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P. Byrd · SciRah

Researcher profile · Semantic Scholar

P. Byrd

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P. Byrd — researcher profile on SciRah

h-index: 26
Works: 55
Citations: 4,469

Most-cited papers

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.
G. Stewart, R. Maser, T. Stankovic, D. Bressan +6 more
1999Cell1,058 citations Open access
Semantic Scholar
Cancer risks and mortality in heterozygous ATM mutation carriers.
Deborah P. Thompson, Silvia Duedal, J. Kirner, L. McGuffog +5 more
2005Journal of the National Cancer Institute571 citations Open access
Semantic Scholar
ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer.
T. Stankovic, A. Kidd, A. Sutcliffe, G. McGuire +9 more
1998American Journal of Human Genetics385 citations Open access
Semantic Scholar
The Wnt Antagonist sFRP1 in Colorectal Tumorigenesis
Germaine M. Caldwell, Carolyn Jones, K. Gensberg, S. Jan +6 more
2004Cancer Research286 citations
Semantic Scholar
Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.
A. M. Taylor, A. Groom, P. Byrd
2004DNA Repair282 citations
Semantic Scholar
Molecular pathology of ataxia telangiectasia
A. Taylor, P. Byrd
2005Journal of Clinical Pathology246 citations Open access
Semantic Scholar
RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling
G. Stewart, T. Stankovic, P. Byrd, Thomas Wechsler +6 more
2007Proceedings of the National Academy of Sciences of the United States of America189 citations Open access
Semantic Scholar
Mutations associated with variant phenotypes in ataxia-telangiectasia.
C. Mcconville, T. Stankovic, P. Byrd, G. McGuire +3 more
1996American Journal of Human Genetics189 citations
Semantic Scholar
Ataxia telangiectasia: more variation at clinical and cellular levels
A. M. Taylor, Z. Lam, J. Last, P. Byrd
2015Clinical Genetics105 citations
Semantic Scholar
Immunodeficiency in ataxia telangiectasia is correlated strongly with the presence of two null mutations in the ataxia telangiectasia mutated gene
E. Staples, E. McDermott, A. Reiman, P. Byrd +3 more
2008Clinical and Experimental Immunology105 citations Open access
Semantic Scholar
Mutations revealed by sequencing the 5' half of the gene for ataxia telangiectasia.
P. Byrd, C. McConville, P. R. Cooper, Julian Parkhill +4 more
1996Human Molecular Genetics100 citations
Semantic Scholar
ATM Mutations in Sporadic Lymphoid Tumours
T. Stankovic, Grant S. Stewart, P. Byrd, Christopher Fegan +2 more
2002Leukemia and Lymphoma93 citations
Semantic Scholar
Serotype-Specific Inactivation of the Cellular DNA Damage Response during Adenovirus Infection
Natalie A Forrester, G. Sedgwick, Anoushka Thomas, Andrew N. Blackford +6 more
2010Journal of Virology71 citations Open access
Semantic Scholar
Malignant transformation of human embryo retinoblasts by cloned adenovirus 12 DNA
P. Byrd, K. Brown, P. Gallimore
1982Nature70 citations
Semantic Scholar
hMRE11: genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decay.
S. Pitts, H. Kullar, T. Stankovic, G. Stewart +7 more
2001Human Molecular Genetics69 citations
Semantic Scholar
Genetic and cellular features of ataxia telangiectasia.
A. Taylor, P. Byrd, C. Mcconville, S. Thacker
1994International Journal of Radiation Biology69 citations
Semantic Scholar
Transformation of human embryo retinoblasts with simian virus 40, adenovirus and ras oncogenes.
P. Gallimore, R. Grand, P. Byrd
1986Anticancer Research58 citations
Semantic Scholar
