PubMed

Population-based survey of cancer risks in chromosome 3 translocation carriers.

Woodward ER, Skytte AB, Cruger DG, Maher ER.

Genes Chromosomes Cancer. 2010 Jan;49(1):52-8.PMID: 19827124 [PubMed - in process]Related articles

Tumour Risks and Genotype-Phenotype-Proteotype Analysis in 358 Patients with Germline Mutations in SDHB and SDHD.

Ricketts CJ, Forman JR, Rattenbury E, Bradshaw N, Lalloo F, Izatt L, Cole TR, Armstrong R, Ajith Kumar VK, Morrison PJ, Atkinson AB, Douglas F, Ball SG, Cook J, Srirangalingam U, Killick P, Kirby G, Aylwin S, Woodward ER, Evans DG, Hodgson SV, Murday V, Chew SL, Connell JM, Blundell TL, Macdonald F, Maher ER.

Hum Mutat. 2009 Oct 2. [Epub ahead of print]PMID: 19802898 [PubMed - as supplied by publisher]Related articles

A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.

Lim DH, Rehal PK, Nahorski MS, Macdonald F, Claessens T, Van Geel M, Gijezen L, Gille JJ, Giraud S, Richard S, van Steensel M, Menko FH, Maher ER.

Hum Mutat. 2009 Oct 2. [Epub ahead of print]PMID: 19802896 [PubMed - as supplied by publisher]Related articles

Genotype-phenotype correlations in VHL exon deletions.

McNeill A, Rattenberry E, Barber R, Killick P, MacDonald F, Maher ER.

Am J Med Genet A. 2009 Oct;149A(10):2147-51.PMID: 19764026 [PubMed - in process]Related articles

Microarray based analysis of 3p25-p26 deletions (3p- syndrome).

Shuib S, McMullan D, Rattenberry E, Barber RM, Rahman F, Zatyka M, Chapman C, Macdonald F, Latif F, Davison V, Maher ER.

Am J Med Genet A. 2009 Oct;149A(10):2099-105.PMID: 19760623 [PubMed - in process]Related articles

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.

van Nederveen FH, Gaal J, Favier J, Korpershoek E, Oldenburg RA, de Bruyn EM, Sleddens HF, Derkx P, Rivière J, Dannenberg H, Petri BJ, Komminoth P, Pacak K, Hop WC, Pollard PJ, Mannelli M, Bayley JP, Perren A, Niemann S, Verhofstad AA, de Bruïne AP, Maher ER, Tissier F, Méatchi T, Badoual C, Bertherat J, Amar L, Alataki D, Van Marck E, Ferrau F, François J, de Herder WW, Peeters MP, van Linge A, Lenders JW, Gimenez-Roqueplo AP, de Krijger RR, Dinjens WN.

Lancet Oncol. 2009 Aug;10(8):764-71. Epub 2009 Jul 1.PMID: 19576851 [PubMed - indexed for MEDLINE]Related articles

The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias.

Hesson LB, Dunwell TL, Cooper WN, Catchpoole D, Brini AT, Chiaramonte R, Griffiths M, Chalmers AD, Maher ER, Latif F.

Mol Cancer. 2009 Jul 1;8:42.PMID: 19570220 [PubMed - indexed for MEDLINE]Related articlesFree article

RAN GTPase is a RASSF1A effector involved in controlling microtubule organization.

Dallol A, Hesson LB, Matallanas D, Cooper WN, O'Neill E, Maher ER, Kolch W, Latif F.

Curr Biol. 2009 Jul 28;19(14):1227-32. Epub 2009 Jun 25.PMID: 19559616 [PubMed - indexed for MEDLINE]Related articles

Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in familial and sporadic renal cell carcinoma.

Ricketts C, Zeegers MP, Lubinski J, Maher ER.

