Skip to Main Content

Author Details

Wei Wei
University of Cambridge
2009
40
20
PMIDPaper TitleJournal TitlePublished Year
36522542Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.Nat Cell Biol2023
37484768Third generation sequencing transforms the way of the screening and diagnosis of thalassemia: a mini-review.Front Pediatr2023
36198798Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes.Nature2022
36044900The human mitochondrial genome contains a second light strand promoter.Mol Cell2022
34002094An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank.Nat Genet2021
34878831Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmission.Sci Adv2021
34732400Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.BMJ2021
34758253100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report.N Engl J Med2021
34428295MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases.Nucleic Acids Res2021
34475388Cell reprogramming shapes the mitochondrial DNA landscape.Nat Commun2021
33990696Oxygen tension modulates the mitochondrial genetic bottleneck and influences the segregation of a heteroplasmic mtDNA variant in vitro.Commun Biol2021
34031572Biparental inheritance of mitochondrial DNA revisited.Nat Rev Genet2021
32694774Cracking the enigma of mitochondrial-DNA variants and cancer.Nat Metab2020
31955222Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.Acta Neuropathol2020
33128823Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency.EMBO J2020
31123110Germline selection shapes human mitochondrial DNA diversity.Science2019
30214067Frequency and signature of somatic variants in 1461 human brain exomes.Genet Med2019
29332010Oligogenic genetic variation of neurodegenerative disease genes in 980 postmortem human brains.J Neurol Neurosurg Psychiatry2018
30323172High prevalence of focal and multi-focal somatic genetic variants in the human brain.Nat Commun2018
29674682Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.Nat Cell Biol2018
29727451Correction: Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations.PLoS Genet2018
29335530Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.Nat Cell Biol2018
28003435Genetic compendium of 1511 human brains available through the UK Medical Research Council Brain Banks Network Resource.Genome Res2017
28228164Erratum to: Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.Acta Neuropathol Commun2017
28454558Response to Simon et al.Acta Neuropathol Commun2017
28349199Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.Acta Neuropathol2017
28153046Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains.Acta Neuropathol Commun2017
29253894Background sequence characteristics influence the occurrence and severity of disease-causing mtDNA mutations.PLoS Genet2017
33473601Phylogenetic studies of <i>Petaurista petauri</i> based on complete mitochondrial DNA sequences.Mitochondrial DNA B Resour2016
25382174Developing a multiplex mtSNP assay for forensic application in Han Chinese based on mtDNA phylogeny and hot spot.Electrophoresis2015
25986439Erratum to: Copy number variation in the human Y chromosome in the UK population.Hum Genet2015
25690121Identification of Saliva Using MicroRNA Biomarkers for Forensic Purpose.J Forensic Sci2015
24242919A novel method for the analysis of 20 multi-Indel polymorphisms and its forensic application.Electrophoresis2014
24858406A strategy for co-analysis of microRNAs and DNA.Forensic Sci Int Genet2014
24854874A global analysis of Y-chromosomal haplotype diversity for 23 STR loci.Forensic Sci Int Genet2014
24528583A case study of SNPSTR efficiency in paternity testing with locus incompatibility.Forensic Sci Int Genet2014
23038768A calibrated human Y-chromosomal phylogeny based on resequencing.Genome Res2013
23768990A comparison of Y-chromosomal lineage dating using either resequencing or Y-SNP plus Y-STR genotyping.Forensic Sci Int Genet2013
21779922Exploring of new Y-chromosome SNP loci using Pyrosequencing and the SNaPshot methods.Int J Legal Med2012
20000052[DNA-based personal identification in disaster].Fa Yi Xue Za Zhi2009
  • 1 - 40 of 40

