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Items: 40

1.

Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants.

Krishnan ML, Van Steenwinckel J, Schang AL, Yan J, Arnadottir J, Le Charpentier T, Csaba Z, Dournaud P, Cipriani S, Auvynet C, Titomanlio L, Pansiot J, Ball G, Boardman JP, Walley AJ, Saxena A, Mirza G, Fleiss B, Edwards AD, Petretto E, Gressens P.

Nat Commun. 2017 Sep 5;8(1):428. doi: 10.1038/s41467-017-00422-w.

2.

Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants.

Krishnan ML, Wang Z, Silver M, Boardman JP, Ball G, Counsell SJ, Walley AJ, Montana G, Edwards AD.

Brain Behav. 2016 Apr 2;6(7):e00434. doi: 10.1002/brb3.434. eCollection 2016 Jul.

3.

Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism.

Alsters SI, Goldstone AP, Buxton JL, Zekavati A, Sosinsky A, Yiorkas AM, Holder S, Klaber RE, Bridges N, van Haelst MM, le Roux CW, Walley AJ, Walters RG, Mueller M, Blakemore AI.

PLoS One. 2015 Jun 29;10(6):e0131417. doi: 10.1371/journal.pone.0131417. eCollection 2015.

4.

Aberrant DNA methylation at genes associated with a stem cell-like phenotype in cholangiocarcinoma tumors.

Sriraksa R, Zeller C, Dai W, Siddiq A, Walley AJ, Limpaiboon T, Brown R.

Cancer Prev Res (Phila). 2013 Dec;6(12):1348-55. doi: 10.1158/1940-6207.CAPR-13-0104. Epub 2013 Oct 2.

5.

Integration of clinical data with a genome-scale metabolic model of the human adipocyte.

Mardinoglu A, Agren R, Kampf C, Asplund A, Nookaew I, Jacobson P, Walley AJ, Froguel P, Carlsson LM, Uhlen M, Nielsen J.

Mol Syst Biol. 2013;9:649. doi: 10.1038/msb.2013.5.

6.

Candidate DNA methylation drivers of acquired cisplatin resistance in ovarian cancer identified by methylome and expression profiling.

Zeller C, Dai W, Steele NL, Siddiq A, Walley AJ, Wilhelm-Benartzi CS, Rizzo S, van der Zee A, Plumb JA, Brown R.

Oncogene. 2012 Oct 18;31(42):4567-76. doi: 10.1038/onc.2011.611. Epub 2012 Jan 16.

7.

ITIH-5 expression in human adipose tissue is increased in obesity.

Anveden Å, Sjöholm K, Jacobson P, Palsdottir V, Walley AJ, Froguel P, Al-Daghri N, McTernan PG, Mejhert N, Arner P, Sjöström L, Carlsson LM, Svensson PA.

Obesity (Silver Spring). 2012 Apr;20(4):708-14. doi: 10.1038/oby.2011.268. Epub 2011 Aug 18.

8.

Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesity.

Clark SJ, Falchi M, Olsson B, Jacobson P, Cauchi S, Balkau B, Marre M, Lantieri O, Andersson JC, Jernås M, Aitman TJ, Richardson S, Sjöström L, Wong HY, Carlsson LM, Froguel P, Walley AJ.

Obesity (Silver Spring). 2012 Jan;20(1):178-85. doi: 10.1038/oby.2011.200. Epub 2011 Jul 14.

9.

famCNV: copy number variant association for quantitative traits in families.

Eleftherohorinou H, Andersson-Assarsson JC, Walters RG, El-Sayed Moustafa JS, Coin L, Jacobson P, Carlsson LM, Blakemore AI, Froguel P, Walley AJ, Falchi M.

Bioinformatics. 2011 Jul 1;27(13):1873-5. doi: 10.1093/bioinformatics/btr264. Epub 2011 May 5.

10.

Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue.

Walley AJ, Jacobson P, Falchi M, Bottolo L, Andersson JC, Petretto E, Bonnefond A, Vaillant E, Lecoeur C, Vatin V, Jernas M, Balding D, Petteni M, Park YS, Aitman T, Richardson S, Sjostrom L, Carlsson LM, Froguel P.

Int J Obes (Lond). 2012 Jan;36(1):137-47. doi: 10.1038/ijo.2011.22. Epub 2011 Mar 22.

11.

Lack of association of CD36 SNPs with early onset obesity: a meta-analysis in 9,973 European subjects.

Choquet H, Labrune Y, De Graeve F, Hinney A, Hebebrand J, Scherag A, Lecoeur C, Tauber M, Balkau B, Elliot P, Jarvelin MR, Walley AJ, Besnard P, Froguel P, Meyre D.

Obesity (Silver Spring). 2011 Apr;19(4):833-9. doi: 10.1038/oby.2010.226. Epub 2010 Oct 21.

12.

A reasoned approach.

Walley AJ.

