David Dyment

David Dyment

UNVERIFIED PROFILE

Are you David Dyment?   Register this Author

Register author
David Dyment

David Dyment

Publications by authors named "David Dyment"

Are you David Dyment?   Register this Author

98Publications

2003Reads

14Profile Views

p21 protein-activated kinase 1 is associated with severe regressive autism, and epilepsy.

Clin Genet 2019 Nov 13;96(5):449-455. Epub 2019 Aug 13.

Department of Pediatrics, Dalhousie University and IWK Health Centre, Halifax, Nova Scotia, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cge.13618DOI Listing
November 2019

De novo substitutions of TRPM3 cause intellectual disability and epilepsy.

Eur J Hum Genet 2019 Oct 5;27(10):1611-1618. Epub 2019 Jul 5.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41431-019-0462-xDOI Listing
October 2019

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.

Nat Commun 2019 07 12;10(1):3094. Epub 2019 Jul 12.

Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41467-019-10910-wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6626132PMC
July 2019

Development of Criteria for Epilepsy Genetic Testing in Ontario, Canada.

Can J Neurol Sci 2019 01 13;46(1):7-13. Epub 2018 Nov 13.

1Epilepsy Program,Division of Neurology,Department of Pediatrics,The Hospital for Sick Children,University of Toronto,Toronto,Ontario,Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/cjn.2018.341DOI Listing
January 2019

The unsolved rare genetic disease atlas? An analysis of the unexplained phenotypic descriptions in OMIM®.

Am J Med Genet C Semin Med Genet 2018 12;178(4):458-463

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.c.31662
Publisher Site
http://dx.doi.org/10.1002/ajmg.c.31662DOI Listing
December 2018

Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further research.

Am J Med Genet C Semin Med Genet 2018 12;178(4):387-397

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.c.31661DOI Listing
December 2018

Unsolved recognizable patterns of human malformation: Challenges and opportunities.

Am J Med Genet C Semin Med Genet 2018 12;178(4):382-386

Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.c.31665DOI Listing
December 2018

Lysosomal dysfunction in hypomyelinating leukodystrophy.

Neurol Genet 2018 Dec 13;4(6):e288. Epub 2018 Nov 13.

Children's Hospital of Eastern Ontario Research Institute (Y.I., T.H., S.B., K.M.B., D.A.D., K.D.K.), Ottawa, Ontario, Canada; Division of Neurology (S.V.), Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada; Institute for Molecular Bioscience (C.S.), University of Queensland, St. Lucia, Queensland, Australia; and Department of Child Neurology (N.I.W.), VU University Medical Center, and Amsterdam Neuroscience, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
Publisher Site
http://dx.doi.org/10.1212/NXG.0000000000000288DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317987PMC
December 2018

Atypical Hepatic Mesenchymal Hamartoma: Histologic Appearance, Immunophenotype, and Molecular Findings.

Pediatr Dev Pathol 2019 Jul-Aug;22(4):365-369. Epub 2018 Nov 29.

9 Department of Pediatric Surgery, Children's Hospital of Eastern Ontario and University of Ottawa Faculty of Medicine, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1093526618806750DOI Listing
November 2018

Periodic breathing in patients with NALCN mutations.

J Hum Genet 2018 Oct 3;63(10):1093-1096. Epub 2018 Jul 3.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s10038-018-0484-1DOI Listing
October 2018

Atypical Rett Syndrome and Intractable Epilepsy With Novel Mutation.

Child Neurol Open 2018 23;5:2329048X18787946. Epub 2018 Aug 23.

Division of Neurology, The Ottawa Hospital Civic Campus, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/2329048X18787946DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108011PMC
August 2018

Reply: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot.

Brain 2018 05;141(5):e37

Department of Child Neurology, VU University Medical Center, and Amsterdam Neuroscience, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/awy030DOI Listing
May 2018

A de novo mutation in RPL10 causes a rare X-linked ribosomopathy characterized by syndromic intellectual disability and epilepsy: A new case and review of the literature.

Eur J Med Genet 2018 Feb 21;61(2):89-93. Epub 2017 Oct 21.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2017.10.011DOI Listing
February 2018

Evaluation of exome filtering techniques for the analysis of clinically relevant genes.

