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Dimitri J. Stavropoulos | Researchclopedia

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Dimitri J. Stavropoulos

University of Toronto ORCID

133

Works

9,900

Citations

43

h-index

81

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Genomics and Rare Diseases Genetics and Neurodevelopmental Disorders

Affiliations

Memorial University of Newfoundland2013–2017

Canadian Cancer Society2013–2013

Université du Québec à Montréal2016–2016

University of Toronto1996–2026

Great Ormond Street Hospital2013–2024

Top Works

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

David T. Miller,Margaret P Adam,et al.

20102,855 citations

Congenital heart defects research

Prenatal Screening and Diagnostics

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

Anath C. Lionel,Gregory Costain,et al.

2017560 citations

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

Kristiina Tammimies,Christian R. Marshall,et al.

2015435 citations

Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

Dimitri J. Stavropoulos,Daniele Merico,et al.

2016375 citations

SHANK1 Deletions in Males with Autism Spectrum Disorder

Daisuke Sato,Anath C. Lionel,et al.

2012322 citations

PhenoTips: Patient Phenotyping Software for Clinical and Research Use

Marta Gîrdea,Sergiu Dumitriu,et al.

2013254 citations

Rare Deletions at the Neurexin 3 Locus in Autism Spectrum Disorder

Andrea K. Vaags,Anath C. Lionel,et al.

2011214 citations

NSD1 mutations generate a genome-wide DNA methylation signature

Sanaa Choufani,Cheryl Cytrynbaum,et al.

2015208 citations

A large data resource of genomic copy number variation across neurodevelopmental disorders

Mehdi Zarrei,Christie L. Burton,et al.

2019198 citations