Zhao, Yingjie, Guo, Tingwei, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, van Amelsvoort, Thérèse, van den Bree, Marianne, Owen, Michael, Niarchou, Maria, Fiksinski, Ania, Campbell, Linda, Breetvelt, Elemi, McDonald-McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann. Wiley-Blackwell; 2018. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects.

Fiksinski, Ania M., Bearden, Carrie E., Morrow, Bernice, Gur, Raquel, Chow, Eva, van den Bree, Marianne, Vermeesch, Joris, Warren, Stephen, Owen, Michael, van Amelsvoort, Therese, Eliez, Stephan, Gothelf, Doron, Bassett, Anne S., Arango, Celso, Kates, W, Simon, T, Murphy, K, Repetto, G, Suner, DH, Vicari, S, Cubells, J, Armando, M, Philip, N, Kahn, René S., Campbell, Linda, Garcia-Minaur, S, Schneider, M, Shashi, V, 22q11DS International Consortium on Brain and Behavior, Vorstman, J, Breetvelt, EJ, Zinkstok, Janneke R., Hooper, Stephen R., Tempelaar, Wanda, McDonald-McGinn, Donna, Swillen, Ann, Emanuel, Beverly. Nature Publishing Group; 2022. A normative chart for cognitive development in a genetically selected population.

Wroe, Jaime, Campbell, Linda, Fletcher, Richard, McLoughland, Carmel. Churchill Livingstone; 2019. "What am I thinking? Is this normal?" A cross-sectional study investigating the nature of negative thoughts, parental self-efficacy and psychological distress in new fathers.

Roche, Laura, Campbell, Linda, Heussler, Helen. Springer; 2020. Communication in 22q11.2 deletion syndrome: a brief overview of the profile, intervention approaches, and future considerations.

Demaerel, Wolfram, Hestand, Matthew S., Breckpot, Jeroen, Devriendt, Koenraad, Vermeesch, Joris R., International 22q11.2 Brain and Behavior Consortium,, Campbell, Linda, , , , , , Vergaelen, Elfi, , , , , , , , , , , Swillen, Ann, , , , , , , , , , , López-Sánchez, Marcos, , , , , , , , , , , Pérez-Jurado, Luis A., , , , , , , , , , , McDonald-McGinn, Donna M., , , , , , , , , , , Zackai, Elaine, , , , , , , , , , , Emanuel, Beverly S., , , , , , , , , , , Morrow, Bernice E., . Cell Press; 2017. Nested inversion polymorphisms predispose chromosome 22q11.2 to meiotic rearrangements.

Fletcher, Richard, Campbell, Linda, Sved Williams, Anne, Rawlinson, Catherine, Dye, Jacob, Baldwin, Andrea, May, Chris, StGeorge, Jennifer. Taylor & Francis; 2019. SMS4 perinatal parents: designing parenting support via text messages for mothers with severe mental illness (SMI) and their partners.

Elliot, Ricki-Leigh, Campbell, Linda, Hunter, Mick, Cooper, Gavin, Melville, Jessica, McCabe, Kathryn, Newman, Louise, Loughland, Carmel. Wiley-Blackwell Publishing; 2014. When I look into my baby's eyes...Infant emotion recognition by mothers with borderline personality disorder.

Kazzi, Christina, Campbell, Linda, Porter, Melanie. Springer; 2023. Psychological therapies for anxiety in autistic individuals with co-occurring intellectual developmental disorder: A systematic review.

Campbell, Linda, McCabe, Kathryn, Leadbeater, Kate, Schall, Ulrich, Loughland, Carmel, Rich, Dominique. Elsevier; 2010. Visual scanning of faces in 22q11.2 deletion syndrome: attention to the mouth or the eyes?.

Campbell, Linda, Hanlon, Mary-Claire, Poon, Abner Weng Cheong, Paolini, Stefania, Stone, Melanie, Galletly, Cherrie, Stain, Helen J., Cohen, Martin. Sage; 2012. The experiences of Australian parents with psychosis: the second Australian national survey of psychosis.

Bassett, Anne S., Lowther, Chelsea, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Merico, Daniele, , , , , , , , , , , Costain, Gregory, , , , , , , , , , , Chow, Eva W. C., , , , , , , , , , , van Amelsvoort, Therese, , McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van den Bree, Marianne. American Psychiatric Association Publishing; 2017. Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome.

Swaab, Linda, Goodwin, Jane, Wroe, Jaime, Woolard, Alix, McCormack, Lynne, Campbell, Linda. Springer; 2023. Stigma Associated with Parenting an Autistic Child with Aggressive Behaviour: a Systematic Review.

Zhao, Yingjie, Wang, Yujue, Johnston, H. Richard, Chow, Eva W. C., Vorstman, Jacob A. S., Vingerhoets, Claudia, van Amelsvoort, Therese, Gothelf, Doron, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Eliez, Stephan, Shi, Lijie, Schneider, Maude, van den Bree, MBM, Owen, MJ, Kates, WR, Repetto, GM, Shashi, V, Schoch, K, Bearden, CE, Digilio, MC, Unolt, M, McDonald-McGinn, Donna M., Putotto, C, Marino, B, Pontillo, M, Armando, M, Vicari, S, Angkustsiri, K, Campbell, Linda, Busa, T, Heine-Suñer, D, Murphy, KC, Crowley, T. Blaine, Murphy, D, García-Miñaúr, S, Fernández, L, International 22q11.2 Brain and Behavior Consortium (IBBC),, Zhang, ZD, Goldmuntz, E, Gur, RE, Emanuel, BS, Zheng, D, Marshall, CR, McGinn, Daniel E., Bassett, AS, Wang, T, Morrow, BE, Tran, Oanh T., Miller, Daniella, Lin, Jhih-Rong, Zackai, Elaine. Nature Publishing Group; 2023. Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS..

Roche, Laura, Flynn, Traci, Campbell, Linda. LIDSEN; 2024. Exploring Education for Children with 22q11.2 Deletion Syndrome: A Qualitative Study of Mothers Perspectives.

Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Campbell, Linda, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, Maria Angeles, Epstein, Michael P., Evers, Rens, Fernandez, L, Fritsch, Rosemarie, Algas, Fernando Garcia, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Terese, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D. A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A. S., Gothelf, Doron, Zackai, Elaine, Agopian, A. J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.. Cell Press; 2020. Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects.

Hutchesson, Melinda, Campbell, Linda, Leonard, Alecia, Vincze, Lisa, Shrewsbury, Vanessa, Collins, Clare, Taylor, Rachael. Elsevier; 2022. Do modifiable risk factors for cardiovascular disease post-pregnancy influence the association between hypertensive disorders of pregnancy and cardiovascular health outcomes? A systematic review of observational studies.