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  • 2022

    Discovery of 42 genome-wide significant loci associated with dyslexia

    23andMe Research Team & Quantitative Trait Working Group of the GenLang Consortium, Nov 2022, In: Nature Genetics. 54, 11, p. 1621-1629 9 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    36 Citations (Scopus)
  • Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

    Eising, E., Mirza-Schreiber, N., de Zeeuw, E. L., Wang, C. A., Truong, D. T., Allegrini, A. G., Shapland, C. Y., Zhu, G., Wigg, K. G., Gerritse, M. L., Molz, B., Alagöz, G., Gialluisi, A., Abbondanza, F., Rimfeld, K., van Donkelaar, M., Liao, Z., Jansen, P. R., Andlauer, T. F. M., Bates, T. C., & 75 othersBernard, M., Blokland, K., Bonte, M., Børglum, A. D., Bourgeron, T., Brandeis, D., Ceroni, F., Csépe, V., Dale, P. S., de Jong, P. F., DeFries, J. C., Démonet, J. F., Demontis, D., Feng, Y., Gordon, S. D., Guger, S. L., Hayiou-Thomas, M. E., Hernández-Cabrera, J. A., Hottenga, J. J., Hulme, C., Kere, J., Kerr, E. N., Koomar, T., Landerl, K., Leonard, G. T., Lovett, M. W., Lyytinen, H., Martin, N. G., Martinelli, A., Maurer, U., Michaelson, J. J., Moll, K., Monaco, A. P., Morgan, A. T., Nöthen, M. M., Pausova, Z., Pennell, C. E., Pennington, B. F., Price, K. M., Rajagopal, V. M., Ramus, F., Richer, L., Simpson, N. H., Smith, S. D., Snowling, M. J., Stein, J., Strug, L. J., Talcott, J. B., Tiemeier, H., van der Schroeff, M. P., Verhoef, E., Watkins, K. E., Wilkinson, M., Wright, M. J., Barr, C. L., Boomsma, D. I., Carreiras, M., Franken, M. C. J., Gruen, J. R., Luciano, M., Müller-Myhsok, B., Newbury, D. F., Olson, R. K., Paracchini, S., Paus, T., Plomin, R., Reilly, S., Schulte-Körne, G., Tomblin, J. B., van Bergen, E., Whitehouse, A. J. O., Willcutt, E. G., St Pourcain, B., Francks, C. & Fisher, S. E., 30 Aug 2022, In: Proceedings of the National Academy of Sciences of the United States of America. 119, 35, p. e2202764119 e2202764119.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    32 Citations (Scopus)
  • Influence of FLG loss-of-function mutations in host–microbe interactions during atopic skin inflammation

    Oláh, P., Szlávicz, E., Kuchner, M., Nemmer, J., Zeeuwen, P., Lefèvre-Utile, A., Fyhrquist, N., Prast-Nielsen, S., Skoog, T., Serra, A., Rodríguez, E., Raap, U., Meller, S., Gyulai, R., Hupé, P., Kere, J., Levi-Schaffer, F., Tsoka, S., Alexander, H., Nestle, F. O., & 11 othersSchröder, J. M., Weidinger, S., van den Bogaard, E., Soumelis, V., Greco, D., Barker, J., Lauerma, A., Ranki, A., Andersson, B., Alenius, H. & Homey, B., Jun 2022, In: Journal of Dermatological Science. 106, 3, p. 132-140 9 p.

    Research output: Contribution to journalArticlepeer-review

    1 Citation (Scopus)
  • 2019

    A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis

    Japan Scoliosis Clinical Research Group (JSCRG), 1 May 2019, In: Journal of Human Genetics. 64, 5, p. 493-498 6 p.

