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C. West · SciRah

Researcher profile · Semantic Scholar

C. West

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C. West — researcher profile on SciRah

h-index: 31
Works: 72
Citations: 4,452

Most-cited papers

The removal of leukocytes and platelets from whole blood.
E. Beutler, C. West, K. Blume
1976Journal of Laboratory and Clinical Medicine746 citations
Semantic Scholar
Mutation analysis in hereditary hemochromatosis.
E. Beutler, T. Gelbart, C. West, P. Lee +11 more
1996Blood Cells, Molecules & Diseases427 citations Open access
Semantic Scholar
The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
P. Lee, T. Gelbart, C. West, Carol Halloran +1 more
1998Blood Cells, Molecules & Diseases328 citations
Semantic Scholar
Hematologic differences between African-Americans and whites: the roles of iron deficiency and alpha-thalassemia on hemoglobin levels and mean corpuscular volume.
E. Beutler, C. West
2005Blood320 citations Open access
Semantic Scholar
Prediction of severity of Gaucher's disease by identification of mutations at DNA level.
A. Zimran, E. Gross, C. West, Joseph A. Sorge +2 more
1989The Lancet285 citations
Semantic Scholar
Gaucher disease: gene frequencies in the Ashkenazi Jewish population.
E. Beutler, N. J. Nguyen, M. Henneberger, J. Smolec +3 more
1993American Journal of Human Genetics237 citations
Semantic Scholar
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features.
R. Sham, P. Phatak, C. West, P. Lee +2 more
2005Blood Cells, Molecules & Diseases148 citations
Semantic Scholar
Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans.
E. Beutler, J. C. Barton, V. Felitti, T. Gelbart +4 more
2003Blood Cells, Molecules & Diseases132 citations
Semantic Scholar
A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorder.
A. Zimran, Joseph A. Sorge, E. Gross, M. Kubitz +2 more
1990Journal of Clinical Investigation120 citations Open access
Semantic Scholar
A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin.
P. Lee, T. Gelbart, C. West, Carol Halloran +2 more
2001Blood Cells, Molecules & Diseases107 citations
Semantic Scholar
Seeking candidate mutations that affect iron homeostasis.
P. Lee, T. Gelbart, C. West, Carol Halloran +1 more
2002Blood Cells, Molecules & Diseases99 citations
Semantic Scholar
Identification of six new Gaucher disease mutations.
E. Beutler, T. Gelbart, C. West
1993Genomics81 citations
Semantic Scholar
Mutations in Jewish patients with Gaucher disease.
E. Beutler, T. Gelbart, Wanda Kuhl, A. Zimran +1 more
1992Blood78 citations Open access
Semantic Scholar
High level transcription of the glucocerebrosidase pseudogene in normal subjects and patients with Gaucher disease.
J. Sorge, E. Gross, C. West, E. Beutler
1990Journal of Clinical Investigation77 citations Open access
Semantic Scholar
Large-scale molecular screening for galactosemia alleles in a pan-ethnic population
Makoto Suzuki, C. West, E. Beutler
2001Human Genetics75 citations
Semantic Scholar
Polymorphisms in the human glucocerebrosidase gene.
E. Beutler, C. West, T. Gelbart
1992Genomics72 citations Open access
Semantic Scholar
Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.
P. Lee, Carol Halloran, C. West, E. Beutler
2001Blood Cells, Molecules & Diseases70 citations
Semantic Scholar
Mutations in Jewish patients with Gaucher disease
E. Beutler, T. Gelbart, Wanda Kuhl, A. Zimran +1 more
199267 citations
Semantic Scholar
A simple rapid radiometric assay for pyrimidine-5'-nucleotidase.
J. Torrance, C. West, E. Beutler
1977Journal of Laboratory and Clinical Medicine64 citations
Semantic Scholar
Genotypic and phenotypic heterogeneity of African Americans with primary iron overload.
J. C. Barton, R. Acton, C. Rivers, L. Bertoli +3 more
2003Blood Cells, Molecules & Diseases62 citations
Semantic Scholar
Homology between a human protein and a protein of the green garden pea.
P. Lee, Wanda Kuhl, T. Gelbart, T. Kamimura +2 more
1994Genomics48 citations
Semantic Scholar
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose‐6‐phosphate dehydrogenase (G‐6‐PD) deficiency
James D. Hoyer, S. L. Allen, E. Beutler, K. Kubik +2 more
2004American journal of hematology/oncology46 citations
Semantic Scholar
Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia.
K. Blume, W. Hryniuk, D. Powars, F. Trinidad +2 more
1972Journal of Laboratory and Clinical Medicine40 citations
Semantic Scholar
HLA-H and Associated Proteins in Patients with Hemochromatosis
E. Beutler, C. West, T. Gelbart
1997Molecular Medicine39 citations Open access
Semantic Scholar
Comment concerning a fluorometric assay for glutathione.
E. Beutler, C. West
1977Analytical Biochemistry39 citations
Semantic Scholar
Iron overload and prolonged ingestion of iron supplements: Clinical features and mutation analysis of hemochromatosis‐associated genes in four cases
J. C. Barton, P. Lee, C. West, S. S. Bottomley
2006American journal of hematology/oncology38 citations
Semantic Scholar
New diallelic markers in the HLA region of chromosome 6.
