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Yasin Memari

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  • Corrigendum: Common genetic variation drives molecular heterogeneity in human iPSCs

    Kilpinen, H., Goncalves, A., Leha, A., Afzal, V., Alasoo, K., Ashford, S., Bala, S., Bensaddek, D., Casale, F. P., Culley, O. J., Danecek, P., Faulconbridge, A., Harrison, P. W., Kathuria, A., McCarthy, D., McCarthy, S. A., Meleckyte, R., Memari, Y., Moens, N., Soares, F., & 23 othersMann, A., Streeter, I., Agu, C. A., Alderton, A., Nelson, R., Harper, S., Patel, M., White, A., Patel, S. R., Clarke, L., Halai, R., Kirton, C. M., Kolb-Kokocinski, A., Beales, P., Birney, E., Danovi, D., Lamond, A. I., Ouwehand, W. H., Vallier, L., Watt, F. M., Durbin, R., Stegle, O. & Gaffney, D. J., 29 Jun 2017, In: NATURE. 546, 7660, p. 686

    Research output: Contribution to journalArticle

    12 Citations (Scopus)
  • Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits

    Tachmazidou, I., Süveges, D., Min, J. L., Ritchie, G. R. S., Steinberg, J., Walter, K., Iotchkova, V., Schwartzentruber, J., Huang, J., Memari, Y., McCarthy, S., Crawford, A. A., Bombieri, C., Cocca, M., Farmaki, A-E., Gaunt, T. R., Jousilahti, P., Kooijman, M. N., Lehne, B., Malerba, G., & 83 othersMännistö, S., Matchan, A., Medina-Gomez, C., Metrustry, S. J., Nag, A., Ntalla, I., Paternoster, L., Rayner, N. W., Sala, C., Scott, W. R., Shihab, H. A., Southam, L., St Pourcain, B., Traglia, M., Trajanoska, K., Zaza, G., Zhang, W., Artigas, M. S., Bansal, N., Benn, M., Chen, Z., Danecek, P., Lin, W-Y., Locke, A., Luan, J., Manning, A. K., Mulas, A., Sidore, C., Tybjaerg-Hansen, A., Varbo, A., Zoledziewska, M., Finan, C., Hatzikotoulas, K., Hendricks, A. E., Kemp, J. P., Moayyeri, A., Panoutsopoulou, K., Szpak, M., Wilson, S. G., Boehnke, M., Cucca, F., Di Angelantonio, E., Langenberg, C., Lindgren, C., McCarthy, M. I., Morris, A. P., Nordestgaard, B. G., Scott, R. A., Tobin, M. D., Wareham, N. J., Burton, P., Chambers, J. C., Smith, G. D., Dedoussis, G., Felix, J. F., Franco, O. H., Gambaro, G., Gasparini, P., Hammond, C. J., Hofman, A., Jaddoe, V. W. V., Kleber, M., Kooner, J. S., Perola, M., Relton, C., Ring, S. M., Rivadeneira, F., Salomaa, V., Spector, T. D., Stegle, O., Toniolo, D., Uitterlinden, A. G., Barroso, I., Greenwood, C. M. T., Perry, J. R. B., Walker, B. R., Butterworth, A. S., Xue, Y., Durbin, R., Small, K. S., Soranzo, N., Timpson, N. J. & Zeggini, E., 1 Jun 2017, In: American Journal of Human Genetics. 100, 6, p. 865–884

    Research output: Contribution to journalArticlepeer-review

    Open Access
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    106 Citations (Scopus)
    179 Downloads (Pure)
  • Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

    Huang, J., Howie, B., McCarthy, S., Memari, Y., Walter, K., Min, J. L., Danecek, P., Malerba, G., Trabetti, E., Zheng, H-F., Gambaro, G., Richards, J. B., Durbin, R., Timpson, N. J., Marchini, J., Soranzo, N. & UK10K Consortium, 14 Sept 2015, In: Nature Communications. 6, p. 1-9 9 p., 8111.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    215 Citations (Scopus)
  • Whole-genome sequence-based analysis of thyroid function

    Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., Memari, Y., Huang, J., Barnes, M. R., Beilby, J. P., Charoen, P., Danecek, P., Dudbridge, F., Forgetta, V., Greenwood, C., Grundberg, E., & 30 othersJohnson, A. D., Hui, J., Lim, E. M., McCarthy, S., Muddyman, D., Panicker, V., Perry, J. R. B., Bell, J. T., Yuan, W., Relton, C., Gaunt, T., Schlessinger, D., Abecasis, G., Cucca, F., Surdulescu, G. L., Woltersdorf, W., Zeggini, E., Zheng, H-F., Toniolo, D., Dayan, C. M., Naitza, S., Walsh, J. P., Spector, T., Davey Smith, G., Durbin, R., Brent Richards, J., Sanna, S., Soranzo, N., Timpson, N. J. & UK0K Consortium, 6 Mar 2015, In: Nature Communications. 6, 10 p., 5681.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    78 Citations (Scopus)
    153 Downloads (Pure)
  • Genes contributing to pain sensitivity in the normal population: an exome sequencing study

    Williams, F. M. K., Scollen, S., Cao, D., Memari, Y., Hyde, C. L., Zhang, B., Sidders, B., Ziemek, D., Shi, Y., Harris, J., Harrow, I., Dougherty, B., Malarstig, A., McEwen, R., Stephens, J. C., Patel, K., Menni, C., Shin, S-Y., Hodgkiss, D., Surdulescu, G., & 7 othersHe, W., Jin, X., McMahon, S. B., Soranzo, N., John, S., Wang, J. & Spector, T. D., 20 Dec 2012, In: PL o S Genetics. 8, 12, p. N/A 10 p., e1003095.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    53 Citations (Scopus)