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Päivi Lahermo

Research Profile

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Physiology

Genes & Molecular Sequences

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V Holmberg; Päivi Lahermo; Elisa Lahtela; Frank P Mockenhaupt; Päivi Onkamo; George Bedu-Addo; Seppo Meri
Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria.
Taina T Nieminen; Ari Ristimäki; Wael M Abdel-Rahman; Heikki J Järvinen; Päivi Lahermo; Maarit Lappalainen; Jukka-Pekka Mecklin; Päivi Peltomäki
BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.
Maria Sandbacka; Marita Lipsanen-Nyman; Minna Puhakka; Kristiina Aittomäki; Sara Bruce; Mervi Halttunen; Katariina Hannula-Jouppi; Juha Kere; Päivi Lahermo; Hannele Laivuori
Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia.

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All Publications

2012: V Holmberg; Päivi Lahermo; Elisa Lahtela; Frank P Mockenhaupt; Päivi Onkamo; George Bedu-Addo; Seppo Meri
Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria.
Malaria journal 2012;11():61.
2011: Taina T Nieminen; Ari Ristimäki; Wael M Abdel-Rahman; Heikki J Järvinen; Päivi Lahermo; Maarit Lappalainen; Jukka-Pekka Mecklin; Päivi Peltomäki
BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.
Gastroenterology 2011;141(1):e23-6.
2011: Maria Sandbacka; Marita Lipsanen-Nyman; Minna Puhakka; Kristiina Aittomäki; Sara Bruce; Mervi Halttunen; Katariina Hannula-Jouppi; Juha Kere; Päivi Lahermo; Hannele Laivuori
Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia.
Fertility and sterility 2011;95(8):2703-6.
2011: Elina Salmela; Tuuli Lappalainen; Jianjun Liu; Pertti Sistonen; Peter M Andersen; Stefan Schreiber; Marja-Liisa Savontaus; Kamila Czene; Päivi Lahermo; Per Hall; Juha Kere
Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.
PloS one 2011;6(2):e16747.
2010: Tuuli Lappalainen; Elina Salmela; Peter M Andersen; Karin Dahlman-Wright; Pertti Sistonen; Marja-Liisa Savontaus; Stefan Schreiber; Päivi Lahermo; Juha Kere
Genomic landscape of positive natural selection in Northern European populations.
European journal of human genetics : EJHG 2010;18(4):471-8.
2010: Johannes Kettunen; Kaisa Silander; Olli Saarela; Najaf Amin; Martina Müller; Nicholas Timpson; Ida Surakka; Samuli Ripatti; Jaana Laitinen; Anna-Liisa Hartikainen; Anneli Pouta; Päivi Lahermo; Verneri Anttila; Satu Männistö; Antti Jula; Jarmo Virtamo; Veikko Salomaa; Terho Lehtimäki; Olli Raitakari; Christian Gieger; Erich H Wichmann; Cornelia M Van Duijn; George Davey Smith; Mark I McCarthy; Marjo-Riitta Järvelin; Markus Perola; Leena Peltonen
European lactase persistence genotype shows evidence of association with increase in body mass index.
Human molecular genetics 2010;19(6):1129-36.
2009: Liisa Tomppo; William Hennah; Päivi Lahermo; Anu Loukola; Annamari Tuulio-Henriksson; Jaana Suvisaari; Timo Partonen; Jesper Ekelund; Jouko Lönnqvist; Leena Peltonen
Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.
Biological psychiatry 2009;65(12):1055-62.
2009: A Marjamaa; Christopher Newton-Cheh; K Porthan; Antti Reunanen; Päivi Lahermo; Heikki Väänänen; Antti Jula; H Karanko; H Swan; Lauri Toivonen; Markku S Nieminen; Matti Viitasalo; Leena Peltonen; L Oikarinen; Aarno Palotie; Kimmo Kontula; Veikko Salomaa
Common candidate gene variants are associated with QT interval duration in the general population.
Journal of internal medicine 2009;265(4):448-58.
2009: Liisa Tomppo; William Hennah; Jouko Miettunen; Marjo-Riitta Järvelin; Juha Veijola; Samuli Ripatti; Päivi Lahermo; Dirk Lichtermann; Leena Peltonen; Jesper Ekelund
Association of variants in DISC1 with psychosis-related traits in a large population cohort.
Archives of general psychiatry 2009;66(2):134-41.
