Publications by authors named "Eneli Oitmaa"

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Single Passage of Human Metapneumovirus in LLC-MK2 Cells Does Not Affect Viral Protein-Coding Capacity.
Simon Loevenich, Aleksandr Ianevski, Eneli Oitmaa, Denis E Kainov, Marit W Anthonsen

Genome Announc· May 2018

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Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia.
Pablo Serrano-Fernandez, Dagmara Dymerska, Grzegorz Kurzawski, Róża Derkacz, Tatiana Sobieszczańska, Eneli Oitmaa

Gastroenterol Res Pract· June 2015

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Arrayed primer extension microarray for the analysis of genes associated with congenital stationary night blindness.
Kadri Vaidla, Janne Uksti, Christina Zeitz, Eneli Oitmaa

Methods Mol Biol· June 2013

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Arrayed primer extension technology simplifies mutation detection in Bardet-Biedl and Alström syndrome.
Ines Pereiro, Bethan E Hoskins, Jan D Marshall, Gayle B Collin, Jürgen K Naggert, Eneli Oitmaa

Eur J Hum Genet· April 2011

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Molecular diagnosis of Down syndrome using quantitative APEX-2 microarrays.
Eneli Oitmaa, Maire Peters, Kadri Vaidla, Reidar Andreson, Reedik Mägi

Prenat Diagn· December 2010

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Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.
Rita Teek, Katrin Kruustük, Riina Zordania, Kairit Joost, Tiia Reimand, Eneli Oitmaa

Int J Pediatr Otorhinolaryngol· September 2010

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Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.
Rita Teek, Eneli Oitmaa, Katrin Kruustük, Riina Zordania, Kairit Joost

Int J Pediatr Otorhinolaryngol· January 2009

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Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up.
Phyllis Gardner, Eneli Oitmaa, Anna Messner, Lies Hoefsloot, Andres Metspalu

Pediatrics· September 2006

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Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations.
Iris Schrijver, Eneli Oitmaa, Andres Metspalu, Phyllis Gardner

J Mol Diagn· August 2005

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