Mutations in AXIN2 Cause Familial Tooth Agenesis and Predispose to Colorectal Cancer

由 Lammi, Laura, Arte, Sirpa, Somer, Mirja, Järvinen, Heikki, Lahermo, Päivi, Thesleff, Irma, Pirinen, Sinikka, Nieminen, Pekka
出版 2004

Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria

由 Holmberg, Ville, Onkamo, Päivi, Lahtela, Elisa, Lahermo, Päivi, Bedu-Addo, George, Mockenhaupt, Frank P, Meri, Seppo
出版 2012

Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs

由 Hannelius, Ulf, Salmela, Elina, Lappalainen, Tuuli, Guillot, Gilles, Lindgren, Cecilia M, von Döbeln, Ulrika, Lahermo, Päivi, Kere, Juha
出版 2008

Susceptibility Loci for Preeclampsia on Chromosomes 2p25 and 9p13 in Finnish Families

由 Laivuori, Hannele, Lahermo, Päivi, Ollikainen, Vesa, Widen, Elisabeth, Häivä-Mällinen, Leena, Sundström, Helena, Laitinen, Tarja, Kaaja, Risto, Ylikorkala, Olavi, Kere, Juha
出版 2003

Association of Variants in DISC1 With Psychosis-Related Traits in a Large Population Cohort

由 Tomppo, Liisa, Hennah, William, Miettunen, Jouko, Järvelin, Marjo-Riitta, Veijola, Juha, Ripatti, Samuli, Lahermo, Päivi, Lichtermann, Dirk, Peltonen, Leena, Ekelund, Jesper
出版 2009

Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental Illnesses

由 Tomppo, Liisa, Hennah, William, Lahermo, Päivi, Loukola, Anu, Tuulio-Henriksson, Annamari, Suvisaari, Jaana, Partonen, Timo, Ekelund, Jesper, Lönnqvist, Jouko, Peltonen, Leena
出版 2009

Genomic landscape of positive natural selection in Northern European populations

由 Lappalainen, Tuuli, Salmela, Elina, Andersen, Peter M, Dahlman-Wright, Karin, Sistonen, Pertti, Savontaus, Marja-Liisa, Schreiber, Stefan, Lahermo, Päivi, Kere, Juha
出版 2010

Genetic background of ataxia in children younger than 5 years in Finland

由 Ignatius, Erika, Isohanni, Pirjo, Pohjanpelto, Max, Lahermo, Päivi, Ojanen, Simo, Brilhante, Virginia, Palin, Eino, Suomalainen, Anu, Lönnqvist, Tuula, Carroll, Christopher J.
發表在 Neurol Genet (2020)

Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes

由 Luukkonen, Tiia Maria, Mehrjouy, Mana M., Pöyhönen, Minna, Anttonen, Anna‐Kaisa, Lahermo, Päivi, Ellonen, Pekka, Paulin, Lars, Tommerup, Niels, Palotie, Aarno, Varilo, Teppo
發表在 Mol Genet Genomic Med (2017)

Swedish Population Substructure Revealed by Genome-Wide Single Nucleotide Polymorphism Data

由 Salmela, Elina, Lappalainen, Tuuli, Liu, Jianjun, Sistonen, Pertti, Andersen, Peter M., Schreiber, Stefan, Savontaus, Marja-Liisa, Czene, Kamila, Lahermo, Päivi, Hall, Per, Kere, Juha
出版 2011

ELMOD2 Is a Candidate Gene for Familial Idiopathic Pulmonary Fibrosis

由 Hodgson, Ulla, Pulkkinen, Ville, Dixon, Morag, Peyrard-Janvid, Myriam, Rehn, Marko, Lahermo, Päivi, Ollikainen, Vesa, Salmenkivi, Kaisa, Kinnula, Vuokko, Kere, Juha, Tukiainen, Pentti, Laitinen, Tarja
出版 2006

Genome-Wide Analysis of Single Nucleotide Polymorphisms Uncovers Population Structure in Northern Europe

由 Salmela, Elina, Lappalainen, Tuuli, Fransson, Ingegerd, Andersen, Peter M., Dahlman-Wright, Karin, Fiebig, Andreas, Sistonen, Pertti, Savontaus, Marja-Liisa, Schreiber, Stefan, Kere, Juha, Lahermo, Päivi
出版 2008

Erratum to: high-resolution SNP array analysis of patients with developmental disorder and normal array CGH result

由 Siggberg, Linda, Ala-Mello, Sirpa, Linnankivi, Tarja, Avela, Kristiina, Scheinin, Ilari, Kristiansson, Kati, Lahermo, Päivi, Hietala, Marja, Metsähonkala, Liisa, Kuusinen, Esa, Laaksonen, Maarit, Saarela, Janna, Knuutila, Sakari
發表在 BMC Med Genet (2014)

COMMON CANDIDATE GENE VARIANTS ARE ASSOCIATED WITH QT INTERVAL DURATION IN THE GENERAL POPULATION

由 Marjamaa, Annukka, Newton-Cheh, Christopher, Porthan, Kimmo, Reunanen, Antti, Lahermo, Päivi, Väänänen, Heikki, Jula, Antti, Karanko, Hannu, Swan, Heikki, Toivonen, Lauri, Nieminen, Markku S., Viitasalo, Matti, Peltonen, Leena, Oikarinen, Lasse, Palotie, Aarno, Kontula, Kimmo, Salomaa, Veikko
出版 2009

High prevalence of four long QT syndrome founder mutations in the Finnish population

