Prentice HL, Schneider PM, Strominger JL. (1986) C4B gene polymorphism
detected in a human cosmid clone. Immunogenetics 23:274-276
Schneider PM, Carroll MC, Alper CA, Rittner C, Whitehead AS, Yunis EJ,
Colten HR. (1986) Polymorphism of the human complement C4 and steroid 21-hydroxylase
genes: Restriction fragment length polymorphisms revealing structural deletions,
homoduplications and size variants. J. Clin. Invest. 78:650-657
Miura N, Prentice HL, Schneider PM, Perlmutter DH. (1987) Synthesis and
regulation of the two human complement C4 genes in stable transfected mouse
fibroblasts. J. Biol. Chem. 262:7298-7305
Schneider PM, Rittner C. (1988) Bgl II restriction fragment polymorphism
of human complement C4A gene coincides with BF*F allele of factor B. Immunogenetics
27:225-228
Whitehead AS, Truedsson L, Schneider PM, Awdeh ZL, Fleischnick E, Blumenthal
M, Costello W, Gerald PS, Yunis EJ, Alper CA. (1988) The distribution of
C4 DNA variants in relation to MHC alleles and extented haplotypes. Human
Immunol. 21:23-32
Herrmann D, Sodetz JM, Rittner C, Schneider PM. (1989) DNA polymorphism
of the human complement C8ß gene: formal genetics and intragenic
localization. Immunogenetics 30:291-295
Braun L, Schneider PM, Giles CM, Bertrams J, Rittner C. (1990) Null alleles
of human complement C4: Evidence for pseudogenes at the C4A locus and for
gene conversion at the C4B locus. J. Exp. Med. 171:129-140
Gianelli-Borradori A, Borradori L, Schneider PM, Gautier E, Späth
PJ. (1990) Combined complete C5 and partial C4 deficiency in humans: Clinical
consequences and complement-mediated functions in vitro. Clin. Immunol.
Immunopathol. 55:41-55
Chu X, Braun-Heimer L, Rittner C, Schneider PM. (1992) Identification of
the recombination site within the steroid 21-hydroxylase gene (CYP21) of
the HLA-B47,DR7 haplotype. Exp. Clin. Immunogenet. 9:80-85
Barba G, Rittner C, Schneider PM. (1993) Genetic basis of human complement
C4A deficiency: detection of a point mutation leading to nonexpression.
J. Clin. Invest. 91:1681-1686
Kaufmann T, Hänsch G, Rittner C, Späth P, Tedesco F, Schneider
PM. (1993) Genetic basis of human complement C8ß deficiency. J. Immunol.
150:4943-4947
Kaufmann T, Rittner C, Schneider PM. (1993) The human complement component
C8B gene: structure and phylogenetic relationship. Hum. Genet. 92:69-75
Barba G, Braun-Heimer L, Rittner C, Schneider PM. (1994) A new PCR-based
typing of the Rodgers and Chido antigenic determinants of the fourth component
of human complement. Eur. J. Immunogenet. 21:325-339
Barba G, Kaufmann TJ, Schneider PM, Rittner C, Brai M. (1994) Polymorphism
of the complement C8A and B genes in two families with C8ß deficiency
and Neissserial infections. Clin. Imunol. Immunopathol. 72:83-89
Zhang L, Würzner R, Stradmann-Bellinghausen B, Rittner C, Schneider
PM. (1994) A combined study of human complement C7 IEF and C7 M/N polymorphism
in the Chinese Han population. Exp. Clin. Immunogenet. 11:17-23
Chu X, Rittner C, Schneider PM (1995) Length polymorphism of the human
complement component C4 is due to an ancient retroviral integration. Exp.
Clin. Immunogenet. 12:53-60
Höhler T, Botto M, Rittner C, Schneider PM, Meyer zum Büschenfelde
KHH (1995) Complement component C3: molecular basis of the C3*S025 variant
and evidence for molecular heterogeneity of other variants. Hum. Genet.
