Nature Genetics, 1061-4036

Journal

View graph of relations

Related Publications
  1. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

    CommonMind Consortium, Psychiat Genomics Consortium, iPSYCH-GEMS Schizophrenia Working, Huckins, L. M., Dobbyn, A., Ruderfer, D. M., Hoffman, G., Wang, W., Pardinas, A. F., Rajagopal, V. M., Als, T. D., Nguyen, H. T., Girdhar, K., Boocock, J., Roussos, P., Fromer, M., Kramer, R., Purcell, S., Demontis, D., Borglum, A. D., Walters, J. T. R., O'Donovan, M. C., Sullivan, P., Owen, M. J., Devlin, B., Sieberts, S. K., Cox, N. J., Im, H. K., Sklar, P. & Stahl, E. A., Apr-2019, In : Nature Genetics. 51, 4, p. 659-674 18 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus

    van den Ouweland, A. M., Dreesen, J. C., Verdijk, M., Knoers, N. V., Monnens, L. A., Rocchi, M. & van Oost, B. A., 1992, In : Nature Genetics. 2, 2, p. 99-102 4 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. Dominant isolated renal magnesium loss is caused by misrouting of the Na(+),K(+)-ATPase gamma-subunit

    Meij, I. C., Koenderink, J. B., van Bokhoven, H., Assink, K. F., Groenestege, W. T., de Pont, J. J., Bindels, R. J., Monnens, L. A., van den Heuvel, L. P. & Knoers, N. V., Nov-2000, In : Nature Genetics. 26, 3, p. 265-6 2 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  4. Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

    Birkenhäger, R., Otto, E., Schürmann, M. J., Vollmer, M., Ruf, E. M., Maier-Lutz, I., Beekmann, F., Fekete, A., Omran, H., Feldmann, D., Milford, D. V., Jeck, N., Konrad, M., Landau, D., Knoers, N. V., Antignac, C., Sudbrak, R., Kispert, A. & Hildebrandt, F., Nov-2001, In : Nature Genetics. 29, 3, p. 310-4 5 p.

    Research output: Contribution to journalArticleAcademicpeer-review

  5. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

    Koolen, D. A., Vissers, L. E. L. M., Pfundt, R., de Leeuw, N., Knight, S. J. L., Regan, R., Kooy, R. F., Reyniers, E., Romano, C., Fichera, M., Schinzel, A., Baumer, A., Anderlid, B-M., Schoumans, J., Knoers, N. V., van Kessel, A. G., Sistermans, E. A., Veltman, J. A., Brunner, H. G. & de Vries, B. B. A., Sep-2006, In : Nature Genetics. 38, 9, p. 999-1001 3 p.

    Research output: Contribution to journalArticleAcademicpeer-review

View all (224) »

ID: 1458704