Concepedia

Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome

Erwin Petek, Christian Windpassinger, John B. Vincent, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer, Peter M. Kroisel, Klaus W. Wagner

The American Journal of Human Genetics · 2001 · 186 citations · 19 references

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19

Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer

H. Telenius, Nigel P. Carter, Charlotte Bebb et al. · Genomics · 1992 · 1.4K citations

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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

Susan E. Hong, Yin Yao Shugart, David T. Huang et al. · Nature Genetics · 2000 · 878 citations

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Online Mendelian Inheritance in Man 'OMIM'.

Sangeeta Amladi · PubMed · 2007 · 870 citations · Full text

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An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries

Roger D. Fréeman, Diane K. Fast, Larry Burd et al. · Developmental Medicine & Child Neurology · 2000 · 867 citations

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A decrease of reelin expression as a putative vulnerability factor in schizophrenia

Francesco Impagnatiello, Alessandro R. Guidotti, Christine Pesold et al. · Proceedings of the National Academy of Sciences · 1998 · 760 citations

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