H.F. Willard
Impact in
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)Kinya Otsu (1 shared paper)Veena Khanna (1 shared paper)Don J. Mahuran (5 shared papers)R A Gravel (5 shared papers)Mark H. Skolnick (4 shared papers)
- Journals
- Cytogenetic and Genome Research (9 papers)Nucleic Acids Research (7 papers)Journal of Biological Chemistry (5 papers)Genomics (5 papers)Proceedings of the National Academy of Sciences (4 papers)
- Partner nations
- CanadaUnited StatesDenmark
In The Last Decade
H.F. Willard
49 papers receiving 3.3k citations
Hit Papers
Peers
Comparison fields: 5 of 112
- Genetics 895
- Neurology 465
- Molecular Biology 2.1k
- Physiology 112
- Cell Biology 256
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 | 520 |
| 2 | Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. Hit paper breakdown → | 1990 | 516 |
| 3 | 1985 | 284 | |
| 4 | 1989 | 197 | |
| 5 | 1987 | 170 | |
| 6 | 1986 | 153 | |
| 7 | 1986 | 115 | |
| 8 | 1998 | 105 | |
| 9 | 1986 | 103 | |
| 10 | 1985 | 92 | |
| 11 | 1986 | 90 | |
| 12 | 1988 | 80 | |
| 13 | 1991 | 70 | |
| 14 | 1986 | 70 | |
| 15 | 1987 | 67 | |
| 16 | 1989 | 65 | |
| 17 | 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 | 61 |
| 18 | 1991 | 59 | |
| 19 | 1992 | 56 | |
| 20 | 1987 | 54 |
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 3.3k 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), CRISPR and Genetic Engineering (5 papers), Lysosomal Storage Disorders Research (5 papers), Animal Genetics and Reproduction (5 papers) and Neurofibromatosis and Schwannoma Cases (4 papers). The work is most often cited by research in Genetics (895 citations), Neurology (465 citations), Molecular Biology (2.1k citations), Physiology (112 citations) and Cell Biology (256 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, Kinya Otsu, Veena Khanna, Don J. Mahuran, R A Gravel, Mark H. Skolnick, Carolyn J. Brown and Brian F. O’Dowd. Their work appears in journals such as Cytogenetic and Genome Research, Nucleic Acids Research, Journal of Biological Chemistry, Genomics and Proceedings of the National Academy of Sciences.
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.