King's College London

Research portal

PL o S Genetics, ‎1553-7390

Journal

  1. AKTIP interacts with ESCRT i and is needed for the recruitment of ESCRT III subunits to the midbody

    Merigliano, C., Burla, R., La Torre, M., Del Giudice, S., Teo, H., Liew, C. W., Chojnowski, A., Goh, W. I., Olmos, Y., MacCaroni, K., Giubettini, M., Chiolo, I., Carlton, J. G., Raimondo, D., Vernì, F., Stewart, C. L., Rhodes, D., Wright, G. D., Burke, B. E. & Saggio, I., 27 Aug 2021, In: PLoS Genetics. 17, 8, e1009757.

    Research output: Contribution to journalArticlepeer-review

  2. Genetic sensitivity analysis: Adjusting for genetic confounding in epidemiological associations

    Pingault, J. B., Rijsdijk, F., Schoeler, T., Choi, S. W., Selzam, S., Krapohl, E., O'Reilly, P. F. & Dudbridge, F., 11 Jun 2021, In: PLoS Genetics. 17, 6, e1009590.

    Research output: Contribution to journalArticlepeer-review

  3. Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images

    Currant, H., Hysi, P., Fitzgerald, T. W., Gharahkhani, P., Bonnemaijer, P. W. M., Senabouth, A., Hewitt, A. W., Atan, D., Aung, T., Charng, J., Choquet, H., Craig, J., Khaw, P. T., Klaver, C. C. W., Kubo, M., Ong, J. S., Pasquale, L. R., Reisman, C. A., Daniszewski, M., Powell, J. E. & 14 others, Pébay, A., Simcoe, M. J., Thiadens, A. A. H. J., van Duijn, C. M., Yazar, S., Jorgenson, E., MacGregor, S., Hammond, C. J., Mackey, D. A., Wiggs, J. L., Foster, P. J., Patel, P. J., Birney, E. & Khawaja, A. P., 12 May 2021, In: PLoS Genetics. 17, 5, e1009497.

    Research output: Contribution to journalArticlepeer-review

  4. Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits

    Early Growth Genetics Consortium, 12 Oct 2020, In: PLoS Genetics. 16, 10, e1008718.

    Research output: Contribution to journalArticlepeer-review

  5. Genomic imprinting: An epigenetic regulatory system

    Bartolomei, M. S., Oakey, R. J. & Wutz, A., 6 Aug 2020, In: PLoS Genetics. 16, 8, p. e1008970 e1008970.

    Research output: Contribution to journalEditorialpeer-review

  6. Is imprinting the result of “friendly fire” by the host defense system?

    Ondičová, M., Oakey, R. J. & Walsh, C. P., Apr 2020, In: PLoS Genetics. 16, 4, e1008599.

    Research output: Contribution to journalReview articlepeer-review

  7. Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma

    Waseem, N. H., Low, S., Shah, A. Z., Avisetti, D., Ostergaard, P., Simpson, M., Niemiec, K. A., Martin-Martin, B., Aldehlawi, H., Usman, S., Lee, P. S., Khawaja, A. P., Ruddle, J. B., Shah, A., Sackey, E., Day, A., Jiang, Y., Swinfield, G., Viswanathan, A., Alfano, G. & 7 others, Chakarova, C., Cordell, H. J., Garway-Heath, D. F., Khaw, P. T., Bhattacharya, S. S., Waseem, A. & Foster, P. J., Apr 2020, In: PLoS Genetics. 16, 4, e1008721.

    Research output: Contribution to journalArticlepeer-review

  8. A meta-analysis of genome-wide association studies of epigenetic age acceleration

    Gibson, J., Russ, T. C., Clarke, T-K., Howard, D. M., Hillary, R., Lewis, K., Walker, R. M., Bermingham, M. L., Morris, S. W., Cambell, A., Hayward, C., Murray, A. D., Porteous, D. J., Horvath, S., Lu, A. T., McIntosh, A., Whalley, H. & Marioni, R., 18 Nov 2019, In: PLoS Genetics. 15, 11

    Research output: Contribution to journalArticlepeer-review

  9. Genomic insights into neonicotinoid sensitivity in the solitary bee Osmia bicornis

    Beadle, K., Singh, K. S., Troczka, B. J., Randall, E., Zaworra, M., Zimmer, C. T., Hayward, A., Reid, R., Kor, L., Kohler, M., Buer, B., Nelson, D. R., Williamson, M. S., Davies, T. G. E., Field, L. M., Nauen, R. & Bass, C., Feb 2019, In: PLoS Genetics. 15, 2, e1007903.

    Research output: Contribution to journalArticlepeer-review

  10. Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis

    Li, Z., Akar, S., Yarkan, H., Lee, S. K., Çetin, P., Can, G., Kenar, G., Çapa, F., Pamuk, O. N., Pehlivan, Y., Cremin, K., De Guzman, E., Harris, J., Wheeler, L., Jamshidi, A., Vojdanian, M., Farhadi, E., Ahmadzadeh, N., Yüce, Z., Dalkılıç, E. & 11 others, Solmaz, D., Akın, B., Dönmez, S., Sarı, I., Leo, P. J., Kenna, T. J., Önen, F., Mahmoudi, M., Brown, M. A., Akkoc, N. & Masters, S. L. (ed.), 2019, In: PLoS Genetics. 15, 4, e1008038.

