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Pertti Sistonen

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Finland

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Founder Effect

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Genetics, Population

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A S Parmar; Jukka Partanen; P Saavalainen; Pertti Sistonen; Ulla Turunen; P Wacklin; Noora Alakulppi; Markus Färkkilä; Leena Halme; Katri Kaukinen; Kimmo Kontula; K Kurppa; Maija Lappalainen; Katri Lindfors; Markku Mäki; Jaana Mättö; Paulina Paavola-Sakki; E Einarsdottir
Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population.
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.
L L E Koskinen; E Einarsdottir; Ilma Korponay-Szabo; K Kurppa; Katri Kaukinen; Pertti Sistonen; Zsuzsa Pocsai; G Széles; Róza Adány; Markku Mäki; Juha Kere; P Saavalainen
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.

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All Publications

2012: A S Parmar; Jukka Partanen; P Saavalainen; Pertti Sistonen; Ulla Turunen; P Wacklin; Noora Alakulppi; Markus Färkkilä; Leena Halme; Katri Kaukinen; Kimmo Kontula; K Kurppa; Maija Lappalainen; Katri Lindfors; Markku Mäki; Jaana Mättö; Paulina Paavola-Sakki; E Einarsdottir
Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population.
Tissue antigens 2012;80(6):488-93.
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.
2009: L L E Koskinen; E Einarsdottir; Ilma Korponay-Szabo; K Kurppa; Katri Kaukinen; Pertti Sistonen; Zsuzsa Pocsai; G Széles; Róza Adány; Markku Mäki; Juha Kere; P Saavalainen
Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.
Tissue antigens 2009;74(5):408-16.
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.
2007: Mia Hedman; A Brandstätter; Ville Pimenoff; Pertti Sistonen; Jukka U Palo; W Parson; Antti Sajantila
Finnish mitochondrial DNA HVS-I and HVS-II population data.
Forensic science international 2007;172(2-3):171-8.
2007: Susanna Lemmelä; Eva Forsman; Pertti Sistonen; Aldur Eriksson; Henrik Forsius; Irma Järvelä
Genome-wide scan of exfoliation syndrome.
Investigative ophthalmology & visual science 2007;48(9):4136-42.
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: 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.
2006: S Sigurdsson; Mia Hedman; Pertti Sistonen; A Sajantila; Ann-Christine Syvänen
A microarray system for genotyping 150 single nucleotide polymorphisms in the coding region of human mitochondrial DNA.
Genomics 2006;87(4):534-42.
2004: Kati Mykkänen; Marja-Liisa Savontaus; Vesa Juvonen; Pertti Sistonen; Seppo Tuisku; Susanna Tuominen; Maila Penttinen; Johan Lundkvist; Matti Viitanen; Hannu Kalimo; Minna Pöyhönen
Detection of the founder effect in Finnish CADASIL families.
European journal of human genetics : EJHG 2004;12(10):813-9.
2004: Jodie N Painter; Miia Savander; Pertti Sistonen; Anna-Elina Lehesjoki; Kristiina Aittomäki
A known polymorphism in the bile salt export pump gene is not a risk allele for intrahepatic cholestasis of pregnancy.
Scandinavian journal of gastroenterology 2004;39(7):694-5.
2004: Mia Hedman; Ville Pimenoff; M Lukka; Pertti Sistonen; Antti Sajantila
Analysis of 16 Y STR loci in the Finnish population reveals a local reduction in the diversity of male lineages.
Forensic science international 2004;142(1):37-43.
2003: Tuija Hienonen; Päivi Laiho; Reijo Salovaara; Jukka-Pekka Mecklin; Heikki Järvinen; Pertti Sistonen; Päivi Peltomäki; Rainer Lehtonen; Nina N Nupponen; Virpi Launonen; Auli Karhu; Lauri A Aaltonen
Little evidence for involvement of MLH3 in colorectal cancer predisposition.
International journal of cancer. Journal international du cancer 2003;106(2):292-6.
2002: Susa Vilkki; Virpi Launonen; Auli Karhu; Pertti Sistonen; I Västrik; Lauri A Aaltonen
Screening for microsatellite instability target genes in colorectal cancers.
Journal of medical genetics 2002;39(11):785-9.
2002: Maaret Ridanpää; Pertti Sistonen; Susanna Rockas; David L Rimoin; Outi Mäkitie; Ilkka Kaitila
Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.
