E.A. Helmbold

2.2k citations
7 papers · 1.6k · 1 hit paper · h-index 6

Impact in

Papers in

    • Vascular Anomalies and Treatments 4
    • BRCA gene mutations in cancer 2
    • Genomic variations and chromosomal abnormalities 1
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema 1
    • Vascular Tumors and Angiosarcomas 1

E.A. Helmbold

7 papers receiving 1.6k citations

E.A. Helmbold's Hit Papers

Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1 1994 · 1.2k citations
1.2k0+10+21Years since publication4008001.2k

Peers

E.A. Helmbold
Comparison fields: 5 of 70
  • Genetics 822
  • Pulmonary and Respiratory Medicine 568
  • Neurology 244
  • Marketing 135
  • Immunology and Allergy 54
Replace Tjeerd J. Haitjema with:
Tjeerd J. Haitjema Netherlands
Ivonne Marondel United States
Sang-Heon Yoon United States
Carmen Langa Spain
Cornelius J.J. Westermann Netherlands
Roberto Zarrabeitia Spain
Sophie Giraud France
S Vera United States
Richard Charlton United Kingdom
Henry Plauchu France
E.A. Helmbold relative to Tjeerd J. Haitjema Netherlands Tjeerd J. Haitjema's profile →
Citations per field
00.5×1.5×
Tjeerd J. Haitjema · 1×
Citations per year

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-authors

The 25 scholars most cited alongside E.A. Helmbold, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E.A. Helmbold Line = papers co-authored together E.A. Helmbold links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Hit paper breakdown →
19941247
2 1994138
3 1995120
4 199480
5
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.
199345
6
Genetic heterogeneity in hereditary hemorrhagic telangiectasia: Possible correlation with clinical phenotype
19948
7 19974

About E.A. Helmbold

E.A. Helmbold is a scholar working on Genetics, Oncology, Genetics, Cancer Research and Pulmonary and Respiratory Medicine, having authored 7 papers that have together received 1.6k indexed citations. Recurring topics across this work include Vascular Anomalies and Treatments (4 papers), BRCA gene mutations in cancer (2 papers), Cancer Genomics and Diagnostics (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Tracheal and airway disorders (1 paper), Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper), Islanding Detection in Power Systems (1 paper) and Vascular Tumors and Angiosarcomas (1 paper). The work is most often cited by research in Genetics (822 citations), Pulmonary and Respiratory Medicine (568 citations), Neurology (244 citations), Marketing (135 citations) and Immunology and Allergy (54 citations). E.A. Helmbold has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Dorene S. Markel, Alan E. Guttmacher, Charles E. Jackson, Douglas A. Marchuk, Wendy C. McKinnon, David Wayne Johnson, Carol J. Gallione, Mary E. Porteous, Margaret A. Pericak‐Vance and Kimberly A. McAllister. Their work appears in journals such as Journal of Medical Genetics, Nature Genetics, Cancer Nursing, The American Journal of Human Genetics and PubMed.

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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