E. J. Maher
Impact in
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 1
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- Prenatal Screening and Diagnostics 5
- Fetal and Pediatric Neurological Disorders 1
- Co-authors
- D. L. N. Cardy (3 shared papers)Jonathan Flint (2 shared papers)Sharon W. Horsley (2 shared papers)N. M. Lawrie (2 shared papers)Samantha J.L. Knight (2 shared papers)Regina Regan (2 shared papers)Eamonn R. Maher (1 shared paper)César Meller (1 shared paper)
- Journals
- Prenatal Diagnosis (2 papers)Clinical Genetics (1 paper)Human Genetics (1 paper)European Journal of Human Genetics (1 paper)Ultrasound in Obstetrics and Gynecology (1 paper)
- Partner nations
- United KingdomUnited StatesArgentina
In The Last Decade
E. J. Maher
11 papers receiving 586 citations
Peers
Comparison fields: 5 of 38
- Pediatrics, Perinatology and Child Health 292
- Genetics 351
- Plant Science 106
- Developmental Biology 5
- Molecular Biology 150
Countries citing papers authored by E. J. Maher
This map shows the geographic impact of E. J. Maher'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 E. J. Maher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. J. Maher more than expected).
Fields of papers citing papers by E. J. Maher
This network shows the impact of papers produced by E. J. Maher. 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 E. J. Maher. The network helps show where E. J. Maher may publish in the future.
Co-authors
The 25 scholars most cited alongside E. J. Maher, 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 | 2013 | 217 | |
| 2 | Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. | 1997 | 141 |
| 3 | 1997 | 110 | |
| 4 | 1996 | 40 | |
| 5 | 1999 | 39 | |
| 6 | 1996 | 26 | |
| 7 | 1997 | 22 | |
| 8 | 1995 | 9 | |
| 9 | 1989 | 7 | |
| 10 | 1989 | 2 | |
| 11 | Novel multiple-colour fluorescence in situ hybridisation technology for the simultaneous identification of the 24 human metaphase chromosomes on a single slide: applications in the analysis of structural chromosomal rearrangements | 1999 | 1 |
About E. J. Maher
E. J. Maher is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cancer Research and Infectious Diseases, having authored 11 papers that have together received 614 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (2 papers), Congenital heart defects research (2 papers), Acute Myeloid Leukemia Research (1 paper), Fetal and Pediatric Neurological Disorders (1 paper), Genomics and Rare Diseases (1 paper) and Acute Lymphoblastic Leukemia research (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (292 citations), Genetics (351 citations), Plant Science (106 citations), Developmental Biology (5 citations) and Molecular Biology (150 citations). E. J. Maher has collaborated with scholars based in United Kingdom, United States and Argentina. Frequent co-authors include D. L. N. Cardy, Jonathan Flint, Sharon W. Horsley, N. M. Lawrie, Samantha J.L. Knight, Regina Regan, Eamonn R. Maher, César Meller, Mark D. Kilby and Gillian C. Hall. Their work appears in journals such as Prenatal Diagnosis, Clinical Genetics, Human Genetics, European Journal of Human Genetics and Ultrasound in Obstetrics and Gynecology.
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.