STEPHANIE SHERMAN to Phenotype
This is a "connection" page, showing publications STEPHANIE SHERMAN has written about Phenotype.
Connection Strength
0.359
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Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. Genet Med. 2009 Feb; 11(2):79-89.
Score: 0.163
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New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics. 2011 May; 12(2):123-35.
Score: 0.047
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Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers. Behav Genet. 2008 Sep; 38(5):493-502.
Score: 0.039
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Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency. Ann N Y Acad Sci. 2008; 1135:99-111.
Score: 0.038
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Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome. Genet Epidemiol. 2004 Nov; 27(3):240-51.
Score: 0.030
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Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypes. Hum Mol Genet. 2020 01 15; 29(2):238-247.
Score: 0.022
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Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology. 2012 Mar; 26(2):156-64.
Score: 0.013
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Examination of the effect of the polymorphic CGG repeat in the FMR1 gene on cognitive performance. Behav Genet. 2005 Jul; 35(4):435-45.
Score: 0.008