H.F. Willard
Impact in
- Neurology top 2%
- Neurofibromatosis and Schwannoma Cases
- Molecular Biology top 5%
- Ion channel regulation and function
- Genomics and Chromatin Dynamics
Papers in
-
- Genomics and Chromatin Dynamics 7
- RNA and protein synthesis mechanisms 6
- CRISPR and Genetic Engineering 5
- Genetics 18
- Genomic variations and chromosomal abnormalities 9
- Animal Genetics and Reproduction 5
- Co-authors
- John S. Waye (4 shared papers)David H. MacLennan (2 shared papers)Francesco Zorzato (2 shared papers)Veena Khanna (1 shared paper)Kinya Otsu (1 shared paper)R A Gravel (5 shared papers)Don J. Mahuran (5 shared papers)Carolyn J. Brown (3 shared papers)
- Journals
- Nucleic Acids Research (7 papers)Genomics (5 papers)Journal of Biological Chemistry (5 papers)Proceedings of the National Academy of Sciences (4 papers)Human Genetics (3 papers)
- Partner nations
- CanadaUnited StatesDenmark
In The Last Decade
H.F. Willard
41 papers receiving 3.0k citations
H.F. Willard's Hit Papers
Peers
Comparison fields: 5 of 103
- Neurology 480
- Molecular Biology 1.9k
- Genetics 767
- Physiology 120
- Cardiology and Cardiovascular Medicine 349
Countries citing papers authored by H.F. Willard
This map shows the geographic impact of H.F. Willard'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 H.F. Willard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H.F. Willard more than expected).
Fields of papers citing papers by H.F. Willard
This network shows the impact of papers produced by H.F. Willard. 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 H.F. Willard. The network helps show where H.F. Willard may publish in the future.
Co-authors
The 25 scholars most cited alongside H.F. Willard, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Hit paper breakdown → | 1987 | 560 |
| 2 | Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. Hit paper breakdown → | 1990 | 545 |
| 3 | 1985 | 306 | |
| 4 | 1987 | 173 | |
| 5 | 1986 | 159 | |
| 6 | 1986 | 117 | |
| 7 | 1986 | 111 | |
| 8 | 1998 | 110 | |
| 9 | 1985 | 103 | |
| 10 | 1986 | 92 | |
| 11 | 1988 | 80 | |
| 12 | 1986 | 78 | |
| 13 | 1987 | 69 | |
| 14 | 1989 | 66 | |
| 15 | 1991 | 66 | |
| 16 | The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy. | 1990 | 64 |
| 17 | 1992 | 57 | |
| 18 | 1987 | 53 | |
| 19 | Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect. | 1989 | 53 |
| 20 | Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation. | 1990 | 47 |
About H.F. Willard
H.F. Willard is a scholar working on Molecular Biology, Genetics, Plant Science, Physiology and Neurology, having authored 49 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (8 papers), Genomics and Chromatin Dynamics (7 papers), RNA and protein synthesis mechanisms (6 papers), Lysosomal Storage Disorders Research (5 papers), Animal Genetics and Reproduction (5 papers), CRISPR and Genetic Engineering (5 papers) and Neurofibromatosis and Schwannoma Cases (4 papers). The work is most often cited by research in Neurology (480 citations), Molecular Biology (1.9k citations), Genetics (767 citations), Physiology (120 citations) and Cardiology and Cardiovascular Medicine (349 citations). H.F. Willard has collaborated with scholars based in Canada, United States and Denmark. Frequent co-authors include John S. Waye, David H. MacLennan, Francesco Zorzato, Veena Khanna, Kinya Otsu, R A Gravel, Don J. Mahuran, Carolyn J. Brown, Mark H. Skolnick and Brian F. O’Dowd. Their work appears in journals such as Nucleic Acids Research, Genomics, Journal of Biological Chemistry, Proceedings of the National Academy of Sciences and 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.