M. Pericak-Vance

Clinical Heterogeneity of Familial Spastic Paraplegia Linked to Chromosome 2p21

J. Haines, M. Pericak-Vance, M. Nance, 1998, Human Heredity.

Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.

M. Pericak-Vance, T. Bird, W. Raskind, 1997, American journal of medical genetics.

Ordered‐subset analysis of savant skills in autism for 15q11‐q13

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Duchenne muscular dystrophy

J. Gilbert, M. Pericak-Vance, R. Bartlett, 1988, Neurology.

Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.

M. Pericak-Vance, J. Vance, J. Stajich, 1999, American journal of human genetics.

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31.

M. Pericak-Vance, W. Hung, T. Siddique, 1996, Human molecular genetics.

Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

M. Pericak-Vance, J. Vance, M. Hamida, 1993, Human molecular genetics.

Analysis of the RELN gene as a genetic risk factor for autism

J. Sutcliffe, S. Folstein, J. Gilbert, 2005, Molecular Psychiatry.

Osteopontin polymorphisms and disease course in multiple sclerosis

J. Haines, M. Pericak-Vance, E. Martin, 2003, Genes and Immunity.

Linkage of a gene for macular corneal dystrophy to chromosome 16.

M. Pericak-Vance, F. Jónasson, K. Damji, 1996, American journal of human genetics.

SLITRK1 mutations in trichotillomania

M. Cuccaro, M. Pericak-Vance, A. Ashley-Koch, 2006, Molecular Psychiatry.

Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

L. Citrigno, Arielle Kushman, S. Züchner, 2011, Clinical genetics.