Song‐Ro Yoon

661 total citations
9 papers, 447 citations indexed

About

Song‐Ro Yoon is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Song‐Ro Yoon has authored 9 papers receiving a total of 447 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Song‐Ro Yoon's work include RNA modifications and cancer (3 papers), Genetic Syndromes and Imprinting (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Song‐Ro Yoon is often cited by papers focused on RNA modifications and cancer (3 papers), Genetic Syndromes and Imprinting (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Song‐Ro Yoon collaborates with scholars based in United States, United Kingdom and South Korea. Song‐Ro Yoon's co-authors include Norman Arnheim, Peter Calabrese, Nancy S. Wexler, Louis Dubeau, Soo‐Kyung Choi, Peggy Shelbourne, Nicola Veitch, Wenya Linda Bi, Jean Paul Vonsattel and Sarah J. Augood and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and PLoS Biology.

In The Last Decade

Song‐Ro Yoon

9 papers receiving 439 citations

Peers

Countries citing papers authored by Song‐Ro Yoon

Since Specialization

Citations

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

Fields of papers citing papers by Song‐Ro Yoon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Song‐Ro Yoon. 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 Song‐Ro Yoon. The network helps show where Song‐Ro Yoon may publish in the future.

Co-authorship network of co-authors of Song‐Ro Yoon

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Germline selection of PTPN11 (HGNC:9644) variants make a major contribution to both Noonan syndrome's high birth rate and the transmission of sporadic cancer variants resulting in fetal abnormality 2022 ·Human Mutation ·(unknown), Soo‐Kyung Choi, Song‐Ro Yoon, Anastasiia Sadybekov, Vsevolod Katritch, Peter Calabrese, Norman Arnheim	4
2	Estimating Exceptionally Rare Germline and Somatic Mutation Frequencies via Next Generation Sequencing 2016 ·PLoS ONE ·(unknown), (unknown), Song‐Ro Yoon, Norman Arnheim, Peter Calabrese	9
3	Age-Dependent Germline Mosaicism of the Most Common Noonan Syndrome Mutation Shows the Signature of Germline Selection 2013 ·The American Journal of Human Genetics ·Song‐Ro Yoon, (unknown), (unknown), Bruce D. Gelb, Peter Calabrese, Norman Arnheim	39
4	Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B 2012 ·PLoS Genetics ·Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim	47
5	A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations 2008 ·Proceedings of the National Academy of Sciences ·Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim	59
6	The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes 2007 ·PLoS Biology ·Jian Qin, Peter Calabrese, Irene Tiemann‐Boege, Deepali N. Shinde, Song‐Ro Yoon, David H. Gelfand, (unknown), Norman Arnheim	52
7	Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain 2007 ·Human Molecular Genetics ·Peggy Shelbourne, Christine E. Keller-McGandy, Wenya Linda Bi, Song‐Ro Yoon, Louis Dubeau, Nicola Veitch, Jean Paul Vonsattel, Nancy S. Wexler, Norman Arnheim, Sarah J. Augood	149
8	Huntington disease expansion mutations in humans can occur before meiosis is completed 2003 ·Proceedings of the National Academy of Sciences ·Song‐Ro Yoon, Louis Dubeau, (unknown), Nancy S. Wexler, Norman Arnheim	83
9	Retroactive DNA analysis for sex determination and dystrophin gene by polymerase chain reaction with archived cytogenetic slides 1999 ·Experimental & Molecular Medicine ·Soo‐Kyung Choi, Jinwoo Kim, So Yeon Park, Young Mi Kim, (unknown), Hyun Mee Ryu, Juan Yang, Song‐Ro Yoon	5

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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