Melissa T Carter

12PUBLICATIONS
27CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseases
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Publications (12)

|Aug 19, 2026
Adult-Onset CTC1-Related Disorder With Kidney Disease, Subcutaneous Dystrophic Calcifications and Telomere Length Conservation.

|Sep 12, 2025
De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.

Samuel M Bradbrook, Gail Graham, Melissa T Carter

|Jul 20, 2024
The diagnostic yield of genetic and metabolic investigations in syndromic and nonsyndromic patients with autism spectrum disorder, global developmental delay, or intellectual disability from a dedicated neurodevelopmental disorders genetics clinic.

Julianne K Postma, Mary-Ann Harrison, Stephen Kutcher

|Aug 16, 2023
Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.

Francesca Peluso, Stefano G Caraffi, Gianluca Contrò

|Feb 23, 2023
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG).

Melissa T Carter, Myriam Srour, Ping-Yee Billie Au

|Aug 13, 2022
Further clinical delineation of microcephaly-capillary malformation syndrome.

Julianne K Postma, Jessica L Zambonin, Ebtissal Khouj

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Frequent Collaborators

3 joint publications

Julianne K Postma

2 joint publications

Kym M Boycott

1 joint publications

Andriy Tomin

1 joint publications

Norbert Weiss