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Päivi Pajukanta

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Daphna Weissglas-Volkov; Prasad M V Linga Reddy; Laura Riba; Janet S Sinsheimer; Marja-Riitta Taskinen; Teresa Tusie-Luna; Carlos A Aguilar-Salinas; Olimpia Arellano-Campos; Rita M Cantor; Ivette Cruz-Bautista; Kerry A Deere; Lizeth Gomez-Munguia; Aldons J Lusis; Niina Matikainen; Linda Liliana Muñoz-Hernandez; Elina Nikkola; Maria Luisa Ordoñez-Sánchez; Päivi Pajukanta
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
M V Prasad Linga Reddy; Miina Juvonen Isabelle Ruel; Janet S Sinsheimer; Daphna Weissglas-Volkov; Miina Juvonen; Isabelle Ruel; Jacques Genest; Blake E Haas; Iulia Iatan; Elina Nikkola; Päivi Pajukanta
Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family.
Alena Stancáková; Aldons J Lusis; Mario A Morken; Jussi Paananen; Päivi Pajukanta; Jussi Pihlajamäki; Niyas K Saleem; Pasi Soininen; Mika Ala-Korpela; Michael Boehnke; Lori L Bonnycastle; Henna Cederberg; Mete Civelek; Francis S Collins; Antti J Kangas; Johanna Kuusisto; Markku Laakso
Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men.

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All Publications

2013: Daphna Weissglas-Volkov; Prasad M V Linga Reddy; Laura Riba; Janet S Sinsheimer; Marja-Riitta Taskinen; Teresa Tusie-Luna; Carlos A Aguilar-Salinas; Olimpia Arellano-Campos; Rita M Cantor; Ivette Cruz-Bautista; Kerry A Deere; Lizeth Gomez-Munguia; Aldons J Lusis; Niina Matikainen; Linda Liliana Muñoz-Hernandez; Elina Nikkola; Maria Luisa Ordoñez-Sánchez; Päivi Pajukanta
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.
Journal of medical genetics 2013;50(5):298-308.
2012: M V Prasad Linga Reddy; Miina Juvonen Isabelle Ruel; Janet S Sinsheimer; Daphna Weissglas-Volkov; Miina Juvonen; Isabelle Ruel; Jacques Genest; Blake E Haas; Iulia Iatan; Elina Nikkola; Päivi Pajukanta
Exome sequencing identifies 2 rare variants for low high-density lipoprotein cholesterol in an extended family.
Circulation. Cardiovascular genetics 2012;5(5):538-46.
2012: Alena Stancáková; Aldons J Lusis; Mario A Morken; Jussi Paananen; Päivi Pajukanta; Jussi Pihlajamäki; Niyas K Saleem; Pasi Soininen; Mika Ala-Korpela; Michael Boehnke; Lori L Bonnycastle; Henna Cederberg; Mete Civelek; Francis S Collins; Antti J Kangas; Johanna Kuusisto; Markku Laakso
Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men.
Diabetes 2012;61(7):1895-902.
2012: Maryam Hosseini; Ching-Mei Lai; Jo-Ling Liao; Hui Z Mao; Elina Nikkola; Päivi Pajukanta; André Bensadoun; Mark H Doolittle; Nicole Ehrhardt; Marja-Riitta Taskinen; Daphna Weissglas-Volkov; Miklós Péterfy
Transgenic expression and genetic variation of Lmf1 affect LPL activity in mice and humans.
Arteriosclerosis, thrombosis, and vascular biology 2012;32(5):1204-10.
2012: Blake E Haas; Steve Horvath; Jaakko Kaprio; Johanna Kuusisto; Markku Laakso; Elina Nikkola; Carlos A Aguilar-Salinas; Rita M Cantor; Mete Civelek; Ivette Cruz-Bautista; Kirsi H Pietiläinen; Laura Riba; Aila Rissanen; Teresa Tusie-Luna; Daphna Weissglas-Volkov; Päivi Pajukanta
Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes.
