Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosis

Por Noponen-Hietala, N, Kyllonen, E, Mannikko, M, Ilkko, E, Karppinen, J, Ott, J, Ala-Kokko, L
Publicado em 2003

Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

Por Männikkö, M, Kestailä, M, Holmberg, C, Norio, R, Ryynänen, M, Olsen, A, Peltonen, L, Tryggvason, K
Publicado em 1995

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.

Por Kestilä, M., Männikkö, M., Holmberg, C., Gyapay, G., Weissenbach, J., Savolainen, E. R., Peltonen, L., Tryggvason, K.
Publicado em 1994

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.

Por Lenkkeri, U, Männikkö, M, McCready, P, Lamerdin, J, Gribouval, O, Niaudet, P M, Antignac C, K, Kashtan, C E, Homberg, C, Olsen, A, Kestilä, M, Tryggvason, K
Publicado em 1999

GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos

Por Sanders, A.E., Jain, D., Sofer, T., Kerr, K.F., Laurie, C.C., Shaffer, J.R., Marazita, M.L., Kaste, L.M., Slade, G.D., Fillingim, R.B., Ohrbach, R., Maixner, W., Kocher, T., Bernhardt, O., Teumer, A., Schwahn, C., Sipilä, K., Lähdesmäki, R., Männikkö, M., Pesonen, P., Järvelin, M., Rizzatti-Barbosa, C.M., Meloto, C.B., Ribeiro-Dasilva, M., Diatchenko, L., Serrano, P., Smith, S.B.
Publicado no J Dent Res (2017)