Jürg Ott - Concepedia

Author

Jürg Ott

Rockefeller University ORCID

Also Known As

J B Ott, J Ott, J. OTT, J. Ott, J. Ott PhD, JURG OTT, Jacob A. Ott, Jan Ott, Jurg Ott, Jurg Ott (5649895)

562

Publications

36.7K

Citations

H-Index

226

Concepts

All Affiliations

Rockefeller University Columbia University Chinese Academy of Sciences Institute of Psychology, Chinese Academy of Sciences Beijing Institute of Genomics

About

Jürg Ott is an author at Rockefeller University specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	63	125	15.2K
2	Health Sciences	16	16	1.1K
3	Engineering	4	4	164
4	Humanities	1	1	12
5	Management	1	1	18

Jürg Ott

269

Publications

30.8K

Citations

H-Index

Page 1

	Year	Citations
Complement Factor H Polymorphism in Age-Related Macular Degeneration Robert J. Klein, Caroline J. Zeiss, Emily Y. Chew, Science	2005	4.5K
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. G.M. Lathrop, J.-M. Lalouel, Cécile Julier, PubMed	1985	1.2K
Handbook of Human Genetic Linkage. A. W. F. Edwards, Joseph D. Terwilliger, Jürg Ott Biometrics Genetic AnalysisComputer SimulationGenetic TestingLinkage DisequilibriumGenetics	1996	873
Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome Karen Hsiao, Harry F. Baker, Tim Crow, Nature Creutzfeldt-jakob DiseaseGenetic DisorderGeneticsPathogenesisProtein Genetics	1989	843
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3 Linda M. Brzustowicz, Thomas Lehner, Lucio H. Castilla, Nature Developmental BiologyGenetic DisorderGeneticsMolecular GeneticsMedical Genetics	1990	617
Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene Rossella Medori, Hans-Juergen Tritschler, Andréa LeBlanc, New England Journal of Medicine	1992	606
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene Konstantin Petrukhin, S G Fischer, Mario Pirastu, Nature Genetics Molecular Diagnostic TechniquesMendelian DisorderDisease MechanismGenetic DisorderWilson Disease Gene	1993	507
A Haplotype-Based Haplotype Relative Risk&rsquo; Approach to Detecting Allelic Associations Joseph D. Terwilliger, Jürg Ott Human Heredity	1992	487
Computer-simulation methods in human linkage analysis. Jürg Ott Proceedings of the National Academy of Sciences Genetic AnalysisLinkage DisequilibriumHuman Linkage AnalysisGenotype-phenotype AssociationMedicine	1989	479
Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene Wasim Ahmad, Muhammad Faiyaz ul Haque, Valeria Brancolini, Science	1998	413

Page 1