Hum Mutat 2018 02 14;39(2):197-201. Epub 2017 Dec 14.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.23374DOI Listing
February 2018

Pointed rhythmic theta waves: a unique EEG pattern in KCNQ2-related neonatal epileptic encephalopathy.

Epileptic Disord 2017 Sep;19(3):351-356

Division of Neurology, Children's Hospital of Eastern Ontario; University of Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1684/epd.2017.0927DOI Listing
September 2017

Benchmarking outcomes in the Neonatal Intensive Care Unit: Cytogenetic and molecular diagnostic rates in a retrospective cohort.

Am J Med Genet A 2017 Jul 9;173(7):1839-1847. Epub 2017 May 9.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.38250DOI Listing
July 2017

Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1.

J Hum Genet 2017 Jun 23;62(6):661-663. Epub 2017 Feb 23.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jhg.2017.18DOI Listing
June 2017

Concordance between whole-exome sequencing and clinical Sanger sequencing: implications for patient care.

Mol Genet Genomic Med 2016 Sep 10;4(5):504-12. Epub 2016 May 10.

Children's Hospital of Eastern Ontario Research InstituteUniversity of OttawaOttawaOntarioCanada; Department of GeneticsChildren's Hospital of Eastern Ontario ResearchOttawaOntarioCanada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mgg3.223DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5023935PMC
September 2016

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.

CMAJ 2016 Aug 30;188(11):E254-E260. Epub 2016 May 30.

Department of Genetics (Daoud, Luco, Beaulieu, Jarinova, Carson, Nikkel, Graham, Richer, Armour, Boycott, Dyment) and Department of Pediatrics (Bulman, Chakraborty, Geraghty, Lines, Lacaze-Masmonteil), Children's Hospital of Eastern Ontario, Ottawa, Ont.; McGill University (Li, Bareke, Majewski) and Genome Quebec Innovation Centre (Li, Bareke, Majewski), Montréal, Que.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1503/cmaj.150823DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4978597PMC
August 2016

Brain malformations in a patient with deletion 2p16.1: A refinement of the phenotype to BCL11A.

Eur J Med Genet 2015 Jun-Jul;58(6-7):351-4. Epub 2015 May 13.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Canada. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2015.04.006DOI Listing
March 2016

Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature.

BMC Med Genet 2016 Feb 27;17:15. Epub 2016 Feb 27.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, K1H 8L1, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12881-016-0276-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769499PMC
February 2016

Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings.

Neurol Genet 2016 Feb 22;2(1):e38. Epub 2015 Dec 22.

Division of Medical Genetics (P.F.), Alberta Children's Hospital, Calgary, Alberta, Canada; Department of Genetics (S.M.L., S.L.S., K.M.B., D.A.D.) and Department of Radiology (J.D., D.A.D.) Children's Hospital of Eastern Ontario, Ottawa, Canada; and Children's Hospital of Eastern Ontario Research Institute (K.M.B.), University of Ottawa, Canada.

View Article

Download full-text PDF

Source
http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
Publisher Site
http://dx.doi.org/10.1212/NXG.0000000000000038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4817904PMC
February 2016

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Am J Med Genet A 2015 Nov 26;167A(11):2867. Epub 2015 Aug 26.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.37270DOI Listing
November 2015

Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2.

Neuromuscul Disord 2015 Oct 5;25(10):794-9. Epub 2015 Aug 5.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada; Division of Neurology, Department of Pediatrics, Children's Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nmd.2015.07.017DOI Listing
October 2015

Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy.

Hum Mol Genet 2015 Sep 17;24(18):5109-14. Epub 2015 Jun 17.

ANZAC Research Institute, University of Sydney, Concord Hospital, New South Wales, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddv229DOI Listing
September 2015

Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.

Curr Neurol Neurosci Rep 2015 Sep;15(9):64

Division of Neurology, The Ottawa Hospital, 1053 Carling Avenue, Ottawa, ON, K1Y 4E9, Canada.

View Article

Download full-text PDF

Source
http://link.springer.com/content/pdf/10.1007/s11910-015-0584
Web Search
http://link.springer.com/10.1007/s11910-015-0584-7
Publisher Site
http://dx.doi.org/10.1007/s11910-015-0584-7DOI Listing
September 2015

Congenital Nemaline Myopathy: The Value of Magnetic Resonance Imaging of Muscle.

