A selected list of publications:
Jew Brandon, Alvarez Marcus, Rahmani Elior, Miao Zong, Ko Arthur, Garske Kristina M, Sul Jae Hoon, Pietiläinen Kirsi H, Pajukanta Päivi, Halperin Eran
Accurate estimation of cell composition in bulk expression through
robust integration of single-cell information
Nature communications,
2020; 11(1):
1971.
Mefford Joel, Park Danny, Zheng Zhili, Ko Arthur, Ala-Korpela Mika, Laakso Markku, Pajukanta Päivi, Yang Jian, Witte John, Zaitlen Noah
Efficient Estimation and Applications of Cross-Validated Genetic
Predictions to Polygenic Risk Scores and Linear Mixed Models
Journal of computational biology : a journal of computational molecular cell biology,
2020; 27(4):
599-612.
Garske Kristina M, Pan David Z, Miao Zong, Bhagat Yash V, Comenho Caroline, Robles Christopher R, Benhammou Jihane N, Alvarez Marcus, Ko Arthur, Ye Chun Jimmie, Pisegna Joseph R, Mohlke Karen L, Sinsheimer Janet S, Laakso Markku, Pajukanta Päivi
Reverse gene-environment interaction approach to identify variants
influencing body-mass index in humans
Nature metabolism,
2019; 1(6):
630-642.
Gallois Apolline, Mefford Joel, Ko Arthur, Vaysse Amaury, Julienne Hanna, Ala-Korpela Mika, Laakso Markku, Zaitlen Noah, Pajukanta Päivi, Aschard Hugues
A comprehensive study of metabolite genetics reveals strong pleiotropy
and heterogeneity across time and context
Nature communications,
2019; 10(1):
4788.
Wu Ying, Broadaway K Alaine, Raulerson Chelsea K, Scott Laura J, Pan Calvin, Ko Arthur, He Aiqing, Tilford Charles, Fuchsberger Christian, Locke Adam E, Stringham Heather M, Jackson Anne U, Narisu Narisu, Kuusisto Johanna, Pajukanta Päivi, Collins Francis S, Boehnke Michael, Laakso Markku, Lusis Aldons J, Civelek Mete, Mohlke Karen L
Colocalization of GWAS and eQTL signals at loci with multiple signals
identifies additional candidate genes for body fat distribution
Human molecular genetics,
2019; 28(24):
4161-4172.
Lea Amanda, Subramaniam Meena, Ko Arthur, Lehtimäki Terho, Raitoharju Emma, Kähönen Mika, Seppälä Ilkka, Mononen Nina, Raitakari Olli T, Ala-Korpela Mika, Pajukanta Päivi, Zaitlen Noah, Ayroles Julien F
Genetic and environmental perturbations lead to regulatory
decoherence
eLife,
2019; 8(4):
e1008009.
Pan David Z, Garske Kristina M, Alvarez Marcus, Bhagat Yash V, Boocock James, Nikkola Elina, Miao Zong, Raulerson Chelsea K, Cantor Rita M, Civelek Mete, Glastonbury Craig A, Small Kerrin S, Boehnke Michael, Lusis Aldons J, Sinsheimer Janet S, Mohlke Karen L, Laakso Markku, Pajukanta Päivi, Ko Arthur
Integration of human adipocyte chromosomal interactions with adipose
gene expression prioritizes obesity-related genes from GWAS
Nature communications,
2018; 9(1):
1512.
Freund Malika Kumar, Burch Kathryn S, Shi Huwenbo, Mancuso Nicholas, Kichaev Gleb, Garske Kristina M, Pan David Z, Miao Zong, Mohlke Karen L, Laakso Markku, Pajukanta Päivi, Pasaniuc Bogdan, Arboleda Valerie A
Phenotype-Specific Enrichment of Mendelian Disorder Genes near GWAS
Regions across 62 Complex Traits
American journal of human genetics,
2018; 103(4):
535-552.
