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.
Published in Clinical genetics (01.01.2018)
Published in Clinical genetics (01.01.2018)
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Journal Article
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.
Published in Andrology (Oxford) (01.05.2017)
Published in Andrology (Oxford) (01.05.2017)
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Journal Article
Factor V Leiden and prothrombin 21210G>A mutation and paediatric ischaemic stroke: a case-control study and two meta-analyses
Laugesaar, R, Kahre, T, Kolk, A, Uustalu, Ü, Kool, P, Talvik, T
Published in Acta Paediatrica (01.08.2010)
Published in Acta Paediatrica (01.08.2010)
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Journal Article
P202 – 2912: Methylenetetrahydrofolate reductase (MTHFR) polymorphisms A1298C and C677T as genetic risk factors for perinatal and childhood arterial ischemic stroke?
Kolk, A, Lorenz, A.-L, Laugessaar, R, Talvik, T, Kahre, T, Nikopensius, T, Mihailov, E, Metspalu, A
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
Hearing impairment in Estonia: An algorithm to investigate genetic causes in pediatric patients
Teek, R, Kruustük, K, Žordania, R, Joost, K, Kahre, T, Tõnisson, N, Nelis, M, Zilina, O, Tranebjaerg, L, Reimand, T, Õunap, K
Published in Advances in medical sciences (01.12.2013)
Published in Advances in medical sciences (01.12.2013)
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Journal Article
374 Clinical and demographic characteristics of Estonian cystic fibrosis patients
Vasar, M, Julge, K, Kivivare, M, Moor, R, Puks, K, Putnik, U, Kahre, T
Published in Journal of cystic fibrosis (2011)
Published in Journal of cystic fibrosis (2011)
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Journal Article
Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia
Joost, K., Õunap, K., Žordania, R., Uudelepp, M.-L., Olsen, R. K., Kall, K., Kilk, K., Soomets, U., Kahre, T.
Published in JIMD Reports - Case and Research Reports, 2011/2 (01.01.2012)
Published in JIMD Reports - Case and Research Reports, 2011/2 (01.01.2012)
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Book Chapter
Journal Article
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, Lidiia, Peters, Maire, Tilk, Kadi, Reimand, Tiia, Ilisson, Piret, Kahre, Tiina, Murumets, Ülle, Ehrenberg, Aivar, Ustav, Eva-Liina, Tõnisson, Neeme, Mölder, Signe, Teder, Hindrek, Krjutškov, Kaarel, Salumets, Andres
Published in BMC pregnancy and childbirth (05.02.2022)
Published in BMC pregnancy and childbirth (05.02.2022)
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Journal Article
Descriptive Epidemiology of Spinal Muscular Atrophy Type I in Estonia
Vaidla, Eve, Talvik, Inga, Kulla, Andres, Kahre, Tiina, Hamarik, Malle, Napa, Aita, Metsvaht, Tuuli, Piirsoo, Andres, Talvik, Tiina
Published in Neuroepidemiology (01.01.2006)
Published in Neuroepidemiology (01.01.2006)
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Journal Article
A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia
Talkop, Ülvi-Astra, Kahre, Tiina, Napa, Aita, Talvik, Inga, Sööt, Anu, Piirsoo, Andres, Sander, Valentin, Talvik, Tiina
Published in European journal of paediatric neurology (01.01.2003)
Published in European journal of paediatric neurology (01.01.2003)
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