Association between sequence variations in genes encoding human zona pellucida glycoproteins and fertilization failure in IVF
Männikkö, M., Törmälä, R.-M., Tuuri, T., Haltia, A., Martikainen, H., Ala-Kokko, L., Tapanainen, J.S., Lakkakorpi, J.T.
Published in Human reproduction (Oxford) (01.06.2005)
Published in Human reproduction (Oxford) (01.06.2005)
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Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome
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Published in Molecular cell (01.03.1998)
Published in Molecular cell (01.03.1998)
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Congenital nephrotic syndrome (NPHS1): Features resulting from different mutations in Finnish patients
Patrakka, Jaakko, Kestilä, Marjo, Wartiovaara, Jorma, Ruotsalainen, Vesa, Tissari, Päivi, Lenkkeri, Ulla, Männikkö, Minna, Visapää, Ilona, Holmberg, Christer, Rapola, Juhani, Tryggvason, Karl, Jalanko, Hannu
Published in Kidney international (01.09.2000)
Published in Kidney international (01.09.2000)
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Knee osteoarthritis genetics in Finnish health 2000 survey
Welling, M, Hämäläinen, S, Ojajärvi, A, Hirvonen, A, Heliövaara, M, Leino-Arjas, P, Männikkö, M, Karppinen, J
Published in Osteoarthritis and cartilage (01.04.2014)
Published in Osteoarthritis and cartilage (01.04.2014)
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Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of Mutations
Lenkkeri, Ulla, Männikkö, Minna, McCready, Paula, Lamerdin, Jane, Gribouval, Olivier, Niaudet, Patrick, Antignac, Corinne, Kashtan, Clifford E., Holmberg, Christer, Olsen, Anne, Kestilä, Marjo, Tryggvason, Karl
Published in American journal of human genetics (1999)
Published in American journal of human genetics (1999)
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Aggrecan core protein of a certain length is protective against hand osteoarthritis
Kämäräinen, O.-P., Solovieva, S., Vehmas, T., Luoma, K., Leino-Arjas, P., Riihimäki, H., Ala-Kokko, L., Männikkö, M.
Published in Osteoarthritis and cartilage (01.10.2006)
Published in Osteoarthritis and cartilage (01.10.2006)
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Targeted inactivation of the type VII collagen gene (Col7a1) in mice results in severe blistering phenotype: a model for recessive dystrophic epidermolysis bullosa
Heinonen, S, Männikkö, M, Klement, J F, Whitaker-Menezes, D, Murphy, G F, Uitto, J
Published in Journal of cell science (01.11.1999)
Published in Journal of cell science (01.11.1999)
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A GWAS meta‐analysis from 5 population‐based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome
Bonfiglio, F., Henström, M., Nag, A., Hadizadeh, F., Zheng, T., Cenit, M. C., Tigchelaar, E., Williams, F., Reznichenko, A., Ek, W. E., Rivera, N. V., Homuth, G., Aghdassi, A. A., Kacprowski, T., Männikkö, M., Karhunen, V., Bujanda, L., Rafter, J., Wijmenga, C., Ronkainen, J., Hysi, P., Zhernakova, A., D'Amato, M.
Published in Neurogastroenterology and motility (01.09.2018)
Published in Neurogastroenterology and motility (01.09.2018)
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GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos
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.
Published in Journal of dental research (01.03.2017)
Published in Journal of dental research (01.03.2017)
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A meta‐analysis of reflux genome‐wide association studies in 6750 Northern Europeans from the general population
Bonfiglio, F., Hysi, P. G., Ek, W., Karhunen, V., Rivera, N. V., Männikkö, M., Nordenstedt, H., Zucchelli, M., Bresso, F., Williams, F., Tornblom, H., Magnusson, P. K., Pedersen, N. L., Ronkainen, J., Schmidt, P. T., D'Amato, M.
