Kerra Pearce

1.7k total citations
15 papers, 444 citations indexed

About

Kerra Pearce is a scholar working on Molecular Biology, Hematology and Epidemiology. According to data from OpenAlex, Kerra Pearce has authored 15 papers receiving a total of 444 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Hematology and 3 papers in Epidemiology. Recurrent topics in Kerra Pearce's work include Protein Degradation and Inhibitors (3 papers), Acute Myeloid Leukemia Research (2 papers) and Congenital Heart Disease Studies (2 papers). Kerra Pearce is often cited by papers focused on Protein Degradation and Inhibitors (3 papers), Acute Myeloid Leukemia Research (2 papers) and Congenital Heart Disease Studies (2 papers). Kerra Pearce collaborates with scholars based in United Kingdom, United States and Netherlands. Kerra Pearce's co-authors include Peter Scambler, Andrew Feber, Stephan Beck, Andrew E. Teschendorff, Matthias Lechner, Christina Thirlwell, Martin Widschwendter, Owen Williams, Tony Brooks and Stuart Adams and has published in prestigious journals such as The Lancet, PLoS ONE and Cancer Research.

In The Last Decade

Kerra Pearce

15 papers receiving 437 citations

Peers

Countries citing papers authored by Kerra Pearce

Since Specialization

Citations

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

Fields of papers citing papers by Kerra Pearce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kerra Pearce

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Review of standard paediatric neuroradiology MRI protocols from 12 UK tertiary paediatric hospitals: is there much variation between centres? 2023 ·Clinical Radiology ·(unknown), (unknown), Daniel Warren, Shivaram Avula, D. S. Bhattacharya, Sun Young Choi, Marcus Likeman, (unknown), Dipayan Mitra, Adam Oates, Kerra Pearce, (unknown), (unknown), Ruth Batty	1
2	The AAA+ATPase RUVBL2 is essential for the oncogenic function of c-MYB in acute myeloid leukemia 2019 ·Leukemia ·Elena Armenteros-Monterroso, Lu Zhao, Luca Gasparoli, Tony Brooks, Kerra Pearce, Marc R. Mansour, Joost H.A. Martens, Jasper de Boer, Owen Williams	17
3	De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes 2019 ·European Journal of Human Genetics ·Nirmal Vadgama, Alan Pittman, Michael A. Simpson, Niranjanan Nirmalananthan, Robin Murray, Takeo Yoshikawa, Peter De Rijk, Elliott Rees, George Kirov, Deborah Hughes, Tomas Fitzgerald, Mark Kristiansen, Kerra Pearce, Eliza Cerveira, Qihui Zhu, Chengsheng Zhang, Charles Lee, John Hardy, Jamal Nasir	19
4	Targeting acute myeloid leukemia by drug-induced c-MYB degradation 2017 ·Leukemia ·(unknown), Kerra Pearce, Tony Brooks, Michael Hubank, (unknown), C. Michel Zwaan, Stuart Adams, Dylan R. Edwards, Jack Bartram, Sujith Samarasinghe, Phil Ancliff, Asim Khwaja, Nicholas Goulden, Gareth Williams, Jasper de Boer, Owen Williams	78
5	Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency 2016 ·Journal of Allergy and Clinical Immunology ·Chiara Bacchelli, Federico A. Moretti, Marlene Carmo, Stuart Adams, Horia Stanescu, Kerra Pearce, Manisha Madkaikar, Kimberly Gilmour, Adeline K. Nicholas, C. Geoffrey Woods, Robert Kleta, Phil Beales, Waseem Qasim, H. Bobby Gaspar	31
6	Comparative Expression Analysis Reveals Lineage Relationships between Human and Murine Gliomas and a Dominance of Glial Signatures during Tumor Propagation In Vitro 2013 ·Cancer Research ·Nico V. Henriquez, Tim Forshew, Ruth Tatevossian, Matthew J. Ellis, Angela Richard-Loendt, Hazel Rogers, Thomas S. Jacques, (unknown), Kerra Pearce, Denise Sheer, Richard G. Grundy, Sebastian Brandner	24
7	Hearing in 44–45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study 2012 ·BMJ Open ·Shamima Rahman, Russell Ecob, Harry Costello, Mary G. Sweeney, Andrew Duncan, Kerra Pearce, David P. Strachan, Andrew Forge, Adrian Davis, Maria Bitner‐Glindzicz	38
8	Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis 2011 ·PLoS ONE ·James F. Meschia, Andrew Singleton, Michael A. Nalls, Stephen S. Rich, Pankaj Sharma, Luigi Ferrucci, Mar Matarín, Dena Hernández, Kerra Pearce, Thomas G. Brott, (unknown), John Hardy, Bradford B. Worrall	12
9	Siblings With Ischemic Stroke Study 2011 ·Stroke ·James F. Meschia, Michael A. Nalls, Mar Matarín, Thomas G. Brott, Robert D. Brown, John Hardy, Brett Kissela, Stephen S. Rich, Andrew Singleton, Dena G. Hernandez, Luigi Ferrucci, Kerra Pearce, (unknown), Bradford B. Worrall, (unknown)	20
10	Genome-wide DNA methylation analysis of archival formalin-fixed paraffin-embedded tissue using the Illumina Infinium HumanMethylation27 BeadChip 2010 ·Methods ·Christina Thirlwell, (unknown), Andrew Feber, Andrew E. Teschendorff, Kerra Pearce, Matthias Lechner, Martin Widschwendter, Stephan Beck	78
11	Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome 2010 ·Developmental Biology ·Kelly Lammerts van Bueren, Irinna Papangeli, Francesca Rochais, Kerra Pearce, Catherine Roberts, Amélie Calmont, Dorota Szumska, Robert G. Kelly, Shoumo Bhattacharya, Peter Scambler	49
12	Molecular study of 33 families with Fraser syndrome new data and mutation review 2008 ·American Journal of Medical Genetics Part A ·Mieke M. van Haelst, (unknown), Geneviève Baujat, Shalini Jadeja, Elena Monti, (unknown), Kerra Pearce, Raoul C. M. Hennekam, Peter Scambler	54
13	Identification of potential Tbx1 targets in a mouse model of DiGeorge syndrome 2007 ·Developmental Biology ·Kelly Lammerts van Bueren, Sarah Ivins, Catherine Roberts, Amélie Calmont, Kerra Pearce, Elizabeth Lindsay, (unknown), Peter Scambler	1
14	Blood groups and brain tumours 1965 ·Journal of the Neurological Sciences ·Kerra Pearce, P. O. Yates	7
15	RECENT CHANGE IN BLOOD-GROUP 1960 ·The Lancet ·(unknown), Kerra Pearce	15

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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