Zhao H - Search Results

1

A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury.

Zhao B, Lu Q, Cheng Y, Belcher JM, Siew ED, Leaf DE, Body SC, Fox AA, Waikar SS, Collard CD, Thiessen-Philbrook H, Ikizler TA, Ware LB, Edelstein CL, Garg AX, Choi M, Schaub JA, Zhao H, Lifton RP, Parikh CR; TRIBE-AKI Consortium *. Zhao B, et al. Among authors: zhao h. Am J Respir Crit Care Med. 2017 Feb 15;195(4):482-490. doi: 10.1164/rccm.201603-0518OC. Am J Respir Crit Care Med. 2017. PMID: 27576016 Free PMC article.

2

Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus.

Mani A, Meraji SM, Houshyar R, Radhakrishnan J, Mani A, Ahangar M, Rezaie TM, Taghavinejad MA, Broumand B, Zhao H, Nelson-Williams C, Lifton RP. Mani A, et al. Among authors: zhao h. Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15054-9. doi: 10.1073/pnas.192582999. Epub 2002 Oct 30. Proc Natl Acad Sci U S A. 2002. PMID: 12409608 Free PMC article.

3

A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

Wilson FH, Hariri A, Farhi A, Zhao H, Petersen KF, Toka HR, Nelson-Williams C, Raja KM, Kashgarian M, Shulman GI, Scheinman SJ, Lifton RP. Wilson FH, et al. Among authors: zhao h. Science. 2004 Nov 12;306(5699):1190-4. doi: 10.1126/science.1102521. Epub 2004 Oct 21. Science. 2004. PMID: 15498972 Free PMC article.

4

Whole-genome association studies on alcoholism comparing different phenotypes using single-nucleotide polymorphisms and microsatellites.

Chen L, Liu N, Wang S, Oh C, Carriero NJ, Zhao H. Chen L, et al. Among authors: zhao h. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S130. doi: 10.1186/1471-2156-6-S1-S130. BMC Genet. 2005. PMID: 16451589 Free PMC article.

5

Whole-genome association analysis to identify markers associated with recombination rates using single-nucleotide polymorphisms and microsatellites.

Huang S, Wang S, Liu N, Chen L, Oh C, Zhao H. Huang S, et al. Among authors: zhao h. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S51. doi: 10.1186/1471-2156-6-S1-S51. BMC Genet. 2005. PMID: 16451663 Free PMC article.

6

Haplotype analysis in the presence of informatively missing genotype data.

Liu N, Beerman I, Lifton R, Zhao H. Liu N, et al. Among authors: zhao h. Genet Epidemiol. 2006 May;30(4):290-300. doi: 10.1002/gepi.20144. Genet Epidemiol. 2006. PMID: 16528706

7

Rare independent mutations in renal salt handling genes contribute to blood pressure variation.

Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP. Ji W, et al. Among authors: zhao h. Nat Genet. 2008 May;40(5):592-599. doi: 10.1038/ng.118. Epub 2008 Apr 6. Nat Genet. 2008. PMID: 18391953 Free PMC article.

8

Genotyping and inflated type I error rate in genome-wide association case/control studies.

Sampson JN, Zhao H. Sampson JN, et al. Among authors: zhao h. BMC Bioinformatics. 2009 Feb 23;10:68. doi: 10.1186/1471-2105-10-68. BMC Bioinformatics. 2009. PMID: 19236714 Free PMC article.

9

Statistical power of model selection strategies for genome-wide association studies.

Wu Z, Zhao H. Wu Z, et al. Among authors: zhao h. PLoS Genet. 2009 Jul;5(7):e1000582. doi: 10.1371/journal.pgen.1000582. Epub 2009 Jul 31. PLoS Genet. 2009. PMID: 19649321 Free PMC article.

10

On optimal pooling designs to identify rare variants through massive resequencing.

Lee JS, Choi M, Yan X, Lifton RP, Zhao H. Lee JS, et al. Among authors: zhao h. Genet Epidemiol. 2011 Apr;35(3):139-47. doi: 10.1002/gepi.20561. Epub 2011 Jan 19. Genet Epidemiol. 2011. PMID: 21254222 Free PMC article.

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