Chromosomes, Human, Pair 6
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Chromosomes, Human, Pair 9
W. K. Scott, Hauser, E. R., Schmechel, D. E., Welsh-Bohmer, K. A., Small, G. W., Roses, A. D., Saunders, A. M., Gilbert, J. R., Vance, J. M., Haines, J. L., and Pericak-Vance, M. A.,
“Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.”,
Am J Hum Genet, vol. 73, no. 5, pp. 1041-51, 2003.
Computer Simulation
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R.,
“Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.”,
Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
Databases, Genetic
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Dementia
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Demography
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
DNA Mutational Analysis
Y. - J. Li, Scott, W. K., Zhang, L., Lin, P. - I., Oliveira, S. A., Skelly, T., Doraiswamy, M. P., Welsh-Bohmer, K. A., Martin, E. R., Haines, J. L., Pericak-Vance, M. A., and Vance, J. M.,
“Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.”,
Neurobiol Aging, vol. 27, no. 8, pp. 1087-93, 2006.
DNA, Mitochondrial
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A.,
“Analysis of European mitochondrial haplogroups with Alzheimer disease risk.”,
Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
European Continental Ancestry Group
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A.,
“Analysis of European mitochondrial haplogroups with Alzheimer disease risk.”,
Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
False Positive Reactions
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R.,
“Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.”,
Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
Female
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A.,
“Analysis of European mitochondrial haplogroups with Alzheimer disease risk.”,
Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
Y. - J. Li, Scott, W. K., Zhang, L., Lin, P. - I., Oliveira, S. A., Skelly, T., Doraiswamy, M. P., Welsh-Bohmer, K. A., Martin, E. R., Haines, J. L., Pericak-Vance, M. A., and Vance, J. M.,
“Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.”,
Neurobiol Aging, vol. 27, no. 8, pp. 1087-93, 2006.
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Y. - J. Li, Oliveira, S. A., Xu, P., Martin, E. R., Stenger, J. E., Scherzer, C. R., Hauser, M. A., Scott, W. K., Small, G. W., Nance, M. A., Watts, R. L., Hubble, J. P., Koller, W. C., Pahwa, R., Stern, M. B., Hiner, B. C., Jankovic, J., Goetz, C. G., Mastaglia, F., Middleton, L. T., Roses, A. D., Saunders, A. M., Schmechel, D. E., Gullans, S. R., Haines, J. L., Gilbert, J. R., Vance, J. M., Pericak-Vance, M. A., Hulette, C., and Welsh-Bohmer, K. A.,
“Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.”,
Hum Mol Genet, vol. 12, no. 24, pp. 3259-67, 2003.
Folic Acid
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Formate-Tetrahydrofolate Ligase
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Gene Frequency
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R.,
“Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.”,
Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
Genetic Heterogeneity
W. K. Scott, Hauser, E. R., Schmechel, D. E., Welsh-Bohmer, K. A., Small, G. W., Roses, A. D., Saunders, A. M., Gilbert, J. R., Vance, J. M., Haines, J. L., and Pericak-Vance, M. A.,
“Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.”,
Am J Hum Genet, vol. 73, no. 5, pp. 1041-51, 2003.
Genetic Linkage
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R.,
“Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.”,
Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
Genetic Loci
A. C. Naj, Beecham, G. W., Martin, E. R., Gallins, P. J., Powell, E. H., Konidari, I., Whitehead, P. L., Cai, G., Haroutunian, V., Scott, W. K., Vance, J. M., Slifer, M. A., Gwirtsman, H. E., Gilbert, J. R., Haines, J. L., Buxbaum, J. D., and Pericak-Vance, M. A.,
“Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.”,
PLoS Genet, vol. 6, no. 9, p. e1001130, 2010.
Genetic Markers
W. K. Scott, Hauser, E. R., Schmechel, D. E., Welsh-Bohmer, K. A., Small, G. W., Roses, A. D., Saunders, A. M., Gilbert, J. R., Vance, J. M., Haines, J. L., and Pericak-Vance, M. A.,
“Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.”,
Am J Hum Genet, vol. 73, no. 5, pp. 1041-51, 2003.
A. L. Boyles, Scott, W. K., Martin, E. R., Schmidt, S., Li, Y. - J., Ashley-Koch, A., Bass, M. P., Schmidt, M., Pericak-Vance, M. A., Speer, M. C., and Hauser, E. R.,
“Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.”,
Hum Hered, vol. 59, no. 4, pp. 220-7, 2005.
Genetic Predisposition to Disease
J. M. van der Walt, Dementieva, Y. A., Martin, E. R., Scott, W. K., Nicodemus, K. K., Kroner, C. C., Welsh-Bohmer, K. A., Saunders, A. M., Roses, A. D., Small, G. W., Schmechel, D. E., P Doraiswamy, M., Gilbert, J. R., Haines, J. L., Vance, J. M., and Pericak-Vance, M. A.,
“Analysis of European mitochondrial haplogroups with Alzheimer disease risk.”,
Neurosci Lett, vol. 365, no. 1, pp. 28-32, 2004.
Y. - J. Li, Scott, W. K., Zhang, L., Lin, P. - I., Oliveira, S. A., Skelly, T., Doraiswamy, M. P., Welsh-Bohmer, K. A., Martin, E. R., Haines, J. L., Pericak-Vance, M. A., and Vance, J. M.,
“Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.”,
Neurobiol Aging, vol. 27, no. 8, pp. 1087-93, 2006.
Genetic Testing
Y. - J. Li, Scott, W. K., Zhang, L., Lin, P. - I., Oliveira, S. A., Skelly, T., Doraiswamy, M. P., Welsh-Bohmer, K. A., Martin, E. R., Haines, J. L., Pericak-Vance, M. A., and Vance, J. M.,
“Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases.”,
Neurobiol Aging, vol. 27, no. 8, pp. 1087-93, 2006.