Connection

RICHARD KELLERMAYER to Female

This is a "connection" page, showing publications RICHARD KELLERMAYER has written about Female.
Connection Strength

0.806
  1. MYO5B and the Polygenic Landscape of Very Early-Onset Inflammatory Bowel Disease in an Ethnically Diverse Population. Inflamm Bowel Dis. 2025 01 06; 31(1):189-199.
    View in: PubMed
    Score: 0.035
  2. Ultrasound was critical in the diagnosis of a late presentation enteric duplication cyst. J Pediatr Gastroenterol Nutr. 2024 Aug; 79(2):446-448.
    View in: PubMed
    Score: 0.034
  3. Routine Histology-Based Diagnosis of CMV Colitis Was Rare in Pediatric Patients. J Pediatr Gastroenterol Nutr. 2022 10 01; 75(4):462-465.
    View in: PubMed
    Score: 0.029
  4. Parental Education May Differentially Impact Pediatric Inflammatory Bowel Disease Phenotype Risk. Inflamm Bowel Dis. 2020 06 18; 26(7):1068-1076.
    View in: PubMed
    Score: 0.026
  5. Fecal microbiota transplantation in a toddler after heart transplant was a safe and effective treatment for recurrent Clostridiodes difficile infection: A case report. Pediatr Transplant. 2020 02; 24(1):e13598.
    View in: PubMed
    Score: 0.024
  6. Diagnostic delay and colectomy risk in pediatric ulcerative colitis. J Pediatr Surg. 2020 Mar; 55(3):403-405.
    View in: PubMed
    Score: 0.023
  7. Giant Cell [Granulomatous] Gastritis in Left-sided Paediatric Ulcerative Colitis. J Crohns Colitis. 2019 03 26; 13(3):396-397.
    View in: PubMed
    Score: 0.023
  8. Right-sided Colonic Juvenile Polyp [Polyps] in Paediatric Primary Sclerosing Cholangitis Patients. J Crohns Colitis. 2018 Nov 15; 12(11):1375-1376.
    View in: PubMed
    Score: 0.023
  9. Academic Stress May Contribute to the Onset of Pediatric Inflammatory Bowel Diseases. J Pediatr Gastroenterol Nutr. 2018 10; 67(4):e73-e76.
    View in: PubMed
    Score: 0.023
  10. Compliance With Fecal Calprotectin Testing in Pediatric Patients With Inflammatory Bowel Disease. J Pediatr Gastroenterol Nutr. 2018 06; 66(6):932-933.
    View in: PubMed
    Score: 0.022
  11. Granulomatous Upper Gastrointestinal Inflammation in Pediatric Ulcerative Colitis. J Pediatr Gastroenterol Nutr. 2018 04; 66(4):620-623.
    View in: PubMed
    Score: 0.022
  12. Composition and function of the pediatric colonic mucosal microbiome in untreated patients with ulcerative colitis. Gut Microbes. 2016 09 02; 7(5):384-96.
    View in: PubMed
    Score: 0.019
  13. Colonic Mucosal Epigenome and Microbiome Development in Children and Adolescents. J Immunol Res. 2016; 2016:9170162.
    View in: PubMed
    Score: 0.019
  14. The forgotten yeast model of Hailey-Hailey disease. Int J Dermatol. 2016 Mar; 55(3):e169-70.
    View in: PubMed
    Score: 0.019
  15. Burdening questions about Clostridium difficile in pediatric inflammatory bowel diseases. J Pediatr Gastroenterol Nutr. 2015 Apr; 60(4):421-2.
    View in: PubMed
    Score: 0.018
  16. Serial fecal microbiota transplantation alters mucosal gene expression in pediatric ulcerative colitis. Am J Gastroenterol. 2015 Apr; 110(4):604-6.
    View in: PubMed
    Score: 0.018
  17. Allopurinol: a useful adjunct to thiopurine therapy for pediatric ulcerative colitis in the biologic era. J Pediatr Gastroenterol Nutr. 2014 Jul; 59(1):22-4.
    View in: PubMed
    Score: 0.017
  18. DNA methylation-associated colonic mucosal immune and defense responses in treatment-na?ve pediatric ulcerative colitis. Epigenetics. 2014 Aug; 9(8):1131-7.
    View in: PubMed
    Score: 0.017
  19. Duration of disease may predict response to infliximab in pediatric ulcerative colitis. J Clin Gastroenterol. 2014 Mar; 48(3):248-52.
    View in: PubMed
    Score: 0.017
  20. Mucosal mast cell counts in pediatric eosinophilic gastrointestinal disease. Pediatr Allergy Immunol. 2014 Feb; 25(1):94-5.
