Edwin P. Kirk
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Molecular Biology top 5%
- Congenital heart defects research
- Mitochondrial Function and Pathology
- RNA modifications and cancer
- ATP Synthase and ATPases Research
Papers in
-
- Congenital heart defects research 21
- Mitochondrial Function and Pathology 10
- Genetics 23
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 7
- Co-authors
- Richard P. Harvey (17 shared papers)David S. Winlaw (15 shared papers)Gary F. Sholler (14 shared papers)Gillian M. Blue (12 shared papers)Michael P. Feneley (5 shared papers)Diane Fatkin (4 shared papers)Rosemary L. Donne (1 shared paper)Timothy H.J. Goodship (1 shared paper)
- Journals
- European Journal of Human Genetics (7 papers)Prenatal Diagnosis (5 papers)Genetics in Medicine (4 papers)Journal of Medical Genetics (3 papers)European Journal of Medical Genetics (3 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Edwin P. Kirk
98 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 114
- Clinical Biochemistry 374
- Molecular Biology 1.5k
- Epidemiology 620
- Genetics 450
- Immunology 324
Countries citing papers authored by Edwin P. Kirk
This map shows the geographic impact of Edwin P. Kirk'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 Edwin P. Kirk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edwin P. Kirk more than expected).
Fields of papers citing papers by Edwin P. Kirk
This network shows the impact of papers produced by Edwin P. Kirk. 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 Edwin P. Kirk. The network helps show where Edwin P. Kirk may publish in the future.
Co-authors
The 25 scholars most cited alongside Edwin P. Kirk, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 103 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 266 | |
| 2 | 2012 | 211 | |
| 3 | 2003 | 196 | |
| 4 | 2004 | 168 | |
| 5 | 2009 | 134 | |
| 6 | 2003 | 126 | |
| 7 | 2010 | 123 | |
| 8 | 2017 | 110 | |
| 9 | 2008 | 106 | |
| 10 | 2013 | 88 | |
| 11 | 2006 | 73 | |
| 12 | 2011 | 71 | |
| 13 | 2014 | 66 | |
| 14 | 2019 | 65 | |
| 15 | 2002 | 62 | |
| 16 | 2011 | 57 | |
| 17 | 2010 | 50 | |
| 18 | 2019 | 46 | |
| 19 | 2015 | 40 | |
| 20 | 2016 | 37 |
About Edwin P. Kirk
Edwin P. Kirk is a scholar working on Molecular Biology, Genetics, Pulmonary and Respiratory Medicine, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 103 papers that have together received 3.0k indexed citations. Recurring topics across this work include Congenital heart defects research (21 papers), Metabolism and Genetic Disorders (14 papers), Congenital Heart Disease Studies (11 papers), Genomic variations and chromosomal abnormalities (10 papers), Mitochondrial Function and Pathology (10 papers), Prenatal Screening and Diagnostics (9 papers), Cystic Fibrosis Research Advances (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Clinical Biochemistry (374 citations), Molecular Biology (1.5k citations), Epidemiology (620 citations), Genetics (450 citations) and Immunology (324 citations). Edwin P. Kirk has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Richard P. Harvey, David S. Winlaw, Gary F. Sholler, Gillian M. Blue, Michael P. Feneley, Diane Fatkin, Rosemary L. Donne, Timothy H.J. Goodship, Michael Venning and Bernard S. Kaplan. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Genetics in Medicine, Journal of Medical Genetics and European Journal of Medical 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.