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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Molecular psychiatry, 2017-02, Vol.22 (2), p.321-322

2017

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Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

Journal of medical genetics, 2011-01, Vol.48 (1), p.1-9

2011

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Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy

Therapeutic innovation & regulatory science, 2015-09, Vol.49 (5), p.632-642

2015

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Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders

Clinical genetics, 2016-02, Vol.89 (2), p.163-172

2016

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Burden of copy number variation in common variable immunodeficiency

Clinical and experimental immunology, 2014-07, Vol.177 (1), p.269-271

2014

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Analysing biological pathways in genome-wide association studies

Nature reviews. Genetics, 2010-12, Vol.11 (12), p.843

2010

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Crohn's Disease and Genetic Hitchhiking at IBD5

Molecular biology and evolution, 2012-01, Vol.29 (1), p.101-111

2012

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Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations

Drug and alcohol dependence, 2013-01, Vol.127 (1), p.122-128

2013

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Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies

Journal of medical genetics, 2009-08, Vol.46 (8), p.553-jmg

2009

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Extended haplotype association study in Crohn's disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3

Genes and immunity, 2013-07, Vol.14 (5), p.310-316

2013

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The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females

Genes and immunity, 2015-10, Vol.16 (7), p.495-498

2015

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Remapping the type I diabetes association of the CTLA4 locus

Genes and immunity, 2009-12, Vol.10 Suppl 1 (S1), p.S27-S32

2009

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Contribution of ADAM33 polymorphisms to the population risk of asthma

Thorax, 2005-04, Vol.60 (4), p.274-276

2005

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OP0282 The Association of PTPN22 RS2476601 with Juvenile Idiopathic Arthritis is Specific to Females

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.179-179

2015

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IL-13-dependent autocrine signaling mediates altered responsiveness of IgE-sensitized airway smooth muscle

American journal of physiology. Lung cellular and molecular physiology, 2002-03, Vol.282 (3), p.520-L528

2002

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Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease

Genes and immunity, 2013-10, Vol.14 (7), p.447-452

2013

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Imaging patterns of brain development and their relationship to cognition

Cerebral cortex (New York, N.Y. 1991), 2015-06, Vol.25 (6), p.1676-1684

2015

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The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

Mucosal immunology, 2011-05, Vol.4 (3), p.314-324

2011

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The type I diabetes association of the IL2RA locus

Genes and immunity, 2009-12, Vol.10 Suppl 1 (S1), p.S42-S48

2009

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Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity

International Journal of Obesity, 2012-01, Vol.36 (1), p.80-83

2012

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876 Loss-of-function EGFR mutation in bartter syndrome with neonatal epithelial autoinflammation

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S150-S150

2023

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Syndromes and the study of autism

Neurotoxicology and teratology, 2013-05, Vol.37, p.79-79

2013

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Role and regulation of interleukin-1 molecules in pro-asthmatic sensitised airway smooth muscle

The European respiratory journal, 2004-10, Vol.24 (4), p.559-567

2004

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Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Human molecular genetics, 2018-09, Vol.27 (18), p.3233-3245

2018

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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients

Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy

Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders

Burden of copy number variation in common variable immunodeficiency

Analysing biological pathways in genome-wide association studies

Crohn's Disease and Genetic Hitchhiking at IBD5

Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations

Association of RASGRP1 with type 1 diabetes is revealed by combined follow-up of two genome-wide studies

Extended haplotype association study in Crohn's disease identifies a novel, Ashkenazi Jewish-specific missense mutation in the NF-κB pathway gene, HEATR3

The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females

Remapping the type I diabetes association of the CTLA4 locus

Contribution of ADAM33 polymorphisms to the population risk of asthma

OP0282 The Association of PTPN22 RS2476601 with Juvenile Idiopathic Arthritis is Specific to Females

IL-13-dependent autocrine signaling mediates altered responsiveness of IgE-sensitized airway smooth muscle

Targeted resequencing identifies defective variants of decoy receptor 3 in pediatric-onset inflammatory bowel disease

Imaging patterns of brain development and their relationship to cognition

The ubiquitin ligase adaptor Ndfip1 regulates T cell-mediated gastrointestinal inflammation and inflammatory bowel disease susceptibility

The type I diabetes association of the IL2RA locus

Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity

876 Loss-of-function EGFR mutation in bartter syndrome with neonatal epithelial autoinflammation

Syndromes and the study of autism

Role and regulation of interleukin-1 molecules in pro-asthmatic sensitised airway smooth muscle

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

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