A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: amino acid sequence, structure and expression studies.
P. Byrd, P. R. Cooper, T. Stankovic, H. Kullar +3 more
1996Human Molecular Genetics56 citations Open access
Semantic Scholar
Variations in ATM protein expression during normal lymphoid differentiation and among B-cell-derived neoplasias.
J. Starczynski, W. Simmons, J. Flavell, P. Byrd +11 more
2003American Journal of Pathology40 citations Open access
Semantic Scholar
Longitudinal analysis of the neurological features of ataxia‐telangiectasia
T. Jackson, G. Chow, M. Suri, P. Byrd +2 more
2016Developmental Medicine & Child Neurology38 citations Open access
Semantic Scholar
Premature ageing of the immune system underlies immunodeficiency in ataxia telangiectasia.
Andrew Exley, S. Buckenham, E. Hodges, Robert Hallam +8 more
2011Clinical Immunology36 citations
Semantic Scholar
Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site.
S. Meyer, H. Kingston, A. Taylor, P. Byrd +6 more
2004Cancer Genetics and Cytogenetics35 citations
Semantic Scholar
The order and orientation of a cluster of metalloproteinase genes, stromelysin 2, collagenase, and stromelysin, together with D11S385, on chromosome 11q22-q23.
C. Formstone, P. Byrd, H. Ambrose, John H. Riley +3 more
1993Genomics29 citations
Semantic Scholar
Irradiation hybrids for human chromosome 11: characterization and use for generating region-specific markers in 11q14-q23.
G. Gillett, C. Mcconville, P. Byrd, T. Stankovic +6 more
1993Genomics29 citations
Semantic Scholar
Sensitivity to ionising radiation of transformed human cells containing mutant ras genes.
M. L. Grant, R. Bruton, P. Byrd, P. Gallimore +3 more
1990Oncogene29 citations
Semantic Scholar
A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development
P. Byrd, G. Stewart, Anna Smith, C. Eaton +11 more
2016PLoS Genetics26 citations Open access
Semantic Scholar
Cloning of DNA fragments from the left end of the adenovirus type 12 genome: transformation by cloned early region 1.
P. Byrd, W. Chia, P. Rigby, P. Gallimore
1982Journal of General Virology26 citations Open access
Semantic Scholar
Schizophrenia-associated chromosome 11q21 translocation: identification of flanking markers and development of chromosome 11q fragment hybrids as cloning and mapping resources.
J. Fletcher, Kathryn L. Evans, David L. Baillie, P. Byrd +6 more
1993American Journal of Human Genetics24 citations
Semantic Scholar
Degradation of a Novel DNA Damage Response Protein, Tankyrase 1 Binding Protein 1, following Adenovirus Infection
Nafiseh Chalabi Hagkarim, Ellis L. Ryan, P. Byrd, R. Hollingworth +8 more
2018Journal of Virology21 citations Open access
Semantic Scholar
DNA profiling reveals remarkably low genetic variability in a herd of SLA homozygous pigs.
E. Signer, A. Jeffreys, S. Licence, R. Miller +2 more
1999Research in Veterinary Science17 citations
Semantic Scholar
The expression of the retinoblastoma gene product Rb1 in primary and adenovirus-transformed human cells.
R. Grand, P. Byrd, P. Grabham, C. Gregory +4 more
1989Oncogene17 citations
Semantic Scholar
Malignant disease and variations in radiosensitivity in ataxia telangiectasia patients
A. M. Taylor, D. Hernandez, C. Mcconville, C. Woods +5 more
199616 citations
Semantic Scholar
A haplotype common to intermediate radiosensitivity variants of ataxia-telangiectasia in the UK.
A. Taylor, C. Mcconville, G. Rotmanj, Y. Shilohj +1 more
1994International Journal of Radiation Biology15 citations
Semantic Scholar
