Literature DB >> 21254448

A genotype resource for postmortem brain samples from the Autism Tissue Program.

Richard F Wintle1, Anath C Lionel, Pingzhao Hu, Stephen D Ginsberg, Dalila Pinto, Bhooma Thiruvahindrapduram, John Wei, Christian R Marshall, Jane Pickett, Edwin H Cook, Stephen W Scherer.   

Abstract

The Autism Tissue Program (ATP), a science program of Autism Speaks, provides researchers with access to well-characterized postmortem brain tissues. Researchers access these tissues through a peer-reviewed, project-based approval process, and obtain related clinical information from a secure, online informatics portal. However, few of these samples have DNA banked from other sources (such as a blood sample from the same individual), hindering genotype-phenotype correlation and interpretation of gene expression data derived from the banked brain tissue. Here, we describe an initiative to extract DNA from Brodmann Area 19, and genotype these samples using both the Affymetrix Genome-Wide Human SNP Array 6.0 and the Illumina Human1M-Duo DNA Analysis BeadChip genome-wide microarray technologies. We additionally verify reported gender, and infer ethnic background from the single nucleotide polymorphism data. We have also used a rigorous, multiple algorithm approach to identify genomic copy number variation (CNV) from these array data. Following an initial proof of principle study using two samples, 52 experimental samples, consisting of 27 subjects with confirmed or suspected autism and related disorders, 5 subjects with cytogenetically visible duplications of 15q, 2 with epilepsy and 18 age-matched normal controls were processed, yielding high-quality genotype data in all cases. The genotype and CNV data are provided via the ATP informatics portal as a resource for the autism research community.
Copyright © 2011, International Society for Autism Research, Wiley Periodicals, Inc.

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Mesh:

Year:  2011        PMID: 21254448      PMCID: PMC4605268          DOI: 10.1002/aur.173

Source DB:  PubMed          Journal:  Autism Res        ISSN: 1939-3806            Impact factor:   5.216


  37 in total

1.  Evaluation of whole genome amplification methods using postmortem brain samples.

Authors:  Kazuya Iwamoto; Junko Ueda; Yoko Nakano; Miki Bundo; Wataru Ukai; Eri Hashimoto; Toshikazu Saito; Tadafumi Kato
Journal:  J Neurosci Methods       Date:  2007-06-02       Impact factor: 2.390

2.  A simple method for comparing microarray genotype data between brain and other tissues.

Authors:  Mark E Ruff; Roger Pamphlett
Journal:  J Neurosci Methods       Date:  2008-07-03       Impact factor: 2.390

3.  A genome-wide association study of alcohol dependence.

Authors:  Laura J Bierut; Arpana Agrawal; Kathleen K Bucholz; Kimberly F Doheny; Cathy Laurie; Elizabeth Pugh; Sherri Fisher; Louis Fox; William Howells; Sarah Bertelsen; Anthony L Hinrichs; Laura Almasy; Naomi Breslau; Robert C Culverhouse; Danielle M Dick; Howard J Edenberg; Tatiana Foroud; Richard A Grucza; Dorothy Hatsukami; Victor Hesselbrock; Eric O Johnson; John Kramer; Robert F Krueger; Samuel Kuperman; Michael Lynskey; Karl Mann; Rosalind J Neuman; Markus M Nöthen; John I Nurnberger; Bernice Porjesz; Monika Ridinger; Nancy L Saccone; Scott F Saccone; Marc A Schuckit; Jay A Tischfield; Jen C Wang; Marcella Rietschel; Alison M Goate; John P Rice
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-02       Impact factor: 11.205

4.  Autism post-mortem neuroinformatic resource: the autism tissue program (ATP) informatics portal.

Authors:  Michael B Brimacombe; Richard Pickett; Jane Pickett
Journal:  J Autism Dev Disord       Date:  2007-03