96:539-541
Höhler T, Hundt M, Rittner C, Schneider PM, Meyer zum Büschenfelde
KH (1995) Cholinesterase variants: rapid characterisation by PCR/SSCP and
evidence for molecular homogeneity. J. Med. Genet. 2:109-112
Späth GF, Ramadori G, Rittner C, Schneider PM. (1995) Expression of
the complement C8 genes during Interleukin 6-mediated in vitro induction
of the acute phase response. Exp. Clin. Immunogenet. 12:74-81
Witzel K, Chu X, Rittner C, Schneider PM (1995) PCR analysis of the Xba
I polymorphism of the human C4 genes provides evidence for strong haplotype
conservation. Hum. Immunol. 43:165-173
Zhang L, Rittner C, Sodetz JM, Schneider PM, Kaufmann T (1995) The eighth
component of human complement: molecular basis of C8A (C81) polymorphism.
Hum. Genet. 96:281-284
Schneider PM, Stradmann-Bellinghausen B, Rittner C (1996) Genetic polymorphism
of the fourth component of human complement: Population study and proposal
for a revised nomenclature based on genomic PCR typing of Rodgers and Chido
determinants. Eur. J. Immunogenet. 23:335-344
Schneider PM, Rittner C. (1997) Complement Genetics. In: Complement - A
Practical Approach (A. Dodds & B. Sim, eds.) Oxford University Press,
165-198
Scheurer B, Rittner C, Schneider PM (1997) Expression of the human complement
C8 subunits is independently regulated by interleukin 1beta, interleukin
6, and interferon-gamma. Immunopharmacol. 38:167-175
Weg-Remers S, Brenden M, Schwarz E, Witzel K, Schneider PM, Guerra LK,
Rehfeldt IR, Lima MT, Hartmann D, Petzl-Erler ML, De Messias IJT, Mauff
G (1997) Major histocompatibility complex (MHC) class III genetics in two
Amerindian tribes from Southern Brazil: the Kaingang and the Guarani. Hum.
Genet. 100:548-556
Witzel-Schlömp K, Späth PJ, Hobart M, Fernie B, Rittner C, Kaufmann
T, Schneider PM (1997) The human complement C9 gene: Identification of
two mutations causing deficiency and revision of the gene structure. J.
Immunol. 158:5043-5049
Fredrikson GN, Gullstrand B, Schneider PM, Witzel-Schlömp K, Sjöholm
A, Alper CA, Awdeh Z, Truedsson L (1998) Characterization of non-expressed
C4 genes in a case of total C4 deficiency: identification of a novel point
mutation leading to a premature stop codon. Hum. Immunol. 59:713-719
Horiuchi T, Nishizaka H, Kojima T, Sawabe T, Niho Y, Schneider PM, Inaba
S, Sakai K, Hayashi K, Hashimura C, Fukumori Y (1998) A non-sense mutation
at Arg95 is predominant in complement C9 deficiency in Japanese. J. Immunol.
160:1509-1513
Witzel-Schlömp K, Hobart MJ, Fernie BA, Orren A, Würzner R, Rittner
C, Kaufmann T, Schneider PM (1998) Heterogeneity in the genetic basis of
human complement C9 deficiency. Immunogenetics 48:144-147
Schneider PM, Würzner R (1999) Complement genetics: biological implications
of polymorphisms and deficiencies. Immunol. Today 20:2-5
Zhang L, Stradmann-Bellinghausen B, Rittner C, Schneider PM (1999) Genetic
polymorphism of human complement factor I (C3b inactivator) in the Chinese
Han population. Exp. Clin. Immunogenet. 16:30-32
MHC and disease
Baur MP, Fimmers R, Fritsche C, Hümmelink M, Neugebauer M, Acton RT,
Hodge T, Barbosa J, Bertrams J, Fehsel K, Kolb H, Rothe H, Boehm B, Cambon-Thomsen
A, Gottschall J, Nepom GT, Robinson DM, Holbeck S, Rittner C, Schneider
PM, Sheehy NJ, and Spielman RS. (1989) Genetic Analysis of IDDM: The GAW5
Multiplex Dataset. Genetic Epidemiol. 6:15-20
Cox NJ, Gogolin KJ, Horvath VJ, Barker DF, Wright E, Tran T, Skolnick M,
Boehm BO, Fehsel K, Bertrams J, Hodge TW, Acton RT, Permutt MA, de Préval
C, Avoustin P, Cambon-Thomsen A, Robinson DM, Holbeck SL, Nepom GT, Schneider
PM, Rittner C, and Spielman RS. (1989) Restriction Fragment Polymorphism
of the HLA-DR, HLA-DQ, and Insulin Gene Regions in IDDM: The GAW5 Data.
