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    Perrier, Rene

    TitleSoftware Developer 5
    SchoolLawrence Berkeley National Lab
    DepartmentJoint Genome Institute
    Address1 Cyclotron Road
    Berkeley CA 94720
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      Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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      1. Bone KM, Chernos JE, Perrier R, Innes AM, Bernier FP, McLeod R, Thomas MA. Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype. Prenat Diagn. 2017 Jun; 37(6):602-610. PMID: 28437579.
        View in: PubMed
      2. Liu DJ, Perrier R, Wei XC, Joseph JT, Strother D. Metachronous Type I pleuropulmonary blastoma and atypical choroid plexus papilloma in a young child. Pediatr Blood Cancer. 2016 Dec; 63(12):2240-2242. PMID: 27442759.
        View in: PubMed
      3. Rambau PF, Duggan MA, Ghatage P, Warfa K, Steed H, Perrier R, Kelemen LE, Köbel M. Significant frequency of MSH2/MSH6 abnormality in ovarian endometrioid carcinoma supports histotype-specific Lynch syndrome screening in ovarian carcinomas. Histopathology. 2016 Aug; 69(2):288-97. PMID: 26799366.
        View in: PubMed
      4. Lazier J, Mah JK, Nikolic A, Wei XC, Samedi V, Fajardo C, Brindle M, Perrier R, Thomas MA. Bilateral congenital lumbar hernias in a patient with central core disease--A case report. Neuromuscul Disord. 2016 Jan; 26(1):56-9. PMID: 26684984.
        View in: PubMed
      5. Innes AM, Boycott KM, Puffenberger EG, Redl D, MacDonald IM, Chudley AE, Beaulieu C, Perrier R, Gillan T, Wade A, Parboosingh JS. A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. Clin Genet. 2010 Nov; 78(5):424-31. PMID: 20618352.
        View in: PubMed

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