Publications by authors named "Celia van der Merwe"

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Autism genetics: perspectives, discourse, and community engagement.
Benjamin E Life, Taylor R Thomas, , Rachel Asher, Zandre Bruwer, Celia van der Merwe

Trends Genet· December 2025

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Pathogenic de novo variants in PPP2R5C cause a neurodevelopmental disorder within the Houge-Janssens syndrome spectrum.
Iris Verbinnen, Sofia Douzgou Houge, Tzung-Chien Hsieh, Hellen Lesmann, Aron Kirchhoff, Celia Van der Merwe

Am J Hum Genet· March 2025

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Phenotype and genetic analysis of data collected within the first year of NeuroDev.
Patricia Kipkemoi, Heesu Ally Kim, Bjorn Christ, Emily O'Heir, Jake Allen, Celia van der Merwe

Neuron· September 2023

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Developmental Variability in Autism Across 17 000 Autistic Individuals and 4000 Siblings Without an Autism Diagnosis: Comparisons by Cohort, Intellectual Disability, Genetic Etiology, and Age at Diagnosis.
Susan S Kuo, Celia van der Merwe, Jack M Fu, Caitlin E Carey, Michael E Talkowski

JAMA Pediatr· September 2022

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The female protective effect against autism spectrum disorder.
Emilie M Wigdor, Daniel J Weiner, Jakob Grove, Jack M Fu, Wesley K Thompson, Celia van der Merwe

Cell Genom· June 2022

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Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations.
Alicia R Martin, Elizabeth G Atkinson, Sinéad B Chapman, Anne Stevenson, Rocky E Stroud, Celia van der Merwe

Am J Hum Genet· April 2021

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Schizophrenia Polygenic Risk and Brain Structural Changes in Methamphetamine-Associated Psychosis in a South African Population.
Ruth V Passchier, Dan J Stein, Anne Uhlmann, Celia van der Merwe, Shareefa Dalvie

Front Genet· October 2020

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ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries.
Paul M Thompson, Neda Jahanshad, Christopher R K Ching, Lauren E Salminen, Sophia I Thomopoulos, Celia van der Merwe

Transl Psychiatry· March 2020

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Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry.
Mary Mufford, Josh Cheung, Neda Jahanshad, Celia van der Merwe, Linda Ding

Transl Psychiatry· March 2019

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Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry.
Celia van der Merwe, Neda Jahanshad, Josh W Cheung, Mary Mufford, Nynke A Groenewold

J Affect Disord· February 2019

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Advancing neuropsychiatric genetics training and collaboration in Africa.
Celia van der Merwe, Emmanuel K Mwesiga, Nathaniel W McGregor, Abebe Ejigu, Abigiya Wondimagegnehu Tilahun

Lancet Glob Health· March 2018

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Curcumin Rescues a PINK1 Knock Down SH-SY5Y Cellular Model of Parkinson's Disease from Mitochondrial Dysfunction and Cell Death.
Celia van der Merwe, Hayley Christy van Dyk, Lize Engelbrecht, Francois Hendrikus van der Westhuizen, Craig Kinnear

Mol Neurobiol· May 2017

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Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients.
Celia van der Merwe, Jonathan Carr, Brigitte Glanzmann, Soraya Bardien

Neurosci Lett· April 2016

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Altered Mitochondrial Respiration and Other Features of Mitochondrial Function in Parkin-Mutant Fibroblasts from Parkinson's Disease Patients.
William Haylett, Chrisna Swart, Francois van der Westhuizen, Hayley van Dyk, Lize van der Merwe, Celia van der Merwe

Parkinsons Dis· April 2016

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Evidence for a common biological pathway linking three Parkinson's disease-causing genes: parkin, PINK1 and DJ-1.
Celia van der Merwe, Zahra Jalali Sefid Dashti, Alan Christoffels, Ben Loos, Soraya Bardien

Eur J Neurosci· May 2015

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Mitochondrial impairment observed in fibroblasts from South African Parkinson's disease patients with parkin mutations.
Celia van der Merwe, Ben Loos, Chrisna Swart, Craig Kinnear, Franclo Henning, Lize van der Merwe

Biochem Biophys Res Commun· May 2014

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Factors influencing the development of early- or late-onset Parkinson's disease in a cohort of South African patients.
Celia van der Merwe, William Haylett, Justin Harvey, Debbie Lombard, Soraya Bardien

S Afr Med J· October 2012

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Mutations in the parkin gene are a minor cause of Parkinson's disease in the South African population.
William L Haylett, Rowena J Keyser, Melissa C du Plessis, Celia van der Merwe, Janine Blanckenberg

Parkinsonism Relat Disord· January 2012

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