Publications by authors named "Melissa Carter"

Claim this Profile
D
Diagnostic Utility of Exome Data Reanalysis After In Silico Multi-Gene Panels or Clinical Exome Testing for Patients With Epilepsy and Developmental Delay/Intellectual Disability: A Retrospective Cohort Study.
Alexanne Cuillerier, Andrea Goodman, Chloe Lawrence, Noémie Villeneuve-Cloutier, Christine M Armour, Melissa T Carter

Clin Genet· January 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De Novo Truncating Variants in ZNF865 Cause a Novel Neurodevelopmental Disorder.
Samuel M Bradbrook, Gail Graham, Melissa T Carter, Maria Kibaek, Christina Fagerberg

Am J Med Genet A· January 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Osmolyte chemical diversity in Lingulaulax polyedra red tides: a critical overlooked factor to respiratory irritations?
Eva Ternon, Evgenia Glukhov, Marine Vallet, Julie Dinasquet, Melissa L Carter

Harmful Algae· January 2026

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Temperature alters interactions and keystone taxa in the marine microbiome.
Ewa Merz, Riley J Hale, Erik Saberski, Kasia M Kenitz, Melissa L Carter

ISME J· December 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exploring the Relationship Between Family Experiences and Behavioral Inflexibility in Young Autistic Children.
Laura de la Roche, Yun-Ju Chen, Caroline Roncadin, Amedeo D'Angiulli, Vivian Lee, Melissa Carter

J Autism Dev Disord· September 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Congenital-onset MLASA2 from a novel variant: A literature review.
Astrid Eisenkölbl, Hanns Lochmüller, Melissa T Carter, Leslie E Hamilton, Hugh J McMillan

J Neuromuscul Dis· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial inheritance of 14q terminal deletion syndrome and review of the literature.
Krista M Vincent, Bradley Prince, Jean McGowan-Jordan, Melissa T Carter

Eur J Med Genet· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Corticosteroid-binding Globulin Dysfunction Due to Homozygous Lyon Variant in a Pediatric Patient.
Mary R Jiang, Caroline Zuijdwijk, Melissa T Carter, Alexandra Ahmet

JCEM Case Rep· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
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, Richard J Webster, Mireille Cloutier, Melissa T Carter

Am J Med Genet A· November 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of a DNA methylation episignature for recurrent constellations of embryonic malformations.
Sadegheh Haghshenas, Karim Karimi, Roger E Stevenson, Michael A Levy, Raissa Relator, Melissa T Carter

Am J Hum Genet· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.
Xueyang Pan, Alice M Tao, Shenzhao Lu, Mengqi Ma, Shabab B Hannan, Melissa T Carter

Am J Hum Genet· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Pediatric Autism Research Cohort (PARC) Study: protocol for a patient-oriented prospective study examining trajectories of functioning in children with autism.
Anna Kata, Patrick G McPhee, Yun-Ju Chen, Lonnie Zwaigenbaum, Deepa Singal, Melissa Carter

BMJ Open· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study.
Taila Hartley, Deborah Marshall, Meryl Acker, Katharine Fooks, Meredith K Gillespie, Melissa Carter

Genet Med· February 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical Utility and Reimbursement of Next-Generation Sequencing-Based Testing for Myeloid Malignancies.
Craig R Soderquist, Christopher Freeman, Wen-Hsuan Lin, Rebecca J Leeman-Neill, Yue Gu, Melissa C Carter

J Mol Diagn· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
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, Lara Valeri, Manuela Napoli, Melissa T Carter

J Med Genet· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
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, Daniela Buhas, Sarah Dyack

J Med Genet· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production.
Frédéric Ebstein, Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie-Pier Scott-Boyer, Melissa T Carter

Sci Transl Med· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rett-like Phenotypes in -Related Neurodevelopmental Disorder.
Joseph Nicho Gonzalez, Sylvie Goldman, Melissa T Carter, Jennifer M Bain

Genes (Basel)· May 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.
Taila Hartley, Élisabeth Soubry, Meryl Acker, Matthew Osmond, Madeline Couse, Melissa T Carter

Clin Genet· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Impact of Community-Based Testing Sites and Gift Incentives on COVID-19 Testing Uptake in Maryland, April 29 - May 9, 2021.
Caitlin Turbyfill, Isabel Thomas, Namita Agravat, Joanna M Prasher, Randall J Nett, Melissa D Carter

Am J Health Promot· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
Elizabeth E Palmer, Michael Pusch, Alessandra Picollo, Caitlin Forwood, Matthew H Nguyen, Melissa Carter

Mol Psychiatry· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Further clinical delineation of microcephaly-capillary malformation syndrome.
Julianne K Postma, Jessica L Zambonin, Ebtissal Khouj, Suad Alyamani, John M Graham, Melissa T Carter

Am J Med Genet A· November 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication.
Irene E Drmic, Bonnie MacKinnon Modi, Beth McConnell, Sanne Jilderda, Ny Hoang, Melissa T Carter

Am J Med Genet A· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction to: Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.
Lijia Huang, Jodi Warman-Chardon, Melissa T Carter, Kathie L Friend, Tracy E Dudding

Orphanet J Rare Dis· March 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis