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Items: 1 to 50 of 80

1.

Correction: Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment.

Chaudhury S, Brookes KJ, Patel T, Fallows A, Guetta-Baranes T, Turton JC, Guerreiro R, Bras J, Hardy J, Francis PT, Croucher R, Holmes C, Morgan K.

Transl Psychiatry. 2019 Jun 11;9(1):167. doi: 10.1038/s41398-019-0503-9.

2.

Alzheimer's disease polygenic risk score as a predictor of conversion from mild-cognitive impairment.

Chaudhury S, Brookes KJ, Patel T, Fallows A, Guetta-Baranes T, Turton JC, Guerreiro R, Bras J, Hardy J, Francis PT, Croucher R, Holmes C, Morgan K, Thomas AJ.

Transl Psychiatry. 2019 May 24;9(1):154. doi: 10.1038/s41398-019-0485-7. Erratum in: Transl Psychiatry. 2019 Jun 11;9(1):167.

3.

The Epistasis Project: A Multi-Cohort Study of the Effects of BDNF, DBH, and SORT1 Epistasis on Alzheimer's Disease Risk.

Belbin O, Morgan K, Medway C, Warden D, Cortina-Borja M, van Duijn CM, Adams HHH, Frank-Garcia A, Brookes K, Sánchez-Juan P, Alvarez V, Heun R, Kölsch H, Coto E, Kehoe PG, Rodriguez-Rodriguez E, Bullido MJ, Ikram MA, Smith AD, Lehmann DJ.

J Alzheimers Dis. 2019;68(4):1535-1547. doi: 10.3233/JAD-181116.

PMID:
30909233
4.

Seasonal and diel acoustic presence of North Atlantic minke whales in the North Sea.

Risch D, Wilson SC, Hoogerwerf M, van Geel NCF, Edwards EWJ, Brookes KL.

Sci Rep. 2019 Mar 5;9(1):3571. doi: 10.1038/s41598-019-39752-8.

5.

Cluster of invasive Mycobacteria chimaera infections following cardiac surgery demonstrating novel clinical features and risks of aortic valve replacement.

Overton K, Mennon V, Mothobi N, Neild B, Martinez E, Masters J, Grant P, Akhunji Z, Su WY, Torda A, Whyte CM, Lloyd A, Weatherall C, Hofmeyr A, Foo H, Brookes K, Marriott D, Sintchenko V, Clezy K, Konecny P, Post JJ.

Intern Med J. 2018 Dec;48(12):1514-1520. doi: 10.1111/imj.14093.

PMID:
30517986
6.

Observations of extensive gene expression differences in the cerebellum and potential relevance to Alzheimer's disease.

Chappell S, Patel T, Guetta-Baranes T, Sang F, Francis PT, Morgan K, Brookes KJ.

BMC Res Notes. 2018 Sep 4;11(1):646. doi: 10.1186/s13104-018-3732-8.

7.

PTTG and PBF Functionally Interact with p53 and Predict Overall Survival in Head and Neck Cancer.

Read ML, Modasia B, Fletcher A, Thompson RJ, Brookes K, Rae PC, Nieto HR, Poole VL, Roberts S, Campbell MJ, Boelaert K, Turnell AS, Smith VE, Mehanna H, McCabe CJ.

Cancer Res. 2018 Oct 15;78(20):5863-5876. doi: 10.1158/0008-5472.CAN-18-0855. Epub 2018 Aug 28.

8.

Ectopic Hedgehog Signaling Causes Cleft Palate and Defective Osteogenesis.

Hammond NL, Brookes KJ, Dixon MJ.

J Dent Res. 2018 Dec;97(13):1485-1493. doi: 10.1177/0022034518785336. Epub 2018 Jul 5.

9.

Genotyping of the Alzheimer's Disease Genome-Wide Association Study Index Single Nucleotide Polymorphisms in the Brains for Dementia Research Cohort.

