Angela T Morgan (Angela Morgan)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 75

Top Venues

European journal of human genetics : EJHG

Molecular psychiatry

Journal of the American Society of Nephrology : JASN

Journal of medical genetics

The University of Queensland (PHD)

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

Education History

The University of Queensland

Australia

PHD

Publications

Michael Stephen Hildebrand, Ruth O Braden, Mariana L Lauretta, Antony Kaspi, Richard J Leventer, Melinda Anderson, Himanshu Goel, Melanie Bahlo, Ingrid Eileen Scheffer, David J Amor, Robert Janowski, Dierk Niessing, Angela T Morgan
Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder. Neurology. Genetics 10 (5) (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN (2024)
Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity (2024)
Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity 14 (4) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry 29 (5) (2024)
Michael Stephen Hildebrand, Ruth O Braden, Mariana L Lauretta, Antony Kaspi, Richard J Leventer, Melinda Anderson, Himanshu Goel, Melanie Bahlo, Ingrid Eileen Scheffer, David J Amor, Robert Janowski, Dierk Niessing, Angela T Morgan
Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder. Neurology. Genetics 10 (5) (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, Tamara Rybak, Floor Wildschut, Dagmar Berghuis, Angela T Morgan, Maria Pilar Trelles, Jeroen Ronald Scheepe, Regina Bökenkamp, Cacha M P C D Peeters-Scholte, Ruth Braden, Gijs W E Santen
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of medical genetics 61 (4) (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry 29 (5) (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, Tamara Rybak, Floor Wildschut, Dagmar Berghuis, Angela T Morgan, Maria Pilar Trelles, Jeroen Ronald Scheepe, Regina Bökenkamp, Cacha M P C D Peeters-Scholte, Ruth Braden, Gijs W E Santen
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of medical genetics 61 (4) (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Patricia J McCabe, Molly Beiting, Elaine R Hitchcock, Edwin Maas, Amy Meredith, Angela T Morgan, Nancy L Potter, Jonathan L Preston, Laura Moorer, Pooja Aggarwal, Kirrie J Ballard, Laura Baskall Smith, Nicole F Caballero, Kathryn L Cabbage, Julie Case, Susan Caspari, Karen V Chenausky, Shina Cook, Ewa Grzelak, Maryane Gomez, Aubrie Hagopian, Chantelle Highman, Anne Hodits, Jenya Iuzzini-Seigel, Jillian LeVos-Carlson, Barbara A Lewis, Patricia Mayro, Jyutika Mehta, Gabrielle Miller, Kimberly D Mory, Elizabeth Murray, Megan S Overby, Lucia Pasquel-Lefebvre, Derrick Peavy, Caitlin V Raaz, Brooke Rea, Denise Santos Ford, Lynn Smith, Michelle T Swartz, Melissa Taberski, Hayo Terband, Donna Claire Thomas, Hannah Valentine, Mirjam van Tellingen, Shelley L Velleman, Emily W Wang, Sarah White, Eddy Chun Ho Wong, Maria I Grigos
Research Priorities for Childhood Apraxia of Speech: A Long View. Journal of speech, language, and hearing research : JSLHR (2024)
Yan Meng, Stephanie Best, David J Amor, Ruth Braden, Angela T Morgan, Ilias Goranitis
The value of genomic testing in severe childhood speech disorders. European journal of human genetics : EJHG 32 (4) (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry 29 (5) (2024)
Marscha M Engelen, Marie-Christine J P Franken, Lottie W Stipdonk, Sarah E Horton, Victoria E Jackson, Sheena Reilly, Angela T Morgan, Simon E Fisher, Sandra van Dulmen, Else Eising
