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Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour

Human molecular genetics, 2011-10, Vol.20 (2), p.R198-R205

2011

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Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p

Human molecular genetics, 2008-03, Vol.17 (6), p.806-814

2008

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Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease

The New England journal of medicine, 2009-12, Vol.361 (26), p.2518-2528

2009

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Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia

Leukemia, 2023-03, Vol.37 (3), p.518-528

2023

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Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

JAMA : the journal of the American Medical Association, 2009-07, Vol.302 (1), p.37

2009

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HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis

Journal of the American Society of Nephrology, 2010-10, Vol.21 (10), p.1791-1797

2010

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APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma

Cancer research (Chicago, Ill.), 2013-12, Vol.73 (24), p.7222-7231

2013

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Variation in the strength of selected codon usage bias among bacteria

Nucleic acids research, 2005-01, Vol.33 (4), p.1141-1153

2005

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Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants

PloS one, 2009-11, Vol.4 (11), p.e7677-e7677

2009

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Situational Influences on Experiences of Long-Distance Hikers

Journal of outdoor recreation, education, and leadership, 2018-12, Vol.10 (3), p.226-237

2018

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Repeat‐associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58

Molecular microbiology, 2000-07, Vol.37 (1), p.207-215

2000

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Preservation amenity, research laboratory, or mineral reserve? International perspectives on the values of Antarctica

Polar record, 2019-03, Vol.55 (2), p.61-71

2019

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Complete Genome Sequence of Neisseria meningitidis Serogroup B Strain MC58

Science (American Association for the Advancement of Science), 2000-03, Vol.287 (5459), p.1809-1815

2000

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Predictors of Coordinated and Comprehensive Care Within a Medical Home for Children With Special Healthcare (CHSCN) Needs

Frontiers in public health, 2018-06, Vol.6, p.170-170

2018

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Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

PLoS genetics, 2006-05, Vol.2 (5), p.e72-e72

2006

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Erratum: The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes

Nature communications, 2016-06, Vol.7 (1), p.11908-11908, Article 11908

2016

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Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori

BMC genomics, 2005-01, Vol.6 (1), p.9-9, Article 9

2005

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Assessing Birth to Age 5 Teaching Methods at a University Laboratory School

Journal of research in childhood education, 2017-04, Vol.31 (2), p.270-280

2017

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Simple sequence repeats in the Helicobacter pylori genome

Molecular microbiology, 1998-03, Vol.27 (6), p.1091-1098

1998

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A Walk in the Forest: Elementary Students’ Perceptions and Knowledge of Forestry Principles

Journal of park and recreation administration, 2016-01, Vol.34 (2)

2016

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Assessing the Transactional Nature of Wilderness Experiences: Construct Validation of the Wilderness-Hassles Appraisal Scale

Environmental management (New York), 2008-09, Vol.42 (3), p.497-510

2008

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Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16

Human molecular genetics, 2001-02, Vol.10 (4), p.339-352

2001

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Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour

The somatic mutation profiles of 2,433 breast cancers refines their genomic and transcriptomic landscapes

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p

Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease

Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma

Variation in the strength of selected codon usage bias among bacteria

Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants

Situational Influences on Experiences of Long-Distance Hikers

Genome sequencing as a generic diagnostic strategy for rare disease

Repeat‐associated phase variable genes in the complete genome sequence of Neisseria meningitidis strain MC58

Preservation amenity, research laboratory, or mineral reserve? International perspectives on the values of Antarctica

Complete Genome Sequence of Neisseria meningitidis Serogroup B Strain MC58

Predictors of Coordinated and Comprehensive Care Within a Medical Home for Children With Special Healthcare (CHSCN) Needs

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

Erratum: The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes

Inter-species horizontal transfer resulting in core-genome and niche-adaptive variation within Helicobacter pylori

Assessing Birth to Age 5 Teaching Methods at a University Laboratory School

Simple sequence repeats in the Helicobacter pylori genome

A Walk in the Forest: Elementary Students’ Perceptions and Knowledge of Forestry Principles

Assessing the Transactional Nature of Wilderness Experiences: Construct Validation of the Wilderness-Hassles Appraisal Scale

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16

The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes

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