Marianne B M van den Bree (Marianne van den Bree, M van den Bree, Marianne Van Den Bree, M B M van den Bree, Marianne Van den Bree)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 52

Top Topics

Intellectual Disability

Depressive Symptoms

Genome Wide Association Study

Top Venues

Translational psychiatry

Nature communications

Research square

medRxiv : the preprint server for health sciences

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

Publications

Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Ruby S M Tsang, Daniel Stow, Alex S F Kwong, Nicholas A Donnelly, Holly Fraser, Inês A Barroso, Peter A Holmans, Michael J Owen, Megan L Wood, null null, Marianne B M van den Bree, Nicholas John Timpson, Golam M Khandaker
Immunometabolic Blood Biomarkers of Developmental Trajectories of Depressive Symptoms: Findings From the ALSPAC Birth Cohort. medRxiv : the preprint server for health sciences (2024)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David H Skuse, Jeremy Hall, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational psychiatry 14 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Ruby S M Tsang, Daniel Stow, Alex S F Kwong, Nicholas A Donnelly, Holly Fraser, Inês A Barroso, Peter A Holmans, Michael J Owen, Megan L Wood, null null, Marianne B M van den Bree, Nicholas John Timpson, Golam M Khandaker
Immunometabolic Blood Biomarkers of Developmental Trajectories of Depressive Symptoms: Findings From the ALSPAC Birth Cohort. medRxiv : the preprint server for health sciences (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David H Skuse, Jeremy Hall, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational psychiatry 14 (1) (2024)
Ruby S M Tsang, Daniel Stow, Alex S F Kwong, Nicholas A Donnelly, Holly Fraser, Inês A Barroso, Peter A Holmans, Michael J Owen, Megan L Wood, null null, Marianne B M van den Bree, Nicholas John Timpson, Golam M Khandaker
Immunometabolic Blood Biomarkers of Developmental Trajectories of Depressive Symptoms: Findings From the ALSPAC Birth Cohort. medRxiv : the preprint server for health sciences (2024)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Sean Gallagher, Emily McClellan, Lauren White, Terrence Blaine Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica H Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles Olivier Martin, Khadije Jizi, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel E Gur
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications. Molecular psychiatry (2024)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David H Skuse, Jeremy Hall, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational psychiatry 14 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert J Zatorre, Sébastien Jacquemont, Danilo Bzdok
Author Correction: Using rare genetic mutations to revisit structural brain asymmetry. Nature communications 15 (1) (2024)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David H Skuse, Jeremy Hall, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). Translational psychiatry 14 (1) (2024)
Erika P Raven, Jelle Veraart, Rogier A Kievit, Sila Genc, Isobel L Ward, Jessica Hall, Adam Cunningham, Joanne Doherty, Marianne B M van den Bree, Derek K Jones
In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome. Molecular psychiatry (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Samuel J R A Chawner, Alexandra Evans, null null, Nigel Williams, Michael J Owen, Jeremy Hall, Marianne B M van den Bree
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational psychiatry 13 (1) (2023)
Jakub Kopal, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A Moreau, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise Douard, Khadije Jizi, Alexis Beauchamp-Chatel, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida Elken Sonderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Robert Zatorre, Sebastien Jacquemont, Danilo Bzdok
Using rare genetic mutations to revisit structural brain asymmetry. bioRxiv : the preprint server for biology (2023)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David Skuse, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences (2023)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David Skuse, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences (2023)
Samuel J R A Chawner, Alexandra Evans, null null, Nigel Williams, Michael J Owen, Jeremy Hall, Marianne B M van den Bree
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational psychiatry 13 (1) (2023)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David Skuse, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Samuel J R A Chawner, Alexandra Evans, null null, Nigel Williams, Michael J Owen, Jeremy Hall, Marianne B M van den Bree