    View in: PubMed
    Score: 0.016
  21. Prenatal methyl-donor supplementation augments colitis in young adult mice. PLoS One. 2013; 8(8):e73162.
    View in: PubMed
    Score: 0.016
  22. Hurdles for epigenetic disease associations from peripheral blood leukocytes. Inflamm Bowel Dis. 2013 Apr; 19(5):E66-7.
    View in: PubMed
    Score: 0.016
  23. Human metastable epiallele candidates link to common disorders. Epigenetics. 2013 Feb; 8(2):157-63.
    View in: PubMed
    Score: 0.015
  24. Microbiota separation and C-reactive protein elevation in treatment-na?ve pediatric granulomatous Crohn disease. J Pediatr Gastroenterol Nutr. 2012 Sep; 55(3):243-50.
    View in: PubMed
    Score: 0.015
  25. Maternal micronutrients can modify colonic mucosal microbiota maturation in murine offspring. Gut Microbes. 2012 Sep-Oct; 3(5):426-33.
    View in: PubMed
    Score: 0.015
  26. Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel diseases. Inflamm Bowel Dis. 2012 Dec; 18(12):2334-41.
    View in: PubMed
    Score: 0.014
  27. SMAD4 haploinsufficiency associates with augmented colonic inflammation in select humans and mice. Ann Clin Lab Sci. 2012; 42(4):401-8.
    View in: PubMed
    Score: 0.014
  28. Congenital tufting enteropathy in the era of molecular genetics. J Pediatr Gastroenterol Nutr. 2011 Sep; 53(3):355.
    View in: PubMed
    Score: 0.014
  29. Maternal methyl-donor supplementation induces prolonged murine offspring colitis susceptibility in association with mucosal epigenetic and microbiomic changes. Hum Mol Genet. 2011 May 01; 20(9):1687-96.
    View in: PubMed
    Score: 0.013
  30. Assessment of DNA methylation at the interferon regulatory factor 5 (IRF5) promoter region in inflammatory bowel diseases. Int J Colorectal Dis. 2010 May; 25(5):553-6.
    View in: PubMed
    Score: 0.012
  31. Further evidence for EpCAM as the gene for congenital tufting enteropathy. Am J Med Genet A. 2010 Jan; 152A(1):222-4.
    View in: PubMed
    Score: 0.012
  32. A cryptic unbalanced translocation resulting in del 13q and dup 15q. Am J Med Genet A. 2008 Oct 01; 146A(19):2570-3.
    View in: PubMed
    Score: 0.011
  33. Steroid responsive eosinophilic gastric outlet obstruction in a child. World J Gastroenterol. 2008 Apr 14; 14(14):2270-1.
    View in: PubMed
    Score: 0.011
  34. Clinical challenges and images in GI. Aortitis as a rare complication of Crohn's disease. Gastroenterology. 2008 Mar; 134(3):668, 898.
    View in: PubMed
    Score: 0.011
  35. Cytomegalovirus esophagitis preceding the diagnosis of systemic lupus erythematosus. Endoscopy. 2007 Feb; 39 Suppl 1:E218.
    View in: PubMed
    Score: 0.010
  36. Upper gastrointestinal malformations in Coffin-Siris syndrome. Am J Med Genet A. 2007 Jul 01; 143A(13):1519-21.
    View in: PubMed
    Score: 0.010
  37. Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation. Am J Med Genet A. 2005 Dec 15; 139(3):234-5.
    View in: PubMed
    Score: 0.009
  38. [The first genetically supported case of chronic benign pemphigus (Hailey-Hailey disease in Hungary]. Orv Hetil. 2005 Sep 11; 146(37):1933-5.
    View in: PubMed
    Score: 0.009
  39. Clinical presentation of parvovirus B19 infection in children with aplastic crisis. Pediatr Infect Dis J. 2003 Dec; 22(12):1100-1.
    View in: PubMed
    Score: 0.008
  40. IFIH1 loss-of-function variants contribute to very early-onset inflammatory bowel disease. Hum Genet. 2021 Sep; 140(9):1299-1312.
    View in: PubMed
    Score: 0.007
  41. Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Am J Hum Genet. 2021 03 04; 108(3):431-445.
    View in: PubMed
    Score: 0.007
  42. Variation in Care in the Management of Children With Crohn's Disease: Data From a Multicenter Inception Cohort Study. Inflamm Bowel Dis. 2019 06 18; 25(7):1208-1217.
    View in: PubMed
    Score: 0.006
  43. Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation. Gastroenterology. 2019 06; 156(8):2254-2265.e3.
    View in: PubMed
    Score: 0.006
  44. Prioritizing Crohn's disease genes by integrating association signals with gene expression implicates monocyte subsets. Genes Immun. 2019 09; 20(7):577-588.
    View in: PubMed
    Score: 0.006
  45. Age-of-diagnosis dependent ileal immune intensification and reduced alpha-defensin in older versus younger pediatric Crohn Disease patients despite already established dysbiosis. Mucosal Immunol. 2019 03; 12(2):491-502.
