C. R. Scriver

5.9k total citations
128 papers, 4.3k citations indexed

About

C. R. Scriver is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, C. R. Scriver has authored 128 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Molecular Biology, 49 papers in Clinical Biochemistry and 26 papers in Genetics. Recurrent topics in C. R. Scriver's work include Metabolism and Genetic Disorders (49 papers), Amino Acid Enzymes and Metabolism (21 papers) and Parathyroid Disorders and Treatments (20 papers). C. R. Scriver is often cited by papers focused on Metabolism and Genetic Disorders (49 papers), Amino Acid Enzymes and Metabolism (21 papers) and Parathyroid Disorders and Treatments (20 papers). C. R. Scriver collaborates with scholars based in Canada, United Kingdom and United States. C. R. Scriver's co-authors include Harriet S. Tenenhouse, C Clow, Francis H. Glorieux, L E Rosenberg, Orval Mamer, E M Eicher, Janice L. Southard, Rima Rozen, John J. Mitchell and Peter Lamm and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

C. R. Scriver

127 papers receiving 4.0k citations

Peers

Countries citing papers authored by C. R. Scriver

Since Specialization

Citations

This map shows the geographic impact of C. R. Scriver's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by C. R. Scriver with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. R. Scriver more than expected).

Fields of papers citing papers by C. R. Scriver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. R. Scriver. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by C. R. Scriver. The network helps show where C. R. Scriver may publish in the future.

Co-authorship network of co-authors of C. R. Scriver

This figure shows the co-authorship network connecting the top 25 collaborators of C. R. Scriver. A scholar is included among the top collaborators of C. R. Scriver based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. R. Scriver. C. R. Scriver is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The Birth Prevalence of PKU in Populations of European, South Asian and Sub‐Saharan African Ancestry Living in South East England 2007 ·Annals of Human Genetics ·Pia Hardelid, Mario Cortina‐Borja, Alastair Munro, Helen Jones, Maureen Cleary, M. P. Champion, (unknown), C. R. Scriver, Carol Dezateux	40
2	CpG methylation accounts for a recurrent mutation (c.1222C>T) in the humanPAH gene 2006 ·Human Mutation ·(unknown), C. R. Scriver, Shiva M. Singh	11
3	Determination of total mercury in biological samples using flow injection CVAAS following tissue solubilization in formic acid 2005 ·Talanta ·(unknown), Scott Willie, C. R. Scriver, Ralph E. Sturgeon	31
4	The human genome project will not replace the physician 2004 ·Canadian Medical Association Journal ·C. R. Scriver	3
5	Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp mice 2003 ·Bone ·(unknown), Rose Travers, Frank Rauch, Francis H. Glorieux, C. R. Scriver, Harriet S. Tenenhouse	16
6	The Oxford Medical Companion 1995 ·BMJ ·C. R. Scriver	11
7	THE HYPERPHENYLALANINEMIAS OF MAN AND MOUSE 1994 ·Annual Review of Genetics ·C. R. Scriver, Randy C. Eisensmith, Savio L.C. Woo, Seymour Kaufman	53
8	Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients 1994 ·Brain ·Paul M. Matthews, R. M. Brown, Lucy J. Otero, David R. Marchington, (unknown), Rosalind E. Howes, Laurence S. Meadows, Michael Shevell, C. R. Scriver, G. K. Brown	30
9	Recommendations on the dietary management of phenylketonuria. Report of Medical Research Council Working Party on Phenylketonuria. 1993 ·Archives of Disease in Childhood ·D. P. Brenton, Jean Chapple, B. J. Clark, G. Curzon, (unknown), (unknown), (unknown), Ian R. McDonald, S.L. Malcolm, R. J. Pollitt, (unknown), G Rylance, Isabel Smith, Ann Stewart, R. Surtees, Alan J. Thompson, Linda Tyfield, M. J. Whittle, C. R. Scriver, (unknown)	217
10	Methylmalonic acidemia with a severe chemical but benign clinical phenotype 1993 ·The Journal of Pediatrics ·Eileen P. Treacy, C Clow, Orval Mamer, C. R. Scriver	11
11	Parental origin of mutant allele does not explain absence of gene dose in X-linked Hyp mice 1993 ·Genetics Research ·(unknown), Harriet S. Tenenhouse, C. R. Scriver	24
12	Familial cold urticaria 1993 ·Clinical and Experimental Dermatology ·(unknown), J. B. Alexander Ross, Malcolm W. Greaves, C. R. Scriver, John J. Mitchell, (unknown)	29
13	Novel Tay-Sachs disease mutations from China 1992 ·Human Mutation ·(unknown), Huiping Shi, George D. Vavougios, Peter Hechtman, Wen-Jyi Lo, C. R. Scriver, Don J. Mahuran, Feige Kaplan	21
14	X-Linked hypophosphatemia. A phenotype in search of a cause 1992 ·International Journal of Biochemistry ·Harriet S. Tenenhouse, C. R. Scriver	13
15	Quantitation of beta-thalassemia genes in Quebec immigrants of Mediterranean, southeast Asian, and Asian Indian origins. 1991 ·PubMed ·Feige Kaplan, (unknown), (unknown), C. R. Scriver	5
16	Initiation and characterization of primary mouse kidney epithelial cultures 1988 ·In Vitro Cellular & Developmental Biology - Plant ·C. L. Bell, Harriet S. Tenenhouse, C. R. Scriver	23
17	Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: Further evidence that they are different diseases 1988 ·Oral Surgery Oral Medicine Oral Pathology ·Steven O. Schwartz, C. R. Scriver, Terry M. Reade, E D Shields	19
18	Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets. 1976 ·Proceedings of the National Academy of Sciences ·E M Eicher, Janice L. Southard, C. R. Scriver, Francis H. Glorieux	319
19	On the screening, diagnosis and investigation of hereditary aminoacidopathies 1973 ·Clinical Biochemistry ·C. R. Scriver, C Clow, Peter Lamm	13
20	X-LINKED HYPOPHOSPHATÆMIC RICKETS: INADEQUATE THERAPEUTIC RESPONSE TO 1,25-DIHYDROXYCHOLECALCIFEROL 1973 ·The Lancet ·Francis H. Glorieux, Michael F. Holick, C. R. Scriver, Hector F. DeLuca	37

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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