Eva W.C. Chow

8.6k total citations
76 papers, 4.6k citations indexed

About

Eva W.C. Chow is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Eva W.C. Chow has authored 76 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 65 papers in Molecular Biology, 46 papers in Genetics and 30 papers in Epidemiology. Recurrent topics in Eva W.C. Chow's work include Congenital heart defects research (59 papers), Congenital Heart Disease Studies (29 papers) and Genomic variations and chromosomal abnormalities (28 papers). Eva W.C. Chow is often cited by papers focused on Congenital heart defects research (59 papers), Congenital Heart Disease Studies (29 papers) and Genomic variations and chromosomal abnormalities (28 papers). Eva W.C. Chow collaborates with scholars based in Canada, United States and Netherlands. Eva W.C. Chow's co-authors include Anne S. Bassett, Rosanna Weksberg, Linda M. Brzustowicz, William G. Honer, Janice Husted, Kathleen Hodgkinson, Kathy Hodgkinson, Nancy J. Butcher, Oana Caluseriu and Michael Α. Gatzoulis and has published in prestigious journals such as Science, PLoS ONE and NeuroImage.

In The Last Decade

Eva W.C. Chow

76 papers receiving 4.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva W.C. Chow Canada 37 3.2k 2.2k 1.4k 930 680 76 4.6k
Rosalie Goldberg United States 30 4.6k 1.4× 3.0k 1.4× 1.4k 1.0× 1.3k 1.4× 361 0.5× 38 6.2k
Michael Knapp Germany 43 1.9k 0.6× 2.4k 1.1× 290 0.2× 271 0.3× 405 0.6× 147 5.2k
E. Schwinger Germany 40 2.7k 0.8× 2.0k 0.9× 451 0.3× 442 0.5× 391 0.6× 210 6.0k
Doron Gothelf Israel 24 1.5k 0.5× 801 0.4× 675 0.5× 608 0.7× 503 0.7× 39 2.1k
Bert B.A. de Vries Netherlands 39 3.6k 1.1× 5.1k 2.3× 196 0.1× 721 0.8× 653 1.0× 114 7.4k
Eric Lancaster United States 34 1.4k 0.4× 1.6k 0.7× 967 0.7× 146 0.2× 251 0.4× 72 7.7k
Richard J. Sinke Netherlands 39 2.2k 0.7× 1.2k 0.5× 188 0.1× 325 0.3× 231 0.3× 119 4.4k
James A. Knowles United States 35 1.4k 0.4× 843 0.4× 131 0.1× 655 0.7× 350 0.5× 67 3.5k
Tiziano Pramparo United States 27 1.7k 0.5× 1.2k 0.6× 340 0.3× 167 0.2× 503 0.7× 50 2.7k
Pablo V. Gejman United States 28 1.5k 0.5× 980 0.4× 183 0.1× 265 0.3× 186 0.3× 58 3.4k

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

20 of 20 papers shown
1.
McGinn, Daniel E., T. Blaine Crowley, Tracy Heung, et al.. (2022). Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13(10). 1800–1800. 2 indexed citations
2.
Malecki, Sarah, Elemi Breetvelt, Maria Corral, et al.. (2019). A genetic model for multimorbidity in young adults. Genetics in Medicine. 22(1). 132–141. 29 indexed citations
3.
Butcher, Nancy J., Connie Marras, Margarita Pondal, et al.. (2017). Neuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease. Brain. 140(5). 1371–1383. 34 indexed citations
4.
Butcher, Nancy J., Daniele Merico, Mehdi Zarrei, et al.. (2017). Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson’s disease. PLoS ONE. 12(4). e0173944–e0173944. 15 indexed citations
5.
Boot, Erik, Nancy J. Butcher, Samantha Cooper, et al.. (2016). Obesity in adults with 22q11.2 deletion syndrome. Genetics in Medicine. 19(2). 204–208. 55 indexed citations
6.
Yuen, Tracy J., Eva W.C. Chow, Candice K. Silversides, & Anne S. Bassett. (2013). Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome. Schizophrenia Research. 151(1-3). 221–225. 19 indexed citations
7.
George, Susan R., et al.. (2013). Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome. Genetics in Medicine. 16(1). 40–44. 60 indexed citations
8.
Butcher, Nancy J., et al.. (2012). Functional outcomes of adults with 22q11.2 deletion syndrome. Genetics in Medicine. 14(10). 836–843. 60 indexed citations
9.
Vorstman, Jacob, et al.. (2012). Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion. Schizophrenia Research. 143(1). 55–59. 55 indexed citations
10.
Costain, Gregory, Eva W.C. Chow, Peter N. Ray, & Anne S. Bassett. (2011). Caregiver and adult patient perspectives on the importance of a diagnosis of 22q11.2 deletion syndrome. Journal of Intellectual Disability Research. 56(6). 641–651. 38 indexed citations
11.
Silversides, Candice K., et al.. (2011). Complex Congenital Heart Disease in Unaffected Relatives of Adults With 22q11.2 Deletion Syndrome. The American Journal of Cardiology. 107(3). 466–471. 14 indexed citations
12.
Husted, Janice, et al.. (2010). Childhood trauma and genetic factors in familial schizophrenia associated with the NOS1AP gene. Schizophrenia Research. 121(1-3). 187–192. 24 indexed citations
13.
Costain, Gregory, Adrian P. Crawley, David J. Mikulis, et al.. (2010). Reduced gray matter in the anterior cingulate gyrus in familial schizophrenia: A preliminary report. Schizophrenia Research. 122(1-3). 81–84. 10 indexed citations
14.
Bassett, Anne S., Christian R. Marshall, Anath C. Lionel, Eva W.C. Chow, & Stephen W. Scherer. (2008). Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Human Molecular Genetics. 17(24). 4045–4053. 128 indexed citations
15.
Vorstman, Jacob, Eva W.C. Chow, Roel A. Ophoff, et al.. (2008). Association of the PIK4CA schizophrenia‐susceptibility gene in adults with the 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(3). 430–433. 35 indexed citations
16.
Bassett, Anne S., Oana Caluseriu, Rosanna Weksberg, Donald A. Young, & Eva W.C. Chow. (2007). Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome. Biological Psychiatry. 61(10). 1135–1140. 77 indexed citations
17.
Brzustowicz, Linda M., et al.. (2004). Linkage Disequilibrium Mapping of Schizophrenia Susceptibility to the CAPON Region of Chromosome 1q22. The American Journal of Human Genetics. 74(5). 1057–1063. 117 indexed citations
18.
Chow, Eva W.C., et al.. (2001). Low platelet count in a 22q11 deletion syndrome subtype of schizophrenia. Schizophrenia Research. 50(3). 177–180. 12 indexed citations
19.
Bassett, Anne S., Eva W.C. Chow, & Rosanna Weksberg. (2000). Chromosomal abnormalities and schizophrenia. American Journal of Medical Genetics. 97(1). 45–51. 84 indexed citations
20.
Brzustowicz, Linda M., William G. Honer, Eva W.C. Chow, et al.. (1999). Linkage of Familial Schizophrenia to Chromosome 13q32. The American Journal of Human Genetics. 65(4). 1096–1103. 166 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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