E. J. Maher
Impact in
-
- 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
-
- Prenatal Screening and Diagnostics 6
- Fetal and Pediatric Neurological Disorders 1
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- D. L. N. Cardy (3 shared papers)N. Martin Lawrie (2 shared papers)Sharon W. Horsley (2 shared papers)Jonathan Flint (2 shared papers)Regina Regan (2 shared papers)Samantha J.L. Knight (2 shared papers)Fiona S. Togneri (1 shared paper)César Hernán Meller (1 shared paper)
- Journals
- Prenatal Diagnosis (3 papers)Human Genetics (1 paper)European Journal of Human Genetics (1 paper)Clinical Genetics (1 paper)Ultrasound in Obstetrics and Gynecology (1 paper)
- Partner nations
- United KingdomArgentinaIndia
In The Last Decade
E. J. Maher
12 papers receiving 657 citations
Peers
Comparison fields: 5 of 42
- Pediatrics, Perinatology and Child Health 354
- Genetics 429
- Plant Science 132
- Developmental Biology 7
- Molecular Biology 183
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 | 241 | |
| 2 | Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. | 1997 | 161 |
| 3 | 1997 | 133 | |
| 4 | 1999 | 57 | |
| 5 | 1996 | 56 | |
| 6 | 1996 | 27 | |
| 7 | 1997 | 24 | |
| 8 | 2013 | 22 | |
| 9 | 1995 | 9 | |
| 10 | 1989 | 8 | |
| 11 | 1989 | 3 | |
| 12 | 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 |
| 13 | 2005 | 0 |
About E. J. Maher
E. J. Maher is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Cancer Research, Infectious Diseases and Molecular Biology, having authored 13 papers that have together received 742 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Cancer Genomics and Diagnostics (2 papers), Congenital heart defects research (2 papers), Parvovirus B19 Infection Studies (2 papers), Acute Myeloid Leukemia Research (1 paper), Chronic Myeloid Leukemia Treatments (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (354 citations), Genetics (429 citations), Plant Science (132 citations), Developmental Biology (7 citations) and Molecular Biology (183 citations). E. J. Maher has collaborated with scholars based in United Kingdom, Argentina and India. Frequent co-authors include D. L. N. Cardy, N. Martin Lawrie, Sharon W. Horsley, Jonathan Flint, Regina Regan, Samantha J.L. Knight, Fiona S. Togneri, César Hernán Meller, Sarah Hillman and Dominic J. McMullan. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, European Journal of Human Genetics, Clinical 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.