Assistant Professor, Pediatrics, Baylor College of Medicine
Pediatric Gastroenterology
Dr. Richard Kellermayer, MD
Richard Kellermayer works in the field of Pediatric Gastroenterology. He researched medicine at Baylor College of Medicine. Dr. Richard Kellermayer has written publications. He has 73 publications published with PubMed. The lastest publication is: 'Colonic Mucosal Epigenome and Microbiome Development in Children and Adolescents.'
Publications
- Detecting Microbial Dysbiosis Associated with Pediatric Crohn Disease Despite the High Variability of the Gut Microbiota.
- Microbiome-Epigenome Interactions and the Environmental Origins of Inflammatory Bowel Diseases.
- Hyperlipasemia in Pediatric Inflammatory Bowel Diseases.
- Evaluating the impact of infliximab use on surgical outcomes in pediatric Crohn's Disease.
- Characterization of Genetic Loci That Affect Susceptibility to Inflammatory Bowel Diseases in African Americans.
- The forgotten yeast model of Hailey-Hailey Disease.
- DNA methylation-associated colonic mucosal immune and defense responses in treatment-naïve pediatric Ulcerative colitis.
- Increased effectiveness of early therapy with anti-tumor necrosis factor-α vs an immunomodulator in children with Crohn's Disease.
- Mucosal mast cell counts in pediatric eosinophilic gastrointestinal Disease.
- Allopurinol: a Useful Adjunct to Thiopurine Therapy for Pediatric Ulcerative Colitis in the Biologic Era.
- Prospects and challenges for Intestinal microbiome therapy in pediatric gastroIntestinal disorders.
- Clostridium difficile Infection in Newly Diagnosed Pediatric Inflammatory Bowel Disease in the Mid-Southern United States.
- Duration of Disease May Predict Response to Infliximab in Pediatric Ulcerative Colitis.
- Perianal Papillomatous Crohn's Disease in a Male Adolescent.
- Cellulose supplementation early in life ameliorates Colitis in adult mice.
- Hurdles for Epigenetic Disease Associations from Peripheral Blood Leukocytes.
- Human metastable epiallele candidates link to common disorders.
- Monotonous Diets Protect Against Acute Colitis in Mice: Epidemiologic and Therapeutic Implications.
- Maternal micronutrients can modify colonic mucosal microbiota maturation in murine offspring.
- Microbiota Separation and C-reactive Protein Elevation in Treatment-naïve Pediatric Granulomatous Crohn Disease.
- Genome-wide peripheral blood leukocyte DNA methylation microarrays identified a single association with inflammatory bowel Diseases.
- Microbiome Associations of Therapeutic Enteral Nutrition.
- Extracellular Ca(2+) sensing contributes to excess Ca(2+) accumulation and vacuolar fragmentation in a pmr1Delta mutant of S. cerevisiae.
- Clinical presentation of parvovirus B19 infection in children with aplastic crisis.
- The intracellular dissipation of cytosolic calcium following glucose re-addition to carbohydrate depleted Saccharomyces cerevisiae.
- Hailey-Hailey Disease and calcium: lessons from yeast.
- Alpha-thalassemia/mental retardation syndrome in a 45,X male.
- Bigenic connexin mutations in a patient with hidrotic ectodermal dysplasia.
- Hailey-Hailey Disease as an orthoDisease of PMR1 deficiency in Saccharomyces cerevisiae.
- A patient with Rothmund-Thomson syndrome and all features of RAPADILINO.
- A novel frame shift mutation in the HMG box of the SRY gene in a patient with complete 46,XY pure gonadal dysgenesis.
- Calcium and magnesium competitively influence the growth of a PMR1 deficient Saccharomyces cerevisiae strain.
- Vertebral defects in a patient with Feingold syndrome.
- Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation.
- Electrically induced gel-to-gel phase-transition in neurons.
- Aminoglycosides as potential pharmacogenetic agents in the treatment of Hailey-Hailey Disease.
- A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency.
- The versatile RECQL4.
- Probability in gene expression.
- Congenital chylothorax in Opitz G/BBB syndrome.
- Translational readthrough induction of pathogenic nonsense mutations.
- Autosomal-dominant calcium ATPase disorders.
- Expanding the clinical spectrum of MYCN-related Feingold syndrome.
- Hailey-Hailey Disease from a clinical perspective.
- Clinical challenges and images in GI. Aortitis as a rare complication of Crohn's Disease.
- Steroid responsive eosinophilic gastric outlet Obstruction in a child.
- Genotype-phenotype correlations in MYCN-related Feingold syndrome.
- A cryptic unbalanced translocation resulting in del 13q and dup 15q.
- Epigenomic profiling indicates a role for DNA methylation in early postnatal liver development.
- Further evidence for EpCAM as the gene for congenital tufting enteropathy.
- Assessment of DNA methylation at the interferon regulatory factor 5 (IRF5) promoter region in inflammatory bowel Diseases.
- Epigenetic maturation in colonic mucosa continues beyond infancy in mice.
- Genetic drift. "Omics"as the filtering gateway between environment and phenotype: The inflammatory bowel Diseases example.
- Season of conception in rural gambia affects DNA methylation at putative human metastable epialleles.
- Colonic mucosal DNA methylation, immune response, and microbiome patterns in Toll-like receptor 2-knockout mice.
- Maternal methyl-donor supplementation induces prolonged murine offspring Colitis susceptibility in association with mucosal epigenetic and microbiomic changes.
- The remarkable capacity for gut microbial and host interactions.
- Congenital tufting enteropathy in the era of molecular genetics.
- Changes of orexin A plasma levels in girls with anorexia nervosa during eight weeks of realimentation.
- Peri-appendiceal inflammation in an 8-year-old child with chronic Ulcerative colitis.
- Presenile cataract: consider cholestanol.
- High incidence of short rib-polydactyly syndrome type IV in a Hungarian Roma subpopulation.
- Lithium suppresses epidermal SERCA2 and PMR1 levels in the rat.
- Genetic drift. Physiologic noise obscures genotype-phenotype correlations.
- Upper gastroIntestinal malformations in Coffin-Siris syndrome.
- Cytomegalovirus esophagitis preceding the diagnosis of systemic lupus erythematosus.
- The Golgi apparatus plays a significant role in the maintenance of Ca2+ homeostasis in the vps33Delta vacuolar biogenesis mutant of Saccharomyces cerevisiae.
- The vacuolar Ca2+/H+ exchanger Vcx1p/Hum1p tightly controls cytosolic Ca2+ levels in S. cerevisiae.
- Mutations in the yeast Hsp40 chaperone protein Ydj1 cause defects in Axl1 biogenesis and pro-a-factor processing.
- Premenstrual exacerbation in calcium ATPase disorders of the skin.
- CYLD mutations underlie Brooke-Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes.
- Colonic Mucosal Epigenome and Microbiome Development in Children and Adolescents.
Procedures Preformed
- Colonoscopy, Proctosigmoidoscopy, and Sigmoidoscopy
Conditions Treated
- Anemia
- Cholecystitis and Gallstones
- Crohn's Disease (Regional Enteritis)
- Gastroesophageal Reflux Disease (GERD)
- View All
Doctors Specialties
- Pediatric Gastroenterology
Accepted Insurances
Education
-
Baylor College of Medicine -
University at Buffalo -
University of Pécs Medical School
Hospital
-
Texas Children's Hospital
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