Kenneth H. Astrin - Concepedia

Author

Kenneth H. Astrin

Icahn School of Medicine at Mount Sinai

Also Known As

K H Astrin, K. Astrin, K. H. ASTRIN, K. H. Astrin, K.H. Astrin, Kenneth Astrin, Kenneth H Astrin, Kenneth H. Astrin

Publications

2.2K

Citations

H-Index

Concepts

All Affiliations

Icahn School of Medicine at Mount Sinai New York University University of California San Diego General Department of Preventive Medicine Universidad de Buenos Aires

About

Kenneth H. Astrin is an author at Icahn School of Medicine at Mount Sinai specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	23	1.2K
2	Natural Sciences	11	12	627
3	Biochemistry	6	6	267
4	Health Sciences	1	1	27
5	Public Health	1	1	101

Kenneth H. Astrin

Publications

Citations

H-Index

Page 1

	Year	Citations
Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease. Christine M. Eng, Lois A. Resnick-Silverman, D J Niehaus, PubMed	1993	220
Human δ-aminolevulinate synthase: Assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome David F. Bishop, A.S. Henderson, Kenneth H. Astrin Genomics ChromatinDevelopmental BiologyChromatin StructureCytogeneticsX Chromosome	1990	166
Fabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase gene. Harold S. Bernstein, David F. Bishop, Kenneth H. Astrin, Journal of Clinical Investigation BiologyResidual Enzyme ActivityFabry DiseaseMendelian DisorderGene Rearrangements	1989	156
Fabry disease: twenty-two novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations in severely and mildly affected hemizygotes and heterozygotes. Patrícia Ashton‐Prolla, Bingdu Tong, Junaid Shabbeer, PubMed	2000	115
δ‐Aminolevulinic Acid Dehydratase Isozymes and Lead Toxicitya Kenneth H. Astrin, David F. Bishop, James G. Wetmur, Annals of the New York Academy of Sciences Lead ExposureBiochemistryMedicineGenetic EpidemiologyHematology	1987	101
Acute Intermittent Porphyria Constanza Solis, A Martínez-Bermejo, Thomas P. Naidich, Archives of Neurology	2004	100
Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria Constanza Solis, G. Aizencang, Kenneth H. Astrin, Journal of Clinical Investigation	2001	94
Twenty Novel Mutations in the α-Galactosidase A Gene Causing Fabry Disease Ali Kemal Topaloğlu, Grace A. Ashley, Bingzheng Tong, Molecular Medicine Mendelian DisorderGenetic DisorderNatural SciencesGeneticsPathogenesis	1999	81
Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation İlhan Tezcan, Weiming Xu, Aytemiz Gürgey, Blood	1998	76
Lesch-Nyhan Syndrome: Preventive Control by Prenatal Diagnosis J. A. Boyle, Kari O. Raivio, Kenneth H. Astrin, Science Down SyndromeInfertilityPediatricsGynecologyMaternal Health	1970	70

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