Autism through midlife: trajectories of symptoms, behavioral functioning, and health

por Hong, Jinkuk, DaWalt, Leann Smith, Taylor, Julie Lounds, Haider, Aasma, Mailick, Marsha
Publicado 2023

Is FMR1 CGG Repeat Number Polymorphism Associated With Phenotypic Variation in the General Population? Report From a Cohort of 5,499 Adults

por Hong, Jinkuk, DaWalt, Leann, Baker, Mei Wang, Berry-Kravis, Elizabeth M., Mailick, Marsha R.
Publicado 2021

Low-normal FMR1 CGG repeat length: phenotypic associations

por Mailick, Marsha R., Hong, Jinkuk, Rathouz, Paul, Baker, Mei W., Greenberg, Jan S., Smith, Leann, Maenner, Matthew
Publicado 2014

LONGITUDINAL CHANGES IN WELL-BEING OF PARENTS OF INDIVIDUALS WITH DEVELOPMENTAL OR MENTAL HEALTH PROBLEMS

por Sloan, Carlie J, Mailick, Marsha R, Hong, Jinkuk, Ha, Jung-Hwa, Greenberg, Jan S, Almeida, David M
Publicado 2019

Longitudinal changes in well-being of parents of individuals with developmental or mental health problems

por Sloan, Carlie J., Mailick, Marsha R., Hong, Jinkuk, Ha, Jung-Hwa, Greenberg, Jan S., Almeida, David M.
Publicado 2020

The effect of college degree attainment on neurodegenerative symptoms in genetically at-risk women

por Hong, Jinkuk, Dembo, Robert S., DaWalt, Leann Smith, Brilliant, Murray, Berry-Kravis, Elizabeth M., Mailick, Marsha
Publicado 2022

Mortality in Women across the FMR1 CGG Repeat Range: The Neuroprotective Effect of Higher Education

por Hong, Jinkuk, Dembo, Robert S., DaWalt, Leann Smith, Baker, Mei Wang, Berry-Kravis, Elizabeth, Mailick, Marsha R.
Publicado 2023

Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness

por Hu, Bowen, Shen, Ning, Li, James J., Kang, Hyunseung, Hong, Jinkuk, Fletcher, Jason, Greenberg, Jan, Mailick, Marsha R., Lu, Qiongshi
Publicado 2019

Artificial intelligence–assisted phenotype discovery of fragile X syndrome in a population-based sample

por Movaghar, Arezoo, Page, David, Scholze, Danielle, Hong, Jinkuk, DaWalt, Leann Smith, Kuusisto, Finn, Stewart, Ron, Brilliant, Murray, Mailick, Marsha
Publicado 2021

FMR1 Low Zone CGG Repeats: Phenotypic Associations in the Context of Parenting Stress

por Mailick, Marsha R., Hong, Jinkuk, DaWalt, Leann Smith, Greenberg, Jan S., Movaghar, Arezoo, Baker, Mei Wang, Rathouz, Paul J., Brilliant, Murray H.
Publicado 2020

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome

por Mailick, Marsha R., Movaghar, Arezoo, Hong, Jinkuk, Greenberg, Jan S., DaWalt, Leann S., Zhou, Lili, Jackson, Jonathan, Rathouz, Paul J., Baker, Mei W., Brilliant, Murray, Page, David, Berry-Kravis, Elizabeth
Publicado 2018

Data-driven phenotype discovery of FMR1 premutation carriers in a population-based sample

por Movaghar, Arezoo, Page, David, Brilliant, Murray, Baker, Mei Wang, Greenberg, Jan, Hong, Jinkuk, DaWalt, Leann Smith, Saha, Krishanu, Kuusisto, Finn, Stewart, Ron, Berry-Kravis, Elizabeth, Mailick, Marsha R.
Publicado 2019