Young Bae Sohn

1.7k total citations
93 papers, 1.1k citations indexed

About

Young Bae Sohn is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Young Bae Sohn has authored 93 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 34 papers in Physiology and 25 papers in Molecular Biology. Recurrent topics in Young Bae Sohn's work include Lysosomal Storage Disorders Research (31 papers), Genetic Syndromes and Imprinting (15 papers) and Trypanosoma species research and implications (14 papers). Young Bae Sohn is often cited by papers focused on Lysosomal Storage Disorders Research (31 papers), Genetic Syndromes and Imprinting (15 papers) and Trypanosoma species research and implications (14 papers). Young Bae Sohn collaborates with scholars based in South Korea, United States and Japan. Young Bae Sohn's co-authors include Dong‐Kyu Jin, Sung Yoon Cho, Sung Won Park, Ah‐Ra Ko, Su Jin Kim, Jung Min Ko, Chang‐Seok Ki, Sang‐Jin Park, Cha Gon Lee and Jieun Lee and has published in prestigious journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Endocrinology.

In The Last Decade

Young Bae Sohn

88 papers receiving 1.1k citations

Peers

Countries citing papers authored by Young Bae Sohn

Since Specialization

Citations

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

Fields of papers citing papers by Young Bae Sohn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Young Bae Sohn. 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 Young Bae Sohn. The network helps show where Young Bae Sohn may publish in the future.

