V. Berry

Publication List Details

Period

1990 - 2009

Number

53

Co-Authors

From Constrained to Unconstrained Maximum Agreement Subtree in Linear Time ∗ (2008)

V. Berry, Z. S. Peng, H. F. Ting

We propose and study the Maximum Constrained Agreement Sub-tree (MCAST) problem, which is a variant of the classical Maximum Agreement Subtree (MAST) problem. Our problem allows users to ap-ply their...

Computational Statistics Data Analysis 38 (2000) 273--283 (2008)

Www Elsevier Com, V. Berry, O. Gascuel, G. Caraux

We consider the problem of phylogenetic reconstruction, which consists in estimating the evolutionary history of a set of species. This unknown history is modelled as a tree and estimated from...

Super-Arbre d'Accord Maximum (2007)

Berry, V.

Super-Arbre d'Accord Maximum

Fast Computation of Supertrees for Compatible Phylogenies with Nested Taxa (2006)

Berry, V., Semple, C.

Typically, supertree methods combine a collection of source trees in which just the leaves are labeled by taxa. In such methods the resulting supertree is also leaf labeled. An underlying assumption...

Improved Parametrized Complexity of the Maximum Agreement Subtree and Maximum Compatible Tree problems (2005)

Berry, V., Nicolas, F.

Improved Parametrized Complexity of the Maximum Agreement Subtree and Maximum Compatible Tree problems

Highly Selective, Electrically Conductive Monolayer of Nanoparticles on Live Bacteria (2004)

Berry, V, S, RangaSwamy, Saraf, Ravi

Using specific peptide−bacteria affinity, a monolayer of 30 nm Au particle is selectively deposited on live bacteria surface to produce electrically conducting bridges spanning over 12 μm. The...

Maximum Agreement and Compatible Supertrees (2004)

Berry, V., Nicolas, F.

Maximum Agreement and Compatible Supertrees

Maximum Agreement and Compatible Supertrees (2004)

Berry, V., Nicolas, F.

Maximum Agreement and Compatible Supertrees

Characterisation of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract (2004)

Reddy, M. Ashwin, Bateman, O. A., Chakarova, C., Ferris, J., Berry, V., Lomas, E., ...

Congenital cataract is a leading cause of visual disability in children. Inherited isolated (non-syndromic) cataract represents a significant proportion of cases and the identification of genes...

Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract (2004)

Reddy, M.A., Bateman, O.A., Chakarova, C., Ferris, J., Berry, V., Lomas, E., ...

Congenital cataract is a leading cause of visual disability in children. Inherited isolated (non-syndromic) cataract represents a significant proportion of cases and the identification of genes...

Characterisation of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract (2004)

Reddy, M. Ashwin, Bateman, O. A., Chakarova, C., Ferris, J., Berry, V., Lomas, E., ...

Congenital cataract is a leading cause of visual disability in children. Inherited isolated (non-syndromic) cataract represents a significant proportion of cases and the identification of genes...

Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. (2001)

Berry, V., Francis, P., Reddy, M. A., Collyer, D., Vithana, E., MacKay, I, ...

Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to...

Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans (2001)

Berry, V., Francis, P., Reddy, M.A., Collyer, D., Vithana, E., MacKay, I., ...

Congenital cataracts are an important cause of bilateral visual impairment in infants. In a four-generation family of English descent, we mapped dominant congenital posterior polar cataract to...

Penetration of amoxycillin, ticarcillin and clavulanic add into lymph after intravenous infusion in rabbits to simulate human serum pharmacokinetics (1990)

Woodnutt, G., Berry, V., Kernutt, I., Mizen, L.

The distribution of amoxycillin, ticarcillin and clavulanic acid into lymph collected from the right lymphatic duct of rabbits was examined after intravenous administration. The compounds were...

Bactericidal and morphological effects of amoxicillin on Helicobacter pylori.

Berry, V, Jennings, K, Woodnutt, G

The growth kinetics of Helicobacter pylori after it has been exposed to amoxicillin have been investigated in conjunction with studies of cell morphology. A potent bactericidal effect was observed at...

Effect of protein binding on penetration of beta-lactams into rabbit peripheral lymph.

Woodnutt, G, Berry, V, Mizen, L

The relevance of protein binding to penetration of beta-lactams into body fluids was investigated by examining the distribution of amoxicillin, ceftriaxone, clavulanic acid, temocillin, and...

Simulation of human serum pharmacokinetics of cefazolin, piperacillin, and BRL 42715 in rats and efficacy against experimental intraperitoneal infections.

Woodnutt, G, Berry, V, Mizen, L

Studies were performed to determine the effects of BRL 42715, a potent beta-lactamase inhibitor, on the activity of cefazolin and piperacillin against experimental intraperitoneal infections caused...

