Samuel John Rupert Allen Chawner - Dissemin

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All papers authored by Samuel John Rupert Allen Chawner

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2023 Natalie M. Papini

ORCID

, Cynthia M. Bulik

ORCID

, Samuel J. R. A. Chawner

ORCID

ORCID

Prevalence and recurrence of pica behaviors in early childhood within the ALSPAC birth cohort

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Joanne L. Doherty

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, Adam C. Cunningham

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, Samuel J. R. A. Chawner

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, Hayley M. Moss

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, Diana C. Dima

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, David E. J. Linden

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, Michael J. Owen

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, Marianne B. M. van den Bree

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, Krish D. Singh

Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders

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Natalie M. Papini

ORCID

, Cynthia M. Bulik, Samuel Jra Chawner

ORCID

, Nadia Micali

Prevalence and Recurrence of Pica Behaviors in Early Childhood: Findings from the ALSPAC Birth Cohort

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Samuel J. R. A. Chawner

ORCID

, Amy L. Paine, Matt J. Dunn, Alice Walsh, Poppy Sloane, Megan Thomas, Alexandra Evans, Lucinda Hopkins‐Jones, Siske Struik, Jeremy Hall, Jonathan T. Erichsen, Susan R. Leekam, Michael J. Owen, Dale Hay, Marianne B. M. van den Bree

Neurodevelopmental dimensional assessment of young children at high genomic risk of neuropsychiatric conditions

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This paper is made freely available by the publisher.

Amy J. Lynham

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, Sarah Knott, Jack F. G. Underwood

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, Leon Hubbard, Sharifah S. Agha, Jonathan I. Bisson, Marianne B. M. van den Bree, Samuel J. R. A. Chawner

ORCID

, Nicholas Craddock, Michael O'Donovan, Ian R. Jones

ORCID

ORCID

, Kate Langley, Joanna Martin

ORCID

, Frances Rice and 7 other authors

DRAGON-Data: a platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts

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Samuel J. R. A. Chawner

ORCID

, Marianne B. M. van den Bree, Jeanne Wolstencroft, Alexandra Evans, Jeremy Hall, Michael J. Owen, F. Lucy Raymond, David Skuse, Nigel Williams, F. Lucy Raymond

Sleep disturbance as a transdiagnostic marker of psychiatric risk in children with neurodevelopmental risk genetic conditions

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2022 Donnelly Na, Cunningham Ac, M. Bracher Smith, S. Chawner

ORCID

, J. Stochl, T. Ford, Raymond Fl, V. Escott Price, van den Bree Mb

Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability

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Marianne B. M. van den Bree, Maria Niarchou, Chawner Sjra, Matthew Sopp, Michael J. Owen, Cunningham Ac, Adam C. Cunningham, Samuel J. R. A. Chawner

ORCID

, Hayley Moulding, Jeremy Hall, Owen Mj, Imagine-Id, van den Bree Mb, van den Bree Mbm

Psychopathology in mothers of children with pathogenic Copy Number Variants

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Samuel J. R. A. Chawner

ORCID

, Michael J. Owen

Autism: A model of neurodevelopmental diversity informed by genomics

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Jeanne Wolstencroft, Francesca Wicks, Ramya Srinivasan, Sarah Wynn, Tamsin Ford, Kate Baker, Samuel J. R. A. Chawner

ORCID

, Jeremy Hall, Marianne B. M. van den Bree, Michael J. Owen, David Skuse, F. Lucy Raymond, Marie Erwood, Amy Lafont, Husne Timur and 54 other authors

Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study

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Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, Samuel J. R. A. Chawner

ORCID

, Kirsten A. Donald, Marianne B. M. van den Bree, Jonathan Sebat, David H. Ledbetter, John N. Constantino, Rachel K. Earl, Donna M. McDonald-Mcginn, Therese van Amelsvoort, Ann Swillen, Anne H. O’Donnell-Luria, David C. Glahn and 10 other authors

Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2021 Joanne L. Doherty, Adam C. Cunningham, Samuel J. R. A. Chawner

ORCID

, Hayley M. Moss, Diana C. Dima, David E. J. Linden, Michael J. Owen, Marianne B. M. van den Bree, Krish D. Singh

Alterations in resting-state activity and functional connectivity in children with 22q11.2 deletion syndrome

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Stefanie C. Linden

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, Cameron J. Watson

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, Jacqueline Smith

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, Samuel J. R. A. Chawner

ORCID

, Thomas M. Lancaster, Ffion Evans, Nigel Williams, David Skuse

ORCID

, F. Lucy Raymond, Jeremy Hall, Michael J. Owen

ORCID

, David E. J. Linden, LeeAnne Green-Snyder, Wendy K. Chung, Anne M. Maillard

ORCID

and 2 other authors

Correction: The psychiatric phenotypes of 1q21 distal deletion and duplication

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Samuel Jra Chawner

ORCID

, Cameron J. Watson

ORCID

, Michael J. Owen

Clinical evaluation of patients with a neuropsychiatric risk copy number variant

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Ania M. Fiksinski

ORCID

, Maude Schneider, Janneke Zinkstok, Danielle Baribeau, Samuel J. R. A. Chawner

ORCID

, Jacob A. S. Vorstman

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

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Stefanie C. Linden

ORCID

, Cameron J. Watson

ORCID

, Jacqueline Smith

ORCID

, Samuel J. R. A. Chawner

ORCID

, Thomas M. Lancaster, Ffion Evans, Nigel Williams, David Skuse

ORCID

, F. Lucy Raymond, Jeremy Hall, Michael J. Owen

ORCID

, David E. J. Linden, LeeAnne Green-Snyder, Wendy K. Chung, Anne M. Maillard

ORCID

and 2 other authors

The psychiatric phenotypes of 1q21 distal deletion and duplication

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Robert T. Schultz, Marianne B. M. van den Bree, Jacob A. Vorstman, Chawner Sjra, Tara L. Wenger, Samuel J. R. A. Chawner

ORCID

, Doherty Jl, Donna M. McDonald-Mcginn, Marina Mihaljevic, Judith S. Miller, Anney Rjl, Hayley Moss, Milica Pejovic-Milovancevic, Anney Rj, Antshel Km and 30 other authors

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.

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2020 Robert W. Davies, Nigel M. Williams, Stephen R. Hooper, Thomas Monfeuga, Michael J. Owen, Bernice E. Morrow, Donna M. McDonald-Mcginn, Ann Swillen, Marianne van den Bree, Joris R. Vermeesch, Therese van Amelsvoort, S. T. Warren, Wendy R. Kates, S. Morrison, Kieran C. Murphy and 67 other authors

Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome

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Samuel J. R. A. Chawner

ORCID

, Marina Mihaljevic, Sinead Morrison, Hale Yapici Eser, Anne M. Maillard

ORCID

, Beata Nowakowska

ORCID

, Marianne B. M. van den Bree, Ann Swillen

Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium

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