Showing 1–15 of 15 results
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Research | | Open
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Research |
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
- anne.bassett@utoronto.ca
- Isabelle Cleynen
- , Worrawat Engchuan
- , Matthew S. Hestand
- , Tracy Heung
- , Aaron M. Holleman
- , H. Richard Johnston
- , Thomas Monfeuga
- , Donna M. McDonald-McGinn
- , Raquel E. Gur
- , Bernice E. Morrow
- , Ann Swillen
- , Jacob A. S. Vorstman
- , Carrie E. Bearden
- , Eva W. C. Chow
- , Marianne van den Bree
- , Beverly S. Emanuel
- , Joris R. Vermeesch
- , Stephen T. Warren
- , Michael J. Owen
- , Pankaj Chopra
- , David J. Cutler
- , Richard Duncan
- , Alex V. Kotlar
- , Jennifer G. Mulle
- , Anna J. Voss
- , Michael E. Zwick
- , Alexander Diacou
- , Aaron Golden
- , Tingwei Guo
- , Jhih-Rong Lin
- , Tao Wang
- , Zhengdong Zhang
- , Yingjie Zhao
- , Christian Marshall
- , Daniele Merico
- , Andrea Jin
- , Brenna Lilley
- , Harold I. Salmons
- , Oanh Tran
- , Peter Holmans
- , Antonio Pardinas
- , James T. R. Walters
- , Wolfram Demaerel
- , Erik Boot
- , Nancy J. Butcher
- , Gregory A. Costain
- , Chelsea Lowther
- , Rens Evers
- , Therese A. M. J. van Amelsvoort
- , Esther van Duin
- , Claudia Vingerhoets
- , Jeroen Breckpot
- , Koen Devriendt
- , Elfi Vergaelen
- , Annick Vogels
- , T. Blaine Crowley
- , Daniel E. McGinn
- , Edward M. Moss
- , Robert J. Sharkus
- , Marta Unolt
- , Elaine H. Zackai
- , Monica E. Calkins
- , Robert S. Gallagher
- , Ruben C. Gur
- , Sunny X. Tang
- , Rosemarie Fritsch
- , Claudia Ornstein
- , Gabriela M. Repetto
- , Elemi Breetvelt
- , Sasja N. Duijff
- , Ania Fiksinski
- , Hayley Moss
- , Maria Niarchou
- , Kieran C. Murphy
- , Sarah E. Prasad
- , Eileen M. Daly
- , Maria Gudbrandsen
- , Clodagh M. Murphy
- , Declan G. Murphy
- , Antonio Buzzanca
- , Fabio Di Fabio
- , Maria C. Digilio
- , Maria Pontillo
- , Bruno Marino
- , Stefano Vicari
- , Karlene Coleman
- , Joseph F. Cubells
- , Opal Y. Ousley
- , Miri Carmel
- , Doron Gothelf
- , Ehud Mekori-Domachevsky
- , Elena Michaelovsky
- , Ronnie Weinberger
- , Abraham Weizman
- , Leila Kushan
- , Maria Jalbrzikowski
- , Marco Armando
- , Stéphan Eliez
- , Corrado Sandini
- , Maude Schneider
- , Frédérique Sloan Béna
- , Kevin M. Antshel
- , Wanda Fremont
- , Wendy R. Kates
- , Raoul Belzeaux
- , Tiffany Busa
- , Nicole Philip
- , Linda E. Campbell
- , Kathryn L. McCabe
- , Stephen R. Hooper
- , Kelly Schoch
- , Vandana Shashi
- , Tony J. Simon
- , Flora Tassone
- , Celso Arango
- , David Fraguas
- , Sixto García-Miñaúr
- , Jaume Morey-Canyelles
- , Jordi Rosell
- , Damià H. Suñer
- , Jasna Raventos-Simic
- , Michael P. Epstein
- , Nigel M. Williams
- & Anne S. Bassett
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Research |
A genetic model for multimorbidity in young adults
- anne.bassett@utoronto.ca
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Research | | Open
All-cause mortality and survival in adults with 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
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Research | | Open
Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot
- anne.bassett@utoronto.ca
- Miriam S. Reuter
- , Rebekah Jobling
- , Rajiv R. Chaturvedi
- , Roozbeh Manshaei
- , Gregory Costain
- , Tracy Heung
- , Meredith Curtis
- , S. Mohsen Hosseini
- , Eriskay Liston
- , Chelsea Lowther
- , Erwin Oechslin
- , Heinrich Sticht
- , Bhooma Thiruvahindrapuram
- , Spencer van Mil
- , Rachel M. Wald
- , Susan Walker
- , Christian R. Marshall
- , Candice K. Silversides
- , Stephen W. Scherer
- , Raymond H. Kim
- & Anne S. Bassett
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Research |
Obesity in adults with 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
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Research |
Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
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Research |
Fetal growth and gestational factors as predictors of schizophrenia in 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
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Research |
1q21.1 Microduplication expression in adults
- anne.bassett@utoronto.ca
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Research |
Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
- anne.bassett@utoronto.ca
- Chelsea Lowther
- , Marsha Speevak
- , Christine M. Armour
- , Elaine S. Goh
- , Gail E. Graham
- , Chumei Li
- , Susan Zeesman
- , Malgorzata J.M. Nowaczyk
- , Lee-Anne Schultz
- , Antonella Morra
- , Rob Nicolson
- , Peter Bikangaga
- , Dawa Samdup
- , Mostafa Zaazou
- , Kerry Boyd
- , Jack H. Jung
- , Victoria Siu
- , Manjulata Rajguru
- , Sharan Goobie
- , Mark A. Tarnopolsky
- , Chitra Prasad
- , Paul T. Dick
- , Asmaa S. Hussain
- , Margreet Walinga
- , Renske G. Reijenga
- , Matthew Gazzellone
- , Anath C. Lionel
- , Christian R. Marshall
- , Stephen W. Scherer
- , Dimitri J. Stavropoulos
- , Elizabeth McCready
- & Anne S. Bassett
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Research |
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Research |
Functional outcomes of adults with 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
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Reviews |
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Reviews | | Open
The importance of copy number variation in congenital heart disease
- anne.bassett@utoronto.ca
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Reviews |
Practical guidelines for managing adults with 22q11.2 deletion syndrome
- anne.bassett@utoronto.ca
- Wai Lun Alan Fung
- , Nancy J. Butcher
- , Gregory Costain
- , Danielle M. Andrade
- , Erik Boot
- , Eva W.C. Chow
- , Brian Chung
- , Cheryl Cytrynbaum
- , Hanna Faghfoury
- , Leona Fishman
- , Sixto García-Miñaúr
- , Susan George
- , Anthony E. Lang
- , Gabriela Repetto
- , Andrea Shugar
- , Candice Silversides
- , Ann Swillen
- , Therese van Amelsvoort
- , Donna M. McDonald-McGinn
- & Anne S. Bassett