European journal of human genetics : EJHG 2002;10(7):439-47.
2002: Reijo Salovaara; S Roth; Anu Loukola; Virpi Launonen; Pertti Sistonen; E Avizienyte; Paula Kristo; Heikki Järvinen; S Souchelnytskyi; Maarit Sarlomo-Rikala; Lauri A Aaltonen
Frequent loss of SMAD4/DPC4 protein in colorectal cancers.
Gut 2002;51(1):56-9.
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: Maija Kiuru; Virpi Launonen; Marja Hietala; Kristiina Aittomäki; Outi Vierimaa; Reijo Salovaara; Johanna Arola; Eero Pukkala; Pertti Sistonen; Riitta Herva; Lauri A Aaltonen
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology.
The American journal of pathology 2001;159(3):825-9.
2001: Virpi Launonen; Outi Vierimaa; Maija Kiuru; Jorma Isola; S Roth; Eero Pukkala; Pertti Sistonen; Riitta Herva; Lauri A Aaltonen
Inherited susceptibility to uterine leiomyomas and renal cell cancer.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(6):3387-92.
2001: M Raitio; Katarina Lindroos; M Laukkanen; Tomi Pastinen; Pertti Sistonen; Antti Sajantila; Ann-Christine Syvänen
Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.
Genome research 2001;11(3):471-82.
2000: Jenni Jonasson; Vesa Juvonen; Pertti Sistonen; Jaakko Ignatius; D Johansson; E J Björck; J Wahlström; A Melberg; Gösta Holmgren; Lars Forsgren; Monica Holmberg
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
European journal of human genetics : EJHG 2000;8(12):918-22.
2000: Annastiina Lund; Bjarne Udd; Vesa Juvonen; Peter M Andersen; K Cederquist; LO Ronnevi; Pertti Sistonen; S A Sörensen; Lisbeth Tranebjaerg; Carina Wallgren-Pettersson; Marja-Liisa Savontaus
Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.
European journal of human genetics : EJHG 2000;8(8):631-6.
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: S Roth; Pertti Sistonen; Reijo Salovaara; Akseli Hemminki; Anu Loukola; M Johansson; E Avizienyte; K A Cleary; P Lynch; C I Amos; Paula Kristo; Jukka-Pekka Mecklin; Ilmo Kellokumpu; Heikki Järvinen; Lauri A Aaltonen
SMAD genes in juvenile polyposis.
Genes, chromosomes & cancer 1999;26(1):54-61.
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.
1999: Antti Ylikorkala; E Avizienyte; Ian P M Tomlinson; Marjaana Tiainen; S Roth; Anu Loukola; Akseli Hemminki; M Johansson; Pertti Sistonen; D Markie; Kay Neale; Robin Phillips; P Zauber; T Twama; J Sampson; Heikki Järvinen; Tomi Mäkelä; Lauri A Aaltonen
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
Human molecular genetics 1999;8(1):45-51.
1998: Anu-Liisa Moisio; Pertti Sistonen; Jukka-Pekka Mecklin; Heikki Järvinen; Päivi Peltomäki
Genetic polymorphisms in carcinogen metabolism and their association to hereditary nonpolyposis colon cancer.
Gastroenterology 1998;115(6):1387-94.
1998: M Wolf; Akseli Hemminki; Aarne Kivioja; Pertti Sistonen; Ilkka Kaitila; H Ervasti; Jaakko Kinnunen; Erkki O Karaharju; Sakari Knuutila
A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. Online.
Human mutation 1998;12(5):362.
1997: Deborah J Marsh; S Roth; Kathryn L Lunetta; Akseli Hemminki; Patricia Dahia; Pertti Sistonen; Z Zheng; S Caron; Nathalie J van Orsouw; Walter F Bodmer; SE Cottrell; Malcolm G Dunlop; Diana Eccles; Shirley V Hodgson; Heikki Järvinen; Ilmo Kellokumpu; D Markie; Kay Neale; Robin Phillips; P Rozen; Sapna Syngal; Jan Vijg; Ian P M Tomlinson; Lauri A Aaltonen; Charis Eng
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
Cancer research 1997;57(22):5017-21.
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.
