Literature DB >> 26067110

CHCHD2 and Parkinson's disease.

Iris E Jansen1, Jose M Bras2, Suzanne Lesage3, Claudia Schulte4, J Raphael Gibbs5, Mike A Nalls5, Alexis Brice3, Nicholas W Wood2, Huw Morris6, John A Hardy7, Andrew B Singleton5, Thomas Gasser4, Peter Heutink8, Manu Sharma9.   

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Year:  2015        PMID： 26067110     DOI： 10.1016/S1474-4422(15)00094-0

Source DB:  PubMed          Journal:  Lancet Neurol        ISSN： 1474-4422            Impact factor:   44.182


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  15 in total

Review 1.  Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.

Authors:  Zhi-Dong Zhou; Wuan-Ting Saw; Eng-King Tan
Journal:  Mol Neurobiol       Date:  2016-09-08       Impact factor: 5.590

2.  Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.

Authors:  Isabella R Straub; Alexandre Janer; Woranontee Weraarpachai; Lorne Zinman; Janice Robertson; Ekaterina Rogaeva; Eric A Shoubridge
Journal:  Hum Mol Genet       Date:  2018-01-01       Impact factor: 6.150

3.  Understanding the role of genetic variability in LRRK2 in Indian population.

Authors:  Asha Kishore; Ashwin Ashok Kumar Sreelatha; Marc Sturm; Felix von-Zweydorf; Lasse Pihlstrøm; Francesco Raimondi; Rob Russell; Peter Lichtner; Moinak Banerjee; Syam Krishnan; Roopa Rajan; Divya Kalikavil Puthenveedu; Sun Ju Chung; Peter Bauer; Olaf Riess; Christian Johannes Gloeckner; Rejko Kruger; Thomas Gasser; Manu Sharma
Journal:  Mov Disord       Date:  2018-11-28       Impact factor: 10.338

Review 4.  Mitochondrial CHCHD2: Disease-Associated Mutations, Physiological Functions, and Current Animal Models.

Authors:  Teresa R Kee; Pamela Espinoza Gonzalez; Jessica L Wehinger; Mohammed Zaheen Bukhari; Aizara Ermekbaeva; Apoorva Sista; Peter Kotsiviras; Tian Liu; David E Kang; Jung-A A Woo
Journal:  Front Aging Neurosci       Date:  2021-04-22       Impact factor: 5.750

Review 5.  New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

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

6.  PD-linked CHCHD2 mutations impair CHCHD10 and MICOS complex leading to mitochondria dysfunction.

Authors:  Wei Zhou; Dongrui Ma; Alfred Xuyang Sun; Hoang-Dai Tran; Dong-Liang Ma; Brijesh K Singh; Jin Zhou; Jinyan Zhang; Danlei Wang; Yi Zhao; Paul M Yen; Eyleen Goh; Eng-King Tan
Journal:  Hum Mol Genet       Date:  2019-04-01       Impact factor: 6.150

Review 7.  Mitochondrial Dysfunction in Parkinson's Disease-Cause or Consequence?

Authors:  Chun Chen; Doug M Turnbull; Amy K Reeve
Journal:  Biology (Basel)       Date:  2019-05-11

8.  A comprehensive screening of copy number variability in dementia with Lewy bodies.

Authors:  Celia Kun-Rodrigues; Tatiana Orme; Susana Carmona; Dena G Hernandez; Owen A Ross; John D Eicher; Claire Shepherd; Laura Parkkinen; Lee Darwent; Michael G Heckman; Sonja W Scholz; Juan C Troncoso; Olga Pletnikova; Ted Dawson; Liana Rosenthal; Olaf Ansorge; Jordi Clarimon; Alberto Lleo; Estrella Morenas-Rodriguez; Lorraine Clark; Lawrence S Honig; Karen Marder; Afina Lemstra; Ekaterina Rogaeva; Peter St George-Hyslop; Elisabet Londos; Henrik Zetterberg; Imelda Barber; Anne Braae; Kristelle Brown; Kevin Morgan; Claire Troakes; Safa Al-Sarraj; Tammaryn Lashley; Janice Holton; Yaroslau Compta; Vivianna Van Deerlin; Geidy E Serrano; Thomas G Beach; Suzanne Lesage; Douglas Galasko; Eliezer Masliah; Isabel Santana; Pau Pastor; Monica Diez-Fairen; Miquel Aguilar; Pentti J Tienari; Liisa Myllykangas; Minna Oinas; Tamas Revesz; Andrew Lees; Brad F Boeve; Ronald C Petersen; Tanis J Ferman; Valentina Escott-Price; Neill Graff-Radford; Nigel J Cairns; John C Morris; Stuart Pickering-Brown; David Mann; Glenda M Halliday; John Hardy; John Q Trojanowski; Dennis W Dickson; Andrew Singleton; David J Stone; Rita Guerreiro; Jose Bras
Journal:  Neurobiol Aging       Date:  2018-10-24       Impact factor: 4.673

9.  A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease.

Authors:  Celia Kun-Rodrigues; Christos Ganos; Rita Guerreiro; Susanne A Schneider; Claudia Schulte; Suzanne Lesage; Lee Darwent; Peter Holmans; Andrew Singleton; Kailash Bhatia; Jose Bras
Journal:  Hum Mol Genet       Date:  2015-09-11       Impact factor: 6.150

10.  Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction.

Authors:  Richard G Lee; Maryam Sedghi; Mehri Salari; Anne-Marie J Shearwood; Maike Stentenbach; Ariana Kariminejad; Hayley Goullee; Oliver Rackham; Nigel G Laing; Homa Tajsharghi; Aleksandra Filipovska
Journal:  Neurol Genet       Date:  2018-10-05
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