5.  Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Authors:  Joseph T Glessner; Kai Wang; Guiqing Cai; Olena Korvatska; Cecilia E Kim; Shawn Wood; Haitao Zhang; Annette Estes; Camille W Brune; Jonathan P Bradfield; Marcin Imielinski; Edward C Frackelton; Jennifer Reichert; Emily L Crawford; Jeffrey Munson; Patrick M A Sleiman; Rosetta Chiavacci; Kiran Annaiah; Kelly Thomas; Cuiping Hou; Wendy Glaberson; James Flory; Frederick Otieno; Maria Garris; Latha Soorya; Lambertus Klei; Joseph Piven; Kacie J Meyer; Evdokia Anagnostou; Takeshi Sakurai; Rachel M Game; Danielle S Rudd; Danielle Zurawiecki; Christopher J McDougle; Lea K Davis; Judith Miller; David J Posey; Shana Michaels; Alexander Kolevzon; Jeremy M Silverman; Raphael Bernier; Susan E Levy; Robert T Schultz; Geraldine Dawson; Thomas Owley; William M McMahon; Thomas H Wassink; John A Sweeney; John I Nurnberger; Hilary Coon; James S Sutcliffe; Nancy J Minshew; Struan F A Grant; Maja Bucan; Edwin H Cook; Joseph D Buxbaum; Bernie Devlin; Gerard D Schellenberg; Hakon Hakonarson
Journal:  Nature       Date:  2009-04-28       Impact factor: 49.962

Review 6.  Challenges and standards in integrating surveys of structural variation.

Authors:  Stephen W Scherer; Charles Lee; Ewan Birney; David M Altshuler; Evan E Eichler; Nigel P Carter; Matthew E Hurles; Lars Feuk
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

Review 7.  PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships.

Authors:  Michael Krawczak; Susanna Nikolaus; Huberta von Eberstein; Peter J P Croucher; Nour Eddine El Mokhtari; Stefan Schreiber
Journal:  Community Genet       Date:  2006

8.  Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.

Authors:  L Palmieri; V Papaleo; V Porcelli; P Scarcia; L Gaita; R Sacco; J Hager; F Rousseau; P Curatolo; B Manzi; R Militerni; C Bravaccio; S Trillo; C Schneider; R Melmed; M Elia; C Lenti; M Saccani; T Pascucci; S Puglisi-Allegra; K-L Reichelt; A M Persico
Journal:  Mol Psychiatry       Date:  2008-07-08       Impact factor: 15.992

9.  Singleton deletions throughout the genome increase risk of bipolar disorder.

Authors:  D Zhang; L Cheng; Y Qian; N Alliey-Rodriguez; J R Kelsoe; T Greenwood; C Nievergelt; T B Barrett; R McKinney; N Schork; E N Smith; C Bloss; J Nurnberger; H J Edenberg; T Foroud; W Sheftner; W B Lawson; E A Nwulia; M Hipolito; W Coryell; J Rice; W Byerley; F McMahon; T G Schulze; W Berrettini; J B Potash; P L Belmonte; P P Zandi; M G McInnis; S Zöllner; D Craig; S Szelinger; D Koller; S L Christian; C Liu; E S Gershon
Journal:  Mol Psychiatry       Date:  2008-12-30       Impact factor: 15.992

10.  Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.

Authors:  Michael S L Ching; Yiping Shen; Wen-Hann Tan; Shafali S Jeste; Eric M Morrow; Xiaoli Chen; Nahit M Mukaddes; Seung-Yun Yoo; Ellen Hanson; Rachel Hundley; Christina Austin; Ronald E Becker; Gerard T Berry; Katherine Driscoll; Elizabeth C Engle; Sandra Friedman; James F Gusella; Fuki M Hisama; Mira B Irons; Tina Lafiosca; Elaine LeClair; David T Miller; Michael Neessen; Jonathan D Picker; Leonard Rappaport; Cynthia M Rooney; Dean P Sarco; Joan M Stoler; Christopher A Walsh; Robert R Wolff; Ting Zhang; Ramzi H Nasir; Bai-Lin Wu
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2010-06-05       Impact factor: 3.568

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  14 in total

1.  Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders.