    Research output: Contribution to journalArticlepeer-review

  11. Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

    the 23andMe Research Team, 1 Dec 2018, In: PLoS Genetics. 14, 12, e1007813.

    Research output: Contribution to journalArticlepeer-review

  12. Dissection of Nidogen function in Drosophila reveals tissue-specific mechanisms of basement membrane assembly

    Dai, J., Estrada, B., Jacobs, S., Sánchez-Sánchez, B. J., Tang, J., Ma, M., Magadán-Corpas, P., Pastor-Pareja, J. C. & Martín-Bermudo, M. D., 27 Sep 2018, In: PLoS Genetics. 14, 9, p. e1007483

    Research output: Contribution to journalArticlepeer-review

  13. Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

    Suri, P., Palmer, M. R., Tsepilov, Y. A., Freidin, M. B., Boer, C. G., Yau, M. S., Evans, D. S., Gelemanovic, A., Bartz, T. M., Nethander, M., Arbeeva, L., Karssen, L., Neogi, T., Campbell, A., Mellstrom, D., Ohlsson, C., Marshall, L. M., Orwoll, E., Uitterlinden, A., Rotter, J. I. & 17 others, Lauc, G., Psaty, B. M., Karlsson, M. K., Lane, N. E., Jarvik, G. P., Polasek, O., Hochberg, M., Jordan, J. M., Van Meurs, J. B. J., Jackson, R., Nielson, C. M., Mitchell, B. D., Smith, B. H., Hayward, C., Smith, N. L., Aulchenko, Y. S. & Williams, F. M. K., Sep 2018, In: PLoS Genetics. 14, 9, p. e1007601

    Research output: Contribution to journalArticlepeer-review

  14. Ras-ERK-ETS inhibition alleviates neuronal mitochondrial dysfunction by reprogramming mitochondrial retrograde signaling

    Duncan, O. F., Granat, L., Ranganathan, R., Singh, V. K., Mazaud, D., Fanto, M., Chambers, D., Ballard, C. G. & Bateman, J. M., 30 Jul 2018, In: PLoS Genetics. 14, 7, 27 p., e1007567.

    Research output: Contribution to journalArticlepeer-review

  15. Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration

    Watson-Scales, S., Kalmar, B., Lana-Elola, E., Gibbins, D., La Russa, F., Wiseman, F., Williamson, M., Saccon, R., Slender, A., Olerinyova, A., Mahmood, R., Nye, E., Cater, H., Wells, S., Yu, Y. E., Bennett, D. L. H., Greensmith, L., Fisher, E. M. C. & Tybulewicz, V. L. J., 10 May 2018, In: PLoS Genetics. 14, 5, e1007383.

    Research output: Contribution to journalArticlepeer-review

  16. Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma

    International Glaucoma Genetics Consortium & NEIGHBORHOOD Consortium, 1 Jan 2018, In: PLoS Genetics. 14, 1, e1007145.

    Research output: Contribution to journalArticlepeer-review

  17. Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development

    Ridge, L. A., Mitchell, K., Al-Anbaki, A., Shaikh Qureshi, W. M., Stephen, L. A., Tenin, G., Lu, Y., Lupu, I. E., Clowes, C., Robertson, A., Barnes, E., Wright, J. A., Keavney, B., Ehler, E., Lovell, S. C., Kadler, K. E. & Hentges, K. E., 30 Oct 2017, (E-pub ahead of print) In: PL o S Genetics. 13, 10, e1007068.

    Research output: Contribution to journalArticlepeer-review

  18. Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons

    Li, H., Reksten, T. R., Ice, J. A., Kelly, J. A., Adrianto, I., Rasmussen, A., Wang, S., He, B., Grundahl, K. M., Glenn, S. B., Miceli-Richard, C., Bowman, S., Lester, S., Eriksson, P., Eloranta, M. L., Brun, J. G., Gøransson, L. G., Harboe, E., Guthridge, J. M., Kaufman, K. M. & 44 others, Kvarnström, M., Cunninghame Graham, D. S., Patel, K., Adler, A. J., Farris, A. D., Brennan, M. T., Chodosh, J., Gopalakrishnan, R., Weisman, M. H., Venuturupalli, S., Wallace, D. J., Hefner, K. S., Houston, G. D., Huang, A. J. W., Hughes, P. J., Lewis, D. M., Radfar, L., Vista, E. S., Edgar, C. E., Rohrer, M. D., Stone, D. U., Vyse, T. J., Harley, J. B., Gaffney, P. M., James, J. A., Turner, S., Alevizos, I., Anaya, J. M., Rhodus, N. L., Segal, B. M., Montgomery, C. G., Scofield, R. H., Kovats, S., Mariette, X., Rönnblom, L., Witte, T., Rischmueller, M., Wahren-Herlenius, M., Omdal, R., Jonsson, R., Ng, W. F., Nordmark, G., Lessard, C. J. & Sivils, K. L., 22 Jun 2017, (E-pub ahead of print) In: PL o S Genetics. 13, 6, e1006820.

