Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Jan S. Greenberg"'
Autor:
Marsha R. Mailick, Jinkuk Hong, Leann Smith DaWalt, Jan S. Greenberg, Arezoo Movaghar, Mei Wang Baker, Paul J. Rathouz, Murray H. Brilliant
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
The FMR1 gene on the X chromosome has varying numbers of CGG repeats. The modal number is 30, and expansion to >200 results in fragile X syndrome, but the copy number extends down to 6. Past research suggests that individuals whose CGGs are in the
Externí odkaz:
https://doaj.org/article/94e54bc9129e4949a87b4b2c7a65bc38
Autor:
Marsha R. Mailick, Arezoo Movaghar, Jinkuk Hong, Jan S. Greenberg, Leann S. DaWalt, Lili Zhou, Jonathan Jackson, Paul J. Rathouz, Mei W. Baker, Murray Brilliant, David Page, Elizabeth Berry-Kravis
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
The FMR1 premutation is of increasing interest to the FXS community, as questions about a primary premutation phenotype warrant research attention. 100 FMR1 premutation carrier mothers (mean age = 58; 67–138 CGG repeats) of adults with fragile X sy
Externí odkaz:
https://doaj.org/article/1612a0afaac644508a0b00e9a6f817c5
Publikováno v:
Journal of Family Issues. 42:2625-2647
Although adoption is a widespread phenomenon in the United States, little research has examined the effects on biological siblings. This article uses two representative datasets to compare educational attainments of individuals who grew up with an ad
Publikováno v:
Psychol Aging
According to family systems theory, strains from parenting an adult with disabilities may spill over to parents' relationships with their other children and disrupt family dynamics and their well-being in later-life. This study examined whether paren
Publikováno v:
J Fam Psychol
Expressed emotion (EE), a measure of the family's emotional climate, is a fundamental measure in caregiving research. A core dimension of EE is the level of criticism expressed by the caregiver to the care recipient, with a high level of criticism a
Publikováno v:
American Journal on Intellectual and Developmental Disabilities. 124:411-426
We examined the benefit of emotional support on daily health in premutation carrier mothers of adolescents and adults with fragile X syndrome (n = 114), and whether this benefit was moderated by the mother's genetic status (FMR1 CGG repeat length). I
Autor:
Jan S. Greenberg, Julie Lounds Taylor, Marsha R. Mailick, Leann Smith DaWalt, Daniel J. Laxman
Publikováno v:
Autism Research. 12:911-921
The present longitudinal study investigated changes in service receipt and unmet service needs spanning 14 years before and after high school exit in a large community-based sample of individuals with autism spectrum disorder (ASD) (n = 204), of whom
Publikováno v:
Journal of Abnormal Psychology. 128:200-211
Neuroticism is a stable and heritable personality trait that is strongly linked to depression. Yet, little is known about its association with late life depression, as well as how neuroticism eventuates into depression. This study used data from the
Apolipoprotein ɛ4 Allele and Subjective Cognitive Functioning in Parents of Adults With Disabilities
Publikováno v:
J Gerontol B Psychol Sci Soc Sci
Objectives Parents of individuals with disabilities face ongoing responsibilities of providing care and support for their children, even during the child’s adulthood. Past research has shown that this caregiving role is linked to chronic stress and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a0c533e9e31793515acf8b791ce0a59
https://europepmc.org/articles/PMC7489093/
https://europepmc.org/articles/PMC7489093/
Autor:
Jan S. Greenberg, Arezoo Movaghar, Marsha R. Mailick, Paul J. Rathouz, Mei W. Baker, Jinkuk Hong, Leann Smith DaWalt, Murray H. Brilliant
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Frontiers in Pediatrics
Frontiers in Pediatrics
The FMR1 gene on the X chromosome has varying numbers of CGG repeats. The modal number is 30, and expansion to >200 results in fragile X syndrome, but the copy number extends down to 6. Past research suggests that individuals whose CGGs are in the