Anne Susan Bassett (Anne S Bassett, Anne Bassett)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 54

Top Venues

Genes

Research square

European journal of human genetics : EJHG

Molecular psychiatry

This page only lists publications with an associated author ORCID identifier.

Publications

Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran, Rajiv R Chaturvedi, Maian Roifman, Xin Chen, Roozbeh Manshaei, Nicole Martin, Simina McDermott, Vanda McNiven, Diane Myles-Reid, Lynne E Nield, Miriam S Reuter, Marci L B Schwartz, Patrick Shannon, Rachel Silver, Cherith Somerville, Ronni Teitelbaum, Laura Zahavich, Anne Susan Bassett, Raymond H Kim, Seema Mital, David Chitayat, Rebekah K Jobling
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease. European journal of human genetics : EJHG 32 (7) (2024)
Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran, Rajiv R Chaturvedi, Maian Roifman, Xin Chen, Roozbeh Manshaei, Nicole Martin, Simina McDermott, Vanda McNiven, Diane Myles-Reid, Lynne E Nield, Miriam S Reuter, Marci L B Schwartz, Patrick Shannon, Rachel Silver, Cherith Somerville, Ronni Teitelbaum, Laura Zahavich, Anne Susan Bassett, Raymond H Kim, Seema Mital, David Chitayat, Rebekah K Jobling
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease. European journal of human genetics : EJHG 32 (7) (2024)
Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran, Rajiv R Chaturvedi, Maian Roifman, Xin Chen, Roozbeh Manshaei, Nicole Martin, Simina McDermott, Vanda McNiven, Diane Myles-Reid, Lynne E Nield, Miriam S Reuter, Marci L B Schwartz, Patrick Shannon, Rachel Silver, Cherith Somerville, Ronni Teitelbaum, Laura Zahavich, Anne Susan Bassett, Raymond H Kim, Seema Mital, David Chitayat, Rebekah K Jobling
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease. European journal of human genetics : EJHG 32 (7) (2024)
Ruiyang Ge, Christopher R K Ching, Anne Susan Bassett, Leila Kushan, Kevin M Antshel, Therese van Amelsvoort, Geor Bakker, Nancy J Butcher, Linda E Campbell, Eva W C Chow, Michael Craig, Nicolas A Crossley, Adam Cunningham, Eileen Daly, Joanne L Doherty, Courtney A Durdle, Beverly S Emanuel, Ania Fiksinski, Jennifer K Forsyth, Wanda Fremont, Naomi J Goodrich-Hunsaker, Maria Gudbrandsen, Raquel E Gur, Maria Jalbrzikowski, Wendy R Kates, Amy Lin, David E J Linden, Kathryn L McCabe, Donna McDonald-McGinn, Hayley Moss, Declan G Murphy, Kieran C Murphy, Michael J Owen, Julio E Villalon-Reina, Gabriela M Repetto, David R Roalf, Kosha Ruparel, J Eric Schmitt, Sanne Schuite-Koops, Kathleen Angkustsiri, Daqiang Sun, Ariana Vajdi, Marianne van den Bree, Jacob Vorstman, Paul M Thompson, Fidel Vila-Rodriguez, Carrie E Bearden
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human brain mapping 45 (1) (2024)
Ruiyang Ge, Christopher R K Ching, Anne Susan Bassett, Leila Kushan, Kevin M Antshel, Therese van Amelsvoort, Geor Bakker, Nancy J Butcher, Linda E Campbell, Eva W C Chow, Michael Craig, Nicolas A Crossley, Adam Cunningham, Eileen Daly, Joanne L Doherty, Courtney A Durdle, Beverly S Emanuel, Ania Fiksinski, Jennifer K Forsyth, Wanda Fremont, Naomi J Goodrich-Hunsaker, Maria Gudbrandsen, Raquel E Gur, Maria Jalbrzikowski, Wendy R Kates, Amy Lin, David E J Linden, Kathryn L McCabe, Donna McDonald-McGinn, Hayley Moss, Declan G Murphy, Kieran C Murphy, Michael J Owen, Julio E Villalon-Reina, Gabriela M Repetto, David R Roalf, Kosha Ruparel, J Eric Schmitt, Sanne Schuite-Koops, Kathleen Angkustsiri, Daqiang Sun, Ariana Vajdi, Marianne van den Bree, Jacob Vorstman, Paul M Thompson, Fidel Vila-Rodriguez, Carrie E Bearden