    Research output: Contribution to journalArticlepeer-review

  19. Alternative exon definition events control the choice between nuclear retention and cytoplasmic export of U11/U12-65K mRNA

    Verbeeren, J., Verma, B., Niemelä, E. H., Yap, K., Makeyev, E. V. & Frilander, M. J., 26 May 2017, (E-pub ahead of print) In: PL o S Genetics. 13, 5, e1006824.

    Research output: Contribution to journalArticlepeer-review

  20. Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults

    CHARGE Consortium, EPIC-InterAct Consortium, PAGE Consortium, Graff, M., Scott, R. A., Justice, A. E., Young, K. L., Feitosa, M. F., Barata, L., Winkler, T. W., Chu, A. Y., Mahajan, A., Hadley, D., Xue, L., Workalemahu, T., Heard-Costa, N. L., den Hoed, M., Ahluwalia, T. S., Qi, Q., Ngwa, J. S. & 33 others, Renström, F., Quaye, L., Eicher, J. D., Hayes, J. E., Cornelis, M., Kutalik, Z., Lim, E., Luan, J., Huffman, J. E., Zhang, W., Zhao, W., Griffin, P. J., Haller, T., Ahmad, S., Marques-Vidal, P. M., Bien, S., Yengo, L., Teumer, A., Smith, A. V., Kumari, M., Harder, M. N., Justesen, J. M., Kleber, M. E., Hollensted, M., Lohman, K., Rivera, N. V., Whitfield, J. B., Zhao, J. H., Stringham, H. M., Lyytikäinen, L. P., Huppertz, C., Willemsen, G. & Peyrot, W. J., 27 Apr 2017, In: PLoS Genetics. 13, 4, e1006528.

    Research output: Contribution to journalArticlepeer-review

  21. Direct Keap1-Nrf2 disruption as a potential therapeutic target for Alzheimer's disease: Keap1 as a therapeutic target for Alzheimer's Disease

    Kerr, F., Sofola-Adesakin, O., Ivanov, D., Gatliff, J., Gomez Perez-Nievas, B., Bertrand, H., Martinez, P., Callard, R., Snoeren, I., Cocheme, H., Adcott, J., Khericha, M., Castillo-Quan, J., Noble, W., Wells, G., Thornton, J. & Partridge, L., 2 Mar 2017, In: PL o S Genetics. 13, 3, 30 p., e1006593.

    Research output: Contribution to journalArticlepeer-review

  22. Genetic variants alter T-bet binding and gene expression in mucosal inflammatory disease

    Soderquest, K., Hertweck, A., Giambartolomei, C., Henderson, S., Mohamed, R., Goldberg, R., Perucha, E., Franke, L., Herrero, J., Plagnol, V., Jenner, R. G. & Lord, G. M., 10 Feb 2017, In: PL o S Genetics. 13, 2, 23 p., e1006587.

    Research output: Contribution to journalArticlepeer-review

  23. Defining the genetic susceptibility to cervical neoplasia—A genome-wide association study

    Leo, P. J., Madeleine, M. M., Wang, S., Schwartz, S. M., Newell, F., Pettersson-Kymmer, U., Hemminki, K., Hallmans, G., Tiews, S., Steinberg, W., Rader, J. S., Castro, F., Safaeian, M., Franco, E. L., Coutlée, F., Ohlsson, C., Cortes, A., Marshall, M., Mukhopadhyay, P., Cremin, K. & 11 others, Johnson, L. G., Garland, S., Tabrizi, S. N., Wentzensen, N., Sitas, F., Little, J., Cruickshank, M., Frazer, I. H., Hildesheim, A., Brown, M. A. & Plagnol, V., 2017, In: PLoS Genetics. 13, 8

    Research output: Contribution to journalArticlepeer-review

  24. Craniofacial Ciliopathies and the Interpretation of Hedgehog Signal Transduction

    Liu, K., 29 Dec 2016, In: PL o S Genetics. 12, 12, 4 p., e1006460.

    Research output: Contribution to journalComment/debatepeer-review

  25. Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation

    Sulaiman, F. A., Nishimoto, S., Murphy, G. R. F., Kucharska, A., Butterfield, N. C., Newbury-Ecob, R. & Logan, M. P. O., 19 Dec 2016, In: PL o S Genetics. 12, 12, p. e1006521

