Literature DB >> 21814258

Growth of genome screening needs debate.

David B Goldstein1.   

Abstract

Mesh：

Year:  2011        PMID： 21814258     DOI： 10.1038/476027a

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  9 in total

1.  Genetic heterogeneity in human disease.

Authors:  Jon McClellan; Mary-Claire King
Journal:  Cell       Date:  2010-04-16       Impact factor: 41.582

2.  Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.

Authors:  Y M Dennis Lo; K C Allen Chan; Hao Sun; Eric Z Chen; Peiyong Jiang; Fiona M F Lun; Yama W Zheng; Tak Y Leung; Tze K Lau; Charles R Cantor; Rossa W K Chiu
Journal:  Sci Transl Med       Date:  2010-12-08       Impact factor: 17.956

Review 3.  Copy-number variants in neurodevelopmental disorders: promises and challenges.

Authors:  Alison K Merikangas; Aiden P Corvin; Louise Gallagher
Journal:  Trends Genet       Date:  2009-11-10       Impact factor: 11.639

Review 4.  Initial impact of the sequencing of the human genome.

Authors:  Eric S Lander
Journal:  Nature       Date:  2011-02-10       Impact factor: 49.962

5.  Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.

Authors:  Erin L Heinzen; Rodney A Radtke; Thomas J Urban; Gianpiero L Cavalleri; Chantal Depondt; Anna C Need; Nicole M Walley; Paola Nicoletti; Dongliang Ge; Claudia B Catarino; John S Duncan; Dalia Kasperaviciūte; Sarah K Tate; Luis O Caboclo; Josemir W Sander; Lisa Clayton; Kristen N Linney; Kevin V Shianna; Curtis E Gumbs; Jason Smith; Kenneth D Cronin; Jessica M Maia; Colin P Doherty; Massimo Pandolfo; David Leppert; Lefkos T Middleton; Rachel A Gibson; Michael R Johnson; Paul M Matthews; David Hosford; Reetta Kälviäinen; Kai Eriksson; Anne-Mari Kantanen; Thomas Dorn; Jörg Hansen; Günter Krämer; Bernhard J Steinhoff; Heinz-Gregor Wieser; Dominik Zumsteg; Marcos Ortega; Nicholas W Wood; Julie Huxley-Jones; Mohamad Mikati; William B Gallentine; Aatif M Husain; Patrick G Buckley; Ray L Stallings; Mihai V Podgoreanu; Norman Delanty; Sanjay M Sisodiya; David B Goldstein
Journal:  Am J Hum Genet       Date:  2010-04-15       Impact factor: 11.025

6.  Carrier testing for severe childhood recessive diseases by next-generation sequencing.

Authors:  Callum J Bell; Darrell L Dinwiddie; Neil A Miller; Shannon L Hateley; Elena E Ganusova; Joann Mudge; Ray J Langley; Lu Zhang; Clarence C Lee; Faye D Schilkey; Vrunda Sheth; Jimmy E Woodward; Heather E Peckham; Gary P Schroth; Ryan W Kim; Stephen F Kingsmore
Journal:  Sci Transl Med       Date:  2011-01-12       Impact factor: 17.956

7.  A genome-wide comparison of the functional properties of rare and common genetic variants in humans.

Authors:  Qianqian Zhu; Dongliang Ge; Jessica M Maia; Mingfu Zhu; Slave Petrovski; Samuel P Dickson; Erin L Heinzen; Kevin V Shianna; David B Goldstein
Journal:  Am J Hum Genet       Date:  2011-03-31       Impact factor: 11.025

8.  Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics.

Authors:  H Christina Fan; Stephen R Quake
Journal:  PLoS One       Date:  2010-05-03       Impact factor: 3.240

9.  Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.

Authors:  Shaun M Purcell; Naomi R Wray; Jennifer L Stone; Peter M Visscher; Michael C O'Donovan; Patrick F Sullivan; Pamela Sklar
Journal:  Nature       Date:  2009-07-01       Impact factor: 49.962
  9 in total
  2 in total

1.  Adolescent idiopathic scoliosis (AIS), environment, exposome and epigenetics: a molecular perspective of postnatal normal spinal growth and the etiopathogenesis of AIS with consideration of a network approach and possible implications for medical therapy.

Authors:  R Geoffrey Burwell; Peter H Dangerfield; Alan Moulton; Theodoros B Grivas
Journal:  Scoliosis       Date:  2011-12-02

2.  Genome-wide meta-analyses of smoking behaviors in African Americans.

Authors:  S P David; A Hamidovic; G K Chen; A W Bergen; J Wessel; J L Kasberger; W M Brown; S Petruzella; E L Thacker; Y Kim; M A Nalls; G J Tranah; Y J Sung; C B Ambrosone; D Arnett; E V Bandera; D M Becker; L Becker; S I Berndt; L Bernstein; W J Blot; U Broeckel; S G Buxbaum; N Caporaso; G Casey; S J Chanock; S L Deming; W R Diver; C B Eaton; D S Evans; M K Evans; M Fornage; N Franceschini; T B Harris; B E Henderson; D G Hernandez; B Hitsman; J J Hu; S C Hunt; S A Ingles; E M John; R Kittles; S Kolb; L N Kolonel; L Le Marchand; Y Liu; K K Lohman; B McKnight; R C Millikan; A Murphy; C Neslund-Dudas; S Nyante; M Press; B M Psaty; D C Rao; S Redline; J L Rodriguez-Gil; B A Rybicki; L B Signorello; A B Singleton; J Smoller; B Snively; B Spring; J L Stanford; S S Strom; G E Swan; K D Taylor; M J Thun; A F Wilson; J S Witte; Y Yamamura; L R Yanek; K Yu; W Zheng; R G Ziegler; A B Zonderman; E Jorgenson; C A Haiman; H Furberg
Journal:  Transl Psychiatry       Date:  2012-05-22       Impact factor: 6.222
  2 in total

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