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Hypophosphatemia during continuous hemodialysis is associated with prolonged respiratory failure in patients with acute kidney injury

Nephrology, dialysis, transplantation, 2011-11, Vol.26 (11), p.3508-3514

2011

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European evidence-based Consensus on the diagnosis and management of ulcerative colitis: Definitions and diagnosis

Journal of Crohn's and colitis, 2008-03, Vol.2 (1), p.1-23

2008

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Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles

Human molecular genetics, 2019-06, Vol.28 (12), p.2078-2092

2019

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High Rates of Subsequent Asymptomatic Sexually Transmitted Infections and Risky Sexual Behavior in Patients Initially Presenting With Primary Human Immunodeficiency Virus-1 Infection

Clinical infectious diseases, 2018-03, Vol.66 (5), p.735-742

2018

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Metagenomic Virome Sequencing in Living Donor and Recipient Kidney Transplant Pairs Revealed JC Polyomavirus Transmission

Clinical infectious diseases, 2019-08, Vol.69 (6), p.987-994

2019

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Disrupted development and integrity of frontal white matter in patients treated for pediatric medulloblastoma

Neuro-oncology (Charlottesville, Va.), 2017-10, Vol.19 (10), p.1408-1418

2017

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Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study

European heart journal, 2014-08, Vol.35 (31), p.2115-2122

2014

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Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes

Brain (London, England : 1878), 2023-11, Vol.146 (11), p.4766-4783

2023

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Human molecular genetics, 2009-10, Vol.18 (19), p.3626-3631

2009

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Y-chromosomal variation in sub-Saharan Africa: insights into the history of Niger-Congo groups

Molecular biology and evolution, 2011-03, Vol.28 (3), p.1255-1269

2011

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Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3

Carcinogenesis (New York), 2014-02, Vol.35 (2), p.315-323

2014

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Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International journal of epidemiology, 2020-06, Vol.49 (3), p.1022-1031

2020

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Detailed Transcriptional Landscape of Peripheral Blood Points to Increased Neutrophil Activation in Treatment-Naïve Inflammatory Bowel Disease

Journal of Crohn's and colitis, 2022, Vol.16 (7), p.1097-1109

2022

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Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

European heart journal, 2011-01, Vol.32 (2), p.158-168

2011

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ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy

Brain (London, England : 1878), 2023-04, Vol.146 (4), p.1357-1372

2023

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The impact of sex in primary glomerulonephritis

Nephrology, dialysis, transplantation, 2008-07, Vol.23 (7), p.2247-2253

2008

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The fate of systemic blood pressure in patients after effectively stented coarctation

European heart journal, 2006-05, Vol.27 (9), p.1100-1105

2006

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Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR)

Human molecular genetics, 2003-12, Vol.12 (24), p.3207-3214

2003

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COGENT (COlorectal cancer GENeTics) revisited

Mutagenesis, 2012-03, Vol.27 (2), p.143-151

Houlston, Richard S.

2012

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Cost-effectiveness of dual-chamber pacemaker therapy: does single lead VDD pacing reduce treatment costs of atrioventricular block?

European heart journal, 2001-01, Vol.22 (2), p.174-180

2001

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The Continued Emergence of Drug-Resistant Streptococcus pneumoniae in the United States: An Update from the Centers for Disease Control and Prevention's Pneumococcal Sentinel Surveillance System

The Journal of infectious diseases, 1996-11, Vol.174 (5), p.986-993

1996

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Mutation screening by denaturing gradient gel electrophoresis in north American patients with acute intermittent porphyria

Clinical chemistry (Baltimore, Md.), 1998-08, Vol.44 (8), p.1766-1768

1998

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Percentage of hypochromic red blood cells as predictor of erythropoietic and iron response after i.v. iron supplementation in maintenance haemodialysis patients

Nephrology, dialysis, transplantation, 1997-06, Vol.12 (6), p.1173-1181

1997

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Hypophosphatemia during continuous hemodialysis is associated with prolonged respiratory failure in patients with acute kidney injury

European evidence-based Consensus on the diagnosis and management of ulcerative colitis: Definitions and diagnosis

Construction and benchmarking of a multi-ethnic reference panel for the imputation of HLA class I and II alleles

High Rates of Subsequent Asymptomatic Sexually Transmitted Infections and Risky Sexual Behavior in Patients Initially Presenting With Primary Human Immunodeficiency Virus-1 Infection

Metagenomic Virome Sequencing in Living Donor and Recipient Kidney Transplant Pairs Revealed JC Polyomavirus Transmission

Disrupted development and integrity of frontal white matter in patients treated for pediatric medulloblastoma

Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study

Models of KPTN-related disorder implicate mTOR signalling in cognitive and overgrowth phenotypes

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance

Y-chromosomal variation in sub-Saharan Africa: insights into the history of Niger-Congo groups

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

Detailed Transcriptional Landscape of Peripheral Blood Points to Increased Neutrophil Activation in Treatment-Naïve Inflammatory Bowel Disease

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy

The ACTTION–APS–AAPM Pain Taxonomy (AAAPT) Multidimensional Approach to Classifying Acute Pain Conditions

The impact of sex in primary glomerulonephritis

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

The fate of systemic blood pressure in patients after effectively stented coarctation

Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR)

COGENT (COlorectal cancer GENeTics) revisited

Cost-effectiveness of dual-chamber pacemaker therapy: does single lead VDD pacing reduce treatment costs of atrioventricular block?

The Continued Emergence of Drug-Resistant Streptococcus pneumoniae in the United States: An Update from the Centers for Disease Control and Prevention's Pneumococcal Sentinel Surveillance System

Mutation screening by denaturing gradient gel electrophoresis in north American patients with acute intermittent porphyria

Percentage of hypochromic red blood cells as predictor of erythropoietic and iron response after i.v. iron supplementation in maintenance haemodialysis patients

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