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Dawn Thiselton

Research Profile

Anatomy

X Chromosome

Chemicals & Drugs

Concepts & Ideas

Disorders

Procedures

Physiology

Geographic Areas

Ireland

Genes & Molecular Sequences

Phenomena

Polymorphism, Single-Stranded Conformational

Co-author Network

Publications

TOP 3
Tom R Webb; Ilaria Zito; Marina Apergi; Dalila Bevilacqua; Michael Cheetham; Alice E Davidson; Jessica C Gardner; Michael B Gorin; Naheed Kanuga; Ariadna Martinez; Michel Michaelides; David A Parfitt; Jacob H C Ressa; Nele Schwarz; Dawn L Thiselton; Alison J Hardcastle
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
B J Crespi; Dawn L Thiselton
Comparative immunogenetics of autism and schizophrenia.
Brion S Maher; Rebecca McNamee; Pierandrea Muglia; E Lenn Murrelle; John Nurnberger; Brien P Riley; Ralph E Tarter; Dawn L Thiselton; Jay A Tischfield; Vladimir I Vladimirov; Arpana Agrawal; Fazil Aliev; Tim B Bigdeli; Xiangning Chen; Howard D Chilcoat; Bernie Devlin; Danielle M Dick; Howard J Edenberg; Robert E Ferrell; Christian Heidbreder; John M Hettema; Moonsu Kang; Kenneth S Kendler; Galina P Kirillova; John Kramer; Shawn J Latendresse; Michael Vanyukov
The AVPR1A gene and substance use disorders: association, replication, and functional evidence.