Genetic Epidemiol. 6:21-26
Schneider PM, Wendler C, Riepert T, Braun L, Schacker U, Horn M, Althoff
H, Mattern R, Rittner C. (1989) Possible association of sudden infant death
(SID) with partial complement C4 deficiency revealed by post-mortem DNA
typing of HLA class II and III genes. Europ. J. Pediatr. 149:170-174
Glöckel U, Schneider PM, Beck JD, Brade V. (1990) Letale Pneumokokkenmeningitis
bei einem 1jährigen Kind mit homozygotem C2-Defekt. Monatsschr. Kinderheilkunde
138:399-402
Hartung K, Coldewey R, Krapf F, Lang B, Specker C, Schendel D, Schneider
PM, Seuchter S, Stangel W, Albert E, Deicher H. (1991) Hetero- and homozygosity
of MHC class II gene products in systemic lupus erythematosus. Tissue Antigens
38:165-168
Manns MP, Bremm A, Schneider PM, Notghi A, Gerken G, Prager-Eberle M, Stradmann-Bellinghausen
B, Meyer zum Büschenfelde KH, Rittner C. (1991) HLA-DRw8 and complement
C4 deficiency as risk factors in primary biliary cirrhosis. Gastroenterology
101:1367-1373
Hartung K, Bauer MP, Coldewey R, Fricke M, Kalden JR, Lakomek HJ, Peter
HH, Schendel DJ, Schneider PM, Seuchter SA, Stangel W, Seicher HRG. (1992)
Major histocompatibility complex haplotypes and complement C4 alleles in
systemic lupus erythematosus. J. Clin. Invest. 90:1346-1351
Schneider PM, Hartung K, Seuchter SA, Albert ED, Baur MP, Coldewey R, Kalden
JR, Lakomek HJ, Peter HH, Rittner C, Schendel DJ, Deicher HRG. (1992) Association
of MHC class I, II, and III genes with systemic lupus erythematosus - results
of a German collaborative study. In: HLA 1991, Vol. 2, Tsuji K, Aizawa
M, Sazazuki T (eds), Oxford University Press, Oxford, p. 525-528
Notghi A, Gerken G, Schneider PM, Meyer zum Büschnefelde KH, Rittner
C. (1995) The use of a new CD4 index for the definition of two distinct
patterns of immune response in HIV-infected patients. AIFO 10:401-405
Heike M, Schlaak J, Schulze-Bergkamen H, Heyl S, Herr W, Schmitt U, Schneider
PM, Meyer zum Büschenfelde KH (1996) Specificities and functions of
CD4+ HLA class II-restricted T cell clones against a human sarcoma. J.
Immunol. 156:2205-2213
Höhler T, Gerken G, Schneider PM, Meyer zum Büschenfelde KH,
Rittner C (1996) Antigen-processing polymorphisms in chronic Hepatitis
C infection. Exp. Clin. Immunogenet. 13:7-11
Höhler T, Weinmann A, Schneider PM, Rittner C, Schopf RE, Knop J,
Hasenclever P, Meyer zum Büschenfelde KH, Märker-Hermann E (1996)
TAP polymorphisms in juvenile onset psoriasis and psoriatic arthritis.
