Dimitri J. Stavropoulos

9.9k citations

66 papers · 1.7k indexed · h-index 23

Genetics top 1%
- Genomic variations and chromosomal abnormalities 41
- Genomics and Rare Diseases 26
- Genetics and Neurodevelopmental Disorders 18
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 10
Molecular Biology top 10%
- Congenital heart defects research 18
- Epigenetics and DNA Methylation 5
Cancer Research
Psychiatry and Mental health top 10%
Cognitive Neuroscience
- Autism Spectrum Disorder Research 5
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 5

Co-authors: Stephen W. Scherer Christian R. Marshall Anath C. Lionel Anne S. Bassett Joyce So David Chitayat Rosanna Weksberg Sébastien Chénier
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Nature Communications (1 paper)SHILAP Revista de lepidopterología (1 paper)Cell Reports (1 paper)
Partner nations: Canada United States United Kingdom

In The Last Decade

Dimitri J. Stavropoulos

64 papers receiving 1.6k citations

Peers

Countries citing papers authored by Dimitri J. Stavropoulos

Since Specialization

Citations

This map shows the geographic impact of Dimitri J. Stavropoulos's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dimitri J. Stavropoulos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dimitri J. Stavropoulos more than expected).

Fields of papers citing papers by Dimitri J. Stavropoulos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dimitri J. Stavropoulos. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dimitri J. Stavropoulos. The network helps show where Dimitri J. Stavropoulos may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Dimitri J. Stavropoulos, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Dimitri J. Stavropoulos Line = papers co-authored together Dimitri J. Stavropoulos links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis Genetics in Medicine ·Wendy J. Ungar,Vercancy Wu,Christian R. Marshall,Jackie Hwang,Robin Z. Hayeems,Kate Tsiplova,Meredith Gillespie,Anna Szuto,Caitlin Chisholm,Dimitri J. Stavropoulos,Viji Venkataramanan,Bowen Xiao,Gregory Costain,Mélanie Beaulieu Bergeron,Sarah L. Sawyer,Lynette Lau,Lijia Huang,Roberto Mendoza‐Londono,Martin J. Somerville,Kym M Boycott,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2025	1
2	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease npj Genomic Medicine ·Christian R. Marshall,Shimul Chowdhury,Ryan J. Taft,Matthew S. Lebo,Jillian G. Buchan,Steven M. Harrison,Ross Rowsey,Eric W. Klee,Pengfei Liu,Elizabeth A. Worthey,Vaidehi Jobanputra,David Dimmock,Hutton M. Kearney,David Bick,Shashikant Kulkarni,Stacie L. Taylor,John W. Belmont,Dimitri J. Stavropoulos,Niall J. Lennon	2020	85
3	Return of genetic and genomic research findings: experience of a pediatric biorepository BMC Medical Genomics ·Tanya Papaz,Eriskay Liston,Laura Zahavich,Dimitri J. Stavropoulos,Rebekah Jobling,Raymond H. Kim,Miriam S. Reuter,Anastasia Miron,Erwin Oechslin,Tapas Mondal,Lynn Bergin,John Smythe,Luis Altamirano‐Diaz,Jane Lougheed,Roderick Yao,Oyediran Akinrinade,Jeroen Breckpot,Seema Mital	2019	19
4	Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants Clinical Epigenetics ·M. Siu,Darci T. Butcher,Andrei L. Turinsky,Cheryl Cytrynbaum,Dimitri J. Stavropoulos,Susan Walker,Oana Caluseriu,M. Carter,Y. Lou,Rob Nicolson,Stelios Georgiades,Péter Szatmári,Evdokia Anagnostou,Stephen W. Scherer,Sanaa Choufani,Michael Brudno,Rosanna Weksberg	2019	43
5	Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders Journal of Neurodevelopmental Disorders ·Gregory Costain,Susan Walker,Bob Argiropoulos,Danielle Baribeau,Anne S. Bassett,Erik Boot,Koenraad Devriendt,Barbara Kellam,Christian R. Marshall,Aparna Prasad,Moises Serrano,Dimitri J. Stavropoulos,Hope Twede,Joris Vermeesch,Jacob Vorstman,Stephen W. Scherer	2019	6
6	Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant Molecular Cytogenetics ·Peter Sabatini,Resham Ejaz,Dimitri J. Stavropoulos,Roberto Mendoza‐Londono,Ann M. Joseph‐George	2018	9
7	Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study npj Genomic Medicine ·Iris Cohn,Tara Paton,Christian R. Marshall,Raveen Basran,Dimitri J. Stavropoulos,Peter N. Ray,Nasim Monfared,Robin Z. Hayeems,M. Stephen Meyn,Sarah Bowdin,Stephen W. Scherer,Ronald D. Cohn,Shinya Ito	2017	38
8	Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray European Journal of Human Genetics ·Robin Z. Hayeems,Jasmin Bhawra,Kate Tsiplova,M. Stephen Meyn,Nasim Monfared,Sarah Bowdin,Dimitri J. Stavropoulos,Christian R. Marshall,Raveen Basran,Cheryl Shuman,Shinya Ito,Iris Cohn,Courtney Hum,Marta Gîrdea,Michael Brudno,Ronald D. Cohn,Stephen W. Scherer,Wendy J. Ungar	2017	27