由 MARJAMAA, ANNUKKA, SALOMAA, VEIKKO, NEWTON-CHEH, CHRISTOPHER, PORTHAN, KIMMO, REUNANEN, ANTTI, KARANKO, HANNU, JULA, ANTTI, LAHERMO, PÄIVI, VÄÄNÄNEN, HEIKKI, TOIVONEN, LAURI, SWAN, HEIKKI, VIITASALO, MATTI, NIEMINEN, MARKKU S., PELTONEN, LEENA, OIKARINEN, LASSE, PALOTIE, AARNO, KONTULA, KIMMO
出版 2009

Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

由 Johari, Mridul, Sarparanta, Jaakko, Vihola, Anna, Jonson, Per Harald, Savarese, Marco, Jokela, Manu, Torella, Annalaura, Piluso, Giulio, Said, Edith, Vella, Norbert, Cauchi, Marija, Magot, Armelle, Magri, Francesca, Mauri, Eleonora, Kornblum, Cornelia, Reimann, Jens, Stojkovic, Tanya, Romero, Norma B., Luque, Helena, Huovinen, Sanna, Lahermo, Päivi, Donner, Kati, Comi, Giacomo Pietro, Nigro, Vincenzo, Hackman, Peter, Udd, Bjarne
發表在 Acta Neuropathol (2021)

European lactase persistence genotype shows evidence of association with increase in body mass index

由 Kettunen, Johannes, Silander, Kaisa, Saarela, Olli, Amin, Najaf, Müller, Martina, Timpson, Nicholas, Surakka, Ida, Ripatti, Samuli, Laitinen, Jaana, Hartikainen, Anna-Liisa, Pouta, Anneli, Lahermo, Päivi, Anttila, Verneri, Männistö, Satu, Jula, Antti, Virtamo, Jarmo, Salomaa, Veikko, Lehtimäki, Terho, Raitakari, Olli, Gieger, Christian, Wichmann, Erich H., Van Duijn, Cornelia M., Smith, George Davey, McCarthy, Mark I., Järvelin, Marjo-Riitta, Perola, Markus, Peltonen, Leena
出版 2010

Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis

由 Tommiska, Johanna, Känsäkoski, Johanna, Skibsbye, Lasse, Vaaralahti, Kirsi, Liu, Xiaonan, Lodge, Emily J., Tang, Chuyi, Yuan, Lei, Fagerholm, Rainer, Kanters, Jørgen K., Lahermo, Päivi, Kaunisto, Mari, Keski-Filppula, Riikka, Vuoristo, Sanna, Pulli, Kristiina, Ebeling, Tapani, Valanne, Leena, Sankila, Eeva-Marja, Kivirikko, Sirpa, Lääperi, Mitja, Casoni, Filippo, Giacobini, Paolo, Phan-Hug, Franziska, Buki, Tal, Tena-Sempere, Manuel, Pitteloud, Nelly, Veijola, Riitta, Lipsanen-Nyman, Marita, Kaunisto, Kari, Mollard, Patrice, Andoniadou, Cynthia L., Hirsch, Joel A., Varjosalo, Markku, Jespersen, Thomas, Raivio, Taneli
發表在 Nat Commun (2017)

New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes

由 Sandholm, Niina, Salem, Rany M., McKnight, Amy Jayne, Brennan, Eoin P., Forsblom, Carol, Isakova, Tamara, McKay, Gareth J., Williams, Winfred W., Sadlier, Denise M., Mäkinen, Ville-Petteri, Swan, Elizabeth J., Palmer, Cameron, Boright, Andrew P., Ahlqvist, Emma, Deshmukh, Harshal A., Keller, Benjamin J., Huang, Huateng, Ahola, Aila J., Fagerholm, Emma, Gordin, Daniel, Harjutsalo, Valma, He, Bing, Heikkilä, Outi, Hietala, Kustaa, Kytö, Janne, Lahermo, Päivi, Lehto, Markku, Lithovius, Raija, Österholm, Anne-May, Parkkonen, Maija, Pitkäniemi, Janne, Rosengård-Bärlund, Milla, Saraheimo, Markku, Sarti, Cinzia, Söderlund, Jenny, Soro-Paavonen, Aino, Syreeni, Anna, Thorn, Lena M., Tikkanen, Heikki, Tolonen, Nina, Tryggvason, Karl, Tuomilehto, Jaakko, Wadén, Johan, Gill, Geoffrey V., Prior, Sarah, Guiducci, Candace, Mirel, Daniel B., Taylor, Andrew, Hosseini, S. Mohsen, Parving, Hans-Henrik, Rossing, Peter, Tarnow, Lise, Ladenvall, Claes, Alhenc-Gelas, François, Lefebvre, Pierre, Rigalleau, Vincent, Roussel, Ronan, Tregouet, David-Alexandre, Maestroni, Anna, Maestroni, Silvia, Falhammar, Henrik, Gu, Tianwei, Möllsten, Anna, Cimponeriu, Danut, Ioana, Mihai, Mota, Maria, Mota, Eugen, Serafinceanu, Cristian, Stavarachi, Monica, Hanson, Robert L., Nelson, Robert G., Kretzler, Matthias, Colhoun, Helen M., Panduru, Nicolae Mircea, Gu, Harvest F., Brismar, Kerstin, Zerbini, Gianpaolo, Hadjadj, Samy, Marre, Michel, Groop, Leif, Lajer, Maria, Bull, Shelley B., Waggott, Daryl, Paterson, Andrew D., Savage, David A., Bain, Stephen C., Martin, Finian, Hirschhorn, Joel N., Godson, Catherine, Florez, Jose C., Groop, Per-Henrik, Maxwell, Alexander P.
出版 2012