III Verzeichnis sämtlicher Publikationen

1. KEIL, W., MADEA B. & ROEWER L. (1988) Zur Hämagglutinationsaktivität des Lektins aus Evonymus europaea. Haima Immunreport 3, 6-7.

2. ROEWER, L., ROSE M., SEMM, K. CORRENS, A. & EPPLEN, J.T. (1989). Typisierung gelagerter, hämolysierter Blutproben durch „DNA-Fingerprinting“. Arch Kriminol 184, 103-107.

3. ROEWER, L., NAGAI, T., PROKOP, O. & EPPLEN J.T. (1989). Oligonucleotide Fingerprints from human urine. Fingerprint News 4 8.

4. NÜRNBERG, P., ROEWER, L., NEITZEL, H., SPERLING, K., PÖPPERL, A., HUNDRIESER J., PÖCHE H., EPPLEN, C., ZISCHLER, H. & EPPLEN, J.T. (1989). DNA fingerprinting with the oligonucleotide probe (CAC)5/(GTG)5: somatic stability and germline mutations. Hum Genet 84, 75-78.

5. ROEWER, L., NAGAI, T., KRÜGER, C. & ROSE, M. (1990). DNA-Analyse aus dem Urin. Krim Forens Wiss 77/78, 181-182.

6. ROEWER, L., NÜRNBERG, P., FUHRMANN, E., ROSE, M., PROKOP, O. & EPPLEN, J.T. (1990). Stain analysis using oligonucleotide probes specific for simple repetitive DNA sequences. Forensic Sci Int 47, 59-70.

7. ROSE, M., NAGAI, T., ROEWER, L., KRÜGER, C. & EPPLEN, J.T. (1990). Praktikabilität digoxigenierter Oligonukleotid-Sonden für den DNA-Fingerprint. Haima Immunreport 5, 9-12.

8. RIEß, O., KAMMERBAUER, C., ROEWER, L., STEIMLE, V., ANDREAS A., ALBERT, E., NAGAI, T. & EPPLEN, J.T. (1990). Hypervariability of intronic simple (gt)n(ga)m repeats in DRB genes. Immunogenetics 32, 110-116.

9. ZISCHLER, H., NÜRNBERG, P., ROEWER, L., PÖCHE, H., NANDA, I., SCHMID, M. & EPPLEN, J.T. (1990). Application of simple repeat oligonucleotides for DNA fingerprinting. In: Advances in Forensic Haemogenetics 3. Edited by POLESKY, H.F. & MAYR, W.R., Springer Verlag Berlin Heidelberg New York, pp. 125-127.

10. PROKOP, O., ROSE, M. & ROEWER, L. (1990). Cesare LOMBROSO, die Serogenetik, DNA, RFLP und kein Ende. In: Past, Present and Future of Forensic Medicine. Tagungsband zum Satellite Symposium anläßlich des 100th Anniversary of the Opening of Department of Forensic Medicine, Faculty of Medicine, University of Tokyo, 9.10.1990.

11. ROEWER, L. (1990). Zur Darstellung und Anwendung simpler repetitiver Oligonukleotidsequenzen in der Gerichtlichen Medizin. Dissertation,Institut für Gerichtliche Medizin der Charité, Humboldt-Universität zu Berlin.

12. EPPLEN, J.T., KAMMERBAUER, C., ZISCHLER, H., STEIMLE, V., EPPLEN, C., ROEWER, L., RIEß, O., ANDREAS, A., ALBERT, E., NANDA, I. & SCHMID, M. (1991). On the meaning of individual hypervariable DNA loci containing stretches of simple repeat sequences. In: Molecular Biology of Tumour Research. Edited by ISSINGER, O.G., HENKE, J., KÖMPF, J. & DRIESEL, A.J., Hüthig-Buch-Verlag Heidelberg, Adv Mol Genet 3, 119-120.

