Struan F A Grant

发表

Role of BMI‐Associated Loci Identified in GWAS Meta‐Analyses in the Context of Common Childhood Obesity in European Americans

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2011, Obesity.

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

Philippe Froguel, Nicholas J Timpson, Dirkje S Postma, 2010, Nature Genetics.

Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study.

Yan Guo, Tie-Lin Yang, Hui Shen, 2013, The Journal of clinical endocrinology and metabolism.

A genome-wide study reveals copy number variants exclusive to childhood obesity cases.

Hakon Hakonarson, Cuiping Hou, J. Glessner, 2010, American journal of human genetics.

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

Constantin Polychronakos, David C Wilson, Joseph T. Glessner, 2010, Human molecular genetics.

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

Common variants at 12q15 and 12q24 are associated with infant head circumference

Aad van der Lugt, Xavier Estivill, Sudha Seshadri, 2013, Nature Genetics.

Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus

Pantelis G Bagos, Niki L Dimou, Evangelos Evangelou, 2017, Nature Communications.

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

Vilmundur Gudnason, Kari Stefansson, Arshed A Quyyumi, 2006, Nature Genetics.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.

Tom M Palmer, Debbie A Lawlor, Marie-France Hivert, 2016, JAMA.

Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.

Hakon Hakonarson, J. Glessner, H. Hakonarson, 2008, Arthritis and rheumatism.

Two novel type 2 diabetes loci revealed through integration of TCF7L2 DNA occupancy and SNP association data

Jonathan Schug, S. Grant, J. Schug, 2014, BMJ Open Diabetes Research and Care.

Genome-wide association studies in type 1 diabetes, inflammatory bowel disease and other immune-mediated disorders.

Hakon Hakonarson, H. Hakonarson, S. Grant, 2009, Seminars in immunology.

Common variants at 6q22 and 17q21 are associated with intracranial volume

Wiro J Niessen, Clifford R Jack, Reinhold Schmidt, 2012, Nature Genetics.

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

Xiaowu Gai, Laura K Conlin, Livija Medne, 2009, Genome research.

Common variants at 12q15 and 12q24 are associated with infant head circumference

Aad van der Lugt, Xavier Estivill, Sudha Seshadri, 2012, Nature Genetics.

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.

Nicholas J Timpson, Clive Osmond, Mark I McCarthy, 2013, Human molecular genetics.

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

Yiran Guo, Joseph T. Glessner, Hakon Hakonarson, 2013, Human molecular genetics.

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

Nazneen Rahman, Joseph T. Glessner, Hakon Hakonarson, 2008, The New England journal of medicine.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Hongzhe Li, Constantin Polychronakos, Yiran Guo, 2015, Nature Communications.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.

Joseph T. Glessner, Hakon Hakonarson, J. Glessner, 2009, The Journal of pediatrics.

Association between a high-risk autism locus on 5p14 and social communication spectrum phenotypes in the general population.

Joseph T. Glessner, Hakon Hakonarson, Jean Golding, 2010, The American journal of psychiatry.

Recent development in pharmacogenomics: from candidate genes to genome-wide association studies

Hakon Hakonarson, H. Hakonarson, S. Grant, 2007, Expert review of molecular diagnostics.

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Joseph T. Glessner, Hakon Hakonarson, Ryan M. Smith, 2008, Nature Genetics.

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.

Christian Gieger, Ingo Ruczinski, Tom R. Gaunt, 2012, American journal of human genetics.

Common variants at five new loci associated with early-onset inflammatory bowel disease

Johan Van Limbergen, David C Wilson, David C. Wilson, 2009, Nature Genetics.