Changsoo Kang

1.5k total citations
27 papers, 747 citations indexed

About

Changsoo Kang is a scholar working on Molecular Biology, Clinical Psychology and Developmental and Educational Psychology. According to data from OpenAlex, Changsoo Kang has authored 27 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Clinical Psychology and 7 papers in Developmental and Educational Psychology. Recurrent topics in Changsoo Kang's work include Stuttering Research and Treatment (7 papers), Language Development and Disorders (7 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Changsoo Kang is often cited by papers focused on Stuttering Research and Treatment (7 papers), Language Development and Disorders (7 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Changsoo Kang collaborates with scholars based in South Korea, Pakistan and United States. Changsoo Kang's co-authors include Dennis Drayna, Changwon Kang, Sang‐Cheol Bae, Hyoungseok Ju, Donna M. Krasnewich, Sheikh Riazuddin, Penelope L. Friedman, James C. Mullikin, Hye‐Soon Lee and Chan‐Bum Choi and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Changsoo Kang

26 papers receiving 724 citations

Peers

Countries citing papers authored by Changsoo Kang

Since Specialization

Citations

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

Fields of papers citing papers by Changsoo Kang

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Changsoo Kang

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

#	Work	Indexed citations
1	Two missense mutations in GPNMB cause autosomal recessive amyloidosis cutis dyschromica in the consanguineous pakistani families 2021 ·Genes & Genomics ·Obaid Ur Rahman, (unknown), Caroline Mahon, Musharraf Jelani, Changsoo Kang	3
2	Biallelic inheritance in a single Pakistani family with intellectual disability implicates new candidate gene RDH14 2021 ·Scientific Reports ·Stephen F. Pastore, Tahir Muhammad, Ricardo Harripaul, Rebecca Lau, Muhammad Tariq Masood Khan, Muhammad Ismail Khan, Omar Islam, Changsoo Kang, Muhammad Ayub, Musharraf Jelani, John B. Vincent	5
3	Prevalence and Genotype Analysis of High Risk-human Papillomavirus Infection in Busan Women 2019 ·JoLS Journal of Life Sciences ·Changsoo Kang, (unknown)	1
4	Whole-exome sequencing analysis reveals co-segregation of a COL20A1 missense mutation in a Pakistani family with striate palmoplantar keratoderma 2018 ·Genes & Genomics ·Muhammad Ismail Khan, Soyeon Choi, Muhammad Zahid, Habib Ahmad, Roshan Ali, Musharraf Jelani, Changsoo Kang	4
5	One-step noninvasive prenatal testing (NIPT) for autosomal recessive homozygous point mutations using digital PCR 2018 ·Scientific Reports ·Mun Young Chang, Soyeon Ahn, Min Young Kim, Jin Hee Han, (unknown), (unknown), (unknown), Seungmin Lee, Doo‐Yi Oh, Changsoo Kang, Byung Yoon Choi	27
6	Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia 2018 ·Congenital Anomalies ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Jumana Y. Al‐Aama, Changsoo Kang, Regina C. Betz, Musharraf Jelani	0
7	Whole exome sequencing identified a novel missense mutation in EPM2A underlying Lafora disease in a Pakistani family 2017 ·Seizure ·(unknown), (unknown), (unknown), Muhammad Naeem, Changsoo Kang	5
8	A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family 2016 ·Archives of Oral Biology ·Musharraf Jelani, Changsoo Kang, (unknown), (unknown), Mona Mohammad Almramhi, (unknown), Huanming Yang, Jumana Y. Al‐Aama, Muhammad Naeem, Yaser M. Alkhiary	22
9	Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR 2016 ·Scientific Reports ·Mun Young Chang, Ah Reum Kim, Min Young Kim, Soyoung Kim, (unknown), Jae Joon Han, Soyeon Ahn, Changsoo Kang, Byung Yoon Choi	19
10	A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans 2015 ·PLoS ONE ·Seongwon Cha, Ah Yeon Park, Changsoo Kang	9
11	A role for inherited metabolic deficits in persistent developmental stuttering 2012 ·Molecular Genetics and Metabolism ·Changsoo Kang, Dennis Drayna	20
12	Genetic approaches to understanding the causes of stuttering 2011 ·Journal of Neurodevelopmental Disorders ·Dennis Drayna, Changsoo Kang	37
13	Genetics of Speech and Language Disorders 2011 ·Annual Review of Genomics and Human Genetics ·Changsoo Kang, Dennis Drayna	57
14	Analysis of Mannose 6-Phosphate Uncovering Enzyme Mutations Associated with Persistent Stuttering 2011 ·Journal of Biological Chemistry ·(unknown), Changsoo Kang, Dennis Drayna, Stuart Kornfeld	20
15	Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation 2010 ·Journal of Human Genetics ·(unknown), Dennis Drayna, Changsoo Kang	19
16	Mutations in the Lysosomal Enzyme–Targeting Pathway and Persistent Stuttering 2010 ·New England Journal of Medicine ·Changsoo Kang, Sheikh Riazuddin, (unknown), Donna M. Krasnewich, Penelope L. Friedman, James C. Mullikin, Dennis Drayna	151
17	Association of Anti–Cyclic citrullinated peptide antibody levels with PADI4 haplotypes in early rheumatoid arthritis and with shared epitope alleles in very late rheumatoid arthritis 2007 ·Arthritis & Rheumatism ·Seongwon Cha, Chan‐Bum Choi, Tae‐Un Han, Changsoo Kang, Changwon Kang, Sang‐Cheol Bae	38
18	The −169C/T polymorphism in FCRL3 is not associated with susceptibility to rheumatoid arthritis or systemic lupus erythematosus in a case–control study of Koreans 2006 ·Arthritis & Rheumatism ·Chan‐Bum Choi, Changsoo Kang, (unknown), Sang‐Cheol Bae, Changwon Kang	33
19	TP53BP2 locus is associated with gastric cancer susceptibility 2005 ·International Journal of Cancer ·Hyoungseok Ju, Kyung‐A Lee, (unknown), Han Jo Kim, Changsoo Kang, (unknown), (unknown), (unknown), Changwon Kang, Jong‐Won Kim	15
20	A functional haplotype of thePADI4gene associated with increased rheumatoid arthritis susceptibility in Koreans 2005 ·Arthritis & Rheumatism ·Changsoo Kang, Hye‐Soon Lee, Hyoungseok Ju, (unknown), Changwon Kang, Sang‐Cheol Bae	127

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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