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Items: 1 to 50 of 127

1.

Androgenic-Anabolic Steroids (AAS) and Violent Behaviour [Internet].

Haug E, Mørland J, Olaisen B, Myhre KI.

Oslo, Norway: Knowledge Centre for the Health Services at The Norwegian Institute of Public Health (NIPH); 2004.

2.

Geographical heterogeneity of Y-chromosomal lineages in Norway.

Dupuy BM, Stenersen M, Lu TT, Olaisen B.

Forensic Sci Int. 2006 Dec 1;164(1):10-9. Epub 2005 Dec 7.

PMID:
16337760
3.

Y-chromosomal microsatellite mutation rates: differences in mutation rate between and within loci.

Dupuy BM, Stenersen M, Egeland T, Olaisen B.

Hum Mutat. 2004 Feb;23(2):117-24.

PMID:
14722915
4.

Paternity Testing Commission of the International Society of Forensic Genetics. Recommendations on genetic investigations in paternity cases.

Morling N, Allen R, Carracedo A, Geada H, Guidet F, Hallenberg C, Martin W, Mayr WR, Olaisen B, Pascali V, Schneider PM; Paternity Testing Commission, International Society of Forensic Genetics.

Int J Legal Med. 2003 Feb;117(1):51-61. No abstract available.

PMID:
12675030
5.

Paternity Testing Commission of the International Society of Forensic Genetics: recommendations on genetic investigations in paternity cases.

Morling N, Allen RW, Carracedo A, Geada H, Guidet F, Hallenberg C, Martin W, Mayr WR, Olaisen B, Pascali VL, Schneider PM; Paternity Testing Commission of the International Society of Forensic Genetics.

Forensic Sci Int. 2002 Oct 9;129(3):148-57.

PMID:
12372685
6.

Mutation at minisatellite locus DYF155S1: allele length mutation rate is affected by age of progenitor.

Andreassen R, Lundsted J, Olaisen B.

Electrophoresis. 2002 Aug;23(15):2377-83.

PMID:
12210191
7.

A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: two identical de novo mutations.

Koss-Harnes D, Høyheim B, Anton-Lamprecht I, Gjesti A, Jørgensen RS, Jahnsen FL, Olaisen B, Wiche G, Gedde-Dahl T Jr.

J Invest Dermatol. 2002 Jan;118(1):87-93.

8.

DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs.

Gill P, Brenner C, Brinkmann B, Budowle B, Carracedo A, Jobling MA, de Knijff P, Kayser M, Krawczak M, Mayr WR, Morling N, Olaisen B, Pascali V, Prinz M, Roewer L, Schneider PM, Sajantila A, Tyler-Smith C.

Forensic Sci Int. 2001 Dec 15;124(1):5-10. Review.

PMID:
11741752
9.

DNA commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs.

Gill P, Brenner C, Brinkmann B, Budowle B, Carracedo A, Jobling MA, de Knijff P, Kayser M, Krawczak M, Mayr WR, Morling N, Olaisen B, Pascali V, Prinz M, Roewer L, Schneider PM, Sajantila A, Tyler-Smith C.

Int J Legal Med. 2001;114(6):305-9. Review.

PMID:
11508794
10.

Microsatellite stability in human post-mortem tissues.

Hoff-Olsen P, Jacobsen S, Mevåg B, Olaisen B.

Forensic Sci Int. 2001 Jul 15;119(3):273-8.

PMID:
11390139
11.

Y-chromosome variation in a Norwegian population sample.

Dupuy BM, Andreassen R, Flønes AG, Tomassen K, Egeland T, Brion M, Carracedo A, Olaisen B.

Forensic Sci Int. 2001 Apr 1;117(3):163-73.

PMID:
11248446
12.

Guidelines for mitochondrial DNA typing. DNA Commission of the International Society for Forensic Genetics.

Bär W, Brinkmann B, Budowle B, Carracedo A, Gill P, Holland M, Lincoln PJ, Mayr W, Morling N, Olaisen B, Schneider PM, Tully G, Wilson M.

Vox Sang. 2000;79(2):121-5. No abstract available.

PMID:
11054055
13.

DXYS267: DYS393 and its X chromosome counterpart.

Dupuy BM, Gedde-Dahl T, Olaisen B.