Nikkola Elina, Ko Arthur, Alvarez Marcus, Cantor Rita M, Garske Kristina, Kim Elliot, Gee Stephanie, Rodriguez Alejandra, Muxel Reinhard, Matikainen Niina, Söderlund Sanni, Motazacker Mahdi M, Borén Jan, Lamina Claudia, Kronenberg Florian, Schneider Wolfgang J, Palotie Aarno, Laakso Markku, Taskinen Marja-Riitta, Pajukanta Päivi
Family-specific aggregation of lipid GWAS variants confers the
susceptibility to familial hypercholesterolemia in a large Austrian
family
Atherosclerosis,
2017; 264(5):
58-66.
Civelek Mete, Wu Ying, Pan Calvin, Raulerson Chelsea K, Ko Arthur, He Aiqing, Tilford Charles, Saleem Niyas K, Stančáková Alena, Scott Laura J, Fuchsberger Christian, Stringham Heather M, Jackson Anne U, Narisu Narisu, Chines Peter S, Small Kerrin S, Kuusisto Johanna, Parks Brian W, Pajukanta Päivi, Kirchgessner Todd, Collins Francis S, Gargalovic Peter S, Boehnke Michael, Laakso Markku, Mohlke Karen L, Lusis Aldons J
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic
Traits
American journal of human genetics,
2017; 100(3):
428-443.
Fejzo Marlena Schoenberg, Myhre Ronny, Colodro-Conde Lucía, MacGibbon Kimber W, Sinsheimer Janet S, Reddy M V Prasad Linga, Pajukanta Päivi, Nyholt Dale R, Wright Margaret J, Martin Nicholas G, Engel Stephanie M, Medland Sarah E, Magnus Per, Mullin Patrick M
Genetic analysis of hyperemesis gravidarum reveals association with
intracellular calcium release channel (RYR2)
Molecular and cellular endocrinology,
2017; 439(3):
308-316.
Gusev Alexander, Ko Arthur, Shi Huwenbo, Bhatia Gaurav, Chung Wonil, Penninx Brenda W J H, Jansen Rick, de Geus Eco J C, Boomsma Dorret I, Wright Fred A, Sullivan Patrick F, Nikkola Elina, Alvarez Marcus, Civelek Mete, Lusis Aldons J, Lehtimäki Terho, Raitoharju Emma, Kähönen Mika, Seppälä Ilkka, Raitakari Olli T, Kuusisto Johanna, Laakso Markku, Price Alkes L, Pajukanta Päivi, Pasaniuc Bogdan
Integrative approaches for large-scale transcriptome-wide association
studies
Nature genetics,
2016; 48(3):
245-52.
Rodríguez Alejandra, Gonzalez Luis, Ko Arthur, Alvarez Marcus, Miao Zong, Bhagat Yash, Nikkola Elina, Cruz-Bautista Ivette, Arellano-Campos Olimpia, Muñoz-Hernández Linda L, Ordóñez-Sánchez Maria-Luisa, Rodriguez-Guillen Rosario, Mohlke Karen L, Laakso Markku, Tusie-Luna Teresa, Aguilar-Salinas Carlos A, Pajukanta Päivi
Molecular Characterization of the Lipid Genome-Wide Association Study
Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of
the TMEM241 Gene
Arteriosclerosis, thrombosis, and vascular biology,
2016; 36(7):
1350-5.
Kaminska Dorota, Käkelä Pirjo, Nikkola Elina, Venesmaa Sari, Ilves Imre, Herzig Karl-Heinz, Kolehmainen Marjukka, Karhunen Leila, Kuusisto Johanna, Gylling Helena, Pajukanta Päivi, Laakso Markku, Pihlajamäki Jussi
Regulation of alternative splicing in human obesity loci
Obesity (Silver Spring, Md.),
2016; 24(10):
2033-7.
