Concepedia

Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing

Anthony M. Musolf, Winson S. Ho, Kyle A. Long, Zhengping Zhuang, Davis P. Argersinger, Haiming Sun, Bilal A. Moiz, Claire L. Simpson, Joan E. Bailey‐Wilson, John D. Heiss

European Journal of Human Genetics · 2019 · 23 citations · 38 references

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Concepts

References

38

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

Shaun Purcell, Benjamin M. Neale, Katherine EO Todd-Brown et al. · The American Journal of Human Genetics · 2007 · 36.1K citations · Full text

, , +13

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

Kai Wang, Man Li, Håkon Håkonarson · Nucleic Acids Research · 2010 · 15.6K citations · Full text

, , +17

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Eric S. Lander, Leonid Kruglyak · Nature Genetics · 1995 · 5.3K citations

, , +16

Merlin—rapid analysis of dense genetic maps using sparse gene flow trees

Gonçalo R. Abecasis, Stacey S. Cherny, William Cookson et al. · Nature Genetics · 2001 · 3.4K citations

, , +15

CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

Alexej Abyzov, Alexander E. Urban, M Snyder et al. · Genome Research · 2011 · 1.8K citations · Full text

, , +17