BMC medical genomics 2012;5():61.
2011: Blake E Haas; Daphna Weissglas-Volkov; Carlos Aguilar Salinas; Elina Nikkola; Laurent Vergnes; Ivette Cruz-Bautista; Laura Riba; Alena Stancakova; Johanna Kuusisto; Pasi Soininen; Antti J Kangas; Mika Ala-Korpela; Teresa Tusie-Luna; Markku Laakso; Päivi Pajukanta
Evidence of how rs7575840 influences apolipoprotein B-containing lipid particles.
Arteriosclerosis, thrombosis, and vascular biology 2011;31(5):1201-7.
2010: Daphna Weissglas-Volkov; Päivi Pajukanta
Genetic causes of high and low serum HDL-cholesterol.
Journal of lipid research 2010;51(8):2032-57.
2010: Zari Dastani; Päivi Pajukanta; Michel Marcil; Nicholas Rudzicz; Isabelle Ruel; Swneke D Bailey; Jenny C Lee; Mathieu Lemire; Janet Faith; Jill Platko; John Rioux; Thomas J Hudson; Daniel Gaudet; James C Engert; Jacques Genest
Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects.
European journal of human genetics : EJHG 2010;18(3):342-7.
2010: Sulin Wu; Rebecca Mar-Heyming; Eric Z Dugum; Nicholas A Kolaitis; Hongxiu Qi; Päivi Pajukanta; Lawrence W Castellani; Aldons J Lusis; Thomas A Drake
Upstream transcription factor 1 influences plasma lipid and metabolic traits in mice.
Human molecular genetics 2010;19(4):597-608.
2010: Daphna Weissglas-Volkov; Carlos A Aguilar-Salinas; Janet S Sinsheimer; Laura Riba; Adriana Huertas-Vazquez; Maria L Ordoñez-Sánchez; Rosario Rodriguez-Guillen; Rita M Cantor; Teresa Tusie-Luna; Päivi Pajukanta
Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples.
Circulation. Cardiovascular genetics 2010;3(1):31-8.
2010: Daphna Weissglas-Volkov; Christopher Plaisier; Adriana Huertas-Vazquez; Ivette Cruz-Bautista; Daniela Riaño-Barros; Miguel Herrera-Hernandez; Laura Riba; Rita M Cantor; Janet S Sinsheimer; Carlos Aguilar Salinas; Teresa Tusie-Luna; Päivi Pajukanta
Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.
Arteriosclerosis, thrombosis, and vascular biology 2010;30(2):353-9.
2010: Adriana Huertas-Vazquez; Christopher Plaisier; Ruishuang Geng; Blake E Haas; Jenny Lee; Marleen M Greevenbroek; Carla van der Kallen; Tjerk W A de Bruin; Marja-Riitta Taskinen; Kumar N Alagramam; Päivi Pajukanta
A nonsynonymous SNP within PCDH15 is associated with lipid traits in familial combined hyperlipidemia.
Human genetics 2010;127(1):83-9.
2009: Iulia Iatan; Zari Dastani; Ron Do; Daphna Weissglas-Volkov; Isabelle L Ruel; Jenny C Lee; Adriana Huertas-Vazquez; Marja-Riitta Taskinen; Annik Prat; Nabil G Seidah; Päivi Pajukanta; James C Engert; Jacques Genest
Genetic variation at the proprotein convertase subtilisin/kexin type 5 gene modulates high-density lipoprotein cholesterol levels.
Circulation. Cardiovascular genetics 2009;2(5):467-75.
2009: Christopher Plaisier; Steve Horvath; Adriana Huertas-Vazquez; Ivette Cruz-Bautista; Miguel F Herrera; Teresa Tusie-Luna; Carlos Aguilar Salinas; Päivi Pajukanta
A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia.
PLoS genetics 2009;5(9):e1000642.
