STEPHANIE SHERMAN to Male
This is a "connection" page, showing publications STEPHANIE SHERMAN has written about Male.
Connection Strength
0.255
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Men with an FMR1 premutation and their health education needs. J Genet Couns. 2021 08; 30(4):1156-1167.
Score: 0.023
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Study of telomere length in men who carry a fragile X premutation or full mutation allele. Hum Genet. 2020 Dec; 139(12):1531-1539.
Score: 0.022
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The association between maternal occupation and down syndrome: A report from the national Down syndrome project. Int J Hyg Environ Health. 2020 01; 223(1):207-213.
Score: 0.020
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An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. PLoS One. 2014; 9(6):e99560.
Score: 0.014
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The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project. Genet Med. 2013 Sep; 15(9):698-705.
Score: 0.013
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Olfactory dysfunction in fragile X tremor ataxia syndrome. Mov Disord. 2012 Oct; 27(12):1556-9.
Score: 0.013
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New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS). Neurogenetics. 2011 May; 12(2):123-35.
Score: 0.011
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Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population. Ann Hum Genet. 2010 Jul; 74(4):316-25.
Score: 0.011
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Examination of FMR1 transcript and protein levels among 74 premutation carriers. J Hum Genet. 2010 Jan; 55(1):66-8.
Score: 0.010
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Investigation of factors associated with paternal nondisjunction of chromosome 21. Am J Med Genet A. 2009 Aug; 149A(8):1685-90.
Score: 0.010
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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: 0.010
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No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. Am J Hum Genet. 2008 Dec; 83(6):692-702.
Score: 0.010
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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: 0.009
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The National Down Syndrome Project: design and implementation. Public Health Rep. 2007 Jan-Feb; 122(1):62-72.
Score: 0.008
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Epidemiology of Down syndrome. Ment Retard Dev Disabil Res Rev. 2007; 13(3):221-7.
Score: 0.008
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A study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum Genet. 2004 Apr; 114(5):439-47.
Score: 0.007
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Prevalence of the fragile X syndrome in African-Americans. Am J Med Genet. 2002 Jul 01; 110(3):226-33.
Score: 0.006
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Identification of PSMB5 as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proc Natl Acad Sci U S A. 2022 05 31; 119(22):e2118124119.
Score: 0.006
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Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. Am J Hum Genet. 2002 Jun; 70(6):1532-44.
Score: 0.006
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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Sci Rep. 2020 10 22; 10(1):18051.
Score: 0.006
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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: 0.005
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Preventive care services and health behaviors in children with fragile X syndrome. Disabil Health J. 2019 10; 12(4):564-573.
Score: 0.005
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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 (Bethesda). 2018 01 04; 8(1):105-111.
Score: 0.005
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Low-level maternal exposure to nicotine associates with significant metabolic perturbations in second-trimester amniotic fluid. Environ Int. 2017 10; 107:227-234.
Score: 0.004
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Parental Perspectives on Pharmacological Clinical Trials: a Qualitative Study in Down Syndrome and Fragile X Syndrome. J Genet Couns. 2017 Dec; 26(6):1333-1340.
Score: 0.004
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Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. Neuropsychology. 2012 Mar; 26(2):156-64.
Score: 0.003
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Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet. 2009 Oct; 85(4):503-14.
Score: 0.003
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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: 0.002