genotype-Phenotype Correlation of Mouse Pde6b Mutations
Hart, Alan W, McKie, Lisa, Morgan, Joanne E, Gautier, Philippe, West, Katrine, Jackson, Ian J, Cross, Sally H
Published in Investigative ophthalmology & visual science (01.09.2005)
Published in Investigative ophthalmology & visual science (01.09.2005)
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Journal Article
Mutation Detection by Clonal Sequencing of PCR Amplicons and Grouped Read Typing is Applicable to Clinical Diagnostics
Chambers, Philip A., Stead, Lucy F., Morgan, Joanne E., Carr, Ian M., Sutton, Kate M., Watson, Christopher M., Crowe, Victoria, Dickinson, Helen, Roberts, Paul, Mulatero, Clive, Seymour, Matthew, Markham, Alexander F., Waring, Paul M., Quirke, Philip, Taylor, Graham R.
Published in Human mutation (01.01.2013)
Published in Human mutation (01.01.2013)
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Journal Article
Novel ENU-induced eye mutations in the mouse: models for human eye disease
Thaung, Caroline, West, Katrine, Clark, Brian J., McKie, Lisa, Morgan, Joanne E., Arnold, Karen, Nolan, Patrick M., Peters, Jo, Hunter, A. Jackie, Brown, Steve D. M., Jackson, Ian J., Cross, Sally H.
Published in Human molecular genetics (01.04.2002)
Published in Human molecular genetics (01.04.2002)
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Journal Article
Illuminator, a desktop program for mutation detection using short-read clonal sequencing
Carr, Ian M., Morgan, Joanne E., Diggle, Christine P., Sheridan, Eamonn, Markham, Alexander F., Logan, Clare V., Inglehearn, Chris F., Taylor, Graham R., Bonthron, David T.
Published in Genomics (San Diego, Calif.) (01.10.2011)
Published in Genomics (San Diego, Calif.) (01.10.2011)
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Journal Article
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor
Lee, Daekee, Cross, Sally H, Strunk, Karen E, Morgan, Joanne E, Bailey, Candice L, Jackson, Ian J, Threadgill, David W
Published in Mammalian genome (01.07.2004)
Published in Mammalian genome (01.07.2004)
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