W35. INDIVIDUAL DIFFERENCES IN DEPRESSIVE SYMPTOMS AFTER THE EARLY RESPONSES TO THE COVID-19 PANDEMIC IN AUSTRALIA

por Conde, Lucia Colodro, Olsen, Catherine, Martin, Nick, Whiteman, David, Medland, Sarah E.
Publicado 2021

Bridging the gap: Short structural variants in the genetics of anorexia nervosa

por Berthold, Natasha, Pytte, Julia, Bulik, Cynthia M., Tschochner, Monika, Medland, Sarah E., Akkari, Patrick Anthony
Publicado 2022

Linkage Analysis of a Model Quantitative Trait in Humans: Finger Ridge Count Shows Significant Multivariate Linkage to 5q14.1

por Medland, Sarah E, Loesch, Danuta Z, Mdzewski, Bogdan, Zhu, Gu, Montgomery, Grant W, Martin, Nicholas G
Publicado 2007

Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHD

por García-Marín, Luis M., Campos, Adrián I., Cuéllar-Partida, Gabriel, Medland, Sarah E., Kollins, Scott H., Rentería, Miguel E.
Publicado 2021

Preliminary results from the Australian Genetics of Bipolar Disorder Study: A nation-wide cohort

por Lind, Penelope A, Siskind, Dan J, Hickie, Ian B, Colodro-Conde, Lucía, Cross, Simone, Parker, Richard, Martin, Nicholas G, Medland, Sarah E
Publicado 2023

“Echoes of a dark past” is a history of maternal childhood maltreatment a perinatal risk factor for pregnancy and postpartum trauma experiences? A longitudinal study

por Mackle, Tracey, Colodro-Conde, Lucía, de Dassel, Therese, Braun, Anastasia, Pope, Adele, Bennett, Elizabeth, Kothari, Alka, Bruxner, George, Medland, Sarah E., Patterson, Sue
Publicado 2023

Attention Deficit Hyperactivity Disorder in Australian Adults: Prevalence, Persistence, Conduct Problems and Disadvantage

por Ebejer, Jane L., Medland, Sarah E., van der Werf, Julius, Gondro, Cedric, Henders, Anjali K., Lynskey, Michael, Martin, Nicholas G., Duffy, David L.
Publicado 2012

Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings

por Visscher, Peter M, Medland, Sarah E, Ferreira, Manuel A. R, Morley, Katherine I, Zhu, Gu, Cornes, Belinda K, Montgomery, Grant W, Martin, Nicholas G
Publicado 2006

Joint genetic analysis of hippocampal size in mouse and human identifies a novel gene linked to neurodegenerative disease

por Ashbrook, David G, Williams, Robert W, Lu, Lu, Stein, Jason L, Hibar, Derrek P, Nichols, Thomas E, Medland, Sarah E, Thompson, Paul M, Hager, Reinmar
Publicado 2014

Effects of ApoE4 and ApoE2 genotypes on subcortical magnetic susceptibility and microstructure in 27,535 participants from the UK Biobank()

por Nir, Talia M., Zhu, Alyssa H., Gari, Iyad Ba, Dixon, Daniel, Islam, Tasfiya, Villalon-Reina, Julio E., Medland, Sarah E., Thompson, Paul M., Jahanshad, Neda
Publicado 2022

Days out of role and somatic, anxious-depressive, hypo-manic, and psychotic-like symptom dimensions in a community sample of young adults

por Crouse, Jacob J., Ho, Nicholas, Scott, Jan, Martin, Nicholas G., Couvy-Duchesne, Baptiste, Hermens, Daniel F., Parker, Richard, Gillespie, Nathan A., Medland, Sarah E., Hickie, Ian B.
Publicado 2021

Unraveling the Genetic Etiology of Adult Antisocial Behavior: A Genome-Wide Association Study

por Tielbeek, Jorim J., Medland, Sarah E., Benyamin, Beben, Byrne, Enda M., Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., Wray, Naomi R., Verweij, Karin J. H.
Publicado 2012

Clinical, demographic, and genetic risk factors of treatment‐attributed suicidality in >10,000 Australian adults taking antidepressants

por Campos, Adrian I., Byrne, Enda M., Iorfino, Frank, Fabbri, Chiara, Hickie, Ian B., Lewis, Cathryn M., Wray, Naomi R., Medland, Sarah E., Rentería, Miguel E., Martin, Nicholas G.
Publicado 2022

Lifetime prevalence and correlates of perinatal depression in a case-cohort study of depression

por Kiewa, Jacqueline, Meltzer-Brody, Samantha, Milgrom, Jeannette, Bennett, Elizabeth, Mackle, Tracey, Guintivano, Jerry, Hickie, Ian B, Colodro-Conde, Lucia, Medland, Sarah E, Martin, Nick, Wray, Naomi, Byrne, Enda
Publicado 2022

The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

por Reed, Danielle R., Zhu, Gu, Breslin, Paul A.S., Duke, Fujiko F., Henders, Anjali K., Campbell, Megan J., Montgomery, Grant W., Medland, Sarah E., Martin, Nicholas G., Wright, Margaret J.
Publicado 2010

Impact of CYP2C19 metaboliser status on SSRI response: a retrospective study of 9500 participants of the Australian Genetics of Depression Study

por Campos, Adrian I., Byrne, Enda M., Mitchell, Brittany L., Wray, Naomi R., Lind, Penelope A., Licinio, Julio, Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E.
Publicado 2022

Understanding genetic risk factors for common side effects of antidepressant medications

por Campos, Adrian I., Mulcahy, Aoibhe, Thorp, Jackson G., Wray, Naomi R., Byrne, Enda M., Lind, Penelope A., Medland, Sarah E., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E.
Publicado 2021

Educational Attainment: A Genome Wide Association Study in 9538 Australians

por Martin, Nicolas W., Medland, Sarah E., Verweij, Karin J. H., Lee, S. Hong, Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Montgomery, Grant W., Wright, Margaret J., Martin, Nicholas G.
Publicado 2011

Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants

por Garcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E., Campos, Adrian I.
Publicado 2023

Head Motion and Inattention/Hyperactivity Share Common Genetic Influences: Implications for fMRI Studies of ADHD

por Couvy-Duchesne, Baptiste, Ebejer, Jane L., Gillespie, Nathan A., Duffy, David L., Hickie, Ian B., Thompson, Paul M., Martin, Nicholas G., de Zubicaray, Greig I., McMahon, Katie L., Medland, Sarah E., Wright, Margaret J.
Publicado 2016