Forensic Sci Int. 2000 Aug 14;112(2-3):111-21.

PMID:
10940596
14.

DNA Commission of the International Society for Forensic Genetics: guidelines for mitochondrial DNA typing.

Bär W, Brinkmann B, Budowle B, Carracedo A, Gill P, Holland M, Lincoln PJ, Mayr W, Morling N, Olaisen B, Schneider PM, Tully G, Wilson M.

Int J Legal Med. 2000;113(4):193-6. No abstract available.

PMID:
10929233
15.

DNA commission of the international society for forensic genetics: guidelines for mitochondrial DNA typing.

Carracedo A, Bär W, Lincoln P, Mayr W, Morling N, Olaisen B, Schneider P, Budowle B, Brinkmann B, Gill P, Holland M, Tully G, Wilson M.

Forensic Sci Int. 2000 May 15;110(2):79-85. No abstract available.

PMID:
10808096
16.

Extraction of DNA from decomposed human tissue. An evaluation of five extraction methods for short tandem repeat typing.

Hoff-Olsen P, Mevåg B, Staalstrøm E, Hovde B, Egeland T, Olaisen B.

Forensic Sci Int. 1999 Nov 8;105(3):171-83.

PMID:
10643651
17.
18.
19.

A computerised method for calculating the probability of pedigrees from genetic data.

Egeland T, Mostad PF, Olaisen B.

Sci Justice. 1997 Oct-Dec;37(4):269-74. No abstract available.

PMID:
9519542
20.

DNA recommendations 1997 of the International Society for Forensic Genetics.

Olaisen B, Bär W, Brinkmann B, Budowle B, Carracedo A, Gill P, Lincoln P, Mayr WR, Rand S.

Vox Sang. 1998;74(1):61-3.

PMID:
9481867
21.

A dedicated internal standard in fragment length analysis of hyperpolymorphic short tandem repeats.

Dupuy BM, Olaisen B.

Forensic Sci Int. 1997 May 5;86(3):207-27.

PMID:
9180030
22.
23.

Identification by DNA analysis of the victims of the August 1996 Spitsbergen civil aircraft disaster.

Olaisen B, Stenersen M, Mevåg B.

Nat Genet. 1997 Apr;15(4):402-5.

PMID:
9090388
24.

[Identification of bodies in mass disasters. The aircraft on Svalbard].

Olaisen B.

Tidsskr Nor Laegeforen. 1997 Mar 20;117(8):1069-70. Norwegian. No abstract available.

PMID:
9148470
25.

DNA recommendations. Further report of the DNA Commission of the ISFH regarding the use of short tandem repeat systems. International Society for Forensic Haemogenetics.

Bär W, Brinkmann B, Budowle B, Carracedo A, Gill P, Lincoln P, Mayr W, Olaisen B.

Int J Legal Med. 1997;110(4):175-6. No abstract available.

PMID:
9274938
27.

Genetics of the Berardinelli-Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping. Berardinelli-Seip Study Group.

Gedde-Dahl T Jr, Trygstad O, Van Maldergem L, Magré J, van der Hagen CB, Olaisen B, Stenersen M, Mevåg B.

Acta Paediatr Suppl. 1996 Jun;413:52-8.

PMID:
8783773
28.
29.

Hybrid PCR sequencing: sequencing of PCR products using a universal primer.

Berg ES, Olaisen B.

Biotechniques. 1994 Nov;17(5):896-901.

PMID:
7840970
30.

Junctional epidermolysis bullosa inversa (locus EBR2A) assigned to 1q31 by linkage and association to LAMC1.

Gedde-Dahl T Jr, Dupuy BM, Jonassen R, Winberg JO, Anton-Lamprecht I, Olaisen B.

Hum Mol Genet. 1994 Aug;3(8):1387-91.

PMID:
7987320
31.

[Concentrate on forensic medicine].

Olaisen B.

Tidsskr Nor Laegeforen. 1994 Apr 30;114(11):1285-6. Norwegian. No abstract available.

PMID:
8079200
32.

Concentrations of lead, cadmium and zinc in the tissues of reproductive organs of men.

Oldereid NB, Thomassen Y, Attramadal A, Olaisen B, Purvis K.