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human brain mapping 45 (1) (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Ruiyang Ge, Christopher R K Ching, Anne Susan Bassett, Leila Kushan, Kevin M Antshel, Therese van Amelsvoort, Geor Bakker, Nancy J Butcher, Linda E Campbell, Eva W C Chow, Michael Craig, Nicolas A Crossley, Adam Cunningham, Eileen Daly, Joanne L Doherty, Courtney A Durdle, Beverly S Emanuel, Ania Fiksinski, Jennifer K Forsyth, Wanda Fremont, Naomi J Goodrich-Hunsaker, Maria Gudbrandsen, Raquel E Gur, Maria Jalbrzikowski, Wendy R Kates, Amy Lin, David E J Linden, Kathryn L McCabe, Donna McDonald-McGinn, Hayley Moss, Declan G Murphy, Kieran C Murphy, Michael J Owen, Julio E Villalon-Reina, Gabriela M Repetto, David R Roalf, Kosha Ruparel, J Eric Schmitt, Sanne Schuite-Koops, Kathleen Angkustsiri, Daqiang Sun, Ariana Vajdi, Marianne van den Bree, Jacob Vorstman, Paul M Thompson, Fidel Vila-Rodriguez, Carrie E Bearden
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human brain mapping 45 (1) (2024)
Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran, Rajiv R Chaturvedi, Maian Roifman, Xin Chen, Roozbeh Manshaei, Nicole Martin, Simina McDermott, Vanda McNiven, Diane Myles-Reid, Lynne E Nield, Miriam S Reuter, Marci L B Schwartz, Patrick Shannon, Rachel Silver, Cherith Somerville, Ronni Teitelbaum, Laura Zahavich, Anne Susan Bassett, Raymond H Kim, Seema Mital, David Chitayat, Rebekah K Jobling
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease. European journal of human genetics : EJHG 32 (7) (2024)
Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M D'Gama, Katherine Howell, Nicole S Y Liang, Amy McTague, Annapurna H Poduri, Kimberly Wiltrout, null null, Anne Susan Bassett, John Chrisodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A S Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. NPJ genomic medicine 9 (1) (2024)
Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran, Rajiv R Chaturvedi, Maian Roifman, Xin Chen, Roozbeh Manshaei, Nicole Martin, Simina McDermott, Vanda McNiven, Diane Myles-Reid, Lynne E Nield, Miriam S Reuter, Marci L B Schwartz, Patrick Shannon, Rachel Silver, Cherith Somerville, Ronni Teitelbaum, Laura Zahavich, Anne Susan Bassett, Raymond H Kim, Seema Mital, David Chitayat, Rebekah K Jobling
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease. European journal of human genetics : EJHG (2024)
Nikolai Gil D Reyes, Nathaniel Bendahan, Emily Swinkin, Anthony E Lang, Anne Susan Bassett
Levodopa-responsive dystonia, parkinsonism, and treatment-resistant schizoaffective disorder in Williams syndrome. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2024)
Ruiyang Ge, Christopher R K Ching, Anne Susan Bassett, Leila Kushan, Kevin M Antshel, Therese van Amelsvoort, Geor Bakker, Nancy J Butcher, Linda E Campbell, Eva W C Chow, Michael Craig, Nicolas A Crossley, Adam Cunningham, Eileen Daly, Joanne L Doherty, Courtney A Durdle, Beverly S Emanuel, Ania Fiksinski, Jennifer K Forsyth, Wanda Fremont, Naomi J Goodrich-Hunsaker, Maria Gudbrandsen, Raquel E Gur, Maria Jalbrzikowski, Wendy R Kates, Amy Lin, David E J Linden, Kathryn L McCabe, Donna McDonald-McGinn, Hayley Moss, Declan G Murphy, Kieran C Murphy, Michael J Owen, Julio E Villalon-Reina, Gabriela M Repetto, David R Roalf, Kosha Ruparel, J Eric Schmitt, Sanne Schuite-Koops, Kathleen Angkustsiri, Daqiang Sun, Ariana Vajdi, Marianne van den Bree, Jacob Vorstman, Paul M Thompson, Fidel Vila-Rodriguez, Carrie E Bearden
Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome. Human brain mapping 45 (1) (2024)
Ali AlMail, Ahmed Jamjoom, Amy Pan, Min Yi Feng, Vann Chau, Alissa M D'Gama, Katherine Howell, Nicole S Y Liang, Amy McTague, Annapurna H Poduri, Kimberly Wiltrout, null null, Anne Susan Bassett, John Chrisodoulou, Lucie Dupuis, Peter Gill, Tess Levy, Paige Siper, Zornitza Stark, Jacob A S Vorstman, Catherine Diskin, Natalie Jewitt, Danielle Baribeau, Gregory Costain
Consensus reporting guidelines to address gaps in descriptions of ultra-rare genetic conditions. NPJ genomic medicine 9 (1) (2024)