Recommended Authors

Martin Kircher
Berlin Institute of Health (BIH) at Charite-Universitatsmedizin Berlin
Career Start Year 2008
Number of shared co-authors 0
Aakrosh Ratan
Center for Public Health Genomics, University of Virginia
Career Start Year 2008
Number of shared co-authors 0
Larry N Singh
Center for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia
Career Start Year 2007
Number of shared co-authors 0
Selina Vattathil
Emory University School of Medicine
Career Start Year 2007
Number of shared co-authors 2
Chad D Huff
University of Texas M.D. Anderson Cancer Center
Career Start Year 2007
Number of shared co-authors 1
Gabriel Renaud
Technical University of Denmark
Career Start Year 2006
Number of shared co-authors 3
Eran Elhaik
Lund University
Career Start Year 2006
Number of shared co-authors 1
Vikas Bansal
University of California San Diego
Career Start Year 2004
Number of shared co-authors 1
Alicia Hawes
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 4
Daniel G MacArthur
Broad Institute of MIT and Harvard
Career Start Year 2003
Number of shared co-authors 28
Ryan E Mills
University of Michigan Medical School ann arbor
Career Start Year 2003
Number of shared co-authors 4
Arcadi Navarro
Barcelonabeta Brain Research Center (BBRC), Pasqual Maragall Foundation
Career Start Year 2003
Number of shared co-authors 7
Jinchuan Xing
The State University of New Jersey
Career Start Year 2003
Number of shared co-authors 1
Christie L Kovar
Baylor College of Medicine
Career Start Year 2002
Number of shared co-authors 4
Fuli Yu
East China University of Science and Technology
Career Start Year 2002
Number of shared co-authors 4
Stacey Gabriel
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 14
Michael C Zody
Broad Institute of Harvard and MIT
Career Start Year 2001
Number of shared co-authors 5
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2000
Number of shared co-authors 7
Xiaoming Liu
College of Electronic Science and Engineering, Jilin University
Career Start Year 1997
Number of shared co-authors 1
Shamil R Sunyaev
Harvard Medical School
Career Start Year 1997
Number of shared co-authors 1
Philip Awadalla
Ontario Institute for Cancer Research
Career Start Year 1997
Number of shared co-authors 2
Gil McVean
Big Data Institute, University of Oxford
Career Start Year 1995
Number of shared co-authors 20
Carlos D Bustamante
Stanford University
Career Start Year 1995
Number of shared co-authors 6
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Career Start Year 1992
Number of shared co-authors 14
Stephen T Sherry
National Center for Biotechnology Information, National Institutes of Health
Career Start Year 1991
Number of shared co-authors 2
David C Samuels
Vanderbilt University
Career Start Year 1990
Number of shared co-authors 9
Donna M Muzny
Baylor College of Medicine
Career Start Year 1988
Number of shared co-authors 16
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 11
Peter Donnelly
University of Oxford
Career Start Year 1985
Number of shared co-authors 24
Richard K Wilson
The Ohio State University
Career Start Year 1983
Number of shared co-authors 9

Collaborators

Patrick F Chinnery
School of Clinical Medicine, University of Cambridge
Co-authored papers 27
Mitinori Saitou
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 5
Safa Al-Sarraj
Co-authored papers 5
Rita Horvath
School of Clinical Medicine, University of Cambridge
Co-authored papers 4
Mark J Caulfield
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 4
Chris Tyler-Smith
Wellcome Sanger Institute
Co-authored papers 4
Frances Lucy Raymond
University of Cambridge, UK Cambridge University Hospitals NHS Foundation Trust
Co-authored papers 3
Henry Houlden
Institute of Neurology, University College London (UCL)
Co-authored papers 3
Thiloka Ratnaike
University of Cambridge
Co-authored papers 3
John A Sayer
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 3
M A Surani
The Gurdon Institute
Co-authored papers 3
Shamima Rahman
UCL Great Ormond Street Institute of Child Health
Co-authored papers 3
Christopher J Penkett
National Health Service Blood and Transplant, University of Cambridge
Co-authored papers 2
Willem H Ouwehand
University of Cambridge
Co-authored papers 2
Ros Quinlivan
The Institute of Neurology, National Hospital for Neurology and Neurosurgery
Co-authored papers 2
Andrew O M Wilkie
NIHR Oxford Biomedical Research Centre
Co-authored papers 2
John R Bradley
Cambridge University Hospitals NHS Foundation
Co-authored papers 2
Maria Bitner-Glindzicz
UCL Great Ormond Street Institute of Child Health Library
Co-authored papers 2
Melita Irving
Guy's and St Thomas' NHS Foundation Trust, Evelina Children's Hospital
Co-authored papers 2
Kathleen Stirrups
University of Cambridge
Co-authored papers 2
Andrew R Webster
Institute of Ophthalmology, University College London
Co-authored papers 2
Kristina Iba??ez
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
Sofie Ashford
University of Cambridge
Co-authored papers 2
Ernest Turro
Icahn School of Medicine at Mount Sinai
Co-authored papers 2
Rodrigo Andres Floto
University of Cambridge
Co-authored papers 2
Louise Izatt
Guy's and St Thomas' NHS Foundation Trust
Co-authored papers 2
Augusto Rendon
Genomics England Ltd
Co-authored papers 2
Charu Deshpande
Guy's Hospital
Co-authored papers 2
Dragana Josifova
Guy's and St Thomas' Hospital
Co-authored papers 2
Daniel Greene
University of Cambridge
Co-authored papers 1
Release 1.2