ROBIN KOCHEL to Phenotype
This is a "connection" page, showing publications ROBIN KOCHEL has written about Phenotype.
Connection Strength
0.918
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Neurocognitive and Neurobehavioral Phenotype of Youth with Schaaf-Yang Syndrome. J Autism Dev Disord. 2020 Jul; 50(7):2491-2500.
Score: 0.168
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The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications. J Autism Dev Disord. 2017 Mar; 47(3):549-562.
Score: 0.133
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The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions. JAMA Psychiatry. 2015 Feb; 72(2):119-26.
Score: 0.115
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Expression of the broad autism phenotype in simplex autism families from the Simons Simplex Collection. J Autism Dev Disord. 2014 Oct; 44(10):2392-9.
Score: 0.113
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Level of functioning in autism spectrum disorders: phenotypic congruence among affected siblings. J Autism Dev Disord. 2008 Jul; 38(6):1019-27.
Score: 0.070
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Clinical phenotype of the recurrent 1q21.1 copy-number variant. Genet Med. 2016 Apr; 18(4):341-9.
Score: 0.059
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The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population. Biol Psychiatry. 2015 May 01; 77(9):785-93.
Score: 0.055
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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. J Med Genet. 2012 Oct; 49(10):660-8.
Score: 0.049
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Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders. Neuron. 2012 Mar 22; 73(6):1063-7.
Score: 0.047
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Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder. J Autism Dev Disord. 2017 Nov; 47(11):3600-3607.
Score: 0.035
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Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia. Eur J Hum Genet. 2011 Feb; 19(2):152-6.
Score: 0.021
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The MTHFR 677C-->T polymorphism and behaviors in children with autism: exploratory genotype-phenotype correlations. Autism Res. 2009 Apr; 2(2):98-108.
Score: 0.019
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Developmental trajectories for young children with 16p11.2 copy number variation. Am J Med Genet B Neuropsychiatr Genet. 2017 Jun; 174(4):367-380.
Score: 0.017
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Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication. J Autism Dev Disord. 2016 Aug; 46(8):2734-2748.
Score: 0.016