Randy C. Eisensmith

2.8k total citations
57 papers, 2.3k citations indexed

About

Randy C. Eisensmith is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Randy C. Eisensmith has authored 57 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 40 papers in Clinical Biochemistry and 20 papers in Rheumatology. Recurrent topics in Randy C. Eisensmith's work include Metabolism and Genetic Disorders (40 papers), Folate and B Vitamins Research (20 papers) and Virus-based gene therapy research (15 papers). Randy C. Eisensmith is often cited by papers focused on Metabolism and Genetic Disorders (40 papers), Folate and B Vitamins Research (20 papers) and Virus-based gene therapy research (15 papers). Randy C. Eisensmith collaborates with scholars based in United States, Italy and China. Randy C. Eisensmith's co-authors include Savio L.C. Woo, Alexei A. Goltsov, Uta Lichter‐Konecki, David Konecki, Y Okano, Kenneth C. Copeland, Patrick Muzzin, Tao Wang, Yoshiyuki Okano and Zong Sheng Guo and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Randy C. Eisensmith

57 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Randy C. Eisensmith United States 28 1.5k 1.2k 805 492 292 57 2.3k
L E Rosenberg United States 23 1.4k 0.9× 777 0.6× 130 0.2× 305 0.6× 118 0.4× 26 1.8k
Yanling Yang China 19 857 0.6× 505 0.4× 209 0.3× 124 0.3× 117 0.4× 138 1.5k
C R Scriver Canada 18 485 0.3× 362 0.3× 161 0.2× 98 0.2× 153 0.5× 37 1.1k
Hubert Carchon Belgium 19 1.2k 0.8× 192 0.2× 154 0.2× 89 0.2× 324 1.1× 43 1.5k
Hitoshi Endo Japan 24 1.4k 1.0× 236 0.2× 133 0.2× 43 0.1× 160 0.5× 63 2.0k
Laurent Baricault France 17 1.6k 1.1× 378 0.3× 91 0.1× 34 0.1× 161 0.6× 22 1.9k
Samantha J. Mentch United States 8 1.2k 0.8× 55 0.0× 135 0.2× 190 0.4× 198 0.7× 8 1.7k
Martin Hřebı́ček Czechia 18 1.0k 0.7× 110 0.1× 91 0.1× 167 0.3× 1.2k 3.9× 39 2.2k
Andrew E. Gal United States 19 904 0.6× 147 0.1× 101 0.1× 444 0.9× 2.0k 6.8× 49 2.6k
Monika B. Dolinska United States 19 499 0.3× 127 0.1× 75 0.1× 89 0.2× 118 0.4× 46 1.5k

Countries citing papers authored by Randy C. Eisensmith

Since Specialization
Citations

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

Fields of papers citing papers by Randy C. Eisensmith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Randy C. Eisensmith

