Alan S. Lidsky

1.1k total citations
10 papers, 855 citations indexed

About

Alan S. Lidsky is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Alan S. Lidsky has authored 10 papers receiving a total of 855 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 6 papers in Rheumatology. Recurrent topics in Alan S. Lidsky's work include Metabolism and Genetic Disorders (9 papers), Folate and B Vitamins Research (6 papers) and Biochemical and Molecular Research (5 papers). Alan S. Lidsky is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Folate and B Vitamins Research (6 papers) and Biochemical and Molecular Research (5 papers). Alan S. Lidsky collaborates with scholars based in United States, Denmark and Germany. Alan S. Lidsky's co-authors include Savio L.C. Woo, Flemming Güttler, Anthony G. DiLella, Kathryn Robson, T.S. Chandra, Joshua Marvit, Stephen P. Daiger, Fred D. Ledley, F. G�ttler and Susan Sullivan and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Alan S. Lidsky

9 papers receiving 808 citations

Peers

Alan S. Lidsky

MB

CB

RHEUM

GENET

PHYSI

A Ponzone Italy

Niels Gregersen Denmark

James G. Coldwell United States

Jack J. Huizenga Canada

R. M. Brown United Kingdom

Andrew A.M. Morris United Kingdom

Nanna Cornelius Denmark

Toshinobu Matsuura Japan

Sze Chern Lim Australia

Teresa Pàmpols Spain

A Ponzone Italy

Alan S. Lidsky

366 ×0.6

MB

468 ×0.8

CB

127 ×0.4

RHEUM

92 ×0.6

GENET

98 ×0.9

PHYSI

Citations per year, relative to Alan S. Lidsky Alan S. Lidsky (= 1×) peers A Ponzone

Countries citing papers authored by Alan S. Lidsky

Since Specialization

Citations

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

Fields of papers citing papers by Alan S. Lidsky

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan S. Lidsky. 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 Alan S. Lidsky. The network helps show where Alan S. Lidsky may publish in the future.

Co-authorship network of co-authors of Alan S. Lidsky

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

All Works

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10 of 10 papers shown

1.

G�ttler, F., Fred D. Ledley, Alan S. Lidsky, et al.. (1987). Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria. The Journal of Pediatrics. 110(1). 68–71. 48 indexed citations

2.

Lidsky, Alan S., Stephen P. Daiger, F. G�ttler, et al.. (1987). Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Human Genetics. 76(1). 40–6. 98 indexed citations

3.

G�ttler, F., Anthony G. DiLella, Fred D. Ledley, et al.. (1987). Molecular biology of phenylketonuria. European Journal of Pediatrics. 146(1). A5–A11. 13 indexed citations

4.

DiLella, Anthony G., Joshua Marvit, Alan S. Lidsky, Flemming Güttler, & Savio L.C. Woo. (1986). Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria. Nature. 322(6082). 799–803. 217 indexed citations

5.

Daiger, Stephen P., Ranajit Chakraborty, Flemming Güttler, et al.. (1986). POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE HYDROXYLASE LOCUS IN PRENATAL DIAGNOSIS OF PHENYLKETONURIA. The Lancet. 327(8475). 229–232. 30 indexed citations

6.

Lidsky, Alan S., Fred D. Ledley, Anthony G. DiLella, et al.. (1985). Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.. PubMed. 37(4). 619–34. 133 indexed citations

7.

Trefz, Friedrich K., et al.. (1985). HAPLOTYPE ANALYSIS OF THE PHENYLALANINE HYDROXYLASE AND PRENATAL DIAGNOSIS OF PKU IN GERMANY. Pediatric Research. 19(10). 1074–1074. 1 indexed citations

8.

Lidsky, Alan S., M L Law, Helvise G. Morse, et al.. (1985). Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome.. Proceedings of the National Academy of Sciences. 82(18). 6221–6225. 64 indexed citations

9.

Morse, Helvise G., et al.. (1984). Genetic mapping of the structural gene for antithrombin III to human chromosome 1. Human Genetics. 67(1). 34–36. 17 indexed citations

10.

Woo, Savio L.C., Alan S. Lidsky, Flemming Güttler, T.S. Chandra, & Kathryn Robson. (1983). Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria. Nature. 306(5939). 151–155. 234 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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