Birgit Funke
Impact in
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- Cardiomyopathy and Myosin Studies
- Cardiovascular Effects of Exercise
- Viral Infections and Immunology Research
- Genetics top 0.5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
Papers in
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- Cardiomyopathy and Myosin Studies 34
- Cardiovascular Effects of Exercise 8
- Genetics 46
- Genomics and Rare Diseases 33
- Genomic variations and chromosomal abnormalities 11
- Genetic Associations and Epidemiology 7
- Co-authors
- Heidi L. Rehm (18 shared papers)Madhuri Hegde (7 shared papers)Neal K. Lakdawala (7 shared papers)Pınar Bayrak‐Toydemir (4 shared papers)Anil K. Malhotra (8 shared papers)Matthew S. Lebo (11 shared papers)Raju Kucherlapati (10 shared papers)Stuart A. Cook (6 shared papers)
- Journals
- Genetics in Medicine (18 papers)Journal of Molecular Diagnostics (10 papers)The American Journal of Human Genetics (8 papers)Human Mutation (5 papers)European Heart Journal (3 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Birgit Funke
112 papers receiving 10.2k citations
Birgit Funke's Hit Papers
Peers
Comparison fields: 5 of 163
- Cardiology and Cardiovascular Medicine 3.0k
- Genetics 3.2k
- Cancer Research 1.1k
- Molecular Biology 4.3k
- Developmental Neuroscience 156
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 116 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome Hit paper breakdown → | 2001 | 806 |
| 2 | ACMG clinical laboratory standards for next-generation sequencing Hit paper breakdown → | 2013 | 744 |
| 3 | Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples Hit paper breakdown → | 2016 | 594 |
| 4 | Genetic Misdiagnoses and the Potential for Health Disparities Hit paper breakdown → | 2016 | 590 |
| 5 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 6 | 2012 | 381 | |
| 7 | Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity Hit paper breakdown → | 2015 | 370 |
| 8 | 2010 | 351 | |
| 9 | 2017 | 333 | |
| 10 | Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes Hit paper breakdown → | 2019 | 330 |
| 11 | 2014 | 299 | |
| 12 | 2014 | 285 | |
| 13 | 2018 | 283 | |
| 14 | 2019 | 248 | |
| 15 | 2020 | 200 | |
| 16 | 2016 | 168 | |
| 17 | 2016 | 160 | |
| 18 | 2012 | 159 | |
| 19 | 2018 | 154 | |
| 20 | 2006 | 148 |
About Birgit Funke
Birgit Funke is a scholar working on Cardiology and Cardiovascular Medicine, Genetics, Molecular Biology, Cancer Research and Industrial and Manufacturing Engineering, having authored 116 papers that have together received 10.5k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (34 papers), Genomics and Rare Diseases (33 papers), Congenital heart defects research (28 papers), Cancer Genomics and Diagnostics (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Cardiovascular Effects of Exercise (8 papers), Genetic Associations and Epidemiology (7 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (3.0k citations), Genetics (3.2k citations), Cancer Research (1.1k citations), Molecular Biology (4.3k citations) and Developmental Neuroscience (156 citations). Birgit Funke has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Heidi L. Rehm, Madhuri Hegde, Neal K. Lakdawala, Pınar Bayrak‐Toydemir, Anil K. Malhotra, Matthew S. Lebo, Raju Kucherlapati, Stuart A. Cook, Roddy Walsh and James S. Ware. Their work appears in journals such as Genetics in Medicine, Journal of Molecular Diagnostics, The American Journal of Human Genetics, Human Mutation and European Heart Journal.
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.