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Jenny Douglas

Medical Research Council

30

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2695

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Correction: Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height

2018 Oncotarget
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Citations (1)
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype

2013 American Journal of Medical Genetics Part A
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Citations (79)
Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer

2012 Breast Cancer Research and Treatment
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Citations (46)
Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma

2011 Familial Cancer
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Citations (52)
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height.

2011 Oncotarget
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Citations (108)
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene

2010 Journal of Medical Genetics
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Citations (43)
Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor

2008 Nature Genetics
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Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth

2007 Nature Genetics
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PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations

2006 American Journal of Medical Genetics Part A
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Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24

2005 Annals of Neurology
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Citations (29)