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All Publications

2012: Tom R Webb; Ilaria Zito; Marina Apergi; Dalila Bevilacqua; Michael Cheetham; Alice E Davidson; Jessica C Gardner; Michael B Gorin; Naheed Kanuga; Ariadna Martinez; Michel Michaelides; David A Parfitt; Jacob H C Ressa; Nele Schwarz; Dawn L Thiselton; Alison J Hardcastle
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23).
Human molecular genetics 2012;21(16):3647-54.
2011: B J Crespi; Dawn L Thiselton
Comparative immunogenetics of autism and schizophrenia.
Genes, brain, and behavior 2011;10(7):689-701.
2011: Brion S Maher; Rebecca McNamee; Pierandrea Muglia; E Lenn Murrelle; John Nurnberger; Brien P Riley; Ralph E Tarter; Dawn L Thiselton; Jay A Tischfield; Vladimir I Vladimirov; Arpana Agrawal; Fazil Aliev; Tim B Bigdeli; Xiangning Chen; Howard D Chilcoat; Bernie Devlin; Danielle M Dick; Howard J Edenberg; Robert E Ferrell; Christian Heidbreder; John M Hettema; Moonsu Kang; Kenneth S Kendler; Galina P Kirillova; John Kramer; Shawn J Latendresse; Michael Vanyukov
The AVPR1A gene and substance use disorders: association, replication, and functional evidence.
Biological psychiatry 2011;70(6):519-27.
2010: Ayman H Fanous; Zhongming Zhao; Edwin J C G van den Oord; Brion S Maher; Dawn L Thiselton; S E Bergen; Brandon Wormley; T Bigdeli; Richard Amdur; F Anthony O'Neill; Dermot Walsh; Kenneth S Kendler; B P Riley
Association study of SNAP25 and schizophrenia in Irish family and case-control samples.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(2):663-74.
2010: Dawn L Thiselton; Brion S Maher; Bradley T Webb; T B Bigdeli; F Anthony O'Neill; Dermot Walsh; Kenneth S Kendler; Brien P Riley
Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS).
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(1):323-31.
2010: Brien Riley; Dawn L Thiselton; Brion S Maher; T Bigdeli; Brandon Wormley; G O McMichael; Ayman H Fanous; vladimir vladimirov; F Anthony O'Neill; Dermot Walsh; Kenneth S Kendler
Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample.
Molecular psychiatry 2010;15(1):29-37.
2008: Dawn L Thiselton; vladimir vladimirov; Po-Hsiu Kuo; Joseph L McClay; Brandon Wormley; Ayman H Fanous; F Anthony O'Neill; Dermot Walsh; Edwin J C G van den Oord; Kenneth S Kendler; Brien P Riley
AKT1 is associated with schizophrenia across multiple symptom dimensions in the Irish study of high density schizophrenia families.
Biological psychiatry 2008;63(5):449-57.
2007: V Vladimirov; Dawn L Thiselton; Po-Hsiu Kuo; Joseph L McClay; Ayman H Fanous; Brandon Wormley; Jen Vittum; R Ribble; B Moher; Edwin J C G van den Oord; F Anthony O'Neill; Dermot Walsh; Kenneth S Kendler; Brien P Riley
A region of 35 kb containing the trace amine associate receptor 6 (TAAR6) gene is associated with schizophrenia in the Irish study of high-density schizophrenia families.
Molecular psychiatry 2007;12(9):842-53.
2006: Po-Hsiu Kuo; Michael C Neale; Brien P Riley; Bradley T Webb; Patrick F Sullivan; Jen Vittum; Diana G Patterson; Dawn L Thiselton; Edwin J C G van den Oord; Dermot Walsh; Kenneth S Kendler; Carol A Prescott
Identification of susceptibility loci for alcohol-related traits in the Irish Affected Sib Pair Study of Alcohol Dependence.
Alcoholism, clinical and experimental research 2006;30(11):1807-16.
2006: Brien P Riley; Gursharan Kalsi; Po-Hsiu Kuo; vladimir vladimirov; Dawn L Thiselton; Jen Vittum; Brandon Wormley; Michael S Grotewiel; Diana G Patterson; Patrick F Sullivan; Edwin J C G van den Oord; Dermot Walsh; Kenneth S Kendler; Carol A Prescott
Alcohol dependence is associated with the ZNF699 gene, a human locus related to Drosophila hangover, in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD) sample.
Molecular psychiatry 2006;11(11):1025-31.
2006: Carol A Prescott; Patrick F Sullivan; Po-Hsiu Kuo; Bradley T Webb; Jen Vittum; Diana G Patterson; Dawn L Thiselton; John M Myers; M Devitt; L J Halberstadt; V P Robinson; Michael C Neale; Edwin J C G van den Oord; Dermot Walsh; Brien P Riley; Kenneth S Kendler
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.
Molecular psychiatry 2006;11(6):603-11.
2004: Dawn L Thiselton; Bradley T Webb; Benjamin M Neale; R C Ribble; F Anthony O'Neill; Dermot Walsh; Brien P Riley; Kenneth S Kendler
No evidence for linkage or association of neuregulin-1 (NRG1) with disease in the Irish study of high-density schizophrenia families (ISHDSF).
Molecular psychiatry 2004;9(8):777-83; image 729.
2003: Lotta Gränse; Ingar C Bergstrand; Dawn L Thiselton; Vesna Ponjavic; Anders Heijl; Marcela Votruba; Sten Andréasson
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene.
Ophthalmic genetics 2003;24(4):233-45.
2003: Marcela Votruba; Dawn L Thiselton; Shomi S Bhattacharya
Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy.
The British journal of ophthalmology 2003;87(1):48-53.
