David J Amor - Murdoch Children's Research Institute

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论文共 333 篇作者统计合作学者相似作者

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The Association Between Human Chorionic Gonadotropin and Adverse Pregnancy Outcomes: a Systematic Review and Meta-Analysis

Monique Peris,Kylie Crompton,Daisy A Shepherd,David J Amor

American Journal of Obstetrics and Gynecologyno. 2 (2024): 118-184

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Fostering Hope and Acknowledging Uncertainty: Meeting Parents’ Needs and Preferences when Communicating Prognosis in Genetic Neurodevelopmental Conditions

Erin Turbitt, Elizabeth Callinan,Pieta Shakes,Alison McEwen,David J. Amor

Current Developmental Disorders Reports（2024）

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Perinatal Outcomes after a Prenatal Diagnosis of a Fetal Copy Number Variant: A Retrospective Population-Based Cohort Study

Cecilia Pynaker,Jacqui McCoy,Jane Halliday,Sharon Lewis,David J. Amor,Susan P. Walker,Lisa Hui

BMC PEDIATRICSno. 1 (2024)

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Parents' Preferences for Receiving and Discussing Prognostic Genetic Information Regarding Their Children's Neurodevelopmental Condition: A Qualitative Study

Erin Turbitt, Meg Bourne,Alison McEwen,David J. Amor

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGYno. 7 (2024): 872-881

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Genetic Architecture of Childhood Speech Disorder: a Review

Angela T. Morgan,David J. Amor,Miya D. St John,Ingrid. E. Scheffer,Michael S. Hildebrand

Molecular Psychiatry（2024）

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Genetic Modifiers and Ascertainment Drive Variable Expressivity of Complex Disorders

Matthew Jensen,Corrine Smolen,Anastasia Tyryshkina,Lucilla Pizzo,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 Bezzina,Marjon van Slegtenhorst,Janneke Kammeraad,Paolo Prontera,Jean-Hubert Caberg, Harry Fraser, Siddhartha 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 Martin,Katrin Mannik,Alexandre Reymond,Laurence Faivre,Erik Sistermans,R Frank Kooy,David J Amor,Corrado Romano,Joris Andrieux,Santhosh Girirajan

medRxiv the preprint server for health sciences (2024)

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Distinct Neurodevelopmental and Epileptic Phenotypes Associated with Gain- and Loss-of-function GABRB2 Variants

Nazanin Azarinejad Mohammadi,Philip Kiaer Ahring,Vivian Wan Yu Liao,Han Chow Chua, Sebastian Ortiz de la Rosa,Katrine Marie Johannesen, Yael Michaeli-Yossef, Aline Vincent-Devulder, Catherine Meridda,Ange-Line Bruel,Alessandra Rossi,Chirag Patel,Joerg Klepper, Paolo Bonanni, Sara Minghetti,Marina Trivisano,Nicola Specchio,David Amor,Stephane Auvin,Sarah Baer,Pierre Meyer,Mathieu Milh, Vincenzo Salpietro, Reza Maroo, Johannes R. Lemke,Sarah Weckhuysen, Palle Christophersen,Guido Rubboli,Mary Chebib,Anders A. Jensen,Nathan L. Absalom, Rikke Steensbjerre Moller

EBIOMEDICINE（2024）

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Inherited PURA Pathogenic Variant Associated with a Mild Neurodevelopmental Disorder

Michael S. Hildebrand,Ruth O. Braden,Mariana L. Lauretta,Antony Kaspi,Richard J. Leventer, Melinda Anderson,Himanshu Goel,Melanie Bahlo,Ingrid E. Scheffer,David J. Amor,Robert Janowski,Dierk Niessing,Angela T. Morgan

NEUROLOGY-GENETICSno. 5 (2024)

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Narrowing the Diagnostic Gap: Genomes, Episignatures, Long-Read Sequencing, and Health Economic Analyses in an Exome-Negative Intellectual Disability Cohort

Kerith-Rae Dias,Rupendra Shrestha,Deborah Schofield,Carey-Anne Evans,Emily O'Heir,Ying Zhu,Futao Zhang, Krystle Standen,Ben Weisburd,Sarah L. Stenton,Alba Sanchis-Juan,Harrison Brand, Michael E. Talkowski,Alan Ma, Sondy Ghedia,Meredith Wilson,Sarah A. Sandaradura,Janine Smith,Benjamin Kamien,Anne Turner,Madhura Bakshi,Lesley C. Ades,David Mowat,Matthew Regan,George McGillivray,Ravi Savarirayan,Susan M. White,Tiong Yang Tan,Zornitza Stark,Natasha J. Brown,Luis A. Perez-Jurado,Emma Krzesinski,Matthew F. Hunter,Lauren Akesson,Andrew Paul Fennell,Alison Yeung,Tiffany Boughtwood,Lisa J. Ewans,Jennifer Kerkhof, Christopher Lucas,Louise Carey, Hugh French,Melissa Rapadas,Igor Stevanovski,Ira W. Deveson,Corrina Cliffe,George Elakis,Edwin P. Kirk,Tracy Dudding-Byth,Janice Fletcher,Rebecca Walsh,Mark A. Corbett,Thessa Kroes,Jozef Gecz,Cliff Meldrum,Simon Cliffe, Meg Wall,Sebastian Lunke,Kathryn North,David J. Amor,Michael Field,Bekim Sadikovic,Michael F. Buckley,Anne O'Donnell-Luria,Tony Roscioli

GENETICS IN MEDICINEno. 5 (2024)

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The Value of Genomic Testing in Severe Childhood Speech Disorders

Yan Meng,Stephanie Best,David J. Amor,Ruth Braden,Angela T. Morgan,Ilias Goranitis

EUROPEAN JOURNAL OF HUMAN GENETICSno. 4 (2024): 440-447

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