Cheryl Halter - Concepedia

Author

Cheryl Halter

Indiana University – Purdue University Indianapolis

Also Known As

Cheryl A Halter, Cheryl A. Halter, Cheryl Halter, Michael W Pauciulo

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Indiana University – Purdue University Indianapolis Cincinnati Children's Hospital Medical Center University of Rochester VA San Diego Healthcare System University Medical Center

About

Cheryl Halter is an author at Indiana University – Purdue University Indianapolis specializing in medicine, parkinson disease, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	1.4K
2	Engineering	1	1	181
3	Public Health	1	1	18
4	Social Sciences	1	1	10
5	Epidemiology	1	1	18

Cheryl Halter

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease William C. Nichols, Nathan Pankratz, Dena Hernández, The Lancet Mendelian DisorderFamilial ParkinsonGenetic DisorderParkinson DiseaseGenetics	2005	453
Genomewide association study for susceptibility genes contributing to familial Parkinson disease Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Human Genetics Familial Parkinson DiseaseGenomewide Association StudyDisease SusceptibilityGenome-wide Association StudyParkinson Disease	2008	442
Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations Nathan Pankratz, William C. Nichols, Sean K. Uniacke, The American Journal of Human Genetics Identify Susceptibility GenesGenetic AnalysisGenome-wide Association StudyEngineeringMedicine	2002	181
Significant Linkage of Parkinson Disease to Chromosome 2q36-37 Nathan Pankratz, William C. Nichols, Sean K. Uniacke, The American Journal of Human Genetics Genetic DisorderGeneticsParkinson DiseaseDisease Gene IdentificationNeurodegeneration	2003	157
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, Movement Disorders	2005	123
Copy Number Variation in Familial Parkinson Disease Nathan Pankratz, Alexandra Dumitriu, Kurt N. Hetrick, PLoS ONE Genome-wide Association StudySingle CnvMendelian DisorderGenetic DisorderGenetics	2011	83
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease Paul J. Hop, Dongbing Lai, Pamela Keagle, Nature Genetics	2024	61
Mutations in DJ-1 are rare in familial Parkinson disease Nathan Pankratz, Michael W. Pauciulo, Veronika E. Elsaesser, Neuroscience Letters Familial Parkinson DiseaseMendelian DisorderParkinson DiseaseDegenerative DiseaseNeurology	2006	54
Alpha‐synuclein and familial Parkinson's disease Nathan Pankratz, William C. Nichols, Veronika E. Elsaesser, Movement Disorders	2009	43
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease William C. Nichols, Sean K. Uniacke, Nathan Pankratz, Movement Disorders	2004	37

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