2009: Annukka Marjamaa; Veikko Salomaa; Christopher Newton-Cheh; Kimmo Porthan; Antti Reunanen; Hannu Karanko; Antti Jula; Päivi Lahermo; Heikki Väänänen; Lauri Toivonen; Heikki Swan; Matti Viitasalo; Markku S Nieminen; Leena Peltonen; Lasse Oikarinen; Aarno Palotie; Kimmo Kontula
High prevalence of four long QT syndrome founder mutations in the Finnish population.
Annals of medicine 2009;41(3):234-40.
2009: T Lappalainen; Ulf Hannelius; Elina Salmela; U von Döbeln; Cecilia M Lindgren; Kirsi Huoponen; Marja-Liisa Savontaus; Juha Kere; Päivi Lahermo
Population structure in contemporary Sweden--a Y-chromosomal and mitochondrial DNA analysis.
Annals of human genetics 2009;73(1):61-73.
2008: T Lappalainen; V Laitinen; Elina Salmela; P Andersen; Kirsi Huoponen; Marja-Liisa Savontaus; Päivi Lahermo
Migration waves to the Baltic Sea region.
Annals of human genetics 2008;72(Pt 3):337-48.
2008: Elina Salmela; Tuuli Lappalainen; Ingegerd Fransson; Peter M Andersen; Karin Dahlman-Wright; Andreas Fiebig; Pertti Sistonen; Marja-Liisa Savontaus; Stefan Schreiber; Juha Kere; Päivi Lahermo
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.
PloS one 2008;3(10):e3519.
2008: Ulf Hannelius; Elina Salmela; Tuuli Lappalainen; Gilles Guillot; Cecilia M Lindgren; Ulrika von Döbeln; Päivi Lahermo; Juha Kere
Population substructure in Finland and Sweden revealed by the use of spatial coordinates and a small number of unlinked autosomal SNPs.
BMC genetics 2008;9():54.
2006: Tuuli Lappalainen; Satu Koivumäki; Elina Salmela; Kirsi Huoponen; Pertti Sistonen; Marja-Liisa Savontaus; Päivi Lahermo
Regional differences among the Finns: a Y-chromosomal perspective.
Gene 2006;376(2):207-15.
2006: Päivi Lahermo; Ulrika Liljedahl; Grethe Alnaes; Tomas Axelsson; Anthony J Brookes; Pekka Ellonen; Per-Henrik Groop; Christer Halldén; Dan Holmberg; Kristina Holmberg; Mauri Keinänen; Katrin Kepp; Juha Kere; Päivi Kiviluoma; Vessela N Kristensen; Cecilia Lindgren; Jacob Odeberg; Pia Osterman; Maija Parkkonen; Janna Saarela; Maria Sterner; Linda Strömqvist; Ulvi Talas; Maija Wessman; Aarno Palotie; Ann-Christine Syvänen
A quality assessment survey of SNP genotyping laboratories.
Human mutation 2006;27(7):711-4.
2006: Ulla Hodgson; Ville Pulkkinen; Morag Dixon; Myriam Peyrard-Janvid; Marko Rehn; Päivi Lahermo; Vesa Ollikainen; Kaisa Salmenkivi; Vuokko Kinnula; Juha Kere; Pentti Tukiainen; Tarja Laitinen
ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.
American journal of human genetics 2006;79(1):149-54.
2006: Elina Salmela; O Taskinen; Jouni K Seppänen; Pertti Sistonen; M J Daly; Päivi Lahermo; Marja-Liisa Savontaus; Juha Kere
Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.
Journal of medical genetics 2006;43(7):590-7.
2005: Hannele Koillinen; Päivi Lahermo; Jorma Rautio; Jyri Hukki; Myriam Peyrard-Janvid; Juha Kere
A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.
Journal of medical genetics 2005;42(2):177-84.
2004: Laura Lammi; Sirpa Arte; Mirja Somer; Heikki Jarvinen; Päivi Lahermo; Irma Thesleff; Sinikka Pirinen; Pekka Nieminen
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.
American journal of human genetics 2004;74(5):1043-50.
2004: Myriam Peyrard-Janvid; Heidi Anthoni; Päivi Onkamo; Päivi Lahermo; Marco Zucchelli; Nina Kaminen; Katariina Hannula-Jouppi; Jaana Nopola-Hemmi; Arja Voutilainen; Heikki Lyytinen; Juha Kere
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Human genetics 2004;114(5):510-6.
2004: Sari Koskenmies; Päivi Lahermo; Heikki Julkunen; Vesa Ollikainen; Juha Kere; Elisabeth Widén
Linkage mapping of systemic lupus erythematosus (SLE) in Finnish families multiply affected by SLE.
Journal of medical genetics 2004;41(1):e2-5.
2003: Kati Asumalahti; Tarja Laitinen; Päivi Lahermo; Sari Suomela; Raija Itkonen-Vatjus; Christer Jansen; Juha T Karvonen; Seija-Liisa Karvonen; Timo Reunala; Erna Snellman; Tutta Uurasmaa; Ulpu Saarialho-Kere; Juha Kere
