review Open AccessTop 1% cited
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
The American Journal of Human Genetics · 2010 · Vol. 86(5) · pp. 749–764
David T. Miller✉(Boston Children's Hospital)Margaret P Adam(Emory University)Swaroop AradhyaLeslie G. Biesecker(National Institutes of Health)Arthur R. Brothman(ARUP Laboratories (United States))Nigel P. Carter(Wellcome Sanger Institute)Deanna M. Church(National Center for Biotechnology Information)John A. Crolla(Wessex Regional Genetics Laboratory)Evan E. Eichler(University of Washington)Charles J. Epstein(University of California, San Francisco)W. Andrew Faucett(Emory University)Lars Feuk(Uppsala University)Jan M. Friedman(University of British Columbia)Ada Hamosh(Johns Hopkins University)Laird Jackson(Drexel University)Erin B. Kaminsky(Emory University)Klaas Kok(University of Groningen)Ian D. Krantz(University of Pennsylvania)Robert M. Kuhn(University of California, Santa Cruz)Charles Lee(Harvard University)James M. Ostell(National Center for Biotechnology Information)Carla RosenbergStephen W. Scherer(SickKids Foundation)Nancy B. Spinner(Philadelphia University)Dimitri J. Stavropoulos(Hospital for Sick Children)James Tepperberg(Triangle)Erik C. Thorland(Mayo Clinic in Arizona)Joris VermeeschDarrel Waggoner(University of Chicago)Michael S. Watson(American College of Medical Genetics)Alastair J. Martin(Emory University)David H. Ledbetter(Emory University)
Genomic variations and chromosomal abnormalitiesCongenital heart defects researchPrenatal Screening and DiagnosticsStatement (logic)Test (biology)MicroarrayMicroarray analysis techniquesIntellectual disabilityMedicinePsychologyGeneticsBiologyGene
MeSH terms
Congenital AbnormalitiesChildDevelopmental DisabilitiesChromosome BandingHumansKaryotypingChromosome Disorders
Funding
- Howard Hughes Medical Institute
- Simons Foundation
- ACMG Foundation for Genetic and Genomic Medicine
- ARUP Laboratories
Citations
2,855
FWCI
116.26
field-weighted impact
References
115
Percentile
100%
vs. same field & year
Citations per year
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References
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The American Journal of Human Genetics · 2009 · 2,072 citations
Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.
Journal of Medical Genetics · 1992 · 418 citations
Structural variation in the human genome
Nature Reviews Genetics · 2006 · 2,063 citations
Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports
Journal of Medical Genetics · 2006 · 417 citations
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
Journal of Medical Genetics · 2004 · 508 citations
Structural Variation of Chromosomes in Autism Spectrum Disorder
The American Journal of Human Genetics · 2008 · 1,832 citations
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
Journal of Medical Genetics · 2005 · 412 citations
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
Journal of Medical Genetics · 2008 · 430 citations
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