Citation map · Study

SZodixStudyAcademic Library

Shelves Open access

Study · an open academic library·Metadata from OpenAlex (CC0)·Shelves·OpenAlex metadata, de-duplicated

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

1 references·16 citing·46 second hop

FromToDepth

this work references cited by second hop

References

2000An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries925 cited

Cited by

2021A Comprehensive Review of Tic Disorders in Children162 cited
2013The genetic basis of Gilles de la Tourette Syndrome117 cited
2010Obsessive-compulsive disorder and its related disorders: a reappraisal of obsessive-compulsive spectrum concepts117 cited
2003Association of Specific Language Impairment (SLI) to the Region of 7q31114 cited
2012Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism114 cited
2003An update on the genetics of Gilles de la Tourette syndrome108 cited
2013Anxiety and affective disorder comorbidity related to serotonin and other neurotransmitter systems: obsessive–compulsive disorder as an example of overlapping clinical and genetic heterogeneity106 cited
2012The genetics of Tourette syndrome97 cited
2004Neurobiology and neuroimmunology of Tourette?s syndrome: an update90 cited
2014The inheritance of Tourette Disorder: A review88 cited
2003Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype81 cited
2011Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome78 cited

Only edges whose both ends are imported exist here. Widen the year window, or show the whole map. Back to the work

2014Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome71 cited

2004Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region70 cited

2013Structural Abnormalities in Early Tourette Syndrome Children: A Combined Voxel-Based Morphometry and Tract-Based Spatial Statistics Study68 cited

2006Genetics and Epidemiology of Tourette Syndrome67 cited