Ernest Turro

9.0k total citations
39 papers, 1.2k citations indexed

About

Ernest Turro is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Ernest Turro has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Hematology and 13 papers in Genetics. Recurrent topics in Ernest Turro's work include Platelet Disorders and Treatments (10 papers), RNA Research and Splicing (5 papers) and Genomics and Rare Diseases (4 papers). Ernest Turro is often cited by papers focused on Platelet Disorders and Treatments (10 papers), RNA Research and Splicing (5 papers) and Genomics and Rare Diseases (4 papers). Ernest Turro collaborates with scholars based in United Kingdom, United States and Belgium. Ernest Turro's co-authors include Sylvia Richardson, Ângela Gonçalves, Kathleen Freson, Daniel Greene, Alex Lewin, Shu-Yi Su, Lachlan Coin, Willem H. Ouwehand, Claire Lentaigne and Michael Laffan and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Nature Medicine.

In The Last Decade

Ernest Turro

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ernest Turro United Kingdom 18 712 282 191 134 118 39 1.2k
Ana-Teresa Maia United Kingdom 15 703 1.0× 276 1.0× 298 1.6× 235 1.8× 174 1.5× 26 1.3k
Jessica Nordlund Sweden 20 591 0.8× 248 0.9× 187 1.0× 161 1.2× 102 0.9× 57 1.1k
Catarina D. Campbell United States 13 534 0.8× 561 2.0× 157 0.8× 220 1.6× 144 1.2× 20 1.2k
Rahul Karnik United States 14 1.6k 2.2× 294 1.0× 122 0.6× 259 1.9× 115 1.0× 25 1.8k
Hanna Davies Sweden 8 447 0.6× 348 1.2× 90 0.5× 148 1.1× 106 0.9× 13 856
Jean McGowan‐Jordan Canada 15 690 1.0× 675 2.4× 158 0.8× 208 1.6× 108 0.9× 31 1.6k
Natalie J. Foot Australia 19 677 1.0× 100 0.4× 230 1.2× 173 1.3× 139 1.2× 29 1.2k
George Mavrothalassitis Greece 22 836 1.2× 171 0.6× 98 0.5× 135 1.0× 201 1.7× 37 1.3k
X. Shirley Liu United States 6 1.8k 2.5× 281 1.0× 380 2.0× 243 1.8× 80 0.7× 10 2.1k
Erikjan Rijkers Netherlands 13 674 0.9× 126 0.4× 66 0.3× 93 0.7× 61 0.5× 17 894

