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Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.

Tan MMX, Malek N, Lawton MA, Hubbard L, Pittman AM, Joseph T, Hehir J, Swallow DMA, Grosset KA, Marrinan SL, Bajaj N, Barker RA, Burn DJ, Bresner C, Foltynie T, Hardy J, Wood N, Ben-Shlomo Y, Grosset DG, Williams NM, Morris HR.

Brain. 2019 Sep 1;142(9):2828-2844. doi: 10.1093/brain/awz191.


Developing and validating Parkinson's disease subtypes and their motor and cognitive progression.

Lawton M, Ben-Shlomo Y, May MT, Baig F, Barber TR, Klein JC, Swallow DMA, Malek N, Grosset KA, Bajaj N, Barker RA, Williams N, Burn DJ, Foltynie T, Morris HR, Wood NW, Grosset DG, Hu MTM.

J Neurol Neurosurg Psychiatry. 2018 Dec;89(12):1279-1287. doi: 10.1136/jnnp-2018-318337. Epub 2018 Jul 25.


Adaptation to milking agropastoralism in Chilean goat herders and nutritional benefit of lactase persistence.

Montalva N, Adhikari K, Liebert A, Mendoza-Revilla J, Flores SV, Mace R, Swallow DM.

Ann Hum Genet. 2019 Jan;83(1):11-22. doi: 10.1111/ahg.12277. Epub 2018 Sep 27.


World-wide distributions of lactase persistence alleles and the complex effects of recombination and selection.

Liebert A, López S, Jones BL, Montalva N, Gerbault P, Lau W, Thomas MG, Bradman N, Maniatis N, Swallow DM.

Hum Genet. 2017 Nov;136(11-12):1445-1453. doi: 10.1007/s00439-017-1847-y. Epub 2017 Oct 23.


Statin usage, vascular diagnosis and vascular risk factors in Parkinson's disease.

Cheng KK, Swallow DM, Grosset KA, Grosset DG.

Scott Med J. 2017 Aug;62(3):104-109. doi: 10.1177/0036933017727432. Epub 2017 Aug 24.


Equating scores of the University of Pennsylvania Smell Identification Test and Sniffin' Sticks test in patients with Parkinson's disease.

Lawton M, Hu MT, Baig F, Ruffmann C, Barron E, Swallow DM, Malek N, Grosset KA, Bajaj N, Barker RA, Williams N, Burn DJ, Foltynie T, Morris HR, Wood NW, May MT, Grosset DG, Ben-Shlomo Y.

Parkinsonism Relat Disord. 2016 Dec;33:96-101. doi: 10.1016/j.parkreldis.2016.09.023. Epub 2016 Sep 25.


In Vitro Functional Analyses of Infrequent Nucleotide Variants in the Lactase Enhancer Reveal Different Molecular Routes to Increased Lactase Promoter Activity and Lactase Persistence.

Liebert A, Jones BL, Danielsen ET, Olsen AK, Swallow DM, Troelsen JT.

Ann Hum Genet. 2016 Nov;80(6):307-318. doi: 10.1111/ahg.12167. Epub 2016 Oct 7.


Statins are underused in recent-onset Parkinson's disease with increased vascular risk: findings from the UK Tracking Parkinson's and Oxford Parkinson's Disease Centre (OPDC) discovery cohorts.

Swallow DM, Lawton MA, Grosset KA, Malek N, Klein J, Baig F, Ruffmann C, Bajaj NP, Barker RA, Ben-Shlomo Y, Burn DJ, Foltynie T, Morris HR, Williams N, Wood NW, Hu MT, Grosset DG.

J Neurol Neurosurg Psychiatry. 2016 Nov;87(11):1183-1190. doi: 10.1136/jnnp-2016-313642. Epub 2016 Sep 26.


Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease.

Malek N, Lawton MA, Swallow DM, Grosset KA, Marrinan SL, Bajaj N, Barker RA, Burn DJ, Hardy J, Morris HR, Williams NM, Wood N, Ben-Shlomo Y, Grosset DG; PRoBaND Clinical Consortium.

Mov Disord. 2016 Oct;31(10):1518-1526. doi: 10.1002/mds.26698.


Escape from epigenetic silencing of lactase expression is triggered by a single-nucleotide change.

Swallow DM, Troelsen JT.

Nat Struct Mol Biol. 2016 Jun 7;23(6):505-7. doi: 10.1038/nsmb.3238. No abstract available.


Variation in Recent Onset Parkinson's Disease: Implications for Prodromal Detection.

Swallow DM, Lawton MA, Grosset KA, Malek N, Smith CR, Bajaj NP, Barker RA, Ben-Shlomo Y, Burn DJ, Foltynie T, Hardy J, Morris HR, Williams N, Wood NW, Grosset DG; PRoBaND Clinical Consortium.

