Eva W. C. Chow

995 total citations
9 papers, 381 citations indexed

About

Eva W. C. Chow is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eva W. C. Chow has authored 9 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eva W. C. Chow's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers) and Genomics and Rare Diseases (3 papers). Eva W. C. Chow is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers) and Genomics and Rare Diseases (3 papers). Eva W. C. Chow collaborates with scholars based in Canada, United Kingdom and Spain. Eva W. C. Chow's co-authors include Anne S. Bassett, Janice Husted, Rosanna Weksberg, Philip AbdelMalik, Gregory Costain, Marsha Speevak, Chelsea Lowther, Dimitrios J. Stavropoulos, Daniele Merico and Tracy J. Yuen and has published in prestigious journals such as Human Molecular Genetics, Schizophrenia Research and Journal of Psychiatric Research.

In The Last Decade

Eva W. C. Chow

9 papers receiving 371 citations

Peers

Eva W. C. Chow

GENET

MB

EPIDE

PMH

CN

A. C. Warren United States

M. A. Mori Spain

Adriana Lo‐Castro Italy

Aude Charollais France

Rachel K. Jonas United States

Yong‐Hui Jiang United States

Laëtitia Lambert France

Jayne Henry United Kingdom

Tracie C. Rosser United States

Delphine Bernoux France

A. C. Warren United States

Eva W. C. Chow

222 ×1.0

GENET

286 ×1.3

MB

37 ×0.5

EPIDE

85 ×1.4

PMH

43 ×1.1

CN

Citations per year, relative to Eva W. C. Chow Eva W. C. Chow (= 1×) peers A. C. Warren

Countries citing papers authored by Eva W. C. Chow

Since Specialization

Citations

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

Fields of papers citing papers by Eva W. C. Chow

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eva W. C. Chow. 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 Eva W. C. Chow. The network helps show where Eva W. C. Chow may publish in the future.

Co-authorship network of co-authors of Eva W. C. Chow

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

All Works

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9 of 9 papers shown

1.

Costain, Gregory, Daniele Merico, Chelsea Lowther, et al.. (2013). Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays. Human Molecular Genetics. 22(22). 4485–4501. 92 indexed citations

2.

Husted, Janice, et al.. (2012). Early environmental exposures influence schizophrenia expression even in the presence of strong genetic predisposition. Schizophrenia Research. 137(1-3). 166–168. 17 indexed citations

3.

Harvard, Chansonette, Eloi Mercier, Rita Colnaghi, et al.. (2011). Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6(1). 54–54. 43 indexed citations

4.

Bassett, Anne S., Gregory Costain, Wai Lun Alan Fung, et al.. (2010). Clinically detectable copy number variations in a Canadian catchment population of schizophrenia. Journal of Psychiatric Research. 44(15). 1005–1009. 51 indexed citations

5.

Caluseriu, Oana, Ghazala Mirza, Jiannis Ragoussis, et al.. (2006). Schizophrenia in an adult with 6p25 deletion syndrome. American Journal of Medical Genetics Part A. 140A(11). 1208–1213. 23 indexed citations

6.

Fañanás, Lourdes, et al.. (2004). Dermatoglyphic profile in 22q deletion syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 128B(1). 46–49. 8 indexed citations

7.

AbdelMalik, Philip, Janice Husted, Eva W. C. Chow, & Anne S. Bassett. (2003). Childhood Head Injury and Expression of Schizophrenia in Multiply Affected Families. Archives of General Psychiatry. 60(3). 231–231. 64 indexed citations

8.

Scutt, L., et al.. (2001). Patterns of dysmorphic features in schizophrenia. American Journal of Medical Genetics. 105(8). 713–723. 19 indexed citations

9.

Chow, Eva W. C., Anne S. Bassett, & Rosanna Weksberg. (1994). Velo‐cardio‐facial syndrome and psychotic disorders: Implications for psychiatric genetics. American Journal of Medical Genetics. 54(2). 107–112. 64 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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