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
Eboreime, Jordan, Choi, Soo‐Kyung, Yoon, Song‐Ro, Sadybekov, Anastasiia, Katritch, Vsevolod, Calabrese, Peter, Arnheim, Norman
Published in Human mutation (01.12.2022)
Published in Human mutation (01.12.2022)
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Estimating Exceptionally Rare Germline and Somatic Mutation Frequencies via Next Generation Sequencing
Eboreime, Jordan, Choi, Soo-Kung, Yoon, Song-Ro, Arnheim, Norman, Calabrese, Peter
Published in PloS one (24.06.2016)
Published in PloS one (24.06.2016)
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Age-Dependent Germline Mosaicism of the Most Common Noonan Syndrome Mutation Shows the Signature of Germline Selection
Yoon, Song-Ro, Choi, Soo-Kung, Eboreime, Jordan, Gelb, Bruce D., Calabrese, Peter, Arnheim, Norman
Published in American journal of human genetics (06.06.2013)
Published in American journal of human genetics (06.06.2013)
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Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain
Shelbourne, Peggy F., Keller-McGandy, Christine, Bi, Wenya Linda, Yoon, Song-Ro, Dubeau, Louis, Veitch, Nicola J., Vonsattel, Jean Paul, Wexler, Nancy S., Arnheim, Norman, Augood, Sarah J.
Published in Human molecular genetics (15.05.2007)
Published in Human molecular genetics (15.05.2007)
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A Germ-Line-Selective Advantage Rather than an Increased Mutation Rate Can Explain Some Unexpectedly Common Human Disease Mutations
Choi, Soo-Kyung, Yoon, Song-Ro, Calabrese, Peter, Arnheim, Norman
Published in Proceedings of the National Academy of Sciences - PNAS (22.07.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (22.07.2008)
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The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect
Yoon, Song-Ro, Qin, Jian, Glaser, Rivka L, Jabs, Ethylin Wang, Wexler, Nancy S, Sokol, Rebecca, Arnheim, Norman, Calabrese, Peter
Published in PLoS genetics (01.07.2009)
Published in PLoS genetics (01.07.2009)
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The molecular anatomy of spontaneous germline mutations in human testes
Qin, Jian, Calabrese, Peter, Tiemann-Boege, Irene, Shinde, Deepali Narendra, Yoon, Song-Ro, Gelfand, David, Bauer, Keith, Arnheim, Norman
Published in PLoS biology (01.09.2007)
Published in PLoS biology (01.09.2007)
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Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse
CHEN, Peng-Chieh, DUDLEY, Sandra, LIPKIN, Steven M, HAGEN, Wayne, DIZON, Diana, PAXTON, Leslie, REICHOW, Denise, YOON, Song-Ro, KAN YANG, ARNHEIM, Norman, LISKAY, R. Michael
Published in Cancer research (Chicago, Ill.) (01.10.2005)
Published in Cancer research (Chicago, Ill.) (01.10.2005)
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Retroactive DNA analysis for sex determination and dystrophin gene by polymerase chain reaction with archived cytogenetic slides
Choi, S K, Kim, J W, Park, S Y, Kim, Y M, Kim, J M, Ryu, H M, Yang, J S, Yoon, S R
Published in Experimental & molecular medicine (31.03.1999)
Published in Experimental & molecular medicine (31.03.1999)
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The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect: e1000558
Yoon, Song-Ro, Qin, Jian, Glaser, Rivka L, Jabs, Ethylin Wang, Wexler, Nancy S, Sokol, Rebecca, Arnheim, Norman, Calabrese, Peter
Published in PLoS genetics (01.07.2009)
Published in PLoS genetics (01.07.2009)
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Korean population genetic data for eleven STR loci
Han, Myun Soo, Kang, Pil Won, Choi, Dong Ho, Lee, Yang Han, Choi, Sang Kyu, Yoon, Song Ro, Shin, Dong Jik, Kim, Jung Min, Jin, Han Jun, Kwak, Kyoung Don, Kim, Wook
Published in Forensic science international (01.12.2001)
Published in Forensic science international (01.12.2001)
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