Joyce So

1.4k citations
36 papers · 1k · h-index 17

Impact in

  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Connective tissue disorders research

Papers in

    • Genomics and Rare Diseases 14
    • Genomic variations and chromosomal abnormalities 8
    • Genetics and Neurodevelopmental Disorders 7
    • Connective tissue disorders research 3
    • Metabolism and Genetic Disorders 4

Joyce So

36 papers receiving 1k citations

Peers

Joyce So
Comparison fields: 5 of 73
  • Genetics 638
  • Developmental Biology 23
  • Psychiatry and Mental health 98
  • Health Informatics 10
  • Developmental Neuroscience 13
Replace Dhavendra Kumar with:
Dhavendra Kumar United Kingdom
Paul A. Mulder Netherlands
Naomi J. L. Meeks United States
Maureen Holvoet Belgium
Paul R. Lee United States
Donatella Greco Italy
Lisa Bradley United Kingdom
Lynne M. Kerr United States
Ricardo Harripaul Canada
Annie Procter United Kingdom
Joyce So relative to Dhavendra Kumar United Kingdom Dhavendra Kumar's profile →
Citations per field
00.5×2×3×4×4.7×
Dhavendra Kumar · 1×
Citations per year

Countries citing papers authored by Joyce So

Since Specialization
Citations

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

Fields of papers citing papers by Joyce So

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013194
2 2014123
3 201476
4 201572
5 200461
6 201561
7 201654
8 201546
9 199833
10 201630
11 201930
12 201427
13 201927
14 200924
15 201522
16 202021
17 201318
18 201916
19 201615
20 201715

About Joyce So

Joyce So is a scholar working on Genetics, Clinical Biochemistry, Developmental Biology, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health, having authored 36 papers that have together received 1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Metabolism and Genetic Disorders (4 papers), Schizophrenia research and treatment (3 papers), Connective tissue disorders research (3 papers), Congenital limb and hand anomalies (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Genetics (638 citations), Developmental Biology (23 citations), Psychiatry and Mental health (98 citations), Health Informatics (10 citations) and Developmental Neuroscience (13 citations). Joyce So has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Dimitri James Stavropoulos, Hanna Faghfoury, Sébastien Chénier, David A. Chitayat, Marc Fiume, Sergiu Dumitriu, M. Stephen Meyn, Peter N. Ray, Marta Gîrdea and Kym M. Boycott. Their work appears in journals such as Human Mutation, Journal of Medical Genetics, European Journal of Medical Genetics, Human Genetics and Schizophrenia Bulletin.

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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