Beth A. Pletcher
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Co-authors
- Deborah A. Driscoll (3 shared papers)Stephanie L. Sherman (1 shared paper)Susan J. Gross (5 shared papers)Kristin G. Monaghan (4 shared papers)Mary Ellen Rimsza (2 shared papers)Scott A. Shipman (2 shared papers)Wayne A. Fenton (1 shared paper)Michael Shevell (1 shared paper)
- Journals
- Genetics in Medicine (9 papers)PEDIATRICS (4 papers)European Journal of Pediatrics (1 paper)Prenatal Diagnosis (1 paper)Human Genetics (1 paper)
- Partner nations
- United StatesGermanyHungary
In The Last Decade
Beth A. Pletcher
48 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 93
- Genetics 506
- Clinical Biochemistry 105
- Rheumatology 153
- Pediatrics, Perinatology and Child Health 183
- Gender Studies 60
Countries citing papers authored by Beth A. Pletcher
This map shows the geographic impact of Beth A. Pletcher'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 Beth A. Pletcher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beth A. Pletcher more than expected).
Fields of papers citing papers by Beth A. Pletcher
This network shows the impact of papers produced by Beth A. Pletcher. 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 Beth A. Pletcher. The network helps show where Beth A. Pletcher may publish in the future.
Co-authors
The 25 scholars most cited alongside Beth A. Pletcher, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 203 | |
| 2 | 1997 | 162 | |
| 3 | 2008 | 153 | |
| 4 | 2010 | 115 | |
| 5 | 2013 | 66 | |
| 6 | 2007 | 43 | |
| 7 | 2013 | 42 | |
| 8 | 1996 | 42 | |
| 9 | 2019 | 39 | |
| 10 | 1995 | 33 | |
| 11 | 2004 | 33 | |
| 12 | 1998 | 30 | |
| 13 | Congenital bifid sternum: repair in early infancy and literature review. | 1991 | 30 |
| 14 | Intrauterine cytomegalovirus infection presenting as fetal meconium peritonitis. | 1991 | 28 |
| 15 | 1994 | 24 | |
| 16 | 2005 | 21 | |
| 17 | 1991 | 19 | |
| 18 | 2008 | 18 | |
| 19 | Health supervision for children with Turner syndrome | 1995 | 18 |
| 20 | 2008 | 17 |
About Beth A. Pletcher
Beth A. Pletcher is a scholar working on Genetics, Surgery, Pulmonary and Respiratory Medicine, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 51 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (4 papers), Metabolism and Genetic Disorders (4 papers), Connective tissue disorders research (4 papers), Child and Adolescent Health (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Lysosomal Storage Disorders Research (3 papers). The work is most often cited by research in Genetics (506 citations), Clinical Biochemistry (105 citations), Rheumatology (153 citations), Pediatrics, Perinatology and Child Health (183 citations) and Gender Studies (60 citations). Beth A. Pletcher has collaborated with scholars based in United States, Germany and Hungary. Frequent co-authors include Deborah A. Driscoll, Stephanie L. Sherman, Susan J. Gross, Kristin G. Monaghan, Mary Ellen Rimsza, Scott A. Shipman, Wayne A. Fenton, Michael Shevell, Anne Aspler and Margretta R. Seashore. Their work appears in journals such as Genetics in Medicine, PEDIATRICS, European Journal of Pediatrics, Prenatal Diagnosis and Human Genetics.
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.