Hum. Immunol. 51:49-54
Höhler T, Schneider PM, Rittner C, Hasenclever P, Meyer zum Büschenfelde
KH, Märker-Hermann E (1996) LMP polymorphisms do not influence disease
expression in psoriatic arthritis. Clin. Exp. Rheumatol. 14:661-664
Höhler T, Gerken G, Notghi A, Lubjuhn R, Taheri H, Protzer U, Löhr
H, Schneider PM, Meyer zum Büschenfelde KH, Rittner C (1997) HLA-DRB1*1301
and *1302 protect against chronic hepatitis B. J. Hepatol. 26:503-507
Höhler T, Gerken G, Notghi A, Knolle P, Lubjuhn R, Taheri H, Schneider
PM, Meyer zum Büschenfelde KH, Rittner C (1997) MHC class II genes
influence the susceptibility to chronic hepatitis C. J. Hepatol. 27:259-264
Höhler T, Kruger A, Schneider PM, Schopf RE, Knop J, Rittner C, Meyer
zum Büschenfelde KH, Märker-Hermann E (1997) A TNF-alpha promoter
polymorphism is associated with juvenile onset psoriasis and psoriatic
arthritis. J. Invest. Dermatol. 509:565-569
Höhler T, Schäper T, Schneider PM, Krummenauer F, Rittner C,
Meyer zum Büschenfelde KH, Märker-Hermann E (1997) No primary
association between LMP2 polymorphisms and extraspinal manifestations in
spondylarthropathies. Ann. Rheum. Dis. 56:741-743
Höhler T, Kruger A, Gerken G, Schneider PM, Meyer zum Büschenfelde
KH, Rittner C (1998) Tumor necrosis factor alpha promoter polymorphism
at position -238 is associated with chronic active hepatitis C infection.
J. Med. Virol. 54:173-177, 1998
Höhler T, Meyer CU, Notghi A, Stradmann-Bellinghausen B, Schneider
PM, Starke R, Zepp F, Sänger R, Clemens R, Meyer zum Büschenfelde
KH, Rittner C (1998) The influence of major histocompatibility complex
class II genes and T-cell Vß repertoire on response to immunization
with HBsAg. Hum. Immunol. 59:212-218
Höhler T, Schäper T, Schneider PM, Meyer zum Büschenfelde
KH, Märker-Hermann E (1998) TNF-alpha promoter alleles TNF308.2 and
TNF238.2 protect against the development of ankylosing spondylitis in HLA-B27
positive individuals. Arthritis Rheum. 41:1489-1493
Höhler T, Wünschel M, Gerken G, Schneider PM, Meyer zum Büschenfelde
KH, Rittner C (1998) No association between mannose-binding lectin alleles
and susceptibility to chronic hepatitis B virus infection in German patients.
Exp. Clin. Immunogenet. 15:130-133
Höhler T, Hug R, Schneider PM, Krummenauer F, Gripenberg-Lerche C,
Granfors K, Märker-Hermann E (1999) Ankylosing spondylitis in monozygotic
twins: studies on immunological parameters. Ann. Rheum. Dis. 58:435-40
Höhler T, Leininger S, Schneider PM (1999) A new polymorphism in the
human HFE gene. Immunogenet. 49:823-824
Boorboor P, Drescher BE, Hartung K, Sachse C, Tsao BP, Schneider PM, Kalden
JR, Lakomek HJ, Peter HH, Schmidt RE, Witte T (2000) Poly (ADP-ribose)
polymerasepolymorphisms are not a genetic risk factor for Systemic Lupus
Erythematosus in German caucasians. J. Rheumatol. 27:2061
Forensic DNA analysis
Rittner C, Schacker U, Schneider PM. (1989) Zum gegenwärtigen Stand
des DNA-Gutachtens (sog. genet. Fingerabdruck) in der Bundesrepublik Deutschland.
