Search Results - Simpson, Michael A

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  1. 1
    Applying for Junior Hospital Posts

    Applying for Junior Hospital Posts by Simpson, Michael A.

    Published 1973
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  2. 2
    Delayed Drug-induced Dystonias

    Delayed Drug-induced Dystonias by Simpson, Michael A.

    Published 1974
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  3. 3
    Fear of ECT

    Fear of ECT by Simpson, Michael A

    Published 1976
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  4. 4
    Registration and the G.M.C

    Registration and the G.M.C by Simpson, Michael A.

    Published 1972
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  5. 5
    Intelligence and Fertility

    Intelligence and Fertility by Simpson, Michael A.

    Published 1972
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  6. 6
    Surgeons and Technical Skill

    Surgeons and Technical Skill by Simpson, Michael A.

    Published 1971
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  7. 7
    Living with the dying

    Living with the dying by Simpson, Michael A.

    Published 1978
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  8. 8
    Student Research

    Student Research by Simpson, Michael A.

    Published 1968
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  9. 9
    The Future of Genomics for Developmentalists

    The Future of Genomics for Developmentalists by Plomin, Robert, Simpson, Michael A.

    Published 2013
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  10. 10
    Psoriasis and Genetics

    Psoriasis and Genetics by DAND, Nick, MAHIL, Satveer K., CAPON, Francesca, SMITH, Catherine H., SIMPSON, Michael A., BARKER, Jonathan N.

    Published 2020
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  11. 11
    Network‐Informed Gene Ranking Tackles Genetic Heterogeneity in Exome‐Sequencing Studies of Monogenic Disease

    Network‐Informed Gene Ranking Tackles Genetic Heterogeneity in Exome‐Sequencing Studies of Monogenic Disease by Dand, Nick, Schulz, Reiner, Weale, Michael E., Southgate, Laura, Oakey, Rebecca J., Simpson, Michael A., Schlitt, Thomas

    Published 2015
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  12. 12
    Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia

    Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia by Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.

    Published 2003
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  13. 13
    MED12, TERT promoter and RBM15 mutations in primary and recurrent phyllodes tumours

    MED12, TERT promoter and RBM15 mutations in primary and recurrent phyllodes tumours by Garcia-Dios, Diego A, Levi, Dina, Shah, Vandna, Gillett, Cheryl, Simpson, Michael A, Hanby, Andrew, Tomlinson, Ian, Sawyer, Elinor J

    Published 2018
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  14. 14
    Mutation in GNE is associated with severe congenital thrombocytopenia

    Mutation in GNE is associated with severe congenital thrombocytopenia by Futterer, Jane, Dalby, Amanda, Lowe, Gillian C., Johnson, Ben, Simpson, Michael A., Motwani, Jayashree, Williams, Mike, Watson, Steve P., Morgan, Neil V.

    Published 2018
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  15. 15
    Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome

    Serpentine fibula polycystic kidney syndrome is part of the phenotypic spectrum of Hajdu–Cheney syndrome by Gray, Mary J, Kim, Chong Ae, Bertola, Debora Romeo, Arantes, Paula Ricci, Stewart, Helen, Simpson, Michael A, Irving, Melita D, Robertson, Stephen P

    Published 2012
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  16. 16
    Thinking positively: The genetics of high intelligence

    Thinking positively: The genetics of high intelligence by Shakeshaft, Nicholas G., Trzaskowski, Maciej, McMillan, Andrew, Krapohl, Eva, Simpson, Michael A., Reichenberg, Avi, Cederlöf, Martin, Larsson, Henrik, Lichtenstein, Paul, Plomin, Robert

    Published 2015
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  17. 17
    A Three-Stage Genome-Wide Association Study of General Cognitive Ability: Hunting the Small Effects

    A Three-Stage Genome-Wide Association Study of General Cognitive Ability: Hunting the Small Effects by Davis, Oliver S. P., Butcher, Lee M., Docherty, Sophia J., Meaburn, Emma L., Curtis, Charles J. C., Simpson, Michael A., Schalkwyk, Leonard C., Plomin, Robert

    Published 2010
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  18. 18
    Fine mapping genetic associations between the HLA region and extremely high intelligence

    Fine mapping genetic associations between the HLA region and extremely high intelligence by Zabaneh, Delilah, Krapohl, Eva, Simpson, Michael A., Miller, Mike B., Iacono, William G., McGue, Matt, Putallaz, Martha, Lubinski, David, Plomin, Robert, Breen, Gerome

    Published 2017
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  19. 19
    EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features

    EGFR mutations cause a lethal syndrome of epithelial dysfunction with progeroid features by Ganetzky, Rebecca, Finn, Erin, Bagchi, Atrish, Zollo, Ornella, Conlin, Laura, Deardorff, Matthew, Harr, Margaret, Simpson, Michael A, McGrath, John A, Zackai, Elaine, Lemmon, Mark A, Sondheimer, Neal

    Published 2015
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  20. 20
    Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years

    Frequency of pathogenic germline variants in BRCA1, BRCA2, PALB2, CHEK2 and TP53 in ductal carcinoma in situ diagnosed in women under the age of 50 years by Petridis, Christos, Arora, Iteeka, Shah, Vandna, Megalios, Anargyros, Moss, Charlotte, Mera, Anca, Clifford, Angela, Gillett, Cheryl, Pinder, Sarah E., Tomlinson, Ian, Roylance, Rebecca, Simpson, Michael A., Sawyer, Elinor J.

    Published 2019
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