Heather Howley
Impact in
- Internal Medicine top 5%
- Venous Thromboembolism Diagnosis and Management
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 5
- Genetics 5
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 3
- BRCA gene mutations in cancer 2
- Co-authors
- Philip S. Wells (3 shared papers)Brenda J. Wilson (4 shared papers)Marc Rodger (5 shared papers)Jodi Heshka (1 shared paper)Mark Walker (8 shared papers)Doug Coyle (3 shared papers)Kym M. Boycott (4 shared papers)Taila Hartley (3 shared papers)
- Journals
- American Journal of Obstetrics and Gynecology (3 papers)Thrombosis Research (2 papers)Genetics in Medicine (2 papers)Annual Review of Genomics and Human Genetics (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Heather Howley
21 papers receiving 756 citations
Peers
Comparison fields: 5 of 86
- Internal Medicine 106
- Genetics 294
- Hematology 100
- Pediatrics, Perinatology and Child Health 145
- Obstetrics and Gynecology 55
Countries citing papers authored by Heather Howley
This map shows the geographic impact of Heather Howley'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 Heather Howley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heather Howley more than expected).
Fields of papers citing papers by Heather Howley
This network shows the impact of papers produced by Heather Howley. 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 Heather Howley. The network helps show where Heather Howley may publish in the future.
Co-authors
The 25 scholars most cited alongside Heather Howley, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 256 | |
| 2 | 2005 | 89 | |
| 3 | 2008 | 61 | |
| 4 | 2020 | 61 | |
| 5 | 2004 | 56 | |
| 6 | 2008 | 49 | |
| 7 | 2007 | 36 | |
| 8 | 2006 | 36 | |
| 9 | 2013 | 35 | |
| 10 | 2003 | 25 | |
| 11 | 2023 | 20 | |
| 12 | 2018 | 16 | |
| 13 | 2022 | 16 | |
| 14 | 2021 | 10 | |
| 15 | 2002 | 5 | |
| 16 | 2023 | 4 | |
| 17 | 2025 | 3 | |
| 18 | 2018 | 3 | |
| 19 | 2023 | 2 | |
| 20 | 2006 | 2 |
About Heather Howley
Heather Howley is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Internal Medicine, Hematology and Emergency Medical Services, having authored 22 papers that have together received 786 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Venous Thromboembolism Diagnosis and Management (4 papers), Genomics and Rare Diseases (3 papers), Blood Coagulation and Thrombosis Mechanisms (3 papers), Genomic variations and chromosomal abnormalities (3 papers), BRCA gene mutations in cancer (2 papers), Autism Spectrum Disorder Research (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Internal Medicine (106 citations), Genetics (294 citations), Hematology (100 citations), Pediatrics, Perinatology and Child Health (145 citations) and Obstetrics and Gynecology (55 citations). Heather Howley has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Philip S. Wells, Brenda J. Wilson, Marc Rodger, Jodi Heshka, Mark Walker, Doug Coyle, Kym M. Boycott, Taila Hartley, Mario Cappelli and Beth K. Potter. Their work appears in journals such as American Journal of Obstetrics and Gynecology, Thrombosis Research, Genetics in Medicine, Annual Review of Genomics and Human Genetics and The American Journal of Human 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.