Andy Itsara
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Psychiatry and Mental health top 10%
- Schizophrenia research and treatment
- Epilepsy research and treatment
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 7
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- Retinal Diseases and Treatments 1
- Co-authors
- Evan E. Eichler (5 shared papers)Carl A. Baker (3 shared papers)Richard M. Myers (2 shared papers)Ronald M. Krauss (2 shared papers)Heather C. Mefford (2 shared papers)Gregory M. Cooper (2 shared papers)Jun Z. Li (2 shared papers)Paul M. Ridker (2 shared papers)
- Journals
- The American Journal of Human Genetics (3 papers)Human Molecular Genetics (1 paper)Blood (1 paper)Nature Protocols (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesAustraliaNetherlands
In The Last Decade
Andy Itsara
9 papers receiving 1.6k citations
Andy Itsara's Hit Papers
Peers
Comparison fields: 5 of 66
- Genetics 1.3k
- Psychiatry and Mental health 154
- Cognitive Neuroscience 169
- Pediatrics, Perinatology and Child Health 93
- Developmental Neuroscience 17
Countries citing papers authored by Andy Itsara
This map shows the geographic impact of Andy Itsara'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 Andy Itsara with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andy Itsara more than expected).
Fields of papers citing papers by Andy Itsara
This network shows the impact of papers produced by Andy Itsara. 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 Andy Itsara. The network helps show where Andy Itsara may publish in the future.
Co-authors
The 25 scholars most cited alongside Andy Itsara, 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 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 2 | A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay Hit paper breakdown → | 2010 | 523 |
| 3 | 2009 | 479 | |
| 4 | 2011 | 44 | |
| 5 | 2009 | 25 | |
| 6 | 2007 | 18 | |
| 7 | 2012 | 17 | |
| 8 | 2014 | 15 | |
| 9 | 2015 | 1 |
About Andy Itsara
Andy Itsara is a scholar working on Genetics, Ophthalmology, Hematology, Immunology and Nuclear Energy and Engineering, having authored 9 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Retinal Diseases and Treatments (1 paper), Platelet Disorders and Treatments (1 paper), Complement system in diseases (1 paper) and Blood groups and transfusion (1 paper). The work is most often cited by research in Genetics (1.3k citations), Psychiatry and Mental health (154 citations), Cognitive Neuroscience (169 citations), Pediatrics, Perinatology and Child Health (93 citations) and Developmental Neuroscience (17 citations). Andy Itsara has collaborated with scholars based in United States, Australia and Netherlands. Frequent co-authors include Evan E. Eichler, Carl A. Baker, Richard M. Myers, Ronald M. Krauss, Heather C. Mefford, Gregory M. Cooper, Jun Z. Li, Paul M. Ridker, Santhosh Girirajan and Deborah A. Nickerson. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, Blood, Nature Protocols and PLoS ONE.
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.