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European Journal of Human Genetics : EJHG|January 28, 2016
Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstructionIvana Matera, Marta Rusmini, Yiran Guo, et al.
Schizophrenia Research|October 3, 2008
Telomerase levels in schizophrenia: a preliminary studyBarbara Porton, Lynn E Delisi, Hilary C Bertisch, et al.
Human Molecular Genetics|December 17, 2013
Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and miceYaqun Zou, Daniela Zwolanek, Yayoi Izu, et al.
BMC Proceedings|May 10, 2008
Mixture modeling of microarray gene expression dataYang Yang, Adam P Tashman, Jung Yeon Lee, et al.
Neurochemical Research|March 8, 2007
Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populationsAbraham M Brown, Derek Gordon, Hsinhwa Lee, et al.
Human Immunology|May 16, 2006
Disease relevant HLA class II alleles isolated by genotypic, haplotypic, and sequence analysis in North American Caucasians with pemphigus vulgarisErica Lee, Katherine A Lendas, Selwyn Chow, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
TNFSF13 insufficiency disrupts human colonic epithelial cell-mediated B cell differentiationXianghui Ma, Noor Dawany, Ayano Kondo, et al.
Genomics|August 12, 2008
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutationLynn Petukhova, Edilson C Sousa, Amalia Martinez-Mir, et al.
Pediatric Research|February 1, 2012
IL-18R1 and IL-18RAP SNPs may be associated with bronchopulmonary dysplasia in African-American infantsJoanna Floros, Douglas Londono, Derek Gordon, et al.
Human Reproduction (Oxford, England)|July 26, 2015
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functionsJulia Spencer Barthold, Yanping Wang, Thomas F Kolon, et al.
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