Automated screening for Fragile X premutation carriers based on linguistic and cognitive computational phenotypes

por Movaghar, Arezoo, Mailick, Marsha, Sterling, Audra, Greenberg, Jan, Saha, Krishanu
Publicado 2017

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

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

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

Associated features in females with an FMR1 premutation

por Wheeler, Anne C, Bailey Jr, Donald B, Berry-Kravis, Elizabeth, Greenberg, Jan, Losh, Molly, Mailick, Marsha, Milà, Montserrat, Olichney, John M, Rodriguez-Revenga, Laia, Sherman, Stephanie, Smith, Leann, Summers, Scott, Yang, Jin-Chen, Hagerman, Randi
Publicado 2014