| Year |
Citation |
Score |
| 2022 |
Young RS, Talmane L, Marion de Procé S, Taylor MS. The contribution of evolutionarily volatile promoters to molecular phenotypes and human trait variation. Genome Biology. 23: 89. PMID 35379293 DOI: 10.1186/s13059-022-02634-w |
0.576 |
|
| 2022 |
Younger NT, Wilson ML, Martinez Lyons A, Jarman EJ, Meynert AM, Grimes GR, Gournopanos K, Waddell SH, Tennant PA, Wilson DH, Guest RV, Wigmore SJ, Acosta JC, Kendall TJ, Taylor MS, et al. In vivo modeling of patient genetic heterogeneity identifies new ways to target cholangiocarcinoma. Cancer Research. PMID 35074757 DOI: 10.1158/0008-5472.CAN-21-2556 |
0.658 |
|
| 2020 |
Ramilowski JA, Yip CW, Agrawal S, Chang JC, Ciani Y, Kulakovskiy IV, Mendez M, Ooi JLC, Ouyang JF, Parkinson N, Petri A, Roos L, Severin J, Yasuzawa K, Abugessaisa I, ... ... Taylor MS, et al. Functional annotation of human long noncoding RNAs via molecular phenotyping. Genome Research. PMID 32718982 DOI: 10.1101/Gr.254219.119 |
0.57 |
|
| 2020 |
Alam T, Agrawal S, Severin J, Young RS, Andersson R, Arner E, Hasegawa A, Lizio M, Ramilowski JA, Abugessaisa I, Ishizu Y, Noma S, Tarui H, Taylor MS, Lassmann T, et al. Comparative transcriptomics of primary cells in vertebrates. Genome Research. PMID 32718981 DOI: 10.1101/Gr.255679.119 |
0.534 |
|
| 2020 |
Longman D, Jackson-Jones KA, Maslon MM, Murphy LC, Young RS, Stoddart JJ, Hug N, Taylor MS, Papadopoulos DK, Cáceres JF. Identification of a localized nonsense-mediated decay pathway at the endoplasmic reticulum. Genes & Development. PMID 32616520 DOI: 10.1101/Gad.338061.120 |
0.476 |
|
| 2020 |
Mordstein C, Savisaar R, Young RS, Bazile J, Talmane L, Luft J, Liss M, Taylor MS, Hurst LD, Kudla G. Codon Usage and Splicing Jointly Influence mRNA Localization. Cell Systems. PMID 32275854 DOI: 10.1016/J.Cels.2020.03.001 |
0.556 |
|
| 2019 |
Halachev M, Meynert A, Taylor MS, Vitart V, Kerr SM, Klaric L, Aitman TJ, Haley CS, Prendergast JG, Pugh C, Hume DA, Harris SE, Liewald DC, Deary IJ, et al. Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions. Plos Genetics. 15: e1008480. PMID 31765389 DOI: 10.1371/Journal.Pgen.1008480 |
0.675 |
|
| 2017 |
Young RS, Kumar Y, Bickmore WA, Taylor MS. Bidirectional transcription initiation marks accessible chromatin and is not specific to enhancers. Genome Biology. 18: 242. PMID 29284524 DOI: 10.1186/S13059-017-1379-8 |
0.517 |
|
| 2017 |
Moss CF, Dalla Rosa I, Hunt LE, Yasukawa T, Young R, Jones AWE, Reddy K, Desai R, Virtue S, Elgar G, Voshol P, Taylor MS, Holt IJ, Reijns MAM, Spinazzola A. Aberrant ribonucleotide incorporation and multiple deletions in mitochondrial DNA of the murine MPV17 disease model. Nucleic Acids Research. PMID 29106596 DOI: 10.1093/Nar/Gkx1009 |
0.484 |
|
| 2015 |
Young RS, Hayashizaki Y, Andersson R, Sandelin A, Kawaji H, Itoh M, Lassmann T, Carninci P, Bickmore WA, Forrest AR, Taylor MS. The frequent evolutionary birth and death of functional promoters in mouse and human. Genome Research. PMID 26228054 DOI: 10.1101/Gr.190546.115 |
