Publications by authors named "Johanna Huttenlocher"

8Publications

Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease.

Hum Mol Genet 2015 Oct 17;24(19):5637-43. Epub 2015 Jul 17.

deCODE Genetics/AMGEN, Reykjavik 101, Iceland, Faculty of Medicine, University of Iceland, Reykjavik IS-101, Iceland

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http://dx.doi.org/10.1093/hmg/ddv277DOI Listing
October 2015

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.

J Neurol Neurosurg Psychiatry 2015 Sep 4;86(9):986-95. Epub 2014 Dec 4.

Sorbonne Universités, Université Pierre et Marie Curie - Paris 06, UMR_S1127, Paris, France Inserm, U1127, Paris, France Cnrs, UMR 7225, Paris, France AP-HP, Groupe Hospitalier Pitié-Salpêtriére, Departement of Genetics and Cytogenetics, Paris, France.

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http://dx.doi.org/10.1136/jnnp-2014-309153DOI Listing
September 2015

EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts.

J Med Genet 2015 Jan 3;52(1):37-41. Epub 2014 Nov 3.

Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1136/jmedgenet-2014-102570DOI Listing
January 2015

Common variants at VRK2 and TCF4 conferring risk of schizophrenia.

Hum Mol Genet 2011 Oct 26;20(20):4076-81. Epub 2011 Jul 26.

deCODE Genetics, IS-101 Reykjavik, Iceland.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/ddr325DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298077PMC
October 2011