    Research output: Contribution to journalArticlepeer-review

    9 Citations (Scopus)
  • A preliminary transcriptome analysis suggests a transitory effect of vitamin D on mitochondrial function in obese young finnish subjects

    Einarsdottir, E., Pekkinen, M., Krjutškov, K., Katayama, S., Kere, J., Mäkitie, O. & Viljakainen, H., May 2019, In: Endocrine Connections. 8, 5, p. 462-467 6 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    8 Citations (Scopus)
    120 Downloads (Pure)
  • Discovering heritable modes of MEG spectral power

    Leppäaho, E., Renvall, H., Salmela, E., Kere, J., Salmelin, R. & Kaski, S., 1 Apr 2019, In: Human Brain Mapping. 40, 5, p. 1391-1402 12 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    12 Citations (Scopus)
  • Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

    Gialluisi, A., Andlauer, T. F. M., Mirza-Schreiber, N., Moll, K., Becker, J., Hoffmann, P., Ludwig, K. U., Czamara, D., St Pourcain, B., Brandler, W., Honbolygó, F., Tóth, D., Csépe, V., Huguet, G., Morris, A. P., Hulslander, J., Willcutt, E. G., DeFries, J. C., Olson, R. K., Smith, S. D., & 25 othersPennington, B. F., Vaessen, A., Maurer, U., Lyytinen, H., Peyrard-Janvid, M., Leppänen, P. H. T., Brandeis, D., Bonte, M., Stein, J. F., Talcott, J. B., Fauchereau, F., Wilcke, A., Francks, C., Bourgeron, T., Monaco, A. P., Ramus, F., Landerl, K., Kere, J., Scerri, T. S., Paracchini, S., Fisher, S. E., Schumacher, J., Nöthen, M. M., Müller-Myhsok, B. & Schulte-Körne, G., 11 Feb 2019, In: Translational psychiatry. 9, 1, 77.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    66 Citations (Scopus)
  • Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions

    Olivé, M., Engvall, M., Ravenscroft, G., Cabrera-Serrano, M., Jiao, H., Bortolotti, C. A., Pignataro, M., Lambrughi, M., Jiang, H., Forrest, A. R. R., Benseny-Cases, N., Hofbauer, S., Obinger, C., Battistuzzi, G., Bellei, M., Borsari, M., Di Rocco, G., Viola, H. M., Hool, L. C., Cladera, J., & 24 othersLagerstedt-Robinson, K., Xiang, F., Wredenberg, A., Miralles, F., Baiges, J. J., Malfatti, E., Romero, N. B., Streichenberger, N., Vial, C., Claeys, K. G., Straathof, C. S. M., Goris, A., Freyer, C., Lammens, M., Bassez, G., Kere, J., Clemente, P., Sejersen, T., Udd, B., Vidal, N., Ferrer, I., Edström, L., Wedell, A. & Laing, N. G., 27 Mar 2019, (E-pub ahead of print) In: Nature Communications. 10, 1, 1396.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    13 Citations (Scopus)
  • 2018

    DNA methylation in childhood asthma: an epigenome-wide meta-analysis

    Xu, C-J., Söderhäll, C., Bustamante, M., Baïz, N., Gruzieva, O., Gehring, U., Mason, D., Chatzi, L., Basterrechea, M., Llop, S., Torrent, M., Forastiere, F., Fantini, M. P., Carlsen, K. C. L., Haahtela, T., Morin, A., Kerkhof, M., Merid, S. K., van Rijkom, B., Jankipersadsing, S. A., & 46 othersBonder, M. J., Ballereau, S., Vermeulen, C. J., Aguirre-Gamboa, R., de Jongste, J. C., Smit, H. A., Kumar, A., Pershagen, G., Guerra, S., Garcia-Aymerich, J., Greco, D., Reinius, L., McEachan, R. R. C., Azad, R., Hovland, V., Mowinckel, P., Alenius, H., Fyhrquist, N., Lemonnier, N., Pellet, J., Auffray, C., van der Vlies, P., van Diemen, C. C., Li, Y., Wijmenga, C., Netea, M. G., Moffatt, M. F., Cookson, W. O. C. M., Anto, J. M., Bousquet, J., Laatikainen, T., Laprise, C., Carlsen, K-H., Gori, D., Porta, D., Iñiguez, C., Bilbao, J. R., Kogevinas, M., Wright, J., Brunekreef, B., Kere, J., Nawijn, M. C., Annesi-Maesano, I., Sunyer, J., Melén, E. & Koppelman, G. H., 26 Feb 2018, (E-pub ahead of print) In: The Lancet Respiratory Medicine.