Lisanne Vervoort, Nicolas Dierckxsens, Marta Sousa Santos, Senne Meynants, Erika Souche, Ruben Cools, Tracy Heung, Koen Devriendt, Hilde Peeters, Donna M McDonald-McGinn, Ann Swillen, Jeroen Breckpot, Beverly S Emanuel, Hilde Van Esch, Anne Susan Bassett, Joris Robert Vermeesch
Multiple paralogues and recombination mechanisms drive the high incidence of 22q11.2 Deletion Syndrome. bioRxiv : the preprint server for biology (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Yingjie Zhao, Yujue Wang, Lijie Shi, Donna M McDonald-McGinn, T Blaine Crowley, Daniel E McGinn, Oanh T Tran, Daniella Miller, Jhih-Rong Lin, Elaine H Zackai, H Richard Johnston, Eva W C Chow, Jacob A S Vorstman, Claudia Vingerhoets, Therese van Amelsvoort, Doron Gothelf, Ann Swillen, Jeroen Breckpot, Joris Robert Vermeesch, Stephan Eliez, Maude Schneider, Marianne B M van den Bree, Michael J Owen, Wendy R Kates, Gabriela M Repetto, Vandana Shashi, Kelly Schoch, Carrie E Bearden, M Cristina Digilio, Marta Unolt, Carolina Putotto, Bruno Marino, Maria Pontillo, Marco Armando, Stefano Vicari, Kathleen Angkustsiri, Linda Campbell, Tiffany Busa, Damian Heine-Suñer, Kieran C Murphy, Declan G M Murphy, Sixto García-Miñaúr, Luis Fernández, null null, Zhengdong D Zhang, Elizabeth Goldmuntz, Raquel E Gur, Beverly S Emanuel, Deyou Zheng, Christian R Marshall, Anne Susan Bassett, Tao Wang, Bernice E Morrow
Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS. NPJ genomic medicine 8 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Lauren K White, Terrence Blaine Crowley, Brenda Finucane, Emily J McClellan, Sarah Donoghue, Sixto Garcia-Minaur, Gabriela M Repetto, Matthias Fischer, Sebastien Jacquemont, Raquel E Gur, Anne Manuela Maillard, Kirsten Ann Donald, Anne Susan Bassett, Ann Swillen, Donna M McDonald-McGinn
Gathering the Stakeholder's Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Jhih-Rong Lin, Yingjie Zhao, M Reza Jabalameli, Nha Nguyen, Joydeep Mitra, null null, Ann Swillen, Jacob A S Vorstman, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Michael J Owen, Nigel M Williams, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur, Carrie E Bearden, Bernice E Morrow, Herbert M Lachman, Zhengdong D Zhang
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular psychiatry (2023)
Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Loo, Lauren A Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S Moldenhauer, Anne Susan Bassett, Donna M McDonald-McGinn
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Bahareh A Mojarad, Worrawat Engchuan, Brett Trost, Ian Backstrom, Yue Yin, Bhooma Thiruvahindrapuram, Linda 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 Susan Bassett, Ryan K C Yuen
Genome-wide tandem repeat expansions contribute to schizophrenia risk. Molecular psychiatry 27 (9) (2022)
Maurice Pasternak, Zahra Shirzadi, Henk-Jan Mm Mutsaerts, Erik Boot, Nancy J Butcher, Bradley J MacIntosh, Tracy Heung, Anne Susan Bassett, Mario Masellis
Elevated regional cerebral blood flow in adults with 22q11.2 deletion syndrome. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry (2022)
Miriam S Reuter, Michael Zech, Maja Hempel, Janine Altmüller, Tracy Heung, Laura Pölsler, René Santer, Holger Thiele, Brett Trost, Christian Kubisch, Stephen W Scherer, Sabine Rudnik-Schöneborn, Anne Susan Bassett, Davor Lessel
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies. European journal of human genetics : EJHG 30 (5) (2022)
Erik Boot, Connie Marras, Anne Susan Bassett
Spectrum of movement disorders and motor abnormalities in adults with a 22q11.2 microdeletion: Comment on the literature and retrospective study of 92 adults. European journal of human genetics : EJHG 30 (12) (2022)
Christina Blagojevic, Tracy Heung, Sarah Malecki, Shengjie Ying, Sabrina Cancelliere, Robert A Hegele, Anne Susan Bassett
Hypertriglyceridemia in young adults with a 22q11.2 microdeletion. European journal of endocrinology 187 (1) (2022)
Daniel E McGinn, Terrence Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H Zackai, Beverly S Emanuel, Eva W C Chow, Bernice E Morrow, Ann Swillen, Anne Susan Bassett, Donna M McDonald-McGinn
Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes 13 (10) (2022)
Lisa D Palmer, Zoë McManus, Tracy Heung, Grace McAlpine, Christina Blagojevic, Maria Corral, Anne Susan Bassett
Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome. Genes 13 (11) (2022)
Irene E Drmic, Bonnie MacKinnon Modi, Beth McConnell, Sanne Jilderda, Ny Hoang, Abdul Noor, Anne Susan Bassett, Marsha Speevak, Dimitri J Stavropoulos, Melissa T Carter
Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication. American journal of medical genetics. Part A 188 (10) (2022)
Jia Wen, Brett Trost, Worrawat Engchuan, Matthew Halvorsen, Linda M Pallotto, Aleksandra Mitina, NaEshia Ancalade, Martilias S Farrell, Ian Backstrom, Keyi Guo, Giovanna Pellecchia, Bhooma Thiruvahindrapuram, Paola Giusti-Rodriguez, Jonathan David Rosen, Yun Li, Hyejung Won, Patrik K E Magnusson, Ulf Gyllensten, Anne Susan Bassett, Christina M Hultman, Patrick F Sullivan, Ryan K C Yuen, Jin P Szatkiewicz
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia. Molecular psychiatry (2022)
Tracy Heung, Brigid Conroy, Sarah Malecki, Joanne Ha, Erik Boot, Maria Corral, Anne Susan Bassett
Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome. Genes 13 (11) (2022)
Doris Skoric-Milosavljevic, Rafik Tadros, Fernanda M Bosada, Federico Tessadori, Jan Hendrik van Weerd, Odilia Ilse Woudstra, Fleur V Y Tjong, Najim Lahrouchi, Fanny Bajolle, Heather J Cordell, A J Agopian, Gillian M Blue, Daniela Qcm Barge-Schaapveld, Stephen Brown, Christoph Preuss, Elisabeth M Lodder, Phil Barnett, Aho Ilgun, Leander Beekman, Karel van Duijvenboden, Regina Bokenkamp, Martina Müller-Nuraysid, Hubert W Vliegen, Thelma C Konings, Joost P van Melle, Arie van Dijk, Roland Rj van Kimmenade, Jolien W Roos-Hesselink, Gertjan Sieswerda, Folkert Meijboom, Hashim Abdul-Khaliq, Felix Berger, Sven Dittrich, Marc-Phillip Hitz, Julia Moosmann, Frank-Thomas Riede, Stephan Schubert, Pilar Galan, G Mark Lathrop, Hans Markus Munter, Ammar Al Chalabi, Christopher E Shaw, Pamela J Shaw, Karen E Morrison, Jan Herman Veldink, Leonard H van den Berg, Sylvia M Evans, Marcelo Aguiar Nobrega, Ivy Aneas, Milena Radivojkov-Blagojevic, Thomas Meitinger, Erwin Oechslin, Tapas Mondal, M Lynn Bergin, John F Smythe, Luis Altamirano-Diaz, Jane Lougheed, Berto Jorrit Bouma, Marie-A Chaix, Jennie Kline, Anne Susan Bassett, Gregor U Andelfinger, Roel L F van der Palen, Patrice Bouvagnet, Sally-Ann B Clur, Jeroen Breckpot, Wilhelmina S Kerstjens-Frederikse, David S Winlaw, Ulrike Bauer, Seema Mital, Elizabeth Goldmuntz, Bernard D Keavney, Damien Bonnet, Barbara J Mulder, Michael W T Tanck, Jeroen Bakkers, Vincent M Christoffels, Cornelis J Boogerd, Alex V Postma, Connie R Bezzina
Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. Circulation research (2021)
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne Susan Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers E F Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl D Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill Anne Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor U Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS genetics 17 (7) (2021)
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, Ian Backstrom, Gregory Costain, Tracy Heung, Daniele Merico, Christian R Marshall, Anne Susan Bassett, Ryan K C Yuen
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia. Translational psychiatry 11 (1) (2021)
Lisa D Palmer, Tracy Heung, Maria Corral, Erik Boot, Stephanie G Brooks, Anne Susan Bassett