    Research output: Contribution to journalArticlepeer-review

  26. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

    Johnson, E. C., Bjelland, D. W., Howrigan, D. P., Abdellaoui, A., Breen, G., Borglum, A., Cichon, S., Degenhardt, F., Forstner, A. J., Frank, J., Genovese, G., Heilmann-Heimbach, S., Herms, S., Hoffman, P., Maier, W., Mattheisen, M., Morris, D., Mowry, B., Müller-Mhysok, B., Neale, B. & 297 others, Nenadic, I., Nöthen, M. M., O’Dushlaine, C., Rietschel, M., Ruderfer, D. M., Rujescu, D., Schulze, T. G., Simonson, M. A., Stahl, E., Strohmaier, J., Witt, S. H., Ripke, S., Neale, B. M., Corvin, A., Walters, J. T. R., Farh, K. H., Holmans, P. A., Lee, P., Bulik-Sullivan, B., Collier, D. A., Huang, H., Pers, T. H., Agartz, I., Agerbo, E., Albus, M., Alexander, M., Amin, F., Bacanu, S. A., Begemann, M., Belliveau, R. A., Bene, J., Bergen, S. E., Bevilacqua, E., Bigdeli, T. B., Black, D. W., Bruggeman, R., Buccola, N. G., Buckner, R. L., Byerley, W., Cahn, W., Cai, G., Campion, D., Cantor, R. M., Carr, V. J., Carrera, N., Catts, S. V., Chambert, K. D., Chan, R. C. K., Chen, R. Y. L., Chen, E. Y. H., Cheng, W., Cheung, E. F. C., Chong, S. A., Robert Cloninger, C., Cohen, D., Cohen, N., Cormican, P., Craddock, N., Crowley, J. J., Curtis, D., Davidson, M., Davis, K. L., Del Favero, J., Demontis, D., Dikeos, D., Dinan, T., Djurovic, S., Donohoe, G., Drapeau, E., Duan, J., Dudbridge, F., Durmishi, N., Eichhammer, P., Eriksson, J., Escott-Price, V., Essioux, L., Fanous, A. H., Farrell, M. S., Franke, L., Freedman, R., Freimer, N. B., Friedl, M., Friedman, J. I., Fromer, M., Georgieva, L., Giegling, I., Giusti-Rodríguez, P., Godard, S., Goldstein, J. I., Golimbet, V., Gopal, S., Gratten, J., de Haan, L., Hammer, C., Hamshere, M. L., Hansen, M., Hansen, T., Haroutunian, V., Hartmann, A. M., Henskens, F. A., Hirschhorn, J. N., Hoffmann, P., Hofman, A., Hollegaard, M. V., Hougaard, D. M., Ikeda, M., Joa, I., Julià, A., Kahn, R. S., Kalaydjieva, L., Karachanak-Yankova, S., Karjalainen, J., Kavanagh, D., Kennedy, J. L., Khrunin, A., Kim, Y., Klovins, J., Knowles, J. A., Konte, B., Kucinskas, V., Kucinskiene, Z. A., Kuzelova-Ptackova, H., Kähler, A. K., Laurent, C., Chee Keong, J. L., Hong Lee, S., Legge, S. E., Lerer, B., Li, M., Li, T., Liang, K. Y., Lieberman, J., Limborska, S., Loughland, C. M., Lubinski, J., Lönnqvist, J., Macek, M., Magnusson, P. K. E., Maher, B. S., Mallet, J., Marsal, S., Mattingsdal, M., McCarley, R. W., McDonald, C., McIntosh, A. M., Meier, S., Meijer, C. J., Melegh, B., Melle, I., Mesholam-Gately, R. I., Metspalu, A., Michie, P. T., Milani, L., Milanova, V., Mokrab, Y., Morris, D. W., Mors, O., Murphy, K. C., Murray, R. M., Myin-Germeys, I., Müller-Myhsok, B., Nelis, M., Nertney, D. A., Nestadt, G., Nicodemus, K. K., Nikitina-Zake, L., Nisenbaum, L., Nordin, A., O'Callaghan, E., O'Dushlaine, C., Anthony O'Neill, F., Oh, S. Y., Olincy, A., Olsen, L., Van Os, J., Pantelis, C., Papadimitriou, G. N., Papiol, S., Parkhomenko, E., Pato, M. T., Paunio, T., Pejovic-Milovancevic, M., Perkins, D. O., Pietiläinen, O., Pimm, J., Pocklington, A. J., Powell, J., Price, A., Pulver, A. E., Purcell, S. M., Quested, D., Rasmussen, H. B., Reichenberg, A., Reimers, M. A., Richards, A. L., Roffman, J. L., Roussos, P., Salomaa, V., Sanders, A. R., Schall, U., Schubert, C. R., Schwab, S. G., Scolnick, E. M., Scott, R. J., Seidman, L. J., Shi, J., Sigurdsson, E., Silagadze, T., Silverman, J. M., Sim, K., Slominsky, P., Smoller, J. W., So, H. C., Spencer, C. C. A., Stahl, E. A., Stefansson, H., Steinberg, S., Stogmann, E., Straub, R. E., Strengman, E., Scott Stroup, T., Subramaniam, M., Suvisaari, J., Svrakic, D. M., Szatkiewicz, J. P., Söderman, E., Thirumalai, S., Toncheva, D., Tosato, S., Veijola, J., Waddington, J., Walsh, D., Wang, D., Wang, Q., Webb, B. T., Weiser, M., Wildenauer, D. B., Williams, N. M., Williams, S., Wolen, A. R., Wong, E. H. M., Wormley, B. K., Xi, H. S., Zai, C. C., Zheng, X., Zimprich, F., Wray, N. R., Stefansson, K., Visscher, P. M., Adolfsson, R., Andreassen, O. A., Blackwood, D. H. R., Bramon, E., Buxbaum, J. D., Børglum, A. D., Darvasi, A., Domenici, E., Ehrenreich, H., Esko, T., Gejman, P. V., Gill, M., Gurling, H., Hultman, C. M., Iwata, N., Jablensky, A. V., Jönsson, E. G., Kendler, K. S., Kirov, G., Knight, J., Lencz, T., Levinson, D. F., Li, Q. S., Liu, J., Malhotra, A. K., McCarroll, S. A., McQuillin, A., Moran, J. L., Mortensen, P. B., Mowry, B. J., Nöthen, M. M., Ophoff, R. A., Owen, M. J., Palotie, A., Pato, C. N., Petryshen, T. L., Posthuma, D., Riley, B. P., Sham, P. C., Sklar, P., Clair, D. S., Weinberger, D. R., Wendland, J. R., Werge, T., Daly, M. J., O'Donovan, M. C., Sullivan, P. F. & Keller, M. C., 28 Oct 2016, In: PL o S Genetics. 12, 10, e1006343.

