David A. Dyment

11.0k citations

129 papers · 5.3k indexed · h-index 37

Impact in

Pathology and Forensic Medicine top 0.2%
- Multiple Sclerosis Research Studies
- Vitamin D Research Studies
Immunology top 1%
- T-cell and B-cell Immunology
- Immunotherapy and Immune Responses
- Reproductive System and Pregnancy

Papers in

Pathology and Forensic Medicine 35
- Multiple Sclerosis Research Studies 30
Genetics 50
- Genomics and Rare Diseases 22
- Genetics and Neurodevelopmental Disorders 18
- Genomic variations and chromosomal abnormalities 10

Co-authors: George C. Ebers A. Dessa Sadovnick Neil Risch Kym M. Boycott Blanca Herrera Matthew R. Lincoln Cristen J. Willer Gabriele C. DeLuca
Journals: Clinical Genetics (9 papers)Neurology (5 papers)Journal of Neuroimmunology (4 papers)Neurology Genetics (4 papers)Human Molecular Genetics (4 papers)
Partner nations: Canada United Kingdom United States

In The Last Decade

David A. Dyment

126 papers receiving 5.1k citations

Peers

Countries citing papers authored by David A. Dyment

Since Specialization

Citations

This map shows the geographic impact of David A. Dyment'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 David A. Dyment with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David A. Dyment more than expected).

Fields of papers citing papers by David A. Dyment

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David A. Dyment. 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 David A. Dyment. The network helps show where David A. Dyment may publish in the future.

