Birgit Funke
Impact in
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
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- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
Papers in
-
- Congenital heart defects research 21
- Genetics 31
- Genomics and Rare Diseases 22
- Genomic variations and chromosomal abnormalities 8
- Genetic Associations and Epidemiology 5
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Heidi L. Rehm (14 shared papers)Madhuri Hegde (7 shared papers)Pınar Bayrak‐Toydemir (4 shared papers)Elaine Lyon (3 shared papers)Anil K. Malhotra (7 shared papers)Sherri J. Bale (2 shared papers)Kerry K. Brown (1 shared paper)Joshua L. Deignan (1 shared paper)
- Journals
- Genetics in Medicine (11 papers)Journal of Molecular Diagnostics (8 papers)Genomics (3 papers)Human Molecular Genetics (3 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Birgit Funke
77 papers receiving 5.5k citations
Birgit Funke's Hit Papers
Peers
Comparison fields: 5 of 148
- Genetics 1.9k
- Cardiology and Cardiovascular Medicine 1.2k
- Cancer Research 625
- Molecular Biology 2.3k
- Sensory Systems 125
Countries citing papers authored by Birgit Funke
This map shows the geographic impact of Birgit Funke'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 Birgit Funke with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Birgit Funke more than expected).
Fields of papers citing papers by Birgit Funke
This network shows the impact of papers produced by Birgit Funke. 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 Birgit Funke. The network helps show where Birgit Funke may publish in the future.
Co-authors
The 25 scholars most cited alongside Birgit Funke, 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 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | ACMG clinical laboratory standards for next-generation sequencing Hit paper breakdown → | 2013 | 677 |
| 2 | Genetic Misdiagnoses and the Potential for Health Disparities Hit paper breakdown → | 2016 | 504 |
| 3 | Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples Hit paper breakdown → | 2016 | 481 |
| 4 | 2010 | 330 | |
| 5 | 2014 | 270 | |
| 6 | 2014 | 256 | |
| 7 | 2017 | 249 | |
| 8 | 2019 | 192 | |
| 9 | 2006 | 144 | |
| 10 | 2016 | 141 | |
| 11 | 2016 | 139 | |
| 12 | 2010 | 130 | |
| 13 | 2012 | 128 | |
| 14 | 2005 | 111 | |
| 15 | 2006 | 99 | |
| 16 | 2010 | 95 | |
| 17 | 2006 | 91 | |
| 18 | 2009 | 90 | |
| 19 | 2019 | 85 | |
| 20 | 1997 | 79 |
About Birgit Funke
Birgit Funke is a scholar working on Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine, Cancer Research and Surgery, having authored 80 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (22 papers), Congenital heart defects research (21 papers), Cardiomyopathy and Myosin Studies (17 papers), Genomic variations and chromosomal abnormalities (8 papers), Cancer Genomics and Diagnostics (7 papers), Genetic Associations and Epidemiology (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Cardiovascular Effects of Exercise (4 papers). The work is most often cited by research in Genetics (1.9k citations), Cardiology and Cardiovascular Medicine (1.2k citations), Cancer Research (625 citations), Molecular Biology (2.3k citations) and Sensory Systems (125 citations). Birgit Funke has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Heidi L. Rehm, Madhuri Hegde, Pınar Bayrak‐Toydemir, Elaine Lyon, Anil K. Malhotra, Sherri J. Bale, Kerry K. Brown, Joshua L. Deignan, Michael J. Friez and Jonathan S. Berg. Their work appears in journals such as Genetics in Medicine, Journal of Molecular Diagnostics, Genomics, Human Molecular Genetics and The American Journal of 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.