Literature DB >> 27787935

Large 3-Mb deletions at 22q11.2 locus in Parkinson's disease and schizophrenia.

Jia Nee Foo1,2, Jimmy Lee3,4, Louis C Tan5, Jianjun Liu2, Eng-King Tan4,5.   

Abstract

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Mesh：

Year:  2016        PMID： 27787935     DOI： 10.1002/mds.26822

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  4 in total

Review 1.  The contribution of CNVs to the most common aging-related neurodegenerative diseases.

Authors:  Giulia Gentile; Valentina La Cognata; Sebastiano Cavallaro
Journal:  Aging Clin Exp Res       Date:  2020-02-06       Impact factor: 3.636

2.  Parkinson's disease with hypocalcaemia: adult presentation of 22q11.2 deletion syndrome.

Authors:  Fradique Moreira; Ana Brás; Joana Ramos Lopes; Cristina Januário
Journal:  BMJ Case Rep       Date:  2018-03-22

Review 3.  New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

Authors:  Andreas Puschmann
Journal:  Curr Neurol Neurosci Rep       Date:  2017-09       Impact factor: 5.081

4.  Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.

Authors:  Nancy J Butcher; Daniele Merico; Mehdi Zarrei; Lucas Ogura; Christian R Marshall; Eva W C Chow; Anthony E Lang; Stephen W Scherer; Anne S Bassett
Journal:  PLoS One       Date:  2017-04-21       Impact factor: 3.240
  4 in total

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