The Association Between Stuttering Burden and Psychosocial Aspects of Life in Adults. Journal of speech, language, and hearing research : JSLHR 67 (5) (2024)
Katherine Hope Kenyon, Myrte Strik, Gustavo Noffs, Angela T Morgan, Scott Kolbe, Ian H Harding, Adam P Vogel, Frederique M C Boonstra, Anneke van der Walt
Volumetric and diffusion MRI abnormalities associated with dysarthria in multiple sclerosis. Brain communications 6 (3) (2024)
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Lotte Kleinendorst, Ozair Abawi, Niels Vos, Elisabeth F C van Rossum, Saskia M Maas, Angela T Morgan, Michael Stephen Hildebrand, Jorge D Da Silva, Ralph J Florijn, Peter Lauffer, Jenny A Visser, Elisabeth F C van Rossum, Erica L T van den Akker, Mieke M van Haelst
GNB1 and obesity: Evidence for a correlation between haploinsufficiency and syndromic obesity. Clinical obesity 14 (4) (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry 29 (5) (2024)
Katherine Hope Kenyon, Myrte Strik, Gustavo Noffs, Angela T Morgan, Scott Kolbe, Ian H Harding, Adam P Vogel, Frederique M C Boonstra, Anneke van der Walt
Volumetric and diffusion MRI abnormalities associated with dysarthria in multiple sclerosis. Brain communications 6 (3) (2024)
Angela T Morgan, Ben Coleman, Adam P Vogel, Alisdair McNeill, Peter Nick Robinson
Speech and language classification in the human phenotype ontology. European journal of human genetics : EJHG (2024)
Angela T Morgan, David J Amor, Miya D St John, Ingrid Eileen Scheffer, Michael Stephen Hildebrand
Genetic architecture of childhood speech disorder: a review. Molecular psychiatry (2024)
Elana J Forbes, Lottie D Morison, Fatma Lelik, Tegan Howell, Simone Debono, Himanshu Goel, Pauline Burger, Jean-Louis Mandel, David Geneviève, David J Amor, Angela T Morgan
Speech and language in DDX3X-neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 195 (6) (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 is Required for Renal Intercalated Dell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN (2024)
Lottie D Morison, Milou G P Kennis, Dmitrijs Rots, Arianne Bouman, Joost Kummeling, Elizabeth Palmer, Adam P Vogel, Frederique Liegeois, Amanda Brignell, Siddharth Srivastava, Zoe Frazier, Di Milnes, Himanshu Goel, David J Amor, Ingrid E Scheffer, Tjitske Kleefstra, Angela T Morgan
Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. Journal of medical genetics 61 (6) (2024)
Patricia J McCabe, Molly Beiting, Elaine R Hitchcock, Edwin Maas, Amy Meredith, Angela T Morgan, Nancy L Potter, Jonathan L Preston, Laura Moorer, Pooja Aggarwal, Kirrie J Ballard, Laura Baskall Smith, Nicole F Caballero, Kathryn L Cabbage, Julie Case, Susan Caspari, Karen V Chenausky, Shina Cook, Ewa Grzelak, Maryane Gomez, Aubrie Hagopian, Chantelle Highman, Anne Hodits, Jenya Iuzzini-Seigel, Jillian LeVos-Carlson, Barbara A Lewis, Patricia Mayro, Jyutika Mehta, Gabrielle Miller, Kimberly D Mory, Elizabeth Murray, Megan S Overby, Lucia Pasquel-Lefebvre, Derrick Peavy, Caitlin V Raaz, Brooke Rea, Denise Santos Ford, Lynn Smith, Michelle T Swartz, Melissa Taberski, Hayo Terband, Donna Claire Thomas, Hannah Valentine, Mirjam van Tellingen, Shelley L Velleman, Emily W Wang, Sarah White, Eddy Chun Ho Wong, Maria I Grigos
Research Priorities for Childhood Apraxia of Speech: A Long View. Journal of speech, language, and hearing research : JSLHR (2024)
