Articles with public access mandates - Caleb WebberLearn more
Not available anywhere: 1
Review
Epistasis in neuropsychiatric disorders
C Webber
Trends in Genetics 33 (4), 256-265, 2017
Mandates: UK Medical Research Council
Available somewhere: 71
Review
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Mandates: US National Institutes of Health, Swedish Research Council, Alzheimers's UK …
Review
Genome analysis of the platypus reveals unique signatures of evolution
Nature 453 (7192), 175-183, 2008
Mandates: US National Institutes of Health, German Research Foundation
Review
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
P Gormley, V Anttila, BS Winsvold, P Palta, T Esko, TH Pers, KH Farh, ...
Nature genetics 48 (8), 856-866, 2016
Mandates: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
Review
Systematic phenomics analysis deconvolutes genes mutated in intellectual disability into biologically coherent modules
K Kochinke, C Zweier, B Nijhof, M Fenckova, P Cizek, F Honti, ...
The American Journal of Human Genetics 98 (1), 149-164, 2016
Mandates: US National Institutes of Health, German Research Foundation, Netherlands …
Review
Natural genetic variation caused by small insertions and deletions in the human genome
RE Mills, WS Pittard, JM Mullaney, U Farooq, TH Creasy, AA Mahurkar, ...
Genome research 21 (6), 830-839, 2011
Mandates: US National Institutes of Health
Review
Addressing variability in iPSC-derived models of human disease: guidelines to promote reproducibility
V Volpato, C Webber
Disease models & mechanisms 13 (1), dmm042317, 2020
Mandates: Alzheimers's UK, UK Medical Research Council
Review
A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders
D Agarwal, C Sandor, V Volpato, TM Caffrey, J Monzón-Sandoval, ...
Nature communications 11 (1), 4183, 2020
Mandates: Alzheimers's UK, UK Medical Research Council, National Institute for Health …
Review
GAT: a simulation framework for testing the association of genomic intervals
A Heger, C Webber, M Goodson, CP Ponting, G Lunter
Bioinformatics 29 (16), 2046-2048, 2013
Mandates: UK Medical Research Council, Wellcome Trust
Review
Diagnostically relevant facial gestalt information from ordinary photos
Q Ferry, J Steinberg, C Webber, DR FitzPatrick, CP Ponting, A Zisserman, ...
elife 3, e02020, 2014
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
Review
CSF1R inhibitor JNJ-40346527 attenuates microglial proliferation and neurodegeneration in P301S mice
R Mancuso, G Fryatt, M Cleal, J Obst, E Pipi, J Monzón-Sandoval, E Ribe, ...
Brain 142 (10), 3243-3264, 2019
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
Review
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill
WM Brandler, AP Morris, DM Evans, TS Scerri, JP Kemp, NJ Timpson, ...
PLoS genetics 9 (9), e1003751, 2013
Mandates: UK Medical Research Council, Wellcome Trust
Review
Reproducibility of molecular phenotypes after long-term differentiation to human iPSC-derived neurons: a multi-site omics study
V Volpato, J Smith, C Sandor, JS Ried, A Baud, A Handel, SE Newey, ...
Stem cell reports 11 (4), 897-911, 2018
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
Review
Single-cell sequencing of iPSC-dopamine neurons reconstructs disease progression and identifies HDAC4 as a regulator of Parkinson cell phenotypes
C Lang, KR Campbell, BJ Ryan, P Carling, M Attar, J Vowles, ...
Cell stem cell 24 (1), 93-106. e6, 2019
Mandates: Cancer Research UK, UK Medical Research Council, National Institute for …
Review
Cellular α-synuclein pathology is associated with bioenergetic dysfunction in Parkinson’s iPSC-derived dopamine neurons
F Zambon, M Cherubini, HJR Fernandes, C Lang, BJ Ryan, V Volpato, ...
Human Molecular Genetics 28 (12), 2001-2013, 2019
Mandates: UK Medical Research Council, Parkinson's UK, Wellcome Trust
Review
Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia
A Hoerder-Suabedissen, FM Oeschger, ML Krishnan, TG Belgard, ...
Proceedings of the National Academy of Sciences 110 (9), 3555-3560, 2013
Mandates: US National Institutes of Health
Review
Extensive microRNA-mediated crosstalk between lncRNAs and mRNAs in mouse embryonic stem cells
JY Tan, T Sirey, F Honti, B Graham, A Piovesan, M Merkenschlager, ...
Genome research 25 (5), 655-666, 2015
Mandates: Swiss National Science Foundation, Natural Sciences and Engineering Research …
Review
Reduced purifying selection prevails over positive selection in human copy number variant evolution
DQ Nguyen, C Webber, J Hehir-Kwa, R Pfundt, J Veltman, CP Ponting
Genome Research 18 (11), 1711-1723, 2008
Mandates: Swiss National Science Foundation
Review
The Parkinson's disease genome‐wide association study locus browser
FP Grenn, JJ Kim, MB Makarious, H Iwaki, A Illarionova, K Brolin, ...
Movement Disorders 35 (11), 2056-2067, 2020
Mandates: US National Institutes of Health, American Heart Association, Alzheimers's …
Publication and funding information is determined automatically by a computer program