Ripatti Pietari, Rämö Joel T, Söderlund Sanni, Surakka Ida, Matikainen Niina, Pirinen Matti, Pajukanta Päivi, Sarin Antti-Pekka, Service Susan K, Laurila Pirkka-Pekka, Ehnholm Christian, Salomaa Veikko, Wilson Richard K, Palotie Aarno, Freimer Nelson B, Taskinen Marja-Riitta, Ripatti Samuli
The Contribution of GWAS Loci in Familial Dyslipidemias
PLoS genetics,
2016; 12(5):
e1006078.
Wiegman Albert, Gidding Samuel S, Watts Gerald F, Chapman M John, Ginsberg Henry N, Cuchel Marina, Ose Leiv, Averna Maurizio, Boileau Catherine, Borén Jan, Bruckert Eric, Catapano Alberico L, Defesche Joep C, Descamps Olivier S, Hegele Robert A, Hovingh G Kees, Humphries Steve E, Kovanen Petri T, Kuivenhoven Jan Albert, Masana Luis, Nordestgaard Børge G, Pajukanta Päivi, Parhofer Klaus G, Raal Frederick J, Ray Kausik K, Santos Raul D, Stalenhoef Anton F H, Steinhagen-Thiessen Elisabeth, Stroes Erik S, Taskinen Marja-Riitta, Tybjærg-Hansen Anne, Wiklund Olov, Wiklund Olov
Familial hypercholesterolaemia in children and adolescents: gaining
decades of life by optimizing detection and treatment
European heart journal,
2015; 36(36):
2425-37.
Nikkola Elina, Laiwalla Azim, Ko Arthur, Alvarez Marcus, Connolly Mark, Ooi Yinn Cher, Hsu William, Bui Alex, Pajukanta Päivi, Gonzalez Nestor R
Remote Ischemic Conditioning Alters Methylation and Expression of Cell
Cycle Genes in Aneurysmal Subarachnoid Hemorrhage
Stroke,
2015; 46(9):
2445-51.
Cuchel Marina, Bruckert Eric, Ginsberg Henry N, Raal Frederick J, Santos Raul D, Hegele Robert A, Kuivenhoven Jan Albert, Nordestgaard Børge G, Descamps Olivier S, Steinhagen-Thiessen Elisabeth, Tybjaerg-Hansen Anne, Watts Gerald F, Averna Maurizio, Boileau Catherine, Borén Jan, Catapano Alberico L, Defesche Joep C, Hovingh G Kees, Humphries Steve E, Kovanen Petri T, Masana Luis, Pajukanta Päivi, Parhofer Klaus G, Ray Kausik K, Stalenhoef Anton F H, Stroes Erik, Taskinen Marja-Riitta, Wiegman Albert, Wiklund Olov, Chapman M John, Chapman M John
[Homozygous familial hypercholesterolaemia: new insights and guidance
for clinicians to improve detection and clinical management. A
position paper from the Consensus Panel on Familial
Hypercholesterolaemia of the European Atherosclerosis Society]
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir,
2015; 43 Suppl 1(9):
1-14.
Ko A, Cantor RM, Weissglas-Volkov D, Nikkola E, Linga Reddy PMV, Sinsheimer JS, Pasaniuc B, Brown R, Alvarez M, Rodriguez A, Rodriguez-Guillen R, Bautista IC, Arellano-Campos O, Muñoz-Hernández LL, Salomaa V, Kaprio J, Jula A, Jauhiainen M, Heliövaara M, Raitakari O, Lehtimäki T, Eriksson JG, Perola M, Lohmueller KE, Matikainen N, Taskinen M-R, Rodriguez-Torres M, Riba L, Tusie-Luna T, Aguilar-Salinas CA, Pajukanta P
Amerindian-specific regions under positive selection harbor new lipid variants in Latinos,
Nature Communications,
2014; (5):
3983.