This figure shows the co-authorship network connecting the top 25 collaborators of Randy C. Eisensmith. A scholar is included among the top collaborators of Randy C. Eisensmith 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 Randy C. Eisensmith. Randy C. Eisensmith 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.
G�ttler, F., Per Guldberg, Randy C. Eisensmith, & Savio L.C. Woo. (1999). Molecular genetics and outcome in PKU. Mental Retardation and Developmental Disabilities Research Reviews. 5(2). 113–116. 1 indexed citations
2.
Muzzin, Patrick, Randy C. Eisensmith, Kenneth C. Copeland, & Savio L.C. Woo. (1997). Hepatic Insulin Gene Expression as Treatment for Type 1 Diabetes Mellitus in Rats. Molecular Endocrinology. 11(6). 833–837. 52 indexed citations
3.
Bowles, Neil E., et al.. (1996). A Simple and Efficient Method for the Concentration and Purification of Recombinant Retrovirus for Increased Hepatocyte Transduction In Vivo. Human Gene Therapy. 7(14). 1735–1742. 105 indexed citations
4.
Eisensmith, Randy C. & Savio L.C. Woo. (1996). Gene therapy for phenylketonuria. European Journal of Pediatrics. 155(S1). S16–S19. 21 indexed citations
5.
Eisensmith, Randy C., et al.. (1996). Phenylketonuria in Costa Rica: Preliminary Spectrum of PAH Mutations and Their Associations with Highly Polymorphic Haplotypes. Human Heredity. 46(3). 128–131. 7 indexed citations
6.
Eisensmith, Randy C. & Savio L.C. Woo. (1995). 6 Molecular Genetics of Phenylketonuria: From Molecular Anthropology to Gene Therapy. Advances in genetics. 32. 199–271. 22 indexed citations
7.
Fang, Bingliang, Randy C. Eisensmith, Igor O. Nasonkin, et al.. (1995). In vivo gene therapy for hyperlipidemia: phenotypic correction in Watanabe rabbits by hepatic delivery of the rabbit LDL receptor gene.. Journal of Clinical Investigation. 95(2). 768–773. 58 indexed citations
8.
Smith, Louis C., Randy C. Eisensmith, & Savio L.C. Woo. (1995). Gene Therapy in Heart Disease. Advances in experimental medicine and biology. 369. 79–88. 6 indexed citations
9.
Fang, B, Randy C. Eisensmith, Mark A. Kay, et al.. (1995). Gene Therapy for Hemophilia B: Host Immunosuppression Prolongs the Therapeutic Effect of Adenovirus-Mediated Factor IX Expression. Human Gene Therapy. 6(8). 1039–1044. 98 indexed citations
10.
Scriver, C. R., Randy C. Eisensmith, Savio L.C. Woo, & Seymour Kaufman. (1994). THE HYPERPHENYLALANINEMIAS OF MAN AND MOUSE. Annual Review of Genetics. 28(1). 141–166. 53 indexed citations
11.
Li, Jia, Randy C. Eisensmith, Tao Wang, et al.. (1994). Phenylketonuria in China: Identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene. Human Mutation. 3(3). 312–314. 2 indexed citations
12.
Eisensmith, Randy C., et al.. (1994). A simple, rapid, and highly informative PCR‐based procedure for prenatal diagnosis and carrier screening of phenylketonuria. Prenatal Diagnosis. 14(12). 1113–1118. 22 indexed citations
13.
Wang, Tao, Yoshiyuki Okano, Randy C. Eisensmith, et al.. (1992). Identification of three novel PKU mutations among Chinese: Evidence for recombination or recurrent mutation at the PAH locus. Genomics. 13(1). 230–231. 17 indexed citations
14.
Goltsov, Alexei A., Randy C. Eisensmith, & Savio L.C. Woo. (1992). Detection of the Xmnl RFLP at the human PAH locus by PCR. Nucleic Acids Research. 20(4). 927–927. 22 indexed citations
15.
Eisensmith, Randy C. & Savio L.C. Woo. (1992). Molecular basis of phenylketonuria and related hyperphenylalaninemias: Mutations and polymorphisms in the human phenylalanine hydroxylase gene. Human Mutation. 1(1). 13–23. 82 indexed citations
16.
Li, Jia, Randy C. Eisensmith, Tao Wang, et al.. (1992). Identification of three novel missense PKU mutations among Chinese. Genomics. 13(3). 894–895. 11 indexed citations
17.
Okano, Yoshiyuki, Randy C. Eisensmith, Flemming Güttler, et al.. (1991). Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria. New England Journal of Medicine. 324(18). 1232–1238. 206 indexed citations
18.
Okano, Yoshiyuki, Tao Wang, Randy C. Eisensmith, et al.. (1991). Phenylketonuria missense mutations in the Mediterranean. Genomics. 9(1). 96–103. 51 indexed citations
19.
Okano, Y, et al.. (1991). A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemia. European Journal of Pediatrics. 150(5). 347–352. 31 indexed citations
20.
Wang, Tao, Yoshiyuki Okano, Randy C. Eisensmith, et al.. (1990). Molecular genetics of PKU in Eastern Europe: A nonsense mutation associated with haplotype 4 of the phenylalanine hydroxylase gene. Somatic Cell and Molecular Genetics. 16(1). 85–90. 32 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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