Stanton Segal

10.1k total citations
344 papers, 8.1k citations indexed

About

Stanton Segal is a scholar working on Biochemistry, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, Stanton Segal has authored 344 papers receiving a total of 8.1k indexed citations (citations by other indexed papers that have themselves been cited), including 163 papers in Biochemistry, 146 papers in Clinical Biochemistry and 144 papers in Molecular Biology. Recurrent topics in Stanton Segal's work include Amino Acid Enzymes and Metabolism (153 papers), Metabolism and Genetic Disorders (145 papers) and Neonatal Health and Biochemistry (70 papers). Stanton Segal is often cited by papers focused on Amino Acid Enzymes and Metabolism (153 papers), Metabolism and Genetic Disorders (145 papers) and Neonatal Health and Biochemistry (70 papers). Stanton Segal collaborates with scholars based in United States, Poland and United Kingdom. Stanton Segal's co-authors include León E. Rosenberg, Alberta Blair, Pedro Cuatrecasas, Gerard T. Berry, Pamela D. McNamara, Marc Yudkoff, Beatrice States, Sylvia J. Downing, Samuel O. Thier and M.R. Spivey Fox and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Stanton Segal

342 papers receiving 7.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Stanton Segal 3.3k 3.2k 2.8k 1.8k 1.4k 344 8.1k
Cornelis Jakobs 5.4k 1.6× 1.6k 0.5× 4.4k 1.6× 1.4k 0.8× 2.1k 1.6× 225 12.0k
C. Jakobs 3.2k 1.0× 896 0.3× 2.8k 1.0× 931 0.5× 1.2k 0.9× 218 7.1k
Stephen I. Goodman 4.8k 1.5× 1.1k 0.4× 4.5k 1.6× 662 0.4× 898 0.7× 177 7.4k
M. Durán 3.8k 1.2× 831 0.3× 3.0k 1.0× 774 0.4× 929 0.7× 263 6.2k
Gerard T. Berry 3.1k 0.9× 947 0.3× 3.3k 1.1× 1.4k 0.8× 1.1k 0.8× 213 7.1k
John M. Lowenstein 4.3k 1.3× 815 0.3× 1.1k 0.4× 456 0.3× 2.0k 1.4× 131 8.1k
Carlo Dionisi‐Vici 4.9k 1.5× 1.2k 0.4× 4.6k 1.6× 1.2k 0.7× 1.7k 1.3× 292 9.3k
Ruud Berger 2.9k 0.9× 1.2k 0.4× 1.3k 0.5× 524 0.3× 1.0k 0.7× 152 7.4k
Dean J. Tuma 2.5k 0.8× 1.1k 0.3× 775 0.3× 368 0.2× 864 0.6× 261 8.3k
Eduard A. Struys 3.3k 1.0× 1.2k 0.4× 2.2k 0.8× 832 0.5× 735 0.5× 149 6.1k

Countries citing papers authored by Stanton Segal

Since Specialization
Citations

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

Fields of papers citing papers by Stanton Segal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stanton Segal

