引用次数
引用: 26,316
H-指数: 70
I10-指数 : 215
出版物: 449
Mutagenesis of three surface-exposed loops of a Bacillus thuringiensis insecticidal toxin reveals residues important for toxicity, receptor recognition and possibly membrane insertion.
D. P. Smedley , D. J. Ellar
Microbiology 142 ( 7) 1617 -1624
79
1996
Channel activity caused by a Bacillus thuringiensis δ-endotoxin preparation depends on the method of activation
Damian P Smedley , Graham Armstrong , David J Ellar
Molecular membrane biology 14 ( 1) 13 -18
24
1997
The Monarch Initiative: An integrative data and analytic platform connecting phenotypes to genotypes across species
Christopher J Mungall , Julie A McMurry , Sebastian Köhler , James P Balhoff
bioRxiv 055756
252
2016
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism
Maya Chopra , Meriel McEntagart , Jill Clayton-Smith , Konrad Platzer
American Journal of Human Genetics 108 ( 6) 1138 -1150
2021
Identification of genes required for eye development by high-throughput screening of mouse knockouts.
Bret A Moore , Brian C Leonard , Lionel Sebbag , Sydney G Edwards
Communications Biology 1 ( 1) 236 -236
17
2018
Ensembl’s 10th year
Nathan Johnson , Andreas Kähäri , Damian Keefe , Stephen Keenan
Nucleic Acids Research 38 557 -562
367
2010
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
Clare Turnbull , Richard H Scott , Ellen Thomas , Louise Jones
BMJ 361
328
2018
Sustaining the Data and Bioresource Commons
Paul N. Schofield , Janan Eppig , Eva Huala , Martin Hrabe de Angelis
Science 330 ( 6004) 592 -593
46
2010
Generation of Silver Standard Concept Annotations from Biomedical Texts with Special Relevance to Phenotypes
Anika Oellrich , Nigel Collier , Damian Smedley , Tudor Groza
PLOS ONE 10 ( 1) e0116040
15
2015
Exomiser and Genomiser
Julius O.B. Jacobsen , Damian Smedley , Peter Robinson
Chapman and Hall/CRC 387 -406
2017
Dual colour fluorescence in situ hybridization to paraffin-embedded samples to deduce the presence of the der(X)t(X;18)(p11.2;q11.2) and involvement of either the SSX1 or SSX2 gene: a diagnostic and prognostic aid for synovial sarcoma.
Yong-Jie Lu , Sandra Birdsall , Brenda Summersgill , Damian Smedley
The Journal of Pathology 187 ( 4) 490 -496
51
1999
The Human Phenotype Ontology in 2021.
Sebastian Köhler , Michael Gargano , Nicolas Matentzoglu , Leigh C Carmody
Nucleic Acids Research 49 1207
5
2021
BioMart Central Portal—unified access to biological data
Syed Haider , Benoit Ballester , Damian Smedley , Junjun Zhang
Nucleic Acids Research 37 23 -27
300
2009
Cre recombinase resources for conditional mouse mutagenesis.
Damian Smedley , Ekaterina Salimova , Nadia Rosenthal
Methods 53 ( 4) 411 -416
40
2011
The influence of disease categories on gene candidate predictions from model organism phenotypes
Anika Oellrich , Sebastian Koehler , Nicole Washington , Chris Mungall
Journal of Biomedical Semantics 5 ( 1) 1 -14
8
2014
The genomic structure of ZNF198 and location of breakpoints in the t(8;13) myeloproliferative syndrome.
Shashikant Kulkarni , Andreas Reiter , Damian Smedley , John M. Goldman
Genomics 55 ( 1) 118 -121
20
1999
Cloning and mapping of members of the MYM family.
Damian Smedley , Rifat Hamoudi , Yong-Jie Lu , Colin Cooper
Genomics 60 ( 2) 244 -247
23
1999
High-throughput mouse phenomics for characterizing mammalian gene function
Steve D. M. Brown , Chris C. Holmes , Ann-Marie Mallon , Terrence F. Meehan
Nature Reviews Genetics 19 ( 6) 357 -370
67
2018
A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease
Damian Smedley , Max Schubach , Julius O.B. Jacobsen , Sebastian Köhler
American Journal of Human Genetics 99 ( 3) 595 -606
130
2016
An Improved Phenotype-Driven Tool for Rare Mendelian Variant Prioritization: Benchmarking Exomiser on Real Patient Whole-Exome Data.
Valentina Cipriani , Nikolas Pontikos , Gavin Arno , Panagiotis I. Sergouniotis
Genes 11 ( 4) 460 -460
3
2020