Leanne Moynihan

813 total citations
7 papers, 226 citations indexed

About

Leanne Moynihan is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Leanne Moynihan has authored 7 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Sensory Systems and 2 papers in Cell Biology. Recurrent topics in Leanne Moynihan's work include RNA regulation and disease (3 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Microtubule and mitosis dynamics (2 papers). Leanne Moynihan is often cited by papers focused on RNA regulation and disease (3 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Microtubule and mitosis dynamics (2 papers). Leanne Moynihan collaborates with scholars based in United Kingdom and United Arab Emirates. Leanne Moynihan's co-authors include Nicholas Lench, Robert F. Mueller, C. Geoffrey Woods, Duncan P. McHale, Gulshan Karbani, Alexander F. Markham, Peter Corry, Andrew P. Jackson, Ian Lewis and G Turner and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Leanne Moynihan

7 papers receiving 221 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leanne Moynihan United Kingdom 7 111 71 46 34 30 7 226
Emmanuelle Ranza Switzerland 12 137 1.2× 103 1.5× 19 0.4× 11 0.3× 11 0.4× 22 295
Janice C. Palumbos United States 8 245 2.2× 161 2.3× 23 0.5× 32 0.9× 13 0.4× 13 391
Sameera Sogaty Saudi Arabia 8 179 1.6× 105 1.5× 52 1.1× 33 1.0× 14 0.5× 8 255
Xavier Zanlonghi France 13 348 3.1× 67 0.9× 74 1.6× 15 0.4× 13 0.4× 44 523
Souad Gherbi France 8 103 0.9× 50 0.7× 13 0.3× 80 2.4× 22 0.7× 11 199
Ivana Ivković France 10 238 2.1× 41 0.6× 73 1.6× 7 0.2× 42 1.4× 17 448
Amjad Khan Pakistan 12 170 1.5× 124 1.7× 39 0.8× 11 0.3× 13 0.4× 40 291
H Dahl Australia 9 300 2.7× 158 2.2× 24 0.5× 69 2.0× 19 0.6× 12 459
Nicola Vanni Italy 5 145 1.3× 122 1.7× 66 1.4× 10 0.3× 5 0.2× 6 278
Xavier Gérard France 10 347 3.1× 126 1.8× 49 1.1× 9 0.3× 13 0.4× 17 404

Countries citing papers authored by Leanne Moynihan

Since Specialization
Citations

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

Fields of papers citing papers by Leanne Moynihan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leanne Moynihan

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

All Works

7 of 7 papers shown
1.
Moynihan, Leanne, Andrew P. Jackson, Emma Roberts, et al.. (2000). A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34. The American Journal of Human Genetics. 66(2). 724–727. 81 indexed citations
2.
McHale, Duncan P., Simon J Mitchell, Sarah Bundey, et al.. (1999). A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25. The American Journal of Human Genetics. 64(2). 526–532. 37 indexed citations
3.
Telford, Elizabeth A.R., Leanne Moynihan, Alexander F. Markham, & Nicholas Lench. (1999). Isolation and characterisation of a cDNA encoding the precursor for a novel member of the Acyl-CoA dehydrogenase gene family. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1446(3). 371–376. 21 indexed citations
4.
Moynihan, Leanne, Mark Houseman, Valerie Newton, Robert F. Mueller, & Nicholas Lench. (1999). DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25–qter. European Journal of Human Genetics. 7(2). 243–246. 16 indexed citations
5.
Moynihan, Leanne, Sarah Bundey, Duncan P. McHale, et al.. (1998). Autozygosity Mapping, to Chromosome 11q25, of a Rare Autosomal Recessive Syndrome Causing Histiocytosis, Joint Contractures, and Sensorineural Deafness. The American Journal of Human Genetics. 62(5). 1123–1128. 27 indexed citations
6.
Campbell, David A., Duncan P. McHale, Kathryn Brown, et al.. (1997). A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.. Journal of Medical Genetics. 34(12). 1015–1017. 31 indexed citations
7.
Brown, Kathryn, L.I. Al-Gazali, Leanne Moynihan, et al.. (1997). Genetic heterogeneity in Schwartz-Jampel syndrome: two families with neonatal Schwartz-Jampel syndrome do not map to human chromosome 1p34-p36.1.. Journal of Medical Genetics. 34(8). 685–687. 13 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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