13. ROEWER, L., RIEß, O. & PROKOP, O. (1991). Hybridization and PCR amplification of simple repeated DNA sequences for the analysis of forensic stains. Electrophoresis 12, 181-186.

14. EPPLEN, J.T., AMMER, H., EPPLEN, C., KAMMERBAUER, C., MITREITER, R., ROEWER, L., SCHWAIGER, W., STEIMLE, V., ZISCHLER, H., ALBERT, E., ANDREAS, A., BEYERMANN, B., MEYER, W., BUITKAMP, J., NANDA, I., SCHMID, M., NÜRNBERG, P., PENA, S.D.J., PÖCHE, H., SPRECHER, W., SCHARTL, M., WEISING, K. & YASSOURIDIS, A. (1991). Oligonucleotide fingerprinting using simple repeat motifs: A convenient, ubiquitously applicable method to detect hypervariability for multiple purposes. In: DNA fingerprinting: Approaches and applications. Edited by BURKE, T., DOLF, G., JEFFREYS, A.J. & WOLFF, R., Birkhäuser-Verlag Basel/Switzerland, pp. 50-69.

15. EPPLEN J.T., ZISCHLER, H., ROEWER, L. & NÜRNBERG, P. (1991). Anwendungen des Genetischen Fingerabdruckes in der Medizin. Deutsches Ärzteblatt 88 (7), D372-D376.

16. EPPLEN, J.T., MÄUELER, W., BUITKAMP, J., GOMOLKA M., PIRCHNER, C., ROEWER, L., SCHWAIGER, F.W., & EPPLEN, C. (1991). On hypervariable, simple, repetitive DNA elements in eucaryote genomes: fact, function, fiction. In: Electrophoresis Forum ´91. Edited by RADOLA, B.J., Bode Verlag München, pp. 97-108.

17. KUNSTMANN, E., BOCKER, T., ROEWER, L., SAUER, H., MEMPEL, W. & EPPLEN, J.T. (1992). Diagnosis of transfusion-associated graft-versus-host disease by genetic fingerprinting and polymerase chain reaction. Transfusion 32, 766-770.

18. ROEWER, L. & NÜRNBERG, P. (1992). DNA Fingerprinting. In: Transfusionsmedizin - Aktuell (2.Auflage). Hrsg. KÖHLER, M. & MAYR, W.R., Verlag Ermer KG, Homburg-Saar, pp. 137-144.

19. NAGY, M. & ROEWER, L. (1992). Die PCR-Analyse. In: Transfusionsmedizin - Aktuell (2.Auflage). Hrsg. KÖHLER, M. & MAYR, W.R., Verlag Ermer KG, Homburg-Saar, pp. 137-144.

20. ROEWER, L., ARNEMANN, J., SPURR, N.K., GRZESCHIK, K.H. & EPPLEN, J.T. (1992). Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum Genet 89, 389-394.

21. ROEWER, L. & EPPLEN, J.T. (1992). Rapid and sensitive typing of forensic stains by PCR amplification of polymorphic simple repeat sequences in case work. Forensic Sci Int 53, 163-171.

22. ROEWER, L., ARNEMANN, J. & EPPLEN, J.T. (1992). Analysis of forensic stains via PCR amplification of polymorphic simple (gata)n repeats. In: Advances in Forensic Haemogenetics 4. Edited by RITTNER, C. & SCHNEIDER, P.M., Springer Verlag Berlin Heidelberg New York, pp. 115-117.

23. EPPLEN, J.T., MELMER, G., SCHMIDT, P., ROEWER, L., HUNDRIESER, J., EPPLEN, C. & BUITKAMP, J. (1992). On the potential of simple repetitive DNA for fingerprinting in clinical, forensic and evolutionary dynamic studies. Clin Investigator 70, 1043-1051.

