Publications by authors named "Aina Rengmark"

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Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Zafar Iqbal, Siri L Rydning, Iselin M Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina H Rengmark

PLoS One· October 2017

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Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Zafar Iqbal, Siri L Rydning, Iselin M Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina H Rengmark

PLoS One· August 2017

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Rare variants in dementia genes and Parkinson's disease.
Zafar Iqbal, Lasse Pihlstrøm, Aina Rengmark, Sandra Pilar Henriksen, Jan Linder

Eur J Hum Genet· December 2016

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Low frequency of GCH1 and TH mutations in Parkinson's disease.
Aina Rengmark, Lasse Pihlstrøm, Jan Linder, Lars Forsgren, Mathias Toft

Parkinsonism Relat Disord· August 2016

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The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.
Christina M Lill, Aina Rengmark, Lasse Pihlstrøm, Isabella Fogh, Aleksey Shatunov

Alzheimers Dement· December 2015

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Fine mapping and resequencing of the PARK16 locus in Parkinson's disease.
Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå, Nil Dizdar, Camilla Fardell

J Hum Genet· July 2015

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Parkinson's disease correlates with promoter methylation in the α-synuclein gene.
Lasse Pihlstrøm, Victoria Berge, Aina Rengmark, Mathias Toft

Mov Disord· April 2015

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Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease.
Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå, Mathias Toft

Ann Hum Genet· May 2014

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