Shi-Ting Wu, Yu Feng, Renhua Song, Yanmiao Qi, Lin Li, Dongbo Lu, Yixuan Wang, Wenrun Wu, Angela T Morgan, Xiaohong Wang, Yin Xia, Renjing Liu, Stephen I Alexander, Justin Jong-Leong Wong, Yuzhen Zhang, Xiangjian Zheng
Foxp1 Is Required for Renal Intercalated Cell Differentiation and Acid-Base Regulation. Journal of the American Society of Nephrology : JASN 35 (5) (2024)
Marscha M Engelen, Marie-Christine J P Franken, Lottie W Stipdonk, Sarah E Horton, Victoria E Jackson, Sheena Reilly, Angela T Morgan, Simon E Fisher, Sandra van Dulmen, Else Eising
The Association Between Stuttering Burden and Psychosocial Aspects of Life in Adults. Journal of speech, language, and hearing research : JSLHR (2024)
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, Tamara Rybak, Floor Wildschut, Dagmar Berghuis, Angela T Morgan, Maria Pilar Trelles, Jeroen Ronald Scheepe, Regina Bökenkamp, Cacha M P C D Peeters-Scholte, Ruth Braden, Gijs W E Santen
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of medical genetics (2023)
Angela T Morgan, Thomas S Scerri, Adam P Vogel, Christopher A Reid, Mara Quach, Victoria E Jackson, Chaseley McKenzie, Emma L Burrows, Mark F Bennett, Samantha J Turner, Sheena Reilly, Sarah E Horton, Susan Block, Elaina Kefalianos, Carlos Frigerio-Domingues, Eduardo Sainz, Kristin A Rigbye, Travis J Featherby, Kay L Richards, Andrew Kueh, Marco J Herold, Mark A Corbett, Jozef Gecz, Ingo Helbig, Daisy G Y Thompson-Lake, Frédérique J Liégeois, Robert J Morell, Andrew Hung, Dennis Drayna, Ingrid E Scheffer, David K Wright, Melanie Bahlo, Michael Stephen Hildebrand
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40. Brain : a journal of neurology (2023)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Lottie D Morison, Olivia van Reyk, Elana Forbes, Flavien Rouxel, Laurence Faivre, Fiona Bruinsma, Marie Vincent, Marie-Line Jacquemont, Natalie L Dykzeul, David Genevieve, David J Amor, Angela T Morgan
CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases. European journal of human genetics : EJHG (2023)
Mariana L Lauretta, Anna I Jarmolowicz, David J Amor, Stephanie Best, Angela T Morgan
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech. Journal of speech, language, and hearing research : JSLHR (2023)
Sarah E Horton, Victoria Jackson, Jessica O Boyce, Marie-Christine J P Franken, Stephanie Siemers, Miya St John, Stephen Hearps, Olivia van Reyk, Ruth Braden, Richard Parker, Adam P Vogel, Else Eising, David J Amor, Janelle Irvine, Simon E Fisher, Nicholas G Martin, Sheena Reilly, Melanie Bahlo, Ingrid Scheffer, Angela T Morgan
Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in Stuttering. Journal of speech, language, and hearing research : JSLHR (2023)
Alexandra F Bonthrone, Dido Green, Angela T Morgan, Kshitij Mankad, Christopher A Clark, Frédérique J Liégeois
Attention and motor profiles in children with developmental coordination disorder: A neuropsychological and neuroimaging investigation. Developmental medicine and child neurology (2023)
Antony Kaspi, Michael Stephen Hildebrand, Victoria E Jackson, Ruth Braden, Olivia van Reyk, Tegan Howell, Simone Debono, Mariana Lauretta, Lottie Morison, Matthew J Coleman, Richard Webster, David Coman, Himanshu Goel, Mathew Wallis, Gabriel Dabscheck, Lilian Downie, Emma K Baker, Bronwyn Parry-Fielder, Kirrie Ballard, Eva Harrold, Shaun Ziegenfusz, Mark F Bennett, Erandee Robertson, Longfei Wang, Amber Boys, Simon E Fisher, David J Amor, Ingrid Eileen Scheffer, Melanie Bahlo, Angela T Morgan
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular psychiatry (2023)
