Time to Break the “Lock-In” Impediments to Chemicals Management

por Blumenthal, Jonathan, Diamond, Miriam L., Hoffmann, Matthew, Wang, Zhanyun
Publicado 2022

Brain and behavior in 48, XXYY syndrome

por Hanley, Alli P., Blumenthal, Jonathan D., Raitano Lee, Nancy, Baker, Eva H., Clasen, Liv S., Giedd, Jay N.
Publicado 2015

Sex-specific associations between subcortical morphometry in childhood and adult alcohol consumption: A 17-year follow-up study

por Mankiw, Catherine, Whitman, Ethan T., Torres, Erin, Lalonde, François, Clasen, Liv S., Blumenthal, Jonathan D., Chakravarty, M. Mallar, Raznahan, Armin
Publicado 2021

Brain morphological abnormalities in 49,XXXXY syndrome: A pediatric magnetic resonance imaging study()()

por Blumenthal, Jonathan D., Baker, Eva H., Lee, Nancy Raitano, Wade, Benjamin, Clasen, Liv S., Lenroot, Rhoshel K., Giedd, Jay N.
Publicado 2013

Persistent Problem: Global Challenges to Managing PCBs

por Melymuk, Lisa, Blumenthal, Jonathan, Sáňka, Ondřej, Shu-Yin, Adriana, Singla, Veena, Šebková, Kateřina, Pullen Fedinick, Kristi, Diamond, Miriam L.
Publicado 2022

Effects of sex chromosome dosage on corpus callosum morphology in supernumerary sex chromosome aneuploidies

por Wade, Benjamin S C, Joshi, Shantanu H, Reuter, Martin, Blumenthal, Jonathan D, Toga, Arthur W, Thompson, Paul M, Giedd, Jay N
Publicado 2014

Modeling familial predictors of proband outcomes in neurogenetic disorders: initial application in XYY syndrome

por Wilson, Kathleen E., Fish, Ari M., Mankiw, Catherine, Xenophontos, Anastasia, Warling, Allysa, Whitman, Ethan, Clasen, Liv, Torres, Erin, Blumenthal, Jonathan, Raznahan, Armin
Publicado 2021

X- vs. Y-Chromosome Influences on Human Behavior: A Deep Phenotypic Comparison of Psychopathology in XXY and XYY Syndromes

por Schaffer, Lukas, Rau, Srishti, Clasen, Liv, Warling, Allysa, Whitman, Ethan T., Nadig, Ajay, McDermott, Cassidy, Xenophontos, Anastasia, Wilson, Kathleen, Blumenthal, Jonathan, Torres, Erin, Raznahan, Armin
Publicado 2023

Everyday executive functions in Down syndrome from early childhood to young adulthood: evidence for both unique and shared characteristics compared to youth with sex chromosome tri...

por Lee, Nancy Raitano, Anand, Payal, Will, Elizabeth, Adeyemi, Elizabeth I., Clasen, Liv S., Blumenthal, Jonathan D., Giedd, Jay N., Daunhauer, Lisa A., Fidler, Deborah J., Edgin, Jamie O.
Publicado 2015

Carriage of Supernumerary Sex Chromosomes Decreases the Volume and Alters the Shape of Limbic Structures

por Nadig, Ajay, Reardon, Paul K., Seidlitz, Jakob, McDermott, Cassidy L., Blumenthal, Jonathan D., Clasen, Liv S., Lalonde, Francois, Lerch, Jason P., Chakravarty, M. Mallar, Raznahan, Armin
Publicado 2018

Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome

por Joseph, Lisa, Farmer, Cristan, Chlebowski, Colby, Henry, Laura, Fish, Ari, Mankiw, Catherine, Xenophontos, Anastasia, Clasen, Liv, Sauls, Bethany, Seidlitz, Jakob, Blumenthal, Jonathan, Torres, Erin, Thurm, Audrey, Raznahan, Armin
Publicado 2018

Deep phenotypic analysis of psychiatric features in genetically defined cohorts: application to XYY syndrome

por Raznahan, Armin, Rau, Srishti, Schaffer, Luke, Liu, Siyuan, Fish, Ari M., Mankiw, Catherine, Xenophontos, Anastasia, Clasen, Liv S., Joseph, Lisa, Thurm, Audrey, Blumenthal, Jonathan D., Bassett, Dani S., Torres, Erin N.
Publicado 2023

Aneuploidy effects on human gene expression across three cell types

por Liu, Siyuan, Akula, Nirmala, Reardon, Paul K., Russ, Jill, Torres, Erin, Clasen, Liv S., Blumenthal, Jonathan, Lalonde, Francois, McMahon, Francis J., Szele, Francis, Disteche, Christine M., Cader, M. Zameel, Raznahan, Armin
Publicado 2023

Sex-biased trajectories of amygdalo-hippocampal morphology change over human development

por Fish, Ari M., Nadig, Ajay, Seidlitz, Jakob, Reardon, Paul K., Mankiw, Catherine, McDermott, Cassidy L., Blumenthal, Jonathan D., Clasen, Liv S., Lalonde, Francois, Lerch, Jason P., Chakravarty, M. Mallar, Shinohara, Russell T., Raznahan, Armin
Publicado 2019

Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

por Seidlitz, Jakob, Nadig, Ajay, Liu, Siyuan, Bethlehem, Richard A. I., Vértes, Petra E., Morgan, Sarah E., Váša, František, Romero-Garcia, Rafael, Lalonde, François M., Clasen, Liv S., Blumenthal, Jonathan D., Paquola, Casey, Bernhardt, Boris, Wagstyl, Konrad, Polioudakis, Damon, de la Torre-Ubieta, Luis, Geschwind, Daniel H., Han, Joan C., Lee, Nancy R., Murphy, Declan G., Bullmore, Edward T., Raznahan, Armin
Publicado 2020

Author Correction: Transcriptomic and cellular decoding of regional brain vulnerability to neurogenetic disorders

por Seidlitz, Jakob, Nadig, Ajay, Liu, Siyuan, Bethlehem, Richard A. I., Vértes, Petra E., Morgan, Sarah E., Váša, František, Romero-Garcia, Rafael, Lalonde, François M., Clasen, Liv S., Blumenthal, Jonathan D., Paquola, Casey, Bernhardt, Boris, Wagstyl, Konrad, Polioudakis, Damon, de la Torre-Ubieta, Luis, Geschwind, Daniel H., Han, Joan C., Lee, Nancy R., Murphy, Declan G., Bullmore, Edward T., Raznahan, Armin
Publicado 2020