Tõnisson N - Search Results

1

Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans.

Putku M, Kepp K, Org E, Sõber S, Comas D, Viigimaa M, Veldre G, Juhanson P, Hallast P, Tõnisson N; HYPertension in ESTonia (HYPEST); Shaw-Hawkins S, Caulfield MJ; BRItish Genetics of HyperTension (BRIGHT); Khusnutdinova E, Kožich V, Munroe PB, Laan M. Putku M, et al. Among authors: tonisson n. Hum Mutat. 2011 Jul;32(7):806-14. doi: 10.1002/humu.21508. Epub 2011 May 10. Hum Mutat. 2011. PMID: 21520334 Free PMC article.

2

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene.

Jaakson K, Zernant J, Külm M, Hutchinson A, Tonisson N, Glavac D, Ravnik-Glavac M, Hawlina M, Meltzer MR, Caruso RC, Testa F, Maugeri A, Hoyng CB, Gouras P, Simonelli F, Lewis RA, Lupski JR, Cremers FP, Allikmets R. Jaakson K, et al. Among authors: tonisson n. Hum Mutat. 2003 Nov;22(5):395-403. doi: 10.1002/humu.10263. Hum Mutat. 2003. PMID: 14517951

3

Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.

Kepp K, Org E, Sõber S, Kelgo P, Viigimaa M, Veldre G, Tõnisson N, Juhanson P, Putku M, Kindmark A, Kozich V, Laan M. Kepp K, et al. Among authors: tonisson n. BMC Med Genet. 2010 Jan 28;11:15. doi: 10.1186/1471-2350-11-15. BMC Med Genet. 2010. PMID: 20109173 Free PMC article.

4

The number of CAG and GGN triplet repeats in the Androgen Receptor gene exert combinatorial effect on hormonal and sperm parameters in young men.

Grigorova M, Punab M, Kahre T, Ivandi M, Tõnisson N, Poolamets O, Vihljajev V, Žilaitienė B, Erenpreiss J, Matulevičius V, Laan M. Grigorova M, et al. Among authors: tonisson n. Andrology. 2017 May;5(3):495-504. doi: 10.1111/andr.12344. Epub 2017 Mar 23. Andrology. 2017. PMID: 28334513 Free article.

5

Genotype-first approach to the detection of hereditary breast and ovarian cancer risk, and effects of risk disclosure to biobank participants.

Leitsalu L, Palover M, Sikka TT, Reigo A, Kals M, Pärn K, Nikopensius T, Esko T, Metspalu A, Padrik P, Tõnisson N. Leitsalu L, et al. Among authors: tonisson n. Eur J Hum Genet. 2021 Mar;29(3):471-481. doi: 10.1038/s41431-020-00760-2. Epub 2020 Nov 23. Eur J Hum Genet. 2021. PMID: 33230308 Free PMC article.

6

From late fatherhood to prenatal screening of monogenic disorders: evidence and ethical concerns.

Zhytnik L, Peters M, Tilk K, Simm K, Tõnisson N, Reimand T, Maasalu K, Acharya G, Krjutškov K, Salumets A. Zhytnik L, et al. Among authors: tonisson n. Hum Reprod Update. 2021 Oct 18;27(6):1056-1085. doi: 10.1093/humupd/dmab023. Hum Reprod Update. 2021. PMID: 34329448 Review.

7

Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank.

Leitsalu L, Reigo A, Palover M, Nikopensius T, Läll K, Krebs K, Reisberg S, Mägi R, Kals M, Alavere H, Nõukas M, Kolk A, Normet I, Tammesoo ML, Käärik E, Puusepp M, Metsalu K, Allik A, Milani L, Fischer K, Tõnisson N, Metspalu A. Leitsalu L, et al. Among authors: tonisson n. Eur J Hum Genet. 2023 Sep;31(9):1048-1056. doi: 10.1038/s41431-022-01196-6. Epub 2022 Oct 3. Eur J Hum Genet. 2023. PMID: 36192438

8

Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.

Teek R, Oitmaa E, Kruustük K, Zordania R, Joost K, Raukas E, Tõnisson N, Gardner P, Schrijver I, Kull M, Ounap K. Teek R, et al. Among authors: tonisson n. Int J Pediatr Otorhinolaryngol. 2009 Jan;73(1):103-7. doi: 10.1016/j.ijporl.2008.10.003. Epub 2008 Nov 22. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19027966

9

Identification of miR-374a as a prognostic marker for survival in patients with early-stage nonsmall cell lung cancer.

Võsa U, Vooder T, Kolde R, Fischer K, Välk K, Tõnisson N, Roosipuu R, Vilo J, Metspalu A, Annilo T. Võsa U, et al. Among authors: tonisson n. Genes Chromosomes Cancer. 2011 Oct;50(10):812-22. doi: 10.1002/gcc.20902. Epub 2011 Jul 11. Genes Chromosomes Cancer. 2011. PMID: 21748820

10

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.

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