B. Olaisen

发表

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

B. Mevåg, B. Olaisen, M. Stenersen, 1997, Nature Genetics.

DNA Recommendations 1997 of the International Society for Forensic Genetics

P. Gill, B. Olaisen, Á. Carracedo, 1998, Vox Sanguinis.

DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome short tandem repeats

C. Tyler-Smith, P. Gill, V. Pascali, 2001 .

Caucasian Y-STR haplotype reference database for forensic application

V. Pascali, M. Krawczak, B. Olaisen, 2000 .

DNA recommendations

A. Carracedo, W. Bär, P. Gill, 1997, International Journal of Legal Medicine.

Interactions of membrane stabilizing drugs affecting human erythrocytes in vitro.

B. Olaisen, I. Oye, 1973, European journal of pharmacology.

Elevated levels of hypoxanthine in vitreous humor indicate prolonged cerebral hypoxia in victims of sudden infant death syndrome.

B. Olaisen, T. Rognum, O. Saugstad, 1988, Pediatrics.

Association analysis of lipid levels and apolipoprotein restriction fragment length polymorphisms

O. Myklebost, B. Olaisen, H. Prydz, 1990, Human Genetics.

Statement on the nomenclature of human C4 allotypes.

B. Olaisen, C. Nerl, P. Demant, 1983, Immunobiology.

Forensic aspects of haptoglobin: Electrophoretic patterns of haptoglobin allotype products and an evaluation of typing procedure

B. Olaisen, B. Teige, P. Teisberg, 1988, Electrophoresis.

Subtyping of haptoglobin — Presentation of a new method

B. Olaisen, B. Teige, L. Pedersen, 1985, Human Genetics.

Electrophoretic Polymorphism of Human C4 is Due to Charge Differences in the α‐Chain, Presumably in the C4d Fragment

B. Mevåg, B. Olaisen, P. Teisberg, 1981, Scandinavian journal of immunology.

Abstracts of workshop presentations (Part 6 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

Genetic Studies of Apolipoprotein A-IV by Two-Dimensional Electrophoresis

B. Olaisen, C. Ehnholm, T. Gedde-Dahl, 1985 .

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

B. Olaisen, B. Høyheim, F. Jahnsen, 2002, The Journal of investigative dermatology.

The Gm‐Pi linkage heterogeneity in view of Pi M subtypes

B. Olaisen, R. Frants, A. Eriksson, 1981, Annals of human genetics.

GPT--epidermolysis bullosa simplex (EBS Ogna) linkage in man.

B. Olaisen, T. Gedde-Dahl, T. Gedde-dahl, 1973, Human heredity.

Characterization of the COL2A1 VNTR polymorphism.

B. Olaisen, E. S. Berg, 1993, Genomics.

Abstracts of workshop presentations (Part 2 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

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

B. Olaisen, G. Markussen, P. Teisberg, 1990, Annals of human genetics.

Genetic analysis of C4 polymorphism by use of DNA amplification (PCR), allele‐specific oligonucleotide probes and allele‐specific restriction enzymes

B. Olaisen, P. Teisberg, E. S. Berg, 1989, Annals of human genetics.

Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway.

B. Olaisen, T. Hovig, J. Blomhoff, 1981, Acta medica Scandinavica.

Abstracts of workshop presentations (Part 12 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

A structural locus for coagulation factor XIIIA (F13A) is located distal to the HLA region on chromosome 6p in man.

E. Thorsby, B. Olaisen, R. Jonassen, 1985, American journal of human genetics.

Restriction fragment length polymorphisms of the complement component C4 loci on chromosome 6: studies with emphasis on the determination of gene number

B. Mevåg, B. Olaisen, R. Jonassen, 1988, Annals of human genetics.

Human complement C4 locus is duplicated on some chromosomes

B. Olaisen, T. Michaelsen, R. Nordhagen, 1979, Nature.

Identification of homozygosity for a human apolipoprotein A-I variant.

R. Mahley, B. Olaisen, K. Weisgraber, 1986, Journal of lipid research.

Genetic polymorphism of the second component of human complement (C2)

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1978, Human Genetics.

The Bf locus in the HLA region of chromosome 6: Linkage and association studies

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1975, Humangenetik.

Complement loci of the HLA complex. Studies on families with intra-HLA crossovers and haplotype associations.