1997: T Lauteala; Pertti Sistonen; Marja-Liisa Savontaus; Juha Mykkänen; J Simell; Mari Lukkarinen; Olli Simell; Pertti Aula
Lysinuric protein intolerance (LPI) gene maps to the long arm of chromosome 14.
American journal of human genetics 1997;60(6):1479-86.
1997: Kristiina Avela; Marita Lipsanen-Nyman; Jaakko Perheentupa; Carina Wallgren-Pettersson; Sylvie Marchand; S Fauré; Pertti Sistonen; Albert de La Chapelle; Anna-Elina Lehesjoki
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis.
American journal of human genetics 1997;60(4):896-902.
1997: T Sulisalo; Outi Mäkitie; Pertti Sistonen; Maaret Ridanpää; Wa'el El-Rifai; O Ruuskanen; Albert de La Chapelle; Ilkka Kaitila
Uniparental disomy in cartilage-hair hypoplasia.
European journal of human genetics : EJHG 1997;5(1):35-42.
1997: Akseli Hemminki; Ian Tomlinson; D Markie; Heikki Järvinen; Pertti Sistonen; AM Björkqvist; Sakari Knuutila; Reijo Salovaara; Walter Bodmer; D Shibata; Albert de La Chapelle; Lauri A Aaltonen
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis.
Nature genetics 1997;15(1):87-90.
1996: T Joensuu; G Blanco; L Pakarinen; Pertti Sistonen; Helena Kääriäinen; S Brown; A Chapelle; Eeva-Marja Sankila
Refined mapping of the Usher syndrome type III locus on chromosome 3, exclusion of candidate genes, and identification of the putative mouse homologous region.
Genomics 1996;38(3):255-63.
1996: Anu-Liisa Moisio; Pertti Sistonen; J Weissenbach; Albert de La Chapelle; Päivi Peltomäki
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer.
American journal of human genetics 1996;59(6):1243-51.
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.
1996: Kimmo Virtaneva; J Miao; A L Träskelin; N Stone; J A Warrington; J Weissenbach; Richard Myers; D R Cox; Pertti Sistonen; Albert de La Chapelle
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q.
American journal of human genetics 1996;58(6):1247-53.
1996: J Schleutker; Pertti Sistonen; Pertti Aula
Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease.
Journal of medical genetics 1996;33(1):36-41.
1995: Esa Tahvanainen; Henrik Forsius; M Damsten; E Karila; J Kolehmainen; J Weissenbach; Pertti Sistonen; Albert de La Chapelle
Linkage disequilibrium mapping of the cornea plana congenita gene CNA2.
Genomics 1995;30(3):409-14.
1995: Kristiina Aittomäki; J L Lucena; Pirjo Pakarinen; Pertti Sistonen; Juha S Tapanainen; J Gromoll; R Kaskikari; Eeva-Marja Sankila; H Lehväslaiho; A R Engel; E Nieschlag; Ilpo Huhtaniemi; Albert de La Chapelle
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure.
Cell 1995;82(6):959-68.
1995: Pia Höglund; Pertti Sistonen; Reijo Norio; Christer Holmberg; A Dimberg; Karl-Henrik Gustavson; Albert de La Chapelle; Juha Kere
Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.
American journal of human genetics 1995;57(1):95-102.
1995: Esa Tahvanainen; Henrik Forsius; E Karila; Sirpa Ranta; M Eerola; J Weissenbach; Pertti Sistonen; Albert de La Chapelle
Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis.
Genomics 1995;26(2):290-3.
1995: T Sulisalo; I van der Burgt; D L Rimoin; J Bonaventure; D Sillence; J B Campbell; D Chitayat; C I Scott; Albert de La Chapelle; Pertti Sistonen
Genetic homogeneity of cartilage-hair hypoplasia.
Human genetics 1995;95(2):157-60.
1995: Eeva-Marja Sankila; L Pakarinen; Helena Kääriäinen; Kristiina Aittomäki; S Karjalainen; Pertti Sistonen; Albert de La Chapelle
Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.
Human molecular genetics 1995;4(1):93-8.
1994: T Sulisalo; J Klockars; Outi Mäkitie; Clair A Francomano; Albert de La Chapelle; Ilkka Kaitila; Pertti Sistonen
High-resolution linkage-disequilibrium mapping of the cartilage-hair hypoplasia gene.
American journal of human genetics 1994;55(5):937-45.
