Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Rowena Ng"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background KAT6A (Arboleda-Tham) syndrome is a Mendelian disorder of the epigenetic machinery caused by pathogenic variants in the lysine acetyltransferase 6 A (KAT6A) gene. Intellectual disability and speech/language impairment (e.g., minim
Externí odkaz:
https://doaj.org/article/12b8a077478e43839a5a1007b81cf0fd
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-9 (2024)
Abstract Background Cornelia de Lange (CdLS) is a rare genetic disorder that affects most body systems. Variants in multiple genes including NIPBL and SMC1A, can cause the syndrome. To date, literature on genotype–phenotype associations in individu
Externí odkaz:
https://doaj.org/article/39c166cf3f294269bcfba60bb9372e91
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101153- (2024)
Externí odkaz:
https://doaj.org/article/44fed12c216e4af9bc326b95dfc75738
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101196- (2024)
Externí odkaz:
https://doaj.org/article/1383267399394971b9ed1d7b9a00525d
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/0a4379cf799d4b92a0a4e1c708f3ea8e
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-11 (2023)
Abstract Epigenetics, one mechanism by which gene expression can change without any changes to the DNA sequence, was described nearly a century ago. However, the importance of epigenetic processes to neurodevelopment and higher order neurological fun
Externí odkaz:
https://doaj.org/article/8863c73caf5d436a91ee84c00e004b5e
Autor:
Tanisha G. Hill-Jarrett, Rowena Ng, Carlos Cardenas-Iniguez, Jemima Akinsanya, Ismary Blanco, Johnathan M. Borland, James S. Brown, Tameka Clemons, Adriana K. Cushnie, Jacqueline Garcia, Brianna George, Cera W. Hassinan, Timothy J. Hines, Dan Landayan, Taylor A. McCorkle, Katherine R. Meckel, Mariajose Metcalfe, Samantha A. Montoya, Deborah K. Rose, Desmond R. Warren
Publikováno v:
Frontiers in Integrative Neuroscience, Vol 17 (2023)
Many early-career neuroscientists with diverse identities may not have mentors who are more advanced in the neuroscience pipeline and have a congruent identity due to historic biases, laws, and policies impacting access to education. Cross-identity m
Externí odkaz:
https://doaj.org/article/14e31cb60d8849d78bd27537a67a3a44
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Wiedemann-Steiner syndrome (WSS) is a rare genetic disorder caused by mutation in KMT2A and characterized by neurodevelopmental delay. This study is the first prospective investigation to examine the sleep and behavioral phenotypes among those with W
Externí odkaz:
https://doaj.org/article/d3b35b03d0c548aeb66e98567de5e89b
Autor:
Michelle P. Brown, Rowena Ng, Joe Lisle, Melissa Koenig, Dane Sannes, Fred Rogosch, Dante Cicchetti
Publikováno v:
Developmental Psychology. 59:1126-1135
Mind-mindedness is associated with positive developmental outcomes. However, much of the literature uses mostly White, middle to high socioeconomic status (SES) samples despite evidence that the benefits of mind-mindedness may vary based on degree of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e53003e45a6cab897221c14b183ea4
https://doi.org/10.1037/dev0001506
https://doi.org/10.1037/dev0001506
Publikováno v:
Child Neuropsychology. :1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88a98413736a340b2d054858f0d2827c
https://doi.org/10.1080/09297049.2023.2170996
https://doi.org/10.1080/09297049.2023.2170996