| A new statistical method for haplotype reconstruction from population data | American Journal of Human Genetics | 2001 | 6.3K |
| Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer | American Journal of Human Genetics | 2001 | 1.5K |
| AP-1 in cell proliferation and survival | Oncogene | 2001 | 1.3K |
| Regulation of the G2/M transition by p53 | Oncogene | 2001 | 1.2K |
| A new approach to decoding life: systems biology | Annual Review of Genomics and Human Genetics | 2001 | 1.2K |
| Are rare variants responsible for susceptibility to complex diseases? | American Journal of Human Genetics | 2001 | 1.2K |
| De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy | American Journal of Human Genetics | 2001 | 929 |
| Linkage disequilibrium in humans: models and data | American Journal of Human Genetics | 2001 | 920 |
| Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma | American Journal of Human Genetics | 2001 | 901 |
| Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST) | Human Molecular Genetics | 2001 | 858 |
| Prediction of deleterious human alleles | Human Molecular Genetics | 2001 | 852 |
| Reverse phase protein microarrays which capture disease progression show activation of pro-survival pathways at the cancer invasion front | Oncogene | 2001 | 844 |
| Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer | American Journal of Human Genetics | 2001 | 809 |
| Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein | American Journal of Human Genetics | 2001 | 791 |
| Nomenclature for the description of human sequence variations | Human Genetics | 2001 | 766 |
| Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs | American Journal of Human Genetics | 2001 | 716 |
| The Rb/E2F pathway and cancer | Human Molecular Genetics | 2001 | 685 |
| The family based association test method: strategies for studying general genotype--phenotype associations | European Journal of Human Genetics | 2001 | 667 |
| Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer | Human Molecular Genetics | 2001 | 661 |
| The ABC of APC | Human Molecular Genetics | 2001 | 646 |
| Denaturing high-performance liquid chromatography: A review | Human Mutation | 2001 | 623 |
| Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family | American Journal of Human Genetics | 2001 | 612 |
| Constitutive activation of Stat3 by the Src and JAK tyrosine kinases participates in growth regulation of human breast carcinoma cells | Oncogene | 2001 | 606 |
| DNA methylation, methyltransferases, and cancer | Oncogene | 2001 | 599 |
| Partners in transcription: NFAT and AP-1 | Oncogene | 2001 | 588 |
