Peer Arts
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
- Immune Response and Inflammation
Papers in
- Genetics 24
- Genomics and Rare Diseases 14
- Blood disorders and treatments 5
- Genomic variations and chromosomal abnormalities 3
- Hematology 10
- Acute Myeloid Leukemia Research 8
- Co-authors
- Alexander Hoischen (15 shared papers)Christian Gilissen (10 shared papers)Joris Andre Veltman (9 shared papers)Marloes Steehouwer (5 shared papers)Han G. Brunner (3 shared papers)Bart van Lier (2 shared papers)Nienke Wieskamp (3 shared papers)Mihai Gheorghe Netea (9 shared papers)
- Journals
- Blood (3 papers)Genetics in Medicine (3 papers)The American Journal of Human Genetics (3 papers)Blood Advances (3 papers)Science Translational Medicine (2 papers)
- Partner nations
- AustraliaNetherlandsUnited States
In The Last Decade
Peer Arts
52 papers receiving 3.6k citations
Peer Arts's Hit Papers
Peers
Comparison fields: 5 of 101
- Genetics 1.5k
- Immunology 702
- Hematology 309
- Infectious Diseases 247
- Developmental Biology 25
Countries citing papers authored by Peer Arts
This map shows the geographic impact of Peer Arts'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 Peer Arts with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peer Arts more than expected).
Fields of papers citing papers by Peer Arts
This network shows the impact of papers produced by Peer Arts. 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 Peer Arts. The network helps show where Peer Arts may publish in the future.
Co-authors
The 25 scholars most cited alongside Peer Arts, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A de novo paradigm for mental retardation Hit paper breakdown → | 2010 | 688 |
| 2 | 2011 | 555 | |
| 3 | 2010 | 387 | |
| 4 | 2010 | 235 | |
| 5 | 2014 | 222 | |
| 6 | 2010 | 182 | |
| 7 | 2013 | 176 | |
| 8 | 2010 | 114 | |
| 9 | 2020 | 114 | |
| 10 | Integrated multi-omics for rapid rare disease diagnosis on a national scale Hit paper breakdown → | 2023 | 99 |
| 11 | 2013 | 83 | |
| 12 | 2010 | 80 | |
| 13 | 2021 | 67 | |
| 14 | 2019 | 61 | |
| 15 | 2019 | 50 | |
| 16 | 2020 | 50 | |
| 17 | 2019 | 49 | |
| 18 | 1999 | 43 | |
| 19 | 2021 | 41 | |
| 20 | 2021 | 36 |
About Peer Arts
Peer Arts is a scholar working on Genetics, Hematology, Pediatrics, Perinatology and Child Health, Immunology and Molecular Biology, having authored 53 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Acute Myeloid Leukemia Research (8 papers), Blood disorders and treatments (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers), Hereditary Neurological Disorders (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Genetics (1.5k citations), Immunology (702 citations), Hematology (309 citations), Infectious Diseases (247 citations) and Developmental Biology (25 citations). Peer Arts has collaborated with scholars based in Australia, Netherlands and United States. Frequent co-authors include Alexander Hoischen, Christian Gilissen, Joris Andre Veltman, Marloes Steehouwer, Han G. Brunner, Bart van Lier, Nienke Wieskamp, Mihai Gheorghe Netea, Leo A. B. Joosten and Theo S. Plantinga. Their work appears in journals such as Blood, Genetics in Medicine, The American Journal of Human Genetics, Blood Advances and Science Translational Medicine.
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.