H.G. Kraft - Concepedia

Author

H.G. Kraft

Universität Innsbruck

Also Known As

H G Kraft, H KRAFT, H Kraft, H. G. KRAFT, H. G. Kraft, H. Kraft, H.-G. Kraft, H.G Kraft, H.G. Kraft, HANS GEORG KRAFT

115

Publications

3.5K

Citations

H-Index

Concepts

All Affiliations

Universität Innsbruck Innsbruck Medical University Roche (United States)Institute of Medical Biology National Institutes of Health

About

H.G. Kraft is an author at Universität Innsbruck specializing in medicine, atherosclerosis, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	2.6K
2	Engineering	3	3	38
3	Health Sciences	3	3	1.1K
4	Natural Sciences	2	2	164
5	Education	1	1	32

H.G. Kraft

Publications

3.4K

Citations

H-Index

Page 1

	Year	Citations
Lp(a) glycoprotein phenotypes. Inheritance and relation to Lp(a)-lipoprotein concentrations in plasma. Gerd Utermann, H. Menzel, H.G. Kraft, Journal of Clinical Investigation ImmunologyGlycobiologyGenetic Epidemiology-Lipoprotein ConcentrationsHyperlipidemia	1987	878
The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration H.G. Kraft, S. K�chl, H. Menzel, Human Genetics BiochemistryTranscribed Hypervariable LocusMedicineGeneticsHyperlipidemia	1992	272
Genetics of the quantitative Lp(a) lipoprotein trait Eric Boerwinkle, Hans J�rgen Menzel, H.G. Kraft, Human Genetics Metabolic SyndromeQuantitative GeneticsGeneticsGenetic EpidemiologyQuantitative Lp	1989	265
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesis. H.G. Kraft, H. Menzel, Fritz Hoppichler, Journal of Clinical Investigation HistocompatibilityApolipoprotein SynthesisPlasma Apo EGeneticsGenetic Epidemiology	1989	253
Apolipoprotein(a) Kringle IV Repeat Number Predicts Risk for Coronary Heart Disease H.G. Kraft, Arno Lingenhel, Silvano Köchl, Arteriosclerosis Thrombosis and Vascular Biology	1996	233
The low density lipoprotein receptor is not required for normal catabolism of Lp(a) in humans. Daniel J. Rader, W. Alexander Mann, William J. Cain, Journal of Clinical Investigation Metabolic SyndromeCardiovascular DiseaseBiochemistryMedicinePhysiology	1995	204
Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome Martina Witsch‐Baumgartner, Barbara U. Fitzky, M. Ogorelkova, The American Journal of Human Genetics Smith-lemli-opitz SyndromeMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2000	188
Cys4057 of apolipoprotein(a) is essential for lipoprotein(a) assembly. Christoph Brunner, H.G. Kraft, Gerd Utermann, Proceedings of the National Academy of Sciences OxysterolBiochemistryCdna PlasmidsNatural SciencesBiochemical Genetics	1993	151
Frequency Distributions ofApolipoprotein(a) Kringle IV RepeatAlleles and Their Effects onLipoprotein(a) Levels in Caucasian,Asian, and African Populations:The Distribution of Null Alleles IsNon-Random H.G. Kraft, Arno Lingenhel, Richard Pang, European Journal of Human Genetics	1996	141
Lipoprotein(a) in Homozygous Familial Hypercholesterolemia H.G. Kraft, Arno Lingenhel, Frederick J. Raal, Arteriosclerosis Thrombosis and Vascular Biology Family MembersGeneticsGenetic EpidemiologyHuman PolymorphismHyperlipidemia	2000	133

Page 1