Peter R Durie


Ontology type: schema:Person     


Person Info

NAME

Peter R

SURNAME

Durie

Publications in SciGraph latest 50 shown

  • 2017-02 Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease in NATURE GENETICS
  • 2016-03 Cystic fibrosis from the gastroenterologist's perspective in NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY
  • 2015-12 Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis in NATURE COMMUNICATIONS
  • 2014-02 Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbidities in HUMAN GENETICS
  • 2013-06 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis in NATURE GENETICS
  • 2012-05 Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis in NATURE GENETICS
  • 2011-12 Intussusception in Adults with Cystic Fibrosis: A Case Series with Review of the Literature in DIGESTIVE DISEASES AND SCIENCES
  • 2011-07 Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection in GENES & IMMUNITY
  • 2011-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 in NATURE GENETICS
  • 2011-01 Outcome in Cystic Fibrosis Liver Disease in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2009-12 Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results in HUMAN GENETICS
  • 2008-03 Distribution of CFTR mutations in Saguenay– Lac-Saint-Jean: proposal of a panel of mutations for population screening in GENETICS IN MEDICINE
  • 2005-12 The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis in HUMAN GENETICS
  • 2004-08 Analysis of Cystic Fibrosis Gener Product (CFTR) Function in Patients with Pancreas Divisum and Recurrent Acute Pancreatitis in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2003-08 Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis in HUMAN GENETICS
  • 2003-01 Mutations in SBDS are associated with Shwachman–Diamond syndrome in NATURE GENETICS
  • 2002-04 Fine mapping of the locus for Shwachman-Diamond syndrome at 7q11, identification of shared disease haplotypes, and exclusion of TPST1 as a candidate gene in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2000-12 Mutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 1999-08 Surface Hydrophobicity Is Increased in the Ileum and Proximal Colon of Cystic Fibrosis Mice in PEDIATRIC RESEARCH
  • 1999-06 Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 in NATURE GENETICS
  • 1999-04 Synergistic Effects of cAMP- and Calcium-Mediated Amylase Secretion in Isolated Pancreatic Acini from Cystic Fibrosis Mice in PEDIATRIC RESEARCH
  • 1998-10 Malignant myeloid transformation with isochromosome 7q in Shwachman–Diamond syndrome in LEUKEMIA
  • 1998-09 LONG-TERM MICROVASCULAR, BUT NOT MACROVASCULAR, DIABETIC COMPLICATIONS ARE COMMON IN CYSTIC FIBROSIS RELATED DIABETES MELLITUS in PEDIATRIC RESEARCH
  • 1996-08 Phenotypic Abnormalities in Long-Term Surviving Cystic Fibrosis Mice in PEDIATRIC RESEARCH
  • 1996-08 Exocrine Pancreatic Alterations in Long-Lived Surviving Cystic Fibrosis Mice in PEDIATRIC RESEARCH
  • 1996-05 Erratum: Modulation of disease severity in cystic f ibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor in NATURE GENETICS
  • 1996-03 Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor in NATURE GENETICS
  • 1992-08 Decline of Exocrine Pancreatic Function in Cystic Fibrosis Patients with Pancreatic Sufficiency in PEDIATRIC RESEARCH
  • 1990-05 INTESTINAL LACTULOSE PERMEABILITY REFLECTS EXOCRINE PANCREATIC DYSFUNCTION in PEDIATRIC RESEARCH
  • 1990-05 GASTROINTESTINAL MANIFESTATIONS OF CF PATIENTS CARRYING THE Δ F5O8 MUTATION in PEDIATRIC RESEARCH
  • 1987-04 TREATMENT OF DISTAL INTESTINAL OBSTRUCTION SYNDROME (DIOS) IN CYSTIC FIBROSIS (CF) WITH AN INTESTINAL LAVAGE SOLUTION in PEDIATRIC RESEARCH
  • 1986-03 Age-Related Alterations of Immunoreactive Pancreatic Cationic Trypsinogen in Sera from Cystic Fibrosis Patients with and without Pancreatic Insufficiency in PEDIATRIC RESEARCH
  • 1986-02 Behçet's syndrome involving the gastrointestinal tract — a diagnostic dilemma in childhood in PEDIATRIC RADIOLOGY
  • 1985-10 Altered PABA pharmacokinetics in cystic fibrosis in DIGESTIVE DISEASES AND SCIENCES
  • 1985-04 684 PANCREATIC FLUID SECRETION IN CYSTIC FIBROSIS (CF) in PEDIATRIC RESEARCH
  • 1984-04 PANCREATIC EXOCRINE FUNCTION IN ISLET CELL DYSPLASIA (ICD)AFTER 95% RESECTION in PEDIATRIC RESEARCH
  • 1984-04 PLASMA BENZOYL-TYROSYL-PABA TEST IN EVALUATING EXOCRINE PANCREATIC FUNCTION IN CF: A PHARMACOKINETIC APPROACH in PEDIATRIC RESEARCH
  • 1982-07 Evidence for a Primary Defect of Pancreatic HCO3− Secretion in Cystic Fibrosis in PEDIATRIC RESEARCH
  • 1981-10 Plasma Immunoreactive Pancreatic Cationic Trypsinogen in Cystic Fibrosis: a Sensitive Indicator of Exocrine Pancreatic Dysfunction in PEDIATRIC RESEARCH
  • 1981-04 542 CIRCULATING IMMUNOREACTIVE PANCREATIC CATIONIC AND ANIONIC TRYPSIN(OGEN) IN PANCREATIC INSUFFICIENCY in PEDIATRIC RESEARCH
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