Almeda-Valdes Paloma, Cuevas-Ramos Daniel, Mehta Roopa, Muñoz-Hernandez Liliana, Cruz-Bautista Ivette, Perez-Mendez Oscar, Tusie-Luna Maria Teresa, Gomez-Perez Francisco J, Pajukanta Päivi, Matikainen Niina, Taskinen Marja-Riitta, Aguilar-Salinas Carlos A
Factors associated with postprandial lipemia and apolipoprotein A-V
levels in individuals with familial combined hyperlipidemia
BMC endocrine disorders,
2014; 14(9):
90.
Cuchel Marina, Bruckert Eric, Ginsberg Henry N, Raal Frederick J, Santos Raul D, Hegele Robert A, Kuivenhoven Jan Albert, Nordestgaard Børge G, Descamps Olivier S, Steinhagen-Thiessen Elisabeth, Tybjærg-Hansen Anne, Watts Gerald F, Averna Maurizio, Boileau Catherine, Borén Jan, Catapano Alberico L, Defesche Joep C, Hovingh G Kees, Humphries Steve E, Kovanen Petri T, Masana Luis, Pajukanta Päivi, Parhofer Klaus G, Ray Kausik K, Stalenhoef Anton F H, Stroes Erik, Taskinen Marja-Riitta, Wiegman Albert, Wiklund Olov, Chapman M John, Chapman M John
Homozygous familial hypercholesterolaemia: new insights and guidance
for clinicians to improve detection and clinical management. A
position paper from the Consensus Panel on Familial
Hypercholesterolaemia of the European Atherosclerosis Society
European heart journal,
2014; 35(32):
2146-57.
Iulia Iatan, Hong Y. Choi, Isabelle Ruel, MV Prasad Linga Reddy, Kil Hyunsuk, Jaeho Lee, Mohammad Abu Odeh, Zaidoun Salah, Muhannad Abu-Remaileh, Daphna Weissglas-Volkov, Elina Nikkola, Mete Civelek, Zuhier Awan, Carlo M. Croce, Rami I. Aqeilan, Päivi Pajukanta, C. Marcelo Aldaz, Jacques Genest
The WW Domain-containing Oxidoreductase Gene Modulates HDL Metabolism and Lipoprotein Gene Expression,
Circulation: Cardiovascular Genetics,
2014; 7:
491-504.
Hegele Robert A, Ginsberg Henry N, Chapman M John, Nordestgaard Børge G, Kuivenhoven Jan Albert, Averna Maurizio, Borén Jan, Bruckert Eric, Catapano Alberico L, Descamps Olivier S, Hovingh G Kees, Humphries Steve E, Kovanen Petri T, Masana Luis, Pajukanta Päivi, Parhofer Klaus G, Raal Frederick J, Ray Kausik K, Santos Raul D, Stalenhoef Anton F H, Stroes Erik, Taskinen Marja-Riitta, Tybjærg-Hansen Anne, Watts Gerald F, Wiklund Olov, Wiklund Olov
The polygenic nature of hypertriglyceridaemia: implications for
definition, diagnosis, and management
The lancet. Diabetes & endocrinology,
2014; 2(8):
655-66.
Mahendran Y, Vangipurapu J, Cederberg H, Stancáková A, Pihlajamäki J, Soininen P, Kangas AJ, Paananen J, Civelek M, Saleem NK, Pajukanta P, Lusis AJ, Bonnycastle LL, Morken MA, Collins FS, Mohlke KL, Boehnke M, Ala-Korpela M, Kuusisto J, Laakso M.
Association of ketone body levels with hyperglycemia and type 2 diabetes in 9,398 Finnish men,
Diabetes,
2013; (62):
3618-3626.
Daphna Weissglas-Volkov, Carlos A. Aguilar-Salinas, Elina Nikkola, Kerry Deere, Ivette Cruz-Bautista, Olimpia Arellano-Campos, Linda Liliana Muñoz-Hernandez, Lizeth Gomez-Munguia, Maria Luisa Ordoñez-Sánchez, Prasad MV Linga Reddy, Aldons J. Lusis, Laura Riba, Rita M. Cantor, Janet S. Sinsheimer, Teresa Tusie-Luna, Päivi Pajukanta
Genome-wide association study in Mexicans identifies a new locus for triglycerides and refines European lipid loci,
Journal of Medical Genetics,
2013; 50:
298-308.
