E. J. Maher

987 total citations
11 papers, 613 citations indexed

About

E. J. Maher is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, E. J. Maher has authored 11 papers receiving a total of 613 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in E. J. Maher's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Fetal and Pediatric Neurological Disorders (2 papers). E. J. Maher is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Fetal and Pediatric Neurological Disorders (2 papers). E. J. Maher collaborates with scholars based in United Kingdom, Argentina and United States. E. J. Maher's co-authors include Regina Regan, Robert E. Kearney, N. M. Lawrie, Samantha J.L. Knight, Jonathan Flint, D. L. N. Cardy, Sharon W. Horsley, Denise Williams, Mark D. Kilby and Ronald J. Wapner and has published in prestigious journals such as British Journal of Cancer, Journal of Medical Genetics and Human Genetics.

In The Last Decade

E. J. Maher

11 papers receiving 584 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
E. J. Maher United Kingdom 8 440 342 173 129 66 11 613
Steven L. Gersen United States 9 410 0.9× 337 1.0× 193 1.1× 158 1.2× 95 1.4× 13 581
Celia Donaghue United Kingdom 14 479 1.1× 437 1.3× 155 0.9× 68 0.5× 46 0.7× 16 629
Jingly Fung United States 8 288 0.7× 359 1.0× 103 0.6× 86 0.7× 83 1.3× 14 509
Jun-Wei Su Taiwan 14 472 1.1× 353 1.0× 197 1.1× 99 0.8× 106 1.6× 75 658
Chen‐Chi Lee Taiwan 17 673 1.5× 550 1.6× 285 1.6× 176 1.4× 185 2.8× 116 929
Sugandhi A. Tharapel United States 10 215 0.5× 142 0.4× 83 0.5× 94 0.7× 31 0.5× 19 337
Shin-Wen Chen Taiwan 12 511 1.2× 548 1.6× 180 1.0× 77 0.6× 166 2.5× 152 747
Paolo Guanciali Franchi Italy 14 298 0.7× 80 0.2× 220 1.3× 71 0.6× 25 0.4× 31 484
Chen‐Wen Pan Taiwan 14 438 1.0× 418 1.2× 136 0.8× 98 0.8× 124 1.9× 68 593
Sandra Peacock United States 9 308 0.7× 207 0.6× 183 1.1× 71 0.6× 25 0.4× 11 489

Countries citing papers authored by E. J. Maher

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of E. J. Maher

This figure shows the co-authorship network connecting the top 25 collaborators of E. J. Maher. A scholar is included among the top collaborators of E. J. Maher based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with E. J. Maher. E. J. Maher is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Hillman, Sarah, Dominic McMullan, Gillian C. Hall, et al.. (2013). Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis. Ultrasound in Obstetrics and Gynecology. 41(6). 610–620. 214 indexed citations
2.
3.
Crooks, Kristy, et al.. (1999). 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. Oxford University Research Archive (ORA) (University of Oxford). 85. 36–37. 1 indexed citations
4.
Slavotinek, Anne, et al.. (1997). The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.. Journal of Medical Genetics. 34(10). 857–861. 22 indexed citations
5.
Knight, Samantha J.L., Sharon W. Horsley, Regina Regan, et al.. (1997). Development and Clinical Application of an Innovative Fluorescence in situ Hybridization Technique Which Detects Submicroscopic Rearrangements Involving Telomeres. European Journal of Human Genetics. 5(1). 1–8. 111 indexed citations
6.
Knight, Samantha J.L., Sharon W. Horsley, Regina Regan, et al.. (1997). Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.. PubMed. 5(1). 1–8. 142 indexed citations
7.
Markie, David, Susan Huson, E. J. Maher, et al.. (1996). A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map. Human Genetics. 98(2). 125–128. 26 indexed citations
8.
Swerdlow, Anthony J., et al.. (1996). Fertility, reproductive outcomes, and health of offspring, of patients treated for Hodgkin's disease: an investigation including chromosome examinations. British Journal of Cancer. 74(2). 291–296. 40 indexed citations
9.
Boyd, Patricia A., et al.. (1995). Maternal 3;13 chromosome insertion, with severe pre‐eclampsia. Clinical Genetics. 47(1). 17–21. 9 indexed citations
10.
11.
Mayne, Keiko & E. J. Maher. (1989). Near-haploid cell line in megakaryoblastic transformation of Philadelphia-positive chronic myeloid leukemia. Cancer Genetics and Cytogenetics. 39(1). 133–136. 2 indexed citations

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.

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