Literature DB >> 20955932

Allelic diversity in human developmental neurogenetics: insights into biology and disease.

Christopher A Walsh1, Elizabeth C Engle.   

Abstract

One of the biggest challenges in neuroscience is illuminating the architecture of developmental brain disorders, which include structural malformations of the brain and nerves, intellectual disability, epilepsy, and some psychiatric conditions like autism and potentially schizophrenia. Ongoing gene identification reveals a great diversity of genetic causes underlying abnormal brain development, illuminating new biochemical pathways often not suspected based on genetic studies in other organisms. Our greater understanding of genetic disease also shows the complexity of allelic diversity, in which distinct mutations in a given gene can cause a wide range of distinct diseases or other phenotypes. These diverse alleles not only provide a platform for discovery of critical protein-protein interactions in a genetic fashion, but also illuminate the likely genetic architecture of as yet poorly characterized neurological disorders.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20955932      PMCID: PMC3010396          DOI: 10.1016/j.neuron.2010.09.042

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  66 in total

1.  Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.

Authors:  Yuanyi Feng; Ming Hui Chen; Ivan P Moskowitz; Ashley M Mendonza; Luis Vidali; Fumihiko Nakamura; David J Kwiatkowski; Christopher A Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-15       Impact factor: 11.205

2.  A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.

Authors:  V des Portes; J M Pinard; P Billuart; M C Vinet; A Koulakoff; A Carrié; A Gelot; E Dupuis; J Motte; Y Berwald-Netter; M Catala; A Kahn; C Beldjord; J Chelly
Journal:  Cell       Date:  1998-01-09       Impact factor: 41.582

3.  Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.

Authors:  J G Gleeson; K M Allen; J W Fox; E D Lamperti; S Berkovic; I Scheffer; E C Cooper; W B Dobyns; S R Minnerath; M E Ross; C A Walsh
Journal:  Cell       Date:  1998-01-09       Impact factor: 41.582

4.  Rac-GAP alpha-chimerin regulates motor-circuit formation as a key mediator of EphrinB3/EphA4 forward signaling.

Authors:  Takuji Iwasato; Hironori Katoh; Hiroshi Nishimaru; Yukio Ishikawa; Haruhisa Inoue; Yoshikazu M Saito; Reiko Ando; Mizuho Iwama; Ryosuke Takahashi; Manabu Negishi; Shigeyoshi Itohara
Journal:  Cell       Date:  2007-08-24       Impact factor: 41.582

5.  Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.

Authors:  Renzo Guerrini; Francesca Moro; Eva Andermann; Elaine Hughes; Daniela D'Agostino; Romeo Carrozzo; Andrea Bernasconi; Frances Flinter; Lucio Parmeggiani; Anna Volzone; Elena Parrini; Davide Mei; Jozef M Jarosz; Robin G Morris; Polly Pratt; Gaetano Tortorella; François Dubeau; Frederick Andermann; William B Dobyns; Soma Das
Journal:  Ann Neurol       Date:  2003-07       Impact factor: 10.422

6.  Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis.

Authors:  Joanna C Jen; Wai-Man Chan; Thomas M Bosley; Jijun Wan; Janai R Carr; Udo Rüb; David Shattuck; Georges Salamon; Lili C Kudo; Jing Ou; Doris D M Lin; Mustafa A M Salih; Tülay Kansu; Hesham Al Dhalaan; Zayed Al Zayed; David B MacDonald; Bent Stigsby; Andreas Plaitakis; Emmanuel K Dretakis; Irene Gottlob; Christina Pieh; Elias I Traboulsi; Qing Wang; Lejin Wang; Caroline Andrews; Koki Yamada; Joseph L Demer; Shaheen Karim; Jeffry R Alger; Daniel H Geschwind; Thomas Deller; Nancy L Sicotte; Stanley F Nelson; Robert W Baloh; Elizabeth C Engle
Journal:  Science       Date:  2004-04-22       Impact factor: 47.728

7.  Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

Authors:  J W Fox; E D Lamperti; Y Z Ekşioğlu; S E Hong; Y Feng; D A Graham; I E Scheffer; W B Dobyns; B A Hirsch; R A Radtke; S F Berkovic; P R Huttenlocher; C A Walsh
Journal:  Neuron       Date:  1998-12       Impact factor: 17.173

8.  A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Authors:  Dan E Arking; David J Cutler; Camille W Brune; Tanya M Teslovich; Kristen West; Morna Ikeda; Alexis Rea; Moltu Guy; Shin Lin; Edwin H Cook; Aravinda Chakravarti
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

9.  A dual phenotype of periventricular nodular heterotopia and frontometaphyseal dysplasia in one patient caused by a single FLNA mutation leading to two functionally different aberrant transcripts.

