Follow
Paul Bevan
Paul Bevan
Wellcome Sanger Institute - Hinxton Cambridge UK
Verified email at sanger.ac.uk - Homepage
Title
Cited by
Cited by
Year
DECIPHER: database of chromosomal imbalance and phenotype in humans using ensembl resources
HV Firth, SM Richards, AP Bevan, S Clayton, M Corpas, D Rajan, ...
The American Journal of Human Genetics 84 (4), 524-533, 2009
18712009
Prevalence and architecture of de novo mutations in developmental disorders
Nature 542 (7642), 433-438, 2017
8662017
Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data
CF Wright, TW Fitzgerald, WD Jones, S Clayton, JF McRae, ...
The Lancet 385 (9975), 1305-1314, 2015
8132015
Large-scale discovery of novel genetic causes of developmental disorders.
DDD Study
Nature 519 (7542), 223-228, 2015
7342015
Peroxovanadium compounds. A new class of potent phosphotyrosine phosphatase inhibitors which are insulin mimetics.
BI Posner, R Faure, JW Burgess, AP Bevan, D Lachance, G Zhang-Sun, ...
Journal of Biological Chemistry 269 (6), 4596-4604, 1994
6571994
An overview of Ensembl
E Birney, TD Andrews, P Bevan, M Caccamo, Y Chen, L Clarke, G Coates, ...
Genome research 14 (5), 925-928, 2004
5572004
Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B. 1.1. 7
B Meng, SA Kemp, G Papa, R Datir, IATM Ferreira, S Marelli, WT Harvey, ...
Cell reports 35 (13), 2021
4162021
Insulin signalling
P Bevan
Journal of cell science 114 (8), 1429-1430, 2001
3402001
Ensembl 2002: accommodating comparative genomics
M Clamp, D Andrews, D Barker, P Bevan, G Cameron, Y Chen, L Clark, ...
Nucleic Acids Research 31 (1), 38-42, 2003
2892003
DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation
E Bragin, EA Chatzimichali, CF Wright, ME Hurles, HV Firth, AP Bevan, ...
Nucleic acids research 42 (D1), D993-D1000, 2014
2412014
Ensembl 2004
E Birney, D Andrews, P Bevan, M Caccamo, G Cameron, Y Chen, ...
Nucleic acids research 32 (suppl_1), D468-D470, 2004
2332004
Cellular and subcellular distribution of polycystin-2, the protein product of the PKD2 gene
L Foggensteiner, AP Bevan, R Thomas, N Coleman, C Boulter, J Bradley, ...
Journal of the American Society of Nephrology 11 (5), 814-827, 2000
2092000
Histone lysine methylases and demethylases in the landscape of human developmental disorders
V Faundes, WG Newman, L Bernardini, N Canham, J Clayton-Smith, ...
The American Journal of Human Genetics 102 (1), 175-187, 2018
2022018
The deciphering developmental disorders (DDD) study
HV Firth, CF Wright
Developmental medicine and child neurology 53 (8), 702, 2011
1862011
Peroxovanadium compounds: biological actions and mechanism of insulin-mimesis
AP Bevan, PG Drake, JF Yale, A Shaver, BI Posner
Vanadium Compounds: Biochemical and Therapeutic Applications, 49-58, 1995
1601995
Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype
LG Sadleir, EI Mountier, D Gill, S Davis, C Joshi, C DeVile, MA Kurian, ...
Neurology 89 (10), 1035-1042, 2017
1242017
Selective activation of the rat hepatic endosomal insulin receptor kinase: role for the endosome in insulin signaling
AP Bevan, JW Burgess, PG Drake, A Shaver, JJM Bergeron, BI Posner
Journal of Biological Chemistry 270 (18), 10784-10791, 1995
1021995
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
L Snijders Blok, J Rousseau, J Twist, S Ehresmann, M Takaku, ...
Nature communications 9 (1), 4619, 2018
952018
Global public perceptions of genomic data sharing: what shapes the willingness to donate DNA and health data?
A Middleton, R Milne, MA Almarri, S Anwer, J Atutornu, EE Baranova, ...
The American Journal of Human Genetics 107 (4), 743-752, 2020
932020
DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders
GJ Swaminathan, E Bragin, EA Chatzimichali, M Corpas, AP Bevan, ...
Human molecular genetics 21 (R1), R37-R44, 2012
882012
The system can't perform the operation now. Try again later.
Articles 1–20