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Items: 1 to 50 of 125

1.

Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population.

Parmar AS, Alakulppi N, Paavola-Sakki P, Kurppa K, Halme L, Färkkilä M, Turunen U, Lappalainen M, Kontula K, Kaukinen K, Mäki M, Lindfors K, Partanen J, Sistonen P, Mättö J, Wacklin P, Saavalainen P, Einarsdottir E.

Tissue Antigens. 2012 Dec;80(6):488-93. doi: 10.1111/tan.12016. Epub 2012 Oct 18.

PMID:
23075394
2.

The i blood group antigen as a marker for umbilical cord blood-derived mesenchymal stem cells.

Hirvonen T, Suila H, Kotovuori A, Ritamo I, Heiskanen A, Sistonen P, Anderson H, Satomaa T, Saarinen J, Tiitinen S, Räbinä J, Laitinen S, Natunen S, Valmu L.

Stem Cells Dev. 2012 Feb 10;21(3):455-64. doi: 10.1089/scd.2011.0405. Epub 2011 Nov 2.

PMID:
21933024
3.

Swedish population substructure revealed by genome-wide single nucleotide polymorphism data.

Salmela E, Lappalainen T, Liu J, Sistonen P, Andersen PM, Schreiber S, Savontaus ML, Czene K, Lahermo P, Hall P, Kere J.

PLoS One. 2011 Feb 9;6(2):e16747. doi: 10.1371/journal.pone.0016747.

4.

Fine mapping of the CELIAC2 locus on chromosome 5q31-q33 in the Finnish and Hungarian populations.

Koskinen LL, Einarsdottir E, Korponay-Szabo IR, Kurppa K, Kaukinen K, Sistonen P, Pocsai Z, Széles G, Adány R, Mäki M, Kere J, Saavalainen P.

Tissue Antigens. 2009 Nov;74(5):408-16. doi: 10.1111/j.1399-0039.2009.01359.x.

PMID:
19845895
5.

Genomic landscape of positive natural selection in Northern European populations.

Lappalainen T, Salmela E, Andersen PM, Dahlman-Wright K, Sistonen P, Savontaus ML, Schreiber S, Lahermo P, Kere J.

Eur J Hum Genet. 2010 Apr;18(4):471-8. doi: 10.1038/ejhg.2009.184. Epub 2009 Oct 21.

6.

International Society of Blood Transfusion Committee on terminology for red blood cell surface antigens: Macao report.

Daniels G, Castilho L, Flegel WA, Fletcher A, Garratty G, Levene C, Lomas-Francis C, Moulds JM, Moulds JJ, Olsson ML, Overbeeke M, Poole J, Reid ME, Rouger P, van der Schoot E, Scott M, Sistonen P, Smart E, Storry JR, Tani Y, Yu LC, Wendel S, Westhoff C, Yahalom V, Zelinski T; International Society of Blood Transfusion Committee on Terminology for Red Blood Cell Surface Antigens.

Vox Sang. 2009 Feb;96(2):153-6. doi: 10.1111/j.1423-0410.2008.01133.x. No abstract available.

PMID:
19152607
7.

Donors with a rare pheno (geno) type.

Reesink HW, Engelfriet CP, Schennach H, Gassner C, Wendel S, Fontão-Wendel R, de Brito MA, Sistonen P, Matilainen J, Peyrard T, Pham BN, Rouger P, Le Pennec PY, Flegel WA, von Zabern I, Lin CK, Tsoi WC, Hoffer I, Barotine-Toth K, Joshi SR, Vasantha K, Yahalom V, Asher O, Levene C, Villa MA, Revelli N, Greppi N, Marconi M, Tani Y, Folman CC, de Haas M, Koopman MM, Beckers E, Gounder DS, Flanagan P, Wall L, Aranburu Urtasun E, Hustinx H, Niederhauser C, Flickinger C, Nance SJ, Meny GM.

Vox Sang. 2008 Oct;95(3):236-53. doi: 10.1111/j.1423-0410.2008.01084.x. No abstract available.

PMID:
19121189
8.

Association study of the IL18RAP locus in three European populations with coeliac disease.

Koskinen LL, Einarsdottir E, Dukes E, Heap GA, Dubois P, Korponay-Szabo IR, Kaukinen K, Kurppa K, Ziberna F, Vatta S, Not T, Ventura A, Sistonen P, Adány R, Pocsai Z, Széles G, Mäki M, Kere J, Wijmenga C, van Heel DA, Saavalainen P.

Hum Mol Genet. 2009 Mar 15;18(6):1148-55. doi: 10.1093/hmg/ddn438. Epub 2008 Dec 22.

PMID:
19103669
9.

Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.

Salmela E, Lappalainen T, Fransson I, Andersen PM, Dahlman-Wright K, Fiebig A, Sistonen P, Savontaus ML, Schreiber S, Kere J, Lahermo P.

PLoS One. 2008;3(10):e3519. doi: 10.1371/journal.pone.0003519. Epub 2008 Oct 24.

10.

Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22.

Pulli K, Karma K, Norio R, Sistonen P, Göring HH, Järvelä I.

J Med Genet. 2008 Jul;45(7):451-6. doi: 10.1136/jmg.2007.056366. Epub 2008 Apr 18.

11.

Genome-wide scan of exfoliation syndrome.

Lemmelä S, Forsman E, Sistonen P, Eriksson A, Forsius H, Järvelä I.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4136-42.

PMID:
17724198
12.

International Society of Blood Transfusion Committee on Terminology for Red Cell Surface Antigens: Cape Town report.

Daniels G, Flegel WA, Fletcher A, Garratty G, Levene C, Lomas-Francis C, Moulds JM, Moulds JJ, Olsson ML, Overbeeke MA, Poole J, Reid ME, Rouger P, van der Schoot CE, Scott M, Sistonen P, Smart E, Storry JR, Tani Y, Yu LC, Wendel S, Westhoff CM, Zelinski T.

Vox Sang. 2007 Apr;92(3):250-3. No abstract available.

PMID:
17348875
13.

Finnish mitochondrial DNA HVS-I and HVS-II population data.

Hedman M, Brandstätter A, Pimenoff V, Sistonen P, Palo JU, Parson W, Sajantila A.

Forensic Sci Int. 2007 Oct 25;172(2-3):171-8. Epub 2007 Mar 2.

PMID:
17336475
14.

Regional differences among the Finns: a Y-chromosomal perspective.

Lappalainen T, Koivumäki S, Salmela E, Huoponen K, Sistonen P, Savontaus ML, Lahermo P.

Gene. 2006 Jul 19;376(2):207-15. Epub 2006 Mar 18.

PMID:
16644145
15.

Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.

Salmela E, Taskinen O, Seppänen JK, Sistonen P, Daly MJ, Lahermo P, Savontaus ML, Kere J.

J Med Genet. 2006 Jul;43(7):590-7. Epub 2006 Jan 27.

16.

A microarray system for genotyping 150 single nucleotide polymorphisms in the coding region of human mitochondrial DNA.

Sigurdsson S, Hedman M, Sistonen P, Sajantila A, Syvänen AC.

Genomics. 2006 Apr;87(4):534-42. Epub 2006 Jan 9. Erratum in: Genomics. 2007 Jan;89(1):166.

17.

Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens.

Daniels GL, Fletcher A, Garratty G, Henry S, Jørgensen J, Judd WJ, Levene C, Lomas-Francis C, Moulds JJ, Moulds JM, Moulds M, Overbeeke M, Reid ME, Rouger P, Scott M, Sistonen P, Smart E, Tani Y, Wendel S, Zelinski T; International Society of Blood Transfusion.

Vox Sang. 2004 Nov;87(4):304-16. No abstract available.

18.

Detection of the founder effect in Finnish CADASIL families.

Mykkänen K, Savontaus ML, Juvonen V, Sistonen P, Tuisku S, Tuominen S, Penttinen M, Lundkvist J, Viitanen M, Kalimo H, Pöyhönen M.

Eur J Hum Genet. 2004 Oct;12(10):813-9.

19.

A known polymorphism in the bile salt export pump gene is not a risk allele for intrahepatic cholestasis of pregnancy.

Painter JN, Savander M, Sistonen P, Lehesjoki AE, Aittomäki K.

Scand J Gastroenterol. 2004 Jul;39(7):694-5. No abstract available.

PMID:
15370693
20.

Analysis of 16 Y STR loci in the Finnish population reveals a local reduction in the diversity of male lineages.

Hedman M, Pimenoff V, Lukka M, Sistonen P, Sajantila A.

Forensic Sci Int. 2004 May 28;142(1):37-43.

PMID:
15110072
21.

High birth weight is associated with human leukocyte antigen (HLA) DRB1*13 in full-term infants.

Aroviita P, Partanen J, Sistonen P, Teramo K, Kekomäki R.

Eur J Immunogenet. 2004 Feb;31(1):21-6.

PMID:
15009177
22.

Little evidence for involvement of MLH3 in colorectal cancer predisposition.

Hienonen T, Laiho P, Salovaara R, Mecklin JP, Järvinen H, Sistonen P, Peltomäki P, Lehtonen R, Nupponen NN, Launonen V, Karhu A, Aaltonen LA.

