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Format : Academic Journals Format : Academic Journals Subject : adhd Subject : fragile x syndrome Subject : habituation Filter by : Author
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Academic Journal

Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.

  • Authors : Tassone F; Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, Sacramento, CA 95817, USA.; MIND Institute, University of California Davis, Davis, CA 95817, USA.

Subjects: Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/metabolism ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/diagnosis Fragile X Tremor Ataxia Syndrome

  • Source: Cells [Cells] 2023 Sep 21; Vol. 12 (18). Date of Electronic Publication: 2023 Sep 21.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409

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Academic Journal

Clustering of comorbid conditions among women who carry an FMR1 premutation.

  • Authors : Allen EG; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA. .; Charen K

Subjects: Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/epidemiology ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2020 Apr; Vol. 22 (4), pp. 758-766. Date of Electronic Publication: 2020 Jan 03.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Feasibility of an app-based mindfulness intervention among women with an FMR1 premutation experiencing maternal stress.

  • Authors : Hunter JE; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, 97227, United States. Electronic address: .; Jenkins CL

Subjects: Communication Barriers* ; Mobile Applications* ; Stress, Psychological*/Stress, Psychological*/Stress, Psychological*/etiology

  • Source: Research in developmental disabilities [Res Dev Disabil] 2019 Jun; Vol. 89, pp. 76-82. Date of Electronic Publication: 2019 Apr 05.Publisher: Pergamon Press Country of Publication: United States NLM ID: 8709782 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Epidemiology of fragile X syndrome: a systematic review and meta-analysis.

  • Authors : Hunter J; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia.; Rivero-Arias O

Subjects: Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*epidemiology; Female ; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/genetics

  • Source: American journal of medical genetics. Part A [Am J Med Genet A] 2014 Jul; Vol. 164A (7), pp. 1648-58. Date of Electronic Publication: 2014 Apr 03.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.

  • Authors : Hunter JE; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.; Leslie M

Subjects: Anxiety/Anxiety/Anxiety/*genetics ; Depression/Depression/Depression/*genetics ; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics

  • Source: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.

  • Authors : Hunter JE; Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.; Sherman S

Subjects: Executive Function* ; Heterozygote* ; Trinucleotide Repeat Expansion*

  • Source: Neuropsychology [Neuropsychology] 2012 Mar; Vol. 26 (2), pp. 156-64. Date of Electronic Publication: 2012 Jan 16.Publisher: American Psychological Association Country of Publication: United States NLM ID: 8904467 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.

Subjects: Memory* ; Trinucleotide Repeat Expansion*; Aging/Aging/Aging/*genetics

  • Source: Neuropsychology [Neuropsychology] 2011 May; Vol. 25 (3), pp. 404-411.Publisher: American Psychological Association Country of Publication: United States NLM ID: 8904467 Publication Model: Print Cited Medium: Internet

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Academic Journal

Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature.

  • Authors : Hunter JE; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.; Abramowitz A

Subjects: Heterozygote* ; Mutation* ; Phenotype*

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2009 Feb; Vol. 11 (2), pp. 79-89.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print Cited Medium: Internet ISSN: 1530-0366

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Academic Journal

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

  • Authors : Hunter JE; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.; Epstein MP

Subjects: Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics ; Menopause/Menopause/Menopause/*genetics

  • Source: Genetic epidemiology [Genet Epidemiol] 2008 Sep; Vol. 32 (6), pp. 553-9.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8411723 Publication Model: Print Cited Medium: Internet ISSN: 1098-2272

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Academic Journal

Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.

  • Authors : Hunter JE; Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Whitehead Biomedical Research Building, Suite 301, Atlanta, GA 30322, USA.; Allen EG

Subjects: Affect* ; Heterozygote* ; Mutation*

  • Source: Behavior genetics [Behav Genet] 2008 Sep; Vol. 38 (5), pp. 493-502. Date of Electronic Publication: 2008 Jun 06.Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0251711 Publication Model: Print-Electronic Cited Medium:

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  • 1-10 of  23 results for ""Hunter, Jessica""