Co-authorship network of co-authors of Young Bae Sohn

This figure shows the co-authorship network connecting the top 25 collaborators of Young Bae Sohn. A scholar is included among the top collaborators of Young Bae Sohn 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 Young Bae Sohn. Young Bae Sohn 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	Long-term outcomes of enzyme replacement therapy from a large cohort of Korean patients with mucopolysaccharidosis IVA (Morquio A syndrome) 2025 ·Molecular Genetics and Metabolism Reports ·(unknown), (unknown), (unknown), (unknown), Sangmi Kim, Ja‐Hyun Jang, Hyung‐Doo Park, Tae Yeon Jeon, Kyung Rae Ko, Se‐Jun Park, Jun Hwa Lee, (unknown), Chong Kun Cheon, Eungu Kang, (unknown), Young Bae Sohn, (unknown), Chih‐Kuang Chuang, Shuan-Pei Lin, Sung Yoon Cho	0
2	Biomarkers of Glycosaminoglycans (GAG) accumulation in patients with mucopolysaccharidosis type VI—LeukoGAG, Corneal Opacification (COM) and Carotid Intima Media Thickening (CIMT) 2023 ·Molecular Genetics and Metabolism Reports ·Young Bae Sohn, Raymond Wang, Jane Ashworth, Pierre Broqua, (unknown), Jean‐Louis Abitbol, (unknown), Laura Pollard, Timothy C. Wood, Tariq Aslam, Paul Harmatz	1
3	The GBA p.G85E mutation in Korean patients with non-neuronopathic Gaucher disease: founder and neuroprotective effects 2020 ·Orphanet Journal of Rare Diseases ·(unknown), Jin Ho Choi, (unknown), Young Bae Sohn, Jung Min Ko, Beom Hee Lee, Chong Kun Cheon, Han Hyuk Lim, (unknown), Han‐Wook Yoo	9
4	Deletion of exons 16–17b of CFTR is frequently identified in Korean patients with cystic fibrosis 2019 ·European Journal of Medical Genetics ·Young Bae Sohn, Jung Min Ko, (unknown), Moon‐Woo Seong, Sung Sup Park, Dong In Suh, Jae Sung Ko, Choong Ho Shin	9
5	Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia 2018 ·International Journal of Hematology ·(unknown), (unknown), Jeong Ok Hah, Young Bae Sohn, Yu Kyung Kim, Joon Hyuk Choi, (unknown), Kyung Mi Jang, Ji Young Ahn, Jae Min Lee	1
6	Skin Barrier Function Is Not Impaired andKallikrein7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization 2016 ·Journal of Korean Medical Science ·(unknown), Na Young Yoon, (unknown), (unknown), Seong Jun Seo, (unknown), Hyeyoung Lee, Young Bae Sohn, Eung Ho Choi	4
7	AAV8-mediated expression of N-acetylglucosamine-1-phosphate transferase attenuates bone loss in a mouse model of mucolipidosis II 2016 ·Molecular Genetics and Metabolism ·Ah‐Ra Ko, Dong‐Kyu Jin, Sung Yoon Cho, Sung Won Park, Malgorzata Przybylska, Nelson S. Yew, Seng H. Cheng, Jung‐Sun Kim, Min Jung Kwak, Su Jin Kim, Young Bae Sohn	12
8	A Phase 2 Multi-center, Open-label, Switch-over Trial to Evaluate the Safety and Efficacy of Abcertin® in Patients with Type 1 Gaucher Disease 2015 ·Journal of Korean Medical Science ·Jin‐Ho Choi, Beom Hee Lee, (unknown), Young Bae Sohn, Jin‐Sung Lee, Gu-Hwan Kim, Sun Hee Heo, (unknown), Yoo‐Mi Kim, (unknown), Han‐Wook Yoo	7
9	Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients 2015 ·Journal of Human Genetics ·Young Bae Sohn, Jung Min Ko, Choong Ho Shin, Sei Won Yang, Jong‐Hee Chae, Kyung‐A Lee	13
10	Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene 2014 ·European Journal of Medical Genetics ·Hyunwoong Park, (unknown), Sung Im Cho, Tae‐Joon Cho, In Ho Choi, Dong‐Kyu Jin, Young Bae Sohn, (unknown), Hyun‐Hae Cho, Jung‐Eun Cheon, So Yeon Kim, Kim J, Sung Sup Park, Moon‐Woo Seong	9
11	An overview of Korean patients with mucopolysaccharidosis and collaboration through the Asia Pacific MPS Network 2014 ·Intractable & Rare Diseases Research ·Sung Yoon Cho, Young Bae Sohn, Dong‐Kyu Jin	29
12	Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome 2014 ·Journal of Human Genetics ·Chong Kun Cheon, Young Bae Sohn, Jung Min Ko, Yeoun Joo Lee, Ji Song, (unknown), Bo Yang, Il Soo Ha, (unknown), Hyun‐Seok Jin, Seon-Yong Jeong	42
13	The proportion of uniparental disomy is increased in Prader–Willi syndrome due to an advanced maternal childbearing age in Korea 2013 ·Journal of Human Genetics ·Sung Yoon Cho, Chang‐Seok Ki, Young Bae Sohn, (unknown), (unknown), Su Jin Kim, Dong‐Kyu Jin	18
14	Array-Based Comparative Genomic Hybridization in 190 Korean Patients with Developmental Delay and/or Intellectual Disability: A Single Tertiary Care University Center Study 2013 ·Yonsei Medical Journal ·Cha Gon Lee, Sang‐Jin Park, (unknown), Jung Min Ko, (unknown), Shin-Young Yim, Young Bae Sohn	10
15	Improvement of CNS Defects Via Continuous Intrathecal Enzyme Replacement by Osmotic Pump in Mucopolysaccharidosis Type II Mice 2013 ·American Journal of Medical Genetics Part A ·Young Bae Sohn, Jeehun Lee, Sung Yoon Cho, Su Jin Kim, Ah‐Ra Ko, (unknown), Dong‐Kyu Jin	23
16	High-dose enzyme replacement therapy attenuates cerebroventriculomegaly in a mouse model of mucopolysaccharidosis type II 2013 ·Journal of Human Genetics ·So Yoon Ahn, Yun Sil Chang, Dong Kyung Sung, Ah‐Ra Ko, (unknown), (unknown), (unknown), Young Bae Sohn, Dong‐Kyu Jin, Won Soon Park	10
17	Enzyme replacement therapy improves joint motion and outcome of the 12‐min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantation 2012 ·American Journal of Medical Genetics Part A ·Young Bae Sohn, Sung Won Park, Se‐Hwa Kim, (unknown), (unknown), Eun Kyung Kwon, (unknown), (unknown), (unknown), Ah‐Ra Ko, (unknown), Jeehun Lee, Dong Hwan Lee, Dong‐Kyu Jin	9
18	Two novel PEX1 mutations in a patient with Zellweger syndrome: the first Korean case confirmed by biochemical, and molecular evidence. 2011 ·PubMed ·Sung Yoon Cho, Young Pyo Chang, (unknown), Hyung‐Doo Park, Young Bae Sohn, (unknown), (unknown), (unknown), Su Jin Kim, Eun Wha Choi, (unknown), Ah‐Ra Ko, (unknown), Dong‐Kyu Jin	5
19	Clinical, biochemical, and genetic analysis of korean patients with pseudohypoparathyroidism type Ia. 2010 ·PubMed ·(unknown), Hyung‐Doo Park, Soo‐Youn Lee, Jong‐Won Kim, Young Bae Sohn, Sung Won Park, Dong‐Kyu Jin	3
20	Plasma adiponectin level and sleep structures in children with Prader-Willi syndrome 2009 ·Journal of Sleep Research ·Eun Yeon Joo, Seung Bong Hong, Young Bae Sohn, Min Jung Kwak, Su Jin Kim, Young Ok Choi, (unknown), (unknown), Dong‐Kyu Jin	16

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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