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational psychiatry 13 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Nicholas A Donnelly, Adam C Cunningham, Sergio Marco Salas, Matthew Bracher-Smith, Samuel J R A Chawner, Jan Stochl, Tamsin Jane Ford, F Lucy Raymond, Valentina Escott-Price, Marianne B M van den Bree
Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach. Molecular autism 14 (1) (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Samuel J R A Chawner, Alexandra Evans, null null, Nigel Williams, Michael J Owen, Jeremy Hall, Marianne B M van den Bree
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational psychiatry 13 (1) (2023)
Samuel J R A Chawner, Alexandra Evans, null null, Nigel Williams, Michael J Owen, Jeremy Hall, Marianne B M van den Bree
Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions. Translational psychiatry 13 (1) (2023)
Jakub Kopal, Kuldeep Kumar, Karin Saltoun, Claudia Modenato, Clara A Moreau, Sandra Martin-Brevet, Guillaume Huguet, Martineau Jean-Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Petra Tamer, Elise Douard, Anne M Maillard, Borja Rodríguez-Herreros, Aurèlie Pain, Sonia Richetin, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Bogdan Draganski, Ida E Sønderby, Ole Andreas Andreassen, David C Glahn, Paul M Thompson, Carrie E Bearden, Sébastien Jacquemont, Danilo Bzdok
Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence. Nature human behaviour (2023)
Jessica H Hall, Samuel J R A Chawner, null null, Jeanne Wolstencroft, David Skuse, Peter A Holmans, Michael J Owen, Marianne B M van den Bree
Irritability in young people with copy number variants associated with neurodevelopmental disorders (ND-CNVs). medRxiv : the preprint server for health sciences (2023)
Raquel C Gur, Carrie E Bearden, Sebastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Marianne B M van den Bree, Jacob A S Vorstman, Jonathan Sebat, Kosha Ruparel, Robert Gallagher, Ann Swillen, Emily McClellan, Lauren White, Terrence Crowley, Victoria Giunta, Leila Kushan, Kathleen O'Hora, Jente Verbesselt, Ans Vandensande, Claudia Vingerhoets, Mieke van Haelst, Jessica Hall, Janet C Harwood, Samuel J R A Chawner, Nishi Patel, Katrina Palad, Oanh Hong, James Guevara, Charles-Olivier Martin, Anne-Marie Bélanger, Stephen W Scherer, Anne Susan Bassett, Donna M McDonald-McGinn, Raquel Gur
Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications. Research square (2023)
Joanne L Doherty, Adam C Cunningham, Samuel J R A Chawner, Hayley M Moss, Diana C Dima, David E J Linden, Michael J Owen, Marianne B M van den Bree, Krish D Singh
Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology (2023)
Mouhamed Alsaqati, Brittany A Davis, Jamie Wood, Megan E Jones, Lora Jones, Aishah Westwood, Olena Petter, Anthony R Isles, David E J Linden, Marianne B M van den Bree, Michael J Owen, Jeremy Hall, Adrian J Harwood
NRSF/REST lies at the intersection between epigenetic regulation, miRNA-mediated gene control and neurodevelopmental pathways associated with Intellectual disability (ID) and Schizophrenia. Translational psychiatry 12 (1) (2022)
Claudia Modenato, Kuldeep Kumar, Clara Moreau, Sandra Martin-Brevet, Guillaume Huguet, Catherine Schramm, Martineau Jean-Louis, Charles-Olivier Martin, Nadine Younis, Petra Tamer, Elise Douard, Fanny Thébault-Dagher, Valérie Côté, Audrey-Rose Charlebois, Florence Deguire, Anne M Maillard, Borja Rodriguez-Herreros, Aurèlie Pain, Sonia Richetin, null null, null null, Lester Melie-García, Leila Kushan, Ana Isabel Silva, Marianne B M van den Bree, David E J Linden, Michael J Owen, Jeremy Hall, Sarah Lippé, Mallar Chakravarty, Danilo Bzdok, Carrie E Bearden, Bogdan Draganski, Sebastien Jacquemont
Effects of eight neuropsychiatric copy number variants on human brain structure. Translational psychiatry 11 (1) (2021)
Maria Rogdaki, Céline Devroye, Mariasole Ciampoli, Mattia Veronese, Abhishekh Hulegar Ashok, Robert A McCutcheon, Sameer Jauhar, Ilaria Bonoldi, Maria Gudbrandsen, Eileen Daly, Therese van Amelsvoort, Marianne B M van den Bree, Michael J Owen, Federico Edoardo Turkheimer, Francesco Papaleo, Oliver D Howes
Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study. Molecular psychiatry (2021)
Stefanie Caroline Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster, Ffion Evans, Nigel Williams, David H Skuse, F Lucy Raymond, Jeremy Hall, Michael J Owen, David E J Linden, LeeAnne Green-Snyder, Wendy K Chung, Anne Manuela Maillard, Sebastien Jacquemont, Marianne B M van den Bree
Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication. Translational psychiatry 11 (1) (2021)
Stefanie Caroline Linden, Cameron J Watson, Jacqueline Smith, Samuel J R A Chawner, Thomas M Lancaster, Ffion Evans, Nigel Williams, David H Skuse, F Lucy Raymond, Jeremy Hall, Michael J Owen, David E J Linden, LeeAnne Green-Snyder, Wendy K Chung, Anne Manuela Maillard, Sebastien Jacquemont, Marianne B M van den Bree
