RICHARD KELLERMAYER to Phenotype
This is a "connection" page, showing publications RICHARD KELLERMAYER has written about Phenotype.
Connection Strength
0.817
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Genetic drift. "Omics"as the filtering gateway between environment and phenotype: The inflammatory bowel diseases example. Am J Med Genet A. 2010 Dec; 152A(12):3022-5.
Score: 0.182
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Genetic drift. Physiologic noise obscures genotype-phenotype correlations. Am J Med Genet A. 2007 Jun 15; 143A(12):1306-7.
Score: 0.143
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Exome Sequencing Implicates DGKZ , ESRRA , and GXYLT1 for Modulating Granuloma Formation in Crohn Disease. J Pediatr Gastroenterol Nutr. 2023 09 01; 77(3):354-357.
Score: 0.109
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Letter: fulminant-onset complicated inflammatory bowel disease (IBD)-a unique subtype? Aliment Pharmacol Ther. 2023 05; 57(10):1192-1193.
Score: 0.108
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Parental Education May Differentially Impact Pediatric Inflammatory Bowel Disease Phenotype Risk. Inflamm Bowel Dis. 2020 06 18; 26(7):1068-1076.
Score: 0.088
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Unique Inflammatory Bowel Disease Phenotype of Pediatric Primary Sclerosing Cholangitis: A Single-Center Study. J Pediatr Gastroenterol Nutr. 2017 10; 65(4):404-409.
Score: 0.073
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The versatile RECQL4. Genet Med. 2006 Apr; 8(4):213-6.
Score: 0.033
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NOD2 Polymorphisms May Direct a Crohn Disease Phenotype in Patients With Very Early-Onset Inflammatory Bowel Disease. J Pediatr Gastroenterol Nutr. 2023 12 01; 77(6):748-752.
Score: 0.027
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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.
Score: 0.020
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Genotype-phenotype correlations in MYCN-related Feingold syndrome. Hum Mutat. 2008 Sep; 29(9):1125-32.
Score: 0.010
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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.
Score: 0.009
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CYLD mutations underlie Brooke-Spiegler, familial cylindromatosis, and multiple familial trichoepithelioma syndromes. Clin Genet. 2006 Sep; 70(3):246-9.
Score: 0.008
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Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation. Pathol Oncol Res. 2005; 11(2):82-6.
Score: 0.008