Andrew Parrish

1.2k citations
21 papers · 953 · h-index 10

Impact in

  • Genetics top 5%
    • Diabetes and associated disorders
    • Genomics and Rare Diseases
    • Genetic and Kidney Cyst Diseases
  • Surgery top 10%
    • Pancreatic function and diabetes

Papers in

    • Genomics and Rare Diseases 6
    • Genomic variations and chromosomal abnormalities 3
    • Diabetes and associated disorders 1
    • Metabolism and Genetic Disorders 2

Andrew Parrish

19 papers receiving 914 citations

Peers

Andrew Parrish
Comparison fields: 5 of 52
  • Genetics 435
  • Surgery 407
  • Clinical Biochemistry 41
  • Developmental Biology 16
  • Health 59
Replace Simone Pötzsch with:
Simone Pötzsch Germany
Steve Holve United States
Claudio Defilippi Italy
Qutub H. Qazi United States
Jamiyah Hassan Malaysia
Franklin Desposito United States
Stephanie Willot France
Catherine Barrey France
Virginia J. Baldwin Canada
Fernando Adrian Poletta Argentina
Andrew Parrish relative to Simone Pötzsch Germany Simone Pötzsch's profile →
Citations per field
00.5×1.5×
Simone Pötzsch · 1×
Citations per year

Countries citing papers authored by Andrew Parrish

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Parrish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2007321
2 2007180
3 201796
4 201783
5 202161
6 201756
7 201443
8 202038
9 202114
10 201213
11 201210
12 20248
13 20177
14 20227
15
Fluconazole-resistant cryptococcal meningitis.
20035
16 20214
17 20254
18 20232
19 20241
20 20250

About Andrew Parrish

Andrew Parrish is a scholar working on Genetics, Clinical Biochemistry, Infectious Diseases, Epidemiology and Psychiatry and Mental health, having authored 21 papers that have together received 953 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (3 papers), Epilepsy research and treatment (2 papers), Metabolism and Genetic Disorders (2 papers), COVID-19 Clinical Research Studies (2 papers), Fungal Infections and Studies (2 papers), Pancreatic function and diabetes (2 papers) and Diabetes and associated disorders (1 paper). The work is most often cited by research in Genetics (435 citations), Surgery (407 citations), Clinical Biochemistry (41 citations), Developmental Biology (16 citations) and Health (59 citations). Andrew Parrish has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include Sian Ellard, Sarah Elizabeth Flanagan, Ann‐Marie Patch, Emma L. Edghill, Andrew Tym Hattersley, Maciej Tadeusz Malecki, Donald F. Steiner, Ritika R. Kapoor, Maggie H. Shepherd and Julie Støy. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Genetics in Medicine, Wellcome Open Research and BMJ Open.

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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