2009: Steven J R Meex; Daphna Weissglas-Volkov; Carla J H van der Kallen; Donna J Thuerauf; Marleen M J van Greevenbroek; Casper G Schalkwijk; Coen D A Stehouwer; Edith J M Feskens; Lonneke Heldens; Torik A Ayoubi; Marten H Hofker; Bradly G Wouters; Robert Francois Vlietinck; Janet S Sinsheimer; Marja-Riitta Taskinen; Johanna Kuusisto; Markku Laakso; Tjerk W A de Bruin; Päivi Pajukanta; Christopher C Glembotski
The ATF6-Met[67]Val substitution is associated with increased plasma cholesterol levels.
Arteriosclerosis, thrombosis, and vascular biology 2009;29(9):1322-7.
2008: Jenny C Lee; Daphna Weissglas-Volkov; Mira Kyttälä; Zari Dastani; Rita M Cantor; Eric M Sobel; Christopher Plaisier; James C Engert; Marleen M J van Greevenbroek; John P Kane; Mary J Malloy; Clive R Pullinger; Adriana Huertas-Vazquez; Carlos Aguilar Salinas; Teresa Tusie-Luna; Tjerk W A de Bruin; Bradley E Aouizerat; Carla C J van der Kallen; Carlo M Croce; Rami I Aqeilan; Michel Marcil; Jorma S A Viikari; Terho Lehtimäki; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Marja-Riitta Taskinen; Jacques Genest; Päivi Pajukanta
WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels.
American journal of human genetics 2008;83(2):180-92.
2008: Rebecca Mar-Heyming; Makoto Miyazaki; Daphna Weissglas-Volkov; Nicholas A Kolaitis; Narimaan Sadaat; Christopher Plaisier; Päivi Pajukanta; Rita M Cantor; Tjerk W A de Bruin; James M Ntambi; Aldons J Lusis
Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.
Arteriosclerosis, thrombosis, and vascular biology 2008;28(6):1193-9.
2008: Janet S Sinsheimer; Christopher Plaisier; Adriana Huertas-Vazquez; Carlos Aguilar Salinas; Teresa Tusie-Luna; Päivi Pajukanta; Kenneth Lange
Estimating ethnic admixture from pedigree data.
American journal of human genetics 2008;82(3):748-55.
2008: Aldons J Lusis; Päivi Pajukanta
A treasure trove for lipoprotein biology.
Nature genetics 2008;40(2):129-30.
2008: Angela P Presson; Eric M Sobel; Päivi Pajukanta; Christopher Plaisier; Daniel E Weeks; Karolina Aberg; Jeanette C Papp
Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis.
BMC bioinformatics 2008;9():317.
2008: Adriana Huertas-Vazquez; Christopher Plaisier; Daphna Weissglas-Volkov; Janet S Sinsheimer; Samuel Canizales-Quinteros; I Cruz-Bautista; E Nikkola; M Herrera-Hernandez; A Davila-Cervantes; Teresa Tusie-Luna; Marja-Riitta Taskinen; Carlos Aguilar Salinas; Päivi Pajukanta
TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia.
Diabetologia 2008;51(1):62-9.
2007: Miklós Péterfy; Osnat Ben-Zeev; Hui Z Mao; Daphna Weissglas-Volkov; Bradley E Aouizerat; Clive R Pullinger; Philip H Frost; John P Kane; Mary J Malloy; Karen Reue; Päivi Pajukanta; Mark H Doolittle
Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia.
Nature genetics 2007;39(12):1483-7.
2007: Jenny C Lee; Daphna Weissglas-Volkov; Mira Kyttälä; Janet S Sinsheimer; Anne Jokiaho; Tjerk W A de Bruin; Aldons J Lusis; Marie-Luise Brennan; Marleen M J van Greevenbroek; Carla J H van der Kallen; Stanley L Hazen; Päivi Pajukanta
USF1 contributes to high serum lipid levels in Dutch FCHL families and U.S. whites with coronary artery disease.
Arteriosclerosis, thrombosis, and vascular biology 2007;27(10):2222-7.