    Research output: Contribution to journalArticlepeer-review

  27. Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis

    Castaño-Betancourt, M. C., Evans, D. S., Ramos, Y. F. M., Boer, C. G., Metrustry, S., Liu, Y., den Hollander, W., van Rooij, J., Kraus, V. B., Yau, M. S., Mitchell, B. D., Muir, K., Hofman, A., Doherty, M., Doherty, S., Zhang, W., Kraaij, R., Rivadeneira, F., Barrett-Connor, E., Maciewicz, R. A. & 17 others, Arden, N., Nelissen, R. G. H. H., Kloppenburg, M., Jordan, J. M., Nevitt, M. C., Slagboom, E. P., Hart, D. J., Lafeber, F., Styrkarsdottir, U., Zeggini, E., Evangelou, E., Spector, T. D., Uitterlinden, A. G., Lane, N. E., Meulenbelt, I., Valdes, A. M. & van Meurs, J. B. J., 4 Oct 2016, In: PL o S Genetics. 12, 10, e1006260.

    Research output: Contribution to journalArticlepeer-review

  28. Reverse Chemical Genetics: Comprehensive Fitness Profiling Reveals the Spectrum of Drug Target Interactions

    Wong, L. H., Sinha, S., Bergeron, J. R., Mellor, J. C., Giaever, G., Flaherty, P. & Nislow, C., Sep 2016, In: PLoS Genetics. 12, 9, p. e1006275

    Research output: Contribution to journalArticlepeer-review

  29. Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

    Winkler, T. W., Justice, A. E., Graff, M., Barata, L., Feitosa, M. F., Chu, S., Czajkowski, J., Esko, T., Fall, T., Kilpeläinen, T. O., Lu, Y., Mägi, R., Mihailov, E., Pers, T. H., Rüeger, S., Teumer, A., Ehret, G. B., Ferreira, T., Heard-Costa, N. L., Karjalainen, J. & 31 others, Lagou, V., Mahajan, A., Neinast, M. D., Prokopenko, I., Simino, J., Teslovich, T. M., Jansen, R., Westra, H-J., White, C. C., Absher, D., Ahluwalia, T. S., Ahmad, S., Albrecht, E., Alves, A. C., Bragg-Gresham, J. L., de Craen, A. J. M., Bis, J. C., Lehne, B., Wilson, J. F., Wong, A., Zhao, J. H., Hysi, P. G., Kyriakou, T., Liu, Y-P., Menni, C., Bennett, D. A., Bornstein, S. R., Chambers, J. C., James, A. L., Spector, T. D. & arcOGEN Consortium, Jun 2016, In: PL o S Genetics. 12, 6, p. e1006166

    Research output: Contribution to journalArticlepeer-review

  30. Bat Accelerated Regions Identify a Bat Forelimb Specific Enhancer in the HoxD Locus

    Booker, B. M., Friedrich, T., Mason, M. K., VanderMeer, J. E., Zhao, J., Eckalbar, W. L., Logan, M., Illing, N., Pollard, K. S. & Ahituv, N., Mar 2016, In: PL o S Genetics. 12, 3, p. e1005738

    Research output: Contribution to journalArticlepeer-review

  31. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

    CHARGE Consortium, DIAGRAM Consortium, GLGC Consortium, Global-BPGen Consortium, ICBP Consortium, MAGIC Consortium & arcOGEN Consortium, 1 Oct 2015, In: PL o S Genetics. 11, 10, p. e1005378

    Research output: Contribution to journalArticlepeer-review

  32. APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans

    Tkatchenko, A. V., Tkatchenko, T. V., Guggenheim, J. A., Verhoeven, V. J. M., Hysi, P. G., Wojciechowski, R., Singh, P. K., Kumar, A., Thinakaran, G. & Williams, C., 27 Aug 2015, In: PL o S Genetics. 11, 8, e1005432.

    Research output: Contribution to journalArticlepeer-review

  33. A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment

    Nyegaard, M., Rendtorff, N. D., Nielsen, M. S., Corydon, T. J., Demontis, D., Starnawska, A., Hedemand, A., Buniello, A., Niola, F., Overgaard, M. T., Leal, S. M., Ahmad, W., Wikman, F. P., Petersen, K. B., Crüger, D. G., Oostrik, J., Kremer, H., Tommerup, N., Frödin, M., Steel, K. P. & 2 others, Tranebjærg, L. & Børglum, A. D., 1 Jul 2015, In: PL o S Genetics. 11, 7, e1005386.