Can J Neurol Sci 2015 Sep;42(5):338-40

2Division of Neurology,University of Ottawa,Children's Hospital of Eastern Ontario,Ottawa,Ontario,Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/cjn.2015.59DOI Listing
September 2015

Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathology.

Neurobiol Aging 2015 Feb 6;36(2):1222.e1-5. Epub 2014 Sep 6.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada; Department of Genetics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2014.09.005DOI Listing
February 2015

Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype.

Cancer Discov 2015 Feb 3;5(2):135-42. Epub 2014 Dec 3.

Department of Cancer Biology, Abramson Family Cancer Research Institute, Basser Research Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. Department of Pathology, Abramson Family Cancer Research Institute, Basser Research Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1158/2159-8290.CD-14-1156DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320660PMC
February 2015

Identification of genes for childhood heritable diseases.

Annu Rev Med 2014 ;65:19-31

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, K1H 8L1 Canada; email: , , , , .

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1146/annurev-med-101712-122108DOI Listing
September 2014

Multiple sclerosis in the Iranian immigrant population of BC, Canada: prevalence and risk factors.

Mult Scler 2014 08 10;20(9):1182-8. Epub 2014 Jan 10.

Department of Medical Genetics, University of British Columbia (BC), Vancouver, Canada Division of Neurology, University of BC, Vancouver, Canada

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/1352458513519179DOI Listing
August 2014

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.

Hum Mol Genet 2014 Jun 8;23(11):2888-900. Epub 2014 Jan 8.

Sektion für Funktionelle Genetik am Institut für Humangenetik, Universität zu Lübeck, Lübeck 23538, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddu002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014191PMC
June 2014

Recent advances in the genetic etiology of brain malformations.

Curr Neurol Neurosci Rep 2013 Aug;13(8):364

Department of Genetics, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, ON, Canada, K1H 8L1.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11910-013-0364-1DOI Listing
August 2013

Early life child exposure and the risk of multiple sclerosis: a population based study.

J Neurol Sci 2011 Aug 23;307(1-2):162-3. Epub 2011 May 23.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S0022510X110021
Publisher Site
http://dx.doi.org/10.1016/j.jns.2011.04.014DOI Listing
August 2011

Multiple sclerosis.

Autoimmune Dis 2011 29;2011:248758. Epub 2011 Jun 29.

Department of Clinical Neurology, University of Oxford, Oxford OX3 9DU, UK.

View Article

Download full-text PDF

Source
http://www.hindawi.com/journals/ad/2011/248758/
Publisher Site
http://dx.doi.org/10.4061/2011/248758DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130332PMC
July 2011

What is Next for the Genetics of Multiple Sclerosis?

Autoimmune Dis 2011 Mar 28;2011:519450. Epub 2011 Mar 28.

Wellcome Trust Centre for Human Genetics, University of Oxford, OX3 7BN Oxford, UK.

View Article

Download full-text PDF

Source
http://www.hindawi.com/journals/ad/2011/519450/
Publisher Site
http://dx.doi.org/10.4061/2011/519450DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3085300PMC
March 2011

Congenital abnormalities and multiple sclerosis.

BMC Neurol 2010 Nov 16;10:115. Epub 2010 Nov 16.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2377-10-115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020672PMC
November 2010

No effect of parental age on risk of multiple sclerosis: a population-based study.

Neuroepidemiology 2010 24;34(2):106-9. Epub 2009 Dec 24.

Wellcome Trust Centre for Human Genetics, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000268822DOI Listing
May 2010

Childhood cow's milk allergy and the risk of multiple sclerosis: a population based study.

J Neurol Sci 2010 Apr 21;291(1-2):86-8. Epub 2010 Jan 21.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jns.2009.10.021DOI Listing
April 2010

A genome-wide scan of male sexual orientation.

J Hum Genet 2010 Feb 8;55(2):131-2. Epub 2010 Jan 8.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jhg.2009.135DOI Listing
February 2010

Parent-of-origin of HLA-DRB1*1501 and age of onset of multiple sclerosis.

J Hum Genet 2009 Sep 24;54(9):547-9. Epub 2009 Jul 24.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jhg.2009.69DOI Listing
September 2009

Age of onset in concordant twins and other relative pairs with multiple sclerosis.