    View in: PubMed
    Score: 0.006
  46. The Effect of Early-Life Environmental Exposures on Disease Phenotype and Clinical Course of Crohn's Disease in Children. Am J Gastroenterol. 2018 10; 113(10):1524-1529.
    View in: PubMed
    Score: 0.006
  47. Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease. Inflamm Bowel Dis. 2018 01 18; 24(2):346-360.
    View in: PubMed
    Score: 0.005
  48. Unique Inflammatory Bowel Disease Phenotype of Pediatric Primary Sclerosing Cholangitis: A Single-Center Study. J Pediatr Gastroenterol Nutr. 2017 10; 65(4):404-409.
    View in: PubMed
    Score: 0.005
  49. Fundic Gland Polyps in the Pediatric Population: Clinical and Histopathologic Studies. Pediatr Dev Pathol. 2017 Nov-Dec; 20(6):482-489.
    View in: PubMed
    Score: 0.005
  50. Prediction of complicated disease course for children newly diagnosed with Crohn's disease: a multicentre inception cohort study. Lancet. 2017 04 29; 389(10080):1710-1718.
    View in: PubMed
    Score: 0.005
  51. Mucosal Expression of Type 2 and Type 17 Immune Response Genes Distinguishes Ulcerative Colitis From Colon-Only Crohn's Disease in Treatment-Naive Pediatric Patients. Gastroenterology. 2017 05; 152(6):1345-1357.e7.
    View in: PubMed
    Score: 0.005
  52. Evaluating the impact of infliximab use on surgical outcomes in pediatric Crohn's disease. J Pediatr Surg. 2016 May; 51(5):786-9.
    View in: PubMed
    Score: 0.005
  53. DNA Methylation Profiling in Inflammatory Bowel Disease Provides New Insights into Disease Pathogenesis. J Crohns Colitis. 2016 Jan; 10(1):77-86.
    View in: PubMed
    Score: 0.005
  54. Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. Gastroenterology. 2015 Nov; 149(6):1575-1586.
    View in: PubMed
    Score: 0.005
  55. Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping. PLoS One. 2015; 10(6):e0128074.
    View in: PubMed
    Score: 0.005
  56. Whole-exome sequencing reveals GPIHBP1 mutations in infantile colitis with severe hypertriglyceridemia. J Pediatr Gastroenterol Nutr. 2014 Jul; 59(1):17-21.
    View in: PubMed
    Score: 0.004
  57. Increased effectiveness of early therapy with anti-tumor necrosis factor-a vs an immunomodulator in children with Crohn's disease. Gastroenterology. 2014 Feb; 146(2):383-91.
    View in: PubMed
    Score: 0.004
  58. Season of conception in rural gambia affects DNA methylation at putative human metastable epialleles. PLoS Genet. 2010 Dec 23; 6(12):e1001252.
    View in: PubMed
    Score: 0.003
  59. Changes of orexin A plasma levels in girls with anorexia nervosa during eight weeks of realimentation. Int J Eat Disord. 2011 Sep; 44(6):547-52.
    View in: PubMed
    Score: 0.003
  60. Epigenomic profiling indicates a role for DNA methylation in early postnatal liver development. Hum Mol Genet. 2009 Aug 15; 18(16):3026-38.
    View in: PubMed
    Score: 0.003
  61. [Psychological aspects of presymptomatic diagnosis in Huntington disease]. Orv Hetil. 2008 Mar 30; 149(13):609-12.
    View in: PubMed
    Score: 0.003
  62. Premenstrual exacerbation in calcium ATPase disorders of the skin. J Eur Acad Dermatol Venereol. 2007 Mar; 21(3):412-3.
    View in: PubMed
    Score: 0.003
  63. High incidence of short rib-polydactyly syndrome type IV in a Hungarian Roma subpopulation. Am J Med Genet A. 2006 Dec 15; 140(24):2816-8.
    View in: PubMed
    Score: 0.003
  64. Presenile cataract: consider cholestanol. Arch Ophthalmol. 2006 Oct; 124(10):1490-2.
    View in: PubMed
    Score: 0.002
  65. CYLD mutations underlie Brooke-Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes. Clin Genet. 2006 Sep; 70(3):246-9.
    View in: PubMed
    Score: 0.002
  66. A novel frame shift mutation in the HMG box of the SRY gene in a patient with complete 46,XY pure gonadal dysgenesis. Diagn Mol Pathol. 2005 Sep; 14(3):159-63.
    View in: PubMed
    Score: 0.002
  67. Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation. Pathol Oncol Res. 2005; 11(2):82-6.
    View in: PubMed
    Score: 0.002
  68. Bigenic connexin mutations in a patient with hidrotic ectodermal dysplasia. Eur J Dermatol. 2005 Mar-Apr; 15(2):75-9.
    View in: PubMed
    Score: 0.002
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.