0.584 |
|
| 2014 |
Ansari M, Poke G, Ferry Q, Williamson K, Aldridge R, Meynert AM, Bengani H, Chan CY, Kayserili H, Avci S, Hennekam RC, Lampe AK, Redeker E, Homfray T, Ross A, ... ... Taylor MS, et al. Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. Journal of Medical Genetics. 51: 659-68. PMID 25125236 DOI: 10.1136/Jmedgenet-2014-102573 |
0.673 |
|
| 2014 |
Zhang Y, Dean C, Chessum L, Nguyen D, Stewart M, Taylor M, Cookson WO, Moffatt MF. Functional analysis of a novel ENU-induced PHD finger 11 (Phf11) mouse mutant. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 25: 573-82. PMID 25091723 DOI: 10.1007/S00335-014-9535-X |
0.353 |
|
| 2014 |
Handley MT, Mégarbané A, Meynert AM, Brown S, Freyer E, Taylor MS, Jackson IJ, Aligianis IA. Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome. Molecular Genetics & Genomic Medicine. 2: 319-25. PMID 25077174 DOI: 10.1002/Mgg3.70 |
0.664 |
|
| 2014 |
Meynert AM, Ansari M, FitzPatrick DR, Taylor MS. Variant detection sensitivity and biases in whole genome and exome sequencing. Bmc Bioinformatics. 15: 247. PMID 25038816 DOI: 10.1186/1471-2105-15-247 |
0.671 |
|
| 2014 |
Rainger J, Pehlivan D, Johansson S, Bengani H, Sanchez-Pulido L, Williamson KA, Ture M, Barker H, Rosendahl K, Spranger J, Horn D, Meynert A, Floyd JA, Prescott T, Anderson CA, ... ... Taylor MS, et al. Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. American Journal of Human Genetics. 94: 915-23. PMID 24906020 DOI: 10.1016/J.Ajhg.2014.05.005 |
0.673 |
|
| 2014 |
Metsu S, Rooms L, Rainger J, Taylor MS, Bengani H, Wilson DI, Chilamakuri CS, Morrison H, Vandeweyer G, Reyniers E, Douglas E, Thompson G, Haan E, Gecz J, Fitzpatrick DR, et al. FRA2A is a CGG repeat expansion associated with silencing of AFF3. Plos Genetics. 10: e1004242. PMID 24763282 DOI: 10.1371/Journal.Pgen.1004242 |
0.315 |
|
| 2014 |
Forrest AR, Kawaji H, Rehli M, Baillie JK, de Hoon MJ, Haberle V, Lassmann T, Kulakovskiy IV, Lizio M, Itoh M, Andersson R, Mungall CJ, Meehan TF, Schmeier S, ... ... Taylor MS, et al. A promoter-level mammalian expression atlas. Nature. 507: 462-70. PMID 24670764 DOI: 10.1038/Nature13182 |
0.723 |
|
| 2014 |
Williamson KA, Rainger J, Floyd JA, Ansari M, Meynert A, Aldridge KV, Rainger JK, Anderson CA, Moore AT, Hurles ME, Clarke A, van Heyningen V, Verloes A, Taylor MS, Wilkie AO, et al. Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. American Journal of Human Genetics. 94: 295-302. PMID 24462371 DOI: 10.1016/J.Ajhg.2014.01.001 |
0.674 |
|
| 2013 |
Meynert AM, Bicknell LS, Hurles ME, Jackson AP, Taylor MS. Quantifying single nucleotide variant detection sensitivity in exome sequencing. Bmc Bioinformatics. 14: 195. PMID 23773188 DOI: 10.1186/1471-2105-14-195 |
0.654 |
|
| 2012 |
Schroder K, Irvine KM, Taylor MS, Bokil NJ, Le Cao KA, Masterman KA, Labzin LI, Semple CA, Kapetanovic R, Fairbairn L, Akalin A, Faulkner GJ, Baillie JK, Gongora M, Daub CO, et al. Conservation and divergence in Toll-like receptor 4-regulated gene expression in primary human versus mouse macrophages. Proceedings of the National Academy of Sciences of the United States of America. 109: E944-53. PMID 22451944 DOI: 10.1073/Pnas.1110156109 |
