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Author Details

Pamela Whittaker
King Edward Memorial Hospital
2000
27
24
PMIDPaper TitleJournal TitlePublished Year
25262025Australian midwives knowledge, attitude and perceived learning needs around perinatal mental health.Midwifery2015
25262025Australian midwives knowledge, attitude and perceived learning needs around perinatal mental health.Midwifery2015
23974872Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Nat Genet2013
23974872Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Nat Genet2013
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
21833088Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.Nature2011
20062062Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.Nat Genet2010
20811451Integrating common and rare genetic variation in diverse human populations.Nature2010
20219945Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.Genome Res2010
20062062Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.Nat Genet2010
20811451Integrating common and rare genetic variation in diverse human populations.Nature2010
20219945Human aging-associated DNA hypermethylation occurs preferentially at bivalent chromatin domains.Genome Res2010
19200524A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.Am J Hum Genet2009
19181680Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.Hum Mol Genet2009
19300499A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.PLoS Genet2009
19200524A genome-wide survey of the prevalence and evolutionary forces acting on human nonsense SNPs.Am J Hum Genet2009
19465909Genome-wide and fine-resolution association analysis of malaria in West Africa.Nat Genet2009
19143810Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.Diabetes Obes Metab2009
19915572Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.Nat Genet2009
19915572Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.Nat Genet2009
19465909Genome-wide and fine-resolution association analysis of malaria in West Africa.Nat Genet2009
19181680Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.Hum Mol Genet2009
19143810Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.Diabetes Obes Metab2009
19300499A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.PLoS Genet2009
18455228Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.Lancet2008
18455228Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.Lancet2008
18728231Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.Diabetes2008
18773191Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathy.Diabetologia2008
18728231Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.Diabetes2008
18773191Genetic association analyses of non-synonymous single nucleotide polymorphisms in diabetic nephropathy.Diabetologia2008
17632285The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans.Neuroreport2007
17952073Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.Nat Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17632285The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans.Neuroreport2007
17952073Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.Nat Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
16998491A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.Nat Genet2006
17008408Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response.Proc Natl Acad Sci U S A2006
16998491A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.Nat Genet2006
17008408Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response.Proc Natl Acad Sci U S A2006
15747258A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.Am J Hum Genet2005
15747258A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.Am J Hum Genet2005
14734624The impact of SNP density on fine-scale patterns of linkage disequilibrium.Hum Mol Genet2004
14734624The impact of SNP density on fine-scale patterns of linkage disequilibrium.Hum Mol Genet2004
13677174Adaptive low-vision and blindness techniques for blood glucose monitoring.Diabetes Educ2003
13677174Adaptive low-vision and blindness techniques for blood glucose monitoring.Diabetes Educ2003
11780052The DNA sequence and comparative analysis of human chromosome 20.Nature2001
11780052The DNA sequence and comparative analysis of human chromosome 20.Nature2001
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Collaborators

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Co-authored papers 25
European Bioinformatics Institute
Co-authored papers 15
The Wellcome Trust Sanger Institute
Co-authored papers 11
Illumina Cambridge Ltd.
Co-authored papers 8
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University of Oxford
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State University of New York at Geneseo
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Regeneron Pharmaceuticals Inc
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Vertex Pharmaceuticals
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The University of Manchester
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Massachusetts General Hospital
Co-authored papers 5
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The Wellcome Trust Sanger Institute
Co-authored papers 5
BioMarin Pharmaceutical Inc.
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Medical Research Council Integrative Epidemiology Unit at the University of Bristol
Co-authored papers 5
Big Data Institute, University of Oxford
Co-authored papers 5
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4Wellcome Trust Sanger Institute
Co-authored papers 4
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Illumina Cambridge Ltd.
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