Wissenschaftliche Kompetenz und Erfahrung
- Seidl S. Incomplete Rh antibody and its method of demonstration]. Z Arztl Fortbild (Jena). 1956 Aug 15;50(16):697-703. German.
- Seidl S. Blutgruppen [Blood groups]. Z Gesamte Inn Med. 1958 Dec 1;13(23):945-9. German.
- Seidl S, Friedrich E, Spielmann W. The frequency of the Lp(a)-factor in Frankfurt/Main. Vox Sang. 1966 Nov-Dec;11(6):730-3.
- Wiebecke D, Spielmann W, Seidl S, Mohs S. [Contribution to population genetics of the Gm and Inv systems]. Klin Wochenschr. 1967 Jul 15;45(14):736-7.
- Wiebecke D, Spielmann W, Seidl S. The frequencies of Gm(1),Gm(2), Gm(4),Gm(12), and Inv(1) in Hessen (Germany). Humangenetik. 1968;5(3):211-5.
- Seidl S, Spielmann W, Martin H. Two siblings with Rh null disease. Vox Sang. 1972;23(3):182-9.
- Spielmann W, Seidl S. The application of the HL-A-system in cases of disputed paternity. Studies on 110 families (author's transl)]. Z Rechtsmed. 1974 May 20;74(2):121-40. German.
- Albert ED, Scholz S, Bertrams J, Ewald RW, Westphal E, Ratschko KW, Spielmann W, Seidl S. Representative HL-A phenotype and haplotype frequencies of the german population. Z Immunitätsforsch Exp Klin Immunol. 1975 May;148(5):367-413.
- Kühnl P, Spielmann W. Investigations on the PGMa1 polymorphism (phosphoglucomutase--EC 2.7.5.1) by isoelectric focusing. Hum Genet. 1978 Jul 12;43(1):57-67.
- Kühnl P, Spielmann W. PiT: a new allele in the alpha 1-antitrypsin system. Hum Genet. 1979;50(2):221-3.
- Spielmann W, Kühnl P. The efficacy of modern blood group genetics with regard to a case of probable superfecundation. Haematologia (Budap). 1980;13(1-4):75-85.
- Constans J, Kühnl P, Viau M, Spielmann W. A new procedure for the determination of transferrin C (Tf C) subtypes by isoelectric focusing. Existence of two additional alleles, Tf C4 and Tf C5. Hum Genet. 1980;55(1):111-4.
- Spielmann W, Kühnl P. Blood group expert evaluation: relation between the extent of testing and the reliability of paternity determination. Reflections on revision and guidelines]. Z Rechtsmed. 1983;90(1):35-44.
- Seidl C, Saraiya C, Osterweil Z, Fu YP, Lee JS. Genetic complexity of regulatory mutant defective for HLA Class II gene expression. J Immunol 1992; 148: 1576-1584.
- Seidl C, Rabold U, Brüggemann B, Kilp M, Teixidor D, Seifried E: Application of single locus probes in cases of disputed paternity. The usefulness of the combination of HLA and DNA. Adv Forensic Haemogenet 1993; 5: 235-239.
- Seidl C, Jäger O, M Kilp, Seifried E. Automated fluorescence PCR based analysis of the STR polymorphism at locus D8S639 and at the CYP19 gene. Adv Forensic Haemogenet 1996; 6: 216-218.
- Seidl C, Rabold U, Brüggemann B, Kilp M, Teixidor D, Seifried E. Population data of the VNTR loci D10S28, D4S139, D16S309 and D5S110 in German Caucasiens. Adv Forensic Haemogenet 1996; 6: 632-634.
- Seidl C, Jäger O, Kilp M, Seifried E. A tetraplex PCR system for the analysis of paternity cases. Adv Forensic Haemogenet 1996; 6: 142-144.
- Seidl C, Jäger O, Seifried E. Analysis of the short tandem repeat polymorphism D21S11 in german caucasians. Adv Forensic Haemogenet 1996; 6: 630-631.
- Seifried E, Seidl C, Grigorean R, Brude R, Jäger O, Langenbeck U, Zang K.D. A rare paternity case with PP 99,99% and exclusion at three loci derived from the 33.15 VNTR sequence. Adv Forensic Haemogenet 1996; 6: 307-309.
- Gärtner H, Seidl C, Luckenbach C, Seifried E ,Ritter H. Genetic analysis of a sarcoma accidentally transplanted from a patient to a surgeon. N Engl J Med 1997; 335: 1494-1496.
- Seidl C, Jäger O, Seifried E. Population and family studies of the sequence polymorphism at short tandem repeat locus D8S639 reveals complex repeat patterns. Prog Forensic Genet 1998; 7: 471-474.
- Seidl C, Müller S, Kilp M, Seifried E. Fluorescence based multiplex analysis of the STR polymorphism FIBRA, VWFA31 and D18S51 in German caucasoid individuals. Prog Forensic Genet 1998; 7: 353-355.
- Seidl C, Müller S, Seifried E. Sequence analysis of the short tandem repeat polymorphisms D11S488 and D19S246 in the German caucasians. Prog Forensic Genet 1998; 7: 356-359
- Seidl C, Müller S, Jäger O, Seifried E. Sequence analysis and population data of short tandem repeat polymorphisms at loci D8S639 and D11S488. Int J Legal Med 1999; 112: 335-359
- Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in German patients with genetic hemochromatosis. Eur J Immunogenet 2000; 27: 129-134
- Koehl U, Beck O, Esser R, Seifried E, Klingebiel T, Schwabe D, Seidl C. Quantitative analysis of chimerism after allogeneic cell transplantation by PCR amplification of microsatellite markers and capillary electrophoresis with fluorescence detection: the Frankfurt experience. Leukemia 2003; 17(1): 232-236
- Beck O, Seidl C, Kreyenberg H, Lehrnbecher T, Schwabe D, Klingebiel Th, Seifried E, Bader P, Koehl U. Quantification of mixed chimerism within peripheral blood, bone marrow and purified leukocyte subsets: Comparison between singleplex versus multiplex PCR amplification of short tandem repeat (STR) loci. Eur J Haematol. 2006 ;76(3):237-44. QB and CS have contributed equally to this sudy
- Fimmers R, Baur M, Rabold U, Seifried E, Seidl C. STR-profiling for differentiation between related and unrelated individuals in cases of citizen rights. Forensic Science International Genetics, 2008; 1: 510-513.
- Brixner V, Martin H, Richter R, Seidl C, Seifried E. A haplotype HLA-A*3201 – B*0702 – Cw*07 with a new HLA-Cw allelic variant closely related to HLA-Cw*0702 found in a Caucasian patient suffering from leukaemia. Tissue Antigens2009; 74(2): 169-170.
- Skrablin PS, Richter R, Brixner V, Seifried E, Seidl C. The novel allele HLA-DQB1*0636 of Caucasian origin has a unique amino acid exchange at position 186 of the beta 2 region. Tissue Antigens. 2010 Jul;76(1):72-4. Epub 2010 Mar 11