24. ROEWER, L., NAGY, M., SCHMIDT, P., EPPLEN, J.T. & HERZOG-SCHRÖDER, G. (1993). Microsatellite and HLA class II oligonucleotide typing in a population of Yanomami Indians. In: DNA fingerprinting: State of the Science. Edited by PENA, S.D.J., CHAKRABORTY, R., EPPLEN, J.T., JEFFREYS, A.J., Birkhäuser Verlag Basel Boston Berlin, pp. 221-230.

25. GOMOLKA, M., HUNDRIESER, J., NÜRNBERG, P., ROEWER, L., EPPLEN, J.T. & EPPLEN, C. (1994). Selected di- and tetranucleotide microsatellites from chromosomes 7, 12, 14 and Y in various Eurasian populations. Hum Genet 93, 592-596.

26. ROEWER, L. (1994). DNA - The code of life. In: The illustrated history of humankind (Volume 5), Weldon Owen Pty Ltd./Bra Bröcker AB, Sydney Australia, pp. 22-23.

27. NAGY, M., ROEWER, L., NÜRNBERG, P., BOCKEL, B, KRAWCZAK, M. & GESERICK, G. (1995). Strategies in paternity testing and forensic case work - the Charité experience. In: Advances in Forensic Sciences 6, Edited by JACOB, B. & BONTE, W., Verlag Dr. Köster Berlin, pp. 90-96.

28. KAYSER, M., NÜRNBERG, P., BERCOVITCH, F., NAGY, M. & ROEWER, L. (1995). Increased microsatellite variability in Macaca mulatta compared to human due to a large scale deletion/insertion event during primate evolution. Electrophoresis 16, 1607-1611.

29. KAYSER, M., RITTER, H., BERCOVITCH, F., MRUG, M., ROEWER, L. & NÜRNBERG, P. (1996). Identification of five highly polymorphic microsatellites in rhesus macaque Macaca mulatta by cross-species amplification. Mol Ecol 5, 157-159.

30. ROEWER, L., KAYSER, M., NAGY, M. & DE KNIJFF, P. (1996). Male identification using Y-chromosomal STR polymorphisms. In: Advances in Forensic Haemogenetics 6, Edited by CARRACEDO, A., BRINKMANN, B., BÄR, W., Springer Verlag Berlin Heidelberg New York, pp. 124-126.

31. ROEWER, L., KAYSER, M., DIELTJES, P., NAGY, M., BAKKER, E., KRAWCZAK, M. & DE KNIJFF, P. (1996). Analysis of Molecular Variance (AMOVA) of Y-chromosome specific microsatellites in two closely related human populations. Hum Mol Genet 5 (7), 1029-1033.

32. DE KNIJFF, P., ROEWER, L., KAYSER, M. & BAKKER, E.B. (1996). Chromosome Y microsatellites and their use in determining population affinities. Am J Hum Genet 59 (4) (suppl.).

33. KAYSER, M., CAGLIÁ, 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., PANDYA, A., PARSON, W., PICCININI, A., PEREZ-LEZAUN, A., PRINZ, M., SCHMITT, C., SCHNEIDER, P.M., SZIBOR, R., TEIFEL-GREDING, J., WEICHHOLD, G., DE KNIJFF, P. & ROEWER, L. (1997). Evaluation of Y chromosomal STRs: A Multicenter Study. Int J Legal Med 110 (3), 125-133, 141-149.

34. DE KNIJFF, P., KAYSER, M., CAGLIÁ, 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., PANDYA, A., PARSON, W., PICCININI, A., PER EZ-LEZAUN, A., PRINZ, M., SCHMITT, C., SCHNEIDER, P.M., SZIBOR, R., TEIFEL-GREDING, J., WEICHHOLD, G. & ROEWER, L. (1997). Chromosome Y microsatellites: population genetic and evolutionary aspects. Int J Legal Med 110 (3), 134-149.