E. Thorsby, B. Olaisen, T. Moen, 1981, Human immunology.

Very close linkage between HLA-B and Bf inferred from allelic association

J. Edwards, B. Olaisen, P. Mackintosh, 1977, Nature.

Genetic polymorphism of complement component C8

B. Mevåg, B. Olaisen, Francesco Saverio Tedesco, 2004, Human Genetics.

Bioassay of kinship using VNTR alleles

B. Olaisen, M. Stenersen, T. Gedde-Dahl, 1994 .

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

B. Olaisen, Y. Thomassen, N. Oldereid, 1993, Journal of reproduction and fertility.

Abstracts of workshop presentations (Part 10 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

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

O. Myklebost, B. Olaisen, B. Høyheim, 1989, Genomics.

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

T. Egeland, B. Mevåg, B. Olaisen, 1999, Forensic science international.

Genetic markers in the Spitsbergen reindeer.

B. Olaisen, A. Storset, M. Wika, 2009, Hereditas.

Y-chromosome variation in a Norwegian population sample.

T. Egeland, B. Olaisen, Á. Carracedo, 2001, Forensic science international.

Genetics of LCAT (lecithin:cholesterol acyltransferase) deficiency

B. Olaisen, E. Gjone, P. Teisberg, 1975, Annals of human genetics.

Close Linkage Between LCAT (Lecithin: Cholesterol Acyltransferase) Locus and α-Haptoglobin Locus on Chromosome No. 16

B. Olaisen, E. Gjone, P. Teisberg, 1975 .

DXYS267: DYS393 and its X chromosome counterpart.

B. Olaisen, T. Gedde-Dahl, B. Dupuy, 2000, Forensic science international.

Abstracts of workshop presentations (Part 11 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

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

B Brinkmann, W R Mayr, P Gill, 2001, Forensic science international.

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

A. Carracedo, M. Kayser, M. Prinz, 2001, International Journal of Legal Medicine.

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

B. Olaisen, B. Dupuy, 1997, Forensic science international.

Two-dimensional electrophoretic characterization (iso-dalt) of fibrinogen and fibrin subunit chains from four different genetic dysfibrinogen variants

B. Olaisen, F. Brosstad, H. Stormorken, 1983 .

De novo mutations and allelic diversity at minisatellite locus D7S22 investigated by allele-specific four-state MVR-PCR analysis.

B. Olaisen, R. Andreassen, 1998, Human molecular genetics.

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

B. Olaisen, R. Andreassen, Rune Andreassen, 2002, Electrophoresis.

Somatic mutations in VNTR‐Locus D1S7 in human colorectal carcinomas are associated with microsatellite instability

B. Olaisen, G. Meling, P. Hoff-Olsen, 1995, Human mutation.

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

B. Olaisen, B. Teige, P. Teisberg, 1992, Human heredity.

Subtyping of haptoglobin

B. Olaisen, B. Teige, Lilian Pedersen, 1986 .

Abstracts of workshop presentations (Part 1 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

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

B. Olaisen, E. Høiby, S. Rogde, 1990, Scandinavian journal of infectious diseases.

A BamH1 RFLP of the C8B gene.

B. Mevåg, B. Olaisen, J. Sodetz, 1989, Nucleic Acids Research.

C8A and C8B polymorphisms in Norwegians and Norwegian lapps.

B. Olaisen, S. Rogde, P. Teisberg, 1989, Human Heredity.

On the localization of the Gb locus within the MHS region of chromosome No. 6.

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1975, Tissue antigens.

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

O. Myklebost, B. Olaisen, S. Rogne, 1991, Journal of medical genetics.

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

B. Olaisen, B. HØyheim, R. Jonassen, 1992, Annals of human genetics.

A Haemolytically Non-Active C4 Gene Products

E. Thorsby, B. Olaisen, R. Nordhagen, 1980 .

Rga (Rodgers) and the HLA region: linkage and associations.

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 2008, Tissue antigens.

Microsatellite stability in human post-mortem tissues.

B. Mevåg, B. Olaisen, P. Hoff-Olsen, 2001, Forensic science international.

The locus for apolipoprotein CII is closely linked to the apolipoprotein E locus on chromosome 19 in man

O. Myklebost, B. Olaisen, H. Prydz, 1984, Human Genetics.

Confirmation of the close linkage between the loci for human apolipoproteins AI and AIV by the use of a cloned cDNA probe and two restriction site polymorphisms

O. Myklebost, B. Olaisen, H. Prydz, 2004, Human Genetics.

Fibrinogen γ chain locus is on chromosome 4 in man

B. Olaisen, T. Gedde-Dahl, P. Teisberg, 2004, Human Genetics.

Gene order and gene distances in the HLA region studied by the haplotype method

E. Thorsby, B. Olaisen, R. Jonassen, 1983, Annals of human genetics.

C4 HAPLOTYPE PRODUCTS AND PARTIAL INHIBITION OF ANTI‐RODGERS SERA

E. Thorsby, B. Olaisen, R. Nordhagen, 1981, Journal of immunogenetics.

Structural complement factor loci and the HLA region.

