Publications by authors named "Zandre Bruwer"

Claim this Profile
A
Autism genetics: perspectives, discourse, and community engagement.
Benjamin E Life, Taylor R Thomas, , Rachel Asher, Zandre Bruwer

Trends Genet· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.
Ghayda M Mirzaa, Keqin Yan, Raissa Relator, Mathieu Levesque, Pranisha Jayasinghe, Zandre Bruwer

Nat Commun· November 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Pascale Sabeh, Samantha A Dumas, Claudia Maios, Hiba Daghar, Marek Korzeniowski, Zandre Bruwer

Am J Hum Genet· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Parental perspectives regarding the return of genomic research results in neurodevelopmental disorders in South Africa: anticipated impact and preferences.
Angelique Diedericks, Zandré Bruwer, Nakita Laing, Emma Eastman, Jantina De Vries

J Community Genet· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic counseling development and milestone in Oman.
Khalsa Al-Kharusi, Chantel Van Wyk, Mariya Al Hinai, Amel Al-Fori, Zandre Bruwer

Genet Med Open· October 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Parental Perspectives Regarding the Return of Genomic Research Results in Neurodevelopmental Disorders in South Africa: Anticipated Impact and Preferences.
Angelique Diedericks, Zandré Bruwer, Nakita Laing, Emma Eastman, Jantina De Vries De Vries

Res Sq· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease.
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, Samantha Baxter, Katherine R Chao, Zandre Bruwer

Am J Hum Genet· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease.
Gabrielle Lemire, Alba Sanchis-Juan, Kathryn Russell, Samantha Baxter, Katherine R Chao, Zandre Bruwer

medRxiv· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.
David Picketts, Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Zandre Bruwer

Res Sq· September 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center Study.
Salem Al-Tamemi, Shoaib Al-Zadjali, Zandre Bruwer, Shafiq-Ur-Rehman Naseem, Nabila Al-Siyabi

J Clin Immunol· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families.
Ghalia Al-Kasbi, Fathiya Al-Murshedi, Adila Al-Kindi, Nadia Al-Hashimi, Khalid Al-Thihli, Zandre Bruwer

Sci Rep· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Uptake of prenatal genetic diagnosis and termination of pregnancy by Omani Muslim families at risk of genetic disorders: experience over a 9-year period.
Zandré Bruwer, Salwa Al Ubaidani, Khalsa Al Kharusi, Fathiya Al Murshedi, Almundher Al-Maawali

J Community Genet· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesis.
Bushra Al-Shamsi, Ghalia Al-Kasbi, Adila Al-Kindi, Zandre Bruwer, Khalsa Al-Kharusi

Eur J Med Genet· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Applying whole exome sequencing in a consanguineous population with autism spectrum disorder.
Watfa Al-Mamari, Ahmed B Idris, Khalid Al-Thihli, Reem Abdulrahim, Saquib Jalees, Zandrè Bruwer

Int J Dev Disabil· June 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The experience of Preimplantation Genetic Testing (PGT) among Muslim couples in Oman in the Middle East.
Khalsa Al-Kharusi, Zandre Bruwer, Tina-Marié Wessels

J Genet Couns· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spinocerebellar ataxia with axonal neuropathy type 1 revisited.
Patrick Scott, Adila Al Kindi, Amira Al Fahdi, Naeema Al Yarubi, Zandre Bruwer

J Clin Neurosci· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Inborn errors of metabolism in a cohort of pregnancies with non-immune hydrops fetalis: a single center experience.
Zandrè Bruwer, Nihal Al Riyami, Tamima Al Dughaishi, Fathiya Al Murshedi, Abeer Al Sayegh

J Perinat Med· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Segmental Spinal Muscular Atrophy Localised to the Lower Limbs: First case from Oman.
Roshan Koul, Amna Al-Futaisi, Khalid Al-Thihli, Zandre Bruwer, Patrick Scott

Sultan Qaboos Univ Med J· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Occurrence of Optic Neuritis and Cervical Cord Schwannoma with Charcot-Marie-Tooth Type 4B1 Disease.
Patrick Scott, Zandre Bruwer, Khalsa Al-Kharusi, Douja Meftah, Fathiya Al-Murshedi

Oman Med J· May 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.
Susan Byrne, Lara Jansen, Jean-Marie U-King-Im, Ata Siddiqui, Hart G W Lidov, Zandre Bruwer

Brain· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population.
Watfa Al-Mamari, Abeer Al-Saegh, Adila Al-Kindy, Zandre Bruwer, Fathiya Al-Murshedi

J Autism Dev Disord· August 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Erratum to: Existing Challenges Associated with Offering Prenatal Genetic Diagnosis in an Arab Society in the Sultanate of Oman.
Zandrè Bruwer, Achandira M Udayakumar, Khalsa Al Kharousi, Adila Al-Kindy

J Genet Couns· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Existing challenges associated with offering prenatal genetic diagnosis in an Arab society in the Sultanate of Oman.
Zandrè Bruwer, Udayakumar Achandira, Khalsa Al Kharousi, Adila Al-Kindy

J Genet Couns· December 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Predictive genetic testing in children: constitutional mismatch repair deficiency cancer predisposing syndrome.
Zandrè Bruwer, Ursula Algar, Alvera Vorster, Karen Fieggen, Alan Davidson

J Genet Couns· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An update on ocular involvement in mucopolysaccharidoses.
Anuradha Ganesh, Zandre Bruwer, Khalid Al-Thihli

Curr Opin Ophthalmol· September 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis