FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Päivi Holopainen

Research Profile

Disorders

Chemicals & Drugs

Physiology

Geographic Areas

Finland

Anatomy

Chromosomes, Human, Pair 2

Concepts & Ideas

Co-author Network

Publications

TOP 3
Sari Suomela; Kati Kainu; Päivi Onkamo; Inkeri Tiala; Johan Himberg; Lotta Koskinen; Erna Snellman; Seija-Liisa Karvonen; Juha T Karvonen; Tutta Uurasmaa; Timo Reunala; Kristiina Kivikäs; Christer T Jansén; Päivi Holopainen; Outi Elomaa; Juha Kere; Ulpu Saarialho-Kere
Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.
Johanna Vendelin; Sara Bruce; Päivi Holopainen; Ville Pulkkinen; Paula Rytilä; Asta Pirskanen; Marko Rehn; Tarja Laitinen; Lauri A Laitinen; Tari Haahtela; Ulpu Saarialho-Kere; Annika Laitinen; Juha Kere
Downstream target genes of the neuropeptide S-NPSR1 pathway.
Ville Pulkkinen; Marja-Leena Majuri; Guoying Wang; Päivi Holopainen; Yasushi Obase; Johanna Vendelin; Henrik Wolff; Paula Rytilä; Lauri A Laitinen; Tari Haahtela; Tarja Laitinen; Harri Alenius; Juha Kere; Marko Rehn
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Päivi Holopainen (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2007: Sari Suomela; Kati Kainu; Päivi Onkamo; Inkeri Tiala; Johan Himberg; Lotta Koskinen; Erna Snellman; Seija-Liisa Karvonen; Juha T Karvonen; Tutta Uurasmaa; Timo Reunala; Kristiina Kivikäs; Christer T Jansén; Päivi Holopainen; Outi Elomaa; Juha Kere; Ulpu Saarialho-Kere
Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.
Acta dermato-venereologica 2007;87(2):127-34.
2006: Johanna Vendelin; Sara Bruce; Päivi Holopainen; Ville Pulkkinen; Paula Rytilä; Asta Pirskanen; Marko Rehn; Tarja Laitinen; Lauri A Laitinen; Tari Haahtela; Ulpu Saarialho-Kere; Annika Laitinen; Juha Kere
Downstream target genes of the neuropeptide S-NPSR1 pathway.
Human molecular genetics 2006;15(19):2923-35.
2006: Ville Pulkkinen; Marja-Leena Majuri; Guoying Wang; Päivi Holopainen; Yasushi Obase; Johanna Vendelin; Henrik Wolff; Paula Rytilä; Lauri A Laitinen; Tari Haahtela; Tarja Laitinen; Harri Alenius; Juha Kere; Marko Rehn
Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.
Human molecular genetics 2006;15(10):1667-79.
2004: Päivi Holopainen; Åsa Torinsson Naluai; Simon J Moodie; Selvaggia Percopo; Iolanda Coto; Fabienne Clot; Henry Ascher; Ludvig M Sollid; Paul J Ciclitira; Luigi Greco; Françoise Clerget-Darpoux; Jukka Partanen
Candidate gene region 2q33 in European families with coeliac disease.
Tissue antigens 2004;63(3):212-22.
2004: K Haimila; T Smedberg; Kirsi Mustalahti; Markku Mäki; Jukka Partanen; Päivi Holopainen
Genetic association of coeliac disease susceptibility to polymorphisms in the ICOS gene on chromosome 2q33.
Genes and immunity 2004;5(2):85-92.
2002: Kirsi Mustalahti; Päivi Holopainen; Kati Karell; Markku Mäki; Jukka Partanen
Genetic dissection between silent and clinically diagnosed symptomatic forms of coeliac disease in multiplex families.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2002;34(12):842-5.
2002: Kati Karell; Ilma Korponay-Szabo; Zs Szalai; Päivi Holopainen; Kirsi Mustalahti; Pekka Collin; Markku Mäki; Jukka Partanen
Genetic dissection between coeliac disease and dermatitis herpetiformis in sib pairs.