Antony Kaspi, Michael Stephen Hildebrand, Victoria E Jackson, Ruth Braden, Olivia van Reyk, Tegan Howell, Simone Debono, Mariana Lauretta, Lottie Morison, Matthew J Coleman, Richard Webster, David Coman, Himanshu Goel, Mathew Wallis, Gabriel Dabscheck, Lilian Downie, Emma K Baker, Bronwyn Parry-Fielder, Kirrie Ballard, Eva Harrold, Shaun Ziegenfusz, Mark F Bennett, Erandee Robertson, Longfei Wang, Amber Boys, Simon E Fisher, David J Amor, Ingrid Eileen Scheffer, Melanie Bahlo, Angela T Morgan
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular psychiatry (2023)
Alison Holm, Olivia van Reyk, Sharon Crosbie, Simone De Bono, Angela T Morgan, Barbara Dodd
Preschool children's consistency of word production. Clinical linguistics & phonetics (2022)
Loretta Gasparini, Daisy A Shepherd, Edith L Bavin, Patricia Eadie, Sheena Reilly, Angela T Morgan, Melissa Wake
Using machine-learning methods to identify early-life predictors of 11-year language outcome. Journal of child psychology and psychiatry, and allied disciplines (2022)
Miya St John, David J Amor, Angela T Morgan
Speech and language development and genotype-phenotype correlation in 49 individuals with KAT6A syndrome. American journal of medical genetics. Part A 188 (12) (2022)
Hayley S Mountford, Ruth Braden, Dianne F Newbury, Angela T Morgan
The Genetic and Molecular Basis of Developmental Language Disorder: A Review. Children (Basel, Switzerland) 9 (5) (2022)
Lottie D Morison, Ruth O Braden, David J Amor, Amanda Brignell, Bregje W M van Bon, Angela T Morgan
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments. European journal of human genetics : EJHG 30 (7) (2022)
Antony Kaspi, Michael Stephen Hildebrand, Victoria E Jackson, Ruth Braden, Olivia van Reyk, Tegan Howell, Simone Debono, Mariana Lauretta, Lottie Morison, Matthew J Coleman, Richard Webster, David Coman, Himanshu Goel, Mathew Wallis, Gabriel Dabscheck, Lilian Downie, Emma K Baker, Bronwyn Parry-Fielder, Kirrie Ballard, Eva Harrold, Shaun Ziegenfusz, Mark F Bennett, Erandee Robertson, Longfei Wang, Amber Boys, Simon E Fisher, David J Amor, Ingrid Eileen Scheffer, Melanie Bahlo, Angela T Morgan
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development. Molecular psychiatry (2022)
Miya St John, Olivia van Reyk, David A Koolen, Bert B A de Vries, David J Amor, Angela T Morgan
Expanding the speech and language phenotype in Koolen-de Vries syndrome: late onset and periodic stuttering a novel feature. European journal of human genetics : EJHG (2022)
Daisy G Y Thompson-Lake, Thomas S Scerri, Susan Block, Samantha J Turner, Sheena Reilly, Elaina Kefalianos, Alexandra F Bonthrone, Ingo Helbig, Melanie Bahlo, Ingrid E Scheffer, Michael S Hildebrand, Frédérique J Liégeois, Angela T Morgan
Atypical development of Broca's area in a large family with inherited stuttering. Brain : a journal of neurology 145 (3) (2022)
Jessica O Boyce, Victoria E Jackson, Olivia van Reyk, Richard Parker, Adam P Vogel, Else Eising, Sarah E Horton, Nathan A Gillespie, Ingrid Eileen Scheffer, David J Amor, Michael S Hildebrand, Simon E Fisher, Nicholas G Martin, Sheena Reilly, Melanie Bahlo, Angela T Morgan
Self-reported impact of developmental stuttering across the lifespan. Developmental medicine and child neurology 64 (10) (2022)