9	Deletion of the MC4R Gene in a 9-Year-Old Obese Boy Childhood Obesity ·Lesley Turner,Anne Gregory,Laurie Twells,Deborah M. Gregory,Dimitri J. Stavropoulos	2015	8
10	Clinically relevant copy number variations detected in cerebral palsy Nature Communications ·Maryam Oskoui,Matthew J. Gazzellone,Bhooma Thiruvahindrapuram,Mehdi Zarrei,John Andersen,John Wei,Zhuozhi Wang,Richard F. Wintle,Christian R. Marshall,Ronald D. Cohn,Rosanna Weksberg,Dimitri J. Stavropoulos,Darcy Fehlings,Michael Shevell,Stephen W. Scherer	2015	103
11	Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus Journal of Medical Genetics ·Janet A. Buchanan,David Chitayat,Elena Kolomietz,Hin C Lee,Stephen W. Scherer,Marsha Speevak,Hana Sroka,Dimitri J. Stavropoulos	2015	4
12	Complex genomic rearrangements in the dystrophin gene due to replication‐based mechanisms Molecular Genetics & Genomic Medicine ·Berivan Baskin,Dimitri J. Stavropoulos,Paige A. Rebeiro,Jennifer Orr,Martin Li,Leslie Steele,Christian R. Marshall,Edmond G. Lemire,Kym M. Boycott,William T. Gibson,Peter N. Ray	2014	17
13	Adult expression of a 3q13.31 microdeletion Molecular Cytogenetics ·Chelsea Lowther,Gregory Costain,Rebecca Melvin,Dimitri J. Stavropoulos,Anath C. Lionel,Christian R. Marshall,Stephen W. Scherer,Anne S. Bassett	2014	9
14	CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems Journal of Neurodevelopmental Disorders ·Sébastien Chénier,Grace Yoon,Bob Argiropoulos,Julie Lauzon,Rachel Laframboise,Joo Wook Ahn,Caroline Mackie Ogilvie,Anath C. Lionel,Christian R. Marshall,Andrea K. Vaags,Bita Hashemi,Karine Boisvert,Géraldine Mathonnet,Frédérique Tihy,Joyce So,Stephen W. Scherer,Emmanuelle Lemyre,Dimitri J. Stavropoulos	2014	63
15	Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature Genetics in Medicine ·Chelsea Lowther,Gregory Costain,Dimitri J. Stavropoulos,Rebecca Melvin,Candice K. Silversides,Danielle M. Andrade,Joyce So,Hanna Faghfoury,Anath C. Lionel,Christian R. Marshall,Stephen W. Scherer,Anne S. Bassett	2014	108
16	High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome Human Genetics ·Berivan Baskin,Sanaa Choufani,Yi‐An Chen,Cheryl Shuman,Nicole Parkinson,Emmanuelle Lemyre,A. Micheil Innes,Dimitri J. Stavropoulos,Peter N. Ray,Rosanna Weksberg	2013	58
17	Osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region Xq11.2 American Journal of Medical Genetics Part A ·Sébastien Chénier,Abdul Noor,Lucie Dupuis,Dimitri J. Stavropoulos,Roberto Mendoza‐Londono	2012	10
18	1q21.1 Microduplication expression in adults Genetics in Medicine ·Alessia Dolcetti,Candice K. Silversides,Christian R. Marshall,Anath C. Lionel,Dimitri J. Stavropoulos,Stephen W. Scherer,Anne S. Bassett	2012	82
19	Severe intellectual disability and autistic features associated with microduplication 2q23.1 European Journal of Human Genetics ·Brian HY Chung,Sureni V. Mullegama,Christian R. Marshall,Anath C. Lionel,Rosanna Weksberg,Lucie Dupuis,Lauren Brick,Chumei Li,Stephen W. Scherer,Swaroop Aradhya,Dimitri J. Stavropoulos,Sarah H. Elsea,Roberto Mendoza‐Londono	2011	27
20	Mosaic microdeletion 18q21 as a cause of mental retardation European Journal of Medical Genetics ·Dimitri J. Stavropoulos,Daune MacGregor,Grace Yoon	2010	15

About Dimitri J. Stavropoulos

Dimitri J. Stavropoulos is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 66 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (41 papers), Genomics and Rare Diseases (26 papers), Congenital heart defects research (18 papers), Genetics and Neurodevelopmental Disorders (18 papers), Prenatal Screening and Diagnostics (10 papers), Autism Spectrum Disorder Research (5 papers), Epigenetics and DNA Methylation (5 papers) and Genetic factors in colorectal cancer (5 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (355 citations) and Molecular Biology (731 citations). Dimitri J. Stavropoulos has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Stephen W. Scherer, Christian R. Marshall, Anath C. Lionel, Anne S. Bassett, Joyce So, David Chitayat, Rosanna Weksberg, Sébastien Chénier, Peter N. Ray and Danielle M. Andrade. Their work appears in journals such as Nature Communications, SHILAP Revista de lepidopterología and Cell Reports.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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