J Reprod Fertil. 1993 Nov;99(2):421-5.

PMID:
8107024
33.

Characterization of the COL2A1 VNTR polymorphism.

Berg ES, Olaisen B.

Genomics. 1993 May;16(2):350-4.

PMID:
8314574
34.

Human VNTR mutation and sex.

Olaisen B, Bekkemoen M, Hoff-Olsen P, Gill P.

EXS. 1993;67:63-9.

PMID:
8400715
35.

The gene encoding human transmembrane secretory component (locus PIGR) is linked to D1S58 on chromosome 1.

Krajci P, Gedde-Dahl T Jr, Høyheim B, Rogde S, Olaisen B, Brandtzaeg P.

Hum Genet. 1992 Nov;90(3):215-9.

PMID:
1487233
36.

Linkage and association studies with C8A and C8B RFLPs on chromosome 1.

Rogde S, Gedde-Dahl T Jr, Teisberg P, Jonassen R, Høyheim B, Olaisen B.

Ann Hum Genet. 1992 Jul;56(3):233-42.

PMID:
1360193
37.

Haptoglobin subtypes in Norway and a review of HP subtypes in various populations.

Teige B, Olaisen B, Teisberg P.

Hum Hered. 1992;42(2):93-106. Review.

PMID:
1572675
38.

The human transmembrane secretory component (poly-Ig receptor): molecular cloning, restriction fragment length polymorphism and chromosomal sublocalization.

Krajci P, Grzeschik KH, Geurts van Kessel AH, Olaisen B, Brandtzaeg P.

Hum Genet. 1991 Oct;87(6):642-8.

PMID:
1682231
39.

The human genes for complement components 6 (C6) and 9 (C9) are closely linked on chromosome 5.

Rogne S, Myklebost O, Olving JH, Kyrkjebø HT, Jonassen R, Olaisen B, Gedde-Dahl T Jr.

J Med Genet. 1991 Sep;28(9):587-90.

40.

A BamHI RFLP of the C8A gene.

Rogde S, Olaisen B, Teisberg P, Sodetz J.

Nucleic Acids Res. 1991 Jul 11;19(13):3762. No abstract available.

41.

Association analysis of lipid levels and apolipoprotein restriction fragment length polymorphisms.

Myklebost O, Rogne S, Hjermann I, Olaisen B, Prydz H.

Hum Genet. 1990 Dec;86(2):209-14.

PMID:
1979958
42.

Use of DNA amplification (PCR) and direct DNA sequencing in the characterization of C4 alleles.

Berg ES, Markussen G, Teisberg P, Olaisen B.

Ann Hum Genet. 1990 Jul;54(3):183-9.

PMID:
2221823
43.

Genetic aspects of complement component C8 in Norwegian meningococcal disease patients.

Rogde S, Høiby EA, Teisberg P, Olaisen B.

Scand J Infect Dis. 1990;22(6):673-9.

PMID:
2284574
44.

[Use of modern gene technology in forensic medicine].

Teisberg P, Mevåg B, Olaisen B.

Tidsskr Nor Laegeforen. 1989 Nov 20;109(32):3337-40. Norwegian.

PMID:
2574505
45.

A BamH1 RFLP of the C8B gene.

Rogde S, Mevåg B, Teisberg P, Olaisen B, Sodetz J.

Nucleic Acids Res. 1989 Aug 25;17(16):6760. No abstract available.

47.

The genes for apolipoprotein all (APOA2) and the Duffy blood group (FY) are linked on chromosome 1 in man.

Rogne S, Myklebost O, Høyheim B, Olaisen B, Gedde-Dahl T Jr.

Genomics. 1989 Feb;4(2):169-73.

PMID:
2500391
48.

C8A and C8B polymorphisms in Norwegians and Norwegian lapps.

Rogde S, Teisberg P, Olaisen B.

Hum Hered. 1989;39(2):81-8.

PMID:
2759635
49.

[The polyposis project].

Gedde-Dahl T Jr, Heim S, Lothe R, Bye R, Geitvik GA, Kyrkjebø HT, Hognestad J, Nygaard K, Bergan A, Olaisen B, et al.

Nord Med. 1989;104(1):12-5. Norwegian.

PMID:
2536147
50.

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