Else Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw, Carol A Wang, Dongnhu T Truong, Andrea G Allegrini, Chin Yang Shapland, Gu Zhu, Karen G Wigg, Margot L Gerritse, Barbara Molz, Gökberk Alagöz, Alessandro Gialluisi, Filippo Abbondanza, Kaili Rimfeld, Marjolein van Donkelaar, Zhijie Liao, Philip R Jansen, Till F M Andlauer, Timothy C Bates, Manon Bernard, Kirsten Blokland, Milene Bonte, Anders D Børglum, Thomas Bourgeron, Daniel Brandeis, Fabiola Ceroni, Valéria Csépe, Philip S Dale, Peter F de Jong, John C DeFries, Jean-François Démonet, Ditte Demontis, Yu Feng, Scott D Gordon, Sharon L Guger, Marianna Emma Hayiou-Thomas, Juan A Hernández-Cabrera, Jouke-Jan Hottenga, Charles Hulme, Juha Kere, Elizabeth N Kerr, Tanner Koomar, Karin Landerl, Gabriel T Leonard, Maureen W Lovett, Heikki Lyytinen, Nicholas G Martin, Angela Martinelli, Urs Maurer, Jacob J Michaelson, Kristina Moll, Anthony P Monaco, Angela T Morgan, Markus Maria Nöthen, Zdenka Pausova, Craig E Pennell, Bruce F Pennington, Kaitlyn M Price, Veera Manikandan Rajagopal, Franck Ramus, Louis Richer, Nuala H Simpson, Shelley D Smith, Margaret J Snowling, John F Stein, Lisa J Strug, Joel B Talcott, Henning Tiemeier, Marc P van der Schroeff, Ellen Verhoef, Kate E Watkins, Margaret Wilkinson, Margaret J Wright, Cathy L Barr, Dorret I Boomsma, Manuel Carreiras, Marie-Christine J Franken, Jeffrey R Gruen, Michelle Luciano, Bertram Müller-Myhsok, Dianne F Newbury, Richard K Olson, Silvia Paracchini, Tomáš Paus, Robert Plomin, Sheena Reilly, Gerd Schulte-Körne, J Bruce Tomblin, Elsje van Bergen, Andrew J O Whitehouse, Erik G Willcutt, Beate St Pourcain, Clyde Francks, Simon E Fisher
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Proceedings of the National Academy of Sciences of the United States of America 119 (35) (2022)
Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer, Katrin Schulze, Tracy Briggs, Ruth Braden, Adam P Vogel, Daisy Thompson-Lake, Chirag Patel, Edward Blair, Himanshu Goel, Samantha Turner, Ute Moog, Angelika Riess, Frederique Liegeois, David A Koolen, David J Amor, Tjitske Kleefstra, Simon E Fisher, Christiane Zweier, Angela T Morgan
In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 . Journal of medical genetics (2022)
Nadieh A Jansen, Ruth O Braden, Siddharth Srivastava, Erin F Otness, Gaëtan Lesca, Massimiliano Rossi, Mathilde Nizon, Raphael A Bernier, Chloé Quelin, Arie van Haeringen, Tjitske Kleefstra, Maggie M K Wong, Sandra Whalen, Simon E Fisher, Angela T Morgan, Bregje W van Bon
Clinical delineation of SETBP1 haploinsufficiency disorder. European journal of human genetics : EJHG 29 (8) (2021)
Ruth O Braden, Jessica O Boyce, Chloe A Stutterd, Kate Pope, Himanshu Goel, Richard J Leventer, Ingrid Eileen Scheffer, Angela T Morgan
Speech, Language, and Oromotor Skills in Patients With Polymicrogyria. Neurology 96 (14) (2021)
Ruth O Braden, David J Amor, Simon E Fisher, Cristina Mei, Candace T Myers, Heather Mefford, Deepak Gill, Siddharth Srivastava, Lindsay C Swanson, Himanshu Goel, Ingrid Eileen Scheffer, Angela T Morgan
Severe speech impairment is a distinguishing feature of FOXP1-related disorder. Developmental medicine and child neurology 63 (12) (2021)
Angela T Morgan, Ruth Braden, Maggie M K Wong, Estelle Colin, David Amor, Frederique Liégeois, Siddharth Srivastava, Adam Vogel, Varoona Bizaoui, Kara Ranguin, Simon E Fisher, Bregje W van Bon
Speech and language deficits are central to SETBP1 haploinsufficiency disorder. European journal of human genetics : EJHG 29 (8) (2021)
Amanda Brignell, Conway Gu, Alison Holm, Bronwyn Carrigg, Daisy A Sheppard, David J Amor, Angela T Morgan
Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome. European journal of human genetics : EJHG 29 (4) (2020)
Miya St John, Georgie Columbus, Amanda Brignell, Peter Carew, Jemma Skeat, Sheena Reilly, Angela T Morgan
Predicting speech-sound disorder outcomes in school-age children with hearing loss: The VicCHILD experience. International journal of language & communication disorders 55 (4) (2020)
Ruth O Braden, Richard J Leventer, Anna C Jansen, Ingrid Eileen Scheffer, Angela T Morgan
Speech and language in bilateral perisylvian polymicrogyria: a systematic review. Developmental medicine and child neurology 61 (10) (2019)
Jessica O Boyce, Katherine Sanchez, David J Amor, Sheena Reilly, Annette Da Costa, Nicky Kilpatrick, Angela T Morgan
Exploring the speech and language of individuals with non-syndromic submucous cleft palate: a preliminary report. International journal of language & communication disorders 54 (5) (2019)
Katherine Sanchez, Angela T Morgan
Music therapy for neurodevelopment in hospitalised infants. Acta paediatrica (Oslo, Norway : 1992) 108 (5) (2019)
Katherine Sanchez, Jessica O Boyce, Cristina Mei, Miya St John, Jodie Smith, Linda Leembruggen, Stephanie Mills, Alicia Jane Spittle, Angela T Morgan
Communication in children born very preterm: a prospective cohort study. Developmental medicine and child neurology 62 (4) (2019)
Barbara Dodd, Sheena Reilly, Kyriaki Ttofari Eecen, Angela T Morgan
Articulation or phonology? Evidence from longitudinal error data. Clinical linguistics & phonetics 32 (11) (2018)
Travis A Wearne, Vicki A Anderson, Cathy Catroppa, Angela T Morgan, Jennie Louise Ponsford, Robyn Tate, Tamara Ownsworth, Leanne Togher, Jennifer Fleming, Professor Jacinta Douglas, Kimberley M Docking, Linda Sigmundsdottir, Heather Francis, Cynthia Alison Honan, Skye McDonald
Psychosocial functioning following moderate-to-severe pediatric traumatic brain injury: recommended outcome instruments for research and remediation studies. Neuropsychological rehabilitation 30 (5) (2018)
Cristina Mei, Evelina Fedorenko, David J Amor, Amber Boys, Caitlyn Hoeflin, Peter Carew, Trent Burgess, Simon E Fisher, Angela T Morgan
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion. European journal of human genetics : EJHG 26 (5) (2018)
Else Eising, Amaia Carrión-Castillo, Arianna Vino, Edythe A Strand, Kathy J Jakielski, Thomas S Scerri, Michael Stephen Hildebrand, Richard Webster, Alan Ma, Bernard Mazoyer, Clyde Francks, Melanie Bahlo, Ingrid Eileen Scheffer, Angela T Morgan, Lawrence D Shriberg, Simon E Fisher
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development. Molecular psychiatry 24 (7) (2018)
Angela T Morgan, Leenke van Haaften, Karen van Hulst, Carol Edley, Cristina Mei, Tiong Yang Tan, David Amor, Simon E Fisher, David A Koolen
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotonia. European journal of human genetics : EJHG 26 (1) (2017)
Cynthia Alison Honan, Skye McDonald, Robyn Tate, Tamara Ownsworth, Leanne Togher, Jennifer Fleming, Vicki A Anderson, Angela T Morgan, Cathy Catroppa, Professor Jacinta Douglas, Heather Francis, Travis A Wearne, Linda Sigmundsdottir, Jennie Louise Ponsford
Outcome instruments in moderate-to-severe adult traumatic brain injury: recommendations for use in psychosocial research. Neuropsychological rehabilitation 29 (6) (2017)

Angela T Morgan.css-eqlu8i{font-size:small;padding-left:4px;} (Angela Morgan)

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Angela T Morgan (Angela Morgan)