Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population
Salo, Perttu P, Havulinna, Aki S, Tukiainen, Taru, Raitakari, Olli, Lehtimäki, Terho, Kähönen, Mika, Kettunen, Johannes, Männikkö, Minna, Eriksson, Johan G, Jula, Antti, Blankenberg, Stefan, Zeller, Tanja, Salomaa, Veikko, Kristiansson, Kati, Perola, Markus
Published in Circulation. Cardiovascular genetics (01.12.2017)
Published in Circulation. Cardiovascular genetics (01.12.2017)
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Journal Article
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population
Salo, Perttu P, Vaara, Satu, Kettunen, Johannes, Pirinen, Matti, Sarin, Antti-Pekka, Huikuri, Heikki, Karhunen, Pekka J, Eskola, Markku, Nikus, Kjell, Lokki, Marja-Liisa, Ripatti, Samuli, Havulinna, Aki S, Salomaa, Veikko, Palotie, Aarno, Nieminen, Markku S, Sinisalo, Juha, Perola, Markus
Published in PloS one (28.10.2015)
Published in PloS one (28.10.2015)
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Journal Article
Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up
Gudelj, Ivan, Salo, Perttu P., Trbojević-Akmačić, Irena, Albers, Malena, Primorac, Dragan, Perola, Markus, Lauc, Gordan
Published in Biochimica et biophysica acta. Molecular basis of disease (01.06.2018)
Published in Biochimica et biophysica acta. Molecular basis of disease (01.06.2018)
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Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium
Marinelli, Marcella, Pappa, Irene, Bustamante, Mariona, Bonilla, Carolina, Suarez, Anna, Tiesler, Carla M., Vilor-Tejedor, Natalia, Zafarmand, Mohammad Hadi, Alvarez-Pedrerol, Mar, Andersson, Sture, Bakermans-Kranenburg, Marian J., Estivill, Xavier, Evans, David M., Flexeder, Claudia, Forns, Joan, Gonzalez, Juan R., Guxens, Monica, Huss, Anke, van IJzendoorn, Marinus H., Jaddoe, Vincent W.V., Julvez, Jordi, Lahti, Jari, López-Vicente, Mónica, Lopez-Espinosa, Maria-Jose, Manz, Judith, Mileva-Seitz, Viara R., Perola, Markus, Pesonen, Anu-Katriina, Rivadeneira, Fernando, Salo, Perttu P., Shahand, Shayan, Schulz, Holger, Standl, Marie, Thiering, Elisabeth, Timpson, Nicholas J., Torrent, Maties, Uitterlinden, André G., Smith, George Davey, Estarlich, Marisa, Heinrich, Joachim, Räikkönen, Katri, Vrijkotte, Tanja G.M., Tiemeier, Henning, Sunyer, Jordi
Published in Sleep (New York, N.Y.) (01.10.2016)
Published in Sleep (New York, N.Y.) (01.10.2016)
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Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
Virtanen, Valtter B., Salo, Perttu P., Cao, Jia, Löf-Granström, Anna, Milani, Lili, Metspalu, Andres, Rintala, Risto J., Saarenpää-Heikkilä, Outi, Paunio, Tiina, Wester, Tomas, Nordenskjöld, Agneta, Perola, Markus, Pakarinen, Mikko P.
Published in European journal of medical genetics (01.04.2019)
Published in European journal of medical genetics (01.04.2019)
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Journal Article
Thyroid cancer and co-occurring RET mutations in Hirschsprung disease
Virtanen, Valtter B, Pukkala, Eero, Kivisaari, Reetta, Salo, Perttu P, Koivusalo, Antti, Arola, Johanna, Miettinen, Päivi J, Rintala, Risto J, Perola, Markus, Pakarinen, Mikko P
Published in Endocrine-related cancer (01.08.2013)
Published in Endocrine-related cancer (01.08.2013)
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Journal Article
Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population: e0140576
Salo, Perttu P, Vaara, Satu, Kettunen, Johannes, Pirinen, Matti, Sarin, Antti-Pekka, Huikuri, Heikki, Karhunen, Pekka J, Eskola, Markku, Nikus, Kjell, Lokki, Marja-Liisa
Published in PloS one (01.01.2015)
Published in PloS one (01.01.2015)
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