Zunyan Dai PhD
Research
Publications
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Caution in interpretation of disease causality for heterozygous loss-of-function variants in the MYH8 gene associated with autosomal dominant disorder.
Eur J Med Genet Volume: 60 Page(s): 312 - 316
06/01/2017 Authors: Dai Z; Whitt Z; Mighion LC; Pontoglio A; Bean LJH; Colombo R; Hegde M -
Paternal duplication of the 11p15 centromeric imprinting control region is associated with increased expression of CDKN1C in a child with Russell-Silver syndrome.
Am J Med Genet A Volume: 167A Page(s): 3229 - 3233
12/01/2015 Authors: Xue Y; Shankar S; Cornell K; Dai Z; Wang C-E; Rudd MK; Coffee B -
Next-Generation Sequencing as a Diagnostic Tool for Hereditary Breast and Ovarian Cancer
Volume: 17 Page(s): 761 - 761
11/01/2015 Authors: Dai Z; Bean LJ; Collins C; Askree SH; Alexander JJ; Hegde M; Tanner A -
Chromothriptic cure of WHIM syndrome.
Cell Volume: 160 Page(s): 686 - 699
02/12/2015 Authors: McDermott DH; Gao J-L; Liu Q; Siwicki M; Martens C; Jacobs P; Velez D; Yim E; Bryke CR; Hsu N -
Haploinsufficiency of HDAC4 does not cause intellectual disability in all affected individuals.
Am J Med Genet A Volume: 164A Page(s): 1826 - 1829
07/01/2014 Authors: Wheeler PG; Huang D; Dai Z -
Incidental Copy Number Findings in Targeted Microarray Gene Testing Explain Clinical Phenotypes
Volume: 142
01/01/2014 Authors: Dai Z; Bunke B; Kunig D; Vena NA; Bean LJH; Collins C; Coffee B; Rudd MK -
Deletions of the PRKAR1A locus at 17q24.2-q24.3 in Carney complex: genotype-phenotype correlations and implications for genetic testing.
J Clin Endocrinol Metab Volume: 99 Page(s): E183 - E188
01/01/2014 Authors: Salpea P; Horvath A; London E; Faucz FR; Vetro A; Levy I; Gourgari E; Dauber A; Holm IA; Morrison PJ -
Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas.
Mol Cytogenet Volume: 5 Page(s): 44
12/03/2012 Authors: Dai Z; Kelly JC; Meloni-Ehrig A; Slovak ML; Boles D; Christacos NC; Bryke CR; Schonberg SA; Otani-Rosa J; Pan Q -
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites.
Eur J Hum Genet Volume: 19 Page(s): 1045 - 1051
10/01/2011 Authors: Chong JX; Oktay AA; Dai Z; Swoboda KJ; Prior TW; Ober C -
Flavopiridol pharmacogenetics: clinical and functional evidence for the role of SLCO1B1/OATP1B1 in flavopiridol disposition.
PLoS One Volume: 5 Page(s): e13792
11/01/2010 Authors: Ni W; Ji J; Dai Z; Papp A; Johnson AJ; Ahn S; Farley KL; Lin TS; Dalton JT; Li X