Karen Chong

2.2k citations

49 papers · 820 indexed · h-index 17

Molecular Biology
Genetics top 10%
Pediatrics, Perinatology and Child Health top 5%
Surgery
Epidemiology

Co-authors: David Chitayat Jennifer J. Johnston Patrick Shannon Leslie G. Biesecker Nancy F. Hansen Jamie K. Teer Stacie K. Loftus Praveen F. Cherukuri
Topics: Prenatal Screening and Diagnostics (18 papers)Genomic variations and chromosomal abnormalities (8 papers)Congenital Diaphragmatic Hernia Studies (7 papers)
Cited by: Pediatrics, Perinatology and Child Health Genetics Sensory Systems
Journals: SHILAP Revista de lepidopterologíaThe American Journal of Human Genetics American Journal of Obstetrics and Gynecology
Partner nations: Canada United States Israel

In The Last Decade

Karen Chong

44 papers receiving 781 citations

Peers

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

#	Work	Indexed citations
1	Diagnosis of TBC1D32‐associated conditions: Expanding the phenotypic spectrum of a complex ciliopathy 2023 ·American Journal of Medical Genetics Part A ·(unknown),Karen Chong,David Chitayat,Kelly L. Gilmore,Alexander A.L. Jorge,Bruna Lucheze Freire,Antônio Marcondes Lerário,Patrick Shannon,Heidi Cope,William B. Gallentine,(unknown),Frédéric Bilan,(unknown),Erica E. Davis,Neeta L. Vora	1
2	Anterior extension of the choroid plexus into the frontal horns of the fetal lateral cerebral ventricles: Prenatal findings and postnatal outcome 2023 ·Prenatal Diagnosis ·Eran Ashwal‏,Susan Blasér,(unknown),(unknown),Pradeep Krishnan,Karen Chong,Maian Roifman,Ants Toi,David Chitayat	1
3	Warsaw breakage syndrome: Further clinical and genetic delineation 2018 ·American Journal of Medical Genetics Part A ·Ebba Alkhunaizi,Ranad Shaheen,Sanjay Kumar Bharti,(unknown),Karen Chong,Ghada M. H. Abdel‐Salam,Mohammed Al‐Owain,Susan Blasér,Blake C. Papsin,(unknown),Mais Hashem,Nicole Martin,(unknown),Robert M. Brosh,Fowzan S. Alkuraya,David Chitayat	16
4	TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism 2018 ·The American Journal of Human Genetics ·Yoshiro Suzuki,David Chitayat,Hirotake Sawada,Matthew A. Deardorff,Heather M. McLaughlin,Amber Begtrup,(unknown),Jennifer Harrington,Karen Chong,Maian Roifman,Katheryn Grand,Makoto Tominaga,Fumio Takada,(unknown),(unknown),H. Mutoh,(unknown),Gen Nishimura	54
5	Severe phenotype of X‐linked dominant chondrodysplasia punctata 2017 ·Clinical Case Reports ·(unknown),Karen Chong,Christian Marshall,Lisa E. Kratz,(unknown),Patrick Shannon,Pekka Kannus	0
6	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 2016 ·European Journal of Medical Genetics ·Karen Wou,Young Se Hyun,David Chitayat,(unknown),Karen Chong,Syed Wasim,Sarah Keating,Patrick Shannon,Elena Kolomietz	28
7	Anesthetic management of a parturient with hypermobility phenotype but possible vascular genotype Ehlers-Danlos syndrome 2015 ·Canadian Journal of Anesthesia/Journal canadien d anesthésie ·(unknown),Karen Chong,Mathew Sermer,José C. A. Carvalho	3
8	Prenatal Diagnosis Procedures and Techniques to Obtain a Diagnostic Fetal Specimen or Tissue: Maternal and Fetal Risks and Benefits 2015 ·Journal of Obstetrics and Gynaecology Canada ·R. Douglas Wilson,Alain Gagnon,François Audibert,Carla Campagnolo,June Carroll,(unknown),Jo‐Ann Brock,Karen Chong,Jo‐Ann Johnson,William MacDonald,Nanette Okun,Melanie Pastuck,(unknown)	30
9	PGD for a carrier of an intrachromosomal insertion using aCGH 2014 ·Systems Biology in Reproductive Medicine ·Claire Jones,Elena Kolomietz,Georges Maire,(unknown),(unknown),(unknown),Karen Chong,David Chitayat,(unknown)	5
