Alan F. Scott
Impact in
- Genetics top 0.5%
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Genomics and Rare Diseases
- Molecular Biology top 1%
- RNA and protein synthesis mechanisms
- CRISPR and Genetic Engineering
- Bioinformatics and Genomic Networks
- RNA modifications and cancer
Papers in
-
- dental development and anomalies 8
- RNA modifications and cancer 7
- Genetics 42
- Cleft Lip and Palate Research 22
- Craniofacial Disorders and Treatments 17
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 9
- Hemoglobinopathies and Related Disorders 7
- Co-authors
- Joanna Amberger (5 shared papers)Carol Bocchini (4 shared papers)Ada Hamosh (4 shared papers)Haig H. Kazazian (6 shared papers)François Schiettecatte (1 shared paper)Stephen L. Mathias (6 shared papers)Stylianos E. Antonarakis (3 shared papers)Jef D. Boeke (3 shared papers)
- Journals
- Genetic Epidemiology (5 papers)Nucleic Acids Research (4 papers)Proceedings of the National Academy of Sciences (4 papers)Genomics (3 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)
- Partner nations
- United StatesTaiwanSingapore
In The Last Decade
Alan F. Scott
74 papers receiving 7.2k citations
Alan F. Scott's Hit Papers
Peers
Comparison fields: 5 of 152
- Genetics 2.5k
- Molecular Biology 5.0k
- Plant Science 1.8k
- Genetics 481
- Pharmacology 328
Countries citing papers authored by Alan F. Scott
This map shows the geographic impact of Alan F. Scott'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 Alan F. Scott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alan F. Scott more than expected).
Fields of papers citing papers by Alan F. Scott
This network shows the impact of papers produced by Alan F. Scott. 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 Alan F. Scott. The network helps show where Alan F. Scott may publish in the future.
Co-authors
The 25 scholars most cited alongside Alan F. Scott, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders Hit paper breakdown → | 2014 | 1646 |
| 2 | Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man Hit paper breakdown → | 1988 | 690 |
| 3 | Reverse Transcriptase Encoded by a Human Transposable Element Hit paper breakdown → | 1991 | 626 |
| 4 | OMIM.org: leveraging knowledge across phenotype–gene relationships Hit paper breakdown → | 2018 | 583 |
| 5 | McKusick's Online Mendelian Inheritance in Man (OMIM(R)) Hit paper breakdown → | 2008 | 519 |
| 6 | 1991 | 366 | |
| 7 | 1994 | 362 | |
| 8 | 1987 | 273 | |
| 9 | 1984 | 172 | |
| 10 | FGFR2 exon IIIa and IIIc mutations in Crouzon, Jackson-Weiss, and Pfeiffer syndromes: evidence for missense changes, insertions, and a deletion due to alternative RNA splicing. | 1996 | 143 |
| 11 | 2013 | 112 | |
| 12 | 2016 | 110 | |
| 13 | 2006 | 106 | |
| 14 | 1993 | 98 | |
| 15 | 2021 | 93 | |
| 16 | 1979 | 93 | |
| 17 | 1981 | 92 | |
| 18 | 2007 | 90 | |
| 19 | 1994 | 80 | |
| 20 | 1985 | 68 |
About Alan F. Scott
Alan F. Scott is a scholar working on Molecular Biology, Genetics, Genetics, Rheumatology and Plant Science, having authored 74 papers that have together received 7.5k indexed citations. Recurring topics across this work include Cleft Lip and Palate Research (22 papers), Craniofacial Disorders and Treatments (17 papers), Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (9 papers), dental development and anomalies (8 papers), RNA modifications and cancer (7 papers), Hemoglobinopathies and Related Disorders (7 papers) and Chromosomal and Genetic Variations (7 papers). The work is most often cited by research in Genetics (2.5k citations), Molecular Biology (5.0k citations), Plant Science (1.8k citations), Genetics (481 citations) and Pharmacology (328 citations). Alan F. Scott has collaborated with scholars based in United States, Taiwan and Singapore. Frequent co-authors include Joanna Amberger, Carol Bocchini, Ada Hamosh, Haig H. Kazazian, François Schiettecatte, Stephen L. Mathias, Stylianos E. Antonarakis, Jef D. Boeke, Abram Gabriel and Corinne Wong. Their work appears in journals such as Genetic Epidemiology, Nucleic Acids Research, Proceedings of the National Academy of Sciences, Genomics and Birth Defects Research Part A Clinical and Molecular Teratology.
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.