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Human Genomics|April 6, 2006
Detecting multiple associations in genome-wide studiesFrank Dudbridge, Arief Gusnanto, Bobby P C KoelemanHuman Genomics|April 6, 2006
A survey of data mining methods for linkage disequilibrium mappingPäivi Onkamo, Hannu ToivonenHuman Genomics|July 20, 2006
Testing groups of genomic locations for enrichment in disease loci using linkage scan data: a method for hypothesis testingDimitrios Avramopoulos, Peter Zandi, Adrian Gherman, et al.Human Genomics|July 20, 2006
A non-parametric approach to population structure inference using multilocus genotypesNianjun Liu, Hongyu ZhaoHuman Genomics|July 20, 2006
Functional single nucleotide polymorphism-based association studiesVictoria E H Carlton, James S Ireland, Francisco Useche, et al.Human Genomics|July 20, 2006
Genetic association studies in cancer: good, bad or no longer ugly?Sharon A Savage, Stephen J ChanockHuman Genomics|December 1, 2022
Lack of association of TP73 rare variants with amyotrophic lateral sclerosis in a Chinese cohortChunyu Li, Yanbing Hou, Qianqian Wei, et al.Human Genomics|December 2, 2022
Phenotypic findings and pregnancy outcomes of fetal rare autosomal aneuploidies detected using chromosomal microarray analysisRong Hu, Weiwei Huang, Weining Zhou, et al.Human Genomics|December 2, 2022
The bridge-like lipid transfer protein (BLTP) gene group: introducing new nomenclature based on structural homology indicating shared functionBryony Braschi, Elspeth A Bruford, Amy T Cavanagh, et al.Human Genomics|December 21, 2022
Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel lociAbdulrahman H Al Anazi, Ahmed S Ammar, Mahmoud Al-Hajj, et al.Pageof 112