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van den Bree, Marianne B. M.

Cardiff University

0H指数
45论文数
0被引数
收录论文 45
发表时间
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs)
err2024-06-18
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errHall, Jessica H.; Chawner, Samuel J. R. A.; Wolstencroft, Jeanne; Skuse, David; Hall, Jeremy; Holmans, Peter; Owen, Michael J.; van den Bree, Marianne B. M.
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Using rare genetic mutations to revisit structural brain asymmetry使用罕见的基因突变来重新审视大脑结构的不对称性
err2024-03-26
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errKopal, Jakub; Kumar, Kuldeep; Shafighi, Kimia; Saltoun, Karin; Modenato, Claudia; Moreau, Clara A.; Huguet, Guillaume; Jean-Louis, Martineau; Martin, Charles-Olivier; Saci, Zohra; Younis, Nadine; Douard, Elise; Jizi, Khadije; Beauchamp-Chatel, Alexis; Kushan, Leila; Silva, Ana I.; van den Bree, Marianne B. M.; Linden, David E. J.; Owen, Michael J.; Hall, Jeremy; Lippe, Sarah; Draganski, Bogdan; Sonderby, Ida E.; Andreassen, Ole A.; Glahn, David C.; Thompson, Paul M.; Bearden, Carrie E.; Zatorre, Robert; Jacquemont, Sebastien; Bzdok, Danilo
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In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome
err2023-07-26
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errRaven, Erika P. P.; Veraart, Jelle; Kievit, Rogier A. A.; Genc, Sila; Ward, Isobel L. L.; Hall, Jessica; Cunningham, Adam; Doherty, Joanne; van den Bree, Marianne B. M.; Jones, Derek K.
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Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders
err2023-07-04
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errDoherty, Joanne L.; Cunningham, Adam C.; Chawner, Samuel J. R. A.; Moss, Hayley M.; Dima, Diana C.; Linden, David E. J.; Owen, Michael J.; van den Bree, Marianne B. M.; Singh, Krish D.
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Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach识别与智力障碍相关的基因组疾病的神经发育和精神病学特征: 机器学习方法
err2023-05-23
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errDonnelly, Nicholas; Cunningham, Adam; Salas, Sergio Marco; Bracher-Smith, Matthew; Chawner, Samuel; Stochl, Jan; Ford, Tamsin; Raymond, F. Lucy; Escott-Price, Valentina; van den Bree, Marianne B. M.
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DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts
err2023-02-08
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errLynham, Amy J.; Knott, Sarah; Underwood, Jack F. G.; Hubbard, Leon; Agha, Sharifah S.; Bisson, Jonathan I.; van den Bree, Marianne B. M.; Chawner, Samuel J. R. A.; Craddock, Nicholas; O'Donovan, Michael; Jones, Ian R.; Kirov, George; Langley, Kate; Martin, Joanna; Rice, Frances; Roberts, Neil P.; Thapar, Anita; Anney, Richard; Owen, Michael J.; Hall, Jeremy; Pardinas, Antonio F. F.; Walters, James T. R.
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Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions
err2023-01-11
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errChawner, Samuel J. R. A.; Evans, Alexandra; Williams, Nigel J.; Owen, Michael; Hall, Jeremy; van den Bree, Marianne B. M.
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Psychopathology in mothers of children with pathogenic Copy Number Variants
err2022-11-29
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errNiarchou, Maria; Cunningham, Adam C.; Chawner, Samuel J. R. A.; Moulding, Hayley; Sopp, Matthew; IMAGINE- ID, Jeremy; Hall, Jeremy J.; Owen, Michael; van den Bree, Marianne B. M.
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Psychopathology in adults with copy number variants
err2022-02-11
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errAdams, Rachael L.; Baird, Alister; Smith, Jacqueline; Williams, Nigel; van den Bree, Marianne B. M.; Linden, David E. J.; Owen, Michael J.; Hall, Jeremy; Linden, Stefanie C.
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Detecting microstructural deviations in individuals with deep diffusion MRI tractometry
err2021-09-22
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errChamberland, Maxime; Genc, Sila; Tax, Chantal M. W.; Shastin, Dmitri; Koller, Kristin; Raven, Erika P.; Cunningham, Adam; Doherty, Joanne; van den Bree, Marianne B. M.; Parker, Greg D.; Hamandi, Khalid; Gray, William P.; Jones, Derek K.