Brookes KJ, McConnell G, Williams K, Chaudhury S, Madhan G, Patel T, Turley C, Guetta-Baranes T, Bras J, Guerreiro R, Hardy J, Francis PT, Morgan K.

J Alzheimers Dis. 2018;64(2):355-362. doi: 10.3233/JAD-180191.

PMID:
29914034
10.

Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer's disease.

Kucukkilic E, Brookes K, Barber I, Guetta-Baranes T; ARUK Consortium, Morgan K, Hollox EJ.

Hum Genet. 2018 Apr;137(4):305-314. doi: 10.1007/s00439-018-1883-2. Epub 2018 Apr 19.

11.

The Many Liberalisms of Serge Audier.

Steinmetz-Jenkins D, Brookes K.

J Hist Ideas. 2018;79(1):45-63. doi: 10.1353/jhi.2018.0002.

PMID:
29398658
12.

Whole-exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer's disease.

Patel T, Brookes KJ, Turton J, Chaudhury S, Guetta-Baranes T, Guerreiro R, Bras J, Hernandez D, Singleton A, Francis PT, Hardy J, Morgan K.

Neuropathol Appl Neurobiol. 2018 Aug;44(5):506-521. doi: 10.1111/nan.12452. Epub 2018 Jan 7.

13.

Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease.

Chaudhury S, Patel T, Barber IS, Guetta-Baranes T, Brookes KJ, Chappell S, Turton J, Guerreiro R, Bras J, Hernandez D, Singleton A, Hardy J, Mann D; ARUK Consortium, Morgan K.

Neurobiol Aging. 2018 Feb;62:244.e1-244.e8. doi: 10.1016/j.neurobiolaging.2017.09.035. Epub 2017 Oct 10.

14.

Methylation Profiling RIN3 and MEF2C Identifies Epigenetic Marks Associated with Sporadic Early Onset Alzheimer's Disease.

Boden KA, Barber IS, Clement N, Patel T, Guetta-Baranes T, Brookes KJ, Chappell S, Craigon J, Chapman NH; ARUK Consortium, Morgan K, Seymour GB, Bottley A.

J Alzheimers Dis Rep. 2017 Sep 13;1(1):97-108. doi: 10.3233/ADR-170015.

15.

Categorizing click trains to increase taxonomic precision in echolocation click loggers.

Palmer KJ, Brookes K, Rendell L.

J Acoust Soc Am. 2017 Aug;142(2):863. doi: 10.1121/1.4996000.

PMID:
28863550
16.

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.

Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, Sleegers K, Vronskaya M, Ruiz A, Graham RR, Olaso R, Hoffmann P, Grove ML, Vardarajan BN, Hiltunen M, Nöthen MM, White CC, Hamilton-Nelson KL, Epelbaum J, Maier W, Choi SH, Beecham GW, Dulary C, Herms S, Smith AV, Funk CC, Derbois C, Forstner AJ, Ahmad S, Li H, Bacq D, Harold D, Satizabal CL, Valladares O, Squassina A, Thomas R, Brody JA, Qu L, Sánchez-Juan P, Morgan T, Wolters FJ, Zhao Y, Garcia FS, Denning N, Fornage M, Malamon J, Naranjo MCD, Majounie E, Mosley TH, Dombroski B, Wallon D, Lupton MK, Dupuis J, Whitehead P, Fratiglioni L, Medway C, Jian X, Mukherjee S, Keller L, Brown K, Lin H, Cantwell LB, Panza F, McGuinness B, Moreno-Grau S, Burgess JD, Solfrizzi V, Proitsi P, Adams HH, Allen M, Seripa D, Pastor P, Cupples LA, Price ND, Hannequin D, Frank-García A, Levy D, Chakrabarty P, Caffarra P, Giegling I, Beiser AS, Giedraitis V, Hampel H, Garcia ME, Wang X, Lannfelt L, Mecocci P, Eiriksdottir G, Crane PK, Pasquier F, Boccardi V, Henández I, Barber RC, Scherer M, Tarraga L, Adams PM, Leber M, Chen Y, Albert MS, Riedel-Heller S, Emilsson V, Beekly D, Braae A, Schmidt R, Blacker D, Masullo C, Schmidt H, Doody RS, Spalletta G, Longstreth WT Jr, Fairchild TJ, Bossù P, Lopez OL, Frosch MP, Sacchinelli E, Ghetti B, Yang Q, Huebinger RM, Jessen F, Li S, Kamboh MI, Morris J, Sotolongo-Grau O, Katz MJ, Corcoran C, Dunstan M, Braddel A, Thomas C, Meggy A, Marshall R, Gerrish A, Chapman J, Aguilar M, Taylor S, Hill M, Fairén MD, Hodges A, Vellas B, Soininen H, Kloszewska I, Daniilidou M, Uphill J, Patel Y, Hughes JT, Lord J, Turton J, Hartmann AM, Cecchetti R, Fenoglio C, Serpente M, Arcaro M, Caltagirone C, Orfei MD, Ciaramella A, Pichler S, Mayhaus M, Gu W, Lleó A, Fortea J, Blesa R, Barber IS, Brookes K, Cupidi C, Maletta RG, Carrell D, Sorbi S, Moebus S, Urbano M, Pilotto A, Kornhuber J, Bosco P, Todd S, Craig D, Johnston J, Gill M, Lawlor B, Lynch A, Fox NC, Hardy J; ARUK Consortium, Albin RL, Apostolova LG, Arnold SE, Asthana S, Atwood CS, Baldwin CT, Barnes LL, Barral S, Beach TG, Becker JT, Bigio EH, Bird TD, Boeve BF, Bowen JD, Boxer A, Burke JR, Burns JM, Buxbaum JD, Cairns NJ, Cao C, Carlson CS, Carlsson CM, Carney RM, Carrasquillo MM, Carroll SL, Diaz CC, Chui HC, Clark DG, Cribbs DH, Crocco EA, DeCarli C, Dick M, Duara R, Evans DA, Faber KM, Fallon KB, Fardo DW, Farlow MR, Ferris S, Foroud TM, Galasko DR, Gearing M, Geschwind DH, Gilbert JR, Graff-Radford NR, Green RC, Growdon JH, Hamilton RL, Harrell LE, Honig LS, Huentelman MJ, Hulette CM, Hyman BT, Jarvik GP, Abner E, Jin LW, Jun G, Karydas A, Kaye JA, Kim R, Kowall NW, Kramer JH, LaFerla FM, Lah JJ, Leverenz JB, Levey AI, Li G, Lieberman AP, Lunetta KL, Lyketsos CG, Marson DC, Martiniuk F, Mash DC, Masliah E, McCormick WC, McCurry SM, McDavid AN, McKee AC, Mesulam M, Miller BL, Miller CA, Miller JW, Morris JC, Murrell JR, Myers AJ, O'Bryant S, Olichney JM, Pankratz VS, Parisi JE, Paulson HL, Perry W, Peskind E, Pierce A, Poon WW, Potter H, Quinn JF, Raj A, Raskind M, Reisberg B, Reitz C, Ringman JM, Roberson ED, Rogaeva E, Rosen HJ, Rosenberg RN, Sager MA, Saykin AJ, Schneider JA, Schneider LS, Seeley WW, Smith AG, Sonnen JA, Spina S, Stern RA, Swerdlow RH, Tanzi RE, Thornton-Wells TA, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Van Eldik LJ, Vinters HV, Vonsattel JP, Weintraub S, Welsh-Bohmer KA, Wilhelmsen KC, Williamson J, Wingo TS, Woltjer RL, Wright CB, Yu CE, Yu L, Garzia F, Golamaully F, Septier G, Engelborghs S, Vandenberghe R, De Deyn PP, Fernadez CM, Benito YA, Thonberg H, Forsell C, Lilius L, Kinhult-Stählbom A, Kilander L, Brundin R, Concari L, Helisalmi S, Koivisto AM, Haapasalo A, Dermecourt V, Fievet N, Hanon O, Dufouil C, Brice A, Ritchie K, Dubois B, Himali JJ, Keene CD, Tschanz J, Fitzpatrick AL, Kukull WA, Norton M, Aspelund T, Larson EB, Munger R, Rotter JI, Lipton RB, Bullido MJ, Hofman A, Montine TJ, Coto E, Boerwinkle E, Petersen RC, Alvarez V, Rivadeneira F, Reiman EM, Gallo M, O'Donnell CJ, Reisch JS, Bruni AC, Royall DR, Dichgans M, Sano M, Galimberti D, St George-Hyslop P, Scarpini E, Tsuang DW, Mancuso M, Bonuccelli U, Winslow AR, Daniele A, Wu CK; GERAD/PERADES, CHARGE, ADGC, EADI, Peters O, Nacmias B, Riemenschneider M, Heun R, Brayne C, Rubinsztein DC, Bras J, Guerreiro R, Al-Chalabi A, Shaw CE, Collinge J, Mann D, Tsolaki M, Clarimón J, Sussams R, Lovestone S, O'Donovan MC, Owen MJ, Behrens TW, Mead S, Goate AM, Uitterlinden AG, Holmes C, Cruchaga C, Ingelsson M, Bennett DA, Powell J, Golde TE, Graff C, De Jager PL, Morgan K, Ertekin-Taner N, Combarros O, Psaty BM, Passmore P, Younkin SG, Berr C, Gudnason V, Rujescu D, Dickson DW, Dartigues JF, DeStefano AL, Ortega-Cubero S, Hakonarson H, Campion D, Boada M, Kauwe JK, Farrer LA, Van Broeckhoven C, Ikram MA, Jones L, Haines JL, Tzourio C, Launer LJ, Escott-Price V, Mayeux R, Deleuze JF, Amin N, Holmans PA, Pericak-Vance MA, Amouyel P, van Duijn CM, Ramirez A, Wang LS, Lambert JC, Seshadri S, Williams J, Schellenberg GD.