Countries citing papers authored by Ernest Turro

Since Specialization
Citations

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

Fields of papers citing papers by Ernest Turro

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ernest Turro

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

All Works

20 of 20 papers shown
1.
Ansari, Shabbir A., et al.. (2025). Human missense variants in F3 impair the initiation of blood coagulation. Blood. 147(6). 689–701.
2.
Greene, Daniel, Chantal Thys, Ian Berry, et al.. (2024). Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders. Nature Medicine. 30(8). 2165–2169. 27 indexed citations
3.
Thomas, Patrick, Joana Batista, Carly Kempster, et al.. (2023). A signature of platelet reactivity in CBC scattergrams reveals genetic predictors of thrombotic disease risk. Blood. 142(22). 1895–1908. 5 indexed citations
4.
Ratnaike, Thiloka, Daniel Greene, Wei Wei, et al.. (2021). MitoPhen database: a human phenotype ontology-based approach to identify mitochondrial DNA diseases. Nucleic Acids Research. 49(17). 9686–9695. 22 indexed citations
5.
Howarth, Karen, Susanna L. Cooke, Suet‐Feung Chin, et al.. (2021). NRG1 fusions in breast cancer. Breast Cancer Research. 23(1). 3–3. 17 indexed citations
6.
Westbury, Sarah K., Claire S. Whyte, Jonathan Stephens, et al.. (2020). A new pedigree with thrombomodulin‐associated coagulopathy in which delayed fibrinolysis is partially attenuated by co‐inherited TAFI deficiency. Journal of Thrombosis and Haemostasis. 18(9). 2209–2214. 21 indexed citations
7.
Schulman, Sol, Mary H.C. Florido, Max Friesen, et al.. (2020). A coagulation defect arising from heterozygous premature termination of tissue factor. Journal of Clinical Investigation. 130(10). 5302–5312. 17 indexed citations
8.
Dalby, Amanda, José Ballester‐Beltrán, Annett Mueller, et al.. (2018). Transcription Factor Levels after Forward Programming of Human Pluripotent Stem Cells with GATA1, FLI1, and TAL1 Determine Megakaryocyte versus Erythroid Cell Fate Decision. Stem Cell Reports. 11(6). 1462–1478. 13 indexed citations
9.
Greene, Daniel, Sylvia Richardson, & Ernest Turro. (2017). A Fast Association Test for Identifying Pathogenic Variants Involved in Rare Diseases. The American Journal of Human Genetics. 101(1). 104–114. 12 indexed citations
10.
Freson, Kathleen & Ernest Turro. (2017). High‐throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders. Journal of Thrombosis and Haemostasis. 15(7). 1262–1272. 33 indexed citations
11.
Jaeken, Jaak, Gepke Visser, Isabelle I. Salles, et al.. (2017). PIGO deficiency: palmoplantar keratoderma and novel mutations. Orphanet Journal of Rare Diseases. 12(1). 101–101. 11 indexed citations
12.
Greene, Daniel, Sylvia Richardson, & Ernest Turro. (2016). Phenotype Similarity Regression for Identifying the Genetic Determinants of Rare Diseases. The American Journal of Human Genetics. 98(3). 490–499. 36 indexed citations
13.
Marneth, Anna E., Ruud van Oorschot, Saskia M. Bergevoet, et al.. (2015). ANALYSIS OF NEW GFI1B VARIANTS IN PATIENTS WITH INHERITED BLEEDING AND PLATELET DISORDERS. Haematologica. 100. 174–174. 2 indexed citations
14.
Rendon, Augusto, Ernest Turro, Yupu Liang, et al.. (2014). αIIbβ3 Variants Defined By Next Generation Sequencing: Implications for Predicting Variants Likely to Cause Glanzmann Thrombasthenia and Alloimmune Disorders. Blood. 124(21). 4151–4151. 1 indexed citations
15.
Shen, Susan Q., Ernest Turro, & Joseph C. Corbo. (2014). Hybrid Mice Reveal Parent-of-Origin and Cis- and Trans-Regulatory Effects in the Retina. PLoS ONE. 9(10). e109382–e109382. 16 indexed citations
16.
Pleines, Irina, Joanne Woods, Ernest Turro, et al.. (2014). Mutations in Tropomyosin 4 Cause Macrothrombocytopenia in Mice and Humans. Blood. 124(21). 571–571. 1 indexed citations
17.
Gonçalves, Ângela, David Thybert, Klara Stefflova, et al.. (2012). Extensive compensatory cis-trans regulation in the evolution of mouse gene expression. Genome Research. 22(12). 2376–2384. 127 indexed citations
18.
Turro, Ernest, Shu-Yi Su, Ângela Gonçalves, et al.. (2011). Haplotype and isoform specific expression estimation using multi-mapping RNA-seq reads. Genome biology. 12(2). R13–R13. 166 indexed citations
19.
Turro, Ernest, et al.. (2009). MMBGX: a method for estimating expression at the isoform level and detecting differential splicing using whole-transcript Affymetrix arrays. Nucleic Acids Research. 38(1). e4–e4. 18 indexed citations
20.
Turro, Ernest, et al.. (2007). BGX: a Bioconductor package for the Bayesian integrated analysis of Affymetrix GeneChips. BMC Bioinformatics. 8(1). 439–439. 16 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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