Tom Stiff

2.3k total citations · 1 hit paper
14 papers, 1.8k citations indexed

About

Tom Stiff is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Tom Stiff has authored 14 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 5 papers in Oncology and 5 papers in Genetics. Recurrent topics in Tom Stiff's work include DNA Repair Mechanisms (7 papers), Moyamoya disease diagnosis and treatment (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Tom Stiff is often cited by papers focused on DNA Repair Mechanisms (7 papers), Moyamoya disease diagnosis and treatment (4 papers) and Genetic and Kidney Cyst Diseases (4 papers). Tom Stiff collaborates with scholars based in United Kingdom, United States and Germany. Tom Stiff's co-authors include Penny A. Jeggo, Mark O’Driscoll, Markus Löbrich, Nicole Rief, Kuniyoshi Iwabuchi, Sarah Walker, Carol-Anne Martin, Andrew P. Jackson, Lisa Woodbine and Gemma Alderton and has published in prestigious journals such as Nature Genetics, The Journal of Cell Biology and The EMBO Journal.

In The Last Decade

Tom Stiff

14 papers receiving 1.8k 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.

ATM and DNA-PK Function Redundantly to Phosphorylate H2AX after Exposure to Ionizing Radiation

2004 811 citations Tom Stiff, Mark O’Driscoll et al. Cancer Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tom Stiff United Kingdom	12	1.6k	553	403	352	288	14	1.8k
Kay Minn United States	14	2.0k 1.3×	1.1k 1.9×	412 1.0×	216 0.6×	171 0.6×	17	2.4k
Joshua M. Francis United States	16	1.5k 0.9×	454 0.8×	540 1.3×	257 0.7×	269 0.9×	26	2.1k
April N. Meyer United States	22	1.2k 0.8×	376 0.7×	169 0.4×	362 1.0×	310 1.1×	38	1.6k
Michela Di Virgilio Germany	17	1.8k 1.1×	600 1.1×	428 1.1×	103 0.3×	152 0.5×	25	2.4k
Michelle Le Beau United States	8	1.2k 0.7×	368 0.7×	360 0.9×	136 0.4×	270 0.9×	9	1.3k
Mélanie Letexier France	12	1.3k 0.8×	304 0.5×	432 1.1×	151 0.4×	372 1.3×	17	2.0k
Sairei So Japan	20	1.2k 0.8×	419 0.8×	184 0.5×	107 0.3×	101 0.4×	28	1.5k
A MacAuley United States	14	1.1k 0.7×	327 0.6×	144 0.4×	336 1.0×	153 0.5×	19	1.6k
Larisa Litovchick United States	24	1.4k 0.8×	669 1.2×	245 0.6×	293 0.8×	151 0.5×	54	1.8k
Ryan B. Jensen United States	15	1.5k 0.9×	597 1.1×	333 0.8×	88 0.3×	275 1.0×	29	1.7k

Countries citing papers authored by Tom Stiff

Since Specialization

Citations

This map shows the geographic impact of Tom Stiff'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 Tom Stiff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tom Stiff more than expected).

Fields of papers citing papers by Tom Stiff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tom Stiff. 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 Tom Stiff. The network helps show where Tom Stiff may publish in the future.

Co-authorship network of co-authors of Tom Stiff

This figure shows the co-authorship network connecting the top 25 collaborators of Tom Stiff. A scholar is included among the top collaborators of Tom Stiff 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 Tom Stiff. Tom Stiff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

Burkhalter, Martin D., Tom Stiff, Lars D. Maerz, et al.. (2024). Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage. Cell Death and Disease. 15(9). 660–660. 1 indexed citations

Stiff, Tom, et al.. (2024). CRISPR screens in 3D tumourspheres identified miR-4787-3p as a transcriptional start site miRNA essential for breast tumour-initiating cell growth. Communications Biology. 7(1). 859–859. 6 indexed citations

Stiff, Tom, et al.. (2020). Prophase-Specific Perinuclear Actin Coordinates Centrosome Separation and Positioning to Ensure Accurate Chromosome Segregation. Cell Reports. 31(8). 107681–107681. 23 indexed citations

Eykelenboom, John K., et al.. (2019). Contractile acto-myosin network on nuclear envelope remnants positions human chromosomes for mitosis. eLife. 8. 37 indexed citations

Stiff, Tom, et al.. (2016). ATR promotes cilia signalling: links to developmental impacts. Human Molecular Genetics. 25(8). 1574–1587. 24 indexed citations

Stiff, Tom, Meryem Alagöz, Diana Alcantara, et al.. (2013). Deficiency in Origin Licensing Proteins Impairs Cilia Formation: Implications for the Aetiology of Meier-Gorlin Syndrome. PLoS Genetics. 9(3). e1003360–e1003360. 52 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

Murray, Johanne M., Tom Stiff, & Penny A. Jeggo. (2012). DNA double-strand break repair within heterochromatic regions. Biochemical Society Transactions. 40(1). 173–178. 24 indexed citations

Bicknell, Louise S., Sarah Walker, Anna Klingseisen, et al.. (2011). Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome. Nature Genetics. 43(4). 350–355. 148 indexed citations

10.

Stiff, Tom, Karen Cerosaletti, Patrick Concannon, Mark O’Driscoll, & Penny A. Jeggo. (2008). Replication independent ATR signalling leads to G2/M arrest requiring Nbs1, 53BP1 and MDC1. Human Molecular Genetics. 17(20). 3247–3253. 31 indexed citations

11.

Griffith, Elen, Sarah Walker, Carol-Anne Martin, et al.. (2007). Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling. Nature Genetics. 40(2). 232–236. 226 indexed citations

12.

Deckbar, Dorothee, Andrea Krempler, Sarah Walker, et al.. (2007). Chromosome breakage after G2 checkpoint release. The Journal of Cell Biology. 176(6). 749–755. 203 indexed citations

13.

Stiff, Tom, Mark O’Driscoll, Nicole Rief, et al.. (2004). ATM and DNA-PK Function Redundantly to Phosphorylate H2AX after Exposure to Ionizing Radiation. Cancer Research. 64(7). 2390–2396. 811 indexed citations breakdown →

14.

Stiff, Tom, et al.. (2004). Nbs1 is required for ATR‐dependent phosphorylation events. The EMBO Journal. 24(1). 199–208. 147 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.

Explore authors with similar magnitude of impact