Maika Malig
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Molecular Biology top 2%
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
Papers in
-
- Genomics and Phylogenetic Studies 11
- Genomics and Chromatin Dynamics 8
- RNA and protein synthesis mechanisms 7
- DNA and Nucleic Acid Chemistry 3
- Genetics 20
- Genomic variations and chromosomal abnormalities 16
- Genomics and Rare Diseases 6
- Co-authors
- Evan E. Eichler (27 shared papers)Peter H. Sudmant (11 shared papers)Francesca Antonacci (12 shared papers)Can Alkan (10 shared papers)Jeffrey M. Kidd (8 shared papers)Richard K. Wilson (10 shared papers)John Huddleston (11 shared papers)Fereydoun Hormozdiari (5 shared papers)
- Journals
- Genome Research (7 papers)Nature Genetics (5 papers)Cell (3 papers)Proceedings of the National Academy of Sciences (3 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesItalySpain
In The Last Decade
Maika Malig
33 papers receiving 4.7k citations
Maika Malig's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 2.2k
- Molecular Biology 2.9k
- Plant Science 1.5k
- Cancer Research 403
- Developmental Neuroscience 63
Countries citing papers authored by Maika Malig
This map shows the geographic impact of Maika Malig'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 Maika Malig with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maika Malig more than expected).
Fields of papers citing papers by Maika Malig
This network shows the impact of papers produced by Maika Malig. 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 Maika Malig. The network helps show where Maika Malig may publish in the future.
Co-authors
The 25 scholars most cited alongside Maika Malig, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Personalized copy number and segmental duplication maps using next-generation sequencing Hit paper breakdown → | 2009 | 508 |
| 2 | Resolving the complexity of the human genome using single-molecule sequencing Hit paper breakdown → | 2014 | 507 |
| 3 | 2010 | 489 | |
| 4 | 2010 | 448 | |
| 5 | 2012 | 415 | |
| 6 | 2012 | 279 | |
| 7 | 2016 | 218 | |
| 8 | 2013 | 212 | |
| 9 | 2010 | 205 | |
| 10 | 2014 | 180 | |
| 11 | 2013 | 160 | |
| 12 | 2012 | 142 | |
| 13 | 2013 | 108 | |
| 14 | 2019 | 98 | |
| 15 | 2010 | 97 | |
| 16 | 2012 | 88 | |
| 17 | 2014 | 86 | |
| 18 | 2010 | 81 | |
| 19 | 2010 | 73 | |
| 20 | 2011 | 64 |
About Maika Malig
Maika Malig is a scholar working on Molecular Biology, Genetics, Plant Science, Hematology and Pediatrics, Perinatology and Child Health, having authored 34 papers that have together received 4.8k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (17 papers), Genomic variations and chromosomal abnormalities (16 papers), Genomics and Phylogenetic Studies (11 papers), Genomics and Chromatin Dynamics (8 papers), RNA and protein synthesis mechanisms (7 papers), Genomics and Rare Diseases (6 papers), DNA and Nucleic Acid Chemistry (3 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Genetics (2.2k citations), Molecular Biology (2.9k citations), Plant Science (1.5k citations), Cancer Research (403 citations) and Developmental Neuroscience (63 citations). Maika Malig has collaborated with scholars based in United States, Italy and Spain. Frequent co-authors include Evan E. Eichler, Peter H. Sudmant, Francesca Antonacci, Can Alkan, Jeffrey M. Kidd, Richard K. Wilson, John Huddleston, Fereydoun Hormozdiari, Megan Y. Dennis and Jacob O. Kitzman. Their work appears in journals such as Genome Research, Nature Genetics, Cell, Proceedings of the National Academy of Sciences 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.