Incidence of infective endocarditis in adults with congenital heart disease and diagnosed 22q11.2 deletion syndrome

by Adonis Ng, Tracy Heung, Erwin Oechslin, Jessica Patzer, Anne Bassett
Published 2021-10-01

Schizophrenia Risk Mediated by microRNA Target Genes Overlapped by Genome-Wide Rare Copy Number Variation in 22q11.2 Deletion Syndrome

by Shengjie Ying, Shengjie Ying, Tracy Heung, Tracy Heung, Zhaolei Zhang, Zhaolei Zhang, Zhaolei Zhang, Ryan K. C. Yuen, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett
Published 2022-04-01

Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome

by Tracy Heung, Brigid Conroy, Sarah Malecki, Joanne Ha, Erik Boot, Maria Corral, Anne S. Bassett
Published 2022-11-01

Abnormal spirometry in adults with 22q11.2 microdeletion and congenital heart disease

by Christina Blagojevic, Tracy Heung, Spencer van Mil, Erwin Oechslin, Candice K. Silversides, John T. Granton, Anne S. Bassett
Published 2021-05-01

Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome

by Lisa D. Palmer, Zoë McManus, Tracy Heung, Grace McAlpine, Christina Blagojevic, Maria Corral, Anne S. Bassett
Published 2022-11-01

Correction: Polygenic risk for triglyceride levels in the presence of a high impact rare variant

by Shengjie Ying, Tracy Heung, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Yue Yin, Christina Blagojevic, Zhaolei Zhang, Robert A. Hegele, Ryan K. C. Yuen, Anne S. Bassett
Published 2023-11-01

Polygenic risk for triglyceride levels in the presence of a high impact rare variant

by Shengjie Ying, Tracy Heung, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Yue Yin, Christina Blagojevic, Zhaolei Zhang, Robert A. Hegele, Ryan K. C. Yuen, Anne S. Bassett
Published 2023-11-01

Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia

by Bahareh A. Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R. Marshall, Anne S. Bassett, Ryan K. C. Yuen
Published 2021-02-01

22q11.2 microdeletion and increased risk for type 2 diabetes

by Lily Van, Tracy Heung, Sarah L. Malecki, Christian Fenn, Andrea Tyrer, Marcos Sanches, Eva W.C. Chow, Erik Boot, Maria Corral, Satya Dash, Susan R. George, Anne S. Bassett
Published 2020-09-01

Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome

by Daniel E. McGinn, T. Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H. Zackai, Beverly S. Emanuel, Eva W. C. Chow, Bernice E. Morrow, Ann Swillen, Anne S. Bassett, Donna M. McDonald-McGinn
Published 2022-10-01

Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences

by Roozbeh Manshaei, Daniele Merico, Daniele Merico, Miriam S. Reuter, Miriam S. Reuter, Worrawat Engchuan, Bahareh A. Mojarad, Rajiv Chaturvedi, Rajiv Chaturvedi, Tracy Heung, Tracy Heung, Giovanna Pellecchia, Mehdi Zarrei, Mehdi Zarrei, Thomas Nalpathamkalam, Reem Khan, John B. A. Okello, Eriskay Liston, Meredith Curtis, Ryan K. C. Yuen, Ryan K. C. Yuen, Ryan K. C. Yuen, Christian R. Marshall, Christian R. Marshall, Christian R. Marshall, Christian R. Marshall, Rebekah K. Jobling, Rebekah K. Jobling, Erwin Oechslin, Rachel M. Wald, Rachel M. Wald, Candice K. Silversides, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Raymond H. Kim, Raymond H. Kim, Raymond H. Kim, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett
Published 2020-09-01