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1Academic Journal
المؤلفون: Nicholas Donnelly, Adam Cunningham, Sergio Marco Salas, Matthew Bracher-Smith, Samuel Chawner, Jan Stochl, Tamsin Ford, F. Lucy Raymond, Valentina Escott-Price, Marianne B. M. van den Bree
المصدر: Molecular Autism, Vol 14, Iss 1, Pp 1-13 (2023)
مصطلحات موضوعية: Intellectual disability, Genetic syndromes, Machine learning, Behavioural phenotypes, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2040-2392
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2Academic Journal
المؤلفون: Diana Baralle, Susan Walker, Ramya Srinivasan, Sarah Davies, Shelagh Joss, Jonathan Berg, Miranda Splitt, Usha Kini, Pradeep Vasudevan, John Dean, William Newman, Yanick Crow, Beverly Searle, Julian Barwell, Lyn Chitty, Peter Holmans, Sarah Law, Virginia Clowes, Rachel Harrison, Muriel Holder, Sahar Mansour, Spiros Denaxas, Ellie Kerry, Frances Flinter, Zheng Ye, Julia Rankin, Oliver Quarrell, Nicola Lewis, Anne Lampe, Astrid Weber, David Skuse, Kate Baker, Annie Procter, Jeremy Hall, Alison Kraus, Neil Walker, Jeanne Wolstencroft, Laura Hull, Lauren Warner, Tooba Nadeem Akhtar, William Mandy, Eleanor Dewhurst, Amy Lafont, F Lucy Raymond, Terry Shirley, Hayley Tilley, Husne Timur, Catherine Titterton, Sarah Wallwork, Francesca Wicks, Marie Erwood, Sophie Andrews, Philippa Birch, Samantha Bowen, Karen Bradley, Aimee Challenger, Samuel Chawner, Andrew Cuthbert, Sinead Morrison, Hayley Moss, Michael Owen, Sinead Ray, Matthew Sopp, Molly Tong, Marianne van den Bree, Nadia Coscini, Hayley Denyer, Nasrtullah Fatih, Manoj Juj, Anna Lucock, Frida Printzlau, Alice Watkins, Anna Pelling, Lisa Robertson, Denise Williams Alan, Donaldson Lucy, Fleur van Dijk
المصدر: BMJ Open, Vol 11, Iss 9 (2021)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
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3
المؤلفون: Jeanne Wolstencroft, Francesca Wicks, Ramya Srinivasan, Sarah Wynn, Tamsin Ford, Kate Baker, Samuel J R A Chawner, Jeremy Hall, Marianne B M van den Bree, Michael J Owen, David Skuse, F Lucy Raymond, Marie Erwood, Amy Lafont, Husne Timur, Zheng Ye, Susan Walker, Frida Printzlau, Manoj Juj, Sarah Davies, Hayley Denyer, Alice Watkins, Eleanor Kerry, Nadia Coscini, Nasrtullah Fatih, Anna Lucock, Spiros Denaxas, William Mandy, Neil Walker, Sarah Wallwork, Eleanor Dewhurst, Andrew Cuthbert, Aimee Challenger, Sophie Andrews, Peter Holmans, Samantha Bowen, Karen Bradley, Philippa Birch, Molly Tong, Nicola Lewis, Sinead Ray, Matthew Sopp, Hayley Moss, Beverley Searle, Lisa Robertson, Jonathan Berg, Anne Lampe, Shelagh Joss, Paul Brennan, Alison Kraus, Nayana Lahiri, Astrid Weber, Myfanwy Rawson, Diana Johnson, Pradeep Vasudevan, Rachel Harrison, Denise Williams, Eamonn Maher, Usha Kini, Fleur Van Dijk, Virginia Clowes, Jana Gurasashvilli, Sahar Mansour, Muriel Holder-Espinasse, Amy Watford, Julia Rankin, Diana Baralle, Annie Procter, Samuel Chawner, Marianne B M Van den Bree
المصدر: The Lancet Psychiatry. 9:715-724
مصطلحات موضوعية: Male, Adolescent, Autism Spectrum Disorder, State Medicine, United Kingdom, Cohort Studies, Psychiatry and Mental health, Child, Preschool, Intellectual Disability, Humans, Female, Prospective Studies, Child, Biological Psychiatry
وصف الملف: application/pdf
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4
المؤلفون: Samuel Chawner
المصدر: Translational Psychiatry. 13
مصطلحات موضوعية: Cellular and Molecular Neuroscience, Psychiatry and Mental health, Biological Psychiatry
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5
المؤلفون: Nicholas A Donnelly, Adam C Cunningham, Matthew Bracher-Smith, Samuel Chawner, Jan Stochl, Tamsin Ford, F Lucy Raymond, Valentina Escott-Price, Marianne BM van den Bree
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6
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المؤلفون: Samuel Chawner, null IMAGINE-ID Consortium, Jeremy Hall, Michael Owen, Marianne van den Bree
المصدر: European Neuropsychopharmacology. 51:e37-e38
مصطلحات موضوعية: Pharmacology, Genetics, Psychiatry and Mental health, Neurology, Pharmacology (medical), Neurology (clinical), Biology, Biological Psychiatry, Genotype phenotype
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8
المؤلفون: Robert Smigiel, Ann Swillen, Branka Polic, Samuel Chawner, Anne M. Maillard, Adrian Harwood, Marina Mihaljevic, Beata Nowakowska, Rumen Stefanov, Paula Jorge, Louise Gallagher, Natália Oliva Teles, Sara Medved, Bernarda Lozic
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, DNA Copy Number Variations, Developmental Disabilities, Population, 030105 genetics & heredity, European, 03 medical and health sciences, Gene Frequency, Pan european, Databases, Genetic, Genetics, medicine, Humans, Medical history, In patient, Genetic Testing, Copy-number variation, Family history, education, Genetics (clinical), Psychiatric genetics, education.field_of_study, Copy number variants, Information Dissemination, Medical genetics, Neurodevelopmental disorders, General Medicine, 3. Good health, Europe, Phenotype, 030104 developmental biology, Geography, Family medicine, Research collaboration, Genome-Wide Association Study
وصف الملف: Print-Electronic; application/pdf
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9
المؤلفون: Am, Maillard, Hippolyte L, Rodriguez-Herreros B, Samuel Chawner, Dremmel D, Agüera Z, Ab, Fagundo, Pain A, Martin-Brevet S, Hilbert A, Kurz S, Etienne R, Draganski B, Jimenez-Murcia S, Männik K, Metspalu A, Reigo A, Isidor B, Le Caignec C, David A
المصدر: Europe PubMed Central