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

Tim Becker

Showing results (61-70 of 142) with videos related to

Pageof 15
Sort By:
Human Heredity|December 16, 2014
Rare variant testing of imputed data: an analysis pipeline typifiedDmitriy Drichel, Christine Herold, André Lacour, et al.
Neuroscience Letters|January 13, 2006
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivitySusanne Lorenz, Armin Heils, Kirsten P Taylor, et al.
Scientific Reports|January 1, 2021
Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1BTim Becker, Andreas Pich, Stephanie Tamm, et al.
BMC Bioinformatics|April 17, 2015
Novel genetic matching methods for handling population stratification in genome-wide association studiesAndré Lacour, Vitalia Schüller, Dmitriy Drichel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected childrenKatharina Domschke, Karen Sheehan, Naomi Lowe, et al.
Nature Communications|April 8, 2023
Predicting compound activity from phenotypic profiles and chemical structuresNikita Moshkov, Tim Becker, Kevin Yang, et al.
European Journal of Human Genetics : EJHG|May 24, 2012
Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expressionIna Schmitt, Ullrich Wüllner, Jan Pierre van Rooyen, et al.
Psychiatric Genetics|July 17, 2008
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorderRami Abou Jamra, Carl Motinda Gobina, Tim Becker, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|July 18, 2019
Evaluation of Deep Learning Strategies for Nucleus Segmentation in Fluorescence ImagesJuan C Caicedo, Jonathan Roth, Allen Goodman, et al.
Human Genetics|February 8, 2006
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosisFrauke Stanke, Tim Becker, Harry Cuppens, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
Human Heredity|December 16, 2014
Rare variant testing of imputed data: an analysis pipeline typifiedDmitriy Drichel, Christine Herold, André Lacour, et al.
Neuroscience Letters|January 13, 2006
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivitySusanne Lorenz, Armin Heils, Kirsten P Taylor, et al.
Scientific Reports|January 1, 2021
Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1BTim Becker, Andreas Pich, Stephanie Tamm, et al.
BMC Bioinformatics|April 17, 2015
Novel genetic matching methods for handling population stratification in genome-wide association studiesAndré Lacour, Vitalia Schüller, Dmitriy Drichel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: preferential transmission of the MAO-A 941G allele to affected childrenKatharina Domschke, Karen Sheehan, Naomi Lowe, et al.
Nature Communications|April 8, 2023
Predicting compound activity from phenotypic profiles and chemical structuresNikita Moshkov, Tim Becker, Kevin Yang, et al.
European Journal of Human Genetics : EJHG|May 24, 2012
Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expressionIna Schmitt, Ullrich Wüllner, Jan Pierre van Rooyen, et al.
Psychiatric Genetics|July 17, 2008
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorderRami Abou Jamra, Carl Motinda Gobina, Tim Becker, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|July 18, 2019
Evaluation of Deep Learning Strategies for Nucleus Segmentation in Fluorescence ImagesJuan C Caicedo, Jonathan Roth, Allen Goodman, et al.
Human Genetics|February 8, 2006
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosisFrauke Stanke, Tim Becker, Harry Cuppens, et al.
Pageof 15