35. ZERJAL, T., DASHNYAM, B., PANDYA, A., KAYSER, M., ROEWER, L., SANTOS, F.R., SCHIEFENHÖVEL, W., FRETWELL, N., JOBLING, M.A., HARIHARA, S., SHIMIZU, K., SEMJIDMAA, D., SAJANTILA, A., SALO, P., CRAWFORD, M.H., GINTER, E.K., EVGRAFOV, O.V. & TYLER-SMITH, C. (1997). Genetic Relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am J Hum Genet 60, 1174-1183.

36. KAYSER, M., DE KNIJFF, P., DIELTJES, P., KRAWCZAK, M., NAGY, M., ZERJAL, T., PANDYA, A., TYLER-SMITH, C. & ROEWER, L. (1997). Applications of microsatellite based Y chromosome haplotyping. Electrophoresis 18, 1602-1607.

37. DE KNIJFF, P., KAYSER, M., HEYER, E., DIELTJES, P., BAKKER, E.B. & ROEWER, L.: Sequence structure, mutation rates and chromosomal localization of a set of Y chromosome microsatellites (Vortrag). 3rd International HUGO Single Chromosome Workshop on the Y Chromosome, 13.-16.4.1997, Heidelberg, Abstract in: Genome Data Base, accession number CIT 766063, Cytogenetic Cell Genet 79, 1-20.

38. KAYSER, M., ROEWER, L., TYLER-SMITH, C. & DE KNIJFF, P.: Genetic variation at Y chromosomal microsatellite loci (Poster). 3rd International HUGO Single Chromosome Workshop on the Y Chromosome 13.-16.4.1997, Heidelberg, Abstract in: Genome Data Base, accession number CIT 765978, Cytogenetic Cell Genet 79, 1-20.

39. NAGY, M., ZIMDAHL, H., KRÜGER, C., ANDERS, P., KAYSER, M., ROEWER, L. & SCHIEFENHÖVEL, W. (1998). Are the Trobriands emigrants of South East Asia? In: Genetic Diversity of HLA: Functional and medical implications. Proceedings of the 12th International Histocompatibility Workshop and Conference. Edited by CHARRON, D.J., EDK Medical and Scientific International Publisher, Sevres, pp. 185-188.

40. ROEWER, L. (1998). Beiträge der modernen Hämogenetik zur Identifikation. DNA-Merkmale. In: Identifikation unbekannter Toter. Interdisziplinäre Methodik, forensische Osteologie. Hrsg. LEOPOLD, D., Verlag Schmidt-Römhild, Lübeck, pp. 327-354

41. FORSTER, P., KAYSER, M., MEYER, E., ROEWER, L., PFEIFFER, H., BENKMANN, H. & BRINKMANN, B. (1998). Phylogenetic resolution of complex mutational features at Y-STR DYS390 in aboriginal Australians and Papuans. Mol Biol Evol 15, 1108-1114.

42. ROEWER, L. (1998). The Y chromosome: Forensic application and evolutionary aspects. In: Progress in Forensic Genetics 7. Proceedings of the 17th International ISFH Congress, Oslo, 2-6 September 1997. Edited by OLAISEN B, BRINKMANN B, LINCOLN PJ, Elsevier Science B.V. Amsterdam, pp. 407-412.

43. CORACH, D., PENACINO, G., SALA, A., IANUCCI, N., MARTINEZ, M., VILLAFANE, A., KAYSER, M. & ROEWER, L. (1998). Validation studies of Y-specific STRs: Forensic casework evaluation. In: Progress in Forensic Genetics 7. Proceedings of the 17th International ISFH Congress, Oslo, 2-6 September 1997. Edited by OLAISEN B, BRINKMANN B, LINCOLN PJ, Elsevier Science B.V. Amsterdam, pp. 407-412.

