Subjects:

Molecular genetics of the complement system

1. Prentice HL, Schneider PM, Strominger JL. (1986) C4B gene polymorphism detected in a human cosmid clone. Immunogenetics 23:274-276
2. 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
3. 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
4. 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
5. 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
6. 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
7. 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
8. 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
9. Mauff G, Alper CA, Dawkins R, Doxiadis G, Giles CM, Hauptmann G, Rittner C, Schneider PM. (1990) C4 nomenclature statement (1990). Complement Inflamm. 7:261-268
10. Mauff G, Brenden M, Braun-Stilwell M, Doxiadis G, Giles C, Hauptmann G, Rittner C, Schneider PM, Stradmann-Bellinghausen B, Uring-Lambert B. (1990) C4 reference typing report. Complement Inflamm. 7:193-212
11. Rittner C, Schneider PM. (1989) Complexity of MHC class III genes and complement polymorphism. Immunol. Today 10:401-403
12. Schneider PM. (1990) C4 DNA RFLP reference typing report. Complement Inflamm. 7:218-224
13. 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
14. 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
15. 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
16. Kaufmann T, Rittner C, Schneider PM. (1993) The human complement component C8B gene: structure and phylogenetic relationship. Hum. Genet. 92:69-75
17. 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
18. 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
19. 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
20. 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
21. 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
22. 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
23. 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
24. 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
25. 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
26. 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
27. Schneider PM, Rittner C. (1997) Complement Genetics. In: Complement - A Practical Approach (A. Dodds & B. Sim, eds.) Oxford University Press, 165-198
28. 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
29. 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
30. 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
31. 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
32. 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
33. 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
34. Schneider PM, Würzner R (1999) Complement genetics: biological implications of polymorphisms and deficiencies. Immunol. Today 20:2-5
35. 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

1. 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
2. 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
3. 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
4. Glöckel U, Schneider PM, Beck JD, Brade V. (1990) Letale Pneumokokkenmeningitis bei einem 1jährigen Kind mit homozygotem C2-Defekt. Monatsschr. Kinderheilkunde 138:399-402
5. 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
6. 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
7. 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
8. 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
9. 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
10. 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
11. 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
12. 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
13. 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
14. 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
15. 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
16. 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
17. 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
18. 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
19. 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
20. 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
21. 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
22. 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
23. Höhler T, Leininger S, Schneider PM (1999) A new polymorphism in the human HFE gene. Immunogenet. 49:823-824
24. 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

1. 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
2. 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
3. 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
4. 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
5. 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
6. 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
7. 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
8. 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
9. 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
10. 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
11. 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
12. 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
13. 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
14. Rittner C, Schneider PM, Rittner G. (1992) Zum Beitrag des DNA-Gutachtens in Fällen mit verstorbenem Putativvater (sog. Defizienzfälle). DAVorm. 65:105-114
15. 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
16. 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
17. 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
18. Pötsch L, Prager-Eberle M, Penzes L, Schneider PM, Rittner C. (1993) Zum Identitätsnachweis an Urinproben mit PCR. Rechtsmedizin 3:128-133
19. 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
20. Brenner CH, Rittner C, Schneider PM. (1994) Calculation of paternity probabilities from multilocus DNA profiles. Electrophoresis 15:170-174
21. 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
22. 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
23. 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
24. 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
25. 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
26. 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
27. 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
28. 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
29. 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
30. Schneider PM (1997) Changes in the DNA profile caused by toxic substances? Forensic Sci. Int. 86:145-148
31. 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
32. 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
33. 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
34. Schneider PM (1998) Datenbanken mit genetischen Merkmalen von Straftätern. Datenschutz und Datensicherheit 22:330-333
35. 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
36. 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
37. 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
38. 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
39. 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
40. 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
41. 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.
42. 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