Eric Haan
Impact in
- Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Craniofacial Disorders and Treatments
- Genetic Associations and Epidemiology
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 104
- Genetics and Neurodevelopmental Disorders 32
- Genomic variations and chromosomal abnormalities 28
- Genomics and Rare Diseases 23
- BRCA gene mutations in cancer 12
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- Prenatal Screening and Diagnostics 21
- Co-authors
- Annabelle C Chan (21 shared papers)Kevin Priest (16 shared papers)Heather M. Scott (10 shared papers)Phillipa van Essen (7 shared papers)Alastair H. MacLennan (23 shared papers)Michael J. Davies (4 shared papers)Vivienne Moore (3 shared papers)Kristyn J. Willson (3 shared papers)
- Journals
- The American Journal of Human Genetics (14 papers)The Medical Journal of Australia (14 papers)Journal of Medical Genetics (13 papers)American Journal of Obstetrics and Gynecology (8 papers)Clinical Genetics (7 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Eric Haan
256 papers receiving 16.5k citations
Eric Haan's Hit Papers
Peers
Comparison fields: 5 of 172
- Genetics 7.0k
- Pediatrics, Perinatology and Child Health 2.4k
- Molecular Biology 6.6k
- Psychiatry and Mental health 1.2k
- Clinical Biochemistry 524
Countries citing papers authored by Eric Haan
This map shows the geographic impact of Eric Haan'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 Eric Haan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Haan more than expected).
Fields of papers citing papers by Eric Haan
This network shows the impact of papers produced by Eric Haan. 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 Eric Haan. The network helps show where Eric Haan may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Haan, 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 258 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome-wide association study identifies novel breast cancer susceptibility loci Hit paper breakdown → | 2007 | 1916 |
| 2 | Reproductive Technologies and the Risk of Birth Defects Hit paper breakdown → | 2012 | 630 |
| 3 | Refining analyses of copy number variation identifies specific genes associated with developmental delay Hit paper breakdown → | 2014 | 533 |
| 4 | 2010 | 521 | |
| 5 | A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation Hit paper breakdown → | 2009 | 508 |
| 6 | Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases Hit paper breakdown → | 2017 | 414 |
| 7 | 2008 | 353 | |
| 8 | A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. | 1997 | 328 |
| 9 | 1995 | 307 | |
| 10 | 2006 | 303 | |
| 11 | 2014 | 295 | |
| 12 | 1997 | 292 | |
| 13 | 1994 | 283 | |
| 14 | 2003 | 255 | |
| 15 | 2015 | 244 | |
| 16 | 2012 | 221 | |
| 17 | 2015 | 218 | |
| 18 | 2002 | 211 | |
| 19 | 1998 | 208 | |
| 20 | 2011 | 200 |
About Eric Haan
Eric Haan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry, Molecular Biology and Rheumatology, having authored 258 papers that have together received 17.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (32 papers), Genomic variations and chromosomal abnormalities (28 papers), Genomics and Rare Diseases (23 papers), Metabolism and Genetic Disorders (22 papers), Prenatal Screening and Diagnostics (21 papers), RNA modifications and cancer (15 papers), BRCA gene mutations in cancer (12 papers) and Cerebral Palsy and Movement Disorders (12 papers). The work is most often cited by research in Genetics (7.0k citations), Pediatrics, Perinatology and Child Health (2.4k citations), Molecular Biology (6.6k citations), Psychiatry and Mental health (1.2k citations) and Clinical Biochemistry (524 citations). Eric Haan has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Annabelle C Chan, Kevin Priest, Heather M. Scott, Phillipa van Essen, Alastair H. MacLennan, Michael J. Davies, Vivienne Moore, Kristyn J. Willson, Catherine S. Gibson and David Frederick Callen. Their work appears in journals such as The American Journal of Human Genetics, The Medical Journal of Australia, Journal of Medical Genetics, American Journal of Obstetrics and Gynecology and Clinical 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.