E. Beutler, C. West
1997Blood Cells, Molecules & Diseases35 citations
Semantic Scholar
SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.
J. C. Barton, R. Acton, P. Lee, C. West
2007Blood Cells, Molecules & Diseases34 citations Open access
Semantic Scholar
A previously undescribed nonsense mutation of the HFE gene
E. Beutler, Mj Griffin, T. Gelbart, C. West
2002Clinical Genetics33 citations
Semantic Scholar
Measurement of the viability of stored red cells by the single‐isotope technique using 51Cr. Analysis of validity
E. Beutler, C. West
1984Transfusion33 citations
Semantic Scholar
Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.
E. Beutler, D. Carson, H. Dannawi, L. Forman +3 more
1983Journal of Clinical Investigation33 citations Open access
Semantic Scholar
Erythrocyte Viability in Blood Salvaged During Total Joint Arthroplasty with Cement
C. Colwell, E. Beutler, C. West, Mary E. Hardwick +1 more
2002Journal of Bone and Joint Surgery. American volume30 citations
Semantic Scholar
The hHFE gene of browsing and grazing rhinoceroses: a possible site of adaptation to a low-iron diet.
E. Beutler, C. West, J. Speir, I. Grant Wilson +1 more
2001Blood Cells, Molecules & Diseases29 citations
Semantic Scholar
Genetic polymorphisms and susceptibility to lung disease
P. Lee, C. West, K. Crain, Lei Wang
2006Journal of Negative Results in Biomedicine28 citations Open access
Semantic Scholar
Red cell glutathione peroxidase polymorphism in Afro-Americans.
E. Beutler, C. West
1974American Journal of Human Genetics26 citations
Semantic Scholar
Electrophoretic polymorphism of glutathione peroxidase
E. Beutler, C. West, B. Beutler
1974Annals of Human Genetics25 citations
Semantic Scholar
Glucosephosphate-isomerase (GPI) deficiency: GPI elyria.
E. Beutler, W. H. Sigalove, W. Muir, F. Matsumoto +1 more
1974Annals of Internal Medicine22 citations
Semantic Scholar
SLC40A1 c.1402G→A Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype
P. Lee, T. Gelbart, C. West, J. C. Barton
2007Acta Haematologica20 citations
Semantic Scholar
Mutations in the gene encoding cytosolic β-glucosidase in Gaucher disease
E. Beutler, L. Beutler, C. West
200420 citations
Semantic Scholar
Storage of red cell concentrates in CPD-A2 for 42 and 49 days.
E. Beutler, C. West
1983Journal of Laboratory and Clinical Medicine20 citations
Semantic Scholar
Effect of oxalate and malonate on red cell metabolism.
E. Beutler, L. Forman, C. West
1987Blood19 citations Open access
Semantic Scholar
The effect of 2,3-DPG on the sickling phenomenon.
E. Beutler, N. Paniker, C. West
1971Blood19 citations Open access
Semantic Scholar
Glucose-6-phosphate dehydrogenase (G6PD) deficiency-type Zurich: a splice site mutation as an uncommon mechanism producing enzyme deficiency.
T. Efferth, E. Bachli, Sonja M. Schwarzl, J. Goede +3 more
2004Blood16 citations Open access
Semantic Scholar
A Chimeric Mouse Model of Gaucher Disease
E. Beutler, C. West, B. Torbett, H. Deguchi
2002Molecular Medicine16 citations Open access
Semantic Scholar
Gaucher disease: retrovirus-mediated correction of the enzymatic defect in cultured cells.
J. Sorge, Wanda Kuhl, C. West, E. Beutler
1986Cold Spring Harbor Symposia on Quantitative Biology16 citations
Semantic Scholar
Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.
J. Corrons, Estefanía García, J. Tusell, K. Varughese +2 more
2003Blood15 citations
Semantic Scholar
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote
J. C. Barton, C. West, P. Lee, E. Beutler
2004Clinical Genetics14 citations
Semantic Scholar
The effect of additives on red cell 2,3 diphosphoglycerate levels in CPDA preservatives
S. Vora, C. West, E. Beutler
1989Transfusion13 citations
Semantic Scholar
Glycolytic enzymes of stored granulocytes
La-Ne Ta, E. Beutler, C. West, G. Lamkin
1984Transfusion13 citations
Semantic Scholar
Uric acid metabolism in starvation.
R. Lloyd-Mostyn, P. S. Lord, R. Glover, C. West +1 more
1970Annals of the Rheumatic Diseases12 citations Open access
Semantic Scholar

Frequent co-authors

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E. Beutler×45
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E. Beutler — researcher profile on SciRah
T. Gelbart×15
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P. Lee×13
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J. C. Barton×5
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Wanda Kuhl — researcher profile on SciRah

Carol Halloran×4

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E. Gross — researcher profile on SciRah

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P. Phatak — researcher profile on SciRah

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A. Zimran — researcher profile on SciRah

Joseph A. Sorge×2

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Joseph A. Sorge — researcher profile on SciRah

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M. Kubitz — researcher profile on SciRah

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V. Felitti — researcher profile on SciRah