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P Michael Conneally

Showing results (1-10 of 18) with videos related to

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American Journal of Human Genetics|February 25, 2003
The complexity of complex diseasesP Michael Conneally
Neuropsychiatry, Neuropsychology, and Behavioral Neurology|September 10, 2002
Longitudinal personality changes among presymptomatic Huntington disease gene carriersSandra Close Kirkwood, Eric Siemers, Richard Viken, et al.
American Journal of Human Genetics|June 12, 2002
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutationsNathan Pankratz, William C Nichols, Sean K Uniacke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 24, 2005
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementiaNathan Pankratz, Lisa Byder, Cheryl Halter, et al.
American Journal of Human Genetics|March 15, 2003
Significant linkage of Parkinson disease to chromosome 2q36-37Nathan Pankratz, William C Nichols, Sean K Uniacke, et al.
Journal of Psychiatric Research|October 24, 2002
Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scalesSandra Close Kirkwood, Eric Siemers, Richard J Viken, et al.
Human Molecular Genetics|August 20, 2003
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease familiesNathan Pankratz, William C Nichols, Sean K Uniacke, et al.
American Journal of Human Genetics|January 20, 2004
Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white womenMichael J Econs, Daniel L Koller, Siu L Hui, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2002
Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13Gwenaelle Carn, Daniel L Koller, Munro Peacock, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|February 25, 2003
The complexity of complex diseasesP Michael Conneally
Neuropsychiatry, Neuropsychology, and Behavioral Neurology|September 10, 2002
Longitudinal personality changes among presymptomatic Huntington disease gene carriersSandra Close Kirkwood, Eric Siemers, Richard Viken, et al.
American Journal of Human Genetics|June 12, 2002
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutationsNathan Pankratz, William C Nichols, Sean K Uniacke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 24, 2005
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementiaNathan Pankratz, Lisa Byder, Cheryl Halter, et al.
American Journal of Human Genetics|March 15, 2003
Significant linkage of Parkinson disease to chromosome 2q36-37Nathan Pankratz, William C Nichols, Sean K Uniacke, et al.
Journal of Psychiatric Research|October 24, 2002
Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scalesSandra Close Kirkwood, Eric Siemers, Richard J Viken, et al.
Human Molecular Genetics|August 20, 2003
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease familiesNathan Pankratz, William C Nichols, Sean K Uniacke, et al.
American Journal of Human Genetics|January 20, 2004
Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white womenMichael J Econs, Daniel L Koller, Siu L Hui, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2002
Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13Gwenaelle Carn, Daniel L Koller, Munro Peacock, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 16, 2004
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's diseaseWilliam C Nichols, Sean K Uniacke, Nathan Pankratz, et al.
Pageof 2