Annals of human genetics 2002;66(Pt 5-6):387-92.
2002: Nina Woolley; Päivi Holopainen; Catherine Bourgain; Kirsi Mustalahti; Pekka Collin; Markku Mäki; Jukka Partanen
CD80 (B7-1) and CD86 (B7-2) genes and genetic susceptibility to coeliac disease.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 2002;29(4):331-3.
2002: Nina Woolley; Päivi Holopainen; Vesa Ollikainen; Kirsi Mustalahti; Markku Mäki; Juha Kere; Jukka Partanen
A new locus for coeliac disease mapped to chromosome 15 in a population isolate.
Human genetics 2002;111(1):40-5.
2002: Katri E Haimila; Jukka Partanen; Päivi Holopainen
Genetic polymorphism of the human ICOS gene.
Immunogenetics 2002;53(12):1028-32.
2002: Kirsi Mustalahti; Satu Sulkanen; Päivi Holopainen; Kaija Laurila; Pekka Collin; Jukka Partanen; Markku Mäki
Coeliac disease among healthy members of multiple case coeliac disease families.
Scandinavian journal of gastroenterology 2002;37(2):161-5.
2002: Kati Karell; Päivi Holopainen; Kirsi Mustalahti; Pekka Collin; Markku Mäki; Jukka Partanen
Not all HLA DR3 DQ2 haplotypes confer equal susceptibility to coeliac disease: transmission analysis in families.
Scandinavian journal of gastroenterology 2002;37(1):56-61.
2002: Jianjun Liu; Suh-Hang Hank Juo; Päivi Holopainen; Joseph D Terwilliger; Xiaomei Tong; Adina Grunn; Miguel Brito; Peter Green; Kirsi Mustalahti; Markku Mäki; T Conrad Gilliam; Jukka Partanen
Genomewide linkage analysis of celiac disease in Finnish families.
American journal of human genetics 2002;70(1):51-9.
2001: Päivi Holopainen; Jukka Partanen
Technical note: linkage disequilibrium and disease-associated CTLA4 gene polymorphisms.
Journal of immunology (Baltimore, Md. : 1950) 2001;167(5):2457-8.
2001: Päivi Holopainen; Kirsi Mustalahti; P Uimari; Pekka Collin; Markku Mäki; Jukka Partanen
Candidate gene regions and genetic heterogeneity in gluten sensitivity.
Gut 2001;48(5):696-701.
2001: M Susi; Päivi Holopainen; Kirsi Mustalahti; Markku Mäki; J Partanen
Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families.
Scandinavian journal of gastroenterology 2001;36(4):372-4.
2001: Catherine Bourgain; Emmanuelle Génin; Päivi Holopainen; Kirsi Mustalahti; Markku Mäki; Jukka Partanen; Françoise Clerget-Darpoux
Use of closely related affected individuals for the genetic study of complex diseases in founder populations.
American journal of human genetics 2001;68(1):154-159.
2000: K Hervonen; Kati Karell; Päivi Holopainen; Pekka Collin; Jukka Partanen; Timo Reunala
Concordance of dermatitis herpetiformis and celiac disease in monozygous twins.
The Journal of investigative dermatology 2000;115(6):990-3.
2000: Antti Levo; K Kuismanen; P Holopainen; Elina Vahtera; Vesa Rasi; Päivi Holopainen; V Rasi; Tom Krusius; Jukka Partanen
Single founder mutation (W380G) in type II protein C deficiency in Finland.
Thrombosis and haemostasis 2000;84(3):424-8.
2000: Kati Karell; N Klinger; Päivi Holopainen; Antti Levo; Jukka Partanen
Major histocompatibility complex (MHC)-linked microsatellite markers in a founder population.
Tissue antigens 2000;56(1):45-51.
1999: Päivi Holopainen; Mikko Arvas; P Sistonen; Kirsi Mustalahti; Pekka Collin; Markku Mäki; Jukka Partanen
CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study.
Tissue antigens 1999;53(5):470-5.