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Ching, Christopher R. K., Gutman, Boris A., Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K., Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K., Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Campbell, Linda E., McCabe, Kathryn L.. American Psychiatric Association (APA); 2020. Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness.
Vorstman, Jacob A. S., Breetvelt, Elemi J., Chow, Eva W. C., Fung, Wai Lun Alan, Butcher, Nancy J., Young, Donald A., McDonald-McGinn, Donna M., Vogels, Annick, van Amelsvoort, Therese, Gothelf, Doron, Weinberger, Ronnie, Weizman, Abraham, Duijff, Sasja N., Klaassen, Petra W. J., Koops, Sanne, Kates, Wendy R., Antshel, Kevin M., Simon, Tony J., Ousley, Opal Y., Swillen, Ann, Gur, Raquel E., Bearden, Carrie E., Kahn, René S., Eliez, Stephan, Bassett, Anne S., Emanuel, Beverly S., Zackai, Elaine H., Kushan, Leila, Fremont, Wanda, Schoch, Kelly, Stoddard, Joel, Cubells, Joseph, Fu, Fiona, Campbell, Linda E., Schneider, Maude, Fritsch, Rosemarie, Vergaelen, Elfi, Neeleman, Marjolein, Boot, Erik, Debbané, Martin, Philip, Nicole, Green, Tamar, van den Bree, Marianne B. M., Murphy, Declan, Canyelles, Jaume Morey, Jalbrzikowski, Maria, Arango, Celso, Murphy, Kieran C., Pontillo, Maria, Armando, Marco, Vicari, Stefano, Shashi, Vandana, Hooper, Stephen R.. American Medical Association; 2015. Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Campbell, Linda E., Hanlon, Mary-Claire, Galletly, Cherrie A., Harvey, Carol, Stain, Helen, Cohen, Martin, van Ravenzwaaij, Don, Brown, Scott. Sage; 2018. Severity of illness and adaptive functioning predict quality of care of children among parents with psychotic disorders: a confirmatory factor analysis.
Cleynen, Isabelle, Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Holleman, Aaron M., Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Bearden, Carrie E., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Warren, Stephen T., Owen, Michael J., Chopra, Pankaj, Campbell, Linda E., McCabe, Kathryn L.. Springer Nature; 2020. Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Woolard, Alix J., Benders, Titia, Campbell, Linda E., Karayanidis, Frini, Mattes, Joerg, Murphy, Vanessa, Whalen, Olivia, Lane, Alison E.. Australasian Speech Science and Technology Association (ASSTA); 2016. Exploring the association of infant temperament on maternal fundamental frequency contours.
Schneider, Maude, Debbané, Martin, Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W. J., Swillen, Ann, Gothelf, Doron, Bassett, Anne S., Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Chow, Eva W. C., Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J., Eliez, Stephan, Fung, Wai Lun Alan, van den Bree, Marianne B. M., Owen, Michael, Murphy, Kieran C., Niarchou, Maria, Kates, Wendy R.. American Psychiatric Association; 2014. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 deletion syndrome.
Azuma, Rayna, Daly, Eileen M., Williams, Steven C. R., Owen, Michael J., Murphy, Declan G. M., Murphy, Kieran C., Campbell, Linda E., Stevens, Angela F., Deeley, Quinton, Giampietro, Vincent, Brammer, Michael J., Glaser, Beate, Ambery, Fiona Z., Morris, Robin G.. Springer; 2009. Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome: an fMRI study.
Stain, Helen J., Galletly, Cherie A., Clark, Scott, Wilson, Jacqueline, Killen, Emily A., Anthes, Lauren, Campbell, Linda E., Hanlon, Mary-Claire, Harvey, Carol. Sage; 2012. Understanding the social costs of psychosis: the experience of adults affected by psychosis identified within the second Australian national survey of psychosis.
Campbell, Linda E., Stevens, Angela, Daly, Eileen, Toal, Fiona, Azuma, Rayna, Karmiloff-Smith, Annette, Murphy, Declan G. M., Murphy, Kieran C.. Elsevier; 2009. A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.
