Literature DB >> 20980985

A common mechanism for microcephaly.

Bernd Wollnik.   

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Year:  2010        PMID： 20980985     DOI： 10.1038/ng1110-923

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  6 in total

Review 1.  Cell-cycle control and cortical development.

Authors:  Colette Dehay; Henry Kennedy
Journal:  Nat Rev Neurosci       Date:  2007-06       Impact factor: 34.870

2.  Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.

Authors:  Timothy W Yu; Ganeshwaran H Mochida; David J Tischfield; Sema K Sgaier; Laura Flores-Sarnat; Consolato M Sergi; Meral Topçu; Marie T McDonald; Brenda J Barry; Jillian M Felie; Christine Sunu; William B Dobyns; Rebecca D Folkerth; A James Barkovich; Christopher A Walsh
Journal:  Nat Genet       Date:  2010-10-03       Impact factor: 38.330

Review 3.  Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options.

Authors:  Renzo Guerrini; William B Dobyns; A James Barkovich
Journal:  Trends Neurosci       Date:  2008-02-08       Impact factor: 13.837

4.  WDR62 is associated with the spindle pole and is mutated in human microcephaly.

Authors:  Adeline K Nicholas; Maryam Khurshid; Julie Désir; Ofélia P Carvalho; James J Cox; Gemma Thornton; Rizwana Kausar; Muhammad Ansar; Wasim Ahmad; Alain Verloes; Sandrine Passemard; Jean-Paul Misson; Susan Lindsay; Fanni Gergely; William B Dobyns; Emma Roberts; Marc Abramowicz; C Geoffrey Woods
Journal:  Nat Genet       Date:  2010-10-03       Impact factor: 38.330

5.  Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.

Authors:  Kaya Bilgüvar; Ali Kemal Oztürk; Angeliki Louvi; Kenneth Y Kwan; Murim Choi; Burak Tatli; Dilek Yalnizoğlu; Beyhan Tüysüz; Ahmet Okay Cağlayan; Sarenur Gökben; Hande Kaymakçalan; Tanyeri Barak; Mehmet Bakircioğlu; Katsuhito Yasuno; Winson Ho; Stephan Sanders; Ying Zhu; Sanem Yilmaz; Alp Dinçer; Michele H Johnson; Richard A Bronen; Naci Koçer; Hüseyin Per; Shrikant Mane; Mehmet Necmettin Pamir; Cengiz Yalçinkaya; Sefer Kumandaş; Meral Topçu; Meral Ozmen; Nenad Sestan; Richard P Lifton; Matthew W State; Murat Günel
Journal:  Nature       Date:  2010-08-22       Impact factor: 49.962

Review 6.  Primary microcephaly: do all roads lead to Rome?

Authors:  Gemma K Thornton; C Geoffrey Woods
Journal:  Trends Genet       Date:  2009-10-21       Impact factor: 11.639
  6 in total
  13 in total

1.  Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders.

Authors:  Elke Gabriel; Jay Gopalakrishnan
Journal:  J Vis Exp       Date:  2017-04-14       Impact factor: 1.355

Review 2.  Recent advances in the genetic etiology of brain malformations.

Authors:  David A Dyment; Sarah L Sawyer; Jodi Warman Chardon; Kym M Boycott
Journal:  Curr Neurol Neurosci Rep       Date:  2013-08       Impact factor: 5.081

3.  Opposing roles for JNK and Aurora A in regulating the association of WDR62 with spindle microtubules.

Authors:  Nicholas R Lim; Yvonne Y C Yeap; Teresa T Zhao; Yan Y Yip; Shu C Wong; Dan Xu; Ching-Seng Ang; Nicholas A Williamson; Zhiheng Xu; Marie A Bogoyevitch; Dominic C H Ng
Journal:  J Cell Sci       Date:  2015-02-01       Impact factor: 5.285

4.  Mutations in WDR62 gene in Pakistani families with autosomal recessive primary microcephaly.

Authors:  Rizwana Kousar; Muhammad Jawad Hassan; Bushra Khan; Sulman Basit; Saqib Mahmood; Asif Mir; Wasim Ahmad; Muhammad Ansar
Journal:  BMC Neurol       Date:  2011-10-01       Impact factor: 2.474

5.  Reciprocal Relationship between Head Size, an Autism Endophenotype, and Gene Dosage at 19p13.12 Points to AKAP8 and AKAP8L.

Authors:  Rebecca A Nebel; Jill Kirschen; Jinlu Cai; Young Jae Woo; Koshi Cherian; Brett S Abrahams
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240

6.  CPAP promotes timely cilium disassembly to maintain neural progenitor pool.

Authors:  Elke Gabriel; Arpit Wason; Anand Ramani; Li Ming Gooi; Patrick Keller; Andrei Pozniakovsky; Ina Poser; Florian Noack; Narasimha Swamy Telugu; Federico Calegari; Tomo Šarić; Jürgen Hescheler; Anthony A Hyman; Marco Gottardo; Giuliano Callaini; Fowzan Sami Alkuraya; Jay Gopalakrishnan
Journal:  EMBO J       Date:  2016-02-29       Impact factor: 11.598

Review 7.  Molecular and cellular insights into Zika virus-related neuropathies.

Authors:  Kai Zhou; Long Wang; Di Yu; Hesuyuan Huang; Hong Ji; Xuming Mo
Journal:  J Neurovirol       Date:  2017-01-26       Impact factor: 2.643

8.  Phf21b imprints the spatiotemporal epigenetic switch essential for neural stem cell differentiation.

Authors:  Amitava Basu; Iván Mestres; Sanjeeb Kumar Sahu; Neha Tiwari; Bimola Khongwir; Jan Baumgart; Aditi Singh; Federico Calegari; Vijay K Tiwari
Journal:  Genes Dev       Date:  2020-08-20       Impact factor: 11.361

9.  The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome.

Authors:  Laura M McDonell; Jodi Warman Chardon; Jeremy Schwartzentruber; Denise Foster; Chandree L Beaulieu; Jacek Majewski; Dennis E Bulman; Kym M Boycott
Journal:  BMC Neurol       Date:  2014-01-31       Impact factor: 2.474

10.  A novel single base pair duplication in WDR62 causes primary microcephaly.

Authors:  Verena Rupp; Sobiah Rauf; Ishrat Naveed; Christian Windpassinger; Asif Mir
Journal:  BMC Med Genet       Date:  2014-10-11       Impact factor: 2.103
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