Jessica X. Chong

17.9k total citations
44 papers, 1.4k citations indexed

About

Jessica X. Chong is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Jessica X. Chong has authored 44 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 16 papers in Molecular Biology and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Jessica X. Chong's work include Genomics and Rare Diseases (16 papers), Cystic Fibrosis Research Advances (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jessica X. Chong is often cited by papers focused on Genomics and Rare Diseases (16 papers), Cystic Fibrosis Research Advances (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jessica X. Chong collaborates with scholars based in United States, Canada and Australia. Jessica X. Chong's co-authors include Michael J. Bamshad, Deborah A. Nickerson, Bobby G. Ng, Hudson H. Freeze, Carole Ober, Holly K. Tabor, Seema M. Jamal, Joon‐Ho Yu, Darrel Waggoner and Jay Shendure and has published in prestigious journals such as Nature Communications, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Jessica X. Chong

41 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jessica X. Chong United States	19	769	687	145	122	108	44	1.4k
Carol Saunders United States	22	744 1.0×	635 0.9×	89 0.6×	95 0.8×	60 0.6×	59	1.3k
Beryl B. Cummings United States	12	862 1.1×	694 1.0×	191 1.3×	75 0.6×	65 0.6×	18	1.6k
Hanan E. Shamseldin Saudi Arabia	24	981 1.3×	590 0.9×	100 0.7×	182 1.5×	85 0.8×	55	1.5k
Tony Roscioli Australia	24	877 1.1×	769 1.1×	77 0.5×	106 0.9×	128 1.2×	85	1.7k
Shagufta Khaliq Pakistan	23	920 1.2×	504 0.7×	69 0.5×	113 0.9×	70 0.6×	64	1.6k
Peter Gustavsson Sweden	20	1.3k 1.6×	476 0.7×	69 0.5×	107 0.9×	86 0.8×	38	1.8k
Eissa Faqeih Saudi Arabia	28	1.5k 1.9×	920 1.3×	159 1.1×	238 2.0×	100 0.9×	80	2.2k
Lora Jh Bean United States	24	862 1.1×	606 0.9×	123 0.8×	64 0.5×	65 0.6×	58	1.6k
Joseph G. Vockley United States	19	730 0.9×	457 0.7×	199 1.4×	65 0.5×	206 1.9×	31	1.4k
Arif O. Khan Saudi Arabia	24	845 1.1×	610 0.9×	94 0.6×	145 1.2×	37 0.3×	131	1.8k

Countries citing papers authored by Jessica X. Chong

Since Specialization

Citations

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

Fields of papers citing papers by Jessica X. Chong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jessica X. Chong

This figure shows the co-authorship network connecting the top 25 collaborators of Jessica X. Chong. A scholar is included among the top collaborators of Jessica X. 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 Jessica X. Chong. Jessica X. 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

Groza, Tudor, Angela Marcello, Melissa Haendel, et al.. (2025). A systematic assessment of large language models’ knowledge of rare diseases: How much do large language models know about rare disease?. Human Genetics and Genomics Advances. 7(1). 100558–100558.

Chong, Jessica X., et al.. (2025). High-dose flecainide for symptomatic relief in paramyotonia congenita/severe neonatal episodic laryngospasm due to SCN4A G1306E: a case report. Journal of Medical Case Reports. 19(1). 224–224.

Xiao, Ming, Jessica X. Chong, Han Wang, et al.. (2024). Physics-based Compact Model for Multi-channel AlGaN/GaN Schottky Barrier Diodes. The HKU Scholars Hub (University of Hong Kong). 327–330. 1 indexed citations

Chong, Jessica X., Seth Berger, Samantha Baxter, et al.. (2024). Considerations for reporting variants in novel candidate genes identified during clinical genomic testing. Genetics in Medicine. 26(10). 101199–101199. 3 indexed citations

Chong, Jessica X., Matthew C. Childers, Colby T. Marvin, et al.. (2023). Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects. Human Genetics and Genomics Advances. 4(3). 100213–100213. 9 indexed citations

Wagner, Matias, Jorge L. Granadillo, Amanda V. Tyndall, et al.. (2023). De novo variants in GATAD2A in individuals with a neurodevelopmental disorder: GATAD2A-related neurodevelopmental disorder. Human Genetics and Genomics Advances. 4(3). 100198–100198. 2 indexed citations

Tran, Thao, Rachel B. Keller, Brecht Guillemyn, et al.. (2021). Biallelic variants in MESD, which encodes a WNT-signaling-related protein, in four new families with recessively inherited osteogenesis imperfecta. SHILAP Revista de lepidopterología. 2(4). 100051–100051. 6 indexed citations

Bamshad, Michael J., Deborah A. Nickerson, & Jessica X. Chong. (2019). Mendelian Gene Discovery: Fast and Furious with No End in Sight. The American Journal of Human Genetics. 105(3). 448–455. 129 indexed citations

Blue, Elizabeth, Tin L. Louie, Jessica X. Chong, et al.. (2018). Variation in Cilia Protein Genes and Progression of Lung Disease in Cystic Fibrosis. Annals of the American Thoracic Society. 15(4). 440–448. 16 indexed citations

10.

Sobreira, Nara, Harindra Arachchi, Orion J. Buske, et al.. (2017). Matchmaker Exchange. Current Protocols in Human Genetics. 95(1). 9.31.1–9.31.15. 32 indexed citations

11.

Said, Edith, Jessica X. Chong, Maja Hempel, et al.. (2017). Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1. American Journal of Medical Genetics Part A. 173(11). 3098–3103. 8 indexed citations

12.

Takamatsu, Junta, et al.. (2016). DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype. Thyroid. 27(1). 129–131. 18 indexed citations

13.

Emond, Mary J., Tin Louie, Julia Emerson, et al.. (2015). Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. PLoS Genetics. 11(6). e1005273–e1005273. 33 indexed citations

14.

Freeze, Hudson H., Jessica X. Chong, Michael J. Bamshad, & Bobby G. Ng. (2014). Solving Glycosylation Disorders: Fundamental Approaches Reveal Complicated Pathways. The American Journal of Human Genetics. 94(2). 161–175. 187 indexed citations

15.

Gripp, Karen W., Cynthia J. Curry, Ann Haskins Olney, et al.. (2014). Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes TSR2 and RPS28. American Journal of Medical Genetics Part A. 164(9). 2240–2249. 98 indexed citations

16.

Tabor, Holly K., Paul L. Auer, Seema M. Jamal, et al.. (2014). Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results. The American Journal of Human Genetics. 95(2). 183–193. 52 indexed citations

17.

Jamal, Seema M., Joon‐Ho Yu, Jessica X. Chong, et al.. (2013). Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications. American Journal of Medical Genetics Part A. 161(5). 935–950. 55 indexed citations

18.

Loucks, Catrina M., Jillian S. Parboosingh, Jessica X. Chong, et al.. (2012). A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America. American Journal of Medical Genetics Part A. 158A(5). 1229–1232. 8 indexed citations

19.

Chong, Jessica X., Rebecca Ouwenga, Rebecca L. Anderson, Darrel Waggoner, & Carole Ober. (2012). A Population-Based Study of Autosomal-Recessive Disease-Causing Mutations in a Founder Population. The American Journal of Human Genetics. 91(4). 608–620. 44 indexed citations

20.

Çalışkan, Minal, Jessica X. Chong, Lawrence H. Uricchio, et al.. (2011). Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13. Human Molecular Genetics. 20(7). 1285–1289. 78 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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