Andrew Singleton

1.5k total citations
6 papers, 250 citations indexed

About

Andrew Singleton is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Andrew Singleton has authored 6 papers receiving a total of 250 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 1 paper in Neurology. Recurrent topics in Andrew Singleton's work include Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (2 papers) and Nutrition, Genetics, and Disease (1 paper). Andrew Singleton is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (2 papers) and Nutrition, Genetics, and Disease (1 paper). Andrew Singleton collaborates with scholars based in United States, Portugal and United Kingdom. Andrew Singleton's co-authors include Rita Guerreiro, Isabel Santana, Catarina R. Oliveira, John Hardy, José Brás, Beatriz Santiago, Hakan Gürvıt, Nicole Gurunlian, J. Raphael Gibbs and Murat Emre and has published in prestigious journals such as PLoS ONE, Neurobiology of Aging and Human Mutation.

In The Last Decade

Andrew Singleton

6 papers receiving 246 citations

Peers

Andrew Singleton

MB

PHYSI

NEURO

GENET

Katharina Heim Germany

Laura Rodríguez‐Pascau Spain

Samira Ait-El-Mkadem France

Yosr Bouhlal Tunisia

Alejandra Darling Spain

Danyu Lin China

Eva Feráková Slovakia

Marzena J. Fabis‐Pedrini Australia

Xianghua He China

Nicole Gurunlian United States

Katharina Heim Germany

Andrew Singleton

135 ×1.1

MB

28 ×0.2

PHYSI

90 ×1.3

NEURO

53 ×0.9

NEURO

31 ×0.6

GENET

Citations per year, relative to Andrew Singleton Andrew Singleton (= 1×) peers Katharina Heim

Countries citing papers authored by Andrew Singleton

Since Specialization

Citations

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

Fields of papers citing papers by Andrew Singleton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Singleton

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Lohmann, Ebba, Rita Guerreiro, Nihan Erginel‐Ünaltuna, et al.. (2012). Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients. Neurobiology of Aging. 33(8). 1850.e17–1850.e27. 34 indexed citations

2.

Guerreiro, Rita, Ebba Lohmann, José Brás, et al.. (2011). Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease. Neurobiology of Aging. 33(5). 1008.e17–1008.e23. 85 indexed citations

3.

Guerreiro, Rita, John S. Beck, J. Raphael Gibbs, et al.. (2010). Genetic Variability in CLU and Its Association with Alzheimer's Disease. PLoS ONE. 5(3). e9510–e9510. 44 indexed citations

4.

Huentelman, Matthew J., Jason J. Corneveaux, Amanda Myers, et al.. (2010). S4‐03‐02: Genome‐Wide Association Study for Alzheimer's Disease Risk in a Large Cohort Of Clinically Characterized And Neuropathologically Verified Subjects. Alzheimer s & Dementia. 6(4S_Part_20). 3 indexed citations

5.

Guerreiro, Rita, Nicole Washecka, John Hardy, & Andrew Singleton. (2009). A thorough assessment of benign genetic variability inGRNandMAPT. Human Mutation. 31(2). E1126–E1140. 17 indexed citations

6.

Guerreiro, Rita, José Brás, Isabel Santana, et al.. (2006). Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort. BMC Neurology. 6(1). 24–24. 67 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.

Explore authors with similar magnitude of impact