Joyce So

1.4k total citations
26 papers, 643 citations indexed

About

Joyce So is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Joyce So has authored 26 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 17 papers in Molecular Biology and 2 papers in Clinical Biochemistry. Recurrent topics in Joyce So's work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Joyce So is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Joyce So collaborates with scholars based in Canada, United States and United Kingdom. Joyce So's co-authors include Dimitri J. Stavropoulos, Hanna Faghfoury, Sébastien Chénier, David Chitayat, Syed Wasim, Anath C. Lionel, Stephen W. Scherer, Christian R. Marshall, Chelsea Lowther and Anne S. Bassett and has published in prestigious journals such as PLoS ONE, Schizophrenia Bulletin and The Journal of Nervous and Mental Disease.

In The Last Decade

Joyce So

26 papers receiving 611 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joyce So Canada 13 438 328 59 40 38 26 643
Adekunle Odunsi United States 11 370 0.8× 336 1.0× 26 0.4× 29 0.7× 26 0.7× 14 730
Nicole Créau France 16 335 0.8× 397 1.2× 47 0.8× 66 1.6× 29 0.8× 25 801
Krystyna Szymańska Poland 14 177 0.4× 218 0.7× 47 0.8× 38 0.9× 49 1.3× 48 485
Deborah Barbouth United States 11 412 0.9× 285 0.9× 118 2.0× 85 2.1× 42 1.1× 32 678
Sébastien Chénier Canada 11 278 0.6× 261 0.8× 29 0.5× 34 0.8× 10 0.3× 17 473
Raúl Sanz Spain 14 206 0.5× 341 1.0× 38 0.6× 80 2.0× 49 1.3× 45 631
Cíntia Barros Santos-Rebouças Brazil 17 311 0.7× 378 1.2× 100 1.7× 82 2.0× 30 0.8× 64 767
Keren Carss United Kingdom 16 303 0.7× 495 1.5× 62 1.1× 118 3.0× 51 1.3× 29 782
Andrej Nikoshkov Sweden 19 270 0.6× 499 1.5× 64 1.1× 25 0.6× 77 2.0× 24 906

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-authorship network of co-authors of Joyce So

This figure shows the co-authorship network connecting the top 25 collaborators of Joyce So. A scholar is included among the top collaborators of Joyce So 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 Joyce So. Joyce So is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Harripaul, Ricardo, et al.. (2024). When rare meets common: Treatable genetic diseases are enriched in the general psychiatric population. American Journal of Medical Genetics Part A. 194(8). e63609–e63609. 2 indexed citations
2.
3.
Waung, Maggie W., et al.. (2023). The Diagnostic Landscape of Adult Neurogenetic Disorders. Biology. 12(12). 1459–1459. 1 indexed citations
4.
5.
Zai, Clement C., et al.. (2019). Copy number variant syndromes are frequent in schizophrenia: Progressing towards a CNV-schizophrenia model. Schizophrenia Research. 209. 171–178. 5 indexed citations
6.
Sohaei, Dorsa, et al.. (2019). Adult patient perspectives on phenylketonuria care: Highlighting the need for dedicated adult management and services. European Journal of Medical Genetics. 63(4). 103818–103818. 8 indexed citations
7.
Silver, Josh, et al.. (2019). Understanding the schizophrenia phenotype in the first patient with the full SCN2A phenotypic spectrum. Psychiatric Genetics. 29(3). 91–94. 12 indexed citations
8.
Harripaul, Ricardo, et al.. (2018). Enrichment of pathogenic variants in genes associated with inborn errors of metabolism in psychiatric populations. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(1). 46–54. 10 indexed citations
9.
Mathieu, François, Erin R. Morgan, Joyce So, et al.. (2017). Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation. World Neurosurgery. 111. 190–193. 12 indexed citations
10.
Mittal, Kirti, Muhammad Rafiq, Rafiullah Rafiullah, et al.. (2016). Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability. Journal of Human Genetics. 61(10). 867–872. 13 indexed citations
11.
Sinajon, Pierre, Dagmar Verbaan, & Joyce So. (2016). The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature. Human Genetics. 135(8). 841–850. 27 indexed citations
12.
Wasim, Syed, et al.. (2015). Psychiatric disorders in Ehlers–Danlos syndrome are frequent, diverse and strongly associated with pain. Rheumatology International. 36(3). 341–348. 60 indexed citations
13.
Sinajon, Pierre, et al.. (2015). Microdeletion 8q22.2-q22.3 in a 40-year-old male. European Journal of Medical Genetics. 58(11). 569–572. 9 indexed citations
14.
Hashemi, Bita, Anne S. Bassett, David Chitayat, et al.. (2015). Deletion of 15q11.2(BP1‐BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population. American Journal of Medical Genetics Part A. 167(9). 2098–2102. 40 indexed citations
15.
Chénier, Sébastien, Grace Yoon, Bob Argiropoulos, et al.. (2014). CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems. Journal of Neurodevelopmental Disorders. 6(1). 9–9. 63 indexed citations
16.
Lowther, Chelsea, Gregory Costain, Dimitri J. Stavropoulos, et al.. (2014). Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature. Genetics in Medicine. 17(2). 149–157. 108 indexed citations
17.
Mir, Asif, Kirti Mittal, Nasim Vasli, et al.. (2014). Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family. Human Genetics. 133(8). 975–984. 17 indexed citations
18.
Guerin, Andrea, et al.. (2014). Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld‐anomaly in a child with PTPN11 mutation. American Journal of Medical Genetics Part A. 167(2). 403–406. 5 indexed citations
19.
So, Joyce, et al.. (2007). Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf–Hirschhorn syndrome. American Journal of Medical Genetics Part A. 146A(1). 103–109. 4 indexed citations
20.
Chan, John, et al.. (1998). Encoding of human basic and glycosylated proline-rich proteins by the PRB gene complex and proteolytic processing of their precursor proteins. Archives of Oral Biology. 43(10). 753–770. 32 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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