J Parkinsons Dis. 2016 Mar 19;6(2):289-300. doi: 10.3233/JPD-150741.


Nonmotor symptoms in patients without evidence of dopaminergic deficit.

Swallow DM, Grosset KA, Grosset DG.

Mov Disord. 2016 Mar;31(3):429-30. doi: 10.1002/mds.26541. Epub 2016 Feb 19. Review. No abstract available.


Olfaction in Parkin single and compound heterozygotes in a cohort of young onset Parkinson's disease patients.

Malek N, Swallow DM, Grosset KA, Lawton MA, Smith CR, Bajaj NP, Barker RA, Ben-Shlomo Y, Bresner C, Burn DJ, Foltynie T, Morris HR, Williams N, Wood NW, Grosset DG; PRoBaND Investigators.

Acta Neurol Scand. 2016 Oct;134(4):271-6. doi: 10.1111/ane.12538. Epub 2015 Dec 1.


Tracking Parkinson's: Study Design and Baseline Patient Data.

Malek N, Swallow DM, Grosset KA, Lawton MA, Marrinan SL, Lehn AC, Bresner C, Bajaj N, Barker RA, Ben-Shlomo Y, Burn DJ, Foltynie T, Hardy J, Morris HR, Williams NM, Wood N, Grosset DG; PRoBaND.

J Parkinsons Dis. 2015;5(4):947-59. doi: 10.3233/JPD-150662.


Evaluation of a protocol-based treatment strategy for postoperative diabetes insipidus in craniopharyngioma.

Pratheesh R, Swallow DM, Joseph M, Natesan D, Rajaratnam S, Jacob KS, Chacko AG.

Neurol India. 2015 Sep-Oct;63(5):712-7. doi: 10.4103/0028-3886.166533.


Diversity of lactase persistence in African milk drinkers.

Jones BL, Oljira T, Liebert A, Zmarz P, Montalva N, Tarekeyn A, Ekong R, Thomas MG, Bekele E, Bradman N, Swallow DM.

Hum Genet. 2015 Aug;134(8):917-25. doi: 10.1007/s00439-015-1573-2. Epub 2015 Jun 9.


Direct evidence of milk consumption from ancient human dental calculus.

Warinner C, Hendy J, Speller C, Cappellini E, Fischer R, Trachsel C, Arneborg J, Lynnerup N, Craig OE, Swallow DM, Fotakis A, Christensen RJ, Olsen JV, Liebert A, Montalva N, Fiddyment S, Charlton S, Mackie M, Canci A, Bouwman A, Rühli F, Gilbert MT, Collins MJ.

Sci Rep. 2014 Nov 27;4:7104. doi: 10.1038/srep07104.


Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.

Horsfall LJ, Hardy R, Wong A, Kuh D, Swallow DM.

J Hepatol. 2014 Dec;61(6):1344-51. doi: 10.1016/j.jhep.2014.07.028. Epub 2014 Jul 31.


Repeatability of cerebrospinal fluid constant rate infusion study.

Swallow DM, Fellner N, Varsos GV, Czosnyka M, Smielewski P, Pickard JD, Czosnyka Z.

Acta Neurol Scand. 2014 Aug;130(2):131-8. doi: 10.1111/ane.12246. Epub 2014 Mar 24.


Diversity of lactase persistence alleles in Ethiopia: signature of a soft selective sweep.

Jones BL, Raga TO, Liebert A, Zmarz P, Bekele E, Danielsen ET, Olsen AK, Bradman N, Troelsen JT, Swallow DM.

Am J Hum Genet. 2013 Sep 5;93(3):538-44. doi: 10.1016/j.ajhg.2013.07.008. Epub 2013 Aug 29.


MUC5AC and inflammatory mediators associated with respiratory outcomes in the British 1946 birth cohort.

Johnson L, Shah I, Loh AX, Vinall LE, Teixeira AS, Rousseau K, Holloway JW, Hardy R, Swallow DM.

Respirology. 2013 Aug;18(6):1003-10. doi: 10.1111/resp.12092.


Apical MUC1 expression revealed on the foveolar epithelium in H. pylori gastritis.

Rashid M, Teixeira AS, Qureshi U, Pereira SP, Novelli MR, Swallow DM.

Br J Cancer. 2013 Mar 19;108(5):1113-8. doi: 10.1038/bjc.2013.54. Epub 2013 Feb 14.


Incidence, predictors and early post-operative course of diabetes insipidus in paediatric craniopharygioma: a comparison with adults.

Pratheesh R, Swallow DM, Rajaratnam S, Jacob KS, Chacko G, Joseph M, Chacko AG.

