Martin Horan

1.1k total citations
24 papers, 797 citations indexed

About

Martin Horan is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Neurology. According to data from OpenAlex, Martin Horan has authored 24 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Endocrinology, Diabetes and Metabolism and 5 papers in Neurology. Recurrent topics in Martin Horan's work include Growth Hormone and Insulin-like Growth Factors (7 papers), Genetic Syndromes and Imprinting (4 papers) and Neuroblastoma Research and Treatments (4 papers). Martin Horan is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (7 papers), Genetic Syndromes and Imprinting (4 papers) and Neuroblastoma Research and Treatments (4 papers). Martin Horan collaborates with scholars based in Australia, United Kingdom and Germany. Martin Horan's co-authors include D.N. Cooper, J. William O. Ballard, Nicolas Pichaud, David Millar, Meena Upadhyaya, Michael Krawczak, Annie Procter, Linda Fryklund, Nadia Chuzhanova and Ying Xu and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Cancer Research and The Journals of Gerontology Series A.

In The Last Decade

Martin Horan

24 papers receiving 776 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin Horan Australia	14	375	185	173	153	132	24	797
Sandra Meulemans Belgium	19	470 1.3×	90 0.5×	58 0.3×	201 1.3×	81 0.6×	29	1.0k
Olivier R. Baris France	20	744 2.0×	108 0.6×	52 0.3×	101 0.7×	133 1.0×	33	1.1k
Daniel Eberhard Germany	19	541 1.4×	160 0.9×	57 0.3×	215 1.4×	122 0.9×	37	1.1k
Michael H. Guo United States	20	603 1.6×	174 0.9×	46 0.3×	509 3.3×	170 1.3×	33	1.2k
Erik-Jan Kamsteeg Netherlands	15	425 1.1×	60 0.3×	66 0.4×	320 2.1×	64 0.5×	21	874
Vittoria Carnicelli Italy	17	457 1.2×	98 0.5×	43 0.2×	66 0.4×	142 1.1×	47	1000
Thomas F. Wienker Germany	20	658 1.8×	56 0.3×	58 0.3×	382 2.5×	139 1.1×	59	1.3k
Rosaria Strammiello Italy	18	1.0k 2.7×	68 0.4×	207 1.2×	47 0.3×	146 1.1×	22	1.3k
Martin G. Bialer United States	18	547 1.5×	258 1.4×	37 0.2×	472 3.1×	248 1.9×	34	1.3k
Eugenio Gutiérrez Jiménez Spain	15	276 0.7×	82 0.4×	131 0.8×	31 0.2×	101 0.8×	33	711

Countries citing papers authored by Martin Horan

Since Specialization

Citations

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

Fields of papers citing papers by Martin Horan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Horan

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

All Works

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20 of 20 papers shown

Fenizia, Francesca, Jennifer A. Fairley, Etienne Rouleau, et al.. (2021). Tumor mutation burden testing: a survey of the International Quality Network for Pathology (IQN Path). Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 479(6). 1067–1072. 5 indexed citations

Peng, Rongxue, Rui Zhang, Martin Horan, et al.. (2019). From Somatic Variants Toward Precision Oncology: An Investigation of Reporting Practice for Next-Generation Sequencing-Based Circulating Tumor DNA Analysis. The Oncologist. 25(3). 218–228. 7 indexed citations

Peng, Rongxue, Rui Zhang, Li Zhou, et al.. (2019). External Quality Assurance of Current Technology for the Testing of Cancer-Associated Circulating Free DNA Variants. Pathology & Oncology Research. 26(3). 1595–1603. 4 indexed citations

Horan, Martin, Kwang Hong Tay, Louise Wienholt, et al.. (2018). High rates of variation in HLA-DQ2/DQ8 testing for coeliac disease: results from an RCPAQAP pilot program. Journal of Clinical Pathology. 71(10). 900–905. 6 indexed citations

Couteur, David G. Le, Szun S. Tay, Samantha M. Solon‐Biet, et al.. (2014). The Influence of Macronutrients on Splanchnic and Hepatic Lymphocytes in Aging Mice. The Journals of Gerontology Series A. 70(12). 1499–1507. 31 indexed citations

