Lisa Edelmann
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Molecular Biology top 5%
- Congenital heart defects research
Papers in
- Genetics 41
- Genomic variations and chromosomal abnormalities 23
- Genomics and Rare Diseases 12
- Genetics and Neurodevelopmental Disorders 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Congenital heart defects research 13
- Co-authors
- Robert J. Desnick (21 shared papers)Ruth Kornreich (28 shared papers)Bernice E. Morrow (6 shared papers)Stuart A. Scott (19 shared papers)Raj K. Pandita (5 shared papers)Winfried Edelmann (3 shared papers)Kurt Hirschhorn (2 shared papers)Tracy Brandt (8 shared papers)
- Journals
- The American Journal of Human Genetics (7 papers)Genetics in Medicine (5 papers)Journal of Molecular Diagnostics (4 papers)Clinical Genetics (4 papers)Human Mutation (3 papers)
- Partner nations
- United StatesFranceNetherlands
In The Last Decade
Lisa Edelmann
78 papers receiving 3.2k citations
Peers
Comparison fields: 5 of 111
- Genetics 1.3k
- Molecular Biology 1.7k
- Pharmacology 199
- Cancer Research 207
- Pediatrics, Perinatology and Child Health 249
Countries citing papers authored by Lisa Edelmann
This map shows the geographic impact of Lisa Edelmann'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 Lisa Edelmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lisa Edelmann more than expected).
Fields of papers citing papers by Lisa Edelmann
This network shows the impact of papers produced by Lisa Edelmann. 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 Lisa Edelmann. The network helps show where Lisa Edelmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Lisa Edelmann, 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 79 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 311 | |
| 2 | 1999 | 239 | |
| 3 | 2007 | 228 | |
| 4 | 2001 | 146 | |
| 5 | 2005 | 122 | |
| 6 | 2014 | 118 | |
| 7 | 2010 | 116 | |
| 8 | 2018 | 111 | |
| 9 | 2008 | 99 | |
| 10 | 2018 | 98 | |
| 11 | 2010 | 89 | |
| 12 | 2008 | 79 | |
| 13 | 1992 | 77 | |
| 14 | 2013 | 74 | |
| 15 | 2010 | 69 | |
| 16 | 2008 | 66 | |
| 17 | 2004 | 64 | |
| 18 | 2010 | 62 | |
| 19 | 2014 | 59 | |
| 20 | 2009 | 58 |
About Lisa Edelmann
Lisa Edelmann is a scholar working on Genetics, Molecular Biology, Plant Science, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health, having authored 79 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Congenital heart defects research (13 papers), Genomics and Rare Diseases (12 papers), Chromosomal and Genetic Variations (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Pharmacogenetics and Drug Metabolism (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Prenatal Screening and Diagnostics (5 papers). The work is most often cited by research in Genetics (1.3k citations), Molecular Biology (1.7k citations), Pharmacology (199 citations), Cancer Research (207 citations) and Pediatrics, Perinatology and Child Health (249 citations). Lisa Edelmann has collaborated with scholars based in United States, France and Netherlands. Frequent co-authors include Robert J. Desnick, Ruth Kornreich, Bernice E. Morrow, Stuart A. Scott, Raj K. Pandita, Winfried Edelmann, Kurt Hirschhorn, Tracy Brandt, Ninette Cohen and Alan Shanske. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Journal of Molecular Diagnostics, Clinical Genetics and Human Mutation.
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.