PLoS One. 2009 Jun 24;4(6):e6037.PMID: 19551141 [PubMed - indexed for MEDLINE]Related articlesFree article

Frequent epigenetic inactivation of the SLIT2 gene in chronic and acute lymphocytic leukemia.

Dunwell TL, Dickinson RE, Stankovic T, Dallol A, Weston V, Austen B, Catchpoole D, Maher ER, Latif F.

Epigenetics. 2009 May;4(4):265-9. Epub 2009 May 1.PMID: 19550140 [PubMed - indexed for MEDLINE]Related articles

CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.

McRonald FE, Morris MR, Gentle D, Winchester L, Baban D, Ragoussis J, Clarke NW, Brown MD, Kishida T, Yao M, Latif F, Maher ER.

Mol Cancer. 2009 Jun 3;8:31.PMID: 19493342 [PubMed - indexed for MEDLINE]Related articlesFree article

Pantothenate kinase-associated neurodegeneration (PKAN): molecular confirmation of a Turkish patient with a rare frameshift mutation in the coding region of the PANK2 gene.

Cangül H, Ozdemir O, Yakut T, Okan M, Morgan NV, Baytan B, Kurian MA, Spiegel R, Maher ER.

Turk J Pediatr. 2009 Mar-Apr;51(2):161-5.PMID: 19480328 [PubMed - indexed for MEDLINE]Related articles

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.

Kurian MA, Zhen J, Cheng SY, Li Y, Mordekar SR, Jardine P, Morgan NV, Meyer E, Tee L, Pasha S, Wassmer E, Heales SJ, Gissen P, Reith ME, Maher ER.

J Clin Invest. 2009 Jun;119(6):1595-603. doi: 10.1172/JCI39060. Epub 2009 May 26.PMID: 19478460 [PubMed - indexed for MEDLINE]Related articlesFree article

Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.

Meyer E, Rahman F, Owens J, Pasha S, Morgan NV, Trembath RC, Stone EM, Moore AT, Maher ER.

Mol Vis. 2009 May 18;15:1014-9.PMID: 19461930 [PubMed - indexed for MEDLINE]Related articlesFree article

Epigenetic analysis of childhood acute lymphoblastic leukemia.

Dunwell TL, Hesson LB, Pavlova T, Zabarovska V, Kashuba V, Catchpoole D, Chiaramonte R, Brini AT, Griffiths M, Maher ER, Zabarovsky E, Latif F.

Epigenetics. 2009 Apr;4(3):185-93. Epub 2009 Apr 12.PMID: 19430199 [PubMed - indexed for MEDLINE]Related articles

X-linked cataract and Nance-Horan syndrome are allelic disorders.

Coccia M, Brooks SP, Webb TR, Christodoulou K, Wozniak IO, Murday V, Balicki M, Yee HA, Wangensteen T, Riise R, Saggar AK, Park SM, Kanuga N, Francis PJ, Maher ER, Moore AT, Russell-Eggitt IM, Hardcastle AJ.

Hum Mol Genet. 2009 Jul 15;18(14):2643-55. Epub 2009 May 4.PMID: 19414485 [PubMed - indexed for MEDLINE]Related articlesFree article

Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.

Jones N, Vogt S, Nielsen M, Christian D, Wark PA, Eccles D, Edwards E, Evans DG, Maher ER, Vasen HF, Hes FJ, Aretz S, Sampson JR.

Gastroenterology. 2009 Aug;137(2):489-94, 494.e1; quiz 725-6. Epub 2009 Apr 23.PMID: 19394335 [PubMed - indexed for MEDLINE]Related articles

Proteomic identification of differentially expressed plasma membrane proteins in renal cell carcinoma by stable isotope labelling of a von Hippel-Lindau transfectant cell line model.

Aggelis V, Craven RA, Peng J, Harnden P, Cairns DA, Maher ER, Tonge R, Selby PJ, Banks RE.

Proteomics. 2009 Apr;9(8):2118-30.PMID: 19337990 [PubMed - indexed for MEDLINE]Related articles

Genetic and epigenetic analysis of recurrent hydatidiform mole.

