Tõnisson N - Search Results

1

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.

Žilina O, Koltšina M, Raid R, Kurg A, Tõnisson N, Salumets A. Žilina O, et al. Among authors: tonisson n. BMC Genomics. 2015 Sep 16;16(1):703. doi: 10.1186/s12864-015-1916-3. BMC Genomics. 2015. PMID: 26376747 Free PMC article.

2

Arrayed primer extension: solid-phase four-color DNA resequencing and mutation detection technology.

Kurg A, Tõnisson N, Georgiou I, Shumaker J, Tollett J, Metspalu A. Kurg A, et al. Among authors: tonisson n. Genet Test. 2000;4(1):1-7. doi: 10.1089/109065700316408. Genet Test. 2000. PMID: 10794354

3

Unravelling genetic data by arrayed primer extension.

Tõnisson N, Kurg A, Kaasik K, Lõhmussaar E, Metspalu A. Tõnisson N, et al. Clin Chem Lab Med. 2000 Feb;38(2):165-70. doi: 10.1515/CCLM.2000.025. Clin Chem Lab Med. 2000. PMID: 10834405

4

Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene.

Tõnisson N, Zernant J, Kurg A, Pavel H, Slavin G, Roomere H, Meiel A, Hainaut P, Metspalu A. Tõnisson N, et al. Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5503-8. doi: 10.1073/pnas.082100599. Proc Natl Acad Sci U S A. 2002. PMID: 11960007 Free PMC article.

5

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.

Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A. Patsalis PC, et al. Among authors: tonisson n. Eur J Hum Genet. 2007 Feb;15(2):162-72. doi: 10.1038/sj.ejhg.5201738. Epub 2006 Nov 22. Eur J Hum Genet. 2007. PMID: 17119536

6

Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.

Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A, Patsalis PC. Kousoulidou L, et al. Among authors: tonisson n. Nat Protoc. 2008;3(5):849-65. doi: 10.1038/nprot.2008.49. Nat Protoc. 2008. PMID: 18451793

7

Molecular diagnosis of Down syndrome using quantitative APEX-2 microarrays.

Oitmaa E, Peters M, Vaidla K, Andreson R, Mägi R, Slavin G, Velthut A, Tõnisson N, Reimand T, Remm M, Schneider M, Ounap K, Salumets A, Metspalu A. Oitmaa E, et al. Among authors: tonisson n. Prenat Diagn. 2010 Dec;30(12-13):1170-7. doi: 10.1002/pd.2639. Prenat Diagn. 2010. PMID: 20949644

8

Methylation markers of early-stage non-small cell lung cancer.

Lokk K, Vooder T, Kolde R, Välk K, Võsa U, Roosipuu R, Milani L, Fischer K, Koltsina M, Urgard E, Annilo T, Metspalu A, Tõnisson N. Lokk K, et al. Among authors: tonisson n. PLoS One. 2012;7(6):e39813. doi: 10.1371/journal.pone.0039813. Epub 2012 Jun 29. PLoS One. 2012. PMID: 22768131 Free PMC article.

9

Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual.

Krjutškov K, Koltšina M, Grand K, Võsa U, Sauk M, Tõnisson N, Salumets A. Krjutškov K, et al. Among authors: tonisson n. Curr Genet. 2014 Feb;60(1):11-6. doi: 10.1007/s00294-013-0398-6. Epub 2013 Jul 11. Curr Genet. 2014. PMID: 23842853 Free PMC article.

10

DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns.

Lokk K, Modhukur V, Rajashekar B, Märtens K, Mägi R, Kolde R, Koltšina M, Nilsson TK, Vilo J, Salumets A, Tõnisson N. Lokk K, et al. Among authors: tonisson n. Genome Biol. 2014 Apr 1;15(4):r54. doi: 10.1186/gb-2014-15-4-r54. Genome Biol. 2014. PMID: 24690455 Free PMC article.

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