Alan E. Guttmacher
Impact in
Papers in
- Genetics 17
- 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
- Co-authors
- Francis S. CollinsDouglas A. MarchukEric D. GreenMark S. GuyerRobert I. WhiteMary PorteousClaire L. ShovlinRobert H. Hyland
- Journals
- New England Journal of Medicine (7 papers)JAMA (3 papers)Nature Genetics (3 papers)Genetics in Medicine (3 papers)American Psychologist (3 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Alan E. Guttmacher
55 papers receiving 7.7k citations
Hit Papers
Peers
Comparison fields: 5 of 171
- Genetics 3.3k
- Marketing 856
- Pulmonary and Respiratory Medicine 2.8k
- Genetics 1.8k
- Neurology 566
Countries citing papers authored by Alan E. Guttmacher
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
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-authorship network
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.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 2 | |
| 2 | 2014 | 192 | |
| 3 | 2013 | 16 | |
| 4 | 2011 | 40 | |
| 5 | 2009 | 7 | |
| 6 | Genomic medicine : articles from the New England Journal of Medicine | 2004 | 14 |
| 7 | A vision for the future of genomics research Hit paper breakdown → | 2003 | 1169 |
| 8 | 2003 | 3 | |
| 9 | 2002 | 401 | |
| 10 | 2001 | 90 | |
| 11 | 2000 | 104 | |
| 12 | 2000 | 3 | |
| 13 | Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) Hit paper breakdown → | 2000 | 1148 |
| 14 | 1998 | 14 | |
| 15 | 1998 | 77 | |
| 16 | 1998 | 6 | |
| 17 | 1997 | 37 | |
| 18 | 1994 | 79 | |
| 19 | Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1 Hit paper breakdown → | 1994 | 1137 |
| 20 | 1993 | 22 |
About Alan E. Guttmacher
Alan E. Guttmacher is a scholar working on Genetics, Developmental Biology, Genetics, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, 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 (9 papers), Genomics and Rare Diseases (6 papers), Genetics, Bioinformatics, and Biomedical Research (5 papers), Nutrition, Genetics, and Disease (4 papers), Neonatal Respiratory Health Research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (3.3k citations), Marketing (856 citations), Pulmonary and Respiratory Medicine (2.8k citations), Genetics (1.8k citations) and Neurology (566 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, Robert H. Hyland, Anette Drøhse Kjeldsen and Cornelius J.J. Westermann. Their work appears in journals such as New England Journal of Medicine, JAMA, Nature Genetics, Genetics in Medicine and American Psychologist.
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.