James Bartley - Concepedia

Concepedia

Author

James Bartley

University of Iowa Hospitals and Clinics

Also Known As

J A Bartley, J Bartley, J. A. Bartley, J. Bartley, James A Bartley, James A. Bartley, James Bartley

63

Publications

2.7K

Citations

30

H-Index

127

Concepts

All Affiliations

University of Iowa Hospitals and Clinics Icahn School of Medicine at Mount Sinai University of Utah Baylor College of Medicine Stanford University

JB

About

James Bartley is an author at University of Iowa Hospitals and Clinics specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	24	1.6K
2	Natural Sciences	7	7	628
3	Engineering	2	2	109
4	Arts	1	1	52
5	Education	1	1	52

James Bartley

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39

Publications

2.7K

Citations

30

H-Index

	Year	Citations
Autosomal XX sex reversal caused by duplication ofSOX9 Bing Huang, Shengbiao Wang, Yi Ning, American Journal of Medical Genetics	1999	425
Abnormality of chromosome 11 in patients withfeatures of Beckwith-Wiedemann syndrome Mary H. Waziri, Shivanand R. Patil, James W. Hanson, The Journal of Pediatrics Developmental AnomalyGenetic DisorderGeneticsCongenital DisordersPathology	1983	233
Phylogenies Inferred from Mitochondrial Gene Orders—A Cautionary Tale from the Parasitic Flatworms Thanh Hoa Le, David Blair, Takeshi Agatsuma, Molecular Biology and Evolution Schistosoma MansoniComparative GenomicsGeneticsMalariaMolecular Genetics	2000	202
Further Studies of a Thymus Nucleohistone-associated Protease James Bartley, Roger Chalkley Journal of Biological Chemistry ProteasomeMolecular BiologyCalf Thymus NucleohistoneEpigeneticsHistone Fractions	1970	190
Deletions of different segments of the long arm of chromosome 4 Joyce A. Mitchell, Seymour Packman, William D. Loughman, American Journal of Medical Genetics	1981	94
Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate George A. Díaz, Lauren Krivitzky, Masoud Mokhtarani, Hepatology	2012	93
Mitochondrial Complex III Deficiency Caused by a Homozygous<i>UQCRC2</i>Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation Noriko Miyake, Shoji Yano, Chika Sakai, Human Mutation Systems BiologyMitochondrial CiiiMitochondrial BiogenesisMitochondrial FunctionGenetic Disorder	2012	88
Characterization of a type II collagen gene (COL2A1) mutation identified in cultured chondrocytes from human hypochondrogenesis. William A. Horton, Marcos Antônio Machado, Jeff Ellard, Proceedings of the National Academy of Sciences Tissue EngineeringHuman HypochondrogenesisBone RepairPathologyCultured Chondrocytes	1992	87
Maternal hyperphenylalaninemia fetal effects Anthony Lipson, Bruce Beuhler, James Bartley, The Journal of Pediatrics Maternal Cardiovascular OutcomePhysiologyFetal MedicineGynecologyMaternal Health	1984	85
The Binding of Deoxyribonucleic Acid and Histone in Native Nucleohistone James Bartley, Roger Chalkley Journal of Biological Chemistry Epigenetic ChangeMolecular BiologyHistones F1Chemical BiologyEpigenetics	1972	79

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