Concepedia

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

Linh T. Duong, Louise K. Hoeffding, Kirsten Bruun Petersen, Charlotte D. Knudsen, Johan H. Thygesen, Laura L. Klitten, Niels Tommerup, Andrés Ingason, Thomas Werge

European Journal of Medical Genetics · 2015 · 17 citations · 19 references

DOI

Concepts

References

19

PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Kai Wang, Mingyao Li, Dexter Hadley et al. · Genome Research · 2007 · 1.9K citations · Full text

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Large recurrent microdeletions associated with schizophrenia

Hreinn Stefánsson, Dan Rujescu, Sven Cichon et al. · Nature · 2008 · 1.8K citations · Full text

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Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature · 2008 · 1.5K citations · Full text

, , +12

Effects of Family History and Place and Season of Birth on the Risk of Schizophrenia

Preben Bo Mortensen, Carsten Bøcker Pedersen, Tine Westergaard et al. · New England Journal of Medicine · 1999 · 822 citations · Full text

, , +12

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

Steven A. McCarroll, Alan Huett, Petric Kuballa et al. · Nature Genetics · 2008 · 661 citations · Full text

, , +12