    Research output: Contribution to journalArticlepeer-review

  34. Aurora-A-Dependent Control of TACC3 Influences the Rate of Mitotic Spindle Assembly

    Burgess, S. G., Peset, I., Joseph, N., Cavazza, T., Vernos, I., Pfuhl, M., Gergely, F. & Bayliss, R., 1 Jul 2015, In: PL o S Genetics. 11, 7, e1005345.

    Research output: Contribution to journalArticlepeer-review

  35. Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

    Villanueva, P., Nudel, R., Hoischen, A., Fernández, M. A., Simpson, N. H., Gilissen, C., Reader, R. H., Jara, L., Echeverry, M. M., Francks, C., Baird, G., Conti-Ramsden, G., O’Hare, A., Bolton, P. F., Hennessy, E. R., Palomino, H., Carvajal-Carmona, L., Veltman, J. A., Cazier, J. B., De Barbieri, Z. & 14 others, Fisher, S. E., Newbury, D. F., Slonims, V., Clark, A., Watson, J., Simonoff, E., Pickles, A., Everitt, A., Seckl, J., Cowie, H., Cohen, W., Nasir, J., Bishop, D. V. M. & Simkin, Z., 17 Mar 2015, In: PL o S Genetics. 11, 3, e1004925.

    Research output: Contribution to journalArticlepeer-review

  36. HDAC4-Myogenin Axis As an Important Marker of HD-Related Skeletal Muscle Atrophy

    Mielcarek, M., Toczek, M., Smeets, C. J. L. M., Franklin, S. A., Bondulich, M. K., Jolinon, N., Muller, T., Ahmed, M., Dick, J. R. T., Piotrowska, I., Greensmith, L., Smolenski, R. T. & Bates, G., 6 Mar 2015, In: PL o S Genetics. 11, 3, e1005021.

    Research output: Contribution to journalArticlepeer-review

  37. An Integrative Multi-scale Analysis of the Dynamic DNA Methylation Landscape in Aging

    Yuan, T., Jiao, Y., de Jong, S., Ophoff, R. A., Beck, S. & Teschendorff, A. E., 18 Feb 2015, In: PL o S Genetics. 11, 2, 21 p., e1004996.

    Research output: Contribution to journalArticlepeer-review

  38. Pooled Sequencing of 531 Genes in Inflammatory Bowel Disease Identifies an Associated Rare Variant in BTNL2 and Implicates Other Immune Related Genes

    Prescott, N. J., Lehne, B., Stone, K., Lee, J. C., Taylor, K., Knight, J., Papouli, E., Mirza, M. M., Simpson, M. A., Spain, S. L., Lu, G., Fraternali, F., Bumpstead, S. J., Gray, E., Amar, A., Bye, H., Green, P., Chung-Faye, G., Hayee, BH., Pollok, R. & 10 others, Satsangi, J., Parkes, M., Barrett, J. C., Mansfield, J. C., Sanderson, J., Lewis, C. M., Weale, M. E., Schlitt, T., Mathew, C. G. & UK IBD Genetics Consortium, 11 Feb 2015, In: PL o S Genetics. 11, 2, 19 p., e1004955.