Nat Genet. 2017 Sep;49(9):1373-1384. doi: 10.1038/ng.3916. Epub 2017 Jul 17.

17.

Underwater noise levels in UK waters.

Merchant ND, Brookes KL, Faulkner RC, Bicknell AW, Godley BJ, Witt MJ.

Sci Rep. 2016 Nov 10;6:36942. doi: 10.1038/srep36942.

18.

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array.

Barber IS, Braae A, Clement N, Patel T, Guetta-Baranes T, Brookes K, Medway C, Chappell S, Guerreiro R, Bras J, Hernandez D, Singleton A, Hardy J, Mann DM; ARUK Consortium, Morgan K.

Neurobiol Aging. 2017 Jan;49:215.e1-215.e8. doi: 10.1016/j.neurobiolaging.2016.09.008. Epub 2016 Sep 23.

19.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease.

Barber IS, García-Cárdenas JM, Sakdapanichkul C, Deacon C, Zapata Erazo G, Guerreiro R, Bras J, Hernandez D, Singleton A, Guetta-Baranes T, Braae A, Clement N, Patel T, Brookes K, Medway C, Chappell S, Mann DM; ARUK Consortium, Morgan K.

Neurobiol Aging. 2016 Mar;39:220.e1-7. doi: 10.1016/j.neurobiolaging.2015.12.011. Epub 2015 Dec 29.

20.

Dysphagia and factors associated with respiratory infections in the first week post stroke.

Brogan E, Langdon C, Brookes K, Budgeon C, Blacker D.

Neuroepidemiology. 2014;43(2):140-4. doi: 10.1159/000366423. Epub 2014 Nov 5.

PMID:
25402187
21.

Assessing environmental impacts of offshore wind farms: lessons learned and recommendations for the future.

Bailey H, Brookes KL, Thompson PM.

