A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome by Fiksinski, Ania M., Hoftman, Gil D., Vorstman, Jacob A. S., Bearden, Carrie E.

Get full text

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome by Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.

Get full text

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome by Fiksinski, Ania M., Schneider, Maude, Murphy, Clodagh M., Armando, Marco, Vicari, Stefano, Canyelles, Jaume M., Gothelf, Doron, Eliez, Stephan, Breetvelt, Elemi J., Arango, Celso, Vorstman, Jacob A. S.

Get full text

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants by Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

Get full text

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model by Fiksinski, Ania M., Heung, Tracy, Corral, Maria, Breetvelt, Elemi J., Costain, Gregory, Marshall, Christian R., Kahn, Rene S., Vorstman, Jacob A.S., Bassett, Anne S.

Get full text

A normative chart for cognitive development in a genetically selected population by Fiksinski, Ania M, Bearden, Carrie E, Bassett, Anne S, Kahn, René S, Zinkstok, Janneke R, Hooper, Stephen R, Tempelaar, Wanda, McDonald-McGinn, Donna, Swillen, Ann, Emanuel, Beverly, Morrow, Bernice, Gur, Raquel, Chow, Eva, van den Bree, Marianne, Vermeesch, Joris, Warren, Stephen, Owen, Michael, van Amelsvoort, Therese, Eliez, Stephan, Gothelf, Doron, Arango, Celso, Kates, Wendy, Simon, Tony, Murphy, Kieran, Repetto, Gabriela, Suner, Damian Heine, Vicari, Stefano, Cubells, Joseph, Armando, Marco, Philip, Nicole, Campbell, Linda, Garcia-Minaur, Sixto, Schneider, Maude, Shashi, Vandana, Vorstman, Jacob, Breetvelt, Elemi J

Get full text

Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome by Korteling, Dorinde, Boks, Marco P., Fiksinski, Ania M., van Hoek, Ilja N., Vorstman, Jacob A. S., Verhoeven-Duif, Nanda M., Jans, Judith J. M., Zinkstok, Janneke R.

Get full text

Low prevalence of substance use in people with 22q11.2 deletion syndrome by Vingerhoets, Claudia, van Oudenaren, Mathilde J.F., Bloemen, Oswald J.N., Boot, Erik, van Duin, Esther D.A., Evers, Laurens J.M., Fiksinski, Ania M., Breetvelt, Elemi J., Palmer, Lisa D., Vergaelen, Elfi, Vogels, Annick, Meijer, Carin, Booij, Jan, de Haan, Liewe, Swillen, Ann, Vorstman, Jacob A.S., Bassett, Anne S., van Amelsvoort, Therese A.M.J.

Get full text

White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline by Nuninga, Jasper Olivier, Bohlken, Marc Marijn, Koops, Sanne, Fiksinski, Ania M., Mandl, René C. W., Breetvelt, Elemi J., Duijff, Sasja N., Kahn, René S., Sommer, Iris E. C., Vorstman, Jacob A. S.

Get full text

Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins by Vervoort, Lisanne, Demaerel, Wolfram, Rengifo, Laura Y, Odrzywolski, Adrian, Vergaelen, Elfi, Hestand, Matthew S, Breckpot, Jeroen, Devriendt, Koen, Swillen, Ann, McDonald-McGinn, Donna M, Fiksinski, Ania M, Zinkstok, Janneke R, Morrow, Bernice E, Heung, Tracy, Vorstman, Jacob A S, Bassett, Anne S, Chow, Eva W C, Shashi, Vandana, Vermeesch, Joris R

Get full text

Transcriptomic profiling of whole blood in 22q11.2 reciprocal copy number variants reveals that cell proportion highly impacts gene expression by Lin, Amy, Forsyth, Jennifer K., Hoftman, Gil D., Kushan-Wells, Leila, Jalbrzikowski, Maria, Dokuru, Deepika, Coppola, Giovanni, Fiksinski, Ania, Zinkstok, Janneke, Vorstman, Jacob, Nachun, Daniel, Bearden, Carrie E.

