| 100,000 genomes pilot on rare-disease diagnosis in health care—preliminary report 100,000 Genomes Project Pilot Investigators New England Journal of Medicine 385 (20), 1868-1880, 2021 | 364 | 2021 |
| A global analysis of Y-chromosomal haplotype diversity for 23 STR loci J Purps, S Siegert, S Willuweit, M Nagy, C Alves, R Salazar, ... Forensic Science International: Genetics 12, 12-23, 2014 | 290 | 2014 |
| A calibrated human Y-chromosomal phylogeny based on resequencing W Wei, Q Ayub, Y Chen, S McCarthy, Y Hou, I Carbone, Y Xue, ... Genome research 23 (2), 388-395, 2013 | 196 | 2013 |
| Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos VI Floros, A Pyle, S Dietmann, W Wei, WCW Tang, N Irie, B Payne, ... Nature cell biology 20 (2), 144-151, 2018 | 184 | 2018 |
| Germline selection shapes human mitochondrial DNA diversity W Wei, S Tuna, MJ Keogh, KR Smith, TJ Aitman, PL Beales, DL Bennett, ... Science 364 (6442), eaau6520, 2019 | 182 | 2019 |
| Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains W Wei, MJ Keogh, I Wilson, J Coxhead, S Ryan, S Rollinson, H Griffin, ... Acta neuropathologica communications 5, 1-8, 2017 | 130* | 2017 |
| Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK DL Ritchie, P Adlard, AH Peden, S Lowrie, M Le Grice, K Burns, ... Acta neuropathologica 134 (2), 221-240, 2017 | 111 | 2017 |
| A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the … SJ Van Der Lee, OJ Conway, I Jansen, MM Carrasquillo, L Kleineidam, ... Acta neuropathologica 138, 237-250, 2019 | 103 | 2019 |
| Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans W Wei, AT Pagnamenta, N Gleadall, A Sanchis-Juan, J Stephens, ... Nature communications 11 (1), 1740, 2020 | 89 | 2020 |
| A comparison of Y-chromosomal lineage dating using either resequencing or Y-SNP plus Y-STR genotyping W Wei, Q Ayub, Y Xue, C Tyler-Smith Forensic Science International: Genetics 7 (6), 568-572, 2013 | 76 | 2013 |
| Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes W Wei, KR Schon, G Elgar, A Orioli, M Tanguy, A Giess, M Tischkowitz, ... Nature 611 (7934), 105-114, 2022 | 71 | 2022 |
| An atlas of mitochondrial DNA genotype–phenotype associations in the UK Biobank E Yonova-Doing, C Calabrese, A Gomez-Duran, K Schon, W Wei, ... Nature genetics 53 (7), 982-993, 2021 | 71 | 2021 |
| Inheritance of mitochondrial DNA in humans: implications for rare and common diseases W Wei, PF Chinnery Journal of internal medicine 287 (6), 634-644, 2020 | 69 | 2020 |
| High prevalence of focal and multi-focal somatic genetic variants in the human brain MJ Keogh, W Wei, J Aryaman, L Walker, J van den Ameele, J Coxhead, ... Nature communications 9 (1), 4257, 2018 | 59 | 2018 |
| Genetic compendium of 1511 human brains available through the UK medical research council brain banks network resource MJ Keogh, W Wei, I Wilson, J Coxhead, S Ryan, S Rollinson, H Griffin, ... Genome research 27 (1), 165-173, 2017 | 54 | 2017 |
| A strategy for co-analysis of microRNAs and DNA Y Li, J Zhang, W Wei, Z Wang, M Prinz, Y Hou Forensic Science International: Genetics 12, 24-29, 2014 | 54 | 2014 |
| Identification of Saliva Using Micro RNA Biomarkers for Forensic Purpose Z Wang, J Zhang, W Wei, D Zhou, H Luo, X Chen, Y Hou Journal of forensic sciences 60 (3), 702-706, 2015 | 52 | 2015 |
| Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations W Wei, A Gomez-Duran, G Hudson, PF Chinnery PLoS genetics 13 (12), e1007126, 2017 | 47 | 2017 |
| Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study KR Schon, R Horvath, W Wei, C Calabrese, A Tucci, K Ibañez, T Ratnaike, ... Bmj 375, 2021 | 46 | 2021 |
| A novel method for the analysis of 20 multi‐I ndel polymorphisms and its forensic application J Huang, H Luo, W Wei, Y Hou Electrophoresis 35 (4), 487-493, 2014 | 44 | 2014 |