    Research output: Contribution to journalArticlepeer-review

    158 Citations (Scopus)
  • FUT2 Variants Confer Susceptibility to Familial Otitis Media

    Santos-Cortez, R. L. P., Chiong, C. M., Frank, D. N., Ryan, A. F., Giese, A. P. J., Bootpetch Roberts, T., Daly, K. A., Steritz, M. J., Szeremeta, W., Pedro, M., Pine, H., Yarza, T. K. L., Scholes, M. A., Llanes, E. G. D. V., Yousaf, S., Friedman, N., Tantoco, M. L. C., Wine, T. M., Labra, P. J., Benoit, J., & 40 othersRuiz, A. G., de la Cruz, R. A. R., Greenlee, C., Yousaf, A., Cardwell, J., Nonato, R. M. A., Ray, D., Ong, K. M. C., So, E., Robertson, C. E., Dinwiddie, J., Lagrana-Villagracia, S. M., Gubbels, S. P., Shaikh, R. S., Cass, S. P., Einarsdottir, E., Lee, N. R., Schwartz, D. A., Gloria-Cruz, T. L. I., Bamshad, M. J., Yang, I. V., Kere, J., Abes, G. T., Prager, J. D., Riazuddin, S., Chan, A. L., Yoon, P. J., Nickerson, D. A., Cutiongco-de la Paz, E. M., Streubel, S-O., Reyes-Quintos, M. R. T., Jenkins, H. A., Mattila, P., Chan, K. H., Mohlke, K. L., Leal, S. M., Hafrén, L., Chonmaitree, T., Sale, M. M. & Ahmed, Z. M., 25 Oct 2018, (E-pub ahead of print) In: American Journal of Human Genetics.

    Research output: Contribution to journalArticlepeer-review

    33 Citations (Scopus)
  • Human pluripotent reprogramming with CRISPR activators

    Weltner, J., Balboa, D., Katayama, S., Bespalov, M., Krjutškov, K., Jouhilahti, E. M., Trokovic, R., Kere, J. & Otonkoski, T., 1 Dec 2018, In: Nature Communications. 9, 1, p. 1-12 2643.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    111 Citations (Scopus)
    140 Downloads (Pure)
  • The psoriasis risk allele HLA-C∗06: 02 shows evidence of association with chronic or recurrent streptococcal tonsillitis

    Haapasalo, K., Koskinen, L. L. E., Suvilehto, J., Jousilahti, P., Wolin, A., Suomela, S., Trembath, R., Barker, J., Vuopio, J., Kere, J., Sakari Jokiranta, T. & Saavalainen, P., 1 Oct 2018, In: Infection and Immunity. 86, 10, e00304-18.

    Research output: Contribution to journalArticlepeer-review

    18 Citations (Scopus)
  • 2016

    Cohort profile: the Finnish Genetics of Pre-eclampsia Consortium (FINNPEC)

    Jääskeläinen, T., Heinonen, S., Kajantie, E., Kere, J., Kivinen, K., Pouta, A., Laivuori, H. & FINNPEC Study Group, 10 Nov 2016, (E-pub ahead of print) In: BMJ open. 6, 11, e013148.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    31 Citations (Scopus)
  • Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1

    Massinen, S., Wang, J., Laivuori, K., Bieder, A., Tapia Paez, I., Jiao, H. & Kere, J., 27 Jan 2016, In: Journal Of Neurodevelopmental Disorders. 8, 1, 4.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    File
    7 Citations (Scopus)
    177 Downloads (Pure)
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