E Quinlan-Jones

2.3k citations
19 papers · 451 · h-index 12

Impact in

Papers in

    • Prenatal Screening and Diagnostics 7
    • Pediatric Urology and Nephrology Studies 3
    • Genomics and Rare Diseases 6
    • Genomic variations and chromosomal abnormalities 5
    • Genetic Syndromes and Imprinting 1

E Quinlan-Jones

18 papers receiving 441 citations

Peers

E Quinlan-Jones
Comparison fields: 5 of 42
  • Pediatrics, Perinatology and Child Health 294
  • Urology 73
  • Genetics 98
  • Surgery 68
  • Molecular Biology 75
Replace Inga J. Murawski with:
Inga J. Murawski Canada
Anne Massez Belgium
Farida Daïkha-Dahmane France
Emmanuel Spaggiari France
Kathleen D’Hauwers Netherlands
Sheau‐Wen Jan Taiwan
An Hindryckx Belgium
S. Kessler France
Donald S. Emerson United States
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Citations per field
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Inga J. Murawski · 1×
Citations per year

Countries citing papers authored by E Quinlan-Jones

Since Specialization
Citations

This map shows the geographic impact of E Quinlan-Jones'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 Quinlan-Jones with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E Quinlan-Jones more than expected).

Fields of papers citing papers by E Quinlan-Jones

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E Quinlan-Jones. 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 Quinlan-Jones. The network helps show where E Quinlan-Jones may publish in the future.

Co-authors

The 25 scholars most cited alongside E Quinlan-Jones, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E Quinlan-Jones Line = papers co-authored together E Quinlan-Jones links everyone, so they are left out of the graph.

All Works

19 of 19 papers shown
#Work
1 2007110
2 201841
3 201336
4 201635
5 201335
6 201532
7 201730
8 201823
9 201921
10 201917
11 202113
12 202013
13 202011
14 201311
15 201710
16 20208
17 20174
18 20141
19
Findings of the randomised controlled trial
20130

About E Quinlan-Jones

E Quinlan-Jones is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Pathology and Forensic Medicine, having authored 19 papers that have together received 451 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Pediatric Urology and Nephrology Studies (3 papers), Congenital heart defects research (3 papers), Kidney Stones and Urolithiasis Treatments (1 paper), Genetic Syndromes and Imprinting (1 paper) and Urological Disorders and Treatments (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (294 citations), Urology (73 citations), Genetics (98 citations), Surgery (68 citations) and Molecular Biology (75 citations). E Quinlan-Jones has collaborated with scholars based in United Kingdom, Hong Kong and China. Frequent co-authors include Mark D. Kilby, R. Katie Morris, Khalid S. Khan, Sarah Hillman, Fionnuala Mone, Dominic McMullan, Sheila Greenfield, Matthew E. Hurles, Amie Wilson and John Skelton. Their work appears in journals such as Prenatal Diagnosis, Archives of Disease in Childhood Fetal & Neonatal, Fetal Diagnosis and Therapy, Health Technology Assessment and European Journal of Obstetrics & Gynecology and Reproductive Biology.

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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