Publications by authors named "Cheryl Halter"

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Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.
Paul J Hop, Dongbing Lai, Pamela J Keagle, Desiree M Baron, Brendan J Kenna, Cheryl Halter

Nat Genet· July 2024

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Novel recruitment strategy to enrich for LRRK2 mutation carriers.
Tatiana Foroud, Danielle Smith, Jacqueline Jackson, Jennifer Verbrugge, Cheryl Halter

Mol Genet Genomic Med· September 2015

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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants.
Roy N Alcalay, Jan Aasly, Daniela Berg, Susan Bressman, Alexis Brice, Cheryl Halter

Genet Med· August 2014

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Copy number variation in familial Parkinson disease.
Nathan Pankratz, Alexandra Dumitriu, Kurt N Hetrick, Mei Sun, Jeanne C Latourelle, Cheryl Halter

PLoS One· December 2011

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Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.
Jeanne C Latourelle, Audrey E Hendricks, Nathan Pankratz, Jemma B Wilk, Cheryl Halter

Mov Disord· September 2011

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Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease.
David K Simon, Nathan Pankratz, Diane K Kissell, Michael W Pauciulo, Cheryl A Halter

BMC Med Genet· April 2010

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Genomewide association study for onset age in Parkinson disease.
Jeanne C Latourelle, Nathan Pankratz, Alexandra Dumitriu, Jemma B Wilk, Stefano Goldwurm, Cheryl Halter

BMC Med Genet· September 2009

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Alpha-synuclein and familial Parkinson's disease.
Nathan Pankratz, William C Nichols, Veronika E Elsaesser, Michael W Pauciulo, Diane K Marek, Cheryl A Halter

Mov Disord· June 2009

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Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Nathan Pankratz, Jemma B Wilk, Jeanne C Latourelle, Anita L DeStefano, Cheryl Halter

Hum Genet· January 2009

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Clinical correlates of depressive symptoms in familial Parkinson's disease.
Nathan Pankratz, Karen S Marder, Cheryl A Halter, Alice Rudolph, Cliff W Shults

Mov Disord· November 2008

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R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
William C Nichols, Diane K Marek, Michael W Pauciulo, Nathan Pankratz, Cheryl A Halter

Mov Disord· January 2007

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Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.
Nathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, Diane K Marek, Cheryl A Halter

Mov Disord· December 2006

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Mutations in DJ-1 are rare in familial Parkinson disease.
Nathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, Diane K Marek, Cheryl A Halter

Neurosci Lett· November 2006

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Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.
Nathan Pankratz, Lisa Byder, Cheryl Halter, Alice Rudolph, Clifford W Shults

Mov Disord· January 2006

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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
William C Nichols, Nathan Pankratz, Dena Hernandez, Coro Paisán-Ruíz, Shushant Jain, Cheryl A Halter

Lancet· February 2005

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Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
William C Nichols, Sean K Uniacke, Nathan Pankratz, Terry Reed, David K Simon, Cheryl Halter

Mov Disord· June 2004

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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
Nathan Pankratz, William C Nichols, Sean K Uniacke, Cheryl Halter, Jill Murrell

Hum Mol Genet· October 2003

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Significant linkage of Parkinson disease to chromosome 2q36-37.
Nathan Pankratz, William C Nichols, Sean K Uniacke, Cheryl Halter, Alice Rudolph

Am J Hum Genet· April 2003

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Reliability of reported age at onset for Parkinson's disease.
Carson R Reider, Cheryl A Halter, Peter F Castelluccio, David Oakes, William C Nichols

Mov Disord· March 2003

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Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.
Nathan Pankratz, William C Nichols, Sean K Uniacke, Cheryl Halter, Alice Rudolph

Am J Hum Genet· July 2002

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