"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

- Wroe, Jaime, Campbell, Linda, Fletcher, Richard, McLoughland, Carmel

A normative chart for cognitive development in a genetically selected population

- 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

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS.

- 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

Communication in 22q11.2 deletion syndrome: a brief overview of the profile, intervention approaches, and future considerations

- Roche, Laura, Campbell, Linda, Heussler, Helen

Complete sequence of the 22q11.2 allele in 1,053 subjects with 22q11.2 deletion syndrome reveals modifiers of conotruncal heart defects

- 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.

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

- Hutchesson, Melinda, Campbell, Linda, Leonard, Alecia, Vincze, Lisa, Shrewsbury, Vanessa, Collins, Clare, Taylor, Rachael

Exploring Education for Children with 22q11.2 Deletion Syndrome: A Qualitative Study of Mothers Perspectives

- Roche, Laura, Flynn, Traci, Campbell, Linda

Nested inversion polymorphisms predispose chromosome 22q11.2 to meiotic rearrangements

- 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.

Psychological therapies for anxiety in autistic individuals with co-occurring intellectual developmental disorder: A systematic review

- Kazzi, Christina, Campbell, Linda, Porter, Melanie

Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome

- 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

SMS4 perinatal parents: designing parenting support via text messages for mothers with severe mental illness (SMI) and their partners

- Fletcher, Richard, Campbell, Linda, Sved Williams, Anne, Rawlinson, Catherine, Dye, Jacob, Baldwin, Andrea, May, Chris, StGeorge, Jennifer

Stigma Associated with Parenting an Autistic Child with Aggressive Behaviour: a Systematic Review

- Swaab, Linda, Goodwin, Jane, Wroe, Jaime, Woolard, Alix, McCormack, Lynne, Campbell, Linda

The experiences of Australian parents with psychosis: the second Australian national survey of psychosis

- Campbell, Linda, Hanlon, Mary-Claire, Poon, Abner Weng Cheong, Paolini, Stefania, Stone, Melanie, Galletly, Cherrie, Stain, Helen J., Cohen, Martin

Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

- 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

Visual scanning of faces in 22q11.2 deletion syndrome: attention to the mouth or the eyes?

- Campbell, Linda, McCabe, Kathryn, Leadbeater, Kate, Schall, Ulrich, Loughland, Carmel, Rich, Dominique

When I look into my baby's eyes...Infant emotion recognition by mothers with borderline personality disorder

- Elliot, Ricki-Leigh, Campbell, Linda, Hunter, Mick, Cooper, Gavin, Melville, Jessica, McCabe, Kathryn, Newman, Louise, Loughland, Carmel