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David J. Amor

university of melbourne

72H-index
503Paper Count
2.0WCitation Count
Published Papers 206
Publication Date
Neuropathic pain in cerebral palsy and related genetic conditions: A scoping review of prevalence, characteristics, and management
err2026-08-18
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PREAI
errAayushi Khillan; Sanya Verma; Hannah Yeomans; Karen Bau; Caitlin Doyle; Monica S. Cooper; David J. Amor; Carolyn Berryman; Adrienne Harvey
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Genomics screening views and practices in South East Asian, Indian and Chinese populations: a scoping review
err2026-08-03
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errOAAI
errYasmin Bylstra; Myrabeth Yeo Juann; Junyu Zhang; Melody Menezes; Jan Hodgson; Saumya S. Jamuar; David J. Amor
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Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants.
err2026-07-08
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errOAAI
errDavid E. Godler; Ling Ling; Dinusha Gamage; Minh Bui; Michael J. Field; David J. Amor
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Functional impact of genetic background on variable expressivity in neurodevelopmental disorders
err2026-05-01
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errOAAI
errJiawan Sun; Serena Noss; Corrine Smolen; Venkata Hemanjani Bhavana; Deepro Banerjee; Maitreya Das; Belinda Giardine; Anisha Prabhu; David J. Amor; Kate Pope; Paul J. Lockhart; Santhosh Girirajan
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Childhood motor speech disorders: who to prioritise for genetic testing
err2026-01-13
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errOAAI
errHalianna Van Niel; Mariana Lauretta; Emma Baker; Lorraine O’Donnell; Charlotte Boulton; Celia Brenchley; David Coman; Evyenia Michellis; Himanshu Goel; Geoff Thompson; Richard Webster; Georgia Paxton; Zornitza Stark; Ingrid E. Scheffer; Michael S. Hildebrand; David J. Amor; Angela T. Morgan
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Unexpected genotypes associated with severe paediatric conditions identified in a healthy population cohort
err2026-01-10
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PREAI
errYasmin Bylstra; Weng Khong Lim; Jing Xian Teo; Melody Menezes; Jan Hodgson; Fabian Yap; John C. Chambers; Khung Keong Yeo; Patrick Tan; David J. Amor; Saumya S. Jamuar
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Expanding carrier screening: beyond the genes, to include underrepresented ancestries
err2025-12-26
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errOAAI
errYasmin Bylstra; Pua Chee Jian; Sui Lin; Jeannette Goh; Christina Choi; Jing Xian Teo; Sandy Lim; Jan Hodgson; Melody Menezes; Ruifen Weng; David J. Amor; Weng Khong Lim; Saumya S. Jamuar
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Robert James McKinlay (“Mac”) Gardner
err2025-12-20
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errOAAI
errDavid J. Amor; Elsdon Storey; Stephen P. Robertson
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Implementing Publicly Funded Fetal Exome Sequencing: A Statewide Multidisciplinary Model for Equitable Integration of Genomics Into Perinatal Care
err2025-12-01
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PREAI
errGheysen, Willem; Hamill, Calder; Fawcett, Susan; Davis, Tenielle; Vasudevan, Anand; Kane, Stefan C.; Graetz, Melissa; Dao, Candice; Amor, David J.; Downie, Lilian; Fahey, Michael C.; Gelfand, Nikki; Palmer, Kirsten R.; Riley, Kate; Said, Joanne M.; Hui, Lisa
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High prevalence of developmental coordination disorder risk in childhood apraxia of speech
err2025-12-01
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errOAAI
errTukel, Sermin; Baker, Emma K.; Tutuncu, G. Yazgi; O'Donnell, Lorraine; Lauretta, Mariana; Brenchley, Celia; Amor, David J.; Morgan, Angela T.
