Jack H. Jung

776 total citations
19 papers, 411 citations indexed

About

Jack H. Jung is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Jack H. Jung has authored 19 papers receiving a total of 411 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Jack H. Jung's work include Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (2 papers). Jack H. Jung is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Chromosomal and Genetic Variations (3 papers) and Prenatal Screening and Diagnostics (2 papers). Jack H. Jung collaborates with scholars based in Canada, United States and Netherlands. Jack H. Jung's co-authors include Victoria Mok Siu, Yao‐Shan Fan, David I. Rodenhiser, Burr G. Atkinson, John M. Graham, David W. Smith, Sandra A. Farrell, Jie Xu, Marsha Speevak and Yang Zhang and has published in prestigious journals such as PEDIATRICS, Human Molecular Genetics and Journal of Cellular Physiology.

In The Last Decade

Jack H. Jung

19 papers receiving 384 citations

Peers

Jack H. Jung

GENET

PPCH

SURGE

G. Bourrouillou France

Barbara Delle Chiaie Belgium

M. Crippa Italy

Nathalie Marle France

Janice Zunich United States

Emma Hobson United Kingdom

F. R. Sergovich Canada

M. G. Daker United Kingdom

Petrea Jacobsen Denmark

Daniela Bettio Italy

G. Bourrouillou France

Jack H. Jung

279 ×1.3

398 ×1.9

GENET

146 ×1.8

PPCH

95 ×1.6

39 ×1.3

SURGE

Citations per year, relative to Jack H. Jung Jack H. Jung (= 1×) peers G. Bourrouillou

Countries citing papers authored by Jack H. Jung

Since Specialization

Citations

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

Fields of papers citing papers by Jack H. Jung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jack H. Jung. 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 Jack H. Jung. The network helps show where Jack H. Jung may publish in the future.

Co-authorship network of co-authors of Jack H. Jung

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

All Works

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19 of 19 papers shown

Zhang, Irene, Murad Husein, Jack H. Jung, et al.. (2012). Neurofibromatosis and velopharyngeal insufficiency: is there an association?. PubMed. 41(1). 58–64. 4 indexed citations

Charames, George S., Lily Ramyar, Terri Berk, et al.. (2008). A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred. Human Genetics. 124(5). 535–541. 20 indexed citations

Chun, Kathy, Ahmad S. Teebi, Jack H. Jung, et al.. (2002). Genetic analysis of patients with the Saethre‐Chotzen phenotype. American Journal of Medical Genetics. 110(2). 136–143. 54 indexed citations

Fan, Yao‐Shan, et al.. (2001). Direct duplication of 8p21.3→p23.1: A cytogenetic anomaly associated with developmental delay without consistent clinical features. American Journal of Medical Genetics. 103(3). 231–234. 4 indexed citations

Fan, Yao‐Shan, Yang Zhang, Marsha Speevak, et al.. (2001). Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes. Genetics in Medicine. 3(6). 416–421. 40 indexed citations

Fan, Yao‐Shan, et al.. (2001). Direct duplication of 8p21.3?p23.1: A cytogenetic anomaly associated with developmental delay without consistent clinical features. American Journal of Medical Genetics. 103(3). 231–234. 27 indexed citations

Fan, Yao‐Shan, Victoria Mok Siu, Jack H. Jung, & Jie Xu. (2000). Sensitivity of Multiple Color Spectral Karyotyping in Detecting Small Interchromosomal Rearrangements. Genetic Testing. 4(1). 9–14. 33 indexed citations

Fan, Yao‐Shan, et al.. (1999). Small terminal deletion of 1p and duplication of 1q: Cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. American Journal of Medical Genetics. 86(2). 118–123. 18 indexed citations

Rodenhiser, David I., Jack H. Jung, Joseph Andrews, et al.. (1997). A five‐basepair deletion (7118 delTTTTA) identified within neurofibromatosis NF1 exon 39. Human Mutation. 9(5). 473–473. 2 indexed citations

10.

Ainsworth, Peter, David I. Rodenhiser, Graham Stuart, & Jack H. Jung. (1994). Characterization of an intron 31 splice junction mutation in the neurofibromatosis type 1 (NF1) gene. Human Molecular Genetics. 3(7). 1179–1181. 8 indexed citations

11.

Gordon, Kevin, Victoria Mok Siu, F. R. Sergovich, & Jack H. Jung. (1993). 18q‐mosaicism associated with Rett syndrome phenotype. American Journal of Medical Genetics. 46(2). 142–144. 12 indexed citations

12.

Trifiro, Mark, Bruce Gottlieb, Leonard Pinsky, et al.. (1991). The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene. Molecular and Cellular Endocrinology. 75(1). 37–47. 39 indexed citations

13.

Siu, Victoria Mok, et al.. (1990). Choroideremia associated with an X-autosomal translocation. Human Genetics. 84(5). 459–464. 20 indexed citations

14.

Rodenhiser, David I., Burr G. Atkinson, & Jack H. Jung. (1988). Synthesis and secretion of immunoglobulin G by lymphocytes from cultured mouse spleen cells is not affected by heat shock. Journal of Cellular Physiology. 135(1). 145–150. 1 indexed citations

15.

Daly, Michael J. & Jack H. Jung. (1987). The Taxation of Corporate Investment Income in Canada: An Analysis of Marginal Effective Tax Rates. Canadian Journal of Economics/Revue canadienne d économique. 20(3). 555–555. 7 indexed citations

16.

Silver, Meredith M., et al.. (1986). Morphologic and morphometric analysis of muscle in X-linked myotubular myopathy. Human Pathology. 17(11). 1167–1178. 15 indexed citations

17.

Rodenhiser, David I., Jack H. Jung, & Burr G. Atkinson. (1986). The synergistic effect of hyperthermia and ethanol on changing gene expression of mouse lymphocytes. Canadian Journal of Genetics and Cytology. 28(6). 1115–1124. 16 indexed citations

18.

Rodenhiser, David I., Jack H. Jung, & Burr G. Atkinson. (1985). Mammalian lymphocytes: stress-induced synthesis of heat-shock proteins in vitro and in vivo. Canadian Journal of Biochemistry and Cell Biology. 63(7). 711–722. 33 indexed citations

19.

Jung, Jack H., et al.. (1984). Congenital Hydranencephaly/Porencephaly Due to Vascular Disruption in Monozygotic Twins. PEDIATRICS. 73(4). 467–469. 58 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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