《AmericanJournalofHumanGenetics》期刊第56页198条数据 

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183.《Enriching the Analysis of Genomewide Association Studies with Hierarchical Modeling》

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184.《Human microRNA-155 on Chromosome 21 Differentially Interacts with Its Polymorphic Target in the AGTR1 3′ Untranslated Region: A Mechanism for Functional Single-Nucleotide Polymorphisms Related to Phenotypes》

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185.《Copy-Number Variations and Human Disease》

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186.《Reply to Dr. Robert A. Hegele》

genetics_thesis/040004248923.html

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187.《The TAF1/DYT3 Multiple Transcript System in X-Linked Dystonia-Parkinsonism》

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188.《TAF1 as the Most Plausible Disease Gene for XDP/DYT3》

genetics_thesis/040004248925.html

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189.《Numbers of Copy-Number Variations and False-Negative Rates Will Be Underestimated If We Do Not Account for the Dependence between Repeated Experiments》

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190.《Reply to Lynch et al.》

genetics_thesis/040004248927.html

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191.《Looking Back; Moving Forward》

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192.《Announcements》

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193.《This Month in the Journal》

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194.《Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H》

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195.《A Genomewide Screen for Late-Onset Alzheimer Disease in a Genetically Isolated Dutch Population》

genetics_thesis/040004248932.html

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196.《Conversion and Compensatory Evolution of the γ-Crystallin Genes and Identification of a Cataractogenic Mutation That Reverses the Sequence of the Human CRYGD Gene to an Ancestral State》

genetics_thesis/040004248933.html

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197.《Evidence of Amino Acid Diversity–Enhancing Selection within Humans and among Primates at the Candidate Sperm-Receptor Gene PKDREJ》

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198.《Identification of Risk-Related Haplotypes with the Use of Multiple SNPs from Nuclear Families》

genetics_thesis/040004248935.html

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