Authors:  Li Zhu; Xiaoming Wang; Xin-Lei Li; Aaron Towers; Xinyu Cao; Ping Wang; Rachel Bowman; Hyuna Yang; Jennifer Goldstein; Yi-Ju Li; Yong-Hui Jiang
Journal:  Hum Mol Genet       Date:  2013-11-01       Impact factor: 6.150

2.  RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.

Authors:  Brent L Fogel; Eric Wexler; Amanda Wahnich; Tara Friedrich; Chandran Vijayendran; Fuying Gao; Neelroop Parikshak; Genevieve Konopka; Daniel H Geschwind
Journal:  Hum Mol Genet       Date:  2012-06-23       Impact factor: 6.150

3.  Increased CYFIP1 dosage alters cellular and dendritic morphology and dysregulates mTOR.

Authors:  A Oguro-Ando; C Rosensweig; E Herman; Y Nishimura; D Werling; B R Bill; J M Berg; F Gao; G Coppola; B S Abrahams; D H Geschwind
Journal:  Mol Psychiatry       Date:  2014-10-14       Impact factor: 15.992

4.  Somatic activation of AKT3 causes hemispheric developmental brain malformations.

Authors:  Annapurna Poduri; Gilad D Evrony; Xuyu Cai; Princess Christina Elhosary; Rameen Beroukhim; Maria K Lehtinen; L Benjamin Hills; Erin L Heinzen; Anthony Hill; R Sean Hill; Brenda J Barry; Blaise F D Bourgeois; James J Riviello; A James Barkovich; Peter M Black; Keith L Ligon; Christopher A Walsh
Journal:  Neuron       Date:  2012-04-12       Impact factor: 17.173

Review 5.  Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder.

Authors:  Brent R Bill; Jennifer K Lowe; Christina T Dybuncio; Brent L Fogel
Journal:  Int Rev Neurobiol       Date:  2013       Impact factor: 3.230

Review 6.  Regulatory genes and pathways disrupted in autism spectrum disorders.

Authors:  Fatma Ayhan; Genevieve Konopka
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2018-08-28       Impact factor: 5.067

7.  RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.

Authors:  Hui Y Xiong; Babak Alipanahi; Leo J Lee; Hannes Bretschneider; Daniele Merico; Ryan K C Yuen; Yimin Hua; Serge Gueroussov; Hamed S Najafabadi; Timothy R Hughes; Quaid Morris; Yoseph Barash; Adrian R Krainer; Nebojsa Jojic; Stephen W Scherer; Benjamin J Blencowe; Brendan J Frey
Journal:  Science       Date:  2014-12-18       Impact factor: 47.728

8.  Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons.

Authors:  Eric Deneault; Sean H White; Deivid C Rodrigues; P Joel Ross; Muhammad Faheem; Kirill Zaslavsky; Zhuozhi Wang; Roumiana Alexandrova; Giovanna Pellecchia; Wei Wei; Alina Piekna; Gaganjot Kaur; Jennifer L Howe; Vickie Kwan; Bhooma Thiruvahindrapuram; Susan Walker; Anath C Lionel; Peter Pasceri; Daniele Merico; Ryan K C Yuen; Karun K Singh; James Ellis; Stephen W Scherer
Journal:  Stem Cell Reports       Date:  2018-11-01       Impact factor: 7.765

9.  Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.

Authors:  Alissa M D'Gama; Sirisha Pochareddy; Mingfeng Li; Saumya S Jamuar; Rachel E Reiff; Anh-Thu N Lam; Nenad Sestan; Christopher A Walsh
Journal:  Neuron       Date:  2015-12-02       Impact factor: 17.173

10.  Brain transcriptional and epigenetic associations with autism.

Authors:  Matthew R Ginsberg; Robert A Rubin; Tatiana Falcone; Angela H Ting; Marvin R Natowicz
Journal:  PLoS One       Date:  2012-09-12       Impact factor: 3.240

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