Aquat Biosyst. 2014 Sep 14;10:8. doi: 10.1186/2046-9063-10-8. eCollection 2014. Review.

22.

Can't swallow, can't transfer, can't toilet: factors predicting infections in the first week post stroke.

Brogan E, Langdon C, Brookes K, Budgeon C, Blacker D.

J Clin Neurosci. 2015 Jan;22(1):92-7. doi: 10.1016/j.jocn.2014.05.035. Epub 2014 Aug 28.

PMID:
25174763
23.

Variation in harbour porpoise activity in response to seismic survey noise.

Pirotta E, Brookes KL, Graham IM, Thompson PM.

Biol Lett. 2014 May;10(5):20131090. doi: 10.1098/rsbl.2013.1090.

24.

Respiratory infections in acute stroke: nasogastric tubes and immobility are stronger predictors than dysphagia.

Brogan E, Langdon C, Brookes K, Budgeon C, Blacker D.

Dysphagia. 2014 Jun;29(3):340-5. doi: 10.1007/s00455-013-9514-5. Epub 2014 Jan 21.

PMID:
24445382
25.

Short-term disturbance by a commercial two-dimensional seismic survey does not lead to long-term displacement of harbour porpoises.

Thompson PM, Brookes KL, Graham IM, Barton TR, Needham K, Bradbury G, Merchant ND.

Proc Biol Sci. 2013 Oct 2;280(1771):20132001. doi: 10.1098/rspb.2013.2001. Print 2013 Nov 22.

26.

Predictions from harbor porpoise habitat association models are confirmed by long-term passive acoustic monitoring.

Brookes KL, Bailey H, Thompson PM.

J Acoust Soc Am. 2013 Sep;134(3):2523-33. doi: 10.1121/1.4816577.

PMID:
23968050
27.

Systematic review: work-related stress and the HSE management standards.

Brookes K, Limbert C, Deacy C, O'Reilly A, Scott S, Thirlaway K.

Occup Med (Lond). 2013 Oct;63(7):463-72. doi: 10.1093/occmed/kqt078. Epub 2013 Jul 11. Review.

PMID:
23847137
28.

The VNTR in complex disorders: the forgotten polymorphisms? A functional way forward?

Brookes KJ.

Genomics. 2013 May;101(5):273-81. doi: 10.1016/j.ygeno.2013.03.003. Epub 2013 Mar 19. Review.

29.

Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler's syndrome after pharmacological enzyme replacement therapy.

Saif MA, Bigger BW, Brookes KE, Mercer J, Tylee KL, Church HJ, Bonney DK, Jones S, Wraith JE, Wynn RF.

Haematologica. 2012 Sep;97(9):1320-8. doi: 10.3324/haematol.2011.058644. Epub 2012 Feb 27.

30.

Down-regulation of XIAP by AEG35156 in paediatric tumour cells induces apoptosis and sensitises cells to cytotoxic agents.

Holt SV, Brookes KE, Dive C, Makin GW.

Oncol Rep. 2011 Apr;25(4):1177-81. doi: 10.3892/or.2011.1167. Epub 2011 Jan 31.

PMID:
21286665
31.

Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression.

Brookes KJ, Hawi Z, Park J, Scott S, Gill M, Kent L.

Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1417-24. doi: 10.1002/ajmg.b.31120. Epub 2010 Sep 22.

32.

The DRD4 receptor Exon 3 VNTR and 5' SNP variants and mRNA expression in human post-mortem brain tissue.

Simpson J, Vetuz G, Wilson M, Brookes KJ, Kent L.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1228-33. doi: 10.1002/ajmg.b.31084.

PMID:
20468066
33.

Issues on fit-for-purpose validation of a panel of ELISAs for application as biomarkers in clinical trials of anti-Angiogenic drugs.

Brookes K, Cummings J, Backen A, Greystoke A, Ward T, Jayson GC, Dive C.

