檢索結果 - Tracy Heung

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  1. 1
    Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context

    Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context 由 Sarah Malecki, Tracy Heung, Walter P. Wodchis, Refik Saskin, Luís Brito Palma, Amol A. Verma, Anne S. Bassett

    出版 2024
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  2. 2
    Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening

    Estimate of the contemporary live-birth prevalence of recurrent 22q11.2 deletions: a cross-sectional analysis from population-based newborn screening 由 Christina Blagojevic, Tracy Heung, Mylène Thériault, Aoy Tomita‐Mitchell, Pranesh Chakraborty, Kristin D. Kernohan, Dennis E. Bulman, Anne S. Bassett

    出版 2021
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  3. 3
    Obesity in adults with 22q11.2 deletion syndrome

    Obesity in adults with 22q11.2 deletion syndrome 由 Sarah L. Voll, Erik Boot, Nancy J. Butcher, Samantha Cooper, Tracy Heung, Eva W.C. Chow, Candice K. Silversides, Anne S. Bassett

    出版 2016
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  4. 4
    All-cause mortality and survival in adults with 22q11.2 deletion syndrome

    All-cause mortality and survival in adults with 22q11.2 deletion syndrome 由 Lily Van, Tracy Heung, Justin Graffi, Enoch Ng, Sarah Malecki, Spencer van Mil, Erik Boot, Maria Corral, Eva W.C. Chow, Kathleen Hodgkinson, Candice K. Silversides, Anne S. Bassett

    出版 2019
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  5. 5
    Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome

    Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome 由 Lisa D. Palmer, Nancy J. Butcher, Erik Boot, Kathleen Hodgkinson, Tracy Heung, Eva W.C. Chow, Alina Guna, T. Blaine Crowley, Elaine H. Zackai, Donna M. McDonald‐McGinn, Anne S. Bassett

    出版 2018
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  6. 6
    Genome-wide tandem repeat expansions contribute to schizophrenia risk

    Genome-wide tandem repeat expansions contribute to schizophrenia risk 由 Bahareh A. Mojarad, Worrawat Engchuan, Brett Trost, Ian Backstrom, Yue Yin, Bhooma Thiruvahindrapuram, Linda M. Pallotto, Aleksandra Mitina, Mahreen Khan, Giovanna Pellecchia, Bushra Haque, Keyi Guo, Tracy Heung, Gregory Costain, Stephen W. Scherer, Christian R. Marshall, Christopher E. Pearson, Anne S. Bassett, Ryan K. C. Yuen

    出版 2022
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  7. 7
    Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot

    Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot 由 Miriam S. Reuter, Rebekah Jobling, Rajiv 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

    出版 2018
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  8. 8
    Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

    Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome 由 Anne S. Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W.C. Chow, Thérèse van Amelsvoort, Donna M. McDonald‐McGinn, Raquel E. Gur, Ann Swillen, Marianne B. M. van den Bree, Kieran C. Murphy, Doron Gothelf, Carrie E. Bearden, Stéphan Eliez, Wendy R. Kates, Nicole Philip, Vandana Sashi, Linda Campbell, Jacob Vorstman, Joseph F. Cubells, Gabriela M. Repetto, Tabassome Simon, Erik Boot, Tracy Heung, Rens Evers, Claudia Vingerhoets, Esther van Duin, Elaine H. Zackai, Elfi Vergaelen, Koenraad Devriendt, Joris Vermeesch, Michael J. Owen, Clodagh M. Murphy, Elena Michaelovosky, Leila Kushan, Maude Schneider, Wanda Fremont, Tiffany Busa, Stephen R. Hooper, Kathryn McCabe, Sasja N. Duijff, Keren Isaev, Giovanna Pellecchia, John Wei, Matthew J. Gazzellone, Stephen W. Scherer, Beverly S. Emanuel, Tingwei Guo, Bernice E. Morrow, Christian R. Marshall

    出版 2017
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  9. 9
    A large data resource of genomic copy number variation across neurodevelopmental disorders

    A large data resource of genomic copy number variation across neurodevelopmental disorders 由 Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, Edwin J. Young, Edward J. Higginbotham, Jeffrey R. MacDonald, Brett Trost, Ada J. S. Chan, Susan Walker, Sylvia Lamoureux, Tracy Heung, Bahareh A. Mojarad, Barbara Kellam, Tara Paton, Muhammad Faheem, Karin Miron, Chao Lu, Ting Wang, Kozue Samler, Xiaolin Wang, Gregory Costain, Ny Hoang, Giovanna Pellecchia, John Wei, Rohan Patel, Bhooma Thiruvahindrapuram, Maian Roifman, Daniele Merico, Tara Goodale, Irene Drmic, Marsha Speevak, Jennifer Howe, Ryan K. C. Yuen, Janet A. Buchanan, Jacob Vorstman, Christian R. Marshall, Richard F. Wintle, David R. Rosenberg, Gregory L. Hanna, Marc Woodbury‐Smith, Cheryl Cytrynbaum, Lonnie Zwaigenbaum, Mayada Elsabbagh, Janine Flanagan, Bridget A. Fernandez, Melissa T. Carter, Peter Szatmari, Wendy Roberts, Jason P. Lerch, Xudong Liu, Rob Nicolson, Stelios Georgiades, Rosanna Weksberg, Paul Arnold, Anne S. Bassett, Jennifer Crosbie, Russell Schachar, Dimitri J. Stavropoulos, Evdokia Anagnostou, Stephen W. Scherer

    出版 2019
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  10. 10
    Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

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

    出版 2019
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  11. 11
    Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

    Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion 由 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 Vorstman, Carrie E. Bearden, Eva W. C. Chow, Marianne B. M. van den Bree, B S Emanuel, Joris Vermeesch, Stephen T. Warren, Michael J. Owen, Pankaj Chopra, David J. Cutler, Richard Duncan, Alex 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 R. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Salmons, Oanh Tran, Peter Holmans, Antonio F. Pardiñas, James Walters, Wolfram Demaerel, Erik Boot, Nancy J. Butcher, Gregory Costain, Chelsea Lowther, Rens Evers, Thérèse van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koenraad Devriendt, Elfi Vergaelen, Annick Vogels, T. Blaine Crowley, Daniel E. McGinn, Edward Moss, Robert 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 Daly, Maria Gudbrandsen, Clodagh M. Murphy, Declan Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Cubells, Opal 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

    出版 2020
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