    Research output: Contribution to journalArticlepeer-review

  39. Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus

    Mahajan, A., Sim, X., Ng, H. J., Manning, A., Rivas, M. A., Highland, H. M., Locke, A. E., Grarup, N., Im, H. K., Cingolani, P., Flannick, J., Fontanillas, P., Fuchsberger, C., Gaulton, K. J., Teslovich, T. M., Rayner, N. W., Robertson, N. R., Beer, N. L., Rundle, J. K., Bork-Jensen, J. & 243 others, Ladenvall, C., Blancher, C., Buck, D., Buck, G., Burtt, N. P., Gabriel, S., Gjesing, A. P., Groves, C. J., Hollensted, M., Huyghe, J. R., Jackson, A. U., Jun, G., Justesen, J. M., Mangino, M., Murphy, J., Neville, M., Onofrio, R., Small, K. S., Stringham, H. M., Syvänen, A. C., Trakalo, J., Abecasis, G., Bell, G. I., Blangero, J., Cox, N. J., Duggirala, R., Hanis, C. L., Seielstad, M., Wilson, J. G., Christensen, C., Brandslund, I., Rauramaa, R., Surdulescu, G. L., Doney, A. S. F., Lannfelt, L., Linneberg, A., Isomaa, B., Tuomi, T., Jørgensen, M. E., Jørgensen, T., Kuusisto, J., Uusitupa, M., Salomaa, V., Spector, T. D., Morris, A. D., Palmer, C. N. A., Collins, F. S., Mohlke, K. L., Bergman, R. N., Ingelsson, E., Lind, L., Tuomilehto, J., Hansen, T., Watanabe, R. M., Prokopenko, I., Dupuis, J., Karpe, F., Groop, L., Laakso, M., Pedersen, O., Florez, J. C., Morris, A. P., Altshuler, D., Meigs, J. B., Boehnke, M., McCarthy, M. I., Lindgren, C. M., Gloyn, A. L., Abboud, H. E., Afzal, U., Aguilar, D., Arya, R., Atzmon, G., Aung, T., Banks, E., Barroso, I., Barzilai, N., Below, J. E., Bharadwaj, D., Blackwell, T. W., Bonnycastle, L. L., Bowden, D., Carey, J., Carneiro, M. O., Chambers, J. C., Chan, E., Chan, J., Chandak, G. R., Chen, P., Chen, Y., Chen, H., Cheng, C. Y., Chia, K. S., Cho, Y. S., Correa, A., Curran, J. E., Daly, M. J., Day-Williams, A. G., DeFronzo, R. A., DePristo, M., Donnelly, P. J., Ebrahim, S. B., Elliott, P., Esko, T., Fadista, J., Farjoun, Y., Farmer, A. J., Farook, V. S., Fennell, T., Ferreira, T., Fingerlin, T., Forsén, T., Fowler, S. P., Franks, P. W., Frayling, T. M., Freedman, B. I., Froguel, P., Gamazon, E. R., Gieger, C., Glaser, B., Go, M. J., Goldstein, J. I., Grallert, H., Grant, G., Green, T., Griswold, M., Hale, D. E., Han, B. G., Hartl, C., Hattersley, A. T., Hicks, P. J., Hodgkiss, D., Horikoshi, M., Hrabé de Angelis, M., Hu, C., Hu, F. B., Huh, I., Kamran Ikram, M., Illig, T., Jablonski, K. A., Jenkinson, C. P., Jia, W., Kang, H. M., Khor, C. C., Kim, Y., Kim, Y. J., Kim, B. J., Kinnunen, L., Kooner, J. S., Kravic, J., Kriebel, J., Kumar, A., Kumar, S., Kuulasmaa, T., Kwon, M. S., Langenberg, C., Lauritzen, T., Lee, S., Lee, J., Lee, J., Lee, J. Y., Lehman, D. M., Lehne, B., Levy, J. C., Li, J., Liang, L., Lim, W. Y., Lin, K. H., Liu, J., Loh, M., Ma, R. C. W., Ma, C., Mägi, R., Maguire, J., Maxwell, T. J., McVean, G., Meisinger, C., Meitinger, T., Melander, O., Metspalu, A., Mihailov, E., Milani, L., Moutsianas, L., Müller-Nurasyid, M., K. Musani, S., Nagai, Y., Narisu, N., Neale, B. M., Ng, M. C. Y., Nilsson, P., O'Rahilly, S. P., Orho-Melander, M., Owen, K. R., Palmer, N. D., Park, T., Pasko, D., Pearson, R. D., Perry, J. R. B., Peters, A., Pollin, T. I., Poplin, R., Prabhakaran, D., Puppala, S., Purcell, S., Qi, L., Qi, Q., Roden, M., Rolandsson, O., Rosengren, A. H., Sandhu, M., Schwarzmayr, T., Scott, L. J., Scott, R. A., Scott, J., Scott, W. R., Sehmi, J., Shakir, K., Sladek, R., Smith, J. D., Stancáková, A., Strauch, K., Strom, T. M., Swift, A., Tai, E. S., Tajes, J. F., Tan, S. T., Tandon, N., Taylor, H. A., Teo, Y. Y., Thameem, F., Thorand, B., van de Bunt, M., Varga, T. V., Walker, M., Wareham, N. J., Welch, R. P., Wieland, T., Wilson, G., Wong, T. Y., Wood, A. R., Yoon, J., Zeggini, E. & Zhang, W., 27 Jan 2015, In: PL o S Genetics. 11, 1, e1004876.

    Research output: Contribution to journalArticlepeer-review

  40. hnRNP K coordinates transcriptional silencing by SETDB1 in embryonic stem cells

    Thompson, P. J., Dulberg, V., Moon, K., Foster, L. J., Chen, C., Karimi, M. M., Lorincz, M. C. & Barsh, G. S. (ed.), Jan 2015, In: PLoS Genetics. 11, 1, p. e1004933

    Research output: Contribution to journalArticlepeer-review

  41. Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss

    Chen, J., Ingham, N., Kelly, J., Jadeja, S., Goulding, D., Pass, J., Mahajan, V. B., Tsang, S. H., Nijnik, A., Jackson, I. J., White, J. K., Forge, A., Jagger, D. & Steel, K. P., 1 Oct 2014, In: PLoS Genetics. 10, 10

    Research output: Contribution to journalArticlepeer-review

  42. Global genetic variations predict brain response to faces

    Dickie, E. W., Tahmasebi, A., French, L., Kovacevic, N., Banaschewski, T., Barker, G. J., Bokde, A., Büchel, C., Conrod, P., Flor, H., Garavan, H., Gallinat, J., Gowland, P., Heinz, A., Ittermann, B., Lawrence, C., Mann, K., Martinot, J-L., Nees, F., Nichols, T. & 10 others, Lathrop, M., Loth, E., Pausova, Z., Rietschel, M., Smolka, M. N., Ströhle, A., Toro, R., Schumann, G., Paus, T. & IMAGEN Consortium, 14 Aug 2014, In: PL o S Genetics. 10, 8, p. e1004523

    Research output: Contribution to journalArticlepeer-review

  43. Dysfunction of the CNS-Heart Axis in Mouse Models of Huntington's Disease

    Mielcarek, M., Inuabasi, L., Bondulich, M. K., Muller, T., Osborne, G. F., Franklin, S. A., Smith, D. L., Neueder, A., Rosinski, J., Rattray, I., Protti, A. & Bates, G. P., 7 Aug 2014, In: PL o S Genetics. 10, 8, p. 1-19 19 p., e1004550.

