H.F. Willard
Impact in
- Genetics top 1%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetics and Neurodevelopmental Disorders 3
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- Genomics and Chromatin Dynamics 6
- DNA and Nucleic Acid Chemistry 4
- RNA and protein synthesis mechanisms 4
- Co-authors
- Christine Clemson (1 shared paper)John A. McNeil (1 shared paper)Jeanne Bentley Lawrence (1 shared paper)Rachel Wevrick (1 shared paper)John S. Waye (2 shared papers)S.A. Latt (3 shared papers)David H. Ledbetter (4 shared papers)Ira Mellman (3 shared papers)
- Journals
- Human Molecular Genetics (3 papers)Proceedings of the National Academy of Sciences (3 papers)Molecular and Cellular Biology (2 papers)Cytogenetic and Genome Research (2 papers)Blood (2 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
H.F. Willard
38 papers receiving 3.1k citations
H.F. Willard's Hit Papers
Peers
Comparison fields: 5 of 101
- Genetics 1.6k
- Molecular Biology 2.1k
- Clinical Biochemistry 147
- Plant Science 829
- Pediatrics, Perinatology and Child Health 383
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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure. Hit paper breakdown → | 1996 | 648 |
| 2 | Uniparental disomy as a mechanism for human genetic disease. | 1988 | 400 |
| 3 | Chromosome-specific organization of human alpha satellite DNA. | 1985 | 225 |
| 4 | 1989 | 184 | |
| 5 | Heritability of X chromosome--inactivation phenotype in a large family. | 1996 | 152 |
| 6 | Five polymorphic microsatellite VNTRs on the human X chromosome. | 1990 | 150 |
| 7 | 1975 | 142 | |
| 8 | 1986 | 137 | |
| 9 | Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. | 1976 | 119 |
| 10 | 1991 | 107 | |
| 11 | Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. | 1978 | 99 |
| 12 | 1979 | 74 | |
| 13 | Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation. | 1996 | 70 |
| 14 | 1995 | 70 | |
| 15 | 1987 | 69 | |
| 16 | 1994 | 69 | |
| 17 | 1993 | 69 | |
| 18 | 1977 | 68 | |
| 19 | Chromosome-specific alpha satellite DNA from the centromere of human chromosome 16. | 1989 | 67 |
| 20 | Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations. | 1994 | 63 |
About H.F. Willard
H.F. Willard is a scholar working on Genetics, Molecular Biology, Plant Science, Immunology and Rheumatology, having authored 43 papers that have together received 3.2k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (12 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genomics and Chromatin Dynamics (6 papers), DNA and Nucleic Acid Chemistry (4 papers), RNA and protein synthesis mechanisms (4 papers), Prenatal Screening and Diagnostics (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (1.6k citations), Molecular Biology (2.1k citations), Clinical Biochemistry (147 citations), Plant Science (829 citations) and Pediatrics, Perinatology and Child Health (383 citations). H.F. Willard has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Christine Clemson, John A. McNeil, Jeanne Bentley Lawrence, Rachel Wevrick, John S. Waye, S.A. Latt, David H. Ledbetter, Ira Mellman, Gillian M. Greig and J. Edward Spence. Their work appears in journals such as Human Molecular Genetics, Proceedings of the National Academy of Sciences, Molecular and Cellular Biology, Cytogenetic and Genome Research and Blood.
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.