Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nancy L Pedersen

Showing results (321-330 of 610) with videos related to

Pageof 61
Sort By:
Journal of Alzheimer'S Disease : JAD|February 8, 2011
Genetic association of sequence variants near AGER/NOTCH4 and dementiaAnna M Bennet, Chandra A Reynolds, Ulrika K Eriksson, et al.
Neuroepidemiology|April 5, 2012
Accuracy and sensitivity of Parkinsonian disorder diagnoses in two Swedish national health registersAdina L Feldman, Anna L V Johansson, Margaret Gatz, et al.
Biological Psychiatry|October 22, 2011
Variation in the oxytocin receptor gene is associated with pair-bonding and social behaviorHasse Walum, Paul Lichtenstein, Jenae M Neiderhiser, et al.
Human Molecular Genetics|September 16, 2004
A cladistic model of ACE sequence variation with implications for myocardial infarction, Alzheimer disease and obesityHagit Katzov, Anna M Bennet, Patrick Kehoe, et al.
International Journal of Epidemiology|October 9, 2012
Cohort profile: The Stockholm Public Health CohortAnna C Svensson, Peeter Fredlund, Lucie Laflamme, et al.
Human Mutation|December 23, 2011
Genome-wide and gene-based association implicates FRMD6 in Alzheimer diseaseMun-Gwan Hong, Chandra A Reynolds, Adina L Feldman, et al.
Developmental Psychology|October 19, 2018
Attained SES as a moderator of adult cognitive performance: Testing gene-environment interaction in various cognitive domainsCatalina Zavala, Christopher R Beam, Brian K Finch, et al.
Neurobiology of Aging|May 29, 2007
Complete ascertainment of Parkinson disease in the Swedish Twin RegistryKarin Wirdefeldt, Margaret Gatz, Stephanie L Bakaysa, et al.
Stroke|September 18, 2010
Genetic epidemiology of spontaneous subarachnoid hemorrhage: Nordic Twin StudyMiikka Korja, Karri Silventoinen, Peter McCarron, et al.
American Journal of Human Genetics|November 7, 2015
Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP ModelsXu Chen, Ralf Kuja-Halkola, Iffat Rahman, et al.
Pageof 61

Showing results (321-330 of 610) with videos related to

Sort By:
Pageof 61
Journal of Alzheimer'S Disease : JAD|February 8, 2011
Genetic association of sequence variants near AGER/NOTCH4 and dementiaAnna M Bennet, Chandra A Reynolds, Ulrika K Eriksson, et al.
Neuroepidemiology|April 5, 2012
Accuracy and sensitivity of Parkinsonian disorder diagnoses in two Swedish national health registersAdina L Feldman, Anna L V Johansson, Margaret Gatz, et al.
Biological Psychiatry|October 22, 2011
Variation in the oxytocin receptor gene is associated with pair-bonding and social behaviorHasse Walum, Paul Lichtenstein, Jenae M Neiderhiser, et al.
Human Molecular Genetics|September 16, 2004
A cladistic model of ACE sequence variation with implications for myocardial infarction, Alzheimer disease and obesityHagit Katzov, Anna M Bennet, Patrick Kehoe, et al.
International Journal of Epidemiology|October 9, 2012
Cohort profile: The Stockholm Public Health CohortAnna C Svensson, Peeter Fredlund, Lucie Laflamme, et al.
Human Mutation|December 23, 2011
Genome-wide and gene-based association implicates FRMD6 in Alzheimer diseaseMun-Gwan Hong, Chandra A Reynolds, Adina L Feldman, et al.
Developmental Psychology|October 19, 2018
Attained SES as a moderator of adult cognitive performance: Testing gene-environment interaction in various cognitive domainsCatalina Zavala, Christopher R Beam, Brian K Finch, et al.
Neurobiology of Aging|May 29, 2007
Complete ascertainment of Parkinson disease in the Swedish Twin RegistryKarin Wirdefeldt, Margaret Gatz, Stephanie L Bakaysa, et al.
Stroke|September 18, 2010
Genetic epidemiology of spontaneous subarachnoid hemorrhage: Nordic Twin StudyMiikka Korja, Karri Silventoinen, Peter McCarron, et al.
American Journal of Human Genetics|November 7, 2015
Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP ModelsXu Chen, Ralf Kuja-Halkola, Iffat Rahman, et al.
Pageof 61