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Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome
err2021-06-10
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errChapman, Gareth; Alsaqati, Mouhamed; Lunn, Sharna; Singh, Tanya; Linden, Stefanie C.; Linden, David E. J.; van den Bree, Marianne B. M.; Ziller, Mike; Owen, Michael J.; Hall, Jeremy; Harwood, Adrian J.; Syed, Yasir Ahmed
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The psychiatric phenotypes of 1q21 distal deletion and duplication
err2021-02-04
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errLinden, Stefanie C.; Watson, Cameron J.; Smith, Jacqueline; Chawner, Samuel J. R. A.; Lancaster, Thomas M.; Evans, Ffion; Williams, Nigel; Skuse, David; Raymond, F. Lucy; Hall, Jeremy; Owen, Michael J.; Linden, David E. J.; Green-Snyder, LeeAnne; Chung, Wendy K.; Maillard, Anne M.; Jacquemont, Sebastien; van den Bree, Marianne B. M.
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants剖析自闭症异质性的遗传学优先方法: 自闭症风险拷贝数变异的表型比较
err2021-01-01
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errChawner, Samuel J. R. A.; Doherty, Joanne L.; Anney, Richard J. L.; Antshel, Kevin M.; Bearden, Carrie E.; Bernier, Raphael; Chung, Wendy K.; Clements, Caitlin C.; Curran, Sarah R.; Cuturilo, Goran; Fiksinski, Ania M.; Gallagher, Louise; Goin-Kochel, Robin P.; Gur, Raquel E.; Hanson, Ellen; Jacquemont, Sebastien; Kates, Wendy R.; Kushan, Leila; Maillard, Anne M.; McDonald-McGinn, Donna M.; Mihaljevic, Marina; Miller, Judith S.; Moss, Hayley; Pejovic-Milovancevic, Milica; Schultz, Robert T.; Green-Snyder, Leeanne; Vorstman, Jacob A.; Wenger, Tara L.; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.
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Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk
err2020-09-21
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errDima, Diana C.; Adams, Rachael; Linden, Stefanie C.; Baird, Alister; Smith, Jacqueline; Foley, Sonya; Perry, Gavin; Routley, Bethany C.; Magazzini, Lorenzo; Drakesmith, Mark; Williams, Nigel; Doherty, Joanne; van den Bree, Marianne B. M.; Owen, Michael J.; Hall, Jeremy; Linden, David E. J.; Singh, Krish D.
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Copy number variants (CNVs): a powerful tool for iPSC-based modelling of ASD
err2020-06-01
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errDrakulic, Danijela; Djurovic, Srdjan; Syed, Yasir Ahmed; Trattaro, Sebastiano; Caporale, Nicolo; Falk, Anna; Ofir, Rivka; Heine, Vivi M.; Chawner, Samuel J. R. A.; Rodriguez-Moreno, Antonio; van den Bree, Marianne B. M.; Testa, Giuseppe; Petrakis, Spyros; Harwood, Adrian J.
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Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome
err2020-05-07
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errCunningham, Adam C.; Fung, Wilson; Massey, Thomas H.; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.; Peall, Kathryn J.
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Response to letter to editor: Knowing when and how to use epilepsy screening questionnaires
err2020-03-02
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errEaton, Christopher B.; Thomas, Rhys H.; Hamandi, Khalid; Payne, Gareth C.; Kerr, Michael P.; Linden, David E. J.; Owen, Michael J.; Cunningham, Adam C.; Bartsch, Ullrich; Struik, Siske S.; van den Bree, Marianne B. M.
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Cognitive deficits in childhood, adolescence and adulthood in 22q11.2 deletion syndrome and association with psychopathology
err2020-02-03
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errMorrison, Sinead; Chawner, Samuel J. R. A.; van Amelsvoort, Therese A. M. J.; Swillen, Ann; Vingerhoets, Claudia; Vergaelen, Elfi; Linden, David E. J.; Linden, Stefanie; Owen, Michael J.; van den Bree, Marianne B. M.
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Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
err2019-06-10
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errCunningham, Adam C.; Hill, Liam; Mon-Williams, Mark; Peall, Kathryn J.; Linden, David E. J.; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.
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