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Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study
err2025-10-09
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errOAAI
errSebastian Lunke; Lilian Downie; Jade Caruana; Nathasha Kugenthiran; Paul De Fazio; Sebastian Hollizeck; Sophie E. Bouffler; David J. Amor; Alison D. Archibald; Yvonne Bombard; John Christodoulou; Marc Clausen; Wendy Fagan; Clara Gaff; Ronda F. Greaves; Christopher Gyngell; Anaita Kanga-Parabia; Nitzan Lang; Crystle Lee; Fiona Lynch; Anthony Marty; Melanie Marty; Candice McGregor; Jessica Riseley; Simon Sadedin; Katrina Scarff; Michelle da Cunha Torres; Erin Tutty; Ching Vang; Meaghan Wall; Ee Ming Wong; Alison Yeung; Ilias Goranitis; Stephanie Best; Danya F. Vears; Zornitza Stark
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Genetic modifiers and ascertainment drive variable expressivity of complex disorders
errCell
IF42.5
err2025-10-07
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errOAAI
errMatthew Jensen; Corrine Smolen; Anastasia Tyryshkina; Lucilla Pizzo; Jiawan Sun; Serena Noss; Deepro Banerjee; Matthew Oetjens; Hermela Shimelis; Cora M. Taylor; Vijay Kumar Pounraja; Hyebin Song; Laura Rohan; Emily Huber; Laila El Khattabi; Ingrid van de Laar; Rafik Tadros; Connie R. Bezzina; Marjon van Slegtenhorst; Janneke Kammeraad; Paolo Prontera; Jean-Hubert Caberg; Harry Fraser; Siddharth Banka; Anke Van Dijck; Charles Schwartz; Els Voorhoeve; Patrick Callier; Anne-Laure Mosca-Boidron; Nathalie Marle; Mathilde Lefebvre; Kate Pope; Penny Snell; Amber Boys; Paul J. Lockhart; Myla Ashfaq; Elizabeth McCready; Margaret Nowacyzk; Lucia Castiglia; Ornella Galesi; Emanuela Avola; Teresa Mattina; Marco Fichera; Maria Grazia Bruccheri; Giuseppa Maria Luana Mandarà; Francesca Mari; Flavia Privitera; Ilaria Longo; Aurora Curró; Alessandra Renieri; Boris Keren; Perrine Charles; Silvestre Cuinat; Mathilde Nizon; Olivier Pichon; Claire Bénéteau; Radka Stoeva; Dominique Martin-Coignard; Sophia Blesson; Cedric Le Caignec; Sandra Mercier; Marie Vincent; Christa L. Martin; Katrin Mannik; Alexandre Reymond; Laurence Faivre; Erik Sistermans; R. Frank Kooy; David J. Amor; Corrado Romano; Joris Andrieux; Santhosh Girirajan
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LONP1 Variants Are Associated With Clinically Diverse Phenotypes
err2025-09-10
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PREAI
errRandee E. Young; Lu Qiao; Rebecca Hernan; David A. Sweetser; Jessica L. Waxler; Daryl A. Scott; Tiana M. Scott; Seema R. Lalani; Mahshid S. Azamian; Jill A. Rosenfeld; Bret Bostwick; Lindsay C. Burrage; Undiagnosed Diseases Network; Lance H. Rodan; Bianca E. Russell; Marina Dutra-Clarke; Michael Kruer; Somayeh Bakhtiarim; Hossein Darvish; David J. Amor; Shamima Rahman; Karen Stals; Lisa Bradley; Susan Byrne; Leandra K. Tolusso; Beatrix Wong; Laura Benedict; Kimberly Wallis; Kestutis Micke; Cindy Colson; Thomas Smol; Sabrina V. Southwick; Kristen A. Miller; Michelle L. Kush; Odelia Chorin; Annick Rothschild; Wei Wang; Yufeng Shen; Wendy K. Chung
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High-throughput assessment of FMR1 and SNRPN methylation-based newborn screening using IsoPure and QIAcube HT systems
err2025-08-13
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errOAAI
errCaleb Cartagena; Mohammed Alshawsh; Minh Q. Bui; Dinusha Gamage; Rajvi P. Thakor; James Pitt; Ronda F. Greaves; Meg Wall; Richard Saffery; David J. Amor; David E. Godler
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Biallelic loss-of-function variants in ZNF142 are associated with a robust DNA methylation signature affecting a limited number of genomic loci
err2025-05-23
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PREAI
errHildonen, Mathis; Ciolfi, Andrea; Ferilli, Marco; Cappelletti, Camilla; Al Alam, Chadi; Amor, David J.; Barakat, Tahsin Stefan; Benoit, Valerie; Birk, Ohad Shmuel; Callewaert, Bert; Cazurro-Gutierrez, Ana; De Wachter, Matthias; Doco-Fenzy, Martine; Gomez-Puertas, Paulino; Hammer, Trine Bjorg; Jamra, Rami Abou; Kaiyrzhanov, Rauan; Kameyama, Shinichi; Keren, Boris; Kresge, Christina; Krey, Ilona; Lederer, Damien; Marcos-Alcalde, Inigo; Maroofian, Reza; Matsumoto, Naomichi; Mizuguchi, Takeshi; Moey, Lip-Hen; Morgan, Angela; Munell, Francina; Platzer, Konrad; Pletcher, Beth A.; Ros-Pardo, David; Rumping, Lynne; Szakszon, Katalin; Van Schil, Kristof; Verdura, Edgard; Vogt, Julie; Wassmer, Evangeline; Zamani, Mina; Tumer, Zeynep; Tartaglia, Marco
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Adaptive functioning in children and young adults with monogenic neurodevelopmental disorders
err2025-01-23
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errOAAI
errBaker, Emma K.; St John, Miya; Braden, Ruth; Morison, Lottie D.; Forbes, Elana J.; Lelik, Fatma; Hearps, Stephen J. C.; Amor, David J.; Morgan, Angela T.
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Parental attitudes and experiences in pursuing genetic testing for their child's motor speech disorder
err2024-12-09
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PREAI
errAtkinson, Christy; Lee, Yong Quan; Lauretta, Mariana L.; Jarmolowicz, Anna; Amor, David J.; Morgan, Angela T.
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