Medizinrecht 1989,1:12-15
Ogata M, Mattern R, Schneider PM, Schacker U, Kaufmann T, Rittner C. (1990)
Quantitative and qualitative analysis of DNA extracted from postmortem
muscle tissues. Rechtsmedizin 103:397-406
Schacker U, Schneider PM, Holtkamp B, Bohnke E, Fimmers R, Sonneborn HH,
Rittner C. (1990) Isolation and characterization of the DNA minisatellite
probe MZ 1.3 and its application to DNA 'fingerprint' analysis. Forensic
Science Intern. 44:209-224
Rittner C, Penzes L, Prager-Eberle M, Schacker U, Schneider PM, Jordan
U, Schmidt V, Busse D, Hildebrand HE, Koops E (1991) DNA-Spurenanalyse.
Kriminalistik 7/91:439-442
Rittner C, Schacker U, Schneider PM. (1991) DNA fingerprinting as a tool
of paternity testing in Germany. In: Berghaus G, Brinkmann B, Rittner C,
Staak M (Hrsg.) DNA Technology and its Forensic Application. Springer Berlin
Heidelberg S. 20-32
Schacker U, Kaufmann T, Schneider PM, Rittner C. (1991) Reliability of
restriction enzyme digestions of genomic DNA for the generation of DNA
fingerprints. In: Berghaus G, Brinkmann B, Rittner C, Staak M (Hrsg.) DNA
Technology and its Forensic Application. Springer Berlin Heidelberg S.
103-108
Schneider PM, Veit A, Rittner C. (1991) PCR typing of the human HLA-DQ
alpha locus: population genetics and application in forensic casework.
In: Berghaus G, Brinkmann B, Rittner C, Staak M (Hrsg.) DNA Technology
and its Forensic Application. Springer Berlin Heidelberg S. 85-91
Schneider PM, Fimmers R, Woodroffe S, Werrett DJ, Bär W, Brinkmann
B, Eriksen B, Jones S, Kloosterman AD, Mevag B, Pascali VL, Rittner C,
Schmitter H, Thomson JA, Gill P. (1991) Report of a European collaborative
exercise comparing DNA typing results using a single locus VNTR probe.
Forensic Science Intern. 49:1-15
Schneider PM, Prager-Eberle M, Rittner C. (1991) Zur Anwendung der Polymerase
Kettenreaktion (PCR) des HLA-DQ alpha Systems in der forensischen Spurenkunde.
Archiv Kriminol. 188:167-174
Schneider PM, Müntefering H, Ruf D, Prager-Eberle M, Rittner C. (1992)
DNA-Technologie zur Täterermittlung: Zum Einsatz der DNA-Analyse bei
Abstammungsuntersuchungen im Zusammenhang mit Straftaten. Kriminalistik
(6) :403-406
Fimmers R, Schneider PM, Baur MP. (1992) Comparison of different methods
for the calculation of indices for paternity. Advances in Forensic Haemogenet.
4:277-284
Gill P, Woodroffe S, Bär W, Brinkmann B, Carracedo A, Eriksen B, Jones
S, Kloosterman AD, Ludes B, Mevag B, Pascali VL, Rudler M, Schmitter H,
Schneider PM, Thomson JA. (1992) A report of an international collaborative
experiment to demonstrate the uniformity obtainable using DNA profiling
techniques. Forensic Science Intern. 53:29-43
Pötsch L, Meyer U, Rothschild S, Schneider PM, Rittner C. (1992) Application
of DNA techniques for identification using human dental pulp as a source
of DNA. Int. J. Legal Med. 105:139-143
Rittner C, Schneider PM, Rittner G. (1992) Zum Beitrag des DNA-Gutachtens
in Fällen mit verstorbenem Putativvater (sog. Defizienzfälle).
DAVorm. 65:105-114
Schneider PM, Fimmers R, Bertrams J, Birkner P, Braunbeck K, Bulnheim U,
Feuerbach M, Henke L, Iten E, Osterhaus E, Prinz M, Simeoni E, Rittner
C. (1992) Biostatistical basis of individualisation and segregation analysis
using the multilocus DNA probe MZ 1.3: results of a collaborative study.
Forensic Science Intern. 55:45-58
Schneider PM, Fimmers R, Schacker U, Rittner C. (1992) Paternity analysis
using the multilocus DNA probe MZ 1.3. Advances in Forensic Haemogenet.
