Volk, Fricke, Strobl, Kolling, Kubisch, Neugebauer: "Analysis of the CHN1 gene in patients with various types of congenital ocular motility disorders." in: Graefe's archive for clinical and experimental ophthalmology, Vol. 248, Issue 9, pp. 1351-7, 2010 (PubMed).
Dick, Meyers, Aliev, Nurnberger, Kramer, Kuperman, Porjesz, Tischfield, Edenberg, Foroud, Schuckit, Goate, Hesselbrock, Bierut: "Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts." in: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, Vol. 153B, Issue 6, pp. 1179-88, 2010 (PubMed).
Rose, Behm, Drgon, Johnson, Uhl: "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score." in: Molecular medicine (Cambridge, Mass.), Vol. 16, Issue 7-8, pp. 247-53, 2010 (PubMed).
Miyake, Andrews, Fan, He, Chan, Engle: "CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome." in: American journal of medical genetics. Part A, Vol. 152A, Issue 1, pp. 215-7, 2009 (PubMed).
Murillo-Correa, Kon-Jara, Engle, Zenteno: "Clinical features associated with an I126M alpha2-chimaerin mutation in a family with autosomal-dominant Duane retraction syndrome." in: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus, Vol. 13, Issue 3, pp. 245-8, 2009 (PubMed).