Eric Haan
Impact in
-
- Prenatal Screening and Diagnostics
- Assisted Reproductive Technology and Twin Pregnancy
- Neonatal and fetal brain pathology
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 64
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 10
- Co-authors
- Annabelle Chan (20 shared papers)Kevin Priest (16 shared papers)Heather Scott (10 shared papers)Phillipa van Essen (7 shared papers)Alastair H. MacLennan (23 shared papers)Michael J. Davies (3 shared papers)Vivienne Moore (3 shared papers)Kristyn Willson (3 shared papers)
- Journals
- Journal of Medical Genetics (11 papers)The Medical Journal of Australia (10 papers)American Journal of Obstetrics and Gynecology (8 papers)Clinical Genetics (7 papers)Journal of Inherited Metabolic Disease (6 papers)
- Partner nations
- AustraliaUnited StatesUnited Kingdom
In The Last Decade
Eric Haan
184 papers receiving 7.0k citations
Eric Haan's Hit Papers
Peers
Comparison fields: 5 of 148
- Pediatrics, Perinatology and Child Health 2.3k
- Genetics 2.3k
- Obstetrics and Gynecology 534
- Clinical Biochemistry 373
- Psychiatry and Mental health 802
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 185 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Reproductive Technologies and the Risk of Birth Defects Hit paper breakdown → | 2012 | 553 |
| 2 | 1995 | 274 | |
| 3 | 1994 | 250 | |
| 4 | 2003 | 227 | |
| 5 | 1998 | 196 | |
| 6 | 2002 | 173 | |
| 7 | 1997 | 164 | |
| 8 | 2015 | 147 | |
| 9 | Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics. | 1991 | 124 |
| 10 | 2005 | 121 | |
| 11 | 2004 | 116 | |
| 12 | 2013 | 115 | |
| 13 | 2001 | 102 | |
| 14 | 2000 | 101 | |
| 15 | 2014 | 100 | |
| 16 | 2001 | 92 | |
| 17 | 2011 | 90 | |
| 18 | 2003 | 86 | |
| 19 | 1996 | 83 | |
| 20 | 2006 | 82 |
About Eric Haan
Eric Haan is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Clinical Biochemistry, having authored 185 papers that have together received 7.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (22 papers), Genomic variations and chromosomal abnormalities (19 papers), Metabolism and Genetic Disorders (19 papers), Cerebral Palsy and Movement Disorders (15 papers), Folate and B Vitamins Research (12 papers), Congenital Anomalies and Fetal Surgery (11 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Genomics and Rare Diseases (10 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.3k citations), Genetics (2.3k citations), Obstetrics and Gynecology (534 citations), Clinical Biochemistry (373 citations) and Psychiatry and Mental health (802 citations). Eric Haan has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Annabelle Chan, Kevin Priest, Heather Scott, Phillipa van Essen, Alastair H. MacLennan, Michael J. Davies, Vivienne Moore, Kristyn Willson, Catherine Gibson and Gustaaf Dekker. Their work appears in journals such as Journal of Medical Genetics, The Medical Journal of Australia, American Journal of Obstetrics and Gynecology, Clinical Genetics and Journal of Inherited Metabolic Disease.
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.