Eli Hatchwell
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 27
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 7
-
- RNA modifications and cancer 9
- Epigenetics and DNA Methylation 5
- Congenital heart defects research 4
- Co-authors
- Jasmin Roohi (8 shared papers)John M. Greally (3 shared papers)Carla J. DeVincent (7 shared papers)Kenneth D. Gadow (7 shared papers)John A. Crolla (5 shared papers)Todd Richmond (3 shared papers)Rebecca R. Selzer (2 shared papers)María E. Figueroa (2 shared papers)
- Journals
- Journal of Medical Genetics (8 papers)Genomics (3 papers)Frontiers in Neurology (3 papers)Clinical Genetics (3 papers)Journal of Autism and Developmental Disorders (3 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Eli Hatchwell
52 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 112
- Genetics 976
- Cognitive Neuroscience 534
- Molecular Biology 1.2k
- Developmental Biology 28
- Psychiatry and Mental health 157
Countries citing papers authored by Eli Hatchwell
This map shows the geographic impact of Eli Hatchwell'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 Eli Hatchwell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eli Hatchwell more than expected).
Fields of papers citing papers by Eli Hatchwell
This network shows the impact of papers produced by Eli Hatchwell. 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 Eli Hatchwell. The network helps show where Eli Hatchwell may publish in the future.
Co-authors
The 25 scholars most cited alongside Eli Hatchwell, 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 52 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 317 | |
| 2 | 2008 | 241 | |
| 3 | 2012 | 152 | |
| 4 | Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis). | 1994 | 139 |
| 5 | 2006 | 132 | |
| 6 | 2009 | 122 | |
| 7 | 1996 | 84 | |
| 8 | 2008 | 84 | |
| 9 | 2007 | 84 | |
| 10 | 2009 | 67 | |
| 11 | 1996 | 57 | |
| 12 | 2009 | 56 | |
| 13 | 2010 | 45 | |
| 14 | 2010 | 43 | |
| 15 | 2007 | 43 | |
| 16 | 2008 | 39 | |
| 17 | 1996 | 37 | |
| 18 | 1998 | 34 | |
| 19 | 2010 | 33 | |
| 20 | 2012 | 32 |
About Eli Hatchwell
Eli Hatchwell is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Surgery, having authored 52 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Autism Spectrum Disorder Research (10 papers), RNA modifications and cancer (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic Syndromes and Imprinting (7 papers), Epigenetics and DNA Methylation (5 papers), Congenital heart defects research (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Genetics (976 citations), Cognitive Neuroscience (534 citations), Molecular Biology (1.2k citations), Developmental Biology (28 citations) and Psychiatry and Mental health (157 citations). Eli Hatchwell has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Jasmin Roohi, John M. Greally, Carla J. DeVincent, Kenneth D. Gadow, John A. Crolla, Todd Richmond, Rebecca R. Selzer, María E. Figueroa, Jacob L. Glass and Ari Melnick. Their work appears in journals such as Journal of Medical Genetics, Genomics, Frontiers in Neurology, Clinical Genetics and Journal of Autism and Developmental Disorders.
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.