Br J Cancer. 2010 May 11;102(10):1524-32. doi: 10.1038/sj.bjc.6605661. Epub 2010 Apr 20.

34.

Evidence that genetic variation in the oxytocin receptor (OXTR) gene influences social cognition in ADHD.

Park J, Willmott M, Vetuz G, Toye C, Kirley A, Hawi Z, Brookes KJ, Gill M, Kent L.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 May 30;34(4):697-702. doi: 10.1016/j.pnpbp.2010.03.029. Epub 2010 Mar 27.

PMID:
20347913
35.

5HTT genotype moderates the influence of early institutional deprivation on emotional problems in adolescence: evidence from the English and Romanian Adoptee (ERA) study.

Kumsta R, Stevens S, Brookes K, Schlotz W, Castle J, Beckett C, Kreppner J, Rutter M, Sonuga-Barke E.

J Child Psychol Psychiatry. 2010 Jul;51(7):755-62. doi: 10.1111/j.1469-7610.2010.02249.x. Epub 2010 Mar 25.

PMID:
20345836
36.

Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies.

Tansey KE, Brookes KJ, Hill MJ, Cochrane LE, Gill M, Skuse D, Correia C, Vicente A, Kent L, Gallagher L, Anney RJL.

Neurosci Lett. 2010 May 3;474(3):163-167. doi: 10.1016/j.neulet.2010.03.035. Epub 2010 Mar 18.

PMID:
20303388
37.

Dopamine transporter gene polymorphism moderates the effects of severe deprivation on ADHD symptoms: developmental continuities in gene-environment interplay.

Stevens SE, Kumsta R, Kreppner JM, Brookes KJ, Rutter M, Sonuga-Barke EJ.

Am J Med Genet B Neuropsychiatr Genet. 2009 Sep 5;150B(6):753-61. doi: 10.1002/ajmg.b.31010.

PMID:
19655343
38.

Replication of an association of a promoter polymorphism of the dopamine transporter gene and Attention Deficit Hyperactivity Disorder.

Doyle C, Brookes K, Simpson J, Park J, Scott S, Coghill DR, Hawi Z, Kirley A, Gill M, Kent L.

Neurosci Lett. 2009 Sep 22;462(2):179-81. doi: 10.1016/j.neulet.2009.06.084. Epub 2009 Jul 2.

PMID:
19576958
39.

Preclinical efficacy of the bioreductive alkylating agent RH1 against paediatric tumours.

Hussein D, Holt SV, Brookes KE, Klymenko T, Adamski JK, Hogg A, Estlin EJ, Ward T, Dive C, Makin GW.

Br J Cancer. 2009 Jul 7;101(1):55-63. doi: 10.1038/sj.bjc.6605100. Epub 2009 Jun 2.

40.

Investigation of the serotonin 2C receptor gene in attention deficit hyperactivity disorder in UK samples.

Xu X, Brookes K, Sun B, Ilott N, Asherson P.

BMC Res Notes. 2009 May 5;2:71. doi: 10.1186/1756-0500-2-71.

41.

ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.

Hawi Z, Kent L, Hill M, Anney RJ, Brookes KJ, Barry E, Franke B, Banaschewski T, Buitelaar J, Ebstein R, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Faraone SV, Asherson P, Gill M.

Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):97-102. doi: 10.1002/ajmg.b.30960.

PMID:
19388000
42.

The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction.

Altink ME, Arias-Vásquez A, Franke B, Slaats-Willemse DI, Buschgens CJ, Rommelse NN, Fliers EA, Anney R, Brookes KJ, Chen W, Gill M, Mulligan A, Sonuga-Barke E, Thompson M, Sergeant JA, Faraone SV, Asherson P, Buitelaar JK.

J Child Psychol Psychiatry. 2008 Oct;49(10):1053-60. doi: 10.1111/j.1469-7610.2008.01998.x.

43.

Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder.

Brookes KJ, Hawi Z, Kirley A, Barry E, Gill M, Kent L.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1531-5. doi: 10.1002/ajmg.b.30873.

