1.Epigenetic regulation of Kcna3-encoding Kv1.3 potassium channel by cereblon contributes to regulation of CD4+ T-cell activation

作　　者：Jung-Ah Kang ;Sang-Heon Park ;Sang Phil Jeong 等

出　　处：Proceedings of the National Academy of Sciences. 2016 ;113(31):8771-8776.doi:10.1073/pnas.1502166113

出版社：The National Academy of Sciences of the United States of America

文章 ID：182290597

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2.Mutational landscape of uterine and ovarian carcinosarcomas implicates histone genes in epithelial–mesenchymal transition

作　　者：Siming Zhao ;Stefania Bellone ;Salvatore Lopez 等

出　　处：Proceedings of the National Academy of Sciences. 2016 ;113(43):12238-12243.doi:10.1073/pnas.1614120113

出版社：The National Academy of Sciences of the United States of America

文章 ID：184627774

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3.Neomorphic effects of recurrent somatic mutations in Yin Yang 1 in insulin-producing adenomas

作　　者：M. Kyle Cromer ;Murim Choi ;Carol Nelson-Williams 等

出　　处：Proceedings of the National Academy of Sciences. 2015 ;112(13):4062-4067.doi:10.1073/pnas.1503696112

出版社：The National Academy of Sciences of the United States of America

文章 ID：103255208

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4.Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia

作　　者：Beryl Royer-Bertrand ;Silvia Castillo-Taucher ;Rodrigo Moreno-Salinas 等

出　　处：Scientific Reports. 2015 ;5.doi:10.1038/srep17154

出版社：Springer Nature

文章 ID：146910404

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5.Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

作　　者：Youngha Lee ;Soojin Park ;Jin Sook Lee 等

出　　处：Scientific Reports. 2020 ;10(1):1-11.doi:10.1038/s41598-020-58101-8

出版社：Springer Nature

文章 ID：244229500

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6.Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia

作　　者：Beryl Royer-Bertrand ;Silvia Castillo-Taucher ;Rodrigo Moreno-Salinas 等

出　　处：Scientific Reports. 2015 ;5(1).doi:10.1038/srep17154

出版社：Springer Nature

文章 ID：235879728

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7.Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

作　　者：Ute I. Scholl ;Murim Choi ;Tiewen Liu 等

出　　处：Proceedings of the National Academy of Sciences. 2009 ;106(14):5842-5847.doi:10.1073/pnas.0901749106

出版社：The National Academy of Sciences of the United States of America

文章 ID：200591292

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8.Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

作　　者：Murim Choi ;Ute I. Scholl ;Weizhen Ji 等

出　　处：Proceedings of the National Academy of Sciences. 2009 ;106(45):19096-19101.doi:10.1073/pnas.0910672106

出版社：The National Academy of Sciences of the United States of America

文章 ID：200592338

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	Murim Choi	8篇
	Richard P. Lifton	4篇
	Carol Nelson-Williams	3篇
	Jong-Hee Chae	3篇
	Shrikant Mane	3篇

	Andrea Superti-Furga	2篇
	Anita Farhi	2篇
	Belinda Campos-Xavier	2篇
	Beryl Royer-Bertrand	2篇
	Carlo Rivolta	2篇
	Enrico Girardi	2篇
	Esra Dikoglu	2篇
	Giulio Superti-Furga	2篇
	Luisa Bonafé	2篇
	Moses Lee	2篇
	Ok-Hwa Kim	2篇
	Rodrigo Moreno-Salinas	2篇
	Sheila Unger	2篇
	Silvia Castillo-Taucher	2篇
	Tae-Joon Cho	2篇
	Tiewen Liu	2篇
	Ute I. Scholl	2篇
	Ahmet Nayir	1篇
	Alessandro D. Santin	1篇
	Amy L. Stiegler	1篇
	Anna Cho	1篇
	Annabelle L. Fonseca	1篇
	Antonella Ravaggi	1篇
	Ayșin Bakkaloğlu	1篇
	Babak Edraki	1篇
	Barton Kenney	1篇
	Byung Chan Lim	1篇
	Carl D. Malchoff	1篇
	Carla Donzelli	1篇
	Carlton Schwab	1篇
	Charles Matthew Quick	1篇
	Chiara Romani	1篇
	Cho-Rong Lee	1篇
	Chul-Seung Park	1篇
	Corrado Terranova	1篇

	美国	5篇
	英国	3篇

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	Proceedings of the National Academy of Sciences	5篇
	Scientific Reports	3篇

	2020	1篇
	2016	2篇
	2015	3篇
	2009	2篇