Kathy Chun

2.4k total citations
59 papers, 1.6k citations indexed

About

Kathy Chun is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, Kathy Chun has authored 59 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Hematology, 19 papers in Genetics and 17 papers in Molecular Biology. Recurrent topics in Kathy Chun's work include Acute Myeloid Leukemia Research (17 papers), Acute Lymphoblastic Leukemia research (10 papers) and Biochemical Acid Research Studies (9 papers). Kathy Chun is often cited by papers focused on Acute Myeloid Leukemia Research (17 papers), Acute Lymphoblastic Leukemia research (10 papers) and Biochemical Acid Research Studies (9 papers). Kathy Chun collaborates with scholars based in Canada, United States and Belgium. Kathy Chun's co-authors include Qilong Yi, Joseph Brandwein, Hong Chang, Mark D. Minden, Peter N. Ray, Andre C. Schuh, Brian H. Robinson, B. H. Robinson, N. MacKay and Vikas Gupta and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Kathy Chun

58 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kathy Chun Canada	22	742	630	319	315	219	59	1.6k
Edward J. Lee United States	17	421 0.6×	858 1.4×	111 0.3×	500 1.6×	22 0.1×	27	1.6k
Bálint Nagy Hungary	20	548 0.7×	140 0.2×	77 0.2×	208 0.7×	43 0.2×	52	1.1k
L A Fitzgerald United States	20	576 0.8×	1.1k 1.8×	219 0.7×	145 0.5×	22 0.1×	27	2.2k
Jacob Baram United States	12	321 0.4×	203 0.3×	37 0.1×	121 0.4×	24 0.1×	16	1.1k
Borys Korchin United States	13	614 0.8×	145 0.2×	48 0.2×	235 0.7×	23 0.1×	18	1.1k
Joseph R. Voland United States	11	502 0.7×	207 0.3×	92 0.3×	355 1.1×	8 0.0×	20	1.2k
Biniam Adane United States	12	1.1k 1.5×	752 1.2×	27 0.1×	188 0.6×	18 0.1×	23	1.6k
Ryan S. Robetorye United States	17	751 1.0×	85 0.1×	237 0.7×	541 1.7×	20 0.1×	41	1.4k
Jan Samuelsson Sweden	26	1.2k 1.6×	1.9k 3.0×	155 0.5×	271 0.9×	11 0.1×	75	2.8k
Sven‐Aage Killmann Denmark	17	284 0.4×	432 0.7×	62 0.2×	127 0.4×	41 0.2×	39	848

Countries citing papers authored by Kathy Chun

Since Specialization

Citations

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

Fields of papers citing papers by Kathy Chun

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathy Chun

This figure shows the co-authorship network connecting the top 25 collaborators of Kathy Chun. A scholar is included among the top collaborators of Kathy Chun 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 Kathy Chun. Kathy Chun 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

Dossa, Fahima, Kelly Metcalfe, Rinku Sutradhar, et al.. (2020). Building the What Comes Next Cohort for BRCA1 and BRCA2 testing: a descriptive analysis. CMAJ Open. 9(3). E874–E885. 2 indexed citations

Chun, Kathy, Gail D. Wenger, Alka Chaubey, et al.. (2018). Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia. Cancer Genetics. 228-229. 236–250. 20 indexed citations

Dawson, Angelika J., et al.. (2012). Origin of a Prenatal Mosaic Supernumerary Neocentromeric Derivative Chromosome 13 Determined by QF-PCR. Fetal Diagnosis and Therapy. 33(1). 75–78. 2 indexed citations

Cherry, Athena M., Marilyn L. Slovak, Lynda J. Campbell, et al.. (2012). Will a peripheral blood (PB) sample yield the same diagnostic and prognostic cytogenetic data as the concomitant bone marrow (BM) in myelodysplasia?. Leukemia Research. 36(7). 832–840. 12 indexed citations

Allingham‐Hawkins, Diane, David Chitayat, Vincenzo Cirigliano, et al.. (2011). Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies. Genetics in Medicine. 13(2). 140–147. 14 indexed citations

McLarty, Kristin, Bart Cornelissen, Deborah A. Scollard, et al.. (2008). Associations between the uptake of 111In-DTPA-trastuzumab, HER2 density and response to trastuzumab (Herceptin) in athymic mice bearing subcutaneous human tumour xenografts. European Journal of Nuclear Medicine and Molecular Imaging. 36(1). 81–93. 103 indexed citations