Childs Nerv Syst. 2013 Jun;29(6):941-9. doi: 10.1007/s00381-013-2041-8. Epub 2013 Feb 6.


Refinement in localization and identification of gene regions associated with Crohn disease.

Elding H, Lau W, Swallow DM, Maniatis N.

Am J Hum Genet. 2013 Jan 10;92(1):107-13. doi: 10.1016/j.ajhg.2012.11.004. Epub 2012 Dec 13.


The impact of cis-acting polymorphisms on the human phenotype.

Jones BL, Swallow DM.

Hugo J. 2011 Dec;5(1-4):13-23. doi: 10.1007/s11568-011-9155-4. Epub 2011 Jul 20.


Mucin methods: genes encoding mucins and their genetic variation with a focus on gel-forming mucins.

Rousseau K, Swallow DM.

Methods Mol Biol. 2012;842:1-26. doi: 10.1007/978-1-61779-513-8_1.


Dissecting the genetics of complex inheritance: linkage disequilibrium mapping provides insight into Crohn disease.

Elding H, Lau W, Swallow DM, Maniatis N.

Am J Hum Genet. 2011 Dec 9;89(6):798-805. doi: 10.1016/j.ajhg.2011.11.006.


Mucin variable number tandem repeat polymorphisms and severity of cystic fibrosis lung disease: significant association with MUC5AC.

Guo X, Pace RG, Stonebraker JR, Commander CW, Dang AT, Drumm ML, Harris A, Zou F, Swallow DM, Wright FA, O'Neal WK, Knowles MR.

PLoS One. 2011;6(10):e25452. doi: 10.1371/journal.pone.0025452. Epub 2011 Oct 6.


Herders of Indian and European cattle share their predominant allele for lactase persistence.

Gallego Romero I, Basu Mallick C, Liebert A, Crivellaro F, Chaubey G, Itan Y, Metspalu M, Eaaswarkhanth M, Pitchappan R, Villems R, Reich D, Singh L, Thangaraj K, Thomas MG, Swallow DM, Mirazón Lahr M, Kivisild T.

Mol Biol Evol. 2012 Jan;29(1):249-60. doi: 10.1093/molbev/msr190. Epub 2011 Aug 11.


The -14010*C variant associated with lactase persistence is located between an Oct-1 and HNF1α binding site and increases lactase promoter activity.

Jensen TG, Liebert A, Lewinsky R, Swallow DM, Olsen J, Troelsen JT.

Hum Genet. 2011 Oct;130(4):483-93. doi: 10.1007/s00439-011-0966-0. Epub 2011 Feb 15.


Serum bilirubin and risk of respiratory disease and death.

Horsfall LJ, Rait G, Walters K, Swallow DM, Pereira SP, Nazareth I, Petersen I.

JAMA. 2011 Feb 16;305(7):691-7. doi: 10.1001/jama.2011.124.


Evolution of lactase persistence: an example of human niche construction.

Gerbault P, Liebert A, Itan Y, Powell A, Currat M, Burger J, Swallow DM, Thomas MG.

Philos Trans R Soc Lond B Biol Sci. 2011 Mar 27;366(1566):863-77. doi: 10.1098/rstb.2010.0268.


Prevalence of clinically relevant UGT1A alleles and haplotypes in African populations.

Horsfall LJ, Zeitlyn D, Tarekegn A, Bekele E, Thomas MG, Bradman N, Swallow DM.

Ann Hum Genet. 2011 Mar;75(2):236-46. doi: 10.1111/j.1469-1809.2010.00638.x.


Cis-acting allelic variation in MUC5B mRNA expression is associated with different promoter haplotypes.

Loh AX, Johnson L, Ng W, Swallow DM.

Ann Hum Genet. 2010 Nov;74(6):498-505. doi: 10.1111/j.1469-1809.2010.00613.x.


A worldwide correlation of lactase persistence phenotype and genotypes.

Itan Y, Jones BL, Ingram CJ, Swallow DM, Thomas MG.

BMC Evol Biol. 2010 Feb 9;10:36. doi: 10.1186/1471-2148-10-36.


Multiple rare variants as a cause of a common phenotype: several different lactase persistence associated alleles in a single ethnic group.

Ingram CJ, Raga TO, Tarekegn A, Browning SL, Elamin MF, Bekele E, Thomas MG, Weale ME, Bradman N, Swallow DM.

J Mol Evol. 2009 Dec;69(6):579-88. doi: 10.1007/s00239-009-9301-y. Epub 2009 Nov 24.


Contribution of functional variation in the IL13 gene to allergy, hay fever and asthma in the NSHD longitudinal 1946 birth cohort.

