|
Tatara, A M; Wurster, S; Lockworth, C R et al. (2018) Immunosuppressed Adult Zebrafish Model of Mucormycosis. Antimicrob Agents Chemother 62:
|
|
Chu, Derrick M; Ma, Jun; Prince, Amanda L et al. (2017) Maturation of the infant microbiome community structure and function across multiple body sites and in relation to mode of delivery. Nat Med 23:314-326
|
|
Chu, Derrick M; Antony, Kathleen M; Ma, Jun et al. (2016) The early infant gut microbiome varies in association with a maternal high-fat diet. Genome Med 8:77
|
|
James, Regis A; Campbell, Ian M; Chen, Edward S et al. (2016) A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnostics. Genome Med 8:13
|
|
Campbell, Ian M; Gambin, Tomasz; Jhangiani, Shalini et al. (2016) Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses. Hum Mutat 37:231-234
|
|
Boone, Philip M; Chan, Yiu Man; Hunter, Jill V et al. (2016) Increased bone turnover, osteoporosis, progressive tibial bowing, fractures, and scoliosis in a patient with a final-exon SATB2 frameshift mutation. Am J Med Genet A 170:3028-3032
|
|
Fleet, Tiffany; Stashi, Erin; Zhu, Bokai et al. (2016) Genetic and Environmental Models of Circadian Disruption Link SRC-2 Function to Hepatic Pathology. J Biol Rhythms 31:443-60
|
|
Cadwell, Cathryn R; Palasantza, Athanasia; Jiang, Xiaolong et al. (2016) Electrophysiological, transcriptomic and morphologic profiling of single neurons using Patch-seq. Nat Biotechnol 34:199-203
|
|
Boone, Philip M; Yuan, Bo; Gu, Shen et al. (2016) Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Mol Genet Genomic Med 4:77-94
|
|
Gu, Shen; Yuan, Bo; Campbell, Ian M et al. (2015) Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3. Hum Mol Genet 24:4061-77
|
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