Horan, Martin, Jon N. Rumbley, Richard G. Melvin, David G. Le Couteur, & J. William O. Ballard. (2013). Quaternary protein modeling to predict the function of DNA variation found in human mitochondrial cytochrome c oxidase. Journal of Human Genetics. 58(3). 127–134. 5 indexed citations

Braidy, Nady, Wei-Ping Gai, Ying Xu, et al.. (2013). Alpha-Synuclein Transmission and Mitochondrial Toxicity in Primary Human Foetal Enteric Neurons In Vitro. Neurotoxicity Research. 25(2). 170–182. 19 indexed citations

Braidy, Nady, Wei‐Ping Gai, Ying Xu, et al.. (2013). Uptake and mitochondrial dysfunction of alpha-synuclein in human astrocytes, cortical neurons and fibroblasts. Translational Neurodegeneration. 2(1). 20–20. 77 indexed citations

Horan, Martin & D.N. Cooper. (2013). The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex disease. Human Genetics. 133(4). 435–458. 24 indexed citations

10.

Horan, Martin, Nicolas Pichaud, & J. William O. Ballard. (2012). Review: Quantifying Mitochondrial Dysfunction in Complex Diseases of Aging. The Journals of Gerontology Series A. 67(10). 1022–1035. 110 indexed citations

11.

Roberts, Kathryn G., Amanda M. Smith, Fiona McDougall, et al.. (2010). Essential Requirement for PP2A Inhibition by the Oncogenic Receptor c-KIT Suggests PP2A Reactivation as a Strategy to Treat c-KIT+ Cancers. Cancer Research. 70(13). 5438–5447. 100 indexed citations

12.

Millar, David, Martin Horan, Nadia Chuzhanova, & D.N. Cooper. (2010). Characterisation of a functional intronic polymorphism in the human growth hormone (GHI) gene. Human Genomics. 4(5). 289–289. 42 indexed citations

13.

Horan, Martin. (2009). Application of serial analysis of gene expression to the study of human genetic disease. Human Genetics. 126(5). 605–614. 17 indexed citations

14.

Wolf, Andreas, David Millar, Amke Caliebe, et al.. (2008). A gene conversion hotspot in the human growth hormone (GH1) gene promoter. Human Mutation. 30(2). 239–247. 12 indexed citations

15.

Millar, David, Mark Lewis, Martin Horan, et al.. (2008). Growth hormone (GH1) gene variation and the growth hormone receptor (GHR) exon 3 deletion polymorphism in a West-African population. Molecular and Cellular Endocrinology. 296(1-2). 18–25. 11 indexed citations

16.

Horan, Martin, Yasmin Yasmin, Mark Lewis, et al.. (2006). Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke. Human Genetics. 119(5). 527–540. 24 indexed citations

17.

Horan, Martin, Michael J. Osborn, D.N. Cooper, & Meena Upadhyaya. (2004). Functional analysis of polymorphic variation within the promoter and 5′ untranslated region of the neurofibromatosis type 1 (NF1) gene. American Journal of Medical Genetics Part A. 131A(3). 227–231. 3 indexed citations

18.

Lewis, Mark, Martin Horan, John W Gregory, et al.. (2003). Novel mutations of the growth hormone 1 (GH1) gene disclosed by modulation of the clinical selection criteria for individuals with short stature. Human Mutation. 21(4). 424–440. 75 indexed citations

19.

Horan, Martin, David Millar, Jürgen Hedderich, et al.. (2003). Human growth hormone 1 (GH1) gene expression: Complex haplotype-dependent influence of polymorphic variation in the proximal promoter and locus control region. Human Mutation. 21(4). 408–423. 88 indexed citations

20.

Horan, Martin, D.N. Cooper, & Meena Upadhyaya. (2000). Hypermethylation of the neurofibromatosis type 1 (NF1) gene promoter is not a common event in the inactivation of the NF1 gene in NF1-specific tumours. Human Genetics. 107(1). 33–39. 23 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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