N. Davis

Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome

Murat Gunel, Brian J. O'Roak, Matthew W. State, 2005, Science.

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

A. Klin, M. State, R. Lifton, 2004, American journal of human genetics.

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population

K. Avraham, M. Frydman, A. Orr-Urtreger, 1999, Human Genetics.

Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

Richard P Lifton, Matthew W State, Ami Klin, 2004, American journal of human genetics.

Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22

D. Ward, M. State, R. King, 2004, American journal of medical genetics. Part A.

Determining the incidence of familiality in ALS

O. Hardiman, R. McLaughlin, N. Pender, 2018, Neurology: Genetics.