2006: Daphna Weissglas-Volkov; Adriana Huertas-Vazquez; Elina Suviolahti; Jenny Lee; Christopher Plaisier; Samuel Canizales-Quinteros; Teresa Tusie-Luna; Carlos Aguilar Salinas; Marja-Riitta Taskinen; Päivi Pajukanta
Common hepatic nuclear factor-4alpha variants are associated with high serum lipid levels and the metabolic syndrome.
Diabetes 2006;55(7):1970-7.
2006: Kati Komulainen; Mervi Alanne; Kirsi Auro; Riika Kilpikari; Päivi Pajukanta; Janna Saarela; Pekka Ellonen; Kaisa Salminen; Sangita Kulathinal; Kari Kuulasmaa; Kaisa Silander; Veikko Salomaa; Markus Perola; Leena Peltonen
Risk alleles of USF1 gene predict cardiovascular disease of women in two prospective studies.
PLoS genetics 2006;2(5):e69.
2006: Jenny C Lee; Aldons J Lusis; Päivi Pajukanta
Familial combined hyperlipidemia: upstream transcription factor 1 and beyond.
Current opinion in lipidology 2006;17(2):101-9.
2006: Zari Dastani; Carole Dangoisse; Betsie Boucher; Katia Desbiens; Larbi Krimbou; Robert Dufour; Robert A Hegele; Päivi Pajukanta; James C Engert; Jacques Genest; Michel Marcil
A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians.
Atherosclerosis 2006;185(1):127-36.
2006: Elina Suviolahti; Karen Reue; Rita M Cantor; Jack Phan; Massimiliano Gentile; Jussi Naukkarinen; Aino Soro-Paavonen; Laura J Oksanen; Jaakko Kaprio; Aila Rissanen; Veikko Salomaa; Kimmo Kontula; Marja-Riitta Taskinen; Päivi Pajukanta; Leena Peltonen
Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism.
Human molecular genetics 2006;15(3):377-86.
2006: Zari Dastani; Leigh Quiogue; Christopher Plaisier; James C Engert; Michel Marcil; Jacques Genest; Päivi Pajukanta
Evidence for a gene influencing high-density lipoprotein cholesterol on chromosome 4q31.21.
Arteriosclerosis, thrombosis, and vascular biology 2006;26(2):392-7.
2006: Elina Suviolahti; Heidi E Lilja; Päivi Pajukanta
Unraveling the complex genetics of familial combined hyperlipidemia.
Annals of medicine 2006;38(5):337-51.
2005: Sampo Sammalisto; Tero Hiekkalinna; Elina Suviolahti; K Sood; A Metzidis; Päivi Pajukanta; Heidi E Lilja; Aino Soro-Paavonen; Marja-Riitta Taskinen; Tiinamaija Tuomi; Peter Almgren; Marju Orho-Melander; L Groop; Leena Peltonen; Markus Perola
A male-specific quantitative trait locus on 1p21 controlling human stature.
Journal of medical genetics 2005;42(12):932-9.
2005: Jussi Naukkarinen; Massimiliano Gentile; Aino Soro-Paavonen; Janna Saarela; Heikki A Koistinen; Päivi Pajukanta; Marja-Riitta Taskinen; Leena Peltonen
USF1 and dyslipidemias: converging evidence for a functional intronic variant.
Human molecular genetics 2005;14(17):2595-605.
2005: Adriana Huertas-Vazquez; Carlos Aguilar Salinas; Aldons J Lusis; Rita M Cantor; Samuel Canizales-Quinteros; Jenny C Lee; Lizzette Mariana-Nuñez; Roopa-Metha Laura Riba-Ramirez; Anne Jokiaho; Teresa Tusie-Luna; Päivi Pajukanta
Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.
Arteriosclerosis, thrombosis, and vascular biology 2005;25(9):1985-91.
2005: Rita M Cantor; Gary K Chen; Päivi Pajukanta; Kenneth Lange
Association testing in a linked region using large pedigrees.