    Research output: Contribution to journalArticlepeer-review

  44. Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes

    The MAGIC Investigators & The GIANT consortium, 7 Aug 2014, In: PLoS Genetics. 10, 8, e1004517.

    Research output: Contribution to journalArticlepeer-review

  45. Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

    Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J. H., Teumer, A., Winkler, T. W., Tšernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Macé, A., Rüeger, S., Bochud, P-Y., Barcella, M., Dauvilliers, Y. & 31 others, Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S., Arking, D. E., Boerwinkle, E., Chambers, J. C., Fiorito, G., Grallert, H., Guarrera, S., Homuth, G., Huffman, J. E., Porteous, D., Moradpour, D., Iranzo, A., Hebebrand, J., Kemp, J. P., Lammers, G. J., Aubert, V., Heim, M. H., Martin, N. G., Montgomery, G. W., Spector, T. D., Yuan, W., Bell, J. T. & Generation Scotland Consortium, 1 Jul 2014, In: PL o S Genetics. 10, 7, 12 p., e1004508.

    Research output: Contribution to journalArticlepeer-review

  46. A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach

    Traylor, M., Mäkelä, K-M., Kilarski, L. L., Holliday, E. G., Devan, W. J., Nalls, M. A., Wiggins, K. L., Zhao, W., Cheng, Y-C., Achterberg, S., Malik, R., Sudlow, C., Bevan, S., Raitoharju, E., METASTROKE, International Stroke Genetics Consortium, Wellcome Trust Case Consortium 2 (WTCCC2), Oksala, N., Thijs, V., Lemmens, R., Lindgren, A., Slowik, A. & 19 others, Maguire, J. M., Walters, M., Algra, A., Sharma, P., Attia, J. R., Boncoraglio, G. B., Rothwell, P. M., de Bakker, P. I. W., Bis, J. C., Saleheen, D., Kittner, S. J., Mitchell, B. D., Rosand, J., Meschia, J. F., Levi, C., Dichgans, M., Lehtimäki, T., Lewis, C. M. & Markus, H. S., Jul 2014, In: PL o S Genetics. 10, 7, p. 1-11 11 p., e1004469.

    Research output: Contribution to journalArticlepeer-review

  47. Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

    Kemp, J. P., Medina-Gomez, C., Estrada, K., St Pourcain, B., Heppe, D. H. M., Warrington, N. M., Oei, L., Ring, S. M., Kruithof, C. J., Timpson, N. J., Wolber, L. E., Reppe, S., Gautvik, K., Grundberg, E., Ge, B., van der Eerden, B., van de Peppel, J., Hibbs, M. A., Ackert-Bicknell, C. L., Choi, K. & 13 others, Koller, D. L., Econs, M. J., Williams, F. M. K., Foroud, T., Zillikens, M. C., Ohlsson, C., Hofman, A., Uitterlinden, A. G., Smith, G. D., Jaddoe, V. W. V., Tobias, J. H., Rivadeneira, F. & Evans, D. M., 19 Jun 2014, In: PL o S Genetics. 10, 6, 18 p., e1004423.

    Research output: Contribution to journalArticlepeer-review

  48. Biased, non-equivalent gene-proximal and -distal binding motifs of orphan nuclear receptor TR4 in primary human erythroid cells

    Shi, L., Sierant, M. C., Gurdziel, K., Zhu, F., Cui, S., Kolodziej, K. E., Strouboulis, J., Guan, Y., Tanabe, O., Lim, K-C. & Engel, J. D., 8 May 2014, In: PLoS Genetics. 10, 5, p. e1004339

    Research output: Contribution to journalArticlepeer-review

  49. Whole Exome Re-Sequencing Implicates CCDC38 and Cilia Structure and Function in Resistance to Smoking Related Airflow Obstruction

    Wain, L. V., Sayers, I., Artigas, M. S., Portelli, M. A., Zeggini, E., Obeidat, M., Sin, D. D., Bosse, Y., Nickle, D., Brandsma, C-A., Malarstig, A., Vangjeli, C., Jelinsky, S. A., John, S., Kilty, I., McKeever, T., Shrine, N. R. G., Cook, J. P., Patel, S., Spector, T. D. & 3 others, Hollox, E. J., Hall, I. P. & Tobin, M. D., May 2014, In: PL o S Genetics. 10, 5, 14 p., e1004314.

    Research output: Contribution to journalArticlepeer-review

Previous 1 2 3 Next

View graph of relations

© 2020 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454