Publications

Publications

Nuytemans, K., Bademci, G., Kohli, M. M., Beecham, G. W., Wang, L., Young, J. I., … & Haines, J. L. (2013). C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease. Annals of human genetics, 77(5), 351-363.

Alsgen Consortium. (2013). Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34. 1. Neurobiology of aging, 34(1), 357-e7.

Deng, H. X., Chen, W., Hong, S. T., Boycott, K. M., Gorrie, G. H., Siddique, N., … & Jiang, H. (2011). Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature, 477(7363), 211-215.

Kwiatkowski, T. J., Bosco, D. A., Leclerc, A. L., Tamrazian, E., Vanderburg, C. R., Russ, C., … & Valdmanis, P. (2009). Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science,323(5918), 1205-1208.

Li, Y. J., Pericak-Vance, M. A., Haines, J. L., Siddique, N., McKenna-Yasek, D., Hung, W. Y., … & Saunders, A. M. (2004). Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis. Neurogenetics, 5(4), 209-213.

Hosler, B. A., Siddique, T., Sapp, P. C., Sailor, W., Huang, M. C., Hossain, A., … & Hung, W. Y. (2000). Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22. Jama, 284(13), 1664-1669.

Hentati, A., Ouahchi, K., Pericak-Vance, M. A., Nijhawan, D., Ahmad, A., Yang, Y., … & Hamida, M. B. (1998). Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.Neurogenetics, 2(1), 55-60.

Siddique, T., Pericak-Vance, M. A., Caliendo, J., Hong, S. T., Hung, W. Y., Kaplan, J., … & Scott, W. K. (1998). Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.Neurogenetics, 1(3), 213-216.

Juneja, T., Pericak-Vance, M. A., Laing, N. G., Dave, S., & Siddique, T. (1997). Prognosis in familial amyotrophic lateral sclerosis progression and survival in patients with Glu100gly and Ala4val mutations in Cu, Zn superoxide dismutase. Neurology, 48(1), 55-57.

Hentati, A., Bejaoui, K., Pericak-Vance, M. A., Hentati, F., Speer, M. C., Hung, W. Y., … & Hamida, M. B. (1994). Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35. Nature genetics,7(3), 425-428.

Siddique, T., Figlewigz, D. A., Pericak-Vance, M. A., Haines, J. L., Rouleau, G., Jeffers, A. J., … & Deng, G. (1991). Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity. New England Journal of Medicine, 324(20), 1381-
1384.

Siddique, T., Hu, P., Hentati, A., Deng, G., Hung, W. Y., McInnis, M. G., … & Pericak-Vance, M. A. (1990). A molecular genetic approach to amyotrophic lateral sclerosis. International journal of neurology, 25, 60-69.

Siddique, T., Pericak-Vance, M. A., Brooks, B. R., Roos, R. P., Hung, W. Y., Antel, J. P., … & Bias, W. B. (1989). Linkage analysis in familial amyotrophic lateral sclerosis. Neurology, 39(7), 919-919.