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[FG] Forensic Genetics

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Senst, A. et al. (2024) ‘Application of the Agilent 2100 Bioanalyzer instrument as quality control for next-generation sequencing’, Journal of Forensic Sciences, 69(6), pp. 2192–2196. Available at: https://doi.org/10.1111/1556-4029.15601.

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Senst, Alina et al. (2024) ‘Application of the Agilent 2100 Bioanalyzer instrument as quality control for next‐generation sequencing’, Journal of Forensic Sciences, 69(6), pp. 2192–2196. Available at: https://doi.org/10.1111/1556-4029.15601.

Schulz, I., Schulte, J. and Dipl-Med, D.W. (2024) ‘Zygotic-splitting after in vitro fertilization and prenatal parenthood testing after suspected embryo mix-up – a case report’, International Journal of Legal Medicine, 138(5), pp. 2057–2064. Available at: https://doi.org/10.1007/s00414-024-03245-9.

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Schulz, Iris, Schulte, Janine and Dipl-Med, Dorothea Wand (2024) ‘Zygotic-splitting after in vitro fertilization and prenatal parenthood testing after suspected embryo mix-up – a case report’, International Journal of Legal Medicine, 138(5), pp. 2057–2064. Available at: https://doi.org/10.1007/s00414-024-03245-9.

Hogg, J. et al. (2024) ‘Targeted recovery of male cells in a male and female same-cell mixture’, Journal of Forensic Sciences, 69(4), pp. 1183–1197. Available at: https://doi.org/10.1111/1556-4029.15514.

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Hogg, Jonathan et al. (2024) ‘Targeted recovery of male cells in a male and female same‐cell mixture’, Journal of Forensic Sciences, 69(4), pp. 1183–1197. Available at: https://doi.org/10.1111/1556-4029.15514.

Schulte, Janine et al. (2024) ‘Exploring the potential of genetic analysis in historical blood spots for patients with iodine-deficient goiter and thyroid carcinomas in Switzerland and Germany (1929–1989)’, BMC Medical Genomics, 17(1). Available at: https://doi.org/10.1186/s12920-024-01947-y.

Schulte, Janine et al. (2024) ‘DEPArray™ single-cell technology: A validation study for forensic applications’, Forensic Science International: Genetics, 70, p. 103026. Available at: https://doi.org/10.1016/j.fsigen.2024.103026.

Schulte, Janine et al. (2024) ‘DEPArray™ single-cell technology: A validation study for forensic applications’, Forensic Science International: Genetics, 70, p. 103026. Available at: https://doi.org/10.1016/j.fsigen.2024.103026.

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Schulz, Iris and Scheurer, Eva (2024) ‘DNA-Analyse in der Forensik - wissenschaftliche Grundlagen und rechtliche Implikationen’, Zeitschrift für Schweizerisches Recht, 1(143), pp. 233–252.

Egloff, Laura et al. (2023) ‘Effect of vaporizing cannabis rich in cannabidiol on cannabinoid levels in blood and on driving ability – a randomized clinical trial’, International Journal of Legal Medicine, 137(6), pp. 1713–1723. Available at: https://doi.org/10.1007/s00414-023-03076-0.

Schulte, Janine et al. (2023) ‘A systematic approach to improve downstream single‐cell analysis for the DEPArray ™ technology’, Journal of Forensic Sciences, 68(6), pp. 1875–1893. Available at: https://doi.org/10.1111/1556-4029.15344.

Schulte, J. et al. (2023) ‘Collecting touch DNA from glass surfaces using different sampling solutions and volumes: Immediate and storage effects on genetic STR analysis’, Journal of Forensic Sciences, 68(4), pp. 1133–1147. Available at: https://doi.org/10.1111/1556-4029.15305.

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Schulte, Janine et al. (2023) ‘Collecting touch DNA from glass surfaces using different sampling solutions and volumes: Immediate and storage effects on genetic STR analysis’, Journal of Forensic Sciences, 68(4), pp. 1133–1147. Available at: https://doi.org/10.1111/1556-4029.15305.

