Sharon L. Wenger
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 30
- Genetics and Neurodevelopmental Disorders 15
- Genetic Syndromes and Imprinting 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Prenatal Screening and Diagnostics 12
- Developmental Biology top 10%
- Molecular Biology top 10%
- DNA Repair Mechanisms 10
- Cognitive Neuroscience top 10%
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- Chromosomal and Genetic Variations 11
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- Acute Myeloid Leukemia Research 5
- Co-authors
- Mark W. SteeleStephen G. GrantMarybeth HummelJames H. CumminsJennifer A. ScottAravinda ChakravartiLinda M. SargentWendy L. Golden
- Journals
- Proceedings of the National Academy of Sciences (1 paper)The Lancet (1 paper)SHILAP Revista de lepidopterología (1 paper)
- Partner nations
- United StatesAustriaIndia
In The Last Decade
Sharon L. Wenger
83 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 108
- Genetics 985
- Pediatrics, Perinatology and Child Health 231
- Developmental Biology 25
- Molecular Biology 790
- Cognitive Neuroscience 155
Countries citing papers authored by Sharon L. Wenger
This map shows the geographic impact of Sharon L. Wenger'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 Sharon L. Wenger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sharon L. Wenger more than expected).
Fields of papers citing papers by Sharon L. Wenger
This network shows the impact of papers produced by Sharon L. Wenger. 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 Sharon L. Wenger. The network helps show where Sharon L. Wenger may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Sharon L. Wenger, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 5 | |
| 2 | 2006 | 22 | |
| 3 | Unusual Pattern of Bone Marrow Somatic Mutation in Pediatric Patients Referred for Cytogenetic Analysis | 2005 | 1 |
| 4 | 2005 | 7 | |
| 5 | 2005 | 85 | |
| 6 | 2004 | 7 | |
| 7 | 2001 | 43 | |
| 8 | 1999 | 29 | |
| 9 | 1997 | 17 | |
| 10 | 1997 | 7 | |
| 11 | 1997 | 1 | |
| 12 | 1996 | 25 | |
| 13 | 1995 | 7 | |
| 14 | 1995 | 25 | |
| 15 | 1995 | 15 | |
| 16 | 1995 | 11 | |
| 17 | 1992 | 15 | |
| 18 | 1992 | 41 | |
| 19 | 1988 | 23 | |
| 20 | 1988 | 5 |
About Sharon L. Wenger
Sharon L. Wenger is a scholar working on Genetics, Developmental Biology and Hematology, having authored 83 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Genetics and Neurodevelopmental Disorders (15 papers), Prenatal Screening and Diagnostics (12 papers), Chromosomal and Genetic Variations (11 papers), DNA Repair Mechanisms (10 papers), Genetic Syndromes and Imprinting (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Acute Myeloid Leukemia Research (5 papers). The work is most often cited by research in Genetics (985 citations), Pediatrics, Perinatology and Child Health (231 citations) and Developmental Biology (25 citations). Sharon L. Wenger has collaborated with scholars based in United States, Austria and India. Frequent co-authors include Mark W. Steele, Stephen G. Grant, Marybeth Hummel, James H. Cummins, Jennifer A. Scott, Aravinda Chakravarti, Linda M. Sargent, Wendy L. Golden, Narendra K. Bairwa and R. Bamezai. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and SHILAP Revista de lepidopterología.
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.