L.G. Shaffer
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
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- Congenital heart defects research 5
- RNA regulation and disease 1
- Chromatin Remodeling and Cancer 1
- Co-authors
- E H Zackai (1 shared paper)Aaron Theisen (1 shared paper)Roger A. Schultz (2 shared papers)Jill A. Rosenfeld (2 shared papers)J. Edward Spence (1 shared paper)Karen D. Tsuchiya (1 shared paper)Lorraine Potocki (1 shared paper)Jerome L. Gorski (1 shared paper)
- Journals
- Clinical Genetics (4 papers)Genetics in Medicine (1 paper)Molecular Syndromology (2 papers)The HKU Scholars Hub (University of Hong Kong) (1 paper)
- Partner nations
- United StatesPolandIsrael
In The Last Decade
L.G. Shaffer
8 papers receiving 276 citations
Peers
Comparison fields: 5 of 42
- Genetics 251
- Developmental Biology 6
- Pediatrics, Perinatology and Child Health 47
- Molecular Biology 155
- Genetics 21
Countries citing papers authored by L.G. Shaffer
This map shows the geographic impact of L.G. Shaffer'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 L.G. Shaffer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L.G. Shaffer more than expected).
Fields of papers citing papers by L.G. Shaffer
This network shows the impact of papers produced by L.G. Shaffer. 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 L.G. Shaffer. The network helps show where L.G. Shaffer may publish in the future.
Co-authors
The 25 scholars most cited alongside L.G. Shaffer, 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 | 2003 | 105 | |
| 2 | 2008 | 63 | |
| 3 | 1999 | 38 | |
| 4 | 2012 | 37 | |
| 5 | 2012 | 31 | |
| 6 | 2001 | 21 | |
| 7 | The first reported case of the DRAGON gene deletion in human. A case with a de-novo interstitial deletion of chromosome 5q15-21.1 | 2009 | 1 |
| 8 | 1999 | 1 |
About L.G. Shaffer
L.G. Shaffer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Epidemiology, having authored 8 papers that have together received 297 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA regulation and disease (1 paper), Tracheal and airway disorders (1 paper), Congenital Heart Disease Studies (1 paper) and Chromatin Remodeling and Cancer (1 paper). The work is most often cited by research in Genetics (251 citations), Developmental Biology (6 citations), Pediatrics, Perinatology and Child Health (47 citations), Molecular Biology (155 citations) and Genetics (21 citations). L.G. Shaffer has collaborated with scholars based in United States, Poland and Israel. Frequent co-authors include E H Zackai, Aaron Theisen, Roger A. Schultz, Jill A. Rosenfeld, J. Edward Spence, Karen D. Tsuchiya, Lorraine Potocki, Jerome L. Gorski, Sung Sup Park and Sarah Zimmerman. Their work appears in journals such as Clinical Genetics, Genetics in Medicine, Molecular Syndromology and The HKU Scholars Hub (University of Hong Kong).
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.