E. Thorsby, B. Olaisen, R. Jonassen, 1978, Cytogenetics and cell genetics.

Genetic polymorphism of C4 in man and localisation of a structural C4 locus to the HLA gene complex of chromosome 6

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1976, Nature.

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

B Brinkmann, W Bär, P Gill, 1997, International journal of legal medicine.

The genetic polymorphism of the fourth component of human complement: methodological aspects and a presentation of linkage and association data relevant to its localization in the HLA region

E. Thorsby, B. Olaisen, R. Jonassen, 1977, The Journal of experimental medicine.

Gpt-EBS1Linkage Group

B. Olaisen, T. Jr.Gedde-Dahl, 1974 .

Gpt-EBS1 linkage group. General linkage relations.

B. Olaisen, T. Gedde-Dahl, 1974, Human heredity.

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

B. Olaisen, E. S. Berg, 1994, BioTechniques.

mtDNA sequences in the Norwegian Saami and main populations

B. Olaisen, B. Dupuy, 1996 .

Analysis of somatic mutations at short tandem repeat loci in colorectal carcinomas

B. Olaisen, G. Meling, P. Hoff-Olsen, 1996 .

The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP

K. Grzeschik, R. Lothe, B. Olaisen, 1987, Human Genetics.

Identification in blood stains through DNA typing with C4 and HLA-DR probes

E. Thorsby, B. Mevåg, B. Olaisen, 2004, Zeitschrift für Rechtsmedizin.

Identification in blood stains through DNA typing with C4 and HLA-DR probes.

E. Thorsby, B. Mevåg, B. Olaisen, 1987 .

Nonlinkage between C6 and chromosome 6 markers

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1977, Human Genetics.

Genetic linkage relations of the sixth component of complement (C6)

B. Olaisen, T. Gedde-Dahl, P. Teisberg, 1979, Human Genetics.

Localization of the human GLO gene locus

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1976, Human Genetics.

Mutation rate in the hypervariable VNTR g3 (D7S22) is affected by allele length and a flanking DNA sequence polymorphism near the repeat array.

T. Egeland, B. Olaisen, R. Andreassen, 1996, American journal of human genetics.

Human VNTR mutation and sex.

P. Gill, B. Olaisen, P. Hoff-Olsen, 1993, EXS.

ASSOCIATION BETWEEN THE ELECTROPHORETICALLY‐DETERMINED C4M HAPLOTYPE PRODUCT AND PARTIAL INHIBITION OF ANTI‐Cha

B. Olaisen, R. Nordhagen, P. Teisberg, 1980, Journal of immunogenetics.

Further investigations on the genetics of the C+ protein polymorphism.

E. Thorsby, B. Olaisen, R. Nordhagen, 1980, Immunobiology.

Genetic linkage relation of the pepsinogen Pg5 locus

E. Thorsby, B. Olaisen, A. Bratlie, 1980, Annals of human genetics.

Studies of HLA, factor B (Bf), complement C2 and C4 haplotypes in type 1 diabetic and control families from northern Sweden.

B. Olaisen, G. Holmgren, G. Holmlund, 1986, Human heredity.

Report of the Committee on the Genetic Constitution of Chromosomes 5 and 6.

B. Olaisen, L. Lamm, 1985, Cytogenetics and cell genetics.

Variation in mutation rate and direction between tetranucleotide STR loci in human colorectal carcinomas

B. Olaisen, G. Meling, P. Hoff-Olsen, 1998, Annals of human genetics.

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

B Brinkmann, W Bär, P Gill, 2000, Forensic science international.

Properdin Factor B (Bf) Polymorphism in Norway 1

B. Olaisen, P. Teisberg, 1977, Vox sanguinis.

A Structural Locus for Coagulation Factor XIIIA (F13A) is Located Distal to HLA on the Short Arm of Chromosome 6 in Man

E. Thorsby, B. Olaisen, T. Gedde-Dahl, 1984 .

A haemolytically non-active C4 gene product.

