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G. Lunter · SciRah

Researcher profile · Semantic Scholar

G. Lunter

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G. Lunter — researcher profile on SciRah

h-index: 47
Works: 156
Citations: 31K

Most-cited papers

A global reference for human genetic variation
Taras K. Oleksyk, Adam Gonçalo R. David M. Richard M. Gonçalo R. David R. Auton Abecasis Altshuler Durbin Abecasis Bentley C, Adam Gonçalo R. Auton Abecasis, Adam Auton +496 more
2015Nature17K citations Open access
Semantic Scholar
A systematic survey of loss-of-function variants in human protein-coding genes
D. MacArthur, S. Balasubramanian, A. Frankish, N. Huang +47 more
2012Science1,247 citations Open access
Semantic Scholar
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications
A. Rimmer, H. Phan, I. Mathieson, Z. Iqbal +4 more
2014Nature Genetics1,032 citations Open access
Semantic Scholar
The Human Pancreatic Islet Transcriptome: Expression of Candidate Genes for Type 1 Diabetes and the Impact of Pro-Inflammatory Cytokines
D. Eizirik, M. Sammeth, T. Bouckenooghe, G. Bottu +14 more
2012PLoS Genetics443 citations Open access
Semantic Scholar
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, H. Martin, S. Lise, J. Broxholme +106 more
2015Nature Genetics389 citations Open access
Semantic Scholar
A fine-scale chimpanzee genetic map from population sequencing
A. Auton, A. Fledel-Alon, S. Pfeifer, O. Venn +19 more
2012Science293 citations Open access
Semantic Scholar
8.2% of the Human Genome Is Constrained: Variation in Rates of Turnover across Functional Element Classes in the Human Lineage
Chris M Rands, S. Meader, C. Ponting, G. Lunter
2014PLoS Genetics263 citations Open access
Semantic Scholar
GAT: a simulation framework for testing the association of genomic intervals
A. Heger, C. Webber, Martin Goodson, C. Ponting +1 more
2013Bioinform.251 citations Open access
Semantic Scholar
The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes
S. Montgomery, D. Goode, E. Kvikstad, C. Albers +17 more
2013Genome Research251 citations Open access
Semantic Scholar
DeepC: predicting 3D genome folding using megabase-scale transfer learning
R. Schwessinger, M. Gosden, D. Downes, Richard C. Brown +5 more
2020Nature Methods193 citations Open access
Semantic Scholar
Improved workflows for high throughput library preparation using the transposome-based nextera system
S. Lamble, E. Batty, M. Attar, D. Buck +5 more
2013BMC Biotechnology171 citations Open access
Semantic Scholar
Sequencing of human genomes with nanopore technology
R. Bowden, R. Davies, A. Heger, A. Pagnamenta +16 more
2019Nature Communications170 citations Open access
Semantic Scholar
Identification of antigen-specific B cell receptor sequences using public repertoire analysis
J. Trück, M. Ramasamy, J. Galson, R. Rance +4 more
2014Journal of Immunology122 citations Open access
Semantic Scholar
scrm: efficiently simulating long sequences using the approximated coalescent with recombination
P. Staab, S. Zhu, D. Metzler, G. Lunter
2015Bioinform.114 citations Open access
Semantic Scholar
A New Isolation with Migration Model along Complete Genomes Infers Very Different Divergence Processes among Closely Related Great Ape Species
T. Mailund, Anders E. Halager, M. Westergaard, J. Dutheil +7 more
2012PLoS Genetics112 citations Open access
Semantic Scholar
Repertoire-wide phylogenetic models of B cell molecular evolution reveal evolutionary signatures of aging and vaccination
Kenneth B. Hoehn, Jason A. Vander Heiden, Julian Q. Zhou, G. Lunter +2 more
2019Proceedings of the National Academy of Sciences of the United States of America108 citations Open access
Semantic Scholar
A unified haplotype-based method for accurate and comprehensive variant calling
Daniel P Cooke, D. Wedge, G. Lunter
2018Nature Biotechnology97 citations Open access
Semantic Scholar
Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN
Anna Fowler, S. Mahamdallie, Elise Ruark, S. Seal +7 more
2016Wellcome Open Research96 citations Open access
Semantic Scholar
Analysis of B Cell Repertoire Dynamics Following Hepatitis B Vaccination in Humans, and Enrichment of Vaccine-specific Antibody Sequences
J. Galson, J. Trück, Anna Fowler, E. Clutterbuck +7 more
2015EBioMedicine92 citations Open access
Semantic Scholar
The Diversity and Molecular Evolution of B-Cell Receptors during Infection
Kenneth B. Hoehn, Anna Fowler, G. Lunter, O. Pybus
2016Molecular biology and evolution91 citations Open access
Semantic Scholar
In-Depth Assessment of Within-Individual and Inter-Individual Variation in the B Cell Receptor Repertoire
J. Galson, J. Trück, Anna Fowler, Márton Münz +4 more
2015Frontiers in Immunology83 citations Open access
Semantic Scholar
BCR repertoire sequencing: different patterns of B cell activation after two Meningococcal vaccines
J. Galson, E. Clutterbuck, J. Trück, M. Ramasamy +6 more
2015Immunology and Cell Biology78 citations Open access
Semantic Scholar
B-cell repertoire dynamics after sequential hepatitis B vaccination and evidence for cross-reactive B-cell activation
J. Galson, J. Trück, E. Clutterbuck, Anna Fowler +4 more
2016Genome Medicine68 citations Open access
Semantic Scholar
CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting
Márton Münz, Elise Ruark, A. Renwick, Emma Ramsay +7 more