Chu, Isabel, Angel Arnaout, Jun Sun, et al.. (2007). Src promotes estrogen-dependent estrogen receptor α proteolysis in human breast cancer. Journal of Clinical Investigation. 117(8). 2205–2215. 72 indexed citations

Medeiros, Bruno C., Kathy Chun, Suzanne Kamel‐Reid, & Jeffrey H. Lipton. (2007). Inv (11)(p15q21) in donor‐derived Ph‐negative cells in a patient with chronic myeloid leukemia in relapse successfully treated with imatinib mesylate post allogeneic stemcell transplantation. American Journal of Hematology. 82(8). 758–760. 3 indexed citations

Yuan, Rui, Fatemeh Haghighi, Susan M. White, et al.. (2006). A Single Nucleotide Polymorphism Chip-Based Method for Combined Genetic and Epigenetic Profiling: Validation in Decitabine Therapy and Tumor/Normal Comparisons. Cancer Research. 66(7). 3443–3451. 46 indexed citations

10.

Carter, Bing Z., Marcela Gronda, Zhiliang Wang, et al.. (2005). Small-molecule XIAP inhibitors derepress downstream effector caspases and induce apoptosis of acute myeloid leukemia cells. Blood. 105(10). 4043–4050. 108 indexed citations

11.

Gronda, Marcela, Joseph Brandwein, Mark D. Minden, et al.. (2005). Assessment of the downstream portion of the mitochondrial pathway of caspase activation in patients with acute myeloid leukemia. APOPTOSIS. 10(6). 1285–1294. 7 indexed citations

12.

Disperati, Patricia, et al.. (2005). Progression of myelodysplasia to acute lymphoblastic leukaemia: Implications for disease biology. Leukemia Research. 30(2). 233–239. 54 indexed citations

13.

Shago, Mary, Derek Bouman, Suzanne Kamel‐Reid, Mark D. Minden, & Kathy Chun. (2004). Cryptic insertion of MLL gene into 9p22 leads to MLL–MLLT3 (AF9) fusion in a case of acute myelogenous leukemia. Genes Chromosomes and Cancer. 40(4). 349–354. 8 indexed citations

14.

Gupta, Vikas, Joseph Brandwein, Mark D. Minden, et al.. (2003). The role of allogeneic bone marrow transplantation in adult patients below the age of 55 years with acute lymphoblastic leukemia in first complete remission: a donor vs no donor comparison. Bone Marrow Transplantation. 33(4). 397–404. 33 indexed citations

15.

Chun, Kathy, et al.. (2003). Screening of patients with craniosynostosis: Molecular strategy. American Journal of Medical Genetics Part A. 120A(4). 470–473. 21 indexed citations

16.

Seyda, Agnieszka, Kathy Chun, Seymour Packman, & B. H. Robinson. (2001). A case of PDH‐E1α mosaicism in a male patient with severe metabolic lactic acidosis. Journal of Inherited Metabolic Disease. 24(5). 551–559. 12 indexed citations

17.

Chitayat, David, Bridget A. Fernandez, Lori L. Moore, et al.. (1999). Compound heterozygosity for the achondroplasia-hypochondroplasia FGFR3 mutations: Prenatal diagnosis and postnatal outcome. American Journal of Medical Genetics. 84(5). 401–405. 19 indexed citations

18.

Chun, Kathy & Brian H. Robinson. (1998). Expression of Normal and Mutant Pyruvate Dehydrogenase Complex E1α cDNAs in Cultured Human Lymphoblasts. Archives of Biochemistry and Biophysics. 349(2). 246–250. 2 indexed citations

19.

Chun, Kathy, et al.. (1993). Mutations in the X-linked E1α subunit of pyruvate dehydrogenase leading to deficiency of the pyruvate dehydrogenase complex. Human Molecular Genetics. 2(4). 449–454. 42 indexed citations

20.

Dahl, H H, Garry K. Brown, R. M. Brown, et al.. (1992). Mutations and polymorphisms in the pyruvate dehydrogenase E1α gene. Human Mutation. 1(2). 97–102. 60 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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