F. J. Dill
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 2
- Co-authors
- DK Kalousek (1 shared paper)Dagmar K. Kalousek (4 shared papers)Barbara McGillivray (2 shared papers)Betty J. Poland (5 shared papers)R. Douglas Wilson (1 shared paper)Siu Li Yong (1 shared paper)Tapio Pantzar (1 shared paper)Diana S. Herbst (2 shared papers)
- Journals
- Human Genetics (4 papers)The Journal of Pediatrics (1 paper)Nature (1 paper)Journal of Medical Genetics (1 paper)Cytogenetic and Genome Research (1 paper)
- Partner nations
- CanadaUnited StatesTunisia
In The Last Decade
F. J. Dill
24 papers receiving 807 citations
Peers
Comparison fields: 5 of 72
- Pediatrics, Perinatology and Child Health 486
- Genetics 579
- Developmental Biology 30
- Obstetrics and Gynecology 48
- Public Health, Environmental and Occupational Health 132
Countries citing papers authored by F. J. Dill
This map shows the geographic impact of F. J. Dill'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 F. J. Dill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F. J. Dill more than expected).
Fields of papers citing papers by F. J. Dill
This network shows the impact of papers produced by F. J. Dill. 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 F. J. Dill. The network helps show where F. J. Dill may publish in the future.
Co-authors
The 25 scholars most cited alongside F. J. Dill, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1983 | 277 | |
| 2 | 1987 | 115 | |
| 3 | 1981 | 48 | |
| 4 | 1980 | 47 | |
| 5 | 2001 | 40 | |
| 6 | 1987 | 39 | |
| 7 | 1979 | 39 | |
| 8 | 1987 | 38 | |
| 9 | 1976 | 36 | |
| 10 | 1964 | 28 | |
| 11 | 1976 | 28 | |
| 12 | 1987 | 27 | |
| 13 | Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos. | 1981 | 22 |
| 14 | 1986 | 21 | |
| 15 | 1980 | 18 | |
| 16 | 1993 | 15 | |
| 17 | 1992 | 13 | |
| 18 | 2008 | 11 | |
| 19 | 1970 | 11 | |
| 20 | 1992 | 10 |
About F. J. Dill
F. J. Dill is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Plant Science, having authored 24 papers that have together received 897 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Chromosomal and Genetic Variations (4 papers), Assisted Reproductive Technology and Twin Pregnancy (3 papers), Genetic Syndromes and Imprinting (2 papers) and Gestational Trophoblastic Disease Studies (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (486 citations), Genetics (579 citations), Developmental Biology (30 citations), Obstetrics and Gynecology (48 citations) and Public Health, Environmental and Occupational Health (132 citations). F. J. Dill has collaborated with scholars based in Canada, United States and Tunisia. Frequent co-authors include DK Kalousek, Dagmar K. Kalousek, Barbara McGillivray, Betty J. Poland, R. Douglas Wilson, Siu Li Yong, Tapio Pantzar, Diana S. Herbst, Stephen Wood and Renée H. Martin. Their work appears in journals such as Human Genetics, The Journal of Pediatrics, Nature, Journal of Medical Genetics and Cytogenetic and Genome Research.
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.