M Lacher

Summary

Affiliation: University of Munich
Country: Germany

Publications

  1. ncbi Association of a CXCL9 polymorphism with pediatric Crohn's disease
    Martin Lacher
    Dr von Haunersches Kinderspital, Pediatric Surgical Clinic, Research Laboratories, Ludwig Maximilians University of Munich, Lindwurmstr 4, D 80337 Munich, Germany
    Biochem Biophys Res Commun 363:701-7. 2007
  2. ncbi Nuclear pregnane X receptor single nucleotide polymorphism (-25385C/T) is not associated with inflammatory bowel disease in pediatric patients
    Martin Lacher
    Department of Pediatric Surgery, Dr von Haunersches Kinderspital, Ludwig Maximilians University of Munich, Lindwurmstr, Munich, Germany
    J Pediatr Gastroenterol Nutr 49:147-50. 2009
  3. ncbi Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children
    Martin Lacher
    Department of Paediatric Surgery, Research Laboratories, University of Munich, Munich, Germany
    Acta Paediatr 98:1835-40. 2009
  4. ncbi Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children
    M Lacher
    Department of Paediatric Surgery, Research Laboratories, University of Munich, Munich, Germany
    Acta Paediatr 99:727-33. 2010
  5. ncbi Early and long term outcome in children with esophageal atresia treated over the last 22 years
    M Lacher
    Pediatric Surgical Clinic, Dr von Haunersches Kinderspital, Ludwig Maximilian University, Munchen, Germany
    Klin Padiatr 222:296-301. 2010
  6. ncbi NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease
    Martin Lacher
    Department of Pediatric Surgery, Research Laboratories, University of Munich, D 80337 Munich, Germany
    J Pediatr Surg 45:1591-7. 2010
  7. ncbi Hirschsprung-associated enterocolitis develops independently of NOD2 variants
    Martin Lacher
    Department of Pediatric Surgery, Research Laboratories, University of Munich, D 80337 Munich, Germany
    J Pediatr Surg 45:1826-31. 2010
  8. ncbi The treatment of supracondylar humeral fractures with elastic stable intramedullary nailing (ESIN) in children
    Martin Lacher
    Department of Pediatric Surgery, University of Munich, Munich, Germany
    J Pediatr Orthop 31:33-8. 2011
  9. ncbi Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease
    Jurgen Glas
    Department of Medicine II, Grosshadern, Ludwig Maximilians University, Munich, Germany
    Am J Gastroenterol 104:1737-44. 2009

Detail Information

Publications9

  1. ncbi Association of a CXCL9 polymorphism with pediatric Crohn's disease
    Martin Lacher
    Dr von Haunersches Kinderspital, Pediatric Surgical Clinic, Research Laboratories, Ludwig Maximilians University of Munich, Lindwurmstr 4, D 80337 Munich, Germany
    Biochem Biophys Res Commun 363:701-7. 2007
    ..1 versus 13.8 years). This is the first report of inverse association of the CXCL9 77147452G-->A polymorphism with pediatric CD. Our data may contribute to a better understanding of the pathophysiology underlying CD...
  2. ncbi Nuclear pregnane X receptor single nucleotide polymorphism (-25385C/T) is not associated with inflammatory bowel disease in pediatric patients
    Martin Lacher
    Department of Pediatric Surgery, Dr von Haunersches Kinderspital, Ludwig Maximilians University of Munich, Lindwurmstr, Munich, Germany
    J Pediatr Gastroenterol Nutr 49:147-50. 2009
    ..Studies in adults characterized the role of the pregnane X receptor (PXR) in the pathophysiology of inflammatory bowel disease (IBD) with conflicting results; pediatric studies are still lacking...
  3. ncbi Autophagy 16-like 1 rs2241880 G allele is associated with Crohn's disease in German children
    Martin Lacher
    Department of Paediatric Surgery, Research Laboratories, University of Munich, Munich, Germany
    Acta Paediatr 98:1835-40. 2009
    ..Therefore, we evaluated this polymorphism in early-onset CD in 152 children and 253 controls and for the first time determined ATG16L1 colonic expression in German CD children...
  4. ncbi Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German children
    M Lacher
    Department of Paediatric Surgery, Research Laboratories, University of Munich, Munich, Germany
    Acta Paediatr 99:727-33. 2010
    ..We investigated the association of rs11209026 (p.Arg381Gln) and rs7517847 (c.799-3588T>G) into German paediatric inflammatory bowel disease (IBD) patients and analysed IL23R transcriptional activity in colonic tissues...
  5. ncbi Early and long term outcome in children with esophageal atresia treated over the last 22 years
    M Lacher
    Pediatric Surgical Clinic, Dr von Haunersches Kinderspital, Ludwig Maximilian University, Munchen, Germany
    Klin Padiatr 222:296-301. 2010
    ..The survival of infants born with esophageal atresia (EA) is > 90% at present. The purpose of this study was to evaluate early complications and long term outcome in children with EA treated at our institution...
  6. ncbi NOD2 mutations predict the risk for surgery in pediatric-onset Crohn's disease
    Martin Lacher
    Department of Pediatric Surgery, Research Laboratories, University of Munich, D 80337 Munich, Germany
    J Pediatr Surg 45:1591-7. 2010
    ..The aim of this study was to investigate the effect of these mutations on disease manifestation and the risk of surgery in a cohort of German childhood-onset CD patients...
  7. ncbi Hirschsprung-associated enterocolitis develops independently of NOD2 variants
    Martin Lacher
    Department of Pediatric Surgery, Research Laboratories, University of Munich, D 80337 Munich, Germany
    J Pediatr Surg 45:1826-31. 2010
    ....
  8. ncbi The treatment of supracondylar humeral fractures with elastic stable intramedullary nailing (ESIN) in children
    Martin Lacher
    Department of Pediatric Surgery, University of Munich, Munich, Germany
    J Pediatr Orthop 31:33-8. 2011
    ..Therefore, the aim of the study was to assess both radiologic and functional outcome of supracondylar humeral fractures treated by elastic stable intramedullary nailing (ESIN) in a large pediatric cohort...
  9. ncbi Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease
    Jurgen Glas
    Department of Medicine II, Grosshadern, Ludwig Maximilians University, Munich, Germany
    Am J Gastroenterol 104:1737-44. 2009
    ..Given the increased prevalence of inflammatory bowel disease (IBD) among celiac disease patients, we investigated the possible involvement of these SNPs in IBD...