Black S, Teixeira AS, Loh AX, Vinall L, Holloway JW, Hardy R, Swallow DM.

Allergy. 2009 Aug;64(8):1172-8. doi: 10.1111/j.1398-9995.2009.01988.x. Epub 2009 Feb 27.


Genetic regulation of MUC1 alternative splicing in human tissues.

Ng W, Loh AX, Teixeira AS, Pereira SP, Swallow DM.

Br J Cancer. 2008 Sep 16;99(6):978-85. doi: 10.1038/sj.bjc.6604617.


Lactose digestion and the evolutionary genetics of lactase persistence.

Ingram CJ, Mulcare CA, Itan Y, Thomas MG, Swallow DM.

Hum Genet. 2009 Jan;124(6):579-91. doi: 10.1007/s00439-008-0593-6. Epub 2008 Nov 26.


MUC4 and MUC5AC are highly specific tumour-associated mucins in biliary tract cancer.

Matull WR, Andreola F, Loh A, Adiguzel Z, Deheragoda M, Qureshi U, Batra SK, Swallow DM, Pereira SP.

Br J Cancer. 2008 May 20;98(10):1675-81. doi: 10.1038/sj.bjc.6604364. Epub 2008 May 13.


Evaluation of a novel reverse-hybridization StripAssay for typing DNA variants useful in diagnosis of adult-type hypolactasia.

Tag CG, Oberkanins C, Kriegshäuser G, Ingram CJ, Swallow DM, Gressner AM, Ledochowski M, Weiskirchen R.

Clin Chim Acta. 2008 Jun;392(1-2):58-62. doi: 10.1016/j.cca.2008.03.006. Epub 2008 Mar 18.


Mouse models of rhinovirus-induced disease and exacerbation of allergic airway inflammation.

Bartlett NW, Walton RP, Edwards MR, Aniscenko J, Caramori G, Zhu J, Glanville N, Choy KJ, Jourdan P, Burnet J, Tuthill TJ, Pedrick MS, Hurle MJ, Plumpton C, Sharp NA, Bussell JN, Swallow DM, Schwarze J, Guy B, Almond JW, Jeffery PK, Lloyd CM, Papi A, Killington RA, Rowlands DJ, Blair ED, Clarke NJ, Johnston SL.

Nat Med. 2008 Feb;14(2):199-204. doi: 10.1038/nm1713. Epub 2008 Feb 3.


Pitfalls in LightCycler diagnosis of the single-nucleotide polymorphism 13.9 kb upstream of the lactase gene that is associated with adult-type hypolactasia.

Weiskirchen R, Tag CG, Mengsteab S, Gressner AM, Ingram CJ, Swallow DM.

Clin Chim Acta. 2007 Sep;384(1-2):93-8. Epub 2007 Jun 16.


Allelic association and recombination hotspots in the mucin gene (MUC) complex on chromosome 11p15.5.

Rousseau K, Byrne C, Griesinger G, Leung A, Chung A, Hill AS, Swallow DM.

Ann Hum Genet. 2007 Sep;71(Pt 5):561-9. Epub 2007 May 29.


A novel polymorphism associated with lactose tolerance in Africa: multiple causes for lactase persistence?

Ingram CJ, Elamin MF, Mulcare CA, Weale ME, Tarekegn A, Raga TO, Bekele E, Elamin FM, Thomas MG, Bradman N, Swallow DM.

Hum Genet. 2007 Feb;120(6):779-88. Epub 2006 Nov 21.


MUC7 haplotype analysis: results from a longitudinal birth cohort support protective effect of the MUC7*5 allele on respiratory function.

Rousseau K, Vinall LE, Butterworth SL, Hardy RJ, Holloway J, Wadsworth ME, Swallow DM.

Ann Hum Genet. 2006 Jul;70(Pt 4):417-27.


DNA test for hypolactasia premature.

Swallow DM.

Gut. 2006 Jan;55(1):131; author reply 131-2. No abstract available.


Expression of ErbB receptors and mucins in the airways of long term current smokers.

O'Donnell RA, Richter A, Ward J, Angco G, Mehta A, Rousseau K, Swallow DM, Holgate ST, Djukanovic R, Davies DE, Wilson SJ.

Thorax. 2004 Dec;59(12):1032-40.


Alpha1-antitrypsin as a risk for infant and adult respiratory outcomes in a national birth cohort.

Wadsworth ME, Vinall LE, Jones AL, Hardy RJ, Whitehouse DB, Butterworth SL, Hilder WS, Lovegrove JU, Swallow DM.

Am J Respir Cell Mol Biol. 2004 Nov;31(5):559-64. Epub 2004 Jul 22.


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