MV Prasad Linga Reddy, Iulia Iatan, Daphna Weissglas-Volkov, Elina Nikkola, Blake E. Haas, Miina Juvonen, Isabelle Ruel, Janet S. Sinsheimer, Jacques Genest, Päivi Pajukanta
Exome sequencing identifies two rare variants for low HDL-C in an extended family,
Circulation: Cardiovascular Genetics. ,
2012; (5):
538-546.
Alena Stancáková, Mete Civelek, Pasi Soininen, Antti J. Kangas, Henna Cederberg, Jussi
Paananen, Jussi Pihlajamäki, Lori L. Bonnycastle, Mario A. Morken, Michael Boehnke, Päivi
Pajukanta, Aldons J. Lusis, Francis S. Collins, Johanna Kuusisto, Mika Ala-Korpela and 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:
1895-1902.
Blake E. Haas, Daphna Weissglas-Volkov, Carlos A. 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:
1201-1207.
Daphna Weisglass-Volkov, Anna C. Calkin, Teresa Tusie-Luna, Janet S. Sinsheimer, Noam Zelcer, Laura Riba, Ana Maria Vargas Tino, Maria Luisa Ordoñez-Sánchez, Ivette Cruz-Bautista, Carlos A. Aguilar-Salinas, Peter Tontonoz and Päivi Pajukanta.
The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL-receptor degradation in humans,
The Journal of Clinical Investigation. ,
2011; 121:
3062-3071.
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 HDL cholesterol and triglycerides levels in Mexican dyslipidemic study samples,
Circulation: Cardiovascular Genetics. ,
2010; 3:
31-38.
Christopher L. 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; Sep;5(9):e1000642.:
.
Christopher L Plaisier, Mira Kyttälä, Daphna Weissglas-Volkov, Janet S. Sinsheimer, Adriana Huertas-Vazquez, Laura Riba, Salvador Ramírez-Jiménez, Tjerk W. A. de Bruin, Teresa Tusié-Luna, Bradley E. Aouizerat, Clive R. Pullinger, Mary J. Malloy, John P. Kane, Ivette Cruz-Bautista, Miguel F. Herrera, Carlos Aguilar-Salinas, Johanna Kuusisto, Markku Laakso, Marja-Riitta Taskinen, Carla J. H. van der Kallen, Päivi Pajukanta
Galanin preproprotein is associated with elevated plasma triglycerides,
Arteriosclerosis Thrombosis and Vascular Biology,
2009; 29:
147-152.
Sinsheimer Janet S, Plaisier Christopher L, Huertas-Vazquez Adriana, Aguilar-Salinas Carlos, Tusie-Luna Teresa, Pajukanta Päivi, Lange Kenneth
Estimating Ethnic Admixture from Pedigree Data.
The American Journal of Human Genetics,
2008; 82(3):
748-55.
Jenny C. Lee, Daphna Weissglas-Volkov, Mira Kyttälä, Zari Dastani, Rita M. Cantor, Eric M. Sobel, Christopher Plaisier, Jamie C. Engert, Marleen M.J. van Greevenbroek, John P. Kane, Mary J. Malloy, Clive R. Pullinger, Adriana Huertaz-Vazquez, Carlos A. Aguilar-Salinas, Teresa Tusie- Luna, Tjerk W. A. de Bruin, Bradley E. Aouizerat, Carla 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,
The American Journal of Human Genetics,
2008; 83:
180-192.
Péterfy M, Ben-Zeev O, Mao HZ, Weissglas-Volkov D, Aouizerat BE, Pullinger CR, Frost PH, Kane JP, Malloy MJ, Reue K, Pajukanta P, Doolittle MH.
Mutations in the novel LMF1 gene cause combined lipase deficiency and severe hypertriglyceridemia. ,
Nature Genetics,
2007; 39:
1483-1487.
