Philip J. Byrd

5.4k total citations · 2 hit papers
47 papers, 4.1k citations indexed

About

Philip J. Byrd is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Philip J. Byrd has authored 47 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 20 papers in Oncology and 19 papers in Genetics. Recurrent topics in Philip J. Byrd's work include DNA Repair Mechanisms (27 papers), Virus-based gene therapy research (15 papers) and Cancer-related Molecular Pathways (13 papers). Philip J. Byrd is often cited by papers focused on DNA Repair Mechanisms (27 papers), Virus-based gene therapy research (15 papers) and Cancer-related Molecular Pathways (13 papers). Philip J. Byrd collaborates with scholars based in United Kingdom, United States and Netherlands. Philip J. Byrd's co-authors include A. Malcolm R. Taylor, Grant S. Stewart, Tatjana Stanković, Debra A. Bressan, Richard S. Maser, John H.J. Petrini, Anja Raams, Mark I. Kaplan, James I. Last and Roger J.A. Grand and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Philip J. Byrd

46 papers receiving 4.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The DNA Double-Strand Break Repair Gene hMRE11 Is Mutated in Individuals with an Ataxia-Telangiectasia-like Disorder

1999 802 citations Grant S. Stewart, Richard S. Maser et al. Cell profile →
The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage

2009 599 citations Grant S. Stewart, Stephanie Panier et al. Cell profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Philip J. Byrd United Kingdom	27	3.4k	1.4k	907	879	359	47	4.1k
Raymonda Varon Germany	30	2.9k 0.8×	783 0.6×	1.0k 1.1×	813 0.9×	213 0.6×	62	3.5k
Frances C. Lucibello Germany	22	2.3k 0.7×	1.8k 1.3×	841 0.9×	582 0.7×	965 2.7×	25	3.9k
Martin Digweed Germany	28	3.6k 1.0×	848 0.6×	1.2k 1.3×	683 0.8×	168 0.5×	76	4.1k
Grant S. Stewart United Kingdom	37	5.3k 1.6×	2.3k 1.7×	1.0k 1.1×	753 0.9×	497 1.4×	87	6.2k
Jin‐Yuh Shew Taiwan	23	2.7k 0.8×	3.1k 2.3×	934 1.0×	1.1k 1.2×	248 0.7×	32	5.2k
Håkan Axelson Sweden	37	2.8k 0.8×	885 0.6×	1.4k 1.6×	311 0.4×	175 0.5×	90	4.1k
Luciana Chessa Italy	28	2.1k 0.6×	693 0.5×	722 0.8×	371 0.4×	115 0.3×	75	2.7k
Jane W. Fountain United States	24	1.7k 0.5×	1.3k 1.0×	730 0.8×	430 0.5×	323 0.9×	37	3.4k
Ellen van Drunen Netherlands	27	2.5k 0.7×	960 0.7×	541 0.6×	529 0.6×	182 0.5×	42	3.7k
Johan P. de Winter Netherlands	41	5.9k 1.7×	916 0.7×	1.7k 1.8×	1.6k 1.8×	270 0.8×	69	6.5k

Countries citing papers authored by Philip J. Byrd

Since Specialization

Citations

This map shows the geographic impact of Philip J. Byrd's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Philip J. Byrd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Philip J. Byrd more than expected).

Fields of papers citing papers by Philip J. Byrd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip J. Byrd. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Philip J. Byrd. The network helps show where Philip J. Byrd may publish in the future.

Co-authorship network of co-authors of Philip J. Byrd

This figure shows the co-authorship network connecting the top 25 collaborators of Philip J. Byrd. A scholar is included among the top collaborators of Philip J. Byrd based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Philip J. Byrd. Philip J. Byrd is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Byrd, Philip J., Grant S. Stewart, Anna Jo Bodurtha Smith, et al.. (2016). A Hypomorphic PALB2 Allele Gives Rise to an Unusual Form of FA-N Associated with Lymphoid Tumour Development. PLoS Genetics. 12(3). e1005945–e1005945. 15 indexed citations

Ogi, Tomoo, Sarah Walker, Tom Stiff, et al.. (2012). Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome. PLoS Genetics. 8(11). e1002945–e1002945. 79 indexed citations

Reiman, Anne, Venkataramanan Srinivasan, Giancarlo Barone, et al.. (2011). Lymphoid tumours and breast cancer in ataxia telangiectasia; substantial protective effect of residual ATM kinase activity against childhood tumours. British Journal of Cancer. 105(4). 586–591. 100 indexed citations