Davies, Robert W., Fiksinski, Ania M., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Breetvelt, Elemi J., Cubells, Joseph F., Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Williams, Nigel M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W., Epstein, Michael P., Warren, Stephen T., Morrison, Sinead, Chawner, Samuel, Vingerhoets, Claudia, Hooper, Stephen R., Breckpot, Jeroen, Vergaelen, Elfi, Vogels, Annick, Monks, Stephen, Prasad, Sarah E., Sandini, Corrado, Schneider, Maude, Maeder, Johanna, Fraguas, David, Evers, Rens, Monfeuga, Thomas, Tassone, Flora, Morey-Canyelles, Jaume, Ousley, Opal Y., Antshel, Kevin M., Fremont, Wanda, Fritsch, Rosemarie, Ornstein, Claudia, Daly, Eileen M., Costain, Gregory A., Boot, Erik, Bassett, Anne S., Heung, Tracy, Crowley, T. Blaine, Zackai, Elaine H., Calkins, Monica E., Gur, Ruben C., McCabe, Kathryn L., Busa, Tiffany, Schoch, Kelly, Pontillo, Maria, Duijff, Sasja N., Owen, Michael J., Kahn, René S., Houben, Michiel, Kushan, Leila, Jalbrzikowski, Maria, Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Bearden, Carrie E., Vorstman, Jacob A. S., Gur, Raquel E., Morrow, Bernice E.. Nature Publishing Group; 2020. Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Frank, Michael C., Alcock, Katherine Jane, Bohland, Maximilian P., Noble, C, Novack, MA, Olesen, NM, Orena, AJ, Ota, M, Panneton, R, Esfahani, SP, Paulus, M, Pletti, C, Polka, L, Bolitho, Petra, Potter, C, Rabagliati, H, Ramachandran, S, Rennels, JL, Reynolds, GD, Roth, KC, Rothwell, C, Rubez, D, Ryjova, Y, Saffran, J, Borovsky, Arielle, Sato, A, Savelkouls, S, Schachner, A, Schafer, G, Schreiner, MS, Seidl, A, Shukla, M, Simpson, EA, National, LS, Skarabela, B, Brady, Shannon M., Soley, G, Sundara, M, Theakston, A, Thompson, A, Trainor, LJ, Trehub, SE, Troan, AS, Tsui, AS-M, Twomey, K, Von Holzen, K, Braun, Bettina, Wang, Y, Waxman, S, Werker, JF, Wermelinger, S, Woolard, A, Yurovsky, D, Zahner, K, Zettersten, M, Soderstrom, M, Brown, Anna, Byers-Heinlein, Krista, Campbell, Linda E., Cashon, Cara, Choi, Mihye, Arias-Trejo, Natalia, Christodoulou, Joan, Cirelli, LK, Conte, S, Cordes, S, Cox, C, Cristia, A, Cusack, R, Davies, C, de Klerk, M, Delle Luche, C, Aschersleben, Gisa, de Ruiter, L, Dinakar, D, Dixon, KC, Durier, V, Durrant, S, Fennell, C, Ferguson, B, Ferry, A, Fikkert, P, Flanagan, T, Baldwin, Dare, Floccia, C, Foley, M, Fritzsche, T, Frost, RLA, Gampe, A, Gervain, J, Gonzalez-Gomez, N, Gupta, A, Hahn, LE, Hamlin, JK, Barbu, Stephanie, Hannon, EE, Havron, N, Hay, J, Hernik, M, Hohle, B, Houston, DM, Howard, LH, Ishikawa, M, Itakura, S, Jackson, I, Bergelson, Elika, Jakobsen, K, Jarto, M, Johnson, SP, Junge, C, Karadag, D, Kartushina, N, Kellier, DJ, Keren-Portnoy, T, Klassen, K, Kline, M, Bergmann, Christina, Ko, E-S, Kominsky, JF, Kosie, JE, Kragness, HE, Krieger, AAR, Krieger, F, Lany, J, Lazo, RJ, Lee, M, Leservoisier, C, Black, Alexis K., Levelt, C, Lew-Williams, C, Lippold, M, Liszkowski, U, Liu, L, Luke, SG, Lundwall, RA, Cassia, VM, Mani, N, Marino, C, Blything, Ryan, Martin, A, Mastroberardino, M, Mateu, V, Mayor, J, Menn, K, Michel, C, Moriguchi, Y, Morris, B, Nave, KM, Nazzi, T. Sage; 2020. Quantifying Sources of Variability in Infancy Research Using the Infant-Directed-Speech Preference.
Sun, Daqiang, Ching, Christopher R. K., Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria, Lin, Amy, Murphy, Clodagh M., Murphy, D, Craig, M, Vorstman, J, Fiksinski, A, Koops, S, Ruparel, K, Roalf, DR, Gur, RE, Schmitt, JE, Forsyth, Jennifer K., Simon, TJ, Goodrich-Hunsaker, NJ, Durdle, CA, Bassett, AS, Chow, EWC, Butcher, NJ, Vila-Rodriguez, F, Doherty, J, Cunningham, A, van den Bree, MBM, Kushan, Leila, Linden, DEJ, Moss, H, Owen, MJ, Murphy, KC, McDonald-McGinn, DM, Emanuel, B, van Erp, TGM, Turner, JA, Thompson, PM, Bearden, CE, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Villalon-Reina, Julio E., Qu, Xiaoping. Nature Publishing Group; 2020. Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Mallise, Carly A., Murphy, Vanessa E., Lane, Alison E., Campbell, Linda E., Woolard, Alix J., Whalen, Olivia M., Milton, Gabrielle, Mattes, Joerg, Collison, Adam, Gibson, Peter G., Karayanidis, Frini. Frontiers Research Foundation; 2021. Early Sensory and Temperament Features in Infants Born to Mothers With Asthma: A Cross-Sectional Study.
