Výsledky vyhledávání - Cheryl Halter
- Zobrazuji výsledky 1 - 7 z 7
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Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families Autor Nathan Pankratz, William C. Nichols, Sean K. Uniacke, Cheryl Halter, Jill R. Murrell, Alice Rudolph, Clifford W. Shults, P. Michael Conneally, Tatiana Foroud
Vydáno 2003Artigo -
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease Autor Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle, Anita L. DeStefano, Cheryl Halter, Elizabeth Pugh, Kimberly F. Doheny, James F. Gusella, William C. Nichols, Tatiana Foroud, Richard H. Myers
Vydáno 2008Artigo -
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Genomewide association study for onset age in Parkinson disease Autor Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio Mariani, Anita L. DeStefano, Cheryl Halter, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud
Vydáno 2009Revisão -
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Copy Number Variation in Familial Parkinson Disease Autor Nathan Pankratz, Alexandra Dumitriu, Kurt N. Hetrick, Mei Sun, Jeanne C. Latourelle, Jemma B. Wilk, Cheryl Halter, Kimberly F. Doheny, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud, Anita L. DeStefano
Vydáno 2011Artigo -
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Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease Autor Paul J. Hop, Dongbing Lai, Pamela Keagle, Desiree M. Baron, Brendan Kenna, Maarten Kooyman, Shankaracharya, Cheryl Halter, Letizia Straniero, Rosanna Asselta, Salvatore Bonvegna, Alexandra I. Soto‐Beasley, Zbigniew K. Wszołek, Ryan J. Uitti, Ioannis U. Isaias, Gianni Pezzoli, Nicola Ticozzi, Owen A. Ross, Jan H. Veldink, Tatiana Foroud, Kevin Kenna, John E. Landers
Vydáno 2024Artigo -
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Significant Linkage of Parkinson Disease to Chromosome 2q36-37 Autor Nathan Pankratz, William C. Nichols, Sean K. Uniacke, Cheryl Halter, Alice Rudolph, Cliff Shults, P. Michael Conneally, Tatiana Foroud, Lawrence I. Golbe, William C. Koller, Kelly Lyons, Karen Marder, Frederick J. Marshall, David Oakes, Aileen Shinaman, Eric Siemers, Joanne Wojcieszek, Joann Belden, Julie Carter, Richard Camicioli, Pamela Andrews, Magali Fernandez, Jean Hubble, Carson Reider, Ali H. Rajput, Alex Rajput, Theresa Shirley, Michel Panisset, Jean Hall, Tilak Mendis, David A. Grimes, Peggy Gray, Carmen Serrano Ramos, Sandra Roque, Stephen G. Reich, Becky Dunlop, Robert A. Hauser, Juan Sanchez‐Ramos, Theresa A. Zesiewicz, Holly Delgado, Joseph H. Friedman, Hubert Fernandez, Margaret C. Lannon, Lauren Seeberger, Christopher OʼBrien, Deborah Judd, Lawrence Elmer, Kathy Davis, Deborah Fontaine, Ronald F. Pfeiffer, Brenda Pfeiffer, Michael J. Aminoff, Mariann DiMinno, Daniel Truong, Mayank Pathak, Anhoa Tran, Robert L. Rodnitzky, Judith Dobson, Rajesh Pahwa, Stephanie Thomas, Danna Jennings, Kenneth Marek, Susan Mendick, Juliette Harris, William J. Weiner, Roger Kurlan, Debra Berry, Peter A. LeWitt, Maryan DeAngelis, Paul Tuite, Robyn Schacherer, W. R. Wayne Martin, Marguerite Wieler, Bala V. Manyam, Patricia Simpson, John M. Bertoni, Carolyn Peterson, Mark Forrest Gordon, Joanna Hamann, Joseph Jankovic, Christine Hunter, Stewart A. Factor, Sharon Evans, Anette Nieves, Julie So, Mark Stacy, Kelli Williamson, Francis O. Walker, Victoria Hunt, Un Jung Kang, Shirley Uy, Karen Blindauer, Jeannine Petit, David K. Simon, Lisa Scollins, Rachel Saunders Pullman, Karyn Boyar, Gordon Gilbert, Joan Stehle Werner
Vydáno 2003Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Disease
Medicine
Parkinson's disease
Genome
Genome-wide association study
Genotype
Internal medicine
Single-nucleotide polymorphism
Allele
Chromosome
Genetic association
Genetic linkage
Linkage (software)
Mutation
Parkin
Pathology
1000 Genomes Project
Age of onset
Bonferroni correction
Candidate gene
Chromosome 9
Computational biology
Copy-number variation
Developmental psychology
Gene mapping
Genotyping
Haplotype