10	Neuropathology of fetal stage Seckel syndrome: A case report providing a morphological correlate for the emerging molecular mechanisms 2011 ·Brain and Development ·Brendan Fitzgerald,Mark O’Driscoll,Karen Chong,Sarah Keating,Patrick Shannon	3
11	Fetal ventriculomegaly secondary to isolated large choroid plexus cysts: prenatal findings and postnatal outcome 2011 ·Prenatal Diagnosis ·Katherine Fong,Karen Chong,Ants Toi,Tami Uster,Susan Blasér,David Chitayat	5
12	Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate 2010 ·The American Journal of Human Genetics ·Jennifer J. Johnston,Jamie K. Teer,Praveen F. Cherukuri,Nancy F. Hansen,Stacie K. Loftus,Karen Chong,James C. Mullikin,Leslie G. Biesecker	120
13	Intracerebral Periventricular Pseudocysts in a Fetus with Mitochondrial Depletion Syndrome: An Association or Coincidence 2009 ·Fetal Diagnosis and Therapy ·Marianne Rohrbach,David Chitayat,Gustavo Maegawa,Sara Shanske,Guido Davidzon,Karen Chong,Joe T.R. Clarke,Ants Toi,Mark A. Tarnopolsky,Brian Robinson,Susan Blasér	18
14	Cornelia de Lange syndrome (CdLS): prenatal and autopsy findings 2009 ·Prenatal Diagnosis ·Karen Chong,Sarah Keating,(unknown),Anne Summers,Howard Berger,Gareth Seaward,Nicole Martin,(unknown),David Chitayat	9
15	Fetal MR imaging of atelosteogenesis type II (AO-II) 2008 ·Pediatric Radiology ·Elka Miller,Susan Blaser,Stephen F. Miller,Sarah Keating,Megan Thompson,Sheila Unger,Ants Toi,Howard Berger,Karen Chong	8
16	Prenatal diagnosis of solitary median maxillary central incisor syndrome by magnetic resonance imaging 2008 ·Ultrasound in Obstetrics and Gynecology ·Neil Johnson,Rory Windrim,Karen Chong,Sandra Viero,Michael P. Thompson,Susan Blasér	9
17	Acrofacial dysostosis syndrome type Rodriguez: Prenatal diagnosis and autopsy findings 2007 ·American Journal of Medical Genetics Part A ·David Sermer,Nada Quercia,Karen Chong,David Chitayat	6
18	Raine syndrome: A rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings 2007 ·American Journal of Medical Genetics Part A ·David Chitayat,Patrick Shannon,Sarah Keating,Ants Toi,Susan Blasér,(unknown),Andrea Superti‐Furga,Karen Chong,Sheila Unger	24
19	Neonatal diabetes, with hypoplastic pancreas, intestinal atresia and gall bladder hypoplasia: search for the aetiology of a new autosomal recessive syndrome 2004 ·Diabetologia ·John J. Mitchell,Zubin Punthakee,Bernard Lo,(unknown),Karen Chong,Catherine E. Newman,Lola Cartier,Valérie Désilets,E. Cutz,(unknown),(unknown),Constantin Polychronakos	79
20	Primary hemangiopericytoma presenting as a pancoast tumor 1993 ·The Annals of Thoracic Surgery ·Karen Chong,S C Lennox,Mary N. Sheppard	13

About Karen Chong

Karen Chong is a scholar working on Pediatrics, Perinatology and Child Health, Developmental Biology and Genetics, having authored 49 papers that have together received 820 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital Diaphragmatic Hernia Studies (7 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (285 citations), Genetics (326 citations) and Sensory Systems (36 citations). Karen Chong has collaborated with scholars based in Canada, United States and Israel. Frequent co-authors include David Chitayat, Jennifer J. Johnston, Patrick Shannon, Leslie G. Biesecker, Nancy F. Hansen, Jamie K. Teer, Stacie K. Loftus, Praveen F. Cherukuri, James C. Mullikin and Susan Blasér. Their work appears in journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and American Journal of Obstetrics and Gynecology.

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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