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

Andreas Zankl

Showing results (11-20 of 77) with videos related to

Pageof 8
Sort By:
BMC Bioinformatics|October 16, 2012
Supervised segmentation of phenotype descriptions for the human skeletal phenome using hybrid methodsTudor Groza, Jane Hunter, Andreas Zankl
Bioinformatics (Oxford, England)|July 16, 2021
Ontoclick: a web browser extension to facilitate biomedical knowledge curationAnthony Xu, Aravind Venkateswaran, Lianguizi Zhou, et al.
Journal of Biomedical Informatics|December 17, 2013
Inferring characteristic phenotypes via class association rule mining in the bone dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
Plos One|December 11, 2012
Decision support methods for finding phenotype--disorder associations in the bone dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
Journal of Biomedical Semantics|February 7, 2014
Semantic interestingness measures for discovering association rules in the skeletal dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
BMC Musculoskeletal Disorders|July 13, 2023
Investigation of a family affected by early-onset osteoarthritis - proposal of a clinical pathway and bioinformatics pipeline for the investigation of cases of familial OALeticia A Deveza, Andreas Zankl, David J Hunter
American Journal of Medical Genetics|September 5, 2002
Growth charts for nose length, nasal protrusion, and philtrum length from birth to 97 yearsAndreas Zankl, Lukas Eberle, Luciano Molinari, et al.
Journal of Biomedical Semantics|May 1, 2015
Capturing domain knowledge from multiple sources: the rare bone disorders use caseTudor Groza, Tania Tudorache, Peter N Robinson, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Natural history of twin disruption sequenceAndreas Zankl, Daniela Brooks, Eugen Boltshauser, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndromeAndreas Zankl, Gudrun Jaeger, Luisa Bonafé, et al.
Pageof 8

Showing results (11-20 of 77) with videos related to

Sort By:
Pageof 8
BMC Bioinformatics|October 16, 2012
Supervised segmentation of phenotype descriptions for the human skeletal phenome using hybrid methodsTudor Groza, Jane Hunter, Andreas Zankl
Bioinformatics (Oxford, England)|July 16, 2021
Ontoclick: a web browser extension to facilitate biomedical knowledge curationAnthony Xu, Aravind Venkateswaran, Lianguizi Zhou, et al.
Journal of Biomedical Informatics|December 17, 2013
Inferring characteristic phenotypes via class association rule mining in the bone dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
Plos One|December 11, 2012
Decision support methods for finding phenotype--disorder associations in the bone dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
Journal of Biomedical Semantics|February 7, 2014
Semantic interestingness measures for discovering association rules in the skeletal dysplasia domainRazan Paul, Tudor Groza, Jane Hunter, et al.
BMC Musculoskeletal Disorders|July 13, 2023
Investigation of a family affected by early-onset osteoarthritis - proposal of a clinical pathway and bioinformatics pipeline for the investigation of cases of familial OALeticia A Deveza, Andreas Zankl, David J Hunter
American Journal of Medical Genetics|September 5, 2002
Growth charts for nose length, nasal protrusion, and philtrum length from birth to 97 yearsAndreas Zankl, Lukas Eberle, Luciano Molinari, et al.
Journal of Biomedical Semantics|May 1, 2015
Capturing domain knowledge from multiple sources: the rare bone disorders use caseTudor Groza, Tania Tudorache, Peter N Robinson, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Natural history of twin disruption sequenceAndreas Zankl, Daniela Brooks, Eugen Boltshauser, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndromeAndreas Zankl, Gudrun Jaeger, Luisa Bonafé, et al.
Pageof 8