Lee JC, Weissglas-Volkov D, Kyttälä M, Sinsheimer JS, Jokiaho A, de Bruin TWA, van Greevenbroek MMJ, Lusis AJ, Brennan M-L, van der Kallen CJH, Hazen SL, Pajukanta P.
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:
2222-2227.
Weissglas-Volkov D, Huertas-Vazquez A, Suviolahti E, Lee J, Plaisier C, Canizales-Quinteros S, Tusie-Luna T, Aguilar-Salinas C, Taskinen M-R, Pajukanta P.
Common hepatic nuclear factor 4 alpha variants are associated with high serum lipid levels and the metabolic syndrome. ,
Diabetes,
2006; 55:
1970-1977.
Huertas-Vazquez, A. Aguilar-Salinas, C. Lusis, A. J. Cantor, R. M. Canizales-Quinteros, S. Lee, J. C. Mariana-Nunez, L. Riba-Ramirez, R. M. Jokiaho, A. Tusie-Luna, T. Pajukanta, P.
Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1
Arterioscler Thromb Vasc Biol,
2005; 25(9):
1985-91.
Pajukanta, P. Lilja, H. E. Sinsheimer, J. S. Cantor, R. M. Lusis, A. J. Gentile, M. Duan, X. J. Soro-Paavonen, A. Naukkarinen, J. Saarela, J. Laakso, M. Ehnholm, C. Taskinen, M. R. Peltonen, L.
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1)
Nat Genet,
2004; 36(4):
371-6.
Pajukanta, P. Allayee, H. Krass, K. L. Kuraishy, A. Soro, A. Lilja, H. E. Mar, R. Taskinen, M. R. Nuotio, I. Laakso, M. Rotter, J. I. de Bruin, T. W. Cantor, R. M. Lusis, A. J. Peltonen, L.
Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q
Am J Hum Genet,
2003; 72(4):
903-17.
Suviolahti, E. Oksanen, L. J. Ohman, M. Cantor, R. M. Ridderstrale, M. Tuomi, T. Kaprio, J. Rissanen, A. Mustajoki, P. Jousilahti, P. Vartiainen, E. Silander, K. Kilpikari, R. Salomaa, V. Groop, L. Kontula, K. Peltonen, L. Pajukanta, P.
The SLC6A14 gene shows evidence of association with obesity
J Clin Invest,
2003; 112(11):
1762-72.
Soro, A. Pajukanta, P. Lilja, H. E. Ylitalo, K. Hiekkalinna, T. Perola, M. Cantor, R. M. Viikari, J. S. Taskinen, M. R. Peltonen, L.
Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families
Am J Hum Genet,
2002; 70(5):
1333-40.
Pajukanta, P. Cargill, M. Viitanen, L. Nuotio, I. Kareinen, A. Perola, M. Terwilliger, J. D. Kempas, E. Daly, M. Lilja, H. Rioux, J. D. Brettin, T. Viikari, J. S. Ronnemaa, T. Laakso, M. Lander, E. S. Peltonen, L.
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
Am J Hum Genet,
2000; 67(6):
1481-93.
Pajukanta, P. Terwilliger, J. D. Perola, M. Hiekkalinna, T. Nuotio, I. Ellonen, P. Parkkonen, M. Hartiala, J. Ylitalo, K. Pihlajamaki, J. Porkka, K. Laakso, M. Viikari, J. Ehnholm, C. Taskinen, M. R. Peltonen, L.
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
Am J Hum Genet,
1999; 64(5):
1453-63.
Pajukanta, P. Nuotio, I. Terwilliger, J. D. Porkka, K. V. Ylitalo, K. Pihlajamaki, J. Suomalainen, A. J. Syvanen, A. C. Lehtimaki, T. Viikari, J. S. Laakso, M. Taskinen, M. R. Ehnholm, C. Peltonen, L.
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
Nat Genet,
1998; 18(4):
369-73.