The psychiatric phenotypes of 1q21 distal deletion and duplication. Translational psychiatry 11 (1) (2021)
Maria Rogdaki, Céline Devroye, Mariasole Ciampoli, Mattia Veronese, Abhishekh Hulegar Ashok, Robert A McCutcheon, Sameer Jauhar, Ilaria Bonoldi, Maria Gudbrandsen, Eileen Daly, Therese van Amelsvoort, Marianne B M van den Bree, Michael J Owen, Federico Edoardo Turkheimer, Francesco Papaleo, Oliver D Howes
Correction: Striatal dopaminergic alterations in individuals with copy number variants at the 22q11.2 genetic locus and their implications for psychosis risk: a [18F]-DOPA PET study. Molecular psychiatry (2021)
Ida Elken Sonderby, Dennis van der Meer, Clara A Moreau, Tobias Kaufmann, G Bragi Walters, Maria Ellegaard, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard, Nicholas B Blackburn, John E Blangero, Dorret I Boomsma, Henry Brodaty, Rachel M Brouwer, Robin Bülow, Rune Bøen, Wiepke Cahn, Vince D Calhoun, Svenja Caspers, Christopher R K Ching, Sven Cichon, Simone Ciufolini, Benedicto Crespo-Facorro, Joanne E Curran, Anders M Dale, Shareefa Dalvie, Paola Dazzan, Eco J C N de Geus, Greig I de Zubicaray, Sonja M C de Zwarte, Sylvane Desrivieres, Joanne L Doherty, Gary Donohoe, Bogdan Draganski, Stefan Ehrlich, Else Eising, Thomas Espeseth, Kim Fejgin, Simon E Fisher, Tormod Fladby, Oleksandr Frei, Vincent Frouin, Masaki Fukunaga, Thomas Gareau, Tian Ge, David C Glahn, Hans Jörgen Grabe, Nynke A Groenewold, Ómar Gústafsson, Jan Haavik, Asta K Haberg, Jeremy Hall, Ryota Hashimoto, Jayne Y Hehir-Kwa, Derrek P Hibar, Manon H J Hillegers, Per Hoffmann, Laurena Holleran, Avram J Homes, Georg Homuth, Jouke- Jan Hottenga, Hilleke E Hulshoff Pol, Kyung Sue Hong, Neda Jahanshad, Christiane Jockwitz, Stefan E Johansson, Erik G Jönsson, Niklas R Jørgensen, Masataka Kikuchi, Emma E M Knowles, Kuldeep Kumar, Stephanie Le Hellard, Costin Leu, David E J Linden, Jingyu Liu, Arvid Lundervold, Astri Johansen Lundervold, Anne Manuela Maillard, Nicholas G Martin, Sandra Martin-Brevet, Karen A Mather, Samuel R Mathias, Katie L Mcmahon, Allan F McRae, Sarah E Medland, Andreas Meyer-Lindenberg, Torgeir Moberget, Claudia Modenato, Jennifer Monereo Sánchez, Derek W Morris, Thomas W Mühleisen, Robin M Murray, Jacob Nielsen, Jan E Nordvik, Lars Nyberg, Loes M Olde Loohuis, Roel A Ophoff, Michael J Owen, Tomáš Paus, Zdenka Pausova, Juan M Peralta, Gilbert Bruce Pike, Carlos Prieto, Erin Burke Quinlan, Céline S Reinbold, Tiago Reis Marques, James J H Rucker, Perminder Singh Sachdev, Sigrid B Sando, Peter R Schofield, Andrew J Schork, Gunter Schumann, Jean Shin, Elena Shumskaya, Ana Isabel Silva, Sanjay M Sisodiya, Vidar M Steen, Dan J Stein, Lachlan T Strike, Ikuo K Suzuki, Christian K Tamnes, Alexander Teumer, Anbupalam Thalamuthu, Diana Tordesillas-Gutiérrez, Anne Uhlmann, Magnus O Ulfarsson, Dennis van 't Ent, Marianne B M van den Bree, Pierre Vanderhaeghen, Evangelos Vassos, Wei Wen, Katharina Wittfeld, Margaret J Wright, Ingrid Agartz, Srdjan Djurovic, Lars Tjelta Westlye, Hreinn Stefánsson, Kári Stefánsson, Sebastien Jacquemont, Paul M Thompson, Ole Andreas Andreassen, null null
1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans. Translational psychiatry 11 (1) (2021)
Gareth Chapman, Mouhamed Alsaqati, Sharna Lunn, Tanya Singh, Stefanie C Linden, David E J Linden, Marianne B M van den Bree, Mike Ziller, Michael J Owen, Jeremy Hall, Adrian J Harwood, Yasir Ahmed Syed
Using induced pluripotent stem cells to investigate human neuronal phenotypes in 1q21.1 deletion and duplication syndrome. Molecular psychiatry (2021)
Ramya Srinivasan, Jeanne Wolstencroft, M Erwood, F L Raymond, Marianne B M van den Bree, J Hall, D Skuse, null null
Mental health and behavioural problems in children with XXYY: a comparison with intellectual disabilities. Journal of intellectual disability research : JIDR 63 (5) (2020)
Christopher B Eaton, Rhys Huw Thomas, Khalid Hamandi, Gareth C Payne, Michael P Kerr, David E J Linden, Michael J Owen, Adam C Cunningham, Ullrich Bartsch, Siske S Struik, Marianne B M van den Bree
Response to letter to editor: "Knowing when and how to use epilepsy screening questionnaires". Epilepsia 61 (4) (2020)
H A Moulding, Ullrich Bartsch, Jeremy Hall, Matthew W Jones, David E J Linden, Michael J Owen, Marianne B M van den Bree
Sleep problems and associations with psychopathology and cognition in young people with 22q11.2 deletion syndrome (22q11.2DS). Psychological medicine 50 (7) (2019)
Christopher B Eaton, Rhys Huw Thomas, Khalid Hamandi, Gareth C Payne, Michael P Kerr, David E J Linden, Michael J Owen, Adam C Cunningham, Ullrich Bartsch, Siske S Struik, Marianne B M van den Bree
Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders. Epilepsia 60 (5) (2019)