H H Kazazian - Concepedia

Author

H H Kazazian

Also Known As

H H Kazazian, H KAZAZIAN, H Kazazian, H. H. KAZAZIAN, H. H. Kazazian, H. Kazazian, H.H. Kazazian, H.H. Kazazian, Jr., Hag H. Kazazian, J N St John

Publications

4.6K

Citations

H-Index

Concepts

All Affiliations

Johns Hopkins University Johns Hopkins Medicine American Red Cross Harvard University Press Howard Hughes Medical Institute

About

H H Kazazian is an author at Johns Hopkins University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	32	2.6K
2	Natural Sciences	10	10	431
3	Public Health	6	6	598
4	Health Sciences	3	3	83
5	Engineering	2	2	304

H H Kazazian

Publications

3.7K

Citations

H-Index

Page 1

	Year	Citations
Molecular characterization of seven beta-thalassemia mutations in Asian Indians. H H Kazazian, Stuart H. Orkin, Stylianos E. Antonarakis, The EMBO Journal Genetic DisorderGeneticsHematologyGenetic VariationBeta-thalassemia Mutations	1984	201
Thalassemia due to a mutation in the cleavage-polyadenylation signal of the human beta-globin gene. Stuart H. Orkin, Tu-Chen Cheng, Stylianos E. Antonarakis, The EMBO Journal Cleavage-polyadenylation SignalGeneticsHematologyMolecular BiologyHeme Transport	1985	193
beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site. Stylianos E. Antonarakis, S H Irkin, Tiffany Cheng, Proceedings of the National Academy of Sciences BiologyMutant GeneHaplotype DeterminationAllelic VariantDevelopmental Biology	1984	192
Single-sperm typing: determination of genetic distance between the G gamma-globin and parathyroid hormone loci by using the polymerase chain reaction and allele-specific oligomers. Xiufang Cui, H H Li, Tushar M. Goradia, Proceedings of the National Academy of Sciences FertilitySingle-sperm TypingGeneticsGenetic EpidemiologyReproductive Health	1989	190
beta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects. Tiffany Cheng, SH Orkin, Stylianos E. Antonarakis, Proceedings of the National Academy of Sciences EngineeringGeneticsHuman PolymorphismMolecular BiologyMolecular Genetics	1984	168
Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene. Miyoko Higuchi, H H Kazazian, L. Kasch, Proceedings of the National Academy of Sciences Genetic DisorderMedicineGeneticsPathogenesisHematology	1991	156
Neurobehavioral effects of the fragile X premutation in adult women: a controlled study. Allan L. Reiss, Lisa S. Freund, Michael T. Abrams, PubMed	1993	150
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, Nucleic Acids Research Second EditionF8 GeneInversional EventsGeneticsPathogenesis	1994	148
Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC. Stuart H. Orkin, Stylianos E. Antonarakis, H H Kazazian Journal of Biological Chemistry	1984	145
Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis. Stuart H. Orkin, Alexander F. Markham, H H Kazazian Journal of Clinical Investigation Genetic TestingEngineeringGeneticsDirect DetectionGenetic Epidemiology	1983	136

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