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

All Works

20 of 20 papers shown
1.
Wehrli, Suzanne, Robert Reynolds, & Stanton Segal. (2007). Evidence for function of UDP galactose pyrophosphorylase in mice with absent galactose-1-phosphate uridyltransferase. Molecular Genetics and Metabolism. 91(2). 191–194. 5 indexed citations
2.
Leslie, Nancy, Claire Yager, Robert Reynolds, & Stanton Segal. (2005). UDP-galactose pyrophosphorylase in mice with galactose-1-phosphate uridyltransferase deficiency. Molecular Genetics and Metabolism. 85(1). 21–27. 14 indexed citations
3.
Yager, Claire, Ning Cong, Robert Reynolds, Nancy Leslie, & Stanton Segal. (2003). Galactitol and galactonate accumulation in heart and skeletal muscle of mice with deficiency of galactose-1-phosphate uridyltransferase. Molecular Genetics and Metabolism. 81(2). 105–111. 9 indexed citations
4.
Wehrli, Suzanne, Robert Reynolds, Jie Chen, Claire Yager, & Stanton Segal. (2002). Metabolism of 13C galactose by lymphoblasts from patients with galactosemia determined by NMR spectroscopy. Molecular Genetics and Metabolism. 77(4). 296–303. 17 indexed citations
5.
Berry, Gerard T., Rani H. Singh, Alice Mazur, et al.. (2000). Galactose Breath Testing Distinguishes Variant and Severe Galactose-1-Phosphate Uridyltransferase Genotypes. Pediatric Research. 48(3). 323–328. 36 indexed citations
6.
Leslie, Nancy D., Karen L. Yager, Pamela D. McNamara, & Stanton Segal. (1996). A Mouse Model of Galactose-1-Phosphate Uridyl Transferase Deficiency. Biochemical and Molecular Medicine. 59(1). 7–12. 70 indexed citations
7.
Berry, Gerard T., et al.. (1996). Sugar nucleotide concentrations in red blood cells of patients on protein- and lactose-limited diets: effect of galactose supplementation. American Journal of Clinical Nutrition. 63(5). 704–708. 8 indexed citations
8.
Berry, Gerard T., Itzhak Nissim, A. Mazur, et al.. (1995). In Vivo Oxidation of [13C]Galactose in Patients with Galactose-1-Phosphate Uridyltransferase Deficiency. Biochemical and Molecular Medicine. 56(2). 158–165. 26 indexed citations
9.
Berry, Gerard T., Itzhak Nissim, Zhang Lin, et al.. (1995). Endogenous synthesis of galactose in normal men and patients with hereditary galactosaemia. The Lancet. 346(8982). 1073–1074. 128 indexed citations
10.
Berry, Gerard T., et al.. (1992). Red blood cell uridine sugar nucleotide levels in patients with classic galactosemia and other metabolic disorders. Metabolism. 41(7). 783–787. 29 indexed citations
11.
12.
States, Beatrice & Stanton Segal. (1990). Cystine and dibasic amino acid uptake by opossum kidney cells. Journal of Cellular Physiology. 143(3). 555–562. 8 indexed citations
13.
Bovée, Kenneth C., Peter F. Jezyk, & Stanton Segal. (1984). Postnatal development of renal tubular amino acid reabsorption in canine pups. American Journal of Veterinary Research. 45(4). 830–832. 9 indexed citations
14.
Segal, Stanton, Joel Y. Rutman, & George W. Frimpter. (1979). Galactokinase deficiency and mental retardation. The Journal of Pediatrics. 95(5). 750–752. 14 indexed citations
15.
Guggenheim, K. & Stanton Segal. (1977). Oral contraceptives and riboflavin nutriture.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 47(3). 234–5. 6 indexed citations
16.
Yudkoff, Marc, et al.. (1977). Phenylalanine-tyrosine deficiency syndrome as a complication of the management of hereditary tyrosinemia. American Journal of Clinical Nutrition. 30(2). 209–214. 11 indexed citations
17.
Segal, Stanton, Henry Roth, & Alberta Blair. (1966). Observations on the influence of orotic acid on galactosemetabolism in congenital galactosemia. The Journal of Pediatrics. 68(1). 135–138. 3 indexed citations
18.
Baker, Lester, William J. Mellman, Thomas A. Tedesco, & Stanton Segal. (1966). Galactosemia: Symptomatic and asymptomatic homozygotes in one Negro sibship. The Journal of Pediatrics. 68(4). 551–558. 42 indexed citations
19.
Segal, Stanton & Howard Bernstein. (1963). Observations on cataract formation in the newborn offspring of rats fed a high-galactose diet. The Journal of Pediatrics. 62(3). 363–370. 30 indexed citations
20.
Topper, Yale J., Leonard Laster, & Stanton Segal. (1962). Galactose Metabolism : Phenotypic Differences among Tissues of a Patient with Congenital Galactosæmia. Nature. 196(4858). 1006–1006. 18 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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