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Search Results - Salo, Perttu P.
Search Results - Salo, Perttu P.
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Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population
by
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
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Low galactosylation of IgG associates with higher risk for future diagnosis of rheumatoid arthritis during 10 years of follow-up
by
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
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Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium
by
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.)
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Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
by
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
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Genetic Variants on Chromosome 1p13.3 Are Associated with Non-ST Elevation Myocardial Infarction and the Expression of DRAM2 in the Finnish Population: e0140576
by
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
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Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
by
Fadista, João
,
Lund, Marie
,
Skotte, Line
,
Geller, Frank
,
Nandakumar, Priyanka
,
Chatterjee, Sumantra
,
Matsson, Hans
,
Granström, Anna Löf
,
Wester, Tomas
,
Salo, Perttu
,
Virtanen, Valtter
,
Carstensen, Lisbeth
,
Bybjerg-Grauholm, Jonas
,
Hougaard, David Michael
,
Pakarinen, Mikko
,
Perola, Markus
,
Nordenskjöld, Agneta
,
Chakravarti, Aravinda
,
Melbye, Mads
,
Feenstra, Bjarke
Published in
European journal of human genetics : EJHG
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Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk
by
Walsh, Kyle M
,
Codd, Veryan
,
Rice, Terri
,
Nelson, Christopher P
,
Smirnov, Ivan V
,
McCoy, Lucie S
,
Hansen, Helen M
,
Elhauge, Edward
,
Ojha, Juhi
,
Francis, Stephen S
,
Madsen, Nils R
,
Bracci, Paige M
,
Pico, Alexander R
,
Molinaro, Annette M
,
Tihan, Tarik
,
Berger, Mitchel S
,
Chang, Susan M
,
Prados, Michael D
,
Jenkins, Robert B
,
Wiemels, Joseph L
,
Samani, Nilesh J
,
Wiencke, John K
,
Wrensch, Margaret R
Published in
Oncotarget
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