Paul M. Thompson, Agatha D. Lee, Rebecca A. Dutton, Jennifer A. Geaga, Kiralee M. Hayashi, Mark A. Eckert, ...
We identified and mapped an anatomically localized failure of cortical maturation in Williams syndrome (WS), a genetic condition associated with deletion of �20 contiguous genes on chromosome 7....
Ming-chang Chiang, Allan L. Reiss, Agatha D. Lee, Ursula Bellugi, Albert M. Galaburda, Julie R. Korenberg, ...
williams syndrome Visualized using tensor-based morphometry, NeuroImage (2007), doi: 10.1016/j.neuroimage.2007.04.024 This is a PDF file of an unedited manuscript that has been accepted for...
Gough, Sheryl M, McDonald, Margaret, Chen, Xiao-Ning, Korenberg, Julie R, Neri, Antonino, Kahn, Tomas, ...
Abstract Background Chromosome band 10q24 is a gene-rich domain and host to a number of cancer, developmental, and neurological genes. Recurring translocations, deletions and mutations involving this...
Mouse Molecular Cytogenetic Resource: 157 BACs Link the Chromosomal and Genetic Maps (1999)
Korenberg, Julie R., Chen, Xiao-Ning, Devon, Keri L., Noya, David, Oster-Granite, Mary L., Birren, Bruce W.
DiDonato, Christine J., Chen, Xiao-Ning, Noya, David, Korenberg, Julie R., Nadeau, Joseph H., Simard, Louise R.
A bacterial artificial chromosome-based framework contig map of human chromosome 22q (1996)
Kim, Ung-Jin, Shizuya, Hiroaki, Kang, Hyung-Lyun, Choi, Sun-Shim, Garrett, Charmain L., Smink, Luc J., ...
We have constructed a physical map of human chromosome 22q using bacterial artificial chromosome (BAC) clones. The map consists of 613 chromosome 22-specific BAC clones that have been localized and...
Kim, Ung-Jin, Shizuya, Hiroaki, Deaven, Larry, Chen, Xiao-Ning, Korenberg, Julie R., Simon, Melvin I.
[No abstract]
Yamakawa, Kazuhiro, Mitchell, Steve, Hubert, René, Chen, Xiao-Ning, Colbern, Steve, Huo, Yong-Kang, ...
The Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1) and autoimmune polyglandular disease type I (APECED) have been mapped to human chromosome 21q22.3 by genetic linkage analysis...
Kim, Ung-Jin, Shizuya, Hiroaki, Deaven, Larry, Chen, Xiao-Ning, Korenberg, Julie R., Simon, Melvin I.
Gough, Sheryl M, McDonald, Margaret, Chen, Xiao-Ning, Korenberg, Julie R, Neri, Antonino, Kahn, Tomas, ...
Mouse Molecular Cytogenetic Resource: 157 BACs Link the Chromosomal and Genetic Maps
Korenberg, Julie R., Chen, Xiao-Ning, Devon, Keri L., Noya, David, Oster-Granite, Mary L., Birren, Bruce W.
We have established a collection of strong molecular cytogenetic markers that span the mouse autosomes and X chromosome at an average spacing of one per 19 Mb and identify 127 distinct band...
Physical and Comparative Mapping of Distal Mouse Chromosome 16
Cabin, Deborah E., McKee-Johnson, Jennifer W., Matesic, Lydia E., Wiltshire, Tim, Rue, Elizabeth E., Mjaatvedt, Anne E., ...
Distal mouse Chromosome 16 (Chr. 16) includes a region of conserved linkage with human Chromosome 21 (Chr. 21). Mouse models of Down syndrome based on trisomy of distal Chr. 16 have several...
Korenberg, Julie R., Chen, Xiao-Ning, Sun, Zhiguang, Shi, Zheng-Yang, Ma, Shaowu, Vataru, Eddy, ...
Human genome sequencing is accelerating rapidly. Multiple genome maps link this sequence to problems in biology and clinical medicine. Because each map represents a different aspect of the structure,...
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
Kamino, Kouzin, Orr, Harry T., Payami, Haydeh, Wijsman, Ellen M., Alonso, Ma. Elisa, Pulst, Stefan M., ...
A large number of familial Alzheimer disease (FAD) kindreds were examined to determine whether mutations in the amyloid precursor protein (APP) gene could be responsible for the disease. Previous...
Korenberg, Julie R., Kawashima, Hiroko, Pulst, Stefan-M., Ikeuchi, T., Ogasawara, N., Yamamoto, K., ...
Down syndrome (DS) is a major cause of mental retardation and heart disease. Although it is usually caused by the presence of an extra chromosome 21, a subset of the diagnostic features may be caused...
Gough, Sheryl M, McDonald, Margaret, Chen, Xiao-Ning, Korenberg, Julie R, Neri, Antonino, Kahn, Tomas, ...
Mouse Molecular Cytogenetic Resource: 157 BACs Link the Chromosomal and Genetic Maps
Korenberg, Julie R., Chen, Xiao-Ning, Devon, Keri L., Noya, David, Oster-Granite, Mary L., Birren, Bruce W.
We have established a collection of strong molecular cytogenetic markers that span the mouse autosomes and X chromosome at an average spacing of one per 19 Mb and identify 127 distinct band...
Physical and Comparative Mapping of Distal Mouse Chromosome 16
Cabin, Deborah E., McKee-Johnson, Jennifer W., Matesic, Lydia E., Wiltshire, Tim, Rue, Elizabeth E., Mjaatvedt, Anne E., ...
Distal mouse Chromosome 16 (Chr. 16) includes a region of conserved linkage with human Chromosome 21 (Chr. 21). Mouse models of Down syndrome based on trisomy of distal Chr. 16 have several...
Korenberg, Julie R., Chen, Xiao-Ning, Sun, Zhiguang, Shi, Zheng-Yang, Ma, Shaowu, Vataru, Eddy, ...
Human genome sequencing is accelerating rapidly. Multiple genome maps link this sequence to problems in biology and clinical medicine. Because each map represents a different aspect of the structure,...
Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region
Kamino, Kouzin, Orr, Harry T., Payami, Haydeh, Wijsman, Ellen M., Alonso, Ma. Elisa, Pulst, Stefan M., ...
A large number of familial Alzheimer disease (FAD) kindreds were examined to determine whether mutations in the amyloid precursor protein (APP) gene could be responsible for the disease. Previous...
Korenberg, Julie R., Kawashima, Hiroko, Pulst, Stefan-M., Ikeuchi, T., Ogasawara, N., Yamamoto, K., ...
Down syndrome (DS) is a major cause of mental retardation and heart disease. Although it is usually caused by the presence of an extra chromosome 21, a subset of the diagnostic features may be caused...
Korbel, Jan O., Tirosh-Wagner, Tal, Urban, Alexander Eckehart, Chen, Xiao-Ning, Kasowski, Maya, Dai, Li, ...
Down syndrome (DS), or trisomy 21, is a common disorder associated with several complex clinical phenotypes. Although several hypotheses have been put forward, it is unclear as to whether particular...