0.507 |
|
| 2010 |
Vandiedonck C, Taylor M, Lockstone H, Plant K, Taylor J, Fairfax B, Durrant C, Broxholme J, Knight J. The First Transcriptional Map of the Human Major Histocompatibility Complex Reveals New Transcripts and Haplotype-specific Pattern of Expression Clinical Immunology. 135: S9. DOI: 10.1016/J.Clim.2010.03.035 |
0.335 |
|
| 2009 |
Taylor JM, Street TL, Hao L, Copley R, Taylor MS, Hayden PJ, Stolper G, Mott R, Hein J, Moffatt MF, Cookson WO. Dynamic and physical clustering of gene expression during epidermal barrier formation in differentiating keratinocytes. Plos One. 4: e7651. PMID 19888454 DOI: 10.1371/Journal.Pone.0007651 |
0.506 |
|
| 2009 |
Huang GJ, Shifman S, Valdar W, Johannesson M, Yalcin B, Taylor MS, Taylor JM, Mott R, Flint J. High resolution mapping of expression QTLs in heterogeneous stock mice in multiple tissues. Genome Research. 19: 1133-40. PMID 19376938 DOI: 10.1101/Gr.088120.108 |
0.512 |
|
| 2008 |
Taylor MS, Massingham T, Hayashizaki Y, Carninci P, Goldman N, Semple CA. Rapidly evolving human promoter regions. Nature Genetics. 40: 1262-3; author reply. PMID 18957975 DOI: 10.1038/Ng1108-1262 |
0.709 |
|
| 2007 |
Taylor M, Valdar W, Kumar A, Flint J, Mott R. Management, presentation and interpretation of genome scans using GSCANDB. Bioinformatics (Oxford, England). 23: 1545-9. PMID 17400728 DOI: 10.1093/Bioinformatics/Btm123 |
0.541 |
|
| 2007 |
Shifman S, Bell JT, Copley RR, Taylor MS, Mott R, Flint J, Williams RW. Evidence of a large-scale functional organization of mammalian chromosomes: Authors' reply [2] Plos Biology. 5: 0984. DOI: 10.1371/Journal.Pbio.0050128 |
0.48 |
|
| 2006 |
Shifman S, Bell JT, Copley RR, Taylor MS, Williams RW, Mott R, Flint J. A high-resolution single nucleotide polymorphism genetic map of the mouse genome. Plos Biology. 4: e395. PMID 17105354 DOI: 10.1371/Journal.Pbio.0040395 |
0.487 |
|
| 2006 |
Valdar W, Solberg LC, Gauguier D, Burnett S, Klenerman P, Cookson WO, Taylor MS, Rawlins JN, Mott R, Flint J. Genome-wide genetic association of complex traits in heterogeneous stock mice. Nature Genetics. 38: 879-87. PMID 16832355 DOI: 10.1038/Ng1840 |
0.507 |
|
| 2004 |
Gibbs RA, Weinstock GM, Metzker ML, Muzny DM, Sodergren EJ, Scherer S, Scott G, Steffen D, Worley KC, Burch PE, Okwuonu G, Hines S, Lewis L, DeRamo C, Delgado O, ... ... Taylor MS, et al. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 428: 493-521. PMID 15057822 DOI: 10.1038/Nature02426 |
0.503 |
|
| 2000 |
Davidson H, Taylor MS, Doherty A, Boyd AC, Porteous DJ. Genomic sequence analysis of Fugu rubripes CFTR and flanking genes in a 60 kb region conserving synteny with 800 kb of human chromosome 7 Genome Research. 10: 1194-1203. PMID 10958637 DOI: 10.1101/gr.10.8.1194 |
0.301 |
|
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