Author/Creator: Chen, Jian‐Min - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Chen, Jian‐Min

1. 5′ splice site GC>GT and GT>GC variants differ markedly in terms of their functionality and pathogenicity. Issue 8 (12th May 2020)

Authors:: Lin, Jin‐Huan; Masson, Emmanuelle; Boulling, Arnaud; Hayden, Matthew; Cooper, David N.; Férec, Claude; Liao, Zhuan; Chen, Jian‐Min
Journal:: Human mutation
Issue:: Volume 41:Issue 8(2020)
Page Start:: 1358
Record Type:: Journal Article
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2. A convenient qualitative and quantitative method to investigate RHD‐RHCE hybrid genes. Issue 11 (3rd April 2013)

Authors:: Fichou, Yann; Le Maréchal, Cédric; Bryckaert, Laurence; Dupont, Isabelle; Jamet, Déborah; Chen, Jian‐Min; Férec, Claude
Journal:: Transfusion
Issue:: Volume 53:Issue 11:Part 2(2013)
Page Start:: 2974
Record Type:: Journal Article
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3. A Mechanistic Link between L1 Retrotransposition and Chromothripsis. Issue 4 (April 2016)

Authors:: Chen, Jian‐Min; Cooper, David N.
Journal:: Human mutation
Issue:: Volume 37:Issue 4(2016)
Page Start:: 329
Record Type:: Journal Article
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4. A New and More Accurate Estimate of the Rate of Concurrent Tandem‐Base Substitution Mutations in the Human Germline: ∼0.4% of the Single‐Nucleotide Substitution Mutation Rate. Issue 3 (16th January 2014)

Authors:: Chen, Jian‐Min; Cooper, David N.; Férec, Claude
Journal:: Human mutation
Issue:: Volume 35:Issue 3(2014:Mar.)
Page Start:: 392
Record Type:: Journal Article
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5. Characterization of the second HFE gross deletion highlights the potential importance of Alu‐mediated recombination in haemochromatosis. (4th October 2014)

Authors:: Ka, Chandran; Chen, Jian‐Min; Gourlaouen, Isabelle; Quemener, Sylvia; Ronsin, Christophe; Massonnet, Simone; Thérond, Jean‐Paul; Férec, Claude; Le Gac, Gérald
Journal:: British journal of haematology
Issue:: Volume 168:Number 5(2015:Mar.)
Page Start:: 759
Record Type:: Journal Article
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6. Complex Multiple‐Nucleotide Substitution Mutations Causing Human Inherited Disease Reveal Novel Insights into the Action of Translesion Synthesis DNA Polymerases. Issue 11 (3rd August 2015)

Authors:: Chen, Jian‐Min; Férec, Claude; Cooper, David N.
Journal:: Human mutation
Issue:: Volume 36:Issue 11(2015:Nov.)
Page Start:: 1034
Record Type:: Journal Article
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7. Concurrent Nucleotide Substitution Mutations in the Human Genome Are Characterized by a Significantly Decreased Transition/Transversion Ratio. Issue 3 (13th March 2015)

Authors:: Zhu, Wenjuan; Cooper, David N.; Zhao, Qiang; Wang, Ye; Liu, Ruihong; Li, Qibin; Férec, Claude; Wang, Yiming; Chen, Jian‐Min
Journal:: Human mutation
Issue:: Volume 36:Issue 3(2015:Mar.)
Page Start:: 333
Record Type:: Journal Article
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8. Concurrent Nucleotide Substitution Mutations in the Human Genome Are Characterized by a Significantly Decreased Transition/Transversion Ratio. Issue 3 (March 2015)

Authors:: Zhu, Wenjuan; Cooper, David N.; Zhao, Qiang; Wang, Ye; Liu, Ruihong; Li, Qibin; Férec, Claude; Wang, Yiming; Chen, Jian‐Min
Journal:: Human mutation
Issue:: Volume 36:Issue 3(2015:Mar.)
Page Start:: 333
Record Type:: Journal Article
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9. Deletions Overlapping VCAN Exon 8 Are New Molecular Defects for Wagner Disease. Issue 1 (23rd November 2016)

Authors:: Burin‐des‐Roziers, Cyril; Rothschild, Pierre‐Raphael; Layet, Valérie; Chen, Jian‐Min; Ghiotti, Tiffany; Leroux, Céline; Cremers, Frans P. M.; Brézin, Antoine P.; Valleix, Sophie
Journal:: Human mutation
Issue:: Volume 38:Issue 1(2017)
Page Start:: 43
Record Type:: Journal Article
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10. Disclosing the Hidden Structure and Underlying Mutational Mechanism of a Novel Type of Duplication CNV Responsible for Hereditary Multiple Osteochondromas. Issue 8 (17th June 2015)

Authors:: Su, Peiqiang; Wang, Ye; Cooper, David N.; Zhu, Wenjuan; Huang, Dongsheng; Férec, Claude; Wang, Yiming; Chen, Jian‐Min
Journal:: Human mutation
Issue:: Volume 36:Issue 8(2015:Aug.)
Page Start:: 758
Record Type:: Journal Article
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