Lorne Lonie

2.6k total citations · 1 hit paper
12 papers, 1.1k citations indexed

About

Lorne Lonie is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Lorne Lonie has authored 12 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Rheumatology. Recurrent topics in Lorne Lonie's work include Bone Tumor Diagnosis and Treatments (3 papers), Wnt/β-catenin signaling in development and cancer (3 papers) and Hereditary Neurological Disorders (2 papers). Lorne Lonie is often cited by papers focused on Bone Tumor Diagnosis and Treatments (3 papers), Wnt/β-catenin signaling in development and cancer (3 papers) and Hereditary Neurological Disorders (2 papers). Lorne Lonie collaborates with scholars based in United Kingdom, United States and Netherlands. Lorne Lonie's co-authors include Jiannis Ragoussis, Serena Ghisletti, Sara Polletti, Lorna Gregory, Iros Barozzi, Flore Mietton, Gioacchino Natoli, Francesca De Santa, Chia‐Lin Wei and Elisa Venturini and has published in prestigious journals such as Immunity, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Lorne Lonie

12 papers receiving 1.1k 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.

Identification and Characterization of Enhancers Controlling the Inflammatory Gene Expression Program in Macrophages

2010 515 citations Serena Ghisletti, Iros Barozzi et al. Immunity profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lorne Lonie United Kingdom	10	591	309	213	158	153	12	1.1k
Xiaoyan M. Zhang United States	7	1.2k 2.0×	49 0.2×	178 0.8×	67 0.4×	360 2.4×	7	1.4k
Christoph Schubert Germany	13	211 0.4×	206 0.7×	91 0.4×	81 0.5×	42 0.3×	30	676
Amy K Hsu United States	14	571 1.0×	78 0.3×	45 0.2×	135 0.9×	113 0.7×	23	1.1k
Axel Bohring Germany	13	361 0.6×	62 0.2×	88 0.4×	58 0.4×	203 1.3×	17	609
Patrick Lombard United Kingdom	10	1.3k 2.2×	74 0.2×	43 0.2×	128 0.8×	94 0.6×	12	1.6k
Paul Bossuyt Belgium	13	440 0.7×	81 0.3×	177 0.8×	111 0.7×	157 1.0×	15	796
Tim C. Cao United States	9	662 1.1×	102 0.3×	57 0.3×	153 1.0×	145 0.9×	11	896
Pierre Bitoun France	17	1.4k 2.3×	52 0.2×	73 0.3×	123 0.8×	818 5.3×	39	1.9k
Peggy P. Lee United States	7	829 1.4×	742 2.4×	63 0.3×	34 0.2×	263 1.7×	11	1.5k
Jiangxia Li China	18	478 0.8×	145 0.5×	85 0.4×	64 0.4×	119 0.8×	40	755

Countries citing papers authored by Lorne Lonie

Since Specialization

Citations

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

Fields of papers citing papers by Lorne Lonie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorne Lonie

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

All Works

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12 of 12 papers shown

Roberts, Hannah, Maria Lopopolo, Alistair T. Pagnamenta, et al.. (2021). Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma. Scientific Reports. 11(1). 6408–6408. 12 indexed citations

Twigg, Stephen R.F., Christian Babbs, Anne Goriely, et al.. (2013). Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes. Human Molecular Genetics. 22(8). 1654–1662. 56 indexed citations

Ghisletti, Serena, Iros Barozzi, Flore Mietton, et al.. (2010). Identification and Characterization of Enhancers Controlling the Inflammatory Gene Expression Program in Macrophages. Immunity. 32(3). 317–328. 515 indexed citations breakdown →

Lonie, Lorne, Daniel Porter, Maria Fraser, et al.. (2006). Determination of the mutation spectrum of theEXT1/EXT2genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes inEXTnegative cases. Human Mutation. 27(11). 1160–1160. 45 indexed citations

Fairclough, Rebecca J., Lorne Lonie, Kurt Van Baelen, et al.. (2004). Hailey–Hailey Disease: Identification of Novel Mutations in ATP2C1 and Effect of Missense Mutation A528P on Protein Expression Levels. Journal of Investigative Dermatology. 123(1). 67–71. 33 indexed citations

Williams, Nic A., et al.. (2004). ProtocadherinX/Y, a candidate gene‐pair for schizophrenia and schizoaffective disorder: A DHPLC investigation of genomic sequence. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 129B(1). 1–9. 36 indexed citations

Porter, D, Lorne Lonie, Maria Fraser, et al.. (2004). Severity of disease and risk of malignant change in hereditary multiple exostoses. Journal of Bone and Joint Surgery - British Volume. 86-B(7). 1041–1046. 149 indexed citations

Winsey, Samantha, et al.. (2004). Genetic variation in COL17A1 and the development of bullous pemphigoid. Experimental Dermatology. 13(3). 140–147. 4 indexed citations

Bitoun, Emmanuelle, Stéphane Chavanas, Alan D. Irvine, et al.. (2002). Netherton Syndrome: Disease Expression and Spectrum of SPINK5 Mutations in 21 Families. Journal of Investigative Dermatology. 118(2). 352–361. 147 indexed citations

10.

Bolino, Alessandra, Lorne Lonie, Michael Zimmer, et al.. (2001). Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy. Neurogenetics. 3(2). 107–109. 28 indexed citations

11.

Dobson‐Stone, Carol, Roger Cox, Lorne Lonie, et al.. (2000). Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses. European Journal of Human Genetics. 8(1). 24–32. 75 indexed citations

12.

Bolino, Alessandra, et al.. (2000). DHPLC analysis of unrelated CMT patients in the Myotubularin related 2 gene, MTMR2, responsible of Charcot-Marie-Tooth disease type 4B. Oxford University Research Archive (ORA) (University of Oxford). 2. 372. 3 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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