Karen Chong

2.2k total citations
49 papers, 820 citations indexed

About

Karen Chong is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Karen Chong has authored 49 papers receiving a total of 820 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 20 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Karen Chong's work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Diaphragmatic Hernia Studies (7 papers). Karen Chong is often cited by papers focused on Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Diaphragmatic Hernia Studies (7 papers). Karen Chong collaborates with scholars based in Canada, United States and Israel. Karen Chong's co-authors include David Chitayat, Stacie K. Loftus, Praveen F. Cherukuri, Nancy F. Hansen, James C. Mullikin, Jamie K. Teer, Leslie G. Biesecker, Jennifer J. Johnston, Patrick Shannon and Susan Blasér and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Karen Chong

44 papers receiving 781 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karen Chong Canada	17	354	326	285	210	56	49	820
Gail Coghlan Canada	15	316 0.9×	157 0.5×	136 0.5×	130 0.6×	62 1.1×	60	896
Can Liao China	17	444 1.3×	359 1.1×	397 1.4×	121 0.6×	104 1.9×	81	923
Mariko Taniguchi‐Ikeda Japan	15	430 1.2×	150 0.5×	144 0.5×	40 0.2×	60 1.1×	60	760
Magalie Lalanne France	16	552 1.6×	148 0.5×	108 0.4×	103 0.5×	36 0.6×	36	859
Fabien Guimiot France	13	113 0.3×	125 0.4×	189 0.7×	92 0.4×	22 0.4×	37	475
Jorge Román Corona‐Rivera Mexico	14	248 0.7×	179 0.5×	88 0.3×	94 0.4×	54 1.0×	81	636
Roberto Quadrelli United States	10	345 1.0×	186 0.6×	72 0.3×	82 0.4×	119 2.1×	26	602
Dorte L. Lildballe Denmark	16	300 0.8×	173 0.5×	256 0.9×	55 0.3×	65 1.2×	52	769
Winnie Courtens Belgium	16	256 0.7×	431 1.3×	158 0.6×	86 0.4×	23 0.4×	29	587
Margo L. Whiteford United Kingdom	12	238 0.7×	239 0.7×	78 0.3×	159 0.8×	51 0.9×	17	627

Countries citing papers authored by Karen Chong

Since Specialization

Citations

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

Fields of papers citing papers by Karen Chong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Chong

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

All Works

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20 of 20 papers shown

Chong, Karen, David Chitayat, Kelly L. Gilmore, et al.. (2023). Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy. American Journal of Medical Genetics Part A. 191(5). 1282–1292. 1 indexed citations

Ashwal‏, Eran, Susan Blasér, Pradeep Krishnan, et al.. (2023). Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcome. Prenatal Diagnosis. 43(6). 756–762. 1 indexed citations

Keunen, Johannes, et al.. (2019). Prenatal detection of isolated bilateral hyperechogenic kidneys: Etiologies and outcomes. Prenatal Diagnosis. 39(9). 693–700. 21 indexed citations

Suzuki, Yoshiro, David Chitayat, Hirotake Sawada, et al.. (2018). TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism. The American Journal of Human Genetics. 102(6). 1104–1114. 54 indexed citations

Alkhunaizi, Ebba, Ranad Shaheen, Sanjay Kumar Bharti, et al.. (2018). Warsaw breakage syndrome: Further clinical and genetic delineation. American Journal of Medical Genetics Part A. 176(11). 2404–2418. 16 indexed citations

Rodan, Lance H., Kwame Anyane‐Yeboa, Karen Chong, et al.. (2018). Gain‐of‐function variants in the ODC1 gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities. American Journal of Medical Genetics Part A. 176(12). 2554–2560. 28 indexed citations

Chong, Karen, et al.. (2017). Severe phenotype of X‐linked dominant chondrodysplasia punctata. Clinical Case Reports. 5(9). 1435–1437.

Wou, Karen, Young Se Hyun, David Chitayat, et al.. (2016). Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol. European Journal of Medical Genetics. 59(8). 417–424. 28 indexed citations

Chong, Karen, et al.. (2015). Anesthetic management of a parturient with hypermobility phenotype but possible vascular genotype Ehlers-Danlos syndrome. Canadian Journal of Anesthesia/Journal canadien d anesthésie. 62(12). 1308–1312. 3 indexed citations

10.

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

11.

Fitzgerald, Brendan, Mark O’Driscoll, Karen Chong, Sarah Keating, & Patrick Shannon. (2011). Neuropathology of fetal stage Seckel syndrome: A case report providing a morphological correlate for the emerging molecular mechanisms. Brain and Development. 34(3). 238–243. 3 indexed citations

12.

Fong, Katherine, Karen Chong, Ants Toi, et al.. (2011). Fetal ventriculomegaly secondary to isolated large choroid plexus cysts: prenatal findings and postnatal outcome. Prenatal Diagnosis. 31(4). 395–400. 5 indexed citations

13.

Johnston, Jennifer J., Jamie K. Teer, Praveen F. Cherukuri, et al.. (2010). Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate. The American Journal of Human Genetics. 86(5). 743–748. 120 indexed citations

14.

Rohrbach, Marianne, David Chitayat, Gustavo Maegawa, et al.. (2009). Intracerebral Periventricular Pseudocysts in a Fetus with Mitochondrial Depletion Syndrome: An Association or Coincidence. Fetal Diagnosis and Therapy. 25(2). 177–182. 18 indexed citations

15.

Chong, Karen, Sarah Keating, Anne Summers, et al.. (2009). Cornelia de Lange syndrome (CdLS): prenatal and autopsy findings. Prenatal Diagnosis. 29(5). 489–494. 9 indexed citations

16.

Miller, Elka, Susan Blaser, Stephen F. Miller, et al.. (2008). Fetal MR imaging of atelosteogenesis type II (AO-II). Pediatric Radiology. 38(12). 1345–1349. 8 indexed citations

17.

Sermer, David, Nada Quercia, Karen Chong, & David Chitayat. (2007). Acrofacial dysostosis syndrome type Rodriguez: Prenatal diagnosis and autopsy findings. American Journal of Medical Genetics Part A. 143A(24). 3286–3289. 6 indexed citations

18.

Mitchell, John J., Zubin Punthakee, Bernard Lo, et al.. (2004). Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome. Diabetologia. 47(12). 2160–2167. 79 indexed citations

19.

McAuliffe, Fionnuala M., Lisa K. Hornberger, Stephanie Winsor, et al.. (2004). Fetal cardiac defects and increased nuchal translucency thickness: A prospective study. American Journal of Obstetrics and Gynecology. 191(4). 1486–1490. 42 indexed citations

20.

Chong, Karen, S C Lennox, & Mary N. Sheppard. (1993). Primary hemangiopericytoma presenting as a pancoast tumor. The Annals of Thoracic Surgery. 55(2). 518–519. 13 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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