Lynne Hobson

943 total citations
11 papers, 684 citations indexed

About

Lynne Hobson is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Lynne Hobson has authored 11 papers receiving a total of 684 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 1 paper in Organic Chemistry. Recurrent topics in Lynne Hobson's work include Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (3 papers) and DNA Repair Mechanisms (2 papers). Lynne Hobson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), RNA modifications and cancer (3 papers) and DNA Repair Mechanisms (2 papers). Lynne Hobson collaborates with scholars based in Australia, United States and Germany. Lynne Hobson's co-authors include Robert I. Richards, Elizabeth Baker, Marie Mangelsdorf, Helen J. Eyre, D. Hewett, Jozef Gécz, Grant R. Sutherland, Marie Shaw, Sui Yu and Karin Ried and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Molecular Cell.

In The Last Decade

Lynne Hobson

11 papers receiving 666 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lynne Hobson Australia	9	563	372	65	52	50	11	684
S. Yu United States	7	430 0.8×	278 0.7×	19 0.3×	59 1.1×	34 0.7×	9	564
Barbara A. Boggs United States	12	691 1.2×	391 1.1×	17 0.3×	100 1.9×	25 0.5×	16	817
Szabolcs Soeroes Germany	10	780 1.4×	132 0.4×	14 0.2×	56 1.1×	39 0.8×	11	858
Manolo Bellotto Switzerland	6	785 1.4×	235 0.6×	33 0.5×	43 0.8×	20 0.4×	11	869
Anne-Claire Lavigne France	12	467 0.8×	100 0.3×	37 0.6×	55 1.1×	33 0.7×	16	558
Shelagh Joss United Kingdom	13	303 0.5×	169 0.5×	25 0.4×	26 0.5×	13 0.3×	19	452
Anna Sawicka Austria	11	546 1.0×	79 0.2×	19 0.3×	70 1.3×	48 1.0×	12	630
R. Vervoort Belgium	13	727 1.3×	233 0.6×	82 1.3×	17 0.3×	15 0.3×	19	910
A. Antonelli Italy	13	392 0.7×	87 0.2×	25 0.4×	38 0.7×	90 1.8×	24	503
Jelle Verbeeck Belgium	12	346 0.6×	170 0.5×	18 0.3×	30 0.6×	49 1.0×	16	469

Countries citing papers authored by Lynne Hobson

Since Specialization

Citations

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

Fields of papers citing papers by Lynne Hobson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lynne Hobson

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

All Works

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11 of 11 papers shown

Serajee, Fatema, Marie Shaw, Lynne Hobson, et al.. (2018). O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling. Journal of Biological Chemistry. 293(27). 10810–10824. 49 indexed citations

Kumar, Raman, Thuong Ha, Duyen Pham, et al.. (2016). A non-coding variant in the 5ʹ UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. European Journal of Human Genetics. 24(11). 1612–1616. 8 indexed citations

Guy, Michael P., Marie Shaw, Catherine L. Weiner, et al.. (2015). Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations inFTSJ1. Human Mutation. 36(12). 1176–1187. 112 indexed citations

Corbett, Mark, Tracy Dudding‐Byth, Patricia Crock, et al.. (2015). A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A. Journal of Medical Genetics. 52(4). 269–274. 40 indexed citations

Kalscheuer, Vera M., Zafar Iqbal, Han Hu, et al.. (2013). RAB40AL loss-of-function mutation does not cause X-linked intellectual disability. Adelaide Research & Scholarship (AR&S) (University of Adelaide). 3 indexed citations

Field, Michael, Ingrid E. Scheffer, Deepak Gill, et al.. (2012). Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations. European Journal of Human Genetics. 20(7). 806–809. 41 indexed citations

Finnis, Merran, Sonia Dayan, Lynne Hobson, et al.. (2005). Common chromosomal fragile site FRA16D mutation in cancer cells. Human Molecular Genetics. 14(10). 1341–1349. 68 indexed citations

Mangelsdorf, Marie, Karin Ried, Erica Woollatt, et al.. (2000). Chromosomal fragile site FRA16D and DNA instability in cancer.. PubMed. 60(6). 1683–9. 103 indexed citations

Hewett, D., Oliva Handt, Lynne Hobson, et al.. (1998). FRA10B Structure Reveals Common Elements in Repeat Expansion and Chromosomal Fragile Site Genesis. Molecular Cell. 1(6). 773–781. 73 indexed citations

10.

Yu, Sui, Marie Mangelsdorf, D. Hewett, et al.. (1997). Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat. Cell. 88(3). 367–374. 155 indexed citations

11.

Horwitz, Marshall S., Kathleen F. Benson, John Wolff, et al.. (1997). Genetic Heterogeneity in Familial Acute Myelogenous Leukemia: Evidence for a Second Locus at Chromosome 16q21-23.2. The American Journal of Human Genetics. 61(4). 873–881. 32 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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