Br Dent J. 2010 Oct 9;209(7):327. doi: 10.1038/sj.bdj.2010.890. No abstract available.

PMID:
20930759
13.

CISH and susceptibility to infectious diseases.

Khor CC, Vannberg FO, Chapman SJ, Guo H, Wong SH, Walley AJ, Vukcevic D, Rautanen A, Mills TC, Chang KC, Kam KM, Crampin AC, Ngwira B, Leung CC, Tam CM, Chan CY, Sung JJ, Yew WW, Toh KY, Tay SK, Kwiatkowski D, Lienhardt C, Hien TT, Day NP, Peshu N, Marsh K, Maitland K, Scott JA, Williams TN, Berkley JA, Floyd S, Tang NL, Fine PE, Goh DL, Hill AV.

N Engl J Med. 2010 Jun 3;362(22):2092-101. doi: 10.1056/NEJMoa0905606. Epub 2010 May 19.

14.

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

Walters RG, Jacquemont S, Valsesia A, de Smith AJ, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa JS, Chèvre JC, Lecoeur C, Vatin V, Bouquillon S, Buxton JL, Boute O, Holder-Espinasse M, Cuisset JM, Lemaitre MP, Ambresin AE, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel JL, Le Caignec C, David A, Isidor B, Cordier MP, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova EG, Henning E, Keogh J, Ellis RJ, Macdermot KD, van Haelst MM, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy RF, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen AL, McCarthy MI, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles ME, O'Rahilly S, Farooqi IS, Männik K, Jarvelin MR, Pattou F, Meyre D, Walley AJ, Coin LJ, Blakemore AI, Froguel P, Beckmann JS.

Nature. 2010 Feb 4;463(7281):671-5. doi: 10.1038/nature08727.

15.

The genetic contribution to non-syndromic human obesity.

Walley AJ, Asher JE, Froguel P.

Nat Rev Genet. 2009 Jul;10(7):431-42. doi: 10.1038/nrg2594. Review.

PMID:
19506576
16.

A rare variant in the visfatin gene (NAMPT/PBEF1) is associated with protection from obesity.

Blakemore AI, Meyre D, Delplanque J, Vatin V, Lecoeur C, Marre M, Tichet J, Balkau B, Froguel P, Walley AJ.

Obesity (Silver Spring). 2009 Aug;17(8):1549-53. doi: 10.1038/oby.2009.75. Epub 2009 Mar 19.

17.

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.

Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, Tichet J, Marre M, Weill J, Heude B, Tauber M, Lemaire K, Schuit F, Elliott P, Jørgensen T, Charpentier G, Hadjadj S, Cauchi S, Vaxillaire M, Sladek R, Visvikis-Siest S, Balkau B, Lévy-Marchal C, Pattou F, Meyre D, Blakemore AI, Jarvelin MR, Walley AJ, Hansen T, Dina C, Pedersen O, Froguel P.

Nat Genet. 2009 Jan;41(1):89-94. doi: 10.1038/ng.277. Epub 2008 Dec 7.

PMID:
19060909
18.

Making it stick....

Walley AJ.

Dent Update. 2008 Jul-Aug;35(6):426-7; author reply 427. No abstract available.

PMID:
18720569
19.

Common nonsynonymous variants in PCSK1 confer risk of obesity.

Benzinou M, Creemers JW, Choquet H, Lobbens S, Dina C, Durand E, Guerardel A, Boutin P, Jouret B, Heude B, Balkau B, Tichet J, Marre M, Potoczna N, Horber F, Le Stunff C, Czernichow S, Sandbaek A, Lauritzen T, Borch-Johnsen K, Andersen G, Kiess W, Körner A, Kovacs P, Jacobson P, Carlsson LM, Walley AJ, Jørgensen T, Hansen T, Pedersen O, Meyre D, Froguel P.

Nat Genet. 2008 Aug;40(8):943-5. doi: 10.1038/ng.177. Epub 2008 Jul 6.

PMID:
18604207
20.

A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis.

Khor CC, Chapman SJ, Vannberg FO, Dunne A, Murphy C, Ling EY, Frodsham AJ, Walley AJ, Kyrieleis O, Khan A, Aucan C, Segal S, Moore CE, Knox K, Campbell SJ, Lienhardt C, Scott A, Aaby P, Sow OY, Grignani RT, Sillah J, Sirugo G, Peshu N, Williams TN, Maitland K, Davies RJ, Kwiatkowski DP, Day NP, Yala D, Crook DW, Marsh K, Berkley JA, O'Neill LA, Hill AV.

Nat Genet. 2007 Apr;39(4):523-8. Epub 2007 Feb 25.

21.

Leptin receptor genotype at Gln223Arg is associated with body composition, BMD, and vertebral fracture in postmenopausal Danish women.

Fairbrother UL, Tankó LB, Walley AJ, Christiansen C, Froguel P, Blakemore AI.