American journal of human genetics 2005;76(3):538-42.
2004: Päivi Pajukanta
Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?
The Journal of clinical investigation 2004;114(9):1244-7.
2004: Heidi E Lilja; Elina Suviolahti; Aino Soro-Paavonen; Tero Hiekkalinna; Aaron Day; Kenneth Lange; Eric Sobel; Marja-Riitta Taskinen; Leena Peltonen; Markus Perola; Päivi Pajukanta
Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with dyslipidemia.
Journal of lipid research 2004;45(10):1876-84.
2004: Rebecca Mar; Päivi Pajukanta; Hooman Allayee; Martine Groenendijk; Geesje M Dallinga-Thie; Ronald M Krauss; Janet S Sinsheimer; Rita M Cantor; Tjerk W A de Bruin; Aldons J Lusis
Association of the APOLIPOPROTEIN A1/C3/A4/A5 gene cluster with triglyceride levels and LDL particle size in familial combined hyperlipidemia.
Circulation research 2004;94(7):993-9.
2004: Päivi Pajukanta; Heidi E Lilja; Janet S Sinsheimer; Rita M Cantor; Aldons J Lusis; Massimiliano Gentile; Xiaoqun Joyce Duan; Aino Soro-Paavonen; Jussi Naukkarinen; Janna Saarela; Markku Laakso; Christian Ehnholm; Marja-Riitta Taskinen; Leena Peltonen
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
Nature genetics 2004;36(4):371-6.
2004: Aldons J Lusis; Rebecca Mar; Päivi Pajukanta
Genetics of atherosclerosis.
Annual review of genomics and human genetics 2004;5():189-218.
2003: Elina Suviolahti; Laura J Oksanen; Miina Ohman; Rita M Cantor; Martin Ridderstrale; Tiinamaija Tuomi; Jaakko Kaprio; Aila Rissanen; Pertti Mustajoki; Pekka Jousilahti; Erkki Vartiainen; Kaisa Silander; Riika Kilpikari; Veikko Salomaa; Leif Groop; Kimmo Kontula; Leena Peltonen; Päivi Pajukanta
The SLC6A14 gene shows evidence of association with obesity.
The Journal of clinical investigation 2003;112(11):1762-72.
2003: Päivi Pajukanta; Hooman Allayee; Kelly L Krass; Ali Kuraishy; Aino Soro; Heidi E Lilja; Rebecca Mar; Marja-Riitta Taskinen; Ilpo Nuotio; Markku Laakso; Jerome I Rotter; Tjerk W A de Bruin; Rita M Cantor; Aldons J Lusis; Leena Peltonen
Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q.
American journal of human genetics 2003;72(4):903-17.
2002: Juha Vakkilainen; Päivi Pajukanta; Rita M Cantor; Ilpo Nuotio; Sanni Lahdenperä; Kati Ylitalo; Jussi Pihlajamäki; Petri T Kovanen; Markku Laakso; Jorma S A Viikari; Leena Peltonen; Marja-Riitta Taskinen
Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia.
European journal of human genetics : EJHG 2002;10(9):547-52.
2002: Heidi E Lilja; Aino Soro; Kati Ylitalo; Ilpo Nuotio; Jorma S A Viikari; Veikko Salomaa; Erkki Vartiainen; Marja-Riitta Taskinen; Leena Peltonen; Päivi Pajukanta
A candidate gene study in low HDL-cholesterol families provides evidence for the involvement of the APOA2 gene and the APOA1C3A4 gene cluster.
Atherosclerosis 2002;164(1):103-11.
2002: Hooman Allayee; Kelly L Krass; Päivi Pajukanta; Rita M Cantor; Carla J H van der Kallen; Rebecca Mar; Jerome I Rotter; Tjerk W A de Bruin; Leena Peltonen; Aldons J Lusis
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia.
Circulation research 2002;90(8):926-31.