1994: F S Leach; N C Nicolaides; Pertti Sistonen; J W Yu; F T Kao; ALBERT DE LA CHAPELLE; Kenneth W Kinzler; Bert Vogelstein
Three dinucleotide repeat polymorphisms proximal to the D2S123 locus.
Human molecular genetics 1994;3(11):2082.
1994: Minna Nyström-Lahti; R Parsons; Pertti Sistonen; Liisa Pylkkänen; Lauri A Aaltonen; F S Leach; Stanley R Hamilton; P Watson; E Bronson; R Fusaro
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.
American journal of human genetics 1994;55(4):659-65.
1994: Henry T Lynch; T Drouhard; Stephen J Lanspa; Thomas C Smyrk; P Lynch; J Lynch; Bert Vogelstein; Minna Nyström-Lahti; Pertti Sistonen; Päivi Peltomäki
Mutation of an mutL homologue in a Navajo family with hereditary nonpolyposis colorectal cancer.
Journal of the National Cancer Institute 1994;86(18):1417-9.
1994: Antti Sajantila; P Pacek; M Lukka; Ann-Christine Syvänen; P Nokelainen; Pertti Sistonen; Leena Peltonen; B Budowle
A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine.
Forensic science international 1994;68(2):91-102.
1994: Jin Jen; H Kim; Steven Piantadosi; Z F Liu; Roy Levitt; Pertti Sistonen; Kenneth W Kinzler; Bert Vogelstein; Stanley R Hamilton
Allelic loss of chromosome 18q and prognosis in colorectal cancer.
The New England journal of medicine 1994;331(4):213-21.
1994: Esa Tahvanainen; Sirpa Ranta; Aune Hirvasniemi; E Karila; Jaakko Leisti; Pertti Sistonen; J Weissenbach; Anna-Elina Lehesjoki; Albert de La Chapelle
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(15):7267-70.
1994: Minna Nyström-Lahti; Pertti Sistonen; Jukka-Pekka Mecklin; Liisa Pylkkänen; Lauri A Aaltonen; Heikki Järvinen; J Weissenbach; Albert de La Chapelle; Päivi Peltomäki
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer families.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(13):6054-8.
1994: Esa Tahvanainen; Reijo Norio; E Karila; Sirpa Ranta; J Weissenbach; Pertti Sistonen; Albert de La Chapelle
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.
Nature genetics 1994;7(2):201-4.
1994: T Sulisalo; Clair A Francomano; Pertti Sistonen; J F Maher; Victor A McKusick; Albert de La Chapelle; Ilkka Kaitila
High-resolution genetic mapping of the cartilage-hair hypoplasia (CHH) gene in Amish and Finnish families.
Genomics 1994;20(3):347-53.
1994: Albert de La Chapelle; J Hästbacka; Anna-Elina Lehesjoki; T Sulisalo; J Kere; Esa Tahvanainen; Pertti Sistonen
[Linkage and linkage disequilibrium in the Finnish disease heritage].
Duodecim; lääketieteellinen aikakauskirja 1994;110(7):654-64.
1993: F S Leach; N C Nicolaides; Nickolas Papadopoulos; B Liu; Jin Jen; R Parsons; Päivi Peltomäki; Pertti Sistonen; Lauri A Aaltonen; Minna Nyström-Lahti
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
Cell 1993;75(6):1215-25.
1993: Juha Kere; Pertti Sistonen; Christer Holmberg; Albert de La Chapelle
The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator.
Proceedings of the National Academy of Sciences of the United States of America 1993;90(22):10686-9.
1993: Pertti Sistonen; A L Träskelin; H Lehväslaiho; Albert de La Chapelle
Genetic mapping of the erythropoietin receptor gene.
Human genetics 1993;92(3):299-301.
1993: Anna-Elina Lehesjoki; Marjaleena Koskiniemi; Reijo Norio; S Tirrito; Pertti Sistonen; Eric S Lander; Albert de La Chapelle
Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping.
Human molecular genetics 1993;2(8):1229-34.
1993: Lauri A Aaltonen; Päivi Peltomäki; F S Leach; Pertti Sistonen; Liisa Pylkkänen; Jukka-Pekka Mecklin; Heikki Järvinen; Steven M Powell; Jin Jen; Stanley R Hamilton
Clues to the pathogenesis of familial colorectal cancer.
