CALHM1 polymorphism is not associated with late-onset Alzheimer Disease

Por Beecham, GW, Schnetz-Boutaud, N, Haines, JL, Pericak-Vance, MA
Publicado em 2009

A Genome-wide Scan in an Amish Pedigree with Parkinsonism

Por LEE, S. L., MURDOCK, D. G., MCCAULEY, J. L., BRADFORD, Y., CRUNK, A., MCFARLAND, L., JIANG, L., WANG, T., SCHNETZ-BOUTAUD, N., HAINES, J. L.
Publicado em 2008

Examination of Association to Autism of Common Genetic Variation in Genes Related to Dopamine

Por Anderson, B.M., Schnetz-Boutaud, N., Bartlett, J., Wright, H.H., Abramson, R.K., Cuccaro, M.L., Gilbert, J.R., Pericak-Vance, M.A., Haines, J.L.
Publicado em 2008

Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer's disease

Por Martin, E, Bronson, P, Li, Y, Wall, N, Chung, R, Schmechel, D, Small, G, Xu, P, Bartlett, J, Schnetz-Boutaud, N, Haines, J, Gilbert, J, Pericak-Vance, M
Publicado em 2005

Examination of Tetrahydrobiopterin Pathway Genes in Autism

Por Schnetz-Boutaud, N.C., Anderson, B.M., Brown, K.D., Wright, H.H., Abramson, R.K., Cuccaro, M.L., Gilbert, J.R., Pericak-Vance, M.A., Haines, J.L.
Publicado em 2009

Examination of Association of Genes in the Serotonin System to Autism

Por Anderson, B.M., Schnetz-Boutaud, N.C., Bartlett, J., Wotawa, A.M., Wright, H.H., Abramson, R.K., Cuccaro, M.L., Gilbert, J.R., Pericak-Vance, M.A., Haines, J.L.
Publicado em 2009

A Second-Generation Genomic Screen for Multiple Sclerosis

Por Kenealy, S. J., Babron, M.-C., Bradford, Y., Schnetz-Boutaud, N., Haines, J. L., Rimmler, J. B., Schmidt, S., Pericak-Vance, M. A., Barcellos, L. F., Lincoln, R. R., Oksenberg, J. R., Hauser, S. L., Clanet, M., Brassat, D., Edan, G., Yaouanq, J., Semana, G., Cournu-Rebeix, I., Lyon-Caen, O., Fontaine, B.
Publicado em 2004