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Items: 14

1.

SD quants-Sensitive detection tetraplex-system for nuclear and mitochondrial DNA quantification and degradation inference.

Xavier C, Eduardoff M, Strobl C, Parson W.

Forensic Sci Int Genet. 2019 Jun 10;42:39-44. doi: 10.1016/j.fsigen.2019.06.004. [Epub ahead of print]

PMID:
31216503
2.

The maternal inheritance of Alto Paraná revealed by full mitogenome sequences.

Simão F, Strobl C, Vullo C, Catelli L, Machado P, Huber N, Schnaller L, Huber G, Xavier C, Carvalho EF, Gusmão L, Parson W.

Forensic Sci Int Genet. 2019 Mar;39:66-72. doi: 10.1016/j.fsigen.2018.12.007. Epub 2018 Dec 19.

PMID:
30594063
3.

Evaluation of the precision ID whole MtDNA genome panel for forensic analyses.

Strobl C, Eduardoff M, Bus MM, Allen M, Parson W.

Forensic Sci Int Genet. 2018 Jul;35:21-25. doi: 10.1016/j.fsigen.2018.03.013. Epub 2018 Mar 29.

PMID:
29626805
4.

Optimized mtDNA Control Region Primer Extension Capture Analysis for Forensically Relevant Samples and Highly Compromised mtDNA of Different Age and Origin.

Eduardoff M, Xavier C, Strobl C, Casas-Vargas A, Parson W.

Genes (Basel). 2017 Sep 21;8(10). pii: E237. doi: 10.3390/genes8100237.

5.

Lack of gene-language correlation due to reciprocal female but directional male admixture in Austronesians and non-Austronesians of East Timor.

Gomes SM, van Oven M, Souto L, Morreira H, Brauer S, Bodner M, Zimmermann B, Huber G, Strobl C, Röck AW, Côrte-Real F, Parson W, Kayser M.

Eur J Hum Genet. 2017 Feb;25(2):246-252. doi: 10.1038/ejhg.2016.101. Epub 2016 Aug 3.

6.

Evaluation of DNA variants associated with androgenetic alopecia and their potential to predict male pattern baldness.

Marcińska M, Pośpiech E, Abidi S, Andersen JD, van den Berge M, Carracedo Á, Eduardoff M, Marczakiewicz-Lustig A, Morling N, Sijen T, Skowron M, Söchtig J, Syndercombe-Court D, Weiler N; EUROFORGEN-NoE Consortium, Schneider PM, Ballard D, Børsting C, Parson W, Phillips C, Branicki W.

PLoS One. 2015 May 22;10(5):e0127852. doi: 10.1371/journal.pone.0127852. eCollection 2015.

7.

Human settlement history between Sunda and Sahul: a focus on East Timor (Timor-Leste) and the Pleistocenic mtDNA diversity.

Gomes SM, Bodner M, Souto L, Zimmermann B, Huber G, Strobl C, Röck AW, Achilli A, Olivieri A, Torroni A, Côrte-Real F, Parson W.

BMC Genomics. 2015 Feb 14;16:70. doi: 10.1186/s12864-014-1201-x.

8.

Evidence for frequent and tissue-specific sequence heteroplasmy in human mitochondrial DNA.

Naue J, Hörer S, Sänger T, Strobl C, Hatzer-Grubwieser P, Parson W, Lutz-Bonengel S.

Mitochondrion. 2015 Jan;20:82-94. doi: 10.1016/j.mito.2014.12.002. Epub 2014 Dec 16.

PMID:
25526677
9.

Full mtGenome reference data: development and characterization of 588 forensic-quality haplotypes representing three U.S. populations.

Just RS, Scheible MK, Fast SA, Sturk-Andreaggi K, Röck AW, Bush JM, Higginbotham JL, Peck MA, Ring JD, Huber GE, Xavier C, Strobl C, Lyons EA, Diegoli TM, Bodner M, Fendt L, Kralj P, Nagl S, Niederwieser D, Zimmermann B, Parson W, Irwin JA.

Forensic Sci Int Genet. 2015 Jan;14:141-55. doi: 10.1016/j.fsigen.2014.09.021. Epub 2014 Oct 5.

10.

Helena, the hidden beauty: Resolving the most common West Eurasian mtDNA control region haplotype by massively parallel sequencing an Italian population sample.

Bodner M, Iuvaro A, Strobl C, Nagl S, Huber G, Pelotti S, Pettener D, Luiselli D, Parson W.

Forensic Sci Int Genet. 2015 Mar;15:21-6. doi: 10.1016/j.fsigen.2014.09.012. Epub 2014 Sep 26.

PMID:
25303789
11.

Development of forensic-quality full mtGenome haplotypes: success rates with low template specimens.

Just RS, Scheible MK, Fast SA, Sturk-Andreaggi K, Higginbotham JL, Lyons EA, Bush JM, Peck MA, Ring JD, Diegoli TM, Röck AW, Huber GE, Nagl S, Strobl C, Zimmermann B, Parson W, Irwin JA.

Forensic Sci Int Genet. 2014 May;10:73-9. doi: 10.1016/j.fsigen.2014.01.010. Epub 2014 Feb 6.

12.

WITHDRAWN: Erratum to "Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM)" [Forensic Sci. Int.: Genet. 7 (2013) 543-549].

Parson W, Strobl C, Huber G, Zimmermann B, Gomes SM, Souto L, Fendt L, Delport R, Langit R, Wootton S, Lagaceé R, Irwin J.

Forensic Sci Int Genet. 2014 Jan 21. pii: S1872-4973(13)00179-8. doi: 10.1016/j.fsigen.2013.08.005. [Epub ahead of print]

PMID:
26898381
13.

Reprint of: Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM).

Parson W, Strobl C, Huber G, Zimmermann B, Gomes SM, Souto L, Fendt L, Delport R, Langit R, Wootton S, Lagacé R, Irwin J.

Forensic Sci Int Genet. 2013 Dec;7(6):632-9. doi: 10.1016/j.fsigen.2013.09.007. Epub 2013 Sep 27.

PMID:
24119954
14.

Evaluation of next generation mtGenome sequencing using the Ion Torrent Personal Genome Machine (PGM).

Parson W, Strobl C, Huber G, Zimmermann B, Gomes SM, Souto L, Fendt L, Delport R, Langit R, Wootton S, Lagacé R, Irwin J.

Forensic Sci Int Genet. 2013 Sep;7(5):543-9. doi: 10.1016/j.fsigen.2013.06.003. Epub 2013 Jul 23.

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