Niamh Spence

868 total citations
6 papers, 457 citations indexed

About

Niamh Spence is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Niamh Spence has authored 6 papers receiving a total of 457 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 3 papers in Molecular Biology and 1 paper in Neurology. Recurrent topics in Niamh Spence's work include Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (2 papers) and Neurological disorders and treatments (1 paper). Niamh Spence is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (2 papers) and Neurological disorders and treatments (1 paper). Niamh Spence collaborates with scholars based in Canada, Italy and Sweden. Niamh Spence's co-authors include Michael R. Hayden, B Kremer, H. Telenius, E. Almqvist, Y. Paul Goldberg, Susan E. Andrew, Ferdinando Squitieri, Maria Anvret, K. Nichol and Jane Theilmann and has published in prestigious journals such as The Journal of Immunology, Human Molecular Genetics and Journal of Medical Genetics.

In The Last Decade

Niamh Spence

6 papers receiving 446 citations

Peers

Countries citing papers authored by Niamh Spence

Since Specialization

Citations

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

Fields of papers citing papers by Niamh Spence

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niamh Spence

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	Sequence and Phylogenetic Analysis of the Untranslated Promoter Regions for HLA Class I Genes 2017 ·The Journal of Immunology ·Veron Ramsuran, (unknown), Colm Ó’hUigín, Gaurav Sharma, Niamh Spence, Danillo G. Augusto, Xiaojiang Gao, Christian A. García‐Sepúlveda, Gurvinder Kaur, Narinder K. Mehra, Mary Carrington	25
2	Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease 1995 ·Human Molecular Genetics ·E. Almqvist, Niamh Spence, K. Nichol, Susan E. Andrew, J. Vesa, Leena Peltonen, Maria Anvret, Jun Goto, Ichiro Kanazawa, Y. Paul Goldberg, Michael R. Hayden	59
3	Somatic mosaicism in sperm is associated with intergenerational (CAG)_n changes in Huntington disease 1995 ·Human Molecular Genetics ·H. Telenius, E. Almqvist, B Kremer, Niamh Spence, Ferdinando Squitieri, K. Nichol, Ulla Grandell, (unknown), Caroline Benjamin, Imma Castaldo, Olga Calabrese, Maria Anvret, Y. Paul Goldberg, Michael R. Hayden	67
4	Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes. 1995 ·PubMed ·B Kremer, E. Almqvist, (unknown), Niamh Spence, H. Telenius, (unknown), Michael R. Hayden	107
5	DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence 1994 ·Human Molecular Genetics ·Ferdinando Squitieri, Susan E. Andrew, Y. Paul Goldberg, B Kremer, Niamh Spence, (unknown), K. Nichol, Jane Theilmann, Jacquie Greenberg, Jun Goto, Ichiro Kanazawa, J. Vesa, Leena Peltonen, E. Almqvist, Maria Anvret, H. Telenius, Binshan Lin, G. Napolitano, Kenneth Morgan, Michael R. Hayden	148
6	Molecular analysis of late onset Huntington's disease. 1993 ·Journal of Medical Genetics ·B Kremer, Ferdinando Squitieri, H. Telenius, Susan E. Andrew, Jane Theilmann, Niamh Spence, Y. Paul Goldberg, Michael R. Hayden	51

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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