Lin Lee - Department of Pathology, University of Washington

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论文共 11 篇作者统计合作学者相似作者

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Targeted Long-Read Sequencing Identifies Missing Pathogenic Variants in Unsolved Werner Syndrome Cases

Danny E. Miller,Lin Lee,Miranda Galey,Renuka Kandhaya-Pillai,Marc Tischkowitz,Deepak Amalnath,Avadh Vithlani,Koutaro Yokote,Hisaya Kato,Yoshiro Maezawa,Aki Takada-Watanabe,Minoru Takemoto,George M. Martin,Evan E. Eichler,Fuki M. Hisama,Junko Oshima

Journal of medical genetics（2022）

引用6浏览0WOS引用

Cell-to-Cell Variation in Gene Expression for Cultured Human Cells Is Controlled in Trans by Diverse Genes: Implications for the Pathobiology of Aging

Jiaming Zhang,Nikolay Burnaevskiy,James Annis,Wenyan Han,Deyin Hou,Paula Ladd,Lin Lee,Alexander R. Mendenhall,Junko Oshima,George M. Martin

JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES（2020）

引用4浏览0WOS引用

ERCC4 Variants Identified in a Cohort of Patients with Segmental Progeroid Syndromes

Takayasu Mori,Matthew J. Yousefzadeh,Maryam Faridounnia,Jessica X. Chong,Fuki M. Hisama,Louanne Hudgins, Gabriela Mercado,Erin A. Wade,Amira S. Barghouthy,Lin Lee,George M. Martin,Deborah A. Nickerson,Michael J. Bamshad,Laura J. Niedernhofer,Junko Oshima

Human mutationno. 2 (2017): 255-265

引用24浏览0WOS引用

A Flanking Gene Problem Leads To The Discovery Of A Gprc5b Splice Variant Predominantly Expressed In C57bl/6j Mouse Brain And In Maturing Neurons

Bethany H. Cool,Guy C. K. Chan,Lin Lee,Junko Oshima,George M. Martin,Qubai Hu

PLOS ONE（2010）

引用18浏览0WOS引用

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Katrin Friedrich,Lin Lee,Dru F. Leistritz,Gudrun Nürnberg,Bidisha Saha,Fuki M. Hisama, Daniel K. Eyman,Davor Lessel,Peter Nürnberg,Chumei Li, María J. Garcia-F-Villalta,Carolien M. Kets,Joerg Schmidtke,Vítor Tedim Cruz,Peter C. Van den Akker,Joseph Boak,Dincy Peter,Goli Compoginis,Kivanc Cefle,Sukru Ozturk, Norberto López, Theda Wessel,Martin Poot,P. F. Ippel,Birgit Groff-Kellermann,Holger Hoehn,George M. Martin,Christian Kubisch,Junko Oshima

Human genetics（2010）

引用91浏览0WOS引用

SOD2 Polymorphisms: Unmasking the Effect of Polymorphism on Splicing

Jing Shao,Lishan Chen,Brian Marrs,Lin Lee,Hai Huang,Kenneth G Manton,George M Martin,Junko Oshima

BMC Medical Geneticsno. 1 (2007)

引用30浏览0WOS引用

The Spectrum of WRN Mutations in Werner Syndrome Patients

Shurong Huang,Lin Lee, Nancy B Hanson, Catherine Lenaerts,Holger Hoehn,Martin Poot, Craig D Rubin,Da-Fu Chen,Chih-Chao Yang,Heike Juch, Thomas Dorn, Roland Spiegel,Elif Arioglu Oral,Mohammed Abid,Carla Battisti,Emanuela Lucci-Cordisco,Giovanni Neri, Erin H Steed, Alexa Kidd, William Isley, David Showalter, Janet L Vittone,Alexander Konstantinow, Johannes Ring,Peter Meyer, Sharon L Wenger, Axel von Herbay,Uwe Wollina,Markus Schuelke, Carin R Huizenga,Dru F Leistritz,George M Martin,I Saira Mian,Junko Oshima

Human mutationno. 6 (2006): 558-67

引用193浏览0WOS引用

193

LMNA mutations identify a new genetic subset of subjects with progeroid features of werner syndrome

Li Chen,Lin Lee,Brian A Kudlow, H G Dos Santos,Olav Sletvold,Yousef Shafeghati,Eleanor G Botha,Amit K Garg,Nancy B Hanson,George M Martin,I S Mian,Brian K Kennedy,Junko Oshima

The Lancet（2003）

引用24浏览0引用

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