Währer J et al. (2023) ‘The DNA‐Buster: The evaluation of an alternative DNA recovery approach’, Forensic Science International: Genetics, 64, p. 102830. Available at: https://doi.org/10.1016/j.fsigen.2023.102830.

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Senst A et al. (2023) ‘Recommendations for the successful identification of altered human remains using standard and emerging technologies: Results of a systematic approach’, Forensic Science International: Genetics, 62, p. 102790. Available at: https://doi.org/10.1016/j.fsigen.2022.102790.

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Senst, Alina et al. (2023) ‘Recommendations for the successful identification of altered human remains using standard and emerging technologies: Results of a systematic approach’, Forensic Science International: Genetics, 62, p. 102790. Available at: https://doi.org/10.1016/j.fsigen.2022.102790.

Egger S et al. (2022) ‘Technical note: Comparison of forensic swabs for intravaginal sampling’, Science and Justice, 62(4), pp. 418–423. Available at: https://doi.org/10.1016/j.scijus.2022.05.006.

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Seiberle I et al. (2022) ‘Collaborative swab performance comparison and the impact of sampling solution volumes on DNA recovery’, Forensic Science International: Genetics, 59, p. 102716. Available at: https://doi.org/10.1016/j.fsigen.2022.102716.

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Senst A et al. (2022) ‘Validation and beyond: Next generation sequencing of forensic casework samples including challenging tissue samples from altered human corpses using the MiSeq FGx system’, Journal of Forensic Sciences, 67(4), pp. 1382–1398. Available at: https://doi.org/10.1111/1556-4029.15028.

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Senst A et al. (2021) ‘Which tissue to take? A retrospective study of the identification success of altered human remains’, Journal of Forensic and Legal Medicine, 84, p. 102271. Available at: https://doi.org/10.1016/j.jflm.2021.102271.

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Egger S. et al. (2021) ‘Erratum to: Erroneous sex typing due to partial deletion of the Y chromosome (Rechtsmedizin, (2020), 30, 2, (94-100), 10.1007/s00194-020-00373-5) Erratum zu: Fehlerhafte Geschlechtsbestimmung aufgrund partieller Deletion des Y-Chromosoms (Rechtsmedizin, (2020), 30, 2, (94-100), 10.1007/s00194-020-00373-5)’, Rechtsmedizin, 31(3), p. 216. Available at: https://doi.org/10.1007/s00194-021-00486-5.

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Ralf A et al. (2020) ‘Identification and characterization of novel rapidly mutating Y-chromosomal short tandem repeat markers’, Human Mutation, 41(9), pp. 1680–1696. Available at: https://doi.org/10.1002/humu.24068.

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Egger S. et al. (2020) ‘Erroneous sex typing due to partial deletion of the Y chromosome Fehlerhafte Geschlechtsbestimmung aufgrund partieller Deletion des Y-Chromosoms’, Rechtsmedizin, 30(2), pp. 94–100. Available at: https://doi.org/10.1007/s00194-020-00373-5.

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Schulz I, Egger S and Senst A (2020) ‘Die Rolle des Speichels in der forensischen Genetik’, in Filippi, Andreas; Waltimo, Tuomas (ed.) Speichel. (Speichel).

Rolf B and Schulz I (2007) ‘Theorie und Praxis der Abstammungsbegutachtung mit molekularbiologischen Methoden.’, in A. Spickhoff; D. Schwab; D. Henrich; P. Gottwald (ed.) Streit um die Abstammung . Gieseking-Verlag (Streit um die Abstammung ), pp. 83–91.

Schulz I et al. (2006) ‘Examination of postmortem animal interference to human remains using cross-species multiplex PCR.’, Forensic science, medicine, and pathology, 2(2), pp. 95–101. Available at: https://doi.org/10.1385/fsmp:2:2:95.

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Schulz I, Schneider PM and Rothschild MA (2006) ‘Absolute quantification of forensic casework samples using quantitative real-time PCR (qPCR) methods’, International Congress Series. 20.04.2006, 1288, pp. 765–767. Available at: https://doi.org/10.1016/j.ics.2005.09.183.

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