Ranade, Koustubh, Hinds, David, Hsiung, Chao Agnes, Chuang, Lee-Ming, Chang, Mau-Song, Chen, Ying-Tsung, ...
Background: Our understanding of genes that predispose to essential hypertension is poor. Methods: A genome-wide scan for linkage at ~10 cM resolution was done on 1425 sibpairs of Chinese and...
High-Throughput Genotyping with Single Nucleotide Polymorphisms
Ranade, Koustubh, Chang, Mau-Song, Ting, Chih-Tai, Pei, Dee, Hsiao, Chin-Fu, Olivier, Michael, ...
To make large-scale association studies a reality, automated high-throughput methods for genotyping with single-nucleotide polymorphisms (SNPs) are needed. We describe PCR conditions that permit the...
Full-Genome Scan for Linkage in 50 Families Segregating the Bipolar Affective Disease Phenotype
Friddle, Carl, Koskela, Rebecca, Ranade, Koustubh, Hebert, Joan, Cargill, Michele, Clark, Chris D., ...
A genome scan of ∼12-cM initial resolution was done on 50 of a set of 51 carefully ascertained unilineal multiplex families segregating the bipolar affective disorder phenotype. In addition to...
High-Throughput Genotyping with Single Nucleotide Polymorphisms
Ranade, Koustubh, Chang, Mau-Song, Ting, Chih-Tai, Pei, Dee, Hsiao, Chin-Fu, Olivier, Michael, ...
To make large-scale association studies a reality, automated high-throughput methods for genotyping with single-nucleotide polymorphisms (SNPs) are needed. We describe PCR conditions that permit the...
Full-Genome Scan for Linkage in 50 Families Segregating the Bipolar Affective Disease Phenotype
Friddle, Carl, Koskela, Rebecca, Ranade, Koustubh, Hebert, Joan, Cargill, Michele, Clark, Chris D., ...
A genome scan of ∼12-cM initial resolution was done on 50 of a set of 51 carefully ascertained unilineal multiplex families segregating the bipolar affective disorder phenotype. In addition to...
Hallmayer, Joachim, Pintado, Elizabeth, Lotspeich, Linda, Spiker, Donna, McMahon, William, Petersen, P. Brent, ...
Approximately 2%–5% of autistic children show cytogenetic evidence of the fragile X syndrome. This report tests whether infantile autism in multiplex autism families arises from an unusual...