PMID:
18937300
44.

Replication of a rare protective allele in the noradrenaline transporter gene and ADHD.

Xu X, Hawi Z, Brookes KJ, Anney R, Bellgrove M, Franke B, Barry E, Chen W, Kuntsi J, Banaschewski T, Buitelaar J, Ebstein R, Fitzgerald M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Faraone SV, Gill M, Asherson P.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1564-7. doi: 10.1002/ajmg.b.30872.

45.

Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity.

Brookes KJ, Xu X, Anney R, Franke B, Zhou K, Chen W, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Asherson P.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1519-23. doi: 10.1002/ajmg.b.30782.

PMID:
18668530
46.

Genetic heterogeneity in ADHD: DAT1 gene only affects probands without CD.

Zhou K, Chen W, Buitelaar J, Banaschewski T, Oades RD, Franke B, Sonuga-Barke E, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Lasky-Su J, Taylor E, Brookes KJ, Xu X, Neale BM, Rijsdijk F, Thompson M, Asherson P, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1481-7. doi: 10.1002/ajmg.b.30644.

47.

Increased cerebral perfusion in adult attention deficit hyperactivity disorder is normalised by stimulant treatment: a non-invasive MRI pilot study.

O'Gorman RL, Mehta MA, Asherson P, Zelaya FO, Brookes KJ, Toone BK, Alsop DC, Williams SC.

Neuroimage. 2008 Aug 1;42(1):36-41. doi: 10.1016/j.neuroimage.2008.04.169. Epub 2008 Apr 20.

PMID:
18511306
48.

No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder.

Xu X, Duman EA, Anney R, Brookes K, Franke B, Zhou K, Buschgens C, Chen W, Christiansen H, Eisenberg J, Gabriëls I, Manor I, Marco R, Müller UC, Mulligan A, Rommelse N, Thompson M, Uebel H, Banaschewski T, Buitelaar J, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Asherson P.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1306-9. doi: 10.1002/ajmg.b.30737. Erratum in: Am J Med Genet B Neuropsychiatr Genet. 2009 Mar 5;150B(2):307. Duman, Elif Aysimi [corrected to Duman, EA]. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):154.. Aysimi, E [corrected to Duman, Elif Aysimi].

PMID:
18452186
49.

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings.

Zhou K, Asherson P, Sham P, Franke B, Anney RJ, Buitelaar J, Ebstein R, Gill M, Brookes K, Buschgens C, Campbell D, Chen W, Christiansen H, Fliers E, Gabriëls I, Johansson L, Marco R, Mulas F, Müller U, Mulligan A, Neale BM, Rijsdijk F, Rommelse N, Uebel H, Psychogiou L, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV.

Biol Psychiatry. 2008 Oct 1;64(7):571-6. doi: 10.1016/j.biopsych.2008.02.024. Epub 2008 Apr 24.

50.

A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16.

Asherson P, Zhou K, Anney RJ, Franke B, Buitelaar J, Ebstein R, Gill M, Altink M, Arnold R, Boer F, Brookes K, Buschgens C, Butler L, Cambell D, Chen W, Christiansen H, Feldman L, Fleischman K, Fliers E, Howe-Forbes R, Goldfarb A, Heise A, Gabriëls I, Johansson L, Lubetzki I, Marco R, Medad S, Minderaa R, Mulas F, Müller U, Mulligan A, Neale B, Rijsdijk F, Rabin K, Rommelse N, Sethna V, Sorohan J, Uebel H, Psychogiou L, Weeks A, Barrett R, Xu X, Banaschewski T, Sonuga-Barke E, Eisenberg J, Manor I, Miranda A, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Steinhausen HC, Taylor E, Thompson M, Faraone SV.

Mol Psychiatry. 2008 May;13(5):514-21. doi: 10.1038/sj.mp.4002140. Epub 2008 Jan 8.

PMID:
18180756

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