Sexual knowledge and behaviour in 22q11.2 deletion syndrome, a complex care condition. Journal of applied research in intellectual disabilities : JARID (2021)
Ania M Fiksinski, Carrie E Bearden, Anne Susan Bassett, Rene S Kahn, Janneke R Zinkstok, Stephen R Hooper, Wanda Tempelaar, null null, Jacob A S Vorstman, Elemi J Breetvelt
A normative chart for cognitive development in a genetically selected population. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology (2021)
Erik Boot, Thierry Q Mentzel, Lisa D Palmer, Peter N van Harten, Connie Marras, Anthony E Lang, Anne Susan Bassett
Age-Related Parkinsonian Signs in Microdeletion 22q11.2. Movement disorders : official journal of the Movement Disorder Society 35 (7) (2020)
Joanne C Y Loo, Erik Boot, Maria Corral, Anne Susan Bassett
Personalized medical information card for adults with 22q11.2 deletion syndrome: An initiative to improve communication between patients and healthcare providers. Journal of applied research in intellectual disabilities : JARID 33 (6) (2020)
Robert William Davies, Ania M Fiksinski, Elemi J Breetvelt, Nigel M Williams, Stephen R Hooper, Thomas Monfeuga, Anne Susan Bassett, Michael J Owen, Raquel E Gur, Bernice E Morrow, Donna M McDonald-McGinn, Ann Swillen, Eva W C Chow, Marianne van den Bree, Beverly S Emanuel, Joris R Vermeesch, Therese van Amelsvoort, Celso Arango, Marco Armando, Linda E Campbell, Joseph F Cubells, Stephan Eliez, Sixto Garcia-Minaur, Doron Gothelf, Wendy R Kates, Kieran C Murphy, Clodagh M Murphy, Declan G M Murphy, Nicole Philip, Gabriela M Repetto, Vandana Shashi, Tony J Simon, Damiàn Heine Suñer, Stefano Vicari, Stephen W Scherer, null null, Carrie E Bearden, Jacob A S Vorstman
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome. Nature medicine 26 (12) (2020)
Lisa D Palmer, Nancy J Butcher, Erik Boot, Kathleen A Hodgkinson, Tracy Heung, Eva W C Chow, Alina Guna, T Blaine Crowley, Elaine Zackai, Donna M McDonald-McGinn, Anne Susan Bassett
Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome. American journal of medical genetics. Part A 176 (4) (2019)
Sarah L Voll, Spencer Van Mil, Justin Graffi, Elemi Breetvelt, Maria Corral, Erik Boot, Eva W C Chow, Marcos Sanches, Amol A Verma, Anne Susan Bassett
A genetic model for multimorbidity in young adults. Genetics in medicine : official journal of the American College of Medical Genetics 22 (1) (2019)
Petra C M Buijs, Anne Susan Bassett, Erik Boot
Non-pharmacological treatment of psychiatric disorders in individuals with 22q11.2 deletion syndrome; a systematic review. American journal of medical genetics. Part A 176 (8) (2018)
Yingjie Zhao, Tingwei Guo, Ania M Fiksinski, Elemi Breetvelt, Donna M McDonald-McGinn, Terrence B Crowley, Alexander Diacou, Maude Schneider, Stephan Eliez, Ann Swillen, Jeroen Breckpot, Joris Vermeesch, Eva W C Chow, Doron Gothelf, Sasja Duijff, Rens Evers, Thérèse A van Amelsvoort, Marianne van den Bree, Michael Owen, Maria Niarchou, Carrie E Bearden, Claudia Ornstein, Maria Pontillo, Antonino Buzzanca, Stefano Vicari, Marco Armando, Kieran C Murphy, Clodagh Murphy, Sixto Garcia-Minaur, Nicole Philip, Linda Campbell, Jaume Morey-Cañellas, Jasna Raventos, Jordi Rosell, Damian Heine-Suner, Robert J Shprintzen, Raquel E Gur, Elaine Zackai, Beverly S Emanuel, Tao Wang, Wendy R Kates, Anne Susan Bassett, Jacob A S Vorstman, Bernice E Morrow, null null
Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American journal of medical genetics. Part A 176 (10) (2018)
Nancy J Butcher, Erik Boot, Anthony E Lang, Danielle Andrade, Jacob Vorstman, Donna McDonald-McGinn, Anne Susan Bassett
Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series. American journal of medical genetics. Part A 176 (10) (2018)

Anne Susan Bassett.css-eqlu8i{font-size:small;padding-left:4px;} (Anne S Bassett, Anne Bassett)

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Anne Susan Bassett (Anne S Bassett, Anne Bassett)