S.A. Latt
Impact in
- Genetics top 1%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
Papers in
-
- DNA and Nucleic Acid Chemistry 20
- DNA Repair Mechanisms 12
- Genomics and Chromatin Dynamics 9
- Genetics 27
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Genomic variations and chromosomal abnormalities 9
- Animal Genetics and Reproduction 7
- Co-authors
- Gail Stetten (4 shared papers)Joan H.M. Knoll (4 shared papers)Louis M. Kunkel (8 shared papers)Rhona Schreck (9 shared papers)Bert L. Vallée (5 shared papers)H.F. Willard (3 shared papers)M. Lalande (8 shared papers)L. Juergens (4 shared papers)
- Journals
- Journal of Histochemistry & Cytochemistry (8 papers)Proceedings of the National Academy of Sciences (8 papers)Experimental Cell Research (8 papers)Human Genetics (5 papers)Molecular and Cellular Biology (4 papers)
- Partner nations
- United StatesHungaryFinland
In The Last Decade
S.A. Latt
68 papers receiving 4.5k citations
S.A. Latt's Hit Papers
Peers
Comparison fields: 5 of 164
- Genetics 1.4k
- Cancer Research 582
- Molecular Biology 2.8k
- Biophysics 183
- Pediatrics, Perinatology and Child Health 507
Countries citing papers authored by S.A. Latt
This map shows the geographic impact of S.A. Latt'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 S.A. Latt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S.A. Latt more than expected).
Fields of papers citing papers by S.A. Latt
This network shows the impact of papers produced by S.A. Latt. 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 S.A. Latt. The network helps show where S.A. Latt may publish in the future.
Co-authors
The 25 scholars most cited alongside S.A. Latt, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Automatic measurement of sister chromatid exchange frequency. Hit paper breakdown → | 1977 | 663 |
| 2 | Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion Hit paper breakdown → | 1989 | 431 |
| 3 | 1985 | 363 | |
| 4 | 1990 | 331 | |
| 5 | 1976 | 310 | |
| 6 | 1975 | 220 | |
| 7 | 1985 | 161 | |
| 8 | 1965 | 135 | |
| 9 | 1975 | 134 | |
| 10 | 1986 | 132 | |
| 11 | Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. | 1976 | 118 |
| 12 | 1983 | 104 | |
| 13 | 1986 | 96 | |
| 14 | Sister chromatid exchange analysis. | 1980 | 92 |
| 15 | 1983 | 84 | |
| 16 | 1971 | 81 | |
| 17 | 1987 | 80 | |
| 18 | 1982 | 78 | |
| 19 | 1985 | 72 | |
| 20 | 1977 | 71 |
About S.A. Latt
S.A. Latt is a scholar working on Molecular Biology, Genetics, Plant Science, Oncology and Cancer Research, having authored 70 papers that have together received 4.9k indexed citations. Recurring topics across this work include DNA and Nucleic Acid Chemistry (20 papers), Chromosomal and Genetic Variations (16 papers), DNA Repair Mechanisms (12 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Genomics and Chromatin Dynamics (9 papers), Animal Genetics and Reproduction (7 papers) and Carcinogens and Genotoxicity Assessment (7 papers). The work is most often cited by research in Genetics (1.4k citations), Cancer Research (582 citations), Molecular Biology (2.8k citations), Biophysics (183 citations) and Pediatrics, Perinatology and Child Health (507 citations). S.A. Latt has collaborated with scholars based in United States, Hungary and Finland. Frequent co-authors include Gail Stetten, Joan H.M. Knoll, Louis M. Kunkel, Rhona Schreck, Bert L. Vallée, H.F. Willard, M. Lalande, L. Juergens, Anthony P. Monaco and William Middlesworth. Their work appears in journals such as Journal of Histochemistry & Cytochemistry, Proceedings of the National Academy of Sciences, Experimental Cell Research, Human Genetics and Molecular and Cellular Biology.
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.