A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.

Mackay, D, Ionides, A, Berry, V, Moore, A, Bhattacharya, S, Shiels, A

Inherited cataract is a clinically and genetically heterogeneous disease that most often presents as a congenital autosomal dominant trait. Here we report the linkage of a new locus for dominant...

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.

Shiels, A, Mackay, D, Ionides, A, Berry, V, Moore, A, Bhattacharya, S

CZP1, a locus for autosomal dominant "zonular pulverulent" cataract, previously had been linked with the Duffy blood-group-antigen locus on chromosome 1q. Here we report genetic refinement of the...

Connexin46 mutations in autosomal dominant congenital cataract.

Mackay, D, Ionides, A, Kibar, Z, Rouleau, G, Berry, V, Moore, A, ...

Loci for autosomal dominant "zonular pulverulent" cataract have been mapped to chromosomes 1q (CZP1) and 13q (CZP3). Here we report genetic refinement of the CZP3 locus and identify underlying...

Bactericidal and morphological effects of amoxicillin on Helicobacter pylori.

Berry, V, Jennings, K, Woodnutt, G

The growth kinetics of Helicobacter pylori after it has been exposed to amoxicillin have been investigated in conjunction with studies of cell morphology. A potent bactericidal effect was observed at...

Effect of protein binding on penetration of beta-lactams into rabbit peripheral lymph.

Woodnutt, G, Berry, V, Mizen, L

The relevance of protein binding to penetration of beta-lactams into body fluids was investigated by examining the distribution of amoxicillin, ceftriaxone, clavulanic acid, temocillin, and...

Simulation of human serum pharmacokinetics of cefazolin, piperacillin, and BRL 42715 in rats and efficacy against experimental intraperitoneal infections.

Woodnutt, G, Berry, V, Mizen, L

Studies were performed to determine the effects of BRL 42715, a potent beta-lactamase inhibitor, on the activity of cefazolin and piperacillin against experimental intraperitoneal infections caused...

A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q.

Shiels, A, Mackay, D, Ionides, A, Berry, V, Moore, A, Bhattacharya, S

CZP1, a locus for autosomal dominant "zonular pulverulent" cataract, previously had been linked with the Duffy blood-group-antigen locus on chromosome 1q. Here we report genetic refinement of the...

Connexin46 mutations in autosomal dominant congenital cataract.

Mackay, D, Ionides, A, Kibar, Z, Rouleau, G, Berry, V, Moore, A, ...

Loci for autosomal dominant "zonular pulverulent" cataract have been mapped to chromosomes 1q (CZP1) and 13q (CZP3). Here we report genetic refinement of the CZP3 locus and identify underlying...

A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.

Mackay, D, Ionides, A, Berry, V, Moore, A, Bhattacharya, S, Shiels, A

Inherited cataract is a clinically and genetically heterogeneous disease that most often presents as a congenital autosomal dominant trait. Here we report the linkage of a new locus for dominant...

Clinical and genetic heterogeneity in autosomal dominant cataract

Ionides, A., Francis, P., Berry, V., Mackay, D., Bhattacharya, S., Shiels, A., ...

AIMS—To determine the different morphologies of autosomal dominant cataract (ADC), assess the intra- and interfamilial variation in cataract morphology, and undertake a genetic linkage study to...

Congenital progressive polymorphic cataract caused by a mutation in the major intrinsic protein of the lens, MIP (AQP0)

Francis, P., Berry, V., Bhattacharya, S., Moore, A.

BACKGROUND—Congenital cataract, when inherited as an isolated abnormality, is phenotypically and genetically heterogeneous. Although there is no agreed nomenclature for the patterns of cataract...

A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma

Reddy, M A, Francis, P J, Berry, V, Bradshaw, K, Patel, R J, Maher, E R, ...

Aim: To phenotype and genetically map the disease locus in a family presenting with autosomal dominant microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.

Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene

Addison, P K F, Berry, V, Ionides, A C W, Francis, P J, Bhattacharya, S S, Moore, A T

Background: The authors recently identified three large genetically unrelated families with an identical 17 base pair duplication mutation in exon 4 of the PITX3 gene. Here, they report the detailed...

The genetics of childhood cataract

Francis, P, Berry, V, Bhattacharya, S, Moore, A

Human congenital cataract has a diverse aetiology. In the proportion of cases where the cause is genetic, the disease shows wide phenotypic and genetic heterogeneity. Over the past few years, much...

A locus for isolated cataract on human Xp

Francis, P, Berry, V, Hardcastle, A, Maher, E, Moore, A, Bhattacharya, S

Purpose: To genetically map the gene causing isolated X linked cataract in a large European pedigree.