Ultralow-volume PCR with a liquid handling system: SNP genotypingEDWARDS, T. O. M; YUILLE, Martin; BROOKING, Justin et al.American biotechnology laboratory. 2003, Vol 21, Num 5, issn 0749-3223, p. 10Article

A high-density SNP genomewide linkage scan for chronic lymphocytic leukemia-susceptibility lociSELLICK, Gabrielle S; WEBB, Emily L; LYTTELTON, Matthew et al.American journal of human genetics. 2005, Vol 77, Num 3, pp 420-429, issn 0002-9297, 10 p.Article

Toward a roadmap in global biobanking for healthHARRIS, Jennifer R; BURTON, Paul; FORTIER, Isabel et al.European journal of human genetics. 2012, Vol 20, Num 11, pp 1105-1111, issn 1018-4813, 7 p.Article

The UK DNA banking network: a fair access biobankYUILLE, Martin; DIXON, Katherine; PLATT, Andrew et al.Cell and tissue banking. 2010, Vol 11, Num 3, pp 241-251, issn 1389-9333, 11 p.Article

Unusual breakpoint distribution of 8p abnormalities in t-prolymphocytic leukemia : A study with YACS mapping to 8p11-p12SOROUR, Amani; BRITO-BABAPULLE, Vasantha; SMEDLEY, Damian et al.Cancer genetics and cytogenetics. 2000, Vol 121, Num 2, pp 128-132, issn 0165-4608Article

Biobanking for EuropeYUILLE, Martin; VAN OMMEN, Gert-Jan; WICHMANN, H-Erich et al.Briefings in bioinformatics. 2008, Vol 9, Num 1, pp 14-24, issn 1467-5463, 11 p.Article

Causation of chronic lymphocytic leukemia: insights from familial diseaseHOULSTON, Richard S; SELLICK, Gabrielle; YUILLE, Martin et al.Leukemia research. 2003, Vol 27, Num 10, pp 871-876, issn 0145-2126, 6 p.Article

Concomitant inactivation of p53 and Chk2 in breast cancerSULLIVAN, Alexandra; YUILLE, Martin; YULUG, Isik et al.Oncogene (Basingstoke). 2002, Vol 21, Num 9, pp 1316-1324, issn 0950-9232Article

Relationship between glutathione S-transferase M1, T1, and P1 polymorphisms and chronic lymphocytic leukemiaYUILLE, Martin; CONDIE, Alison; HUDSON, Chantelle et al.Blood. 2002, Vol 99, Num 11, pp 4216-4218, issn 0006-4971Article

Breakpoints in the ataxia telangiectasia gene arise at the RGYW somatic hypermutation motifBRADSHAW, Paul S; CONDIE, Alison; MATUTES, Estella et al.Oncogene (Basingstoke). 2002, Vol 21, Num 3, pp 483-487, issn 0950-9232Article

Recurrent ATM mutations in T-PLL on diverse haplotypes : no support for their germline originSTANKOVIC, Tatjana; TAYLOR, A. Malcolm R; YUILLE, Martin R et al.Blood. 2001, Vol 97, Num 5, pp 1517-1518, issn 0006-4971Article

Disruption of the ATM gene in breast cancerLU, Yong-Jie; CONDIE, Alison; BENNETT, Julie D et al.Cancer genetics and cytogenetics. 2001, Vol 126, Num 2, pp 97-101, issn 0165-4608Article

Inherited predisposition to CLL is detectable as subclinical monoclonal B-lymphocyte expansionRAWSTRON, Andy C; YUILLE, Martin R; HOULSTON, Richard S et al.Blood. 2002, Vol 100, Num 7, pp 2289-2291, issn 0006-4971, 3 p.Article

ATM mutations are rare in familial chronic lymphocytic leukemiaYUILLE, Martin R; CONDIE, Alison; HUDSON, Chantelle D et al.Blood. 2002, Vol 100, Num 2, pp 603-609, issn 0006-4971Article

Linkage analysis for major histocompatibility complex-related genetic susceptibility in familial chronic lymphocytic leukemiaBEVAN, Stephen; CATOVSKY, Daniel; MAURO, Francesca R et al.Blood. 2000, Vol 96, Num 12, pp 3982-3984, issn 0006-4971Article