Science (New York, N.Y.) 1993;260(5109):812-6.
1993: Päivi Peltomäki; Lauri A Aaltonen; Pertti Sistonen; Liisa Pylkkänen; Jukka-Pekka Mecklin; Heikki Järvinen; J S Green; J R Jass; J L Weber; F S Leach
Genetic mapping of a locus predisposing to human colorectal cancer.
Science (New York, N.Y.) 1993;260(5109):810-2.
1993: T Sulisalo; Pertti Sistonen; J Hästbacka; Claes Wadelius; Outi Mäkitie; Albert de La Chapelle; Ilkka Kaitila
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis.
Nature genetics 1993;3(4):338-41.
1993: Albert de La Chapelle; Pertti Sistonen; H Lehväslaiho; E Ikkala; E Juvonen
Familial erythrocytosis genetically linked to erythropoietin receptor gene.
Lancet 1993;341(8837):82-4.
1992: J Hästbacka; Albert de La Chapelle; Ilkka Kaitila; Pertti Sistonen; A Weaver; Eric S Lander
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland.
Nature genetics 1992;2(3):204-11.
1992: Rigmor Solberg; Pertti Sistonen; A L Träskelin; D Bérubé; Jacques Simard; Peter Krajci; Tore Jahnsen; Albert de La Chapelle
Mapping of the regulatory subunits RI beta and RII beta of cAMP-dependent protein kinase genes on human chromosome 7.
Genomics 1992;14(1):63-9.
1992: Päivi Peltomäki; Pertti Sistonen; Jukka-Pekka Mecklin; Liisa Pylkkänen; Lauri A Aaltonen; S Nordling; Juha Kere; Heikki Järvinen; Stanley R Hamilton; G Petersen
Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.
Cancer research 1992;52(16):4530-3.
1992: Anna-Elina Lehesjoki; Marjaleena Koskiniemi; M Pandolfo; A Antonelli; M Kyllerman; J Wahlström; A Nergårdh; Margit Burmeister; Pertti Sistonen; Reijo Norio
Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases.
Neurology 1992;42(8):1545-50.
1992: Anna-Elina Lehesjoki; Marjaleena Koskiniemi; Pertti Sistonen; Reijo Norio; ALBERT DE LA CHAPELLE
[Localization of progressive myoclonus epilepsy gene opens new horizons for epilepsy research].
Duodecim; lääketieteellinen aikakauskirja 1992;108(4):355-7.
1991: J Hästbacka; Pertti Sistonen; Ilkka Kaitila; B Weiffenbach; Kenneth K Kidd; Albert de La Chapelle
A linkage map spanning the locus for diastrophic dysplasia (DTD).
Genomics 1991;11(4):968-73.
1991: Päivi Peltomäki; Pertti Sistonen; Jukka-Pekka Mecklin; Liisa Pylkkänen; Heikki Järvinen; J W Simons; Kathleen R Cho; Bert Vogelstein; Albert de La Chapelle
Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindreds.
Cancer research 1991;51(16):4135-40.
1991: Eeva-Marja Sankila; Pertti Sistonen; Frans P M Cremers; Albert de La Chapelle
Choroideremia: linkage analysis with physically mapped close DNA-markers.
Human genetics 1991;87(3):348-52.
1991: Anna-Elina Lehesjoki; Marjaleena Koskiniemi; Pertti Sistonen; J Miao; J Hästbacka; Reijo Norio; Albert de La Chapelle
Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(9):3696-9.
1991: Anna-Elina Lehesjoki; Pertti Sistonen; Vesa Rasi; Albert de La Chapelle
Hemophilia A: genetic prediction and linkage studies in all available families in Finland.
Clinical genetics 1991;39(3):199-209.
1991: Ilkka Kaitila; J Hästbacka; ALBERT DE LA CHAPELLE; Pertti Sistonen
[Defective gene causing diastrophic dysplasia has been localized].
Duodecim; lääketieteellinen aikakauskirja 1991;107(17):1418-9.
1990: J Hästbacka; Ilkka Kaitila; Pertti Sistonen; Albert de La Chapelle
Diastrophic dysplasia gene maps to the distal long arm of chromosome 5.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(20):8056-9.
1987: M Lindlöf; Pertti Sistonen; Albert de La Chapelle
Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
Annals of human genetics 1987;51(Pt 4):317-28.