Glenn L. Renforth

1.0k total citations
5 papers, 798 citations indexed

About

Glenn L. Renforth is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Glenn L. Renforth has authored 5 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Glenn L. Renforth's work include Genetic Syndromes and Imprinting (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Glenn L. Renforth is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Glenn L. Renforth collaborates with scholars based in United Kingdom, France and United States. Glenn L. Renforth's co-authors include David I. Wilson, C. Mirella Spalluto, Tom Hearn, Neil A. Hanley, Jan Ure, Trevor Jowett, Douglas A. Marchuk, John Burn, Dinah V. Parums and Richard Charlton and has published in prestigious journals such as Nature Genetics, Diabetes and Developmental Biology.

In The Last Decade

Glenn L. Renforth

5 papers receiving 787 citations

Author Peers

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

Author						Papers	Cites
Glenn L. Renforth	448	355	161	139	121	5	798
Elizabeth Salisbury	489 1.1×	193 0.5×	82 0.5×	64 0.5×	194 1.6×	24	951
Martin P. Powers	349 0.8×	292 0.8×	133 0.8×	69 0.5×	38 0.3×	18	805
Susan Schelley	342 0.8×	258 0.7×	337 2.1×	385 2.8×	263 2.2×	17	1.0k
John Garcia	597 1.3×	441 1.2×	102 0.6×	49 0.4×	60 0.5×	16	1.3k
Ilaria Lapini	202 0.5×	122 0.3×	107 0.7×	114 0.8×	114 0.9×	19	582
Fatema Alzahrani	430 1.0×	386 1.1×	44 0.3×	55 0.4×	73 0.6×	25	724
Maarten Bergwerff	602 1.3×	107 0.3×	211 1.3×	51 0.4×	172 1.4×	10	840
Christelle Arrondel	457 1.0×	271 0.8×	79 0.5×	139 1.0×	58 0.5×	17	980
Kristiina Avela	633 1.4×	402 1.1×	40 0.2×	49 0.4×	74 0.6×	34	1.1k

Countries citing papers authored by Glenn L. Renforth

Since Specialization

Citations

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

Fields of papers citing papers by Glenn L. Renforth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Glenn L. Renforth

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

All Works

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5 of 5 papers shown

Cox, Helen, Anneke Lucassen, Marlène Rio, et al.. (2009). Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings. Clinical Dysmorphology. 18(2). 98–102. 3 indexed citations

Hearn, Tom, C. Mirella Spalluto, Glenn L. Renforth, et al.. (2005). Subcellular Localization of ALMS1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity, Insulin Resistance, and Type 2 Diabetes. Diabetes. 54(5). 1581–1587. 173 indexed citations

Phillips, Helen M., Glenn L. Renforth, C. Mirella Spalluto, et al.. (2002). Narrowing the Critical Region within 11q24–qter for Hypoplastic Left Heart and Identification of a Candidate Gene, JAM3, Expressed during Cardiogenesis. Genomics. 79(4). 475–478. 34 indexed citations

Hearn, Tom, Glenn L. Renforth, C. Mirella Spalluto, et al.. (2002). Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome. Nature Genetics. 31(1). 79–83. 215 indexed citations

Arthur, Helen M., Jan Ure, Andrew J. H. Smith, et al.. (2000). Endoglin, an Ancillary TGFβ Receptor, Is Required for Extraembryonic Angiogenesis and Plays a Key Role in Heart Development. Developmental Biology. 217(1). 42–53. 373 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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