Get full text

TU48. THE COMPLETE IQ PROFILE OVER THE LIFESPAN IN INDIVIDUALS WITH 22Q11DS AND ASSOCIATIONS WITH COMMON GENETIC VARIATION FOR IQ AND SCHIZOPHRENIA by Fiksinski, Ania, Wierenga, Rielle, Vorstman, Jacob, van Amelsvoort, Therese

Get full text

S210. A Normative Chart for the Trajectory of Cognitive Functioning in a Genetically Selected Population: Longitudinal Findings From the International Brain and Behavior Consortium... by Fiksinski, Ania, Vorstman, Jacob, Bassett, Anne, Breetvelt, Elemi

Get full text

TU64. UNTARGETED METABOLIC PROFILING IN DRIED BLOOD SPOTS REVEALS METABOLIC FINGERPRINT FOR 22Q11.2 DELETION SYNDROME by Zinkstok, Janneke, Korteling, Dorinde, Fiksinski, Ania, Jans, Judith, Verhoeven, Nanda, Boks, Marco

Get full text

S132. A NORMATIVE CHART FOR THE TRAJECTORY OF COGNITIVE FUNCTIONING IN INDIVIDUALS AT HIGH RISK FOR SCHIZOPHRENIA: LONGITUDINAL FINDINGS FROM THE INTERNATIONAL BRAIN AND BEHAVIOR C... by Ania, Fiksinski, Vorstman, Jacob, Bassett, Anne, Breetvelt, Elemi

Get full text

Psychiatric phenotypes associated with hyperprolinemia: A systematic review by Namavar, Yasmin, Duineveld, Denise Joanne, Both, Geertje Ingena Angelique, Fiksinski, Ania Maria, Vorstman, Jacob Abraham Schrey, Verhoeven‐Duif, Nanda Margriet, Zinkstok, Janneke Rozemarijn

Get full text

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs by Meer, Dennis, Agartz, Ingrid, Arango, Celso, Ayesa‐Arriola, Rosa, Bakker, Geor, Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Caspers, Svenja, Crespo‐Facorro, Benedicto, Dale, Anders M., Dazzan, Paola, Zubicaray, Greig I., Donohoe, Gary, Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Håberg, Asta K., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hulshoff Pol, Hilleke E., Kushan, Leila, Liu, Jingyu, Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., Medland, Sarah E., Modenato, Claudia, Mühleisen, Thomas W., Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Ulfarsson, Magnus O., Vajdi, Ariana, Ent, Dennis, Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Zackai, Elaine H., Thompson, Paul M., Bearden, Carrie E., Blackburn, Nicholas B., Bøen, Rune, Zwarte, Sonja M. C., Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir‐Kwa, Jayne Y., Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Nyberg, Lars, Shumskaya, Elena, Sisodiya, Sanjay M., Steen, Vidar M., Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J., Campbell, Linda E., Crossley, Nicolas A., Crowley, T. Blaine, Daly, Eileen, Fiksinski, Ania M., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Jonas, Rachel K., Kates, Wendy R., Lin, Amy, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J., Simon, Tony. J., Amelsvoort, Therese, Vorstman, Jacob A. S.

Get full text

F207. Neurocognition and Adaptive Functioning in the 22q11.2 Deletion Syndrome Model of Schizophrenia by Fiksinski, Ania, Breetvelt, Elemi, Vorstman, Jacob, Lee, Erin, Boot, Erik, Butcher, Nancy, Palmer, Lisa, Chow, Eva, Kahn, René, Bassett, Anne

Get full text

F72. NEUROCOGNITION AND ADAPTIVE FUNCTIONING IN THE 22Q11.2 DELETION SYNDROME MODEL OF SCHIZOPHRENIA by Ania, Fiksinski, Breetvelt, Elemi, Vorstman, Jacob, Chow, Eva, Lee, Erin, Palmer, Lisa, Boot, Erik, Butcher, Nancy, Kahn, Rene, Bassett, Anne

Get full text

Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics by Forsyth, Jennifer K, Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R K, Villalon-Reina, Julio E, Thompson, Paul M, Bearden, Carrie E

Get full text