Am J Epidemiol 2009 Aug 22;170(3):289-96. Epub 2009 Jun 22.

Department of Medical Genetics, Vancouver Coastal Health Authority-University of British Columbia Hospital, G-920 Detwiller Pavilion, Vancouver, British Columbia, Canada.

View Article

Download full-text PDF

Source
https://academic.oup.com/aje/article-lookup/doi/10.1093/aje/
Publisher Site
http://dx.doi.org/10.1093/aje/kwp143DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714951PMC
August 2009

Association of infectious mononucleosis with multiple sclerosis. A population-based study.

Neuroepidemiology 2009 11;32(4):257-62. Epub 2009 Feb 11.

Wellcome Trust Centre for Human Genetics, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000201564DOI Listing
June 2009

Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility.

Proc Natl Acad Sci U S A 2009 May 20;106(18):7542-7. Epub 2009 Apr 20.

University Department of Clinical Neurology, Third Floor, West Wing, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DU, United Kingdom.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1073/pnas.0812664106DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2678609PMC
May 2009

No effect of birth weight on the risk of multiple sclerosis. A population-based study.

Neuroepidemiology 2008 11;31(3):181-4. Epub 2008 Sep 11.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/154931
Publisher Site
http://dx.doi.org/10.1159/000154931DOI Listing
February 2009

Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex.

Hum Mol Genet 2009 Jan;18(2):261-6

Department of Clinical Neurology, Level 3 West Wing, John Radcliffe Hospital, University of Oxford, Oxford OX3 7BN, UK.

View Article

Download full-text PDF

Source
https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
Publisher Site
http://dx.doi.org/10.1093/hmg/ddn353DOI Listing
January 2009

Genetic epidemiology: the use of old and new tools for multiple sclerosis.

Trends Neurosci 2008 Dec 24;31(12):645-52. Epub 2008 Oct 24.

Wellcome Trust Centre for Human Genetics and Department of Clinical Neurology, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tins.2008.09.001DOI Listing
December 2008

No effect of preterm birth on the risk of multiple sclerosis: a population based study.

BMC Neurol 2008 Aug 1;8:30. Epub 2008 Aug 1.

Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Headington, Oxford, OX3 7BN, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2377-8-30DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518551PMC
August 2008

A genome-wide scan in forty large pedigrees with multiple sclerosis.

J Hum Genet 2007 15;52(12):955-62. Epub 2007 Nov 15.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10038-007-0194-6DOI Listing
February 2008

Parental transmission of HLA-DRB1*15 in multiple sclerosis.

Hum Genet 2008 Jan 31;122(6):661-3. Epub 2007 Oct 31.

Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-007-0442-zDOI Listing
January 2008

Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium.

Hum Mol Genet 2007 Aug 20;16(16):1951-8. Epub 2007 Jun 20.

Department of Clinical Neurology, University of Oxford, John Radcliffe Hospital, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddm142DOI Listing
August 2007

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis.

Nat Genet 2005 Oct 25;37(10):1108-12. Epub 2005 Sep 25.

Department of Clinical Neurology, Radcliffe Infirmary, University of Oxford, Oxford OX2 6HE, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ng1647DOI Listing
October 2005

Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance.

Hum Mol Genet 2005 Jul 1;14(14):2019-26. Epub 2005 Jun 1.

The Wellcome Trust Centre for Human Genetics, University of Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddi206DOI Listing
July 2005

Timing of birth and risk of multiple sclerosis: population based study.

BMJ 2005 Jan 7;330(7483):120. Epub 2004 Dec 7.

Department of Biostatistics, University of Michigan, Ann Arbor, MI 48109, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1136/bmj.38301.686030.63DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC544426PMC
January 2005

Genetics of multiple sclerosis.

Lancet Neurol 2004 Feb;3(2):104-10

The Wellcome Trust Center for Human Genetics, University of Oxford, Oxford, UK.

View Article

Download full-text PDF

Source
February 2004

Different patterns of gene silencing in position-effect variegation.

Genome 2003 Dec;46(6):1104-17

Department of Zoology, University of British Columbia, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1139/g03-070DOI Listing
December 2003