Co-authors

The 25 scholars most cited alongside David A. Dyment, 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 David A. Dyment Line = papers co-authored together David A. Dyment links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The Clinician-reported Genetic Testing Utility Index (C-GUIDE) for Prenatal Care: Initial evidence of content and construct validity Genetics in Medicine ·Robin Z. Hayeems, Stephanie Luca, E Ingals, Zhan-yu Mo, Maciej Gwóźdź, Abigail Aquino, (unknown), 황인창, Lauren Chad, David A. Dyment, Kym M. Boycott, Joanna Lazier, Wendy J. Ungar, Christine M. Armour	2024	1
2	Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction Neurology Genetics ·Jodi Warman‐Chardon, Taila Hartley, Aren E. Marshall, Arran McBride, Madeline Couse, William MacDonald, Mellissa R.W. Mann, Pierre R. Bourque, Ari Breiner, Hanns Lochmüller, John Woulfe, V. Sottke, Gerd Melkus, Bernard Brais, David A. Dyment, Kym M. Boycott, Kristin D. Kernohan	2023	2
3	The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile Annals of Clinical and Translational Neurology ·Michelle M. Lee, 王家奎, Darryl C. De Vivo, Daniel Friedman, Samuel F. Berkovic, Se-Jin Jung, Argirios Dinopoulos, Katheryn Grand, Pedro A. Sanchez‐Lara, Remigio Marin Ibarra, Jodi Warman‐Chardon, М.К. Черняков, Thierry Levade, Edward H. Schuchman, Steffany A. L. Bennett, David A. Dyment, Toni S. Pearson	2022	5
4	Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery The American Journal of Human Genetics ·Kym M. Boycott, Taila Hartley, Kristin D. Kernohan, David A. Dyment, Heather Howley, A. Micheil Innes, François P. Bernier, Michael Brudno	2022	15
5	A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia European Journal of Medical Genetics ·Keith Backman, Wendy Mears, Cilwyn Braganza, فاطمه جوادیان, Ivchenko Vn, Joseph de Nanassy, Joseph Reisman, Matthew Osmond, Taila Hartley, Alan J. Mears, Kristin D. Kernohan, David A. Dyment	2021	5
6	A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features Scientific Reports ·日本社会党中央本部, Jane S. Green, Somayyeh Fahiminiya, Jacek Majewski, Bridget A. Fernandez, Matthew A. Deardorff, (unknown), Alicia Vanessa Ceballos Salinas, Dirk Hubmacher, Suneel Apte, Kym M. Boycott, Dennis E. Bulman, David A. Dyment, 洗介福士, Michael Brudno, Michael O. Woods	2020	14
7	Epilepsy genetics: Current knowledge, applications, and future directions Clinical Genetics ·Kenneth A. Myers, Devon L. Johnstone, David A. Dyment	2018	75
8	Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1 Journal of Human Genetics ·Puja T. Pape, Taila Hartley, Eric Bareke, Kym M. Boycott, Alex MacKenzie, Jacek Majewski, Michael Brudno, Dennis E. Bulman, David A. Dyment, Sarah M. Nikkel	2017	11
9	Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE American Journal of Medical Genetics Part A ·Julie Richer, Hussein Daoud, Pavel Geier, Olga Jarinova, Nancy Carson, Ch. Konstadilaki-Savvapoulou, Chen Qida, Hassan Saber, Eric Bareke, Karine Khatchadourian, Dennis E. Bulman, Jacek Majewski, Kym M. Boycott, David A. Dyment	2015	12
10	Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study Clinical Genetics ·David A. Dyment, Martine Tétreault, Chandree L. Beaulieu, Taila Hartley, Patrick Ferreira, (unknown), Janet Marcadier, Sarah L. Sawyer, Taenikon Land Techniques, A. Micheil Innes, Jillian S. Parboosingh, Dennis E. Bulman, Jeremy Schwartzentruber, Jacek Majewski, Mark A. Tarnopolsky, Kym M. Boycott, (unknown)	2014	64
11	Whole‐exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation Epilepsia ·Sunita Venkateswaran, Kenneth A. Myers, Amanda Smith, Chandree L. Beaulieu, Jeremy Schwartzentruber, Jacek Majewski, Dennis E. Bulman, Kym M. Boycott, David A. Dyment	2014	32
12	Mutations in PIK3R1 Cause SHORT Syndrome The American Journal of Human Genetics ·David A. Dyment, Amanda Smith, Diana Alcantara, Jeremy Schwartzentruber, Lina Basel‐Vanagaite, Cynthia J. Curry, I. Karen Temple, William Reardon, Sahar Mansour, Mushfequr R. Haq, Rodney D. Gilbert, Ordan J. Lehmann, Megan R. Vanstone, Chandree L. Beaulieu, Jacek Majewski, Dennis E. Bulman, Mark O’Driscoll, Kym M. Boycott, A. Micheil Innes	2013	130
13	Association of Infectious Mononucleosis with Multiple Sclerosis Neuroepidemiology ·Sreeram V Ramagopalan, William Valdar, David A. Dyment, Gabriele C. DeLuca, Irene M. Yee, Gavin Giovannoni, George C. Ebers, A. Dessa Sadovnick	2009	74
14	Prenatal, perinatal and early life factors in MS susceptibility Oxford University Research Archive (ORA) (University of Oxford) ·Sreeram V Ramagopalan, Colleen Guimond, Maria Criscuoli, Irene M. Yee, David A. Dyment, George C. Ebers, A. Dessa Sadovnick	2009	1
15	An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1gene BMC Medical Genetics ·Sreeram V. Ramagopalan, Róisín M. McMahon, David A. Dyment, A. Dessa Sadovnick, George C. Ebers, Knut M. Wittkowski	2009	18
16	Genetic epidemiology: the use of old and new tools for multiple sclerosis Trends in Neurosciences ·Sreeram V. Ramagopalan, David A. Dyment, George C. Ebers	2008	40
17	Autoimmune disease in families with multiple sclerosis: a population-based study The Lancet Neurology ·Sreeram V. Ramagopalan, David A. Dyment, William Valdar, Blanca Herrera, Maria Criscuoli, A Anasiewicz, A. Dessa Sadovnick, George C. Ebers	2007	133
18	A first stage genome‐wide screen for regions shared identical‐by‐descent in hutterite families with multiple sclerosis American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·David A. Dyment, M. Zameel Cader, Anita Datta, Jiang Jiayou, Stacey S. Cherny, Cristen J. Willer, Sreeram V. Ramagopalan, Blanca Herrera, Sarah Orton, Michael J. Chao, A. Dessa Sadovnick, Jeffery Gilchriest, Walter Hader, George C. Ebers	2007	4
19	Genetics of multiple sclerosis The Lancet Neurology ·David A. Dyment, George C. Ebers, A. Dessa Sadovnick	2004	383
20	No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study Journal of Neuroimmunology ·David A. Dyment, J. L. Steckley, Cristen J. Willer, Holly Armstrong, A. Dessa Sadovnick, Neil Risch, George C. Ebers	2002	39

About David A. Dyment

David A. Dyment is a scholar working on Pathology and Forensic Medicine, Genetics, Immunology, Clinical Biochemistry and Rheumatology, having authored 129 papers that have together received 5.3k indexed citations. Recurring topics across this work include Multiple Sclerosis Research Studies (30 papers), Genomics and Rare Diseases (22 papers), T-cell and B-cell Immunology (18 papers), Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (10 papers), RNA modifications and cancer (10 papers), Systemic Lupus Erythematosus Research (9 papers) and Metabolism and Genetic Disorders (9 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.3k citations), Immunology (1.6k citations), Rheumatology (675 citations), Genetics (1.2k citations) and Neurology (227 citations). David A. Dyment has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include George C. Ebers, A. Dessa Sadovnick, Neil Risch, Kym M. Boycott, Blanca Herrera, Matthew R. Lincoln, Cristen J. Willer, Gabriele C. DeLuca, Sreeram V. Ramagopalan and Jacek Majewski. Their work appears in journals such as Clinical Genetics, Neurology, Journal of Neuroimmunology, Neurology Genetics and Human Molecular Genetics.

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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