Sung‐Hae Kang

2.4k total citations
30 papers, 1.4k citations indexed

About

Sung‐Hae Kang is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Sung‐Hae Kang has authored 30 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Sung‐Hae Kang's work include Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Rare Diseases (6 papers). Sung‐Hae Kang is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Rare Diseases (6 papers). Sung‐Hae Kang collaborates with scholars based in United States, Poland and Canada. Sung‐Hae Kang's co-authors include Sau Wai Cheung, Chad A. Shaw, Ankita Patel, James R. Lupski, Arthur L. Beaudet, Paweł Stankiewicz, Weimin Bi, Amber N. Pursley, Carlos A. Bacino and A. Craig Chinault and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Molecular Cell.

In The Last Decade

Sung‐Hae Kang

30 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sung‐Hae Kang United States 20 925 737 348 180 153 30 1.4k
Erica Andersen United States 16 773 0.8× 612 0.8× 340 1.0× 85 0.5× 86 0.6× 28 1.5k
Andreas Dufke Germany 22 865 0.9× 695 0.9× 351 1.0× 310 1.7× 83 0.5× 60 1.4k
Kosuke Izumi United States 19 635 0.7× 606 0.8× 185 0.5× 126 0.7× 169 1.1× 77 1.1k
Holger Tönnies Germany 23 833 0.9× 927 1.3× 179 0.5× 221 1.2× 122 0.8× 55 1.6k
Udo Trautmann Germany 23 1.1k 1.1× 930 1.3× 328 0.9× 331 1.8× 132 0.9× 65 1.7k
Shola M. Richards Switzerland 5 929 1.0× 711 1.0× 142 0.4× 86 0.5× 102 0.7× 5 1.3k
Jannine D. Cody United States 25 971 1.0× 729 1.0× 275 0.8× 312 1.7× 90 0.6× 63 1.5k
Fabiola Quintero‐Rivera United States 16 907 1.0× 634 0.9× 357 1.0× 57 0.3× 99 0.6× 54 1.4k
Zhishuo Ou United States 14 862 0.9× 602 0.8× 230 0.7× 214 1.2× 80 0.5× 26 1.1k
Anas M. Alazami Saudi Arabia 22 584 0.6× 857 1.2× 128 0.4× 62 0.3× 95 0.6× 55 1.5k

Countries citing papers authored by Sung‐Hae Kang

Since Specialization
Citations

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

Fields of papers citing papers by Sung‐Hae Kang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sung‐Hae Kang. 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 Sung‐Hae Kang. The network helps show where Sung‐Hae Kang may publish in the future.

Co-authorship network of co-authors of Sung‐Hae Kang

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

All Works

20 of 20 papers shown
1.
Wang, Jasmine J., Rong Rong Huang, Sung‐Hae Kang, et al.. (2025). ELOC-Mutated Renal Cell Carcinoma is a Rare Indolent Tumor With Distinctive Genomic Characteristics. Modern Pathology. 38(8). 100777–100777. 3 indexed citations
2.
Yenamandra, Ashwini, Rebecca B. Smith, Sung‐Hae Kang, et al.. (2022). Evidence-based review of genomic aberrations in diffuse large B cell lymphoma, not otherwise specified (DLBCL, NOS): Report from the cancer genomics consortium lymphoma working group. Cancer Genetics. 268-269. 1–21. 4 indexed citations
3.
Hao, Yi-Heng, Michael D. Fountain, Klementina Fon Tacer, et al.. (2015). USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder. Molecular Cell. 59(6). 956–969. 149 indexed citations
4.
Tsai, Michaela L., et al.. (2015). Utility of Oncotype DX Risk Assessment in Patients With Invasive Lobular Carcinoma. Clinical Breast Cancer. 16(1). 45–50. 35 indexed citations
5.
Shaw, Chad A., Amber N. Pursley, Patricia Hixson, et al.. (2014). Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases. European Journal of Human Genetics. 22(8). 969–978. 35 indexed citations
6.
Tsai, Michaela L., et al.. (2014). Utility of Oncotype DX risk assessment in patients with invasive lobular carcinoma (ILC).. Journal of Clinical Oncology. 32(26_suppl). 28–28. 1 indexed citations
7.
Campbell, Ian M., Mitchell Rao, Seema R. Lalani, et al.. (2013). Fusion of Large-Scale Genomic Knowledge and Frequency Data Computationally Prioritizes Variants in Epilepsy. PLoS Genetics. 9(9). e1003797–e1003797. 18 indexed citations
8.
Wiszniewska, Joanna, Weimin Bi, Chad A. Shaw, et al.. (2013). Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing. European Journal of Human Genetics. 22(1). 79–87. 77 indexed citations
9.
Harris, R. Alan, Chad A. Shaw, Jian Li, et al.. (2013). Confounding by Repetitive Elements and CpG Islands Does Not Explain the Association between Hypomethylation and Genomic Instability. PLoS Genetics. 9(2). e1003333–e1003333. 3 indexed citations
10.
Kang, Sung‐Hae, et al.. (2011). High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy. BMC Medical Genetics. 12(1). 154–154. 46 indexed citations
11.
Richards, Elliott G., et al.. (2011). Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22. American Journal of Medical Genetics Part A. 155(7). 1729–1734. 24 indexed citations
12.
Sanchez‐Valle, Amarilis, Xueqing Wang, Lorraine Potocki, et al.. (2010). HERV‐mediated genomic rearrangement of EYA1 in an individual with branchio‐oto‐renal syndrome. American Journal of Medical Genetics Part A. 152A(11). 2854–2860. 29 indexed citations
13.
Breman, Amy M., Melissa B. Ramocki, Sung‐Hae Kang, et al.. (2010). MECP2 duplications in six patients with complex sex chromosome rearrangements. European Journal of Human Genetics. 19(4). 409–415. 25 indexed citations
14.
Kang, Sung‐Hae, Chad A. Shaw, Zhishuo Ou, et al.. (2010). Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results. American Journal of Medical Genetics Part A. 152A(5). 1111–1126. 79 indexed citations
15.
Tannour‐Louet, Mounia, Shuo Han, Sean T. Corbett, et al.. (2010). Identification of De Novo Copy Number Variants Associated with Human Disorders of Sexual Development. PLoS ONE. 5(10). e15392–e15392. 107 indexed citations
16.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Joseph Shen, et al.. (2009). Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12. European Journal of Human Genetics. 18(3). 278–284. 103 indexed citations
17.
El‐Hattab, Ayman W., Teresa A. Smolarek, Elizabeth K. Schorry, et al.. (2009). Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping. Human Genetics. 126(4). 589–602. 56 indexed citations
18.
Wat, Margaret, Oleg A. Shchelochkov, Ashley M. Holder, et al.. (2009). Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. American Journal of Medical Genetics Part A. 149A(8). 1661–1677. 129 indexed citations
19.
Ou, Zhishuo, Sung‐Hae Kang, Chad A. Shaw, et al.. (2008). Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses. Genetics in Medicine. 10(4). 278–289. 64 indexed citations
20.
Veyver, Ignatia B. Van den, Ankita Patel, Chad A. Shaw, et al.. (2008). Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenatal Diagnosis. 29(1). 29–39. 155 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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