Arthur S. Schneider - Concepedia

Author

Arthur S. Schneider

Rosalind Franklin University of Medicine and Science

Also Known As

A Schneider, A. S. Schneider, A. Schneider, A.S. Schneider, Arthur S. Schneider, Arthur Schneider

Publications

Citations

H-Index

Concepts

All Affiliations

Rosalind Franklin University of Medicine and Science University of California, Los Angeles Wadsworth Center Scripps Research Institute

About

Arthur S. Schneider is an author at Rosalind Franklin University of Medicine and Science specializing in medicine, hematology, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	724
2	Biochemistry	5	5	621
3	Health Sciences	3	3	393
4	Biology	1	1	50
5	Cellular Physiology	1	1	50

Arthur S. Schneider

Publications

900

Citations

H-Index

Page 1

	Year	Citations
Hereditary Hemolytic Anemia with Triosephosphate Isomerase Deficiency Arthur S. Schneider, Henry L. Heins New England Journal of Medicine AnemiaInherited DeficienciesHealth SciencesBiochemistryGenetics	1965	193
Hereditary Hemolytic Anemia with Hexokinase Deficiency William N. Valentine, Frank A. Oski, Donald E. Paglia, New England Journal of Medicine Iron MetabolismPathologyMolecular BiologyIron DeficiencyRedox Biology	1967	185
Hereditary hemolytic anemia with triosephosphate isomerase deficiency William N. Valentine, Arthur S. Schneider, Marjorie A. Baughan, The American Journal of Medicine AnemiaBiochemistryHematologyIron DeficiencyMedicine	1966	182
Studies on Chromated Erythrocytes. Effect of Sodium Chromate on Erythrocyte Glutathione Reductase* George A. Koutras, Masao Hattori, Arthur S. Schneider, Journal of Clinical Investigation	1964	103
On the role of arginine kinase in insect flight muscle Arthur S. Schneider, Rudolf J. Wiesner, M. K. Grieshaber Insect Biochemistry BiologyMuscle FunctionMolecular PhysiologySignal TransductionSkeletal Muscle	1989	50
Studies on Chromated Erythrocytes. MECHANISMS OF CHROMATE INHIBITION OF GLUTATHIONE REDUCTASE George A. Koutras, Arthur S. Schneider, Masaya Hattori, British Journal of Haematology Reductive StressRedox SignalingBiochemistryChromated ErythrocytesRedox Regulator	1965	46
Triosephosphate isomerase deficiency: Repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated families Arthur S. Schneider, Beryl Westwood, Catherine Yim, American Journal of Hematology	1995	32
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris). Colette Valentin, Serge Pissard, Josiane Martin, PubMed	2000	27
Hematologically Important Mutations: Triosephosphate Isomerase Arthur S. Schneider, Michel Cohen‐Solal Blood Cells Molecules and Diseases GeneticsTriosephosphate IsomeraseHematologyMolecular BiologyMolecular Genetics	1996	20
The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families Arthur S. Schneider, Beryl Westwood, Catherine Yim, Blood Cells Molecules and Diseases Common HaplotypeAllelic VariantGenetic DisorderGeneticsTriosephosphate Isomerase	1996	18

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