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The Journal of Infectious Diseases|July 12, 2011
Genetic and functional evidence implicating DLL1 as the gene that influences susceptibility to visceral leishmaniasis at chromosome 6q27Michaela Fakiola, E Nancy Miller, Manal Fadl, et al.
Scientific Reports|January 10, 2018
Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 25, 2020
A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in BrazilLéa C Castellucci, Lucas Almeida, Svetlana Cherlin, et al.
Alcoholism, Clinical and Experimental Research|April 16, 2015
Brief report: genetics of alcoholic cirrhosis-GenomALC multinational studyJohn B Whitfield, Khairunnessa Rahman, Paul S Haber, et al.
Human Genetics|April 18, 2003
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetesRebecca C J Twells, Charles A Mein, Felicity Payne, et al.
Circulation. Cardiovascular Genetics|April 17, 2012
A common variant in the PTPN11 gene contributes to the risk of tetralogy of FallotJudith A Goodship, Darroch Hall, Ana Topf, et al.
BMC Proceedings|December 19, 2014
Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigreesHeike Bickeböller, Julia N Bailey, Joseph Beyene, et al.
Scientific Reports|November 4, 2017
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric refluxJohn M Darlow, Rebecca Darlay, Mark G Dobson, et al.
Journal of Medical Genetics|October 9, 2023
Genetic complexity of diagnostically unresolved Ehlers-Danlos syndromeAnthony M Vandersteen, Ruwan A Weerakkody, David A Parry, et al.
The British Journal of Dermatology|March 25, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populationsH Chen, J E A Common, R L Haines, et al.
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