Martina Brueckner
- Genetics top 0.5%
- Genetic and Kidney Cyst Diseases 16
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 7
- Molecular Biology top 2%
- Congenital heart defects research 37
- Developmental Biology and Gene Regulation 11
- Renal and related cancers 7
- Protist diversity and phylogeny 7
- Epidemiology top 2%
- Congenital Heart Disease Studies 20
- Cell Biology top 5%
- Aging top 5%
- Co-authors
- James McGrathSamir ZaidiSvetlana MakovaS. Steven PotterDorothy M. SuppDavid P. WitteXin TianStefan Somlo
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Martina Brueckner
63 papers receiving 4.4k citations
Hit Papers
Peers
Comparison fields: 5 of 124
- Genetics 1.9k
- Molecular Biology 3.4k
- Epidemiology 1.1k
- Cell Biology 451
- Aging 39
Countries citing papers authored by Martina Brueckner
This map shows the geographic impact of Martina Brueckner'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 Martina Brueckner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martina Brueckner more than expected).
Fields of papers citing papers by Martina Brueckner
This network shows the impact of papers produced by Martina Brueckner. 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 Martina Brueckner. The network helps show where Martina Brueckner may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Martina Brueckner, 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 | 2025 | 2 | |
| 2 | 2023 | 4 | |
| 3 | 2023 | 1 | |
| 4 | 2023 | 3 | |
| 5 | 2021 | 35 | |
| 6 | 2019 | 29 | |
| 7 | 2019 | 49 | |
| 8 | 2018 | 32 | |
| 9 | 2016 | 1 | |
| 10 | 2014 | 87 | |
| 11 | 2011 | 41 | |
| 12 | 2008 | 102 | |
| 13 | 2007 | 49 | |
| 14 | 2004 | 82 | |
| 15 | Two Populations of Node Monocilia Initiate Left-Right Asymmetry in the Mousebreakdown → | 2003 | 610 |
| 16 | 2002 | 288 | |
| 17 | 1998 | 15 | |
| 18 | 1996 | 30 | |
| 19 | 1995 | 5 | |
| 20 | 1990 | 24 |
About Martina Brueckner
Martina Brueckner is a scholar working on Genetics, Molecular Biology and Epidemiology, having authored 64 papers that have together received 4.4k indexed citations. Recurring topics across this work include Congenital heart defects research (37 papers), Congenital Heart Disease Studies (20 papers), Genetic and Kidney Cyst Diseases (16 papers), Developmental Biology and Gene Regulation (11 papers), Genomics and Rare Diseases (7 papers), Renal and related cancers (7 papers), Protist diversity and phylogeny (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (3.4k citations) and Epidemiology (1.1k citations). Martina Brueckner has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include James McGrath, Samir Zaidi, Svetlana Makova, S. Steven Potter, Dorothy M. Supp, David P. Witte, Xin Tian, Stefan Somlo, H. Joseph Yost and Basudha Basu. Their work appears in journals such as Nature, Science and Cell.
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.