Beth A. Torchia
Impact in
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- Prenatal Screening and Diagnostics
- Pediatric Urology and Nephrology Studies
- Fetal and Pediatric Neurological Disorders
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 10
- Genetic Syndromes and Imprinting 2
- Genomics and Rare Diseases 1
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- Prenatal Screening and Diagnostics 3
- Co-authors
- Lisa G. Shaffer (8 shared papers)Blake C. Ballif (6 shared papers)Bassem A. Bejjani (6 shared papers)Aaron Theisen (4 shared papers)Jill A. Rosenfeld (3 shared papers)Arthur S. Aylsworth (2 shared papers)Justine Coppinger (3 shared papers)Sarah Alliman (2 shared papers)
- Journals
- Molecular Cytogenetics (2 papers)Obstetrical & Gynecological Survey (1 paper)Fetal Diagnosis and Therapy (1 paper)Prenatal Diagnosis (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesCanada
In The Last Decade
Beth A. Torchia
11 papers receiving 329 citations
Peers
Comparison fields: 5 of 30
- Pediatrics, Perinatology and Child Health 155
- Genetics 235
- Urology 17
- Molecular Biology 118
- Genetics 16
Countries citing papers authored by Beth A. Torchia
This map shows the geographic impact of Beth A. Torchia'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. Torchia 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. Torchia more than expected).
Fields of papers citing papers by Beth A. Torchia
This network shows the impact of papers produced by Beth A. Torchia. 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. Torchia. The network helps show where Beth A. Torchia may publish in the future.
Co-authors
The 25 scholars most cited alongside Beth A. Torchia, 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 | 2008 | 102 | |
| 2 | 2009 | 94 | |
| 3 | 2009 | 41 | |
| 4 | 2010 | 40 | |
| 5 | 2009 | 40 | |
| 6 | 2008 | 28 | |
| 7 | 2011 | 15 | |
| 8 | 2009 | 5 | |
| 9 | 2008 | 2 | |
| 10 | 2008 | 2 | |
| 11 | 2012 | 1 |
About Beth A. Torchia
Beth A. Torchia is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 11 papers that have together received 370 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (3 papers), Genetic Syndromes and Imprinting (2 papers), Chromosomal and Genetic Variations (2 papers), Congenital heart defects research (2 papers), Genomics and Chromatin Dynamics (1 paper), Genomics and Rare Diseases (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (155 citations), Genetics (235 citations), Urology (17 citations), Molecular Biology (118 citations) and Genetics (16 citations). Beth A. Torchia has collaborated with scholars based in United States and Canada. Frequent co-authors include Lisa G. Shaffer, Blake C. Ballif, Bassem A. Bejjani, Aaron Theisen, Jill A. Rosenfeld, Arthur S. Aylsworth, Justine Coppinger, Sarah Alliman, Ann Lucas and Cynthia M. Powell. Their work appears in journals such as Molecular Cytogenetics, Obstetrical & Gynecological Survey, Fetal Diagnosis and Therapy, Prenatal Diagnosis and PLoS ONE.
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.