E.A. Helmbold

2.2k total citations · 1 hit paper
8 papers, 1.6k citations indexed

About

E.A. Helmbold is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Oncology. According to data from OpenAlex, E.A. Helmbold has authored 8 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Pulmonary and Respiratory Medicine and 2 papers in Oncology. Recurrent topics in E.A. Helmbold's work include Vascular Anomalies and Treatments (5 papers), BRCA gene mutations in cancer (2 papers) and Tracheal and airway disorders (2 papers). E.A. Helmbold is often cited by papers focused on Vascular Anomalies and Treatments (5 papers), BRCA gene mutations in cancer (2 papers) and Tracheal and airway disorders (2 papers). E.A. Helmbold collaborates with scholars based in United States, United Kingdom and Netherlands. E.A. Helmbold's co-authors include Dorene S. Markel, Douglas A. Marchuk, Charles E. Jackson, David W. Johnson, Carol J. Gallione, Kimberly A. McAllister, Mary Porteous, Wendy McKinnon, Alan E. Guttmacher and M. A. Pericak‐Vance and has published in prestigious journals such as Nature Genetics, Genome Research and The American Journal of Human Genetics.

In The Last Decade

E.A. Helmbold

8 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

1994 1.1k citations Kimberly A. McAllister, David W. Johnson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E.A. Helmbold United States	7	911	769	431	421	257	8	1.6k
T. Haitjema Netherlands	14	1.1k 1.2×	1.2k 1.5×	440 1.0×	454 1.1×	233 0.9×	19	1.9k
Ivonne Marondel United States	6	482 0.5×	403 0.5×	209 0.5×	357 0.8×	131 0.5×	7	972
Sang-Heon Yoon United States	5	477 0.5×	386 0.5×	199 0.5×	337 0.8×	123 0.5×	5	913
Cornelius J.J. Westermann Netherlands	16	2.1k 2.3×	1.8k 2.3×	689 1.6×	189 0.4×	273 1.1×	18	2.5k
Carmen Langa Spain	22	625 0.7×	656 0.9×	317 0.7×	1.2k 2.8×	109 0.4×	36	2.3k
Sophie Giraud France	28	405 0.4×	984 1.3×	328 0.8×	889 2.1×	428 1.7×	71	2.4k
Tom G.W. Letteboer Netherlands	16	353 0.4×	336 0.4×	191 0.4×	410 1.0×	75 0.3×	27	1.2k
S. Pinson France	19	216 0.2×	254 0.3×	242 0.6×	205 0.5×	399 1.6×	39	1.1k
S Vera Canada	6	356 0.4×	335 0.4×	143 0.3×	635 1.5×	52 0.2×	8	1.3k
Evelyn Torsney United Kingdom	15	377 0.4×	474 0.6×	444 1.0×	928 2.2×	95 0.4×	22	1.8k

Countries citing papers authored by E.A. Helmbold

Since Specialization

Citations

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

Fields of papers citing papers by E.A. Helmbold

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E.A. Helmbold

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

All Works

Sort: Min cites: Since: Top N: Style:

8 of 8 papers shown

1.

Middelton, Lindsay, Kathryn F. Peters, & E.A. Helmbold. (1997). Programmed Instruction: Genetics and Gene Therapy. Cancer Nursing. 20(2). 129–151. 3 indexed citations

2.

Johnson, David W., Jonathan Berg, Carol J. Gallione, et al.. (1995). A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.. Genome Research. 5(1). 21–28. 124 indexed citations

3.

Gallione, Carol J., Krystyna A. Pasyk, Laurence M. Boon, et al.. (1995). A gene for familial venous malformations maps to chromosome 9p in a second large kindred.. Journal of Medical Genetics. 32(3). 197–199. 105 indexed citations

4.

Lennon, Felicia, et al.. (1994). Genetic heterogeneity in hereditary hemorrhagic telangiectasia: Possible correlation with clinical phenotype. The American Journal of Human Genetics. 55. 9 indexed citations

5.

McAllister, Kimberly A., Felicia Lennon, Wendy McKinnon, et al.. (1994). Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.. Journal of Medical Genetics. 31(12). 927–932. 79 indexed citations

6.

McAllister, Kimberly A., David W. Johnson, Carol J. Gallione, et al.. (1994). Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1. Nature Genetics. 8(4). 345–351. 1137 indexed citations breakdown →

7.

McDonald, Marie, Soumitra Ghosh, Arthur A. Glatfelter, et al.. (1994). A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33–34. Nature Genetics. 6(2). 197–204. 120 indexed citations

8.

Chamberlain, Jeffrey S., Michael Boehnke, Thomas Frank, et al.. (1993). BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.. PubMed. 52(4). 792–8. 39 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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