Jun Liao

798 total citations
18 papers, 310 citations indexed

About

Jun Liao is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Jun Liao has authored 18 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Jun Liao's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers) and Cancer Genomics and Diagnostics (4 papers). Jun Liao is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers) and Cancer Genomics and Diagnostics (4 papers). Jun Liao collaborates with scholars based in United States, Jordan and Brazil. Jun Liao's co-authors include Urvashi Surti, Jie Hu, Ruth Kornreich, Malini Sathanoori, Svetlana A. Yatsenko, Suneeta Madan‐Khetarpal, Stephanie J. DeWard, Victoria M. Pratt, Jessica Sebastian and Praful Aggarwal and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and American Journal of Clinical Pathology.

In The Last Decade

Jun Liao

17 papers receiving 304 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jun Liao United States	8	161	122	79	54	39	18	310
Stefan Rentas United States	11	200 1.2×	73 0.6×	16 0.2×	43 0.8×	17 0.4×	17	332
Y. Lachance Canada	7	280 1.7×	160 1.3×	35 0.4×	21 0.4×	14 0.4×	13	558
Maxwell N. Skor United States	8	237 1.5×	164 1.3×	10 0.1×	68 1.3×	13 0.3×	14	488
Jungsoo Gim South Korea	13	200 1.2×	49 0.4×	10 0.1×	41 0.8×	7 0.2×	34	429
Peter Bazeley United States	10	333 2.1×	68 0.6×	24 0.3×	127 2.4×	9 0.2×	29	460
Michelle Wang United States	10	316 2.0×	21 0.2×	26 0.3×	22 0.4×	9 0.2×	28	426
Sophie Pâquet France	12	300 1.9×	31 0.3×	40 0.5×	33 0.6×	7 0.2×	15	417
Arindam Paul United States	8	300 1.9×	88 0.7×	4 0.1×	75 1.4×	33 0.8×	8	398
Jucimara Colombo Brazil	11	249 1.5×	57 0.5×	8 0.1×	70 1.3×	7 0.2×	21	472
Masakazu Doshida Japan	11	174 1.1×	96 0.8×	8 0.1×	24 0.4×	46 1.2×	22	485

Countries citing papers authored by Jun Liao

Since Specialization

Citations

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

Fields of papers citing papers by Jun Liao

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jun Liao

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

All Works

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18 of 18 papers shown

Webb, Bryn D., et al.. (2024). Familial RPL26 Variant Causing Congenital Anomalies Without Hematological Features of Diamond Blackfan Anemia. American Journal of Medical Genetics Part A. 197(5). e63954–e63954.

Aggarwal, Vimla S., et al.. (2024). P641: Application of AlphaMissense prediction to pathogenicity classification of missense variants from clinical exome sequencing. SHILAP Revista de lepidopterología. 2. 101547–101547. 1 indexed citations

Dharmadhikari, Avinash V., Elaine M. Pereira, Michael J. Macera, et al.. (2022). Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl. Frontiers in Genetics. 13. 906077–906077. 1 indexed citations

Ganapathi, Mythily, Amanda Thomas‐Wilson, Christie M. Buchovecky, et al.. (2022). Clinical exome sequencing for inherited retinal degenerations at a tertiary care center. Scientific Reports. 12(1). 9358–9358. 10 indexed citations

Pereira, Elaine M., et al.. (2022). 3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities. Molecular Cytogenetics. 15(1). 7–7. 3 indexed citations

Liao, Jun, Keith A. Coffman, Joseph Locker, et al.. (2021). Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea. Molecular Genetics & Genomic Medicine. 9(4). e1647–e1647. 4 indexed citations

Abdelhakim, Aliaa H., Avinash V. Dharmadhikari, Sara D. Ragi, et al.. (2020). Compound heterozygous inheritance of two novel COQ2 variants results in familial coenzyme Q deficiency. Orphanet Journal of Rare Diseases. 15(1). 320–320. 7 indexed citations

Liao, Jun & Lakshmi Mehta. (2019). Molecular Genetics of Noonan Syndrome and RASopathies.. PubMed. 16(Suppl 2). 435–446. 12 indexed citations

Pratt, Victoria M., Robin E. Everts, Praful Aggarwal, et al.. (2016). Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project. 3 indexed citations

10.

Pratt, Victoria M., Robin E. Everts, Praful Aggarwal, et al.. (2015). Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes. Journal of Molecular Diagnostics. 18(1). 109–123. 107 indexed citations

11.

Wang, Jinlian, Jun Liao, Jinglan Zhang, et al.. (2015). ClinLabGeneticist: a tool for clinical management of genetic variants from whole exome sequencing in clinical genetic laboratories. Genome Medicine. 7(1). 77–77. 5 indexed citations

12.

Hu, Jie, Jun Liao, Malini Sathanoori, et al.. (2015). CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Journal of Neurodevelopmental Disorders. 7(1). 26–26. 52 indexed citations

13.

Masri, Amira, Jun Liao, Ruth Kornreich, & Alireza Haghighi. (2014). Homozygous p.R284* mutation in HEXB gene causing Sandhoff disease with nystagmus. European Journal of Paediatric Neurology. 18(3). 399–403. 2 indexed citations

14.

Martignetti, John A., Olga Camacho‐Vanegas, Nolan Priedigkeit, et al.. (2014). Personalized Ovarian Cancer Disease Surveillance and Detection of Candidate Therapeutic Drug Target in Circulating Tumor DNA. Neoplasia. 16(1). 97–W29. 46 indexed citations

15.

Gibson, Sarah E., Jianhua Luo, Malini Sathanoori, et al.. (2014). Whole-Genome Single Nucleotide Polymorphism Array Analysis Is Complementary to Classical Cytogenetic Analysis in the Evaluation of Lymphoid Proliferations. American Journal of Clinical Pathology. 141(2). 247–255. 6 indexed citations

16.

Webb, Bryn D., Tracy Brandt, Chaim Jalas, et al.. (2013). A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population. Clinical Genetics. 86(2). 155–160. 12 indexed citations

17.

Liao, Jun, Malini Sathanoori, Svetlana A. Yatsenko, et al.. (2012). Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype. Prenatal Diagnosis. 32(12). 1166–1169. 1 indexed citations

18.

Liao, Jun, Stephanie J. DeWard, Suneeta Madan‐Khetarpal, Urvashi Surti, & Jie Hu. (2011). A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features. American Journal of Medical Genetics Part A. 155(11). 2795–2800. 38 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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