Psoriasis susceptibility locus on 18p revealed by genome scan in Finnish families not associated with PSORS1.
The Journal of investigative dermatology 2003;121(4):735-40.
2003: Nina Kaminen; Katariina Hannula-Jouppi; Marjo Kestilä; Päivi Lahermo; K Muller; M Kaaranen; Birgitta Myllyluoma; Arja Voutilainen; Heikki Lyytinen; Jaana Nopola-Hemmi; Juha Kere
A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32.
Journal of medical genetics 2003;40(5):340-5.
2003: Paulina Paavola-Sakki; Vesa Ollikainen; Tiina Heliö; Leena Halme; Ulla Turunen; Päivi Lahermo; Maija Lappalainen; Markus Färkkilä; Kimmo Kontula
Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility loci.
European journal of human genetics : EJHG 2003;11(2):112-20.
2003: Hannele Laivuori; Päivi Lahermo; Vesa Ollikainen; Elisabeth Widen; Leena Häivä-Mällinen; Helena Sundström; Tarja Laitinen; Risto Kaaja; Olavi Ylikorkala; Juha Kere
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families.
American journal of human genetics 2003;72(1):168-77.
2002: Niina Paunu; Päivi Lahermo; Päivi Onkamo; Vesa Ollikainen; Immo Rantala; Pauli Helén; Kalle O J Simola; Juha Kere; Hannu Haapasalo
A novel low-penetrance locus for familial glioma at 15q23-q26.3.
Cancer research 2002;62(13):3798-802.
2002: Päivi Laiho; Virpi Launonen; Päivi Lahermo; Manel Esteller; Mingzhou Guo; James G Herman; Jukka-Pekka Mecklin; Heikki Järvinen; Pertti Sistonen; Kyoung-Mee Kim; Darryl Shibata; richard Houlston; Lauri A Aaltonen
Low-level microsatellite instability in most colorectal carcinomas.
Cancer research 2002;62(4):1166-70.
2002: Virpi Laitinen; Päivi Lahermo; Pertti Sistonen; Marja-Liisa Savontaus
Y-chromosomal diversity suggests that Baltic males share common Finno-Ugric-speaking forefathers.
Human heredity 2002;53(2):68-78.
2001: Hannele Koillinen; FK Wong; Jorma Rautio; Vesa Ollikainen; Agneta Karsten; Ola Larson; Bin Tean Teh; Jan Huggare; Päivi Lahermo; Catharina Larsson; Juha Kere
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
European journal of human genetics : EJHG 2001;9(10):747-52.
2001: Hans-Jürgen Bandelt; Päivi Lahermo; M Richards; Vincent Macaulay
Detecting errors in mtDNA data by phylogenetic analysis.
International journal of legal medicine 2001;115(2):64-9.
2000: Päivi Lahermo; V Laitinen; Pertti Sistonen; J Béres; Veronika Karcagi; Marja-Liisa Savontaus
MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populations.
Hereditas 2000;132(1):35-42.
1999: Päivi Lahermo; Marja-Liisa Savontaus; Pertti Sistonen; J Béres; P de Knijff; Pertti Aula; Antti Sajantila
Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami.
European journal of human genetics : EJHG 1999;7(4):447-58.
1998: Antonio Torroni; Hans-Jürgen Bandelt; L D'Urbano; Päivi Lahermo; Pedro Moral; Daniele Sellitto; Chiara Rengo; Peter Forster; Marja-Liisa Savontaus; B Bonné-Tamir; Rosaria Scozzari
mtDNA analysis reveals a major late Paleolithic population expansion from southwestern to northeastern Europe.
American journal of human genetics 1998;62(5):1137-52.
1997: Tarja Lamminen; Kirsi Huoponen; Pertti Sistonen; Vesa Juvonen; Päivi Lahermo; Pertti Aula; Eeva Nikoskelainen; Marja-Liisa Savontaus
mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.
European journal of human genetics : EJHG 1997;5(5):271-9.
1996: Päivi Lahermo; Antti Sajantila; Pertti Sistonen; M Lukka; Pertti Aula; Leena Peltonen; Marja-Liisa Savontaus
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.
American journal of human genetics 1996;58(6):1309-22.
1995: Antti Sajantila; Päivi Lahermo; T Anttinen; M Lukka; P Sistonen; M L Savontaus; P Aula; L Beckman; L Tranebjaerg; T Gedde-Dahl; L Issel-Tarver; A DiRienzo; S Pääbo
Genes and languages in Europe: an analysis of mitochondrial lineages.
Genome research 1995;5(1):42-52.