E. Thorsby, B. Olaisen, R. Nordhagen, 1980, Immunobiology.

The C4 system

B. Olaisen, R. Jonassen, T. Gedde-Dahl, 2004, Human Genetics.

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

P. Krajči, B. Olaisen, B. Høyheim, 1992, Human Genetics.

Genetics of the Berardinelli‐Seip syndrome (congenital generalized lipodystrophy) in Norway: epidemiology and gene mapping

B. Mevåg, B. Olaisen, M. Stenersen, 1996, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Abstracts of workshop presentations (Part 13 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Corresponding Repeats in STRs and the Internal Standard in Fragment Analysis

B. Olaisen, B. Dupuy, 1996 .

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

K. Grzeschik, P. Krajči, B. Olaisen, 1991, Human Genetics.

The C8A and C8B loci are closely linked on chromosome 1

B. Olaisen, S. ROGDE, B. OLAISEN, 1986, Annals of human genetics.

Post-mortem hypoxanthine levels in the vitreous humour. An introductory report.

B. Olaisen, O. Saugstad, 1978, Forensic science.

Y‐chromosomal microsatellite mutation rates: Differences in mutation rate between and within loci

T. Egeland, B. Olaisen, M. Stenersen, 2004, Human mutation.

Abstracts of workshop presentations (Part 3 of 16)

J. N. Guidi, C. Bloomfield, K. Kidd, 1987 .

The two apolipoprotein loci apoA-I and apoA-IV are closely linked in man

B. Mevåg, B. Olaisen, C. Ehnholm, 2004, Human Genetics.

Genetic studies of an apoA-I lipoprotein variant

B. Olaisen, T. Gedde-Dahl, P. Teisberg, 2004, Human Genetics.

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

A. Carracedo, N. Morling, W. Bär, 2000, Forensic science international.

The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man

B. Olaisen, T. Gedde-Dahl, P. Teisberg, 2004, Human Genetics.

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

Niels Morling, Peter M Schneider, Angel Carracedo, 2002, Forensic science international.

The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19

B. Mevåg, B. Olaisen, T. Gedde-Dahl, 2004, Human Genetics.

Abstracts of workshop presentations (Part 12 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

The C4 system: quantitative studies of different genotypes.

B. Olaisen, R. Jonassen, P. Teisberg, 1980, Immunobiology.

Abstracts of workshop presentations (Part 4 of 13)

R. L. Miller, D. Cox, C. Bloomfield, 1985 .

Three intriguing identification cases

B. Mevåg, B. Olaisen, S. Jacobsen, 1996 .

Genetic basis of acquired C4 deficiency

B. Olaisen, J. Cream, P. Teisberg, 1979, Clinical genetics.

Y‐chromosomal microsatellite mutation rates: Differences in mutation rate between and within loci

B. Olaisen, M. Stenersen, B. Dupuy, 2004 .

Very close linkage between D2S1 and ACP1 on chromosome 2p

R. Lothe, B. Olaisen, P. Pearson, 1986, Annals of human genetics.

GLO polymorphism in Norway.

B. Olaisen, R. Jonassen, P. Teisberg, 1976, Human heredity.

Two rare GPT phenotypes in a Norwegian family

B. Olaisen, 1973, Humangenetik.

Distribution of GPT types in Norway.

B. Olaisen, 1975, Human heredity.

ESD polymorphism in Norway

B. Olaisen, R. Jonassen, P. Teisberg, 1976, Human Genetics.

Geographical heterogeneity of Y-chromosomal lineages in Norway.

B. Olaisen, M. Stenersen, Tim Lu, 2006, Forensic science international.

Fluorescent stains in protein detection on immunoblots

B. Olaisen, R. Jonassen, B. Teige, 1986 .

Patterns and frequencies of common and rare Hp α-chain variants

B. Olaisen, B. Teige, H. Lie, 1988 .

Atypical segregation of erythrocyte glutamic-pyruvic transaminase in a Norwegian family. Evidence of a silent allele.

B. Olaisen, 1973, Human heredity.

Decision-making in paternity diagnostics using SLPs

B. Olaisen, M. Stenersen, 1996 .

The legal situation of forensic DNA analysis in Norway

B. Olaisen, 1997 .

Application of the GPT system in paternity cases.

B. Olaisen, 1975, Human heredity.

Length and sequence variation in D7S22 (g3) alleles studied by high resolution length measurements and nucleotide sequencing

B. Olaisen, R. Andreassen, Bjørnar Olaisen, 1997, Electrophoresis.

Mutation rate variation in the hypervariable VNTR g3 (D7S22) is associated with a flanking DNA sequence polymorphism near the repeat array

B. Olaisen, R. Andreassen, 1996 .

A study of Y-chromosomal microsatellites and biallelic markers in Norway

B. Olaisen, M. Stenersen, B. Dupuy, 2004 .

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

P. Gill, G. Tully, M. Holland, 2000, International Journal of Legal Medicine.

Guidelines for Mitochondrial DNA Typing

Mark R. Wilson, P. Gill, G. Tully, 2000, Vox Sanguinis.