Authors:  Martin Zenker; Anita Rauch; Andreas Winterpacht; Andreas Tagariello; Cornelia Kraus; Thomas Rupprecht; Heinrich Sticht; André Reis
Journal:  Am J Hum Genet       Date:  2004-02-25       Impact factor: 11.025

10.  Clinical genetic testing for patients with autism spectrum disorders.

Authors:  Yiping Shen; Kira A Dies; Ingrid A Holm; Carolyn Bridgemohan; Magdi M Sobeih; Elizabeth B Caronna; Karen J Miller; Jean A Frazier; Iris Silverstein; Jonathan Picker; Laura Weissman; Peter Raffalli; Shafali Jeste; Laurie A Demmer; Heather K Peters; Stephanie J Brewster; Sara J Kowalczyk; Beth Rosen-Sheidley; Caroline McGowan; Andrew W Duda; Sharyn A Lincoln; Kathryn R Lowe; Alison Schonwald; Michael Robbins; Fuki Hisama; Robert Wolff; Ronald Becker; Ramzi Nasir; David K Urion; Jeff M Milunsky; Leonard Rappaport; James F Gusella; Christopher A Walsh; Bai-Lin Wu; David T Miller
Journal:  Pediatrics       Date:  2010-03-15       Impact factor: 7.124

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  21 in total

1.  X11/Mint genes control polarized localization of axonal membrane proteins in vivo.

Authors:  Garrett G Gross; G Mohiddin Lone; Lok Kwan Leung; Volker Hartenstein; Ming Guo
Journal:  J Neurosci       Date:  2013-05-08       Impact factor: 6.167

Review 2.  Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations.

Authors:  Max A Tischfield; Gustav Y Cederquist; Mohan L Gupta; Elizabeth C Engle
Journal:  Curr Opin Genet Dev       Date:  2011-02-01       Impact factor: 5.578

3.  FLNA genomic rearrangements cause periventricular nodular heterotopia.

Authors:  K R Clapham; T W Yu; V S Ganesh; B Barry; Y Chan; D Mei; E Parrini; B Funalot; L Dupuis; M M Nezarati; C du Souich; C van Karnebeek; R Guerrini; C A Walsh
Journal:  Neurology       Date:  2012-01-11       Impact factor: 9.910

4.  Using whole-exome sequencing to identify inherited causes of autism.

Authors:  Timothy W Yu; Maria H Chahrour; Michael E Coulter; Sarn Jiralerspong; Kazuko Okamura-Ikeda; Bulent Ataman; Klaus Schmitz-Abe; David A Harmin; Mazhar Adli; Athar N Malik; Alissa M D'Gama; Elaine T Lim; Stephan J Sanders; Ganesh H Mochida; Jennifer N Partlow; Christine M Sunu; Jillian M Felie; Jacqueline Rodriguez; Ramzi H Nasir; Janice Ware; Robert M Joseph; R Sean Hill; Benjamin Y Kwan; Muna Al-Saffar; Nahit M Mukaddes; Asif Hashmi; Soher Balkhy; Generoso G Gascon; Fuki M Hisama; Elaine LeClair; Annapurna Poduri; Ozgur Oner; Samira Al-Saad; Sadika A Al-Awadi; Laila Bastaki; Tawfeg Ben-Omran; Ahmad S Teebi; Lihadh Al-Gazali; Valsamma Eapen; Christine R Stevens; Leonard Rappaport; Stacey B Gabriel; Kyriacos Markianos; Matthew W State; Michael E Greenberg; Hisaaki Taniguchi; Nancy E Braverman; Eric M Morrow; Christopher A Walsh
Journal:  Neuron       Date:  2013-01-23       Impact factor: 17.173

5.  Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects.

Authors:  Jong G Park; Max A Tischfield; Alicia A Nugent; Long Cheng; Silvio Alessandro Di Gioia; Wai-Man Chan; Gail Maconachie; Thomas M Bosley; C Gail Summers; David G Hunter; Caroline D Robson; Irene Gottlob; Elizabeth C Engle
Journal:  Am J Hum Genet       Date:  2016-05-12       Impact factor: 11.025

6.  Roles of heat shock factor 1 in neuronal response to fetal environmental risks and its relevance to brain disorders.

Authors:  Kazue Hashimoto-Torii; Masaaki Torii; Mitsuaki Fujimoto; Akira Nakai; Rachid El Fatimy; Valerie Mezger; Min J Ju; Seiji Ishii; Shih-Hui Chao; Kristen J Brennand; Fred H Gage; Pasko Rakic
Journal:  Neuron       Date:  2014-04-10       Impact factor: 17.173

7.  Canonical TGF-β Signaling Negatively Regulates Neuronal Morphogenesis through TGIF/Smad Complex-Mediated CRMP2 Suppression.

Authors:  Hideyuki Nakashima; Keita Tsujimura; Koichiro Irie; Masataka Ishizu; Miao Pan; Tomonori Kameda; Kinichi Nakashima
Journal:  J Neurosci       Date:  2018-04-25       Impact factor: 6.167

Review 8.  What disorders of cortical development tell us about the cortex: one plus one does not always make two.

Authors:  M Chiara Manzini; Christopher A Walsh
Journal:  Curr Opin Genet Dev       Date:  2011-02-01       Impact factor: 5.578

Review 9.  Toward developmental models of psychiatric disorders in zebrafish.

Authors:  William H J Norton
Journal:  Front Neural Circuits       Date:  2013-04-26       Impact factor: 3.492

10.  Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.

Authors:  Martin Breuss; Julian Ik-Tsen Heng; Karine Poirier; Guoling Tian; Xavier Hubert Jaglin; Zhengdong Qu; Andreas Braun; Thomas Gstrein; Linh Ngo; Matilda Haas; Nadia Bahi-Buisson; Marie-Laure Moutard; Sandrine Passemard; Alain Verloes; Pierre Gressens; Yunli Xie; Kathryn J H Robson; Deepa Selvi Rani; Kumarasamy Thangaraj; Tim Clausen; Jamel Chelly; Nicholas Justin Cowan; David Anthony Keays
Journal:  Cell Rep       Date:  2012-12-13       Impact factor: 9.423

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