Anna Hackett
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
-
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- RNA Research and Splicing
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
-
- Congenital heart defects research 2
- RNA modifications and cancer 2
- Co-authors
- Jozef Gécz (11 shared papers)Lindsay Rowe (1 shared paper)F. Lucy Raymond (2 shared papers)Michael Field (5 shared papers)Mark Corbett (4 shared papers)Gillian Turner (3 shared papers)Patrick Tarpey (3 shared papers)Vera M. Kalscheuer (3 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)Clinical Genetics (2 papers)Human Molecular Genetics (2 papers)The American Journal of Human Genetics (2 papers)Genes Brain & Behavior (1 paper)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Anna Hackett
20 papers receiving 498 citations
Peers
Comparison fields: 5 of 68
- Genetics 281
- Molecular Biology 289
- Cognitive Neuroscience 47
- Developmental Neuroscience 8
- Clinical Biochemistry 12
Countries citing papers authored by Anna Hackett
This map shows the geographic impact of Anna Hackett'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 Anna Hackett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Hackett more than expected).
Fields of papers citing papers by Anna Hackett
This network shows the impact of papers produced by Anna Hackett. 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 Anna Hackett. The network helps show where Anna Hackett may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Hackett, 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 | 2014 | 89 | |
| 2 | 2012 | 75 | |
| 3 | 2009 | 50 | |
| 4 | 2012 | 44 | |
| 5 | 2015 | 41 | |
| 6 | 2010 | 33 | |
| 7 | 2017 | 26 | |
| 8 | 2018 | 23 | |
| 9 | 2015 | 21 | |
| 10 | 2006 | 21 | |
| 11 | 2017 | 18 | |
| 12 | 2011 | 16 | |
| 13 | 2015 | 13 | |
| 14 | 2019 | 12 | |
| 15 | 2016 | 11 | |
| 16 | 2019 | 10 | |
| 17 | 2016 | 8 | |
| 18 | 2012 | 7 | |
| 19 | 2012 | 5 | |
| 20 | 2023 | 1 |
About Anna Hackett
Anna Hackett is a scholar working on Genetics, Molecular Biology, Surgery, Cognitive Neuroscience and Cellular and Molecular Neuroscience, having authored 20 papers that have together received 524 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Autism Spectrum Disorder Research (2 papers), Congenital heart defects research (2 papers), Pancreatic function and diabetes (2 papers), RNA modifications and cancer (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (281 citations), Molecular Biology (289 citations), Cognitive Neuroscience (47 citations), Developmental Neuroscience (8 citations) and Clinical Biochemistry (12 citations). Anna Hackett has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Jozef Gécz, Lindsay Rowe, F. Lucy Raymond, Michael Field, Mark Corbett, Gillian Turner, Patrick Tarpey, Vera M. Kalscheuer, Michael Field and Charles E. Schwartz. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, Human Molecular Genetics, The American Journal of Human Genetics and Genes Brain & Behavior.
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.