1.Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis

作　　者：Patrick Maffucci ;Patrick Maffucci ;Benedetta Bigio 等

出　　处：Proceedings of the National Academy of Sciences. 2019 ;116(3):950-959.doi:10.1073/pnas.1808403116

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

文章 ID：225725501

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2.Implicit Hypotheses Are Hidden Power Droppers in Family-Based Association Studies of Secondary Outcomes

作　　者：Jean Gaschignard 1,2 , Quentin B. Vincent 1,2 , Jean-Philippe Jaïs 1,2,3 , Aurélie Cobat 1,2 , Alexandre Alcaïs 1,

出　　处：Open Journal of Statistics. 2015 ;05(01):35-45.doi:10.4236/ojs.2015.51005

出版社：Scientific Research Publishing

文章 ID：103874616

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3.Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage

作　　者：Aziz Belkadi ;Vincent Pedergnana ;Aurélie Cobat 等

出　　处：Proceedings of the National Academy of Sciences. 2016 ;113(24):6713-6718.doi:10.1073/pnas.1606460113

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

文章 ID：179204169

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4.An eQTL variant of ZXDC is associated with IFN-γ production following Mycobacterium tuberculosis antigen-specific stimulation

作　　者：Fabienne Jabot-Hanin ;Aurélie Cobat ;Jacqueline Feinberg 等

出　　处：Scientific Reports. 2017 ;7(1).doi:10.1038/s41598-017-13017-8

出版社：Springer Nature

文章 ID：235895870

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5.A genome-wide case-only test for the detection of digenic inheritance in human exomes

作　　者：Gaspard Kerner ;Matthieu Bouaziz ;Aurélie Cobat 等

出　　处：Proceedings of the National Academy of Sciences. 2020 ;117(32):19367-19375.doi:10.1073/pnas.1920650117

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

文章 ID：260995290

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6.Reply to Zhang et al.: The differential role of LRRK2 variants in nested leprosy phenotypes

作　　者：Vinicius M. Fava ;Aurélie Cobat ;Chaïma Gzara 等

出　　处：Proceedings of the National Academy of Sciences. 2020 ;117(19):10124-10125.doi:10.1073/pnas.2002654117

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

文章 ID：260996376

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7.Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants

作　　者：Aziz Belkadi ;Alexandre Bolze ;Yuval Itan 等

出　　处：Proceedings of the National Academy of Sciences. 2015 ;112(17):5473-5478.doi:10.1073/pnas.1418631112

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

文章 ID：101155462

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8.Controlling for human population stratification in rare variant association studies

作　　者：Matthieu Bouaziz ;Jimmy Mullaert ;Benedetta Bigio 等

出　　处：Scientific Reports. 2021 ;11.doi:10.1038/s41598-021-98370-5

出版社：Springer Nature

文章 ID：1035674116

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