Kahre T[au] - Search Results

Year	Number of Results
2003	1
2004	1
2006	3
2008	1
2010	2
2011	1
2012	2
2013	1
2014	1
2015	3
2016	1
2017	2
2018	2
2019	2
2021	3
2022	5
2023	0

1

Pharmacogenetics may explain part of the interindividual variability of dobutamine pharmacodynamics in neonates.

Hallik M, Soeorg H, Kahre T, Murumets Ü, Ilmoja ML, Kipper K, Metsvaht T. Hallik M, et al. Among authors: kahre t. Br J Clin Pharmacol. 2022 Sep;88(9):4155-4162. doi: 10.1111/bcp.15357. Epub 2022 Apr 29. Br J Clin Pharmacol. 2022. PMID: 35437830

2

Aortic arch thrombosis in a neonate with heterozygous carrier status of factor V Leiden mutation.

Metsvaht T, Hermlin T, Kern H, Kahre T, Starkopf J. Metsvaht T, et al. Among authors: kahre t. Congenit Heart Dis. 2006 Jan;1(1-2):40-5. doi: 10.1111/j.1747-0803.2006.00007.x. Congenit Heart Dis. 2006. PMID: 18373789 Review.

3

Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.

Jürgens H, Roht L, Leitsalu L, Nõukas M, Palover M, Nikopensius T, Reigo A, Kals M, Kallak K, Kütner R, Budrikas K, Kuusk S, Valvere V, Laidre P, Toome K, Rekker K, Tooming M, Ülle Murumets, Kahre T, Kruuv-Käo K, Õunap K, Padrik P, Metspalu A, Esko T, Fischer K, Tõnisson N. Jürgens H, et al. Among authors: kahre t. Front Genet. 2022 Jul 22;13:881100. doi: 10.3389/fgene.2022.881100. eCollection 2022. Front Genet. 2022. PMID: 35938029 Free PMC article.

4

The Birth Prevalence of Spinal Muscular Atrophy: A Population Specific Approach in Estonia.

Sarv S, Kahre T, Vaidla E, Pajusalu S, Muru K, Põder H, Gross-Paju K, Ütt S, Žordania R, Talvik I, Õiglane-Shlik E, Muhu K, Õunap K. Sarv S, et al. Among authors: kahre t. Front Genet. 2021 Dec 22;12:796862. doi: 10.3389/fgene.2021.796862. eCollection 2021. Front Genet. 2021. PMID: 35003227 Free PMC article.

5

The prevalence of germline pathogenic variants in Estonian colorectal cancer patients: results from routine clinical setting 2016-2021.

Roht L, Tooming M, Rekker K, Roomere H, Toome K, Murumets Ü, Šamarina U, Õunap K, Kahre T. Roht L, et al. Among authors: kahre t. Front Genet. 2022 Nov 8;13:1020543. doi: 10.3389/fgene.2022.1020543. eCollection 2022. Front Genet. 2022. PMID: 36425062 Free PMC article.

6

The prevalence of inherited metabolic disorders in Estonian population over 30 years: A significant increase during study period.

Tiivoja E, Reinson K, Muru K, Rähn K, Muhu K, Mauring L, Kahre T, Pajusalu S, Õunap K. Tiivoja E, et al. Among authors: kahre t. JIMD Rep. 2022 Aug 24;63(6):604-613. doi: 10.1002/jmd2.12325. eCollection 2022 Nov. JIMD Rep. 2022. PMID: 36341167 Free PMC article.

7

Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection: a case report.

Zhytnik L, Peters M, Tilk K, Reimand T, Ilisson P, Kahre T, Murumets Ü, Ehrenberg A, Ustav EL, Tõnisson N, Mölder S, Teder H, Krjutškov K, Salumets A. Zhytnik L, et al. Among authors: kahre t. BMC Pregnancy Childbirth. 2022 Feb 5;22(1):105. doi: 10.1186/s12884-022-04431-6. BMC Pregnancy Childbirth. 2022. PMID: 35123446 Free PMC article.

8

Presumed Perinatal Stroke: Risk Factors, Clinical and Radiological Findings.

Ilves P, Laugesaar R, Loorits D, Kolk A, Tomberg T, Lõo S, Talvik I, Kahre T, Talvik T. Ilves P, et al. Among authors: kahre t. J Child Neurol. 2016 Apr;31(5):621-8. doi: 10.1177/0883073815609149. Epub 2015 Oct 7. J Child Neurol. 2016. PMID: 26446909

9

Large gene panel sequencing in clinical diagnostics-results from 501 consecutive cases.

Pajusalu S, Kahre T, Roomere H, Murumets Ü, Roht L, Simenson K, Reimand T, Õunap K. Pajusalu S, et al. Among authors: kahre t. Clin Genet. 2018 Jan;93(1):78-83. doi: 10.1111/cge.13031. Epub 2017 Aug 21. Clin Genet. 2018. PMID: 28378410

10

A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016.

Yakoreva M, Kahre T, Žordania R, Reinson K, Teek R, Tillmann V, Peet A, Õiglane-Shlik E, Pajusalu S, Murumets Ü, Vals MA, Mee P, Wojcik MH, Õunap K. Yakoreva M, et al. Among authors: kahre t. Eur J Hum Genet. 2019 Nov;27(11):1649-1658. doi: 10.1038/s41431-019-0446-x. Epub 2019 Jun 11. Eur J Hum Genet. 2019. PMID: 31186545 Free PMC article.

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