Published in Neurogastroenterology and motility (01.02.2017)
Published in Neurogastroenterology and motility (01.02.2017)
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Congenital nephrotic syndrome of the finnish type maps to the long arm of chromosome 19
KESTILÄ, M, MÄNNIKKÖ, M, HOLMBERG, C, GYAPAY, G, WEISSENBACH, J, SAVOLAINEN, E.-R, PELTONEN, L, TRYGGVASON, K
Published in American journal of human genetics (01.05.1994)
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Published in American journal of human genetics (01.05.1994)
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Targeted re-sequencing of linkage region on 2q21 identifies a novel functional variant for hip and knee osteoarthritis
Taipale, M, Jakkula, E, Kämäräinen, O.-P, Gao, P, Skarp, S, Barral, S, Kiviranta, I, Kröger, H, Ott, J, Wei, G.-H, Ala-Kokko, L, Männikkö, M
Published in Osteoarthritis and cartilage (01.04.2016)
Published in Osteoarthritis and cartilage (01.04.2016)
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Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1
MÄNNIKKÖ, M, KESTILÄ, M, HOLMBERG, C, NORIO, R, RYYNÄNEN, M, OLSEN, A, PELTONEN, L, TRYGGVASON, K
Published in American journal of human genetics (01.12.1995)
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Published in American journal of human genetics (01.12.1995)
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Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis
Männikkö, Minna, Kestilä, Marjo, Lenkkeri, Ulla, Alakurtti, Heli, Holmberg, Christer, Leisti, Jaakko, Salonen, Riitta, Aula, Pertti, Mustonen, Aki, Peltonen, Leena, Tryggvason, Karl
Published in Kidney international (01.03.1997)
Published in Kidney international (01.03.1997)
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Conference Proceeding
Congenital Nephrotic Syndrome of the Finnish Type Is Not Associated with the Pax-2 Gene Despite the Promising Transgenic Animal Model
Kestilä, Marjo, Männikkö, Minna, Holmberg, Christer, Tryggvason, Karl, Peltonen, Leena
Published in Genomics (San Diego, Calif.) (01.02.1994)
Published in Genomics (San Diego, Calif.) (01.02.1994)
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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
Singh, Tarjinder, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S, Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B, Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, Georg, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M, Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A, McGuffin, Peter, McIntosh, Andrew M, McQuillin, Andrew, Moilanen, Jukka S, Moore, Carmel, Murray, Robin M, Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, St Clair, David, Veijola, Juha, Walters, James T R, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E, O'Donovan, Michael C, Palotie, Aarno, Owen, Michael J, Barrett, Jeffrey C
Published in Nature neuroscience (01.04.2016)
Published in Nature neuroscience (01.04.2016)
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Exome Sequencing Reveals a Phenotype Modifying Variant in ZNF528 in Primary Osteoporosis With a COL1A2 Deletion
Skarp, Sini, Xia, Ji‐Han, Zhang, Qin, Löija, Marika, Costantini, Alice, Ruddock, Lloyd W, Mäkitie, Outi, Wei, Gong‐Hong, Männikkö, Minna
Published in Journal of bone and mineral research (01.12.2020)
Published in Journal of bone and mineral research (01.12.2020)
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Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland
Martin, Alicia R., Karczewski, Konrad J., Kerminen, Sini, Kurki, Mitja I., Sarin, Antti-Pekka, Artomov, Mykyta, Eriksson, Johan G., Esko, Tõnu, Genovese, Giulio, Havulinna, Aki S., Kaprio, Jaakko, Konradi, Alexandra, Korányi, László, Kostareva, Anna, Männikkö, Minna, Metspalu, Andres, Perola, Markus, Prasad, Rashmi B., Raitakari, Olli, Rotar, Oxana, Salomaa, Veikko, Groop, Leif, Palotie, Aarno, Neale, Benjamin M., Ripatti, Samuli, Pirinen, Matti, Daly, Mark J.
Published in American journal of human genetics (03.05.2018)
Published in American journal of human genetics (03.05.2018)
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