J Bone Miner Res. 2007 Apr;22(4):544-50.

22.

No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.

Bell CG, Meyre D, Petretto E, Levy-Marchal C, Hercberg S, Charles MA, Boyle C, Weill J, Tauber M, Mein CA, Aitman TJ, Froguel P, Walley AJ.

Eur J Hum Genet. 2007 Mar;15(3):320-7. Epub 2006 Dec 13.

23.

Genetics of obesity and the prediction of risk for health.

Walley AJ, Blakemore AI, Froguel P.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R124-30. Review.

PMID:
16987875
24.

Association of melanin-concentrating hormone receptor 1 5' polymorphism with early-onset extreme obesity.

Bell CG, Meyre D, Samson C, Boyle C, Lecoeur C, Tauber M, Jouret B, Jaquet D, Levy-Marchal C, Charles MA, Weill J, Gibson F, Mein CA, Froguel P, Walley AJ.

Diabetes. 2005 Oct;54(10):3049-55.

25.

The genetics of human obesity.

Bell CG, Walley AJ, Froguel P.

Nat Rev Genet. 2005 Mar;6(3):221-34. Review.

PMID:
15703762
26.

Association of Fcgamma receptor IIa (CD32) polymorphism with severe malaria in West Africa.

Cooke GS, Aucan C, Walley AJ, Segal S, Greenwood BM, Kwiatkowski DP, Hill AV.

Am J Trop Med Hyg. 2003 Dec;69(6):565-8.

PMID:
14740869
27.

Common apolipoprotein E polymorphisms and risk of clinical malaria in the Gambia.

Aucan C, Walley AJ, Hill AV.

J Med Genet. 2004 Jan;41(1):21-4. No abstract available.

28.

Interleukin-1 gene cluster polymorphisms and susceptibility to clinical malaria in a Gambian case-control study.

Walley AJ, Aucan C, Kwiatkowski D, Hill AV.

Eur J Hum Genet. 2004 Feb;12(2):132-8.

29.

Interferon-alpha receptor-1 (IFNAR1) variants are associated with protection against cerebral malaria in the Gambia.

Aucan C, Walley AJ, Hennig BJ, Fitness J, Frodsham A, Zhang L, Kwiatkowski D, Hill AV.

Genes Immun. 2003 Jun;4(4):275-82.

PMID:
12761564
30.

Haptoglobin genotypes are not associated with resistance to severe malaria in The Gambia.

Aucan C, Walley AJ, Greenwood BM, Hill AV.

Trans R Soc Trop Med Hyg. 2002 May-Jun;96(3):327-8.

PMID:
12174790
31.

Gene polymorphism in Netherton and common atopic disease.

Walley AJ, Chavanas S, Moffatt MF, Esnouf RM, Ubhi B, Lawrence R, Wong K, Abecasis GR, Jones EY, Harper JI, Hovnanian A, Cookson WO.

Nat Genet. 2001 Oct;29(2):175-8.

PMID:
11544479
32.

Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility loci.

Cookson WO, Ubhi B, Lawrence R, Abecasis GR, Walley AJ, Cox HE, Coleman R, Leaves NI, Trembath RC, Moffatt MF, Harper JI.

Nat Genet. 2001 Apr;27(4):372-3.

PMID:
11279517
33.

Linkage and allelic association of chromosome 5 cytokine cluster genetic markers with atopy and asthma associated traits.

Walley AJ, Wiltshire S, Ellis CM, Cookson WO.

Genomics. 2001 Feb 15;72(1):15-20.

PMID:
11247662
34.

Delta 32 deletion of CCR5 gene and association with asthma or atopy.

Mitchell TJ, Walley AJ, Pease JE, Venables PJ, Wiltshire S, Williams TJ, Cookson WO.

Lancet. 2000 Oct 28;356(9240):1491-2.

PMID:
11081537
35.

Association of atopic dermatitis to the beta subunit of the high affinity immunoglobulin E receptor.

Cox HE, Moffatt MF, Faux JA, Walley AJ, Coleman R, Trembath RC, Cookson WO, Harper JI.

Br J Dermatol. 1998 Jan;138(1):182-7.

PMID:
9536245
36.
37.
38.

A novel point mutation (D380A) and a rare deletion (1255del55) in the glucocerebrosidase gene causing Gaucher's disease.

Walley AJ, Harris A.

Hum Mol Genet. 1993 Oct;2(10):1737-8. No abstract available.

PMID:
8268935
39.

Gaucher's disease in the United Kingdom: screening non-Jewish patients for the two common mutations.

Walley AJ, Barth ML, Ellis I, Fensom AH, Harris A.

J Med Genet. 1993 Apr;30(4):280-3.

40.

Direct RNA binding by the rev product of HIV-1.

Walley AJ, Heaphy S, Jones IM.

AIDS. 1989 Dec;3(12):859-61. No abstract available.

PMID:
2517208

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