2002: Dawn L Thiselton; Christiane Alexander; Jan-Willem Taanman; Simon Brooks; Thomas Rosenberg; Hans Eiberg; sten andreasson; Nicole Van Regemorter; Francis L Munier; Anthony T Moore; Shomi S Bhattacharya; Marcela Votruba
A comprehensive survey of mutations in the OPA1 gene in patients with autosomal dominant optic atrophy.
Investigative ophthalmology & visual science 2002;43(6):1715-24.
2002: Dawn L Thiselton; Jennifer McDowall; Oliver Brandau; Juliane Ramser; Fabiana d'Esposito; Shomi S Bhattacharya; Mark T Ross; Alison J Hardcastle; Alfons Meindl
An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disorders.
Genomics 2002;79(4):560-72.
2002: Tin Aung; Louise Ocaka; Neil D Ebenezer; Alex G Morris; Michael Krawczak; Dawn L Thiselton; Christiane Alexander; Marcela Votruba; Glen Brice; Anne Child; Peter J Francis; Roger A Hitchings; Ordan J Lehmann; Shomi S Bhattacharya
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
Human genetics 2002;110(1):52-6.
2001: Dawn L Thiselton; Christiane Alexander; A Morris; S Brooks; Thomas Rosenberg; Hans Eiberg; Birgit Kjer; P Kjer; Shomi S Bhattacharya; Marcela Votruba
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.
Human genetics 2001;109(5):498-502.
2000: Christiane Alexander; Marcela Votruba; Ulrike E A Pesch; Dawn L Thiselton; S Mayer; A Moore; M Rodriguez; Ulrich Kellner; Beate Leo-Kottler; G Auburger; Shomi S Bhattacharya; Bernd Wissinger
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
Nature genetics 2000;26(2):211-5.
2000: Ilaria Zito; A Morris; P Tyson; I Winship; D Sharp; D Gilbert; Dawn L Thiselton; Shomi S Bhattacharya; Alison J Hardcastle
Sequence variation within the RPGR gene: evidence for a founder complex allele.
Human mutation 2000;16(3):273-4.
2000: Alison J Hardcastle; Dawn L Thiselton; Ilaria Zito; Neil D Ebenezer; Tammy S Mah; Michael B Gorin; Shomi S Bhattacharya
Evidence for a new locus for X-linked retinitis pigmentosa (RP23).
Investigative ophthalmology & visual science 2000;41(8):2080-6.
2000: Dawn L Thiselton; Ilaria Zito; C Plant; MR Jay; Shirley V Hodgson; Alan C Bird; Shomi S Bhattacharya; Alison J Hardcastle
Novel frameshift mutations in the RP2 gene and polymorphic variants.
Human mutation 2000;15(6):580.
1999: Christina J Flaxel; MR Jay; Dawn L Thiselton; M Nayudu; Alison J Hardcastle; A Wright; Alan C Bird
Difference between RP2 and RP3 phenotypes in X linked retinitis pigmentosa.
The British journal of ophthalmology 1999;83(10):1144-8.
1999: Ilaria Zito; Dawn L Thiselton; Michael B Gorin; J Timothy Stout; C Plant; Alan C Bird; Shomi S Bhattacharya; Alison J Hardcastle
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus.
Human genetics 1999;105(1-2):57-62.
1999: Alison J Hardcastle; Dawn L Thiselton; L Van Maldergem; bratin saha; MR Jay; C Plant; R Taylor; Alan C Bird; S Bhattacharya
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study.
American journal of human genetics 1999;64(4):1210-5.
1997: Alison J Hardcastle; Dawn L Thiselton; M Nayudu; R M Hampson; Shomi S Bhattacharya
Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2.
Investigative ophthalmology & visual science 1997;38(9):1893-6.
1996: Dawn L Thiselton; R M Hampson; M Nayudu; L Van Maldergem; M L Wolf; B K Saha; Shomi S Bhattacharya; Alison J Hardcastle
Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping.
Genome research 1996;6(11):1093-102.
1995: Dawn L Thiselton; S Lindsay; S Kamakari; Alison J Hardcastle; P Roustan; Shomi S Bhattacharya
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.
Genomics 1995;25(1):279-81.
1995: S Kamakari; Dawn L Thiselton; S Lindsay; Alison J Hardcastle; Shomi Bhattacharya
FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp.
Cytogenetics and cell genetics 1995;71(2):151-4.
1993: S Lindsay; A R Curtis; P Roustan; S Kamakari; Dawn L Thiselton; A Stephenson; Shomi S Bhattacharya
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome.
Genomics 1993;17(1):208-10.
1993: Dawn L Thiselton; S Kamakari; A R Curtis; M P Coleman; Kay E Davies; S Lindsay; Shomi Bhattacharya
Dinucleotide repeat polymorphism at the DXS556 locus.
Human molecular genetics 1993;2(5):613.
1993: P Roustan; A R Curtis; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Dinucleotide repeat polymorphism at the DXS573 locus.
Human molecular genetics 1993;2(1):92.
1992: P Roustan; A R Curtis; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Dinucleotide repeat polymorphism at the DXS559 locus.
Human molecular genetics 1992;1(9):778.
1992: A R Curtis; P Roustan; S Kamakari; Dawn L Thiselton; S Lindsay; Shomi S Bhattacharya
Two dinucleotide repeat polymorphisms at the DXS571 locus.
Human molecular genetics 1992;1(9):776.
1992: S Lindsay; Dawn L Thiselton; J B Bateman; J T Ngo; RS Sparkes; M Coleman; Kay E Davies; Shomi S Bhattacharya
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Human genetics 1992;88(3):349-50.