44. KAYSER, M., KRÜGER, C., NAGY, M., GESERICK, G., DE KNIJFF, P. & ROEWER, L. (1998). Chromosome Y analysis in paternity testing: Experiences and recommendations. In: Progress in Forensic Genetics 7. Proceedings of the 17th International ISFH Congress, Oslo, 2-6 September 1997. Edited by OLAISEN B, BRINKMANN B, LINCOLN PJ, Elsevier Science B.V. Amsterdam, pp. 407-412.

45. ZIMDAHL, H., KRÜGER, C., ANDERS, P., GESERICK, G., ROEWER, L. & NAGY, M. (1998). Evaluation and application of highly informative and sensitive HLA-DRB and -DPB INNO-LIPA typing systems in forensic practice. In: Progress in Forensic Genetics 7. Proceedings of the 17th International ISFH Congress, Oslo, 2-6 September 1997. Edited by OLAISEN B, BRINKMANN B, LINCOLN PJ, Elsevier Science B.V. Amsterdam, pp. 407-412.

46. ROEWER, L. (1998) Paternitätsdiagnostik. DNA Short Tandem repeat (STR) Systeme. In: DGI Technisches Handbuch Histokompatibilität & Immungenetik. Hrsg. BEIN, G., NAGY, M., WAßMUTH, R., WEGENER, S., Methodenkommission der Deutschen Gesellschaft für Immungenetik, pp. 230-234.

47. ROEWER, L., DE KNIJFF, P. & KAYSER, M. (1999) Y chromosome STR analysis in Forensic Practice In: Proceedings from the Second European Symposium on Human Identification. Ed. Promega Corporation Madison, USA, pp. 13-16.

48. HAGELBERG, E., KAYSER, M., NAGY, M., ROEWER, L., ZIMDAHL, H., KRAWCZAK, M., LIÓ, P. & SCHIEFENHÖVEL, W. (1999) Molecular genetic evidence for the human settlement of the Pacific: analysis of mitochondrial DNA, Y chromosome and HLA markers. Philos T Roy Soc B 354, 141-152.

49. ROEWER, L., NAGY, M. & GESERICK, G. (1999) Der genetische Fingerabdruck. Humboldt-Spektrum 6 (1), 4-15.

50. HONDA, K., ROEWER, L. & DE KNIJFF, P. (1999). Male DNA typing from 25-year-old vaginal swabs using Y STR polymorphisms in retrial request case. J Forensic Sci 44(4), 868-872.

51. KRAWCZAK, M. & ROEWER,L. (1999) Frequency estimation for rare Y-chromosomal haplotypes. (Poster) Abstract cited in: Am J Hum Genet 65 (4), A 208.

52. ZIMDAHL, H., SCHIEFENHÖVEL, W., KAYSER, M., ROEWER, L. & NAGY, M. (1999) Towards understanding the origin and dispersal of Austronesians in the Solomon Sea: HLA class II polymorphism in eight distinct populations of Asia-Oceania. Eur J Immunogenet 26, 405-416.

53. ROEWER, L., KAYSER, M., ANSLINGER, K., AUGUSTIN, C., CAGLIÁ, A., CORACH, D., FÜREDI, S., GESERICK, G., HENKE, L., HIDDING, M., KÄRGEL, H.-J., DE KNIJFF, P., LESSIG, R., PASCALI, V.L., PARSON, W., PRINZ, M., ROLF, B., SCHMITT, C., SCHNEIDER, P., SZIBOR, R., TEIFEL-GREDING, J., KRAWCZAK, M. (1999). Caucasian Y-STR haplotype reference database for forensic application. In: Progress in Forensic Genetics 8. Proceedings of the 18th International ISFH Congress, San Francisco, 17-21 August 1999. Edited by SENSABAUGH, G.F., LINCOLN, P.J., OLAISEN B, Elsevier Science B.V. Amsterdam, pp. 613-615.

