Dawn L. Thiselton - Concepedia

Author

Dawn L. Thiselton

Also Known As

D L Thiselton, D Thiselton, D. L Thiselton, D. L. Thiselton, D. Thiselton, D.L. Thiselton, DAWN L. THISELTON, Dawn L Thiselton, Dawn L. Thiselton, Dawn Thiselton

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

Virginia Commonwealth University University College London Health Research Board Medical Diagnostic Laboratories (United States)Washington DC VA Medical Center

About

Dawn L. Thiselton is an author at Virginia Commonwealth University specializing in medicine, genetics, and psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	2.4K
2	Social Sciences	3	3	407
3	Health Sciences	2	2	78
4	Natural Sciences	2	2	65
5	Public Health	2	2	26

Dawn L. Thiselton

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 Christiane Alexander, Marcela Votruba, Ulrike E. A. Pesch, Nature Genetics Mendelian DisorderDynamin-related GtpaseGenetic DisorderGeneticsMolecular Genetics	2000	1.3K
Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample Brien P. Riley, Dawn L. Thiselton, Brion S. Maher, Molecular Psychiatry Schizophrenia SamplePsychiatryPsychotic DisorderPsychiatric GeneticsIrish Case–control Study	2009	228
AKT1 Is Associated with Schizophrenia Across Multiple Symptom Dimensions in the Irish Study of High Density Schizophrenia Families Dawn L. Thiselton, Vladimir I. Vladimirov, Po‐Hsiu Kuo, Biological Psychiatry PsychiatryRisk PredictionPsychotic DisorderPsychiatric GeneticsPsychology	2007	157
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23) Tom R. Webb, David A. Parfitt, J.C. Gardner, Human Molecular Genetics	2012	151
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Tin Aung, Louise Ocaka, Neil D. Ebenezer, Human Genetics Opa1 GeneOcular DiseaseOphthalmologyExperimental OphthalmologyGenetics	2001	139
Genomewide linkage study in the Irish affected sib pair study of alcohol dependence: evidence for a susceptibility region for symptoms of alcohol dependence on chromosome 4 Carol A. Prescott, Patrick F. Sullivan, Po‐Hsiu Kuo, Molecular Psychiatry Genome-wide Association StudySubstance UsePsychiatryAlcohol DependenceGenetics	2006	110
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy. Dawn L. Thiselton, Christiane Alexander, Jan‐Willem Taanman, PubMed	2002	105
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF) Dawn L. Thiselton, Bradley T. Webb, Benjamin M. Neale, Molecular Psychiatry PsychiatryPsychotic DisorderPsychiatric GeneticsSchizophreniaHigh-density Schizophrenia Families	2004	103
Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis Zhongming Zhao, Bradley T. Webb, Peilin Jia, PLoS ONE	2013	102
An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders Dawn L. Thiselton, Jennifer McDowall, Oliver Brandau, Genomics Neurodegenerative DiseasesDxs8026–elk1 IntervalGenetic DisorderGeneticsHuman Xp11.3–xp11.23	2002	89

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