Int J Cancer. 2003 Aug 20;106(2):292-6.

23.

International Society of Blood Transfusion Committee on terminology for red cell surface antigens: Vancouver Report.

Daniels GL, Cartron JP, Fletcher A, Garratty G, Henry S, Jørgensen J, Judd WJ, Levene C, Lin M, Lomas-Francis C, Moulds JJ, Moulds JM, Moulds M, Overbeeke M, Reid ME, Rouger P, Scott M, Sistonen P, Smart E, Tani Y, Wendel S, Zelinski T.

Vox Sang. 2003 Apr;84(3):244-7. No abstract available.

PMID:
12670376
24.

Screening for microsatellite instability target genes in colorectal cancers.

Vilkki S, Launonen V, Karhu A, Sistonen P, Västrik I, Aaltonen LA.

J Med Genet. 2002 Nov;39(11):785-9.

25.

A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families.

Tyynismaa H, Sistonen P, Tuupanen S, Tervo T, Dammert A, Latvala T, Alitalo T.

Invest Ophthalmol Vis Sci. 2002 Oct;43(10):3160-4.

PMID:
12356819
26.

Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.

Ridanpää M, Sistonen P, Rockas S, Rimoin DL, Mäkitie O, Kaitila I.

Eur J Hum Genet. 2002 Jul;10(7):439-47.

27.

Frequent loss of SMAD4/DPC4 protein in colorectal cancers.

Salovaara R, Roth S, Loukola A, Launonen V, Sistonen P, Avizienyte E, Kristo P, Järvinen H, Souchelnytskyi S, Sarlomo-Rikala M, Aaltonen LA.

Gut. 2002 Jul;51(1):56-9.

28.

Y-chromosomal diversity suggests that Baltic males share common Finno-Ugric-speaking forefathers.

Laitinen V, Lahermo P, Sistonen P, Savontaus ML.

Hum Hered. 2002;53(2):68-78.

PMID:
12037406
29.

Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot.

Howe JR, Shellnut J, Wagner B, Ringold JC, Sayed MG, Ahmed AF, Lynch PM, Amos CI, Sistonen P, Aaltonen LA.

Am J Hum Genet. 2002 May;70(5):1357-62. Epub 2002 Mar 27.

30.

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.

Tomlinson IP, Alam NA, Rowan AJ, Barclay E, Jaeger EE, Kelsell D, Leigh I, Gorman P, Lamlum H, Rahman S, Roylance RR, Olpin S, Bevan S, Barker K, Hearle N, Houlston RS, Kiuru M, Lehtonen R, Karhu A, Vilkki S, Laiho P, Eklund C, Vierimaa O, Aittomäki K, Hietala M, Sistonen P, Paetau A, Salovaara R, Herva R, Launonen V, Aaltonen LA; Multiple Leiomyoma Consortium.

Nat Genet. 2002 Apr;30(4):406-10. Epub 2002 Feb 25.

PMID:
11865300
31.

Low-level microsatellite instability in most colorectal carcinomas.

Laiho P, Launonen V, Lahermo P, Esteller M, Guo M, Herman JG, Mecklin JP, Järvinen H, Sistonen P, Kim KM, Shibata D, Houlston RS, Aaltonen LA.

Cancer Res. 2002 Feb 15;62(4):1166-70.

32.

Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology.

Kiuru M, Launonen V, Hietala M, Aittomäki K, Vierimaa O, Salovaara R, Arola J, Pukkala E, Sistonen P, Herva R, Aaltonen LA.

Am J Pathol. 2001 Sep;159(3):825-9.

33.

International Society of Blood Transfusion Working Party on Terminology for Red Cell Surface Antigens.

Daniels GL, Anstee DJ, Cartron JP, Dahr W, Fletcher A, Garratty G, Henry S, Jørgensen J, Judd WJ, Kornstad L, Levene C, Lin M, Lomas-Francis C, Lubenko A, Moulds JJ, Moulds JM, Moulds M, Overbeeke M, Reid ME, Rouger P, Scott M, Sistonen P, Smart E, Tani Y, Wendel S, Zelinski T.

Vox Sang. 2001 Apr;80(3):193-7. No abstract available.

PMID:
11449960
34.

Inherited susceptibility to uterine leiomyomas and renal cell cancer.

Launonen V, Vierimaa O, Kiuru M, Isola J, Roth S, Pukkala E, Sistonen P, Herva R, Aaltonen LA.

Proc Natl Acad Sci U S A. 2001 Mar 13;98(6):3387-92. Epub 2001 Feb 27.

35.

Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays.

Raitio M, Lindroos K, Laukkanen M, Pastinen T, Sistonen P, Sajantila A, Syvänen AC.

