C Clow

1.0k total citations
28 papers, 732 citations indexed

About

C Clow is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Clow has authored 28 papers receiving a total of 732 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Clinical Biochemistry, 10 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Clow's work include Metabolism and Genetic Disorders (14 papers), Hemoglobinopathies and Related Disorders (6 papers) and Biochemical and Molecular Research (5 papers). C Clow is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Hemoglobinopathies and Related Disorders (6 papers) and Biochemical and Molecular Research (5 papers). C Clow collaborates with scholars based in Canada, United States and India. C Clow's co-authors include C. R. Scriver, John J. Mitchell, Susan A. MacKenzie, C R Scriver, E. Delvin, Eileen P. Treacy, Feige Kaplan, Orval Mamer, David Chitayat and Claude Laberge and has published in prestigious journals such as The Lancet, PEDIATRICS and American Journal of Public Health.

In The Last Decade

C Clow

27 papers receiving 686 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C Clow Canada	14	355	254	138	129	122	28	732
Carol L. Clow Canada	14	319 0.9×	218 0.9×	194 1.4×	100 0.8×	141 1.2×	23	731
N. J. Brandt Denmark	24	773 2.2×	729 2.9×	216 1.6×	152 1.2×	147 1.2×	66	1.4k
Hélène Ogier France	13	415 1.2×	443 1.7×	76 0.6×	87 0.7×	86 0.7×	16	877
Alice Masurel‐Paulet France	15	164 0.5×	344 1.4×	105 0.8×	79 0.6×	386 3.2×	26	800
Dimitar Gavrilov United States	15	437 1.2×	403 1.6×	200 1.4×	57 0.4×	121 1.0×	35	901
Philip P. Dembure United States	16	606 1.7×	403 1.6×	304 2.2×	256 2.0×	91 0.7×	26	1.0k
J. T. R. Clarke Canada	15	131 0.4×	225 0.9×	65 0.5×	29 0.2×	85 0.7×	23	560
Ubaldo Caruso Italy	15	338 1.0×	349 1.4×	108 0.8×	89 0.7×	48 0.4×	21	662
François Eyskens Belgium	17	331 0.9×	462 1.8×	75 0.5×	83 0.6×	94 0.8×	38	779
Lynn Hall United States	15	125 0.4×	437 1.7×	49 0.4×	34 0.3×	76 0.6×	22	741

Countries citing papers authored by C Clow

Since Specialization

Citations

This map shows the geographic impact of C Clow'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 Clow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Clow more than expected).

Fields of papers citing papers by C Clow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C Clow. 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 Clow. The network helps show where C Clow may publish in the future.

Co-authorship network of co-authors of C Clow

This figure shows the co-authorship network connecting the top 25 collaborators of C Clow. A scholar is included among the top collaborators of C Clow 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 Clow. C Clow is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Treacy, Eileen P., C Clow, Orval Mamer, & C. R. Scriver. (1993). Methylmalonic acidemia with a severe chemical but benign clinical phenotype. The Journal of Pediatrics. 122(3). 428–429. 11 indexed citations

Mitchell, John J., C. R. Scriver, C Clow, & Feige Kaplan. (1993). What young people think and do when the option for cystic fibrosis carrier testing is available.. Journal of Medical Genetics. 30(7). 538–542. 52 indexed citations

Mitchell, John J., et al.. (1992). Newborn screening for sickle cell and other hemoglobinopathies: a Canadian pilot study.. PubMed. 15(4). 376–83. 11 indexed citations

Treacy, Eileen P., et al.. (1991). Maple syrup urine disease: Interrelations between branched‐chain amino‐, oxo‐ and hydroxyacids; implications for treatment; associations with CNS dysmyelination. Journal of Inherited Metabolic Disease. 15(1). 121–135. 79 indexed citations

Kaplan, Feige, C Clow, & C R Scriver. (1991). Cystic fibrosis carrier screening by DNA analysis: a pilot study of attitudes among participants.. PubMed. 49(1). 240–2. 25 indexed citations

Chitayat, David, et al.. (1991). Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: Intrafamilial variation in phenotype; absence of parental phenotype effects on the fetus. Journal of Inherited Metabolic Disease. 15(2). 198–203. 12 indexed citations

Cartier, Lola, et al.. (1989). B-Thalassemia disease prevention: Genetic medicine applied. 2 indexed citations

Prévost, Chantal, et al.. (1988). [The beta-thalassemia gene in French Canada: reappearance in Portneuf County].. PubMed. 118(3). 241, 243–4. 2 indexed citations

Scriver, C. R., C Clow, Paige Kaplan, & A. Niederwieser. (1987). Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase. Human Genetics. 77(2). 168–171. 14 indexed citations

10.

Scriver, C. R., Barbara E. Mahon, Harvey L. Levy, et al.. (1987). The Hartnup phenotype: Mendelian transport disorder, multifactorial disease.. PubMed. 40(5). 401–12. 49 indexed citations

11.

Scriver, C. R., et al.. (1984). Beta-thalassemia disease prevention: genetic medicine applied.. PubMed. 36(5). 1024–38. 42 indexed citations

12.

Rosenmann, Ada, C. R. Scriver, C Clow, & Harvey L. Levy. (1983). Histidinaemia. Part II: Impact; a retrospective study. Journal of Inherited Metabolic Disease. 6(2). 54–57. 7 indexed citations

13.

Cartier, Lola, C Clow, A Lippman-Hand, J Morissette, & C R Scriver. (1982). Prevention of mental retardation in offspring of hyperphenylalaninemic mothers.. American Journal of Public Health. 72(12). 1386–1390. 13 indexed citations

14.

Scriver, C. R., C Clow, & Peter Lamm. (1973). On the screening, diagnosis and investigation of hereditary aminoacidopathies. Clinical Biochemistry. 6(3). 142–188. 13 indexed citations

15.

Delvin, Edgar, et al.. (1972). Maladie de Tay-Sachs: dépistage et diagnostic prénatal.. 101(4). 4 indexed citations

16.

Glorieux, Francis H., et al.. (1971). X-linked hypophosphatemic rickets: A PTH-insensitive transport effect responsive to phosphate. Pediatric Research. 5(8). 392–392. 1 indexed citations

17.

Scriver, C. R., C Clow, Susan A. MacKenzie, & E. Delvin. (1971). THIAMINE-RESPONSIVE MAPLE-SYRUP-URINE DISEASE. The Lancet. 297(7694). 310–312. 122 indexed citations

18.

Klein, Marina B., Donald T. Whelan, C Clow, & C. R. Scriver. (1969). Urine Screening for Disorders of Mucopolysaccharide Metabolism. PEDIATRICS. 44(5). 768–769. 2 indexed citations

19.

Scriver, C R, Mark S. Silverberg, & C Clow. (1967). Hereditary tyrosinemia and tyrosyluria: clinical report of four patients.. PubMed. 97(18). 1047–50. 15 indexed citations

20.

Scriver, C R, C Clow, & Mark S. Silverberg. (1966). HYPERMETHIONINÆMIA IN ACUTE TYROSINOSIS. The Lancet. 287(7429). 153–154. 11 indexed citations

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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