Hayward BE, De Vos M, Talati N, Abdollahi MR, Taylor GR, Meyer E, Williams D, Maher ER, Setna F, Nazir K, Hussaini S, Jafri H, Rashid Y, Sheridan E, Bonthron DT.

Hum Mutat. 2009 May;30(5):E629-39.PMID: 19309689 [PubMed - indexed for MEDLINE]Related articles

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

Meyer E, Lim D, Pasha S, Tee LJ, Rahman F, Yates JR, Woods CG, Reik W, Maher ER.

PLoS Genet. 2009 Mar;5(3):e1000423. Epub 2009 Mar 20.PMID: 19300480 [PubMed - indexed for MEDLINE]Related articlesFree article

Germline mutation in DOK7 associated with fetal akinesia deformation sequence.

Vogt J, Morgan NV, Marton T, Maxwell S, Harrison BJ, Beeson D, Maher ER.

J Med Genet. 2009 May;46(5):338-40. Epub 2009 Mar 3.PMID: 19261599 [PubMed - indexed for MEDLINE]Related articles

Succinate dehydrogenase subunit B (SDHB) gene deletion associated with a composite paraganglioma/neuroblastoma.

Armstrong R, Greenhalgh KL, Rattenberry E, Judd B, Shukla R, Losty PD, Maher ER.

J Med Genet. 2009 Mar;46(3):215-6. No abstract available. PMID: 19251979 [PubMed - indexed for MEDLINE]Related articles

Contrasting clinical manifestations of SDHB and VHL associated chromaffin tumours.

Srirangalingam U, Khoo B, Walker L, MacDonald F, Skelly RH, George E, Spooner D, Johnston LB, Monson JP, Grossman AB, Drake WM, Akker SA, Pollard PJ, Plowman N, Avril N, Berney DM, Burrin JM, Reznek RH, Kumar VK, Maher ER, Chew SL.

Endocr Relat Cancer. 2009 Jun;16(2):515-25. Epub 2009 Feb 10.PMID: 19208735 [PubMed - indexed for MEDLINE]Related articles

SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosis.

Henderson A, Douglas F, Perros P, Morgan C, Maher ER.

Fam Cancer. 2009;8(3):257-60. Epub 2009 Jan 29.PMID: 19184535 [PubMed - in process]Related articles

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome.

Burn J, Bishop DT, Mecklin JP, Macrae F, Möslein G, Olschwang S, Bisgaard ML, Ramesar R, Eccles D, Maher ER, Bertario L, Jarvinen HJ, Lindblom A, Evans DG, Lubinski J, Morrison PJ, Ho JW, Vasen HF, Side L, Thomas HJ, Scott RJ, Dunlop M, Barker G, Elliott F, Jass JR, Fodde R, Lynch HT, Mathers JC; CAPP2 Investigators.

N Engl J Med. 2008 Dec 11;359(24):2567-78. Erratum in: N Engl J Med. 2009 Apr 2;360(14):1470. PMID: 19073976 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.

Lim D, Bowdin SC, Tee L, Kirby GA, Blair E, Fryer A, Lam W, Oley C, Cole T, Brueton LA, Reik W, Macdonald F, Maher ER.

Hum Reprod. 2009 Mar;24(3):741-7. Epub 2008 Dec 10.PMID: 19073614 [PubMed - indexed for MEDLINE]Related articles

Molecular investigations to improve diagnostic accuracy in patients with ARC syndrome.

Cullinane AR, Straatman-Iwanowska A, Seo JK, Ko JS, Song KS, Gizewska M, Gruszfeld D, Gliwicz D, Tuysuz B, Erdemir G, Sougrat R, Wakabayashi Y, Hinds R, Barnicoat A, Mandel H, Chitayat D, Fischler B, Garcia-Cazorla A, Knisely AS, Kelly DA, Maher ER, Gissen P.

Hum Mutat. 2009 Feb;30(2):E330-7.PMID: 18853461 [PubMed - indexed for MEDLINE]Related articles

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.

Scott RH, Douglas J, Baskcomb L, Huxter N, Barker K, Hanks S, Craft A, Gerrard M, Kohler JA, Levitt GA, Picton S, Pizer B, Ronghe MD, Williams D; Factors Associated with Childhood Tumours (FACT) Collaboration, Cook JA, Pujol P, Maher ER, Birch JM, Stiller CA, Pritchard-Jones K, Rahman N.

Nat Genet. 2008 Nov;40(11):1329-34. Epub 2008 Oct 5.PMID: 18836444 [PubMed - indexed for MEDLINE]Related articles

Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN.

Woodward ER, Ricketts C, Killick P, Gad S, Morris MR, Kavalier F, Hodgson SV, Giraud S, Bressac-de Paillerets B, Chapman C, Escudier B, Latif F, Richard S, Maher ER.

Clin Cancer Res. 2008 Sep 15;14(18):5925-30.PMID: 18794106 [PubMed - indexed for MEDLINE]Related articlesFree article

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.

Pittman AM, Webb E, Carvajal-Carmona L, Howarth K, Di Bernardo MC, Broderick P, Spain S, Walther A, Price A, Sullivan K, Twiss P, Fielding S, Rowan A, Jaeger E, Vijayakrishnan J, Chandler I, Penegar S, Qureshi M, Lubbe S, Domingo E, Kemp Z, Barclay E, Wood W, Martin L, Gorman M, Thomas H, Peto J, Bishop T, Gray R, Maher ER, Lucassen A, Kerr D, Evans GR; CORGI Consortium, van Wezel T, Morreau H, Wijnen JT, Hopper JL, Southey MC, Giles GG, Severi G, Castellví-Bel S, Ruiz-Ponte C, Carracedo A, Castells A; EPICOLON Consortium, Försti A, Hemminki K, Vodicka P, Naccarati A, Lipton L, Ho JW, Cheng KK, Sham PC, Luk J, Agúndez JA, Ladero JM, de la Hoya M, Caldés T, Niittymäki I, Tuupanen S, Karhu A, Aaltonen LA, Cazier JB, Tomlinson IP, Houlston RS.

Hum Mol Genet. 2008 Dec 1;17(23):3720-7. Epub 2008 Aug 27.PMID: 18753146 [PubMed - indexed for MEDLINE]Related articles

Germline SDHB mutations and familial renal cell carcinoma.

Ricketts C, Woodward ER, Killick P, Morris MR, Astuti D, Latif F, Maher ER.

J Natl Cancer Inst. 2008 Sep 3;100(17):1260-2. Epub 2008 Aug 26.PMID: 18728283 [PubMed - indexed for MEDLINE]Related articlesFree article

Deciphering the genetics of hereditary non-syndromic colorectal cancer.

Papaemmanuil E, Carvajal-Carmona L, Sellick GS, Kemp Z, Webb E, Spain S, Sullivan K, Barclay E, Lubbe S, Jaeger E, Vijayakrishnan J, Broderick P, Gorman M, Martin L, Lucassen A, Bishop DT, Evans DG, Maher ER, Steinke V, Rahner N, Schackert HK, Goecke TO, Holinski-Feder E, Propping P, Van Wezel T, Wijnen J, Cazier JB, Thomas H, Houlston RS, Tomlinson I; CORGI Consortium.

Eur J Hum Genet. 2008 Dec;16(12):1477-86. Epub 2008 Jul 16.PMID: 18628789 [PubMed - indexed for MEDLINE]Related articles

Better life expectancy in women with BRCA2 compared with BRCA1 mutations is attributable to lower frequency and later onset of ovarian cancer.

Byrd LM, Shenton A, Maher ER, Woodward E, Belk R, Lim C, Lalloo F, Howell A, Jayson GC, Evans GD.

Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1535-42.PMID: 18559571 [PubMed - indexed for MEDLINE]Related articlesFree article

Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3.

Dallosso AR, Dolwani S, Jones N, Jones S, Colley J, Maynard J, Idziaszczyk S, Humphreys V, Arnold J, Donaldson A, Eccles D, Ellis A, Evans DG, Frayling IM, Hes FJ, Houlston RS, Maher ER, Nielsen M, Parry S, Tyler E, Moskvina V, Cheadle JP, Sampson JR.

Gut. 2008 Sep;57(9):1252-5. Epub 2008 May 30.PMID: 18515411 [PubMed - indexed for MEDLINE]Related articles

Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer burden in the family.

Evans DG, Shenton A, Woodward E, Lalloo F, Howell A, Maher ER.

BMC Cancer. 2008 May 30;8:155.PMID: 18513387 [PubMed - indexed for MEDLINE]Related articlesFree article

Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastoma.

Margetts CD, Morris M, Astuti D, Gentle DC, Cascon A, McRonald FE, Catchpoole D, Robledo M, Neumann HP, Latif F, Maher ER.

Endocr Relat Cancer. 2008 Sep;15(3):777-86. Epub 2008 May 22.PMID: 18499731 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN).

Kurian MA, Morgan NV, MacPherson L, Foster K, Peake D, Gupta R, Philip SG, Hendriksz C, Morton JE, Kingston HM, Rosser EM, Wassmer E, Gissen P, Maher ER.

Neurology. 2008 Apr 29;70(18):1623-9.PMID: 18443314 [PubMed - indexed for MEDLINE]Related articles

Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.

Srirangalingam U, Walker L, Khoo B, MacDonald F, Gardner D, Wilkin TJ, Skelly RH, George E, Spooner D, Monson JP, Grossman AB, Akker SA, Pollard PJ, Plowman N, Avril N, Berney DM, Burrin JM, Reznek RH, Kumar VK, Maher ER, Chew SL.

Clin Endocrinol (Oxf). 2008 Oct;69(4):587-96. Epub 2008 Apr 14.PMID: 18419787 [PubMed - indexed for MEDLINE]Related articles

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.

Tomlinson IP, Webb E, Carvajal-Carmona L, Broderick P, Howarth K, Pittman AM, Spain S, Lubbe S, Walther A, Sullivan K, Jaeger E, Fielding S, Rowan A, Vijayakrishnan J, Domingo E, Chandler I, Kemp Z, Qureshi M, Farrington SM, Tenesa A, Prendergast JG, Barnetson RA, Penegar S, Barclay E, Wood W, Martin L, Gorman M, Thomas H, Peto J, Bishop DT, Gray R, Maher ER, Lucassen A, Kerr D, Evans DG; CORGI Consortium, Schafmayer C, Buch S, Völzke H, Hampe J, Schreiber S, John U, Koessler T, Pharoah P, van Wezel T, Morreau H, Wijnen JT, Hopper JL, Southey MC, Giles GG, Severi G, Castellví-Bel S, Ruiz-Ponte C, Carracedo A, Castells A; EPICOLON Consortium, Försti A, Hemminki K, Vodicka P, Naccarati A, Lipton L, Ho JW, Cheng KK, Sham PC, Luk J, Agúndez JA, Ladero JM, de la Hoya M, Caldés T, Niittymäki I, Tuupanen S, Karhu A, Aaltonen L, Cazier JB, Campbell H, Dunlop MG, Houlston RS.

Nat Genet. 2008 May;40(5):623-30. Epub 2008 Mar 30.PMID: 18372905 [PubMed - indexed for MEDLINE]Related articles

Beckwith Weidemann syndrome: a behavioral phenotype-genotype study.

Kent L, Bowdin S, Kirby GA, Cooper WN, Maher ER.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1295-7.PMID: 18314872 [PubMed - indexed for MEDLINE]Related articles

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.

Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A.

Hum Mol Genet. 2008 May 15;17(10):1427-35. Epub 2008 Feb 1.PMID: 18245780 [PubMed - indexed for MEDLINE]Related articlesFree article

Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation.

Scott RH, Douglas J, Baskcomb L, Nygren AO, Birch JM, Cole TR, Cormier-Daire V, Eastwood DM, Garcia-Minaur S, Lupunzina P, Tatton-Brown K, Bliek J, Maher ER, Rahman N.

J Med Genet. 2008 Feb;45(2):106-13. Epub 2007 Oct 15.PMID: 18245390 [PubMed - indexed for MEDLINE]Related articles

Functional epigenomics approach to identify methylated candidate tumour suppressor genes in renal cell carcinoma.

Morris MR, Gentle D, Abdulrahman M, Clarke N, Brown M, Kishida T, Yao M, Teh BT, Latif F, Maher ER.

Br J Cancer. 2008 Jan 29;98(2):496-501. Epub 2008 Jan 15.PMID: 18195710 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.

Vogt J, Harrison BJ, Spearman H, Cossins J, Vermeer S, ten Cate LN, Morgan NV, Beeson D, Maher ER.

Am J Hum Genet. 2008 Jan;82(1):222-7.PMID: 18179903 [PubMed - indexed for MEDLINE]Related articlesFree article

Beckwith-Wiedemann-like macroglossia and 18q23 haploinsufficiency.

Lirussi F, Jonard L, Gaston V, Sanlaville D, Kooy RF, Winnepenninckx B, Maher ER, Fitzpatrick DR, Gicquel C, Portnoï MF, Couderc R, Vazquez MP, Bahuau M.

Am J Med Genet A. 2007 Dec 1;143A(23):2796-803.PMID: 17994567 [PubMed - indexed for MEDLINE]Related articles

Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11.2.

Khaliq S, Abid A, White DR, Johnson CA, Ismail M, Khan A, Ayub Q, Sultana S, Maher ER, Mehdi SQ.

Am J Med Genet A. 2007 Dec 1;143A(23):2768-74.PMID: 17975799 [PubMed - indexed for MEDLINE]Related articles

Loss of PL6 protein expression in renal clear cell carcinomas and other VHL-deficient tumours.

Ivanova AV, Vortmeyer A, Ivanov SV, Nickerson ML, Maher ER, Lerman MI.

J Pathol. 2008 Jan;214(1):46-57.PMID: 17973242 [PubMed - indexed for MEDLINE]Related articles

Methylation-specific MLPA (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation.

Scott RH, Douglas J, Baskcomb L, Nygren AO, Birch JM, Cole TR, Cormier-Daire V, Eastwood DM, Garcia-Minaur S, Lapunzina P, Tatton-Brown K, Bliek J, Maher ER, Rahman N.

J Med Genet. 2007 Oct 15. [Epub ahead of print]PMID: 17938164 [PubMed - as supplied by publisher]Related articles

A survey of assisted reproductive technology births and imprinting disorders.

Bowdin S, Allen C, Kirby G, Brueton L, Afnan M, Barratt C, Kirkman-Brown J, Harrison R, Maher ER, Reardon W.

Hum Reprod. 2007 Dec;22(12):3237-40. Epub 2007 Oct 5.PMID: 17921133 [PubMed - indexed for MEDLINE]Related articlesFree article

Epigenetic regulation of the ras effector/tumour suppressor RASSF2 in breast and lung cancer.

Cooper WN, Dickinson RE, Dallol A, Grigorieva EV, Pavlova TV, Hesson LB, Bieche I, Broggini M, Maher ER, Zabarovsky ER, Clark GJ, Latif F.

Oncogene. 2008 Mar 13;27(12):1805-11. Epub 2007 Sep 24.PMID: 17891178 [PubMed - indexed for MEDLINE]Related articles