Genome Res. 2001 Mar;11(3):471-82.

36.

Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.

Jonasson J, Juvonen V, Sistonen P, Ignatius J, Johansson D, Björck EJ, Wahlström J, Melberg A, Holmgren G, Forsgren L, Holmberg M.

Eur J Hum Genet. 2000 Dec;8(12):918-22.

37.

Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia.

Lund A, Udd B, Juvonen V, Andersen PM, Cederquist K, Ronnevi LO, Sistonen P, Sörensen SA, Tranebjaerg L, Wallgren-Pettersson C, Savontaus ML.

Eur J Hum Genet. 2000 Aug;8(8):631-6.

38.

Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns.

Sidoux-Walter F, Lucien N, Nissinen R, Sistonen P, Henry S, Moulds J, Cartron JP, Bailly P.

Blood. 2000 Aug 15;96(4):1566-73.

PMID:
10942407
39.

MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populations.

Lahermo P, Laitinen V, Sistonen P, Béres J, Karcagi V, Savontaus ML.

Hereditas. 2000;132(1):35-42.

40.

A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. Online.

Wolf M, Hemminki A, Kivioja A, Sistonen P, Kaitila I, Ervasti H, Kinnunen J, Karaharju E, Knuutila S.

Hum Mutat. 1998;12(5):362.

PMID:
10671060
41.

Terminology for red cell surface antigens. ISBT Working Party Oslo Report. International Society of Blood Transfusion.

Daniels GL, Anstee DJ, Cartron JP, Dahr W, Garratty G, Henry S, Jørgensen J, Judd WJ, Kornstad L, Levene C, Lomas-Francis C, Lubenko A, Moulds JJ, Moulds JM, Moulds M, Overbeeke M, Reid ME, Rouger P, Scott M, Seidl S, Sistonen P, Tani Y, Wendel S, Zelinski T.

Vox Sang. 1999;77(1):52-7. No abstract available.

42.

SMAD genes in juvenile polyposis.

Roth S, Sistonen P, Salovaara R, Hemminki A, Loukola A, Johansson M, Avizienyte E, Cleary KA, Lynch P, Amos CI, Kristo P, Mecklin JP, Kellokumpu I, Järvinen H, Aaltonen LA.

Genes Chromosomes Cancer. 1999 Sep;26(1):54-61.

PMID:
10441006
43.

CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study.

Holopainen P, Arvas M, Sistonen P, Mustalahti K, Collin P, Mäki M, Partanen J.

Tissue Antigens. 1999 May;53(5):470-5.

PMID:
10372542
44.

The LWb blood group as a marker of prehistoric Baltic migrations and admixture.

Sistonen P, Virtaranta-Knowles K, Denisova R, Kucinskas V, Ambrasiene D, Beckman L.

Hum Hered. 1999 Jun;49(3):154-8.

PMID:
10364680
45.

Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami.

Lahermo P, Savontaus ML, Sistonen P, Béres J, de Knijff P, Aula P, Sajantila A.

Eur J Hum Genet. 1999 May-Jun;7(4):447-58.

46.

Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland.

Levo A, Jääskeläinen J, Sistonen P, Sirén MK, Voutilainen R, Partanen J.

Eur J Hum Genet. 1999 Feb-Mar;7(2):188-96.

47.

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

Ylikorkala A, Avizienyte E, Tomlinson IP, Tiainen M, Roth S, Loukola A, Hemminki A, Johansson M, Sistonen P, Markie D, Neale K, Phillips R, Zauber P, Twama T, Sampson J, Järvinen H, Mäkelä TP, Aaltonen LA.

Hum Mol Genet. 1999 Jan;8(1):45-51.

PMID:
9887330
48.

Genetic polymorphisms in carcinogen metabolism and their association to hereditary nonpolyposis colon cancer.

Moisio AL, Sistonen P, Mecklin JP, Järvinen H, Peltomäki P.

Gastroenterology. 1998 Dec;115(6):1387-94.

PMID:
9834266
49.

Mutations in the SMAD4/DPC4 gene in juvenile polyposis.

Howe JR, Roth S, Ringold JC, Summers RW, Järvinen HJ, Sistonen P, Tomlinson IP, Houlston RS, Bevan S, Mitros FA, Stone EM, Aaltonen LA.

Science. 1998 May 15;280(5366):1086-8.

50.

mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy.

Lamminen T, Huoponen K, Sistonen P, Juvonen V, Lahermo P, Aula P, Nikoskelainen E, Savontaus ML.

Eur J Hum Genet. 1997 Sep-Oct;5(5):271-9.

PMID:
9412783

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