A L Beaudet

2.3k total citations
23 papers, 1.8k citations indexed

About

A L Beaudet is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, A L Beaudet has authored 23 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Pulmonary and Respiratory Medicine and 6 papers in Genetics. Recurrent topics in A L Beaudet's work include Cystic Fibrosis Research Advances (7 papers), Cell Adhesion Molecules Research (5 papers) and Genetic Syndromes and Imprinting (4 papers). A L Beaudet is often cited by papers focused on Cystic Fibrosis Research Advances (7 papers), Cell Adhesion Molecules Research (5 papers) and Genetic Syndromes and Imprinting (4 papers). A L Beaudet collaborates with scholars based in United States, Canada and Switzerland. A L Beaudet's co-authors include W E O'Brien, J. Edward Spence, J. Fielding Hejtmancik, M S Pollack, Gillian Greig, H.F. Willard, David H. Ledbetter, N. D. Staite, W M Quinlan and N A Doyle and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Blood.

In The Last Decade

A L Beaudet

23 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A L Beaudet United States	16	688	678	390	389	312	23	1.8k
Suzanna G.M. Frints Netherlands	21	878 1.3×	1.1k 1.5×	98 0.3×	193 0.5×	416 1.3×	39	1.9k
Mohnish Suri United Kingdom	24	1.2k 1.8×	736 1.1×	57 0.1×	131 0.3×	180 0.6×	82	2.2k
Ragnar Mattsson Sweden	23	622 0.9×	332 0.5×	176 0.5×	1.1k 2.7×	108 0.3×	61	2.1k
Hanne Jensen Denmark	25	576 0.8×	167 0.2×	51 0.1×	141 0.4×	188 0.6×	107	2.0k
J.J. Cassiman Belgium	20	567 0.8×	229 0.3×	83 0.2×	138 0.4×	60 0.2×	53	1.4k
Ulrike Hüffmeier Germany	24	534 0.8×	586 0.9×	61 0.2×	813 2.1×	132 0.4×	45	1.8k
Diana C. Blaydon United Kingdom	18	846 1.2×	293 0.4×	71 0.2×	155 0.4×	97 0.3×	29	1.6k
Athena Milatovich United States	19	1.1k 1.6×	442 0.7×	113 0.3×	767 2.0×	56 0.2×	32	2.3k
Francesca Faravelli Italy	22	869 1.3×	1.2k 1.7×	50 0.1×	1.2k 3.2×	294 0.9×	61	2.9k
Lesley Vanes United Kingdom	21	897 1.3×	390 0.6×	99 0.3×	942 2.4×	51 0.2×	26	2.2k

Countries citing papers authored by A L Beaudet

Since Specialization

Citations

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

Fields of papers citing papers by A L Beaudet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A L Beaudet. 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 A L Beaudet. The network helps show where A L Beaudet may publish in the future.

Co-authorship network of co-authors of A L Beaudet

This figure shows the co-authorship network connecting the top 25 collaborators of A L Beaudet. A scholar is included among the top collaborators of A L Beaudet 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 A L Beaudet. A L Beaudet 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

Beaudet, A L, et al.. (2004). Autism in Angelman syndrome: implications for autism research. Clinical Genetics. 66(6). 530–536. 147 indexed citations

Bercovich, Dani & A L Beaudet. (2003). Denaturing High-Performance Liquid Chromatography for the Detection of Mutations and Polymorphisms in UBE3A. Genetic Testing. 7(3). 189–194. 20 indexed citations

Jiang, Yao-Hui, et al.. (1999). Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing to Prader-Willi Syndrome. Human Molecular Genetics. 8(8). 1357–1364. 128 indexed citations

Qin, Li, W M Quinlan, N A Doyle, et al.. (1996). The roles of CD11/CD18 and ICAM-1 in acute Pseudomonas aeruginosa-induced pneumonia in mice. The Journal of Immunology. 157(11). 5016–5021. 108 indexed citations

Bullard, Daniel C., et al.. (1996). Reduced susceptibility to collagen-induced arthritis in mice deficient in intercellular adhesion molecule-1. The Journal of Immunology. 157(7). 3153–3158. 50 indexed citations

Doerschuk, Claire M., W M Quinlan, N A Doyle, et al.. (1996). The role of P-selectin and ICAM-1 in acute lung injury as determined using blocking antibodies and mutant mice. The Journal of Immunology. 157(10). 4609–4614. 138 indexed citations

King, Philip D., et al.. (1995). Novel isoforms of murine intercellular adhesion molecule-1 generated by alternative RNA splicing.. The Journal of Immunology. 154(11). 6080–6093. 134 indexed citations

Beaudet, A L, et al.. (1994). Somatic gene therapy for cystic fibrosis. Human Molecular Genetics. 3(suppl_1). 1497–1502. 27 indexed citations

Beaudet, A L, et al.. (1992). Molecular cloning and analysis of in vivo expression of murine P- selectin. Blood. 80(3). 795–800. 10 indexed citations

10.

Beaudet, A L, et al.. (1991). Mutation Analysis for Cystic Fibrosis in a North American Population. Advances in experimental medicine and biology. 290. 53–54. 5 indexed citations

11.

Caskey, C. T., Michael M. Kaback, & A L Beaudet. (1990). The American Society of Human Genetics statement on cystic fibrosis screening.. PubMed. 46(2). 393–393. 70 indexed citations

12.

Northrup, Hope, C L Rosenbloom, W E O'Brien, & A L Beaudet. (1989). Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplification. Nucleic Acids Research. 17(4). 1784–1784. 14 indexed citations

13.

Meisler, Miriam H., et al.. (1987). Exclusion of close linkage between the loci for cystic fibrosis and neuropeptide Y on human chromosome 7. Cytogenetic and Genome Research. 44(2-3). 175–176. 5 indexed citations

14.

Berchtold, Martin W., Paul N. Epstein, A L Beaudet, et al.. (1987). Structural organization and chromosomal assignment of the parvalbumin gene.. Journal of Biological Chemistry. 262(18). 8696–8701. 64 indexed citations

15.

Nussbaum, Robert L., et al.. (1986). New mutation and prenatal diagnosis in ornithine transcarbamylase deficiency.. PubMed. 38(2). 149–58. 34 indexed citations

16.

Beaudet, A L, A. Bowcock, Manuel Buchwald, et al.. (1986). Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study.. PubMed. 39(6). 681–93. 143 indexed citations

17.

Spence, J. Edward, C L Rosenbloom, W E O'Brien, et al.. (1986). Linkage of DNA markers to cystic fibrosis in 26 families.. PubMed. 39(6). 729–34. 13 indexed citations

18.

Rostène, William, R. Quirion, A L Beaudet, & B. Mazièré. (1985). Images des récepteurs des messagers chimiques et des médicaments dans le cerveau. médecine/sciences. 1(8). 419–419. 1 indexed citations

19.

Beaudet, A L. (1985). Bibliography of cloned human and other selected DNAs.. PubMed. 37(2). 386–406. 13 indexed citations

20.

Robinson, B. H., et al.. (1983). Lacticacidosis, neurological deterioration and compromised cellular pyruvate oxidation due to a defect in the reoxidation of cytoplasmically generated NADH. European Journal of Pediatrics. 140(2). 98–101. 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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