S. L. Sherman
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 5%
- Cognitive Neuroscience top 10%
- Public Health, Environmental and Occupational Health top 10%
- Co-authors
- Terry HassoldSallie B. FreemanDorothy PettayNeil E. LambMichelle MerrillP. A. JacobsDavid C. PageAllison E. Ashley‐Koch
- Topics
- Genetics and Neurodevelopmental Disorders (8 papers)Genomic variations and chromosomal abnormalities (8 papers)Prenatal Screening and Diagnostics (4 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
S. L. Sherman
18 papers receiving 996 citations
Peers
Comparison fields: 5 of 70
- Genetics 642
- Molecular Biology 424
- Pediatrics, Perinatology and Child Health 392
- Cognitive Neuroscience 199
- Public Health, Environmental and Occupational Health 156
Countries citing papers authored by S. L. Sherman
This map shows the geographic impact of S. L. Sherman'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. L. Sherman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. L. Sherman more than expected).
Fields of papers citing papers by S. L. Sherman
This network shows the impact of papers produced by S. L. Sherman. 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. L. Sherman. The network helps show where S. L. Sherman may publish in the future.
Co-authorship network of co-authors of S. L. Sherman
This figure shows the co-authorship network connecting the top 25 collaborators of S. L. Sherman. A scholar is included among the top collaborators of S. L. Sherman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with S. L. Sherman. S. L. Sherman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 71 | |
| 2 | 70 | |
| 3 | 121 | |
| 4 | 1 | |
| 5 | FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 2 |
| 6 | 59 | |
| 7 | 2 | |
| 8 | 14 | |
| 9 | 7 | |
| 10 | Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study. | 145 |
| 11 | Familial transmission of the FMR1 CGG repeat. | 146 |
| 12 | Statistical models for trisomic phenotypes. | 4 |
| 13 | Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. | 177 |
| 14 | Population dynamics of a meiotic/mitotic expansion model for the fragile X syndrome. | 29 |
| 15 | XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. | 148 |
| 16 | 6 | |
| 17 | 1 | |
| 18 | 21 |
About S. L. Sherman
S. L. Sherman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 18 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (642 citations), Pediatrics, Perinatology and Child Health (392 citations) and Cognitive Neuroscience (199 citations). S. L. Sherman has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Terry Hassold, Sallie B. Freeman, Dorothy Pettay, Neil E. Lamb, Michelle Merrill, P. A. Jacobs, David C. Page, Allison E. Ashley‐Koch, Paula W. Yoon and W. Dana Flanders. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics and Epidemiologic Reviews.
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.