Gareth Cross

2.7k citations
39 papers · 1.4k · h-index 19

Impact in

  • Genetics top 5%
    • Genetics and Neurodevelopmental Disorders
    • Neurogenetic and Muscular Disorders Research
    • Autism Spectrum Disorder Research

Papers in

    • Muscle Physiology and Disorders 10
    • RNA Research and Splicing 5
    • Congenital heart defects research 4
    • Genetics and Neurodevelopmental Disorders 7

Gareth Cross

37 papers receiving 1.4k citations

Peers

Gareth Cross
Comparison fields: 5 of 104
  • Genetics 532
  • Genetics 141
  • Cognitive Neuroscience 232
  • Molecular Biology 835
  • Developmental Neuroscience 47
Replace Susan Moore with:
Susan Moore United Kingdom
María Clara Bonaglia Italy
C. T. R. M. Schrander‐Stumpel Netherlands
Takeo Kato Japan
Siddharth Srivastava United States
Valérie Matagne United States
Tomonari Awaya Japan
Stefan Herms Germany
Trilochan Sahoo United States
Marc R. Pelletier Canada
Gareth Cross relative to Susan Moore United Kingdom Susan Moore's profile →
Citations per field
00.5×12×
Susan Moore · 1×
Citations per year

Countries citing papers authored by Gareth Cross

Since Specialization
Citations

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

Fields of papers citing papers by Gareth Cross

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gareth Cross. 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 Gareth Cross. The network helps show where Gareth Cross may publish in the future.

Co-authors

The 25 scholars most cited alongside Gareth Cross, 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 Gareth Cross Line = papers co-authored together Gareth Cross links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2005178
2 1987164
3 1988147
4 200195
5 199983
6 198674
7 199460
8 199460
9 198759
10 199852
11 199148
12 198741
13 198740
14
A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.
199637
15 200036
16 199931
17 201530
18 202428
19 198718
20 198815

About Gareth Cross

Gareth Cross is a scholar working on Molecular Biology, Genetics, Infectious Diseases, Cellular and Molecular Neuroscience and Pollution, having authored 39 papers that have together received 1.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), SARS-CoV-2 detection and testing (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Pharmaceutical and Antibiotic Environmental Impacts (6 papers), Viral gastroenteritis research and epidemiology (5 papers), RNA Research and Splicing (5 papers), Genetic Neurodegenerative Diseases (4 papers) and Congenital heart defects research (4 papers). The work is most often cited by research in Genetics (532 citations), Genetics (141 citations), Cognitive Neuroscience (232 citations), Molecular Biology (835 citations) and Developmental Neuroscience (47 citations). Gareth Cross has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Kim Cornish, Fehmidah Munir, Andreas Speer, S. M. Forrest, K. E. Davies, Hugh R. Woodland, Tracey Flint, Clive Wilson, John Burn and D. Gardner‐Medwin. Their work appears in journals such as Water Research, Nucleic Acids Research, Breast Cancer Research and Treatment, Genomics and Nature.

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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