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Times Co-cited
Similarity
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Lionel Willatt, James Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David R FitzPatrick, Eddy Maher, Howard Martin, Josep Parnau,[...]. Am J Hum Genet 2005
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Microdeletions of 3q29 confer high risk for schizophrenia.
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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
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3q29 interstitial microduplication: a new syndrome in a three-generation family.
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Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.
Fabiola Quintero-Rivera, Pantea Sharifi-Hannauer, Julian A Martinez-Agosto. Am J Med Genet A 2010
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Association between microdeletion and microduplication at 16p11.2 and autism.
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Large recurrent microdeletions associated with schizophrenia.
Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp,[...]. Nature 2008
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Structural variation of chromosomes in autism spectrum disorder.
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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
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Microduplications of 16p11.2 are associated with schizophrenia.
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Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
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Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.
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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
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Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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Functional impact of global rare copy number variation in autism spectrum disorders.
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Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
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Phenotypic variability and genetic susceptibility to genomic disorders.
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De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
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1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
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Strong association of de novo copy number mutations with autism.
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Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
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Detection of large-scale variation in the human genome.
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3q29 Microdeletion: a mental retardation disorder unassociated with a recognizable phenotype in two mother-daughter pairs.
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
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The 3q29 deletion confers >40-fold increase in risk for schizophrenia.
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A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.
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Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
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Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
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A clinical case report and literature review of the 3q29 microdeletion syndrome.
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3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
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Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.
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Population analysis of large copy number variants and hotspots of human genetic disease.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.