Heather E. McDermid
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Molecular Biology top 5%
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 35
- Genetic Associations and Epidemiology 3
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- Genomics and Chromatin Dynamics 6
- Developmental Biology and Gene Regulation 5
- Chromatin Remodeling and Cancer 3
- Co-authors
- Katy Phelan (1 shared paper)Bernice E. Morrow (2 shared papers)Jonathan Flint (2 shared papers)Andrew O.M. Wilkie (1 shared paper)R M Winter (1 shared paper)Veronica J. Buckle (1 shared paper)Anthony John Holland (1 shared paper)Marcia L. Budarf (10 shared papers)
- Journals
- Genomics (10 papers)Human Molecular Genetics (4 papers)Journal of Medical Genetics (3 papers)Physiological Genomics (3 papers)Nature (2 papers)
- Partner nations
- CanadaUnited StatesJapan
In The Last Decade
Heather E. McDermid
64 papers receiving 4.2k citations
Heather E. McDermid's Hit Papers
Peers
Comparison fields: 5 of 109
- Genetics 2.4k
- Molecular Biology 1k
- Endocrinology, Diabetes and Metabolism 226
- Physiology 42
- Pediatrics, Perinatology and Child Health 135
Countries citing papers authored by Heather E. McDermid
This map shows the geographic impact of Heather E. McDermid'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 E. McDermid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heather E. McDermid more than expected).
Fields of papers citing papers by Heather E. McDermid
This network shows the impact of papers produced by Heather E. McDermid. 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 E. McDermid. The network helps show where Heather E. McDermid may publish in the future.
Co-authors
The 25 scholars most cited alongside Heather E. McDermid, 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 64 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The DNA sequence of human chromosome 22 Hit paper breakdown → | 1999 | 834 |
| 2 | 1995 | 419 | |
| 3 | 2011 | 382 | |
| 4 | 1987 | 370 | |
| 5 | 2001 | 236 | |
| 6 | 2002 | 214 | |
| 7 | 2005 | 201 | |
| 8 | 1986 | 127 | |
| 9 | 2005 | 127 | |
| 10 | Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardation. | 1997 | 115 |
| 11 | 1998 | 83 | |
| 12 | Molecular characterization of the marker chromosome associated with cat eye syndrome. | 1994 | 73 |
| 13 | 2008 | 65 | |
| 14 | 2005 | 58 | |
| 15 | 1986 | 57 | |
| 16 | 2000 | 55 | |
| 17 | 1992 | 54 | |
| 18 | 1997 | 53 | |
| 19 | 1999 | 51 | |
| 20 | Molecular studies of DiGeorge syndrome. | 1990 | 49 |
About Heather E. McDermid
Heather E. McDermid is a scholar working on Genetics, Molecular Biology, Immunology, Cellular and Molecular Neuroscience and Public Health, Environmental and Occupational Health, having authored 64 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (35 papers), Genomics and Chromatin Dynamics (6 papers), Developmental Biology and Gene Regulation (5 papers), Chromosomal and Genetic Variations (4 papers), Spinal Dysraphism and Malformations (4 papers), Genetic Associations and Epidemiology (3 papers), Chromatin Remodeling and Cancer (3 papers) and T-cell and B-cell Immunology (2 papers). The work is most often cited by research in Genetics (2.4k citations), Molecular Biology (1k citations), Endocrinology, Diabetes and Metabolism (226 citations), Physiology (42 citations) and Pediatrics, Perinatology and Child Health (135 citations). Heather E. McDermid has collaborated with scholars based in Canada, United States and Japan. Frequent co-authors include Katy Phelan, Bernice E. Morrow, Jonathan Flint, Andrew O.M. Wilkie, R M Winter, Veronica J. Buckle, Anthony John Holland, Marcia L. Budarf, Alessandra M.V. Duncan and Bradley N. White. Their work appears in journals such as Genomics, Human Molecular Genetics, Journal of Medical Genetics, Physiological Genomics and Nature.
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.