Publications by authors named "Erik Simons"

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LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
Marialuisa Quadri, Wim Mandemakers, Martyna M Grochowska, Roy Masius, Hanneke Geut, Erik Simons

Lancet Neurol· July 2018

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XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination.
Hanna IJspeert, Jacob Rozmus, Klaus Schwarz, René L Warren, David van Zessen, Erik Simons

Blood· August 2016

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CD21 and CD19 deficiency: Two defects in the same complex leading to different disease modalities.
Marjolein W J Wentink, Annechien J A Lambeck, Menno C van Zelm, Erik Simons, Jacques J M van Dongen

Clin Immunol· December 2015

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Strategies for B-cell receptor repertoire analysis in primary immunodeficiencies: from severe combined immunodeficiency to common variable immunodeficiency.
Hanna IJspeert, Marjolein Wentink, David van Zessen, Gertjan J Driessen, Virgil A S H Dalm, Erik J Simons

Front Immunol· April 2015

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Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants.
Lei Zhang, Marialuisa Quadri, Leonor Correia Guedes, Miguel Coelho, Anabela Valadas, Erik Simons

Parkinsonism Relat Disord· October 2013

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Detection of mutant NPM1 mRNA in acute myeloid leukemia using custom gene expression arrays.
Martin H van Vliet, Belinda Dumee, Erik Simons, Lars Bullinger, Konstanze Döhner

Genet Test Mol Biomarkers· April 2013

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Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease.
Ekaterina Yonova-Doing, Masharip Atadzhanov, Marialuisa Quadri, Paul Kelly, Nyambura Shawa, Erik J Simons

Parkinsonism Relat Disord· June 2012

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The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy.
Chiara Criscuolo, Anna De Rosa, Anna Guacci, Erik J Simons, Guido J Breedveld

Mov Disord· August 2011

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Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
Marialuisa Quadri, Giovanni Cossu, Valeria Saddi, Erik J Simons, Daniela Murgia

Neurogenetics· August 2011

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Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation.
Roberto Di Fabio, Alessandra Tessa, Erik J Simons, Filippo M Santorelli, Carlo Casali

Parkinsonism Relat Disord· August 2010

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Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
Antonetta M G Sas, Alessio Di Fonzo, Stef L M Bakker, Erik J Simons, Ben A Oostra

Mov Disord· August 2010

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GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
Alessio Di Fonzo, Edito Fabrizio, Astrid Thomas, Emiliana Fincati, Roberto Marconi, Erik J Simons

Parkinsonism Relat Disord· November 2009

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A reliable cell-based assay for testing unclassified TSC2 gene variants.
Ricardo Coevoets, Sermin Arican, Marianne Hoogeveen-Westerveld, Erik Simons, Ans van den Ouweland

Eur J Hum Genet· March 2009

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The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population.
Chin-Song Lu, Yah-Huei Wu-Chou, Marina van Doeselaar, Erik J Simons, Hsiu-Chen Chang

Neurogenetics· October 2008

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LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample.
Stefano Goldwurm, Michela Zini, Alessio Di Fonzo, Danilo De Gaspari, Chiara Siri, Erik J Simons

Parkinsonism Relat Disord· October 2006

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A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan.
Alessio Di Fonzo, Yah-Huei Wu-Chou, Chin-Song Lu, Marina van Doeselaar, Erik J Simons

Neurogenetics· July 2006

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Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
Alessio Di Fonzo, Cristina Tassorelli, Michele De Mari, Hsin F Chien, Joaquim Ferreira, Erik J Simons

Eur J Hum Genet· March 2006

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Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the Netherlands.
Aida M Bertoli-Avella, Marieke C J Dekker, Yurii S Aulchenko, Jeanine J Houwing-Duistermaat, Erik Simons

Hum Genet· March 2006

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The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.
Chin-Song Lu, Erik J Simons, Yah-Huei Wu-Chou, Alessio Di Fonzo, Hsiu-Chen Chang

Parkinsonism Relat Disord· December 2005

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Multiple regulatory elements contribute to the vascular-specific expression of the rice HD-Zip gene Oshox1 in Arabidopsis.
Enrico Scarpella, Erik J Simons, Annemarie H Meijer

Plant Cell Physiol· August 2005

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