Down‐regulation of ATM protein in HRS cells of nodular sclerosis Hodgkin's lymphoma in children occurs in the absence of ATM gene inactivation
S. Bose, J. Starczynski, M. Chukwuma, K. Baumforth +10 more
2007Journal of Pathology14 citations
Semantic Scholar
Genetic and physical mapping of the ataxia-telangiectasia locus on chromosome 11q22-q23.
C. Mcconville, P. Byrd, H. Ambrose, A. Taylor
1994International Journal of Radiation Biology13 citations
Semantic Scholar
Dopa‐Responsive Dystonia and Chorea as a Presenting Feature in Ataxia‐Telangiectasia
Sarah Thompson, A. Iyer, P. Byrd, Malcolm Taylor +1 more
2014Movement Disorders Clinical Practice12 citations Open access
Semantic Scholar
Clinical and cellular heterogeneity in ataxia-telangiectasia
A. Taylor, C. Mcconville, C. Woods, P. Byrd +1 more
199310 citations
Semantic Scholar
hMRE 11 : genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decay
S. Pitts, H. Kullar, T. Stankovic, G. Stewart +8 more
20015 citations
Semantic Scholar
The binding of guanine nucleotide to N-ras p21--a phosphorous and proton magnetic resonance study.
R. Grand, B. Levine, P. Byrd, P. Gallimore
1989Oncogene5 citations
Semantic Scholar
Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly.
M. Serey-Gaut, M. Cortés, P. Makrythanasis, M. Suri +45 more
2023American Journal of Human Genetics3 citations Open access
Semantic Scholar
Biallelic Mutation of SETX and Additional Likely “In Cis” SETX Sequence Change in Ataxia with Oculomotor Apraxia Type 2
Michael D. Perry, Martin Evans, P. Byrd, Malcolm R. Taylor
2020Journal of Pediatric Genetics2 citations Open access
Semantic Scholar
PALB2 variant status in hematological malignancies – a potential therapeutic target?
C. Oldreive, P. Byrd, G. Stewart, Alexander J. Taylor +14 more
2019Leukemia and Lymphoma2 citations
Semantic Scholar
Identification of ATM Mutations in Multiple Myeloma Tumours.
B. Austen, M. Podinovskaia, J. Starcynski, G. Barone +5 more
20051 citations
Semantic Scholar
PALB2 Mutational Status in Haematopoeitic Malignancies - a Potential Therapeutic Target?
C. Oldreive, T. Stankovic, P. Byrd, G. Stewart +7 more
20160 citations
Semantic Scholar
A Novel Role of PALB2 in Lymphoid Tumour Development
T. Stankovic, P. Byrd, G. Stewart, Alexander J. Taylor +7 more
20160 citations
Semantic Scholar
damage response and unrepaired chromosome damage leukemia occurs in pregerminal center cells and results in defective deficient B-cell chronic lymphocytic - Ataxia telangiectasia mutated
D. Keenan, P. Moss, A. M. Taylor, T. Stankovic +4 more
20130 citations
Semantic Scholar
The Ataxia Telangiectasia Nude Mouse with No Risk of Thymoma: A Model to Investigate Tumour Development of B Cell and Myeloid Origin Associated with ATM Loss
T. Stankovic, P. Byrd, T. Francis, T. Marafioti +2 more
20120 citations
Semantic Scholar
Increased chromosome breakage in lymphocytes exposed to ionizing radiation can be used to distinguish FANCD1 caused by biallelic BRCA2 mutations from more common forms of Fanconi anaemia
S. Holden, G. Stewart, P. Byrd, C. Turnbull +8 more
20110 citations
Semantic Scholar
Clinical, cellular and mutational variations in ataxia telangiectasia
A. Taylor, G. Stewart, T. Stankovic, S. Man +1 more
20040 citations
Semantic Scholar
Genetic and physical mapping of the ataxia-telangiectasia locus on chromosome Ilq22-q23.
C. Mcconville, P. Byrd, H. Ambrose, A. Taylor
1994International Journal of Radiation Biology0 citations
Semantic Scholar

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