4:179-181
Schneider PM, Rittner C. (1993) Experience with the PCR-based HLA-DQalpha
DNA typing system in routine forensic casework. Int. J. Legal Med. 105:295-299
Pötsch L, Prager-Eberle M, Penzes L, Schneider PM, Rittner C. (1993)
Zum Identitätsnachweis an Urinproben mit PCR. Rechtsmedizin 3:128-133
Zhang L, Stradmann-Bellinghausen B, Schneider PM, Rittner C. (1993) Genetic
polymorphisms of the A and B subunits of coagulation factor XIII in the
Chinese population. Exp. Clin. Immunogenet. 10:137-140
Brenner CH, Rittner C, Schneider PM. (1994) Calculation of paternity probabilities
from multilocus DNA profiles. Electrophoresis 15:170-174
Gill P, Kimpton C, D'Aloja E, Andersen JF, Bär W, Brinkmann B, Holgerssen
S, Johnsson V, Kloosterman AD, Lareu MV, Nellemann L, Pfitzinger H, Phillips
CP, Schmitter H, Schneider PM, Stenersen M. (1994) Report of the European
DNA profiling group (EDNAP) - towards standardization of short tandem repeat
(STR) loci. Forensic Science Intern. 65:51-59
Kimpton C, Gill P, D'Aloja E, Andersen JF, Bär W, Holgerssen S, Jacobsen
S, Johnsson V, Kloosterman AD, Lareu MV, Nellemann L, Pfitzinger H, Phillips
CP, Rand S, Schmitter H, Schneider PM, Stenersen M, Vide MC (1995) Report
on the second EDNAP collaborative STR exercise. Forensic Sci. Int. 71:137-152
Lessig R, Edelmann J, Christmann A, Grigorean R, Weichhold G, Zehner R,
Morling N, Brenner CH, Schneider PM (1995) Vergleich populationsgenetischer
Daten verschiedener Laboratorien zu den Eizel-Locus-Systemen MS31 und MS43a.
Rechtsmedizin 6:10-16
Andersen J, Martin P, Carracedo A, Dobosz M, Eriksen B, Johnsson V, Kimpton
C, Kloosterman A, Konialis C, Kratzer A, Phillips P, Mevag B, Pfitzinger
H, Rand S, Rosen B, Schmitter H, Schneider PM, Vide M (1996) Report on
the third EDNAP collaborative STR exercise. Forensic Sci. Int. 78:83-93
Schneider PM, Lummer J, Rittner G, Rittner C (1996) Populationsgenetik
und forensische Anwendung der PCR-typisierten Genorte LDL Rezeptor, Glycophorin
A, Hämoglobin G-gamma, D7S8 und gruppenspezifische Komponente. Rechtsmedizin
6:83-87
Schneider PM, Zhang L, Esdar C, Rittner G, Batzer MA, Rittner C (1996)
PCR typing of Alu elements - molecular genetics and forensic application.
Advances in Forensic Haemogenet. 5:118-120
Kayser M, Caglia A, Corach D, Fretwell N, Gehrig C, Graziosi G, Heidorn
F, Herrmann S, Herzog B, Hidding M, Honda K, Jobling M, Krawczak M, Leim
K, Meuser S, Meyer E, Oesterreich W, Schneider PM, Szibor R, Teifel-Greding
J, Weichhold G, De Knijf P, Roewer L. (1997) Evaluation of Y-chromosomal
STRs: a multicenter study. Int. J. Legal Med. 110:125-133
De Knijf P, Kayser M, Caglia A, Corach D, Fretwell N, Gehrig C, Graziosi
G, Heidorn F, Herrmann S, Herzog B, Hidding M, Honda K, Jobling M, Krawczak
M, Leim K, Meuser S, Meyer E, Oesterreich W, .. Schneider PM, Szibor R,
Teifel-Greding J, Weichhold G, Roewer L. (1997) Chromosome Y microsatellites:
population genetics and evolutionary aspects. Int. J. Legal Med.110:134-140
Gill P, d'Ajola A, Andersen J, Dupuy B, Jangblad M, Johnsson V, Kloosterman
AD, Kratzer A, Lareu MV, Meldegaard M, Philips C, Pfitzinger H, Rand S,
Sabatier M, Scheithauer R, Schmitter H, Schneider PM, Vide MC. (1997) Report
of the European DNA profiling group (EDNAP): an investigation of the complex
STR loci D21S11 and HUMFIBRA (FGA). Forensic Sci. Int. 86:25-33
Schneider PM (1997) Changes in the DNA profile caused by toxic substances?