2015Genome Medicine68 citations Open access
Semantic Scholar
A Phylogenetic Codon Substitution Model for Antibody Lineages
Kenneth B. Hoehn, G. Lunter, O. Pybus
2016Genetics67 citations Open access
Semantic Scholar
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
A. Pagnamenta, Carme Camps, E. Giacopuzzi, John M. Taylor +93 more
2023Genome Medicine66 citations Open access
Semantic Scholar
Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations
Katherine R. Bull, A. Rimmer, O. Siggs, L. Miosge +13 more
2013PLoS Genetics46 citations Open access
Semantic Scholar
Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis
T. Tapmeier, N. Rahmioglu, Jiang-Hai Lin, B. De Leo +30 more
2021Science Translational Medicine44 citations Open access
Semantic Scholar
Recurrence and survival after laparoscopy versus laparotomy without lymphadenectomy in early-stage endometrial cancer: Long-term outcomes of a randomised trial.
B. Reijntjes, Mieke van Suijlichem, J. Woolderink, M. Bongers +14 more
2021Gynecologic Oncology29 citations Open access
Semantic Scholar
Lifestyle factors related to prevalent chronic disease multimorbidity: A population-based cross-sectional study
J. Niebuur, J. Vonk, Yihui Du, G. H. de Bock +7 more
2023PLoS ONE28 citations Open access
Semantic Scholar
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.
Sophie Wang, V. Agarwala, J. Flannick, Charleston W. K. Chiang +79 more
2014American Journal of Human Genetics28 citations Open access
Semantic Scholar
Insertions and Deletions: Computational Methods, Evolutionary Dynamics, and Biological Applications
B. Redelings, Ian Holmes, G. Lunter, T. Pupko +1 more
2024Molecular biology and evolution26 citations Open access
Semantic Scholar
Lifestyle factors and incident multimorbidity related to chronic disease: a population-based cohort study
Yihui Du, G. D. de Bock, J. Vonk, An Thanh Pham +7 more
2024European Journal of Ageing26 citations Open access
Semantic Scholar
Unsupervised learning for medical data: A review of probabilistic factorization methods
D. Neijzen, G. Lunter
2023Statistics in Medicine25 citations Open access
Semantic Scholar
Respiratory Syncytial Virus, Human Metapneumovirus, and Parainfluenza Virus Infections in Lung Transplant Recipients: A Systematic Review of Outcomes and Treatment Strategies
A. D. de Zwart, A. Riezebos-Brilman, G. Lunter, J. Vonk +6 more
2021Clinical Infectious Diseases23 citations Open access
Semantic Scholar
Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
H. Roberts, M. Lopopolo, A. Pagnamenta, Eshita Sharma +11 more
2020Scientific Reports20 citations Open access
Semantic Scholar
Benchmarking small-variant genotyping in polyploids
Daniel P Cooke, D. Wedge, G. Lunter
2021bioRxiv19 citations Open access
Semantic Scholar
An equivariant Bayesian convolutional network predicts recombination hotspots and accurately resolves binding motifs
Richard C. Brown, G. Lunter
2018bioRxiv18 citations Open access
Semantic Scholar
Timely referral for device-aided therapy in Parkinson's disease. Development of a screening tool.
H. Moes, J. T. ten Kate, A. Portman, B. van Harten +5 more
2023Parkinsonism & Related Disorders17 citations Open access
Semantic Scholar
An integrated platform to systematically identify causal variants and genes for polygenic human traits
D. Downes, R. Schwessinger, Stephanie J. Hill, L. Nussbaum +28 more
2019bioRxiv17 citations Open access
Semantic Scholar
Haplotype matching in large cohorts using the Li and Stephens model
G. Lunter
2018Bioinform.16 citations Open access
Semantic Scholar
A high throughput screen for active human transposable elements
E. Kvikstad, P. Piazza, Jenny C. Taylor, G. Lunter
2017BMC Genomics15 citations Open access
Semantic Scholar
DeepC: Predicting chromatin interactions using megabase scaled deep neural networks and transfer learning
R. Schwessinger, M. Gosden, D. Downes, Richard E. Brown +4 more
2019bioRxiv14 citations Open access
Semantic Scholar
Mutations in CDC 45 , Encoding an Essential Component of the Pre-initiation Complex , Cause Meier-Gorlin Syndrome and Craniosynostosis
John Bell, David L. Bentley, G. McVean, P. Ratcliffe +37 more
201713 citations
Semantic Scholar
MacArthur Protein-Coding Genes A Systematic Survey of Loss-of-Function Variants in Human
D. MacArthur, S. Balasubramanian, A. Frankish, N. Huang +47 more
201211 citations
Semantic Scholar
OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis
Elise Ruark, Márton Münz, M. Clarke, A. Renwick +5 more
2016Scientific Reports10 citations Open access
Semantic Scholar
Topic modeling identifies novel genetic loci associated with multimorbidities in UK Biobank
Yi-Dong Zhang, Xi-Lin Jiang, A. Mentzer, G. McVean +1 more
2023Cell Genomics9 citations Open access
Semantic Scholar
Multi Locus View: an extensible web-based tool for the analysis of genomic data.
M. Sergeant, J. Hughes, L. Hentges, G. Lunter +2 more
2020Communications Biology8 citations Open access
Semantic Scholar
Inferring B cell specificity for vaccines using a Bayesian mixture model
Anna Fowler, J. Galson, J. Trück, D. Kelly +1 more
2020BMC Genomics8 citations Open access
Semantic Scholar
Fast haplotype matching in very large cohorts using the Li and Stephens model
G. Lunter
2016bioRxiv8 citations Open access
Semantic Scholar

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