Alan E. Guttmacher

23.9k citations
56 papers · 8.0k · 5 hit papers · h-index 28

Impact in

  • Genetics top 0.1%
    • Vascular Anomalies and Treatments
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Tracheal and airway disorders
    • Pulmonary Hypertension Research and Treatments

Papers in

    • Vascular Anomalies and Treatments 16
    • BRCA gene mutations in cancer 13
    • Genomics and Rare Diseases 6
    • Nutrition, Genetics, and Disease 4
    • Genomic variations and chromosomal abnormalities 4
    • Tracheal and airway disorders 8
    • Neonatal Respiratory Health Research 4

Alan E. Guttmacher

55 papers receiving 7.8k citations

Alan E. Guttmacher's Hit Papers

A vision for the future of genomics research 2003 · 1.2k citations
1.2k0+10+21Years since publication2505007501000

Peers

Alan E. Guttmacher
Comparison fields: 5 of 167
  • Genetics 3.2k
  • Pulmonary and Respiratory Medicine 2.1k
  • Marketing 584
  • Genetics 1.7k
  • Neurology 480
Replace Mary Porteous with:
Mary Porteous United Kingdom
Michael Walker United States
Sophia Wang United States
Lijun Chen China
Ingrid Winship Australia
Hidetoshi Yamashita Japan
Kathleen N. Moore United States
John Park United States
Wendy Liu United States
Michael Lim United States
Alan E. Guttmacher relative to Mary Porteous United Kingdom Mary Porteous's profile →
Citations per field
00.5×1.5×2.1×
Mary Porteous · 1×
Citations per year

Countries citing papers authored by Alan E. Guttmacher

Since Specialization
Citations

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

Fields of papers citing papers by Alan E. Guttmacher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Alan E. Guttmacher, 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 Alan E. Guttmacher Line = papers co-authored together Alan E. Guttmacher links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A vision for the future of genomics research
Hit paper breakdown →
20031176
2
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)
Hit paper breakdown →
20001154
3
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1
Hit paper breakdown →
19941140
4
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2
Hit paper breakdown →
1996848
5
Hereditary Hemorrhagic Telangiectasia
Hit paper breakdown →
1995762
6 2002401
7 2004361
8 2010274
9 2007226
10 2014193
11 1994121
12 2000104
13 201096
14 200592
15 199692
16 200190
17 200185
18 199480
19 199877
20
A vision for the future of genomics research A blueprint for the genomic era.
200377

About Alan E. Guttmacher

Alan E. Guttmacher is a scholar working on Genetics, Genetics, Pulmonary and Respiratory Medicine, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 56 papers that have together received 8.0k indexed citations. Recurring topics across this work include Vascular Anomalies and Treatments (16 papers), BRCA gene mutations in cancer (13 papers), Tracheal and airway disorders (8 papers), Genomics and Rare Diseases (6 papers), Genetics, Bioinformatics, and Biomedical Research (5 papers), Nutrition, Genetics, and Disease (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Neonatal Respiratory Health Research (4 papers). The work is most often cited by research in Genetics (3.2k citations), Pulmonary and Respiratory Medicine (2.1k citations), Marketing (584 citations), Genetics (1.7k citations) and Neurology (480 citations). Alan E. Guttmacher has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Francis S. Collins, Douglas A. Marchuk, Eric D. Green, Mark S. Guyer, Robert I. White, Mary Porteous, Claire L. Shovlin, Marie E. Faughnan, Robert H. Hyland and Elisabetta Buscarini. Their work appears in journals such as New England Journal of Medicine, JAMA, American Psychologist, Human Mutation and Nature Genetics.

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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