2002: Aino Soro; Päivi Pajukanta; Heidi E Lilja; Kati Ylitalo; Tero Hiekkalinna; Markus Perola; Rita M Cantor; Jorma S A Viikari; Marja-Riitta Taskinen; Leena Peltonen
Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families.
American journal of human genetics 2002;70(5):1333-40.
2002: G Hu; Barmak Modrek; H M F Riise Stensland; Janna Saarela; Päivi Pajukanta; Vlad Kustanovich; Leena Peltonen; Stanley F Nelson; Christopher Lee
Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes.
The pharmacogenomics journal 2002;2(4):236-42.
2002: Jenny Ekholm; P Pekkarinen; Päivi Pajukanta; Tuula Kieseppä; Timo Partonen; Tiina Paunio; Teppo Varilo; Markus Perola; Jouko Lönnqvist; Leena Peltonen
Bipolar disorder susceptibility region on Xq24-q27.1 in Finnish families.
Molecular psychiatry 2002;7(5):453-9.
2001: Markus Perola; Miina Ohman; Tero Hiekkalinna; J Leppävuori; Päivi Pajukanta; Maija Wessman; M Koskenvuo; Aarno Palotie; Kenneth Lange; Jaakko Kaprio; Leena Peltonen
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.
American journal of human genetics 2001;69(1):117-23.
2001: Kati Ylitalo; Päivi Pajukanta; Seppo Meri; Rita M Cantor; N Mero-Matikainen; Juha Vakkilainen; Ilpo Nuotio; Marja-Riitta Taskinen
Serum C3 but not plasma acylation-stimulating protein is elevated in Finnish patients with familial combined hyperlipidemia.
Arteriosclerosis, thrombosis, and vascular biology 2001;21(5):838-43.
2001: Päivi Pajukanta; Jackie S Bodnar; Riitta Sallinen; M Chu; T Airaksinen; Q Xiao; Lawrence W Castellani; Sonal S Sheth; Maija Wessman; Aarno Palotie; Janet S Sinsheimer; Peter Demant; Aldons J Lusis; Leena Peltonen
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(3):238-45.
2000: Kati Ylitalo; V Large; Päivi Pajukanta; S Reynisdottir; Kimmo Porkka; Juha Vakkilainen; Ilpo Nuotio; Marja-Riitta Taskinen; Peter Arner
Reduced hormone-sensitive lipase activity is not a major metabolic defect in Finnish FCHL families.
Atherosclerosis 2000;153(2):373-81.
2000: Päivi Pajukanta; M Cargill; Laura Viitanen; Ilpo Nuotio; Anu Kareinen; Markus Perola; Joseph D Terwilliger; E Kempas; Mark J Daly; Heidi E Lilja; JD Rioux; T Brettin; Jorma S A Viikari; T Rönnemaa; Markku Laakso; Eric S Lander; Leena Peltonen
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
American journal of human genetics 2000;67(6):1481-93.
2000: Markus Perola; K Kainulainen; Päivi Pajukanta; Joseph D Terwilliger; Tero Hiekkalinna; Pekka Ellonen; Jaakko Kaprio; Markku Koskenvuo; Kimmo Kontula; Leena Peltonen
Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings.
Journal of hypertension 2000;18(11):1579-85.
1999: Päivi Pajukanta; Kimmo Porkka
Genetics of familial combined hyperlipidemia.
Current atherosclerosis reports 1999;1(1):79-86.
1999: Päivi Pajukanta; Joseph D Terwilliger; Markus Perola; Tero Hiekkalinna; Ilpo Nuotio; Pekka Ellonen; Maija Parkkonen; Jaana Hartiala; Kati Ylitalo; Jussi Pihlajamäki; Kimmo Porkka; Markku Laakso; Jorma Viikari; Christian Ehnholm; Marja-Riitta Taskinen; Leena Peltonen
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.
American journal of human genetics 1999;64(5):1453-63.
