Liam Carroll

2.1k total citations
14 papers, 483 citations indexed

About

Liam Carroll is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Liam Carroll has authored 14 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Liam Carroll's work include Genetic Neurodegenerative Diseases (4 papers), Genomics and Rare Diseases (4 papers) and Genetic Associations and Epidemiology (4 papers). Liam Carroll is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Genomics and Rare Diseases (4 papers) and Genetic Associations and Epidemiology (4 papers). Liam Carroll collaborates with scholars based in United Kingdom, Australia and China. Liam Carroll's co-authors include Michael J. Owen, Michael O’Donovan, Mark Wardle, Thomas H. Massey, Hywel Williams, George Kirov, Sarah Dwyer, James Walters, Nigel Williams and Nadine Norton and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Immunological Methods and Schizophrenia Research.

In The Last Decade

Liam Carroll

14 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liam Carroll United Kingdom	9	221	185	163	113	97	14	483
Stacy Steinberg Iceland	12	378 1.7×	241 1.3×	109 0.7×	109 1.0×	73 0.8×	14	785
John Burke United Kingdom	6	290 1.3×	142 0.8×	100 0.6×	102 0.9×	91 0.9×	6	498
Л. И. Абрамова Russia	13	126 0.6×	174 0.9×	112 0.7×	154 1.4×	115 1.2×	45	482
Sibylle G. Schwab Germany	11	336 1.5×	259 1.4×	170 1.0×	121 1.1×	122 1.3×	14	609
Tetsuya Marui Japan	12	149 0.7×	119 0.6×	124 0.8×	54 0.5×	93 1.0×	16	372
Luigi Balasco Italy	8	116 0.5×	95 0.5×	242 1.5×	74 0.7×	61 0.6×	14	395
Michael John Owen United Kingdom	8	182 0.8×	216 1.2×	54 0.3×	125 1.1×	173 1.8×	27	485
H. Gurling United Kingdom	4	306 1.4×	103 0.6×	110 0.7×	134 1.2×	50 0.5×	7	497
В. Г. Каледа Russia	12	114 0.5×	193 1.0×	111 0.7×	179 1.6×	119 1.2×	109	549
Margaret K. King United States	9	452 2.0×	375 2.0×	380 2.3×	53 0.5×	150 1.5×	11	783

Countries citing papers authored by Liam Carroll

Since Specialization

Citations

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

Fields of papers citing papers by Liam Carroll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liam Carroll

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

All Works

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14 of 14 papers shown

Carroll, Liam, Sarah Ennis, Nicola Foulds, & Simon Hammans. (2023). HNRNPA2B1 myopathy presenting in a family with an early onset oculopharyngeal muscular dystrophy-like phenotype. Neuromuscular Disorders. 34. 27–31. 1 indexed citations

Carroll, Liam, Mark Walker, David R. Allen, et al.. (2021). Desminopathy presenting as late onset bilateral facial weakness, with diagnosis supported by lower limb MRI. Neuromuscular Disorders. 31(3). 249–252. 1 indexed citations

Carroll, Liam, et al.. (2018). Dentatorubral-Pallidoluysian Atrophy: An Update. SHILAP Revista de lepidopterología. 8. 577–577. 31 indexed citations

Carroll, Liam, et al.. (2018). Dentatorubral-pallidoluysian Atrophy: An Update. Tremor and Other Hyperkinetic Movements. 8(0). 577–577. 30 indexed citations

Carroll, Liam, et al.. (2017). Zinc containing dental fixative causing copper deficiency myelopathy. BMJ Case Reports. 2017. bcr–2017. 7 indexed citations

Carroll, Liam, Hywel Williams, Sarah Dwyer, et al.. (2015). Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation. Psychiatric Genetics. 26(2). 60–65. 43 indexed citations

Carroll, Liam, Hywel Williams, James Walters, et al.. (2011). Mutation screening of the 3q29 microdeletion syndrome candidate genes DLG1 and PAK2 in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(7). 844–849. 23 indexed citations

Mantripragada, Kiran K., Liam Carroll, & Nigel Williams. (2010). Experimental Approaches for Identifying Schizophrenia Risk Genes. Current topics in behavioral neurosciences. 4. 587–610. 3 indexed citations

Carroll, Liam, Kimberley Kendall, Michael O’Donovan, Michael J. Owen, & Nigel Williams. (2010). EVIDENCE THAT PUTATIVE ADHD LOW RISK ALLELES AT SNAP25 MAY INCREASE THE RISK OF SCHIZOPHRENIA. Schizophrenia Research. 117(2-3). 337–337. 1 indexed citations

10.

Carroll, Liam & Michael J. Owen. (2009). Genetic overlap between autism, schizophrenia and bipolar disorder. Genome Medicine. 1(10). 102–102. 246 indexed citations

11.

Dwyer, Sarah, Liam Carroll, Kiran K. Mantripragada, et al.. (2009). Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high‐resolution melting analysis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(3). 766–774. 11 indexed citations

12.

Liu, Yang, Gang Chen, Nadine Norton, et al.. (2009). Whole Genome Association Study in a Homogenous Population in Shandong Peninsula of China Reveals JARID2 as a Susceptibility Gene for Schizophrenia. BioMed Research International. 2009(1). 536918–536918. 30 indexed citations

13.

Norton, Nadine, Hywel Williams, Sarah Dwyer, et al.. (2007). Association analysis of AKT1 and schizophrenia in a UK case control sample. Schizophrenia Research. 93(1-3). 58–65. 48 indexed citations

14.

Carroll, Liam & Wayne K. Potts. (2001). Accumulated background variation among H2 mutant congenic strains: elimination through PCR-based genotyping of F2 segregants. Journal of Immunological Methods. 257(1-2). 137–143. 8 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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