Stewart, Grant S., Stephanie Panier, Kelly Townsend, et al.. (2009). The RIDDLE Syndrome Protein Mediates a Ubiquitin-Dependent Signaling Cascade at Sites of DNA Damage. Cell. 136(3). 420–434. 599 indexed citations breakdown →

Austen, Belinda, Giancarlo Barone, Anne Reiman, et al.. (2008). Pathogenic ATM mutations occur rarely in a subset of multiple myeloma patients. British Journal of Haematology. 142(6). 925–933. 19 indexed citations

Shahwan, Amre, et al.. (2006). Atypical presentation of ataxia–oculomotor apraxia type 1. Developmental Medicine & Child Neurology. 48(6). 529–529. 8 indexed citations

Taylor, A. Malcolm R. & Philip J. Byrd. (2005). Molecular pathology of ataxia telangiectasia. Journal of Clinical Pathology. 58(10). 1009–1015. 158 indexed citations

Barral, Paola M., Andrew S. Turnell, Phillip H. Gallimore, et al.. (2005). The interaction of the hnRNP family member E1B‐AP5 with p53. FEBS Letters. 579(13). 2752–2758. 19 indexed citations

Sutton, Ian, et al.. (2004). Adult‐onset ataxia telangiectasia due to ATM 5762ins137 mutation homozygosity. Annals of Neurology. 55(6). 891–895. 44 indexed citations

10.

Clements, Paula, Claire Breslin, Philip J. Byrd, et al.. (2004). The ataxia–oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4. DNA repair. 3(11). 1493–1502. 156 indexed citations

11.

Stewart, Grant S., James I. Last, Tatjana Stanković, et al.. (2001). Residual Ataxia Telangiectasia Mutated Protein Function in Cells from Ataxia Telangiectasia Patients, with 5762ins137 and 7271T→G Mutations, Showing a Less Severe Phenotype. Journal of Biological Chemistry. 276(32). 30133–30141. 78 indexed citations

12.

Stewart, Grant S., Richard S. Maser, Tatjana Stanković, et al.. (1999). The DNA Double-Strand Break Repair Gene hMRE11 Is Mutated in Individuals with an Ataxia-Telangiectasia-like Disorder. Cell. 99(6). 577–587. 802 indexed citations breakdown →

13.

Stanković, Tatjana, Philip J. Byrd, Paul R. Cooper, et al.. (1997). Construction of a Transcription Map around the Gene for Ataxia Telangiectasia: Identification of at Least Four Novel Genes. Genomics. 40(2). 267–276. 19 indexed citations

14.

Byrd, Philip J.. (1996). A gene transcribed from the bidirectional ATM promoter coding for a serine rich protein: amino acid sequence, structure and expression studies. Human Molecular Genetics. 5(11). 1785–1791. 50 indexed citations

15.

Gillett, Godfrey T., Carmel McConville, Philip J. Byrd, et al.. (1993). Irradiation Hybrids for Human Chromosome 11: Characterization and Use for Generating Region-Specific Markers in 11q14-q23. Genomics. 15(2). 332–341. 26 indexed citations

16.

Mitchison, Hannah M., Roger J.A. Grand, Philip J. Byrd, et al.. (1990). The Expression of the Adenovirus 12 Early Region 1B 19K Protein Using a Recombinant Simian Virus 40 System. Journal of General Virology. 71(8). 1713–1722. 2 indexed citations

17.

Grand, Roger J.A., et al.. (1988). Differentiation of normal and adenovirus-12 E1 transformed human embryo retinal cells. Experimental Eye Research. 47(1). 123–133. 14 indexed citations

18.

Byrd, Philip J., Roger J.A. Grand, & P. H. Gallimore. (1988). Differential transformation of primary human embryo retinal cells by adenovirus E1 regions and combinations of E1A + ras.. PubMed. 2(5). 477–84. 33 indexed citations

19.

Breiding, David E., Jennifer Y. Tong, Philip J. Byrd, et al.. (1988). Isolation and characterization of adenovirus type 12 E1 host-range mutants defective for growth in nontransformed human cells. Virology. 164(2). 390–402. 20 indexed citations

20.

Byrd, Philip J., Roger J.A. Grand, David E. Breiding, Jim Williams, & Phillip H. Gallimore. (1988). Host range mutants of adenovirus type 12 E1 defective for lytic infection, transformation, and oncogenicity. Virology. 163(1). 155–165. 27 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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