J.C. Murray - Concepedia

Author

J.C. Murray

Also Known As

Fisher Khan-Cattsz, J C Murray, J Murray, J. C Murray, J. C. Murray, J. Murray, J.C. MURRAY, J.C. Murray, JEFFREY C. MURRAY

Publications

743

Citations

H-Index

Concepts

All Affiliations

University of Iowa University of Bergen

About

J.C. Murray is an author at University of Iowa specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	506
2	Public Health	3	3	257
3	Natural Sciences	1	1	67
4	Biochemistry	1	1	67
5	Cell Biology	1	1	23

J.C. Murray

Publications

694

Citations

H-Index

Page 1

	Year	Citations
Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Kenneth H. Buetow, J.C. Murray, Jonathan Israel, Proceedings of the National Academy of Sciences Primary Hepatocellular CarcinomaGeneticsGenetic EpidemiologyPathologyTumor Biology	1989	186
Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA) K. Mills, D. Even, J.C. Murray Human Molecular Genetics GeneticsImmunodeficienciesGenetic EpidemiologyHuman PolymorphismMolecular Biology	1992	119
Prenatal care effectiveness and utilization in Brazil George L. Wehby, J.C. Murray, Eduardo E. Castilla, Health Policy and Planning Maternity ServiceHigh-risk PregnancyPrimary CarePrenatal Care EffectivenessSouth American Countries	2009	105
Maternal Alcohol Consumption, Alcohol Metabolism Genes, and the Risk of Oral Clefts: A Population-based Case-Control Study in Norway, 1996-2001 Abee L. Boyles, Lisa A. DeRoo, Rolv T. Lie, American Journal of Epidemiology	2010	83
Molecular genetics of human serum albumin: restriction enzyme fragment length polymorphisms and analbuminemia. J.C. Murray, Christina M. Demopulos, R.M. Lawn, Proceedings of the National Academy of Sciences Cdna ProbesHuman Albumin GeneGeneticsHuman PolymorphismMolecular Biology	1983	67
Report of the committee on the genetic constitution of chromosome 4 J.C. Murray, Gert‐Jan B. van Ommen, R.J. Daniels Cytogenetic and Genome Research ChromatinGenetic DisorderGeneticsMolecular BiologyChromosome Biology	1990	35
Platelet glycoprotein Ibα and integrin α2β1 polymorphisms: gene frequencies and linkage disequilibrium in a population diversity panel Jorge Di Paola, Astanand Jugessur, T. Goldman, Journal of Thrombosis and Haemostasis Allelic VariantIntegrin α2β1 PolymorphismsBlood PlateletGenotype-phenotype AssociationMedicine	2005	33
Phenotypic and Pathologic Evaluation of the myd Mouse. A Candidate Model for Facioscapulohumeral Dystrophy Katherine D. Mathews, Douglas Rapisarda, Holly L. Bailey, Journal of Neuropathology & Experimental Neurology Human Disease FshdDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1995	31
Linkage Localization of TGFB2 and the Human Homeobox Gene HLX1 to Chromosome 1q Darryl Nishimura, A F Purchio, J.C. Murray Genomics ChromatinGenetic DisorderGeneticsGene CharacterizationMolecular Genetics	1993	23
<scp>HCV</scp> genotype 4, 5 and 6: Distribution of viral subtypes and sustained virologic response rates in clinical trials of approved direct‐acting antiviral regimens Sarita D. Boyd, Patrick R. Harrington, T. Komatsu, Journal of Viral Hepatitis HepatologyHepatitis CVirologic Response RatesViral HepatitisImmunodeficiencies	2018	12

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