McCabe, Kathryn L., Marlin, Stuart, Cooper, Gavin, Morris, Robin, Schall, Ulrich, Murphy, Declan G., Murphy, Kieran C., Campbell, Linda E.. BioMed Central; 2016. Visual perception and processing in children with 22q11.2 deletion syndrome: associations with social cognition measures of face identity and emotion recognition.
Villalon-Reina, Julio E., Ching, Christopher R. K., Kothapalli, Deydeep, Sun, Dagiang, Nir, Talia, Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L., Daly, Eileen, Gudbrandsen, Maria. Society of Photo-Optical Instrumentation Engineers (SPIE); 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome.
Villalón-Reina, Julio E., Martínez, Kenia, Qu, Xiaoping, Ching, Christopher R. K., Nir, Talia M., Kothapalli, Deydeep, Corbin, Conor, Sun, Daqiang, Lin, Amy, Forsyth, Jennifer K., Kushan, Leila, Vajdi, Ariana, Jalbrzikowski, Maria, Hansen, Laura, Jonas, Rachel K., van Amelsvoort, Therese, Bakker, Geor, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, Campbell, Linda E., McCabe, Kathryn L.. Nature Publishing Group; 2020. Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Campbell, Linda E., Hughes, Matthew, Schall, Ulrich, Budd, Timothy W., Cooper, Gavin, Fulham, W. Ross, Karayanidis, Frini, Hanlon, Mary-Claire, Stojanov, Wendy, Johnston, Patrick, Case, Vanessa. Wiley-Blackwell; 2007. Primary and secondary neural networks of auditory prepulse inhibition: a functional magnetic resonance imaging study of sensorimotor gating of the human acoustic startle response.
Woolard, Alix, Benders, Titia, Korostenski, Larissa, Lane, Alison E., Campbell, Linda E., Whalen, Olivia M., Mallise, Carly, Karayanidis, Frini, Barker, Daniel, Murphy, Vanessa E., Tait, Jordan, Gibson, Peter. Elsevier; 2023. The relationship between pitch contours in infant-directed speech and early signs of autism in infancy.
Hutchesson, Melinda J., Taylor, Rachael, Shrewsbury, Vanessa A., Vincze, Lisa, Campbell, Linda E., Callister, Robin, Park, Felicity, Schumacher, Tracy L., Collins, Clare E.. MDPI AG; 2020. Be Healthe for your heart: a pilot randomized controlled trial evaluating a web-based behavioral intervention to improve the cardiovascular health of women with a history of preeclampsia.
Ge, Ruiyang, Ching, Christopher R. K., Craig, Michael, Crossley, Nicolas A., Cunningham, Adam, Daly, Eileen, Doherty, Joanne L., Durdle, Courtney A., Emanuel, Beverly S., Fiksinski, Ania, Forsyth, Jennifer K., Fremont, Wanda, Bassett, Anne S., Goodrich-Hunsaker, Naomi J., Gudbrandsen, M, Gur, RE, Jalbrzikowski, M, Kates, WR, Lin, A, Linden, DEJ, McCabe, Kathryn L., McDonald-McGinn, D, Moss, H, Kushan, Leila, Murphy, DG, Murphy, KC, Owen, MJ, Villalon-Reina, JE, Repetto, GM, Roalf, DR, Ruparel, K, Schmitt, JE, Schuite-Koops, S, Angkustsiri, K, Antshel, Kevin M., Sun, D, Vajdi, A, van den Bree, M, Vorstman, J, Thompson, PM, Vila-Rodriguez, F, Bearden, CE, van Amelsvoort, Therese, Bakker, Geor, Butcher, Nancy J., Campbell, Linda E., Chow, Eva W. C.. John Wiley & Sons; 2024. Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome.
Woolard, Alix, Lane, Alison E., Campbell, Linda E., Whalen, Olivia M., Swaab, Linda, Karayanidis, Frini, Barker, Daniel, Murphy, Vanessa, Benders, Titia. Springer; 2022. Infant and Child-Directed Speech Used with Infants and Children at Risk or Diagnosed with Autism Spectrum Disorder: a Scoping Review.
Whalen, Olivia M., Campbell, Linda E., Murphy, Vanessa E., Lane, Alison E., Karayanidis, Frini, Mallise, Carly A., Woolard, Alix J., Holliday, Elizabeth G., Mattes, Joerg, Collison, Adam, Gibson, Peter G.. Springer; 2024. Effect of fractional exhaled nitric oxide (FENO)-based asthma management during pregnancy versus usual care on infant development, temperament, sensory function and autism signs.
Whalen, Olivia M., Campbell, Linda E., Murphy, Vanessa E., Lane, Alison E., Gibson, Peter G., Mattes, Joerg, Collison, Adam, Mallise, Carly A., Woolard, Alix, Karayanidis, Frini. Taylor & Francis; 2020. Observational study of mental health in asthmatic women during the prenatal and postnatal periods.