Paul Sandor

Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families

P. Paschou, J. Hebebrand, G. Lehmkuhl, 2012, Molecular Psychiatry.

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.

K. Kidd, P. Paschou, J. Kidd, 2004, American journal of human genetics.

Genome scan for linkage to Gilles de la Tourette syndrome.

K. Kidd, L. Tsui, A. Pakstis, 1994, American journal of medical genetics.

No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families.

L. Tsui, P. Sandor, C. Barr, 1996, American journal of medical genetics.

Genome-wide association study identifies new locus associated with OCD

Laurent F. Thomas, Jason A. Elias, Zachary F. Gerring, 2022 .