Hasil Pencarian - Mihail Halachev

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  1. 1
    Regionally enriched rare deleterious exonic variants in the UK and Ireland

    Regionally enriched rare deleterious exonic variants in the UK and Ireland oleh Mihail Halachev, Viktoria-Eleni Gountouna, Alison Meynert, Gannie Tzoneva, Alan R. Shuldiner, Colin A. Semple, James F. Wilson

    Diterbitkan 2024-10-01
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  2. 2
    Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP

    Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP oleh Anja Thormann, Mihail Halachev, William McLaren, David J. Moore, Victoria Svinti, Archie Campbell, Shona M. Kerr, Marc Tischkowitz, Sarah E. Hunt, Malcolm G. Dunlop, Matthew E. Hurles, Caroline F. Wright, Helen V. Firth, Fiona Cunningham, David R. FitzPatrick

    Diterbitkan 2019-05-01
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  3. 3
    Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.

    Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. oleh Mihail Halachev, Alison Meynert, Martin S Taylor, Veronique Vitart, Shona M Kerr, Lucija Klaric, S. G. P. Consortium, Timothy J Aitman, Chris S Haley, James G Prendergast, Carys Pugh, David A Hume, Sarah E Harris, David C Liewald, Ian J Deary, Colin A Semple, James F Wilson

    Diterbitkan 2019-11-01
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  4. 4
    ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.

    ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy. oleh Mark T Handley, Kaalak Reddy, Jimi Wills, Elisabeth Rosser, Archith Kamath, Mihail Halachev, Gavin Falkous, Denise Williams, Phillip Cox, Alison Meynert, Eleanor S Raymond, Harris Morrison, Stephen Brown, Emma Allan, Irene Aligianis, Andrew P Jackson, Bernard H Ramsahoye, Alex von Kriegsheim, Robert W Taylor, Andrew J Finch, David R FitzPatrick

    Diterbitkan 2019-03-01
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  5. 5
    Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability.

    Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability. oleh Hemant Bengani, Detelina Grozeva, Lambert Moyon, Shipra Bhatia, Susana R Louros, Jilly Hope, Adam Jackson, James G Prendergast, Liusaidh J Owen, Magali Naville, Jacqueline Rainger, Graeme Grimes, Mihail Halachev, Laura C Murphy, Olivera Spasic-Boskovic, Veronica van Heyningen, Peter Kind, Catherine M Abbott, Emily Osterweil, F Lucy Raymond, Hugues Roest Crollius, David R FitzPatrick

    Diterbitkan 2021-01-01
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