Forensic Sci. Int. 86:145-148
Bein G, Driller B, Schürmann M, Schneider PM, Kirchner H (1998) Pseudo-exclusion
from paternity due to maternal uniparental disomy 16. Int. J. Legal Med.
111:328-330
Gill P, d'Aloja E, Dupuy B, Eriksen B, Jangblad A, Johnsson V, Kloosterman
AD, Lareu MV, Mevag B, Morling N, Phillips C, Pfitzinger H, Rand S, Sabatier
M, Scheithauer R, Schmitter H, Schneider PM, Skitsa I, Vide MC. Report
of the European DNA Profiling group (EDNAP) - an investigation of the hypervariable
loci ACTBP2, APOA11 and D11S554 and the compound loci D12S391 and D1S1656.
Forensic Sci. Int. 98:193-200
Schneider PM, Rittner C (1998) DNA-Profile von Sexualstraftätern:
Rechtliche und organisatorische Aspekte zur Einrichtung eines zentralen
Registers für DNA-Profile von Straftätern (sog. Gen-Datenbanken).
Zeitschrift f. Rechtspolitik 31:64-68
Schneider PM (1998) Datenbanken mit genetischen Merkmalen von Straftätern.
Datenschutz und Datensicherheit 22:330-333
Schneider PM (1998) DNA databases for offender identification in Europe
- the need for technical, legal and political harmonization. In: Proceedings
of the 2nd European Symposium on Human Identification, Promega Corp., Madison,
WI, USA
Schneider PM, Meuser S, Waiyawuth W, Seo Y, Rittner C (1998) Tandem repeat
structure of the duplicated Y-chromosomal STR locus DYS385 and frequency
studies in the German and three Asian populations. Forensic Sci. Int. 97:61-70
Seo Y, Stradmann-Bellinghausen B, Rittner C, Takahama K, Schneider PM (1998)
Sequence polymorphism of mitochondrial DNA control region in Japanese.
Forensic Sci. Int. 97:155-164
Waiyawuth W, Zhang L, Rittner C, Schneider PM (1998) Genetic analysis of
the short tandem repeat system D12S391 in the German and three Asian populations.
Forensic Sci. Int. 94:25-31
Schneider PM, d'Aloja E, Dupuy BM, Eriksen B, Jangblad A, Kloosterman AD,
Kratzer A, Lareu MV, Pfitzinger H, Rand S, Scheithauer R, Schmitter H,
Skitsa I, Syndercombe-Court D, Vide MC (1999) Results of a collaborative
study regarding the standardization of the Y-linked STR system DYS385 by
the European DNA Profiling (EDNAP) group. Forensic Sci. Int. 102:159-165
Schneider PM, Seo Y, Rittner C (1999) Forensic mtDNA hair analysis excludes
a dog from having caused a traffic accident. Int. J. Legal Med. 112:315-316
Carracedo A, Bär W, Lincoln P, Mayr W, Morling N, Olaisen B, Schneider
PM, Budowle B, Brinkmann B, Gill P, Holland M, Tully G, Wilson M (2000)
DNA Commission of the International Society for Forensic Genetics: guidelines
for mitochondrial DNA typing. Forensic Sci Int 110:79-85.
Bender K, Schneider PM, Rittner C (2000) Application of mtDNA sequence
analysis in forensic casework for the identification of human remains.
Forensic Sci. Int. 113:103-107