54. KAYSER, M., ROEWER, L., HEDMAN, M., HENKE, L., HENKE, J., BRAUER, S., KRÜGER, C., KRAWCZAK, M., NAGY, M., DOBOSZ, T., SZIBOR, R., DE KNIJFF, P., STONEKING, M. & SAJANTILA, A. (2000) Characteristics and frequency of germline mutations at microsatellite loci from the human Y chromosome, as revealed by direct observation in father / son pairs. Am J Hum Genet 66, 1580-1588.

55. SZIBOR, R., KAYSER, M. & ROEWER, L. (2000). Identification of the Human Y-Chromosomal Microsatellite DYS19 from degraded DNA. Am J Foren Med Path 21(3), 252-254.

56. ROEWER, L., KAYSER, M., DE KNIJFF, P., ANSLINGER, K., CAGLIÁ, A., CORACH, D., FÜREDI, S., HENKE, L., HIDDING, M., KÄRGEL, H.-J., LESSIG, R., NAGY, M., PASCALI, V.L., PARSON, W., ROLF, B., SCHMITT, C., SZIBOR, R., TEIFEL-GREDING, J. & KRAWCZAK, M. (2000). A new method for the evaluation of matches in non-recombining genomes: application to Y-chromosomal short tandem repeat (STR) haplotypes in European males. For Sci International 114 (1), 31- 43.

57. ROLF, B., KEIL, W., BRINKMANN, B., ROEWER, L., FIMMERS, R. (2000) Paternity testing using Y-STR haplotypes: Assigning a probability for paternity in cases of mutations. Int J Legal Med (in press)

58. KAYSER, M., KRAWCZAK, M., EXCOFFIER, L., DIELTJES, CORACH, D., PASCALI, V., GEHRIG, C., SCHIEFENHÖVEL, W., BERNINI, JESPERSEN, BAKKER, ROEWER, L., DE KNIJFF, P. (2001) Extensive analysis of chromosome Y microsatellite haplotypes from globally dispersed human populations. Am J Hum Genet 68, 990-1018.

59. KAYSER, M., BRAUER, S., WEISS, G., UNDERHILL, P., ROEWER, L., SCHIEFENHÖVEL, W. & STONEKING, M. (2000). Melanesian Origin of Polynesian Y Chromosomes. Curr Biol 10, 1237-1246. Corrigendum (2001) Curr Biol, 11(2).

60. ROSSER, Z.H., ZERJAL, T., HURLES,M.E., ADOJAAN, M., ALAVANTIC, D., AMORIM, A., AMOS, W., ARMENTEROS, M., ARROYO, E., BARBUJANI, G., BECKMAN, L., BERTRANPETIT, J., BOSCH, E., BRADLEY, D.G., BREDE, G., COOPER, G.C., CORTE-REAL, H., DE KNIJFF, P., DECORTE, R., DUBROVA, Y.E., EVGRAFOV, O., GILISSEN, A., GLISIC, S., GÖLGE, M., HILL, E.W., JEZIOROVSKA, A., KALAYDIJEVA, L., KAYSER, M., KRAVCHENKO, S.A., LAVINHA, J., LIVSHITS, L.A., MARIA, S., MCELREAVEY, K., MEITINGER, T.A., MELEGH, B., MITCHELL, R.J., NICHOLSON, J., NORBY, S., NOVELETTO, A., PANDYA, A., PARIK, J., PATSALIS, P.C., PEREIRA, L., PETERLIN, B., PIELBERG, G., PRATA, M.J., PREVIDERÉ, C., RAJCZY, K., ROEWER, L., ROOTSI, S., RUBINSZTEIN, D.C., SAILLARD, J., SANTOS, F.R., SHLUMUKOVA, M., STEFANESCU, G., SYKES, B.C., TOLUN, A., VILLEMS, R., TYLER-SMITH, C. & JOBLING, M.A. (2000). Y-chromosomal diversity within Europe is clinal and influenced primarily by geography rather than language. Am J Hum Genet 67, 1526-1543. Erratum (2001). Am J Hum Genet 68, 1075.


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