1998: Esa Tahvanainen; Päivi Pajukanta; Kimmo Porkka; S Nieminen; L Ikävalko; Ilpo Nuotio; Marja-Riitta Taskinen; L Peltonen; Christian Ehnholm
Haplotypes of the ApoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia.
Arteriosclerosis, thrombosis, and vascular biology 1998;18(11):1810-7.
1998: Päivi Pajukanta; Ilpo Nuotio; Joseph D Terwilliger; Kimmo Porkka; Kati Ylitalo; Jussi Pihlajamäki; Anu Suomalainen; Ann-Christine Syvänen; T Lehtimäki; Jorma S A Viikari; Markku Laakso; Marja-Riitta Taskinen; Christian Ehnholm; Leena Peltonen
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
Nature genetics 1998;18(4):369-73.
1998: Juha Vakkilainen; Kimmo Porkka; Ilpo Nuotio; Päivi Pajukanta; L Suurinkeroinen; Kati Ylitalo; Jorma S A Viikari; Christian Ehnholm; Marja-Riitta Taskinen
Glucose intolerance in familial combined hyperlipidaemia. EUFAM study group.
European journal of clinical investigation 1998;28(1):24-32.
1997: Kimmo Porkka; Ilpo Nuotio; Päivi Pajukanta; Christian Ehnholm; L Suurinkeroinen; Mikko Syvänne; Terho Lehtimäki; Anne-Tiina Lahdenkari; Sanni Lahdenperä; Kati Ylitalo; Marjatta Antikainen; Markus Perola; Olli T Raitakari; Petri T Kovanen; Jorma S A Viikari; Leena Peltonen; Marja-Riitta Taskinen
Phenotype expression in familial combined hyperlipidemia.
Atherosclerosis 1997;133(2):245-53.
1997: QH Meng; Päivi Pajukanta; L Valsta; A Aro; Pirjo Pietinen; Matti J Tikkanen
Influence of apolipoprotein A-1 promoter polymorphism on lipid levels and responses to dietary change in Finnish adults.
Journal of internal medicine 1997;241(5):373-8.
1997: Päivi Pajukanta; Kimmo Porkka; Marjatta Antikainen; Marja-Riitta Taskinen; Markus Perola; S Murtomäki-Repo; Sonja Jaari; Ilpo Nuotio; L Suurinkeroinen; Anne-Tiina Lahdenkari; Ann-Christine Syvänen; Jorma S A Viikari; Christian Ehnholm; Leena Peltonen
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families.
Arteriosclerosis, thrombosis, and vascular biology 1997;17(5):841-50.
1997: Päivi Pajukanta; Leena Peltonen
How to tackle genetic loci predisposing to atherosclerosis?
Current opinion in lipidology 1997;8(2):95-100.
1997: Kati Ylitalo; Kimmo Porkka; Seppo Meri; Ilpo Nuotio; L Suurinkeroinen; Juha Vakkilainen; Päivi Pajukanta; Jorma S A Viikari; Leena Peltonen; Christian Ehnholm; Marja-Riitta Taskinen
Serum complement and familial combined hyperlipidemia.
Atherosclerosis 1997;129(2):271-7.
1996: QH Meng; Päivi Pajukanta; M Ilmonen; H Schuster; C K Schewe; L C Andersson; Matti J Tikkanen
Analysis of novel apolipoprotein B mutations using a modified U937 cell line LDL binding assay.
Clinica chimica acta; international journal of clinical chemistry 1996;256(1):27-36.
1996: Päivi Pajukanta; L M Valsta; A Aro; P Pietinen; T Heliö; Matti J Tikkanen
The effects of the apolipoprotein B signal peptide (ins/del) and XbaI polymorphisms on plasma lipid responses to dietary change.
Atherosclerosis 1996;122(1):1-10.
1995: Matti J Tikkanen; J K Huttunen; Päivi Pajukanta; P Pietinen
Apolipoprotein E polymorphism and dietary plasma cholesterol response.
The Canadian journal of cardiology 1995;11 Suppl G():93G-96G.