Viv Maloney

2.0k total citations
18 papers, 587 citations indexed

About

Viv Maloney is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Viv Maloney has authored 18 papers receiving a total of 587 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Viv Maloney's work include Genomic variations and chromosomal abnormalities (15 papers), Congenital Ear and Nasal Anomalies (8 papers) and Congenital heart defects research (7 papers). Viv Maloney is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Congenital Ear and Nasal Anomalies (8 papers) and Congenital heart defects research (7 papers). Viv Maloney collaborates with scholars based in United Kingdom, Germany and United States. Viv Maloney's co-authors include John Barber, Shuwen Huang, N. Simon Thomas, John A. Crolla, Patricia A. Jacobs, Catherine Mercer, Elena Prigmore, Susan Gribble, Nigel P. Carter and Júlia Baptista and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Viv Maloney

18 papers receiving 518 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Viv Maloney United Kingdom 14 453 256 135 119 57 18 587
Courtney Sebold United States 16 437 1.0× 216 0.8× 97 0.7× 141 1.2× 32 0.6× 27 616
Azzedine Aboura France 17 525 1.2× 311 1.2× 110 0.8× 258 2.2× 53 0.9× 40 767
Mauro Pierluigi Italy 14 379 0.8× 248 1.0× 152 1.1× 98 0.8× 43 0.8× 26 496
Rachel D. Burnside United States 11 460 1.0× 229 0.9× 79 0.6× 173 1.5× 29 0.5× 26 576
Cristina Cuoco Italy 15 396 0.9× 275 1.1× 89 0.7× 214 1.8× 52 0.9× 38 647
Joo Wook Ahn United Kingdom 13 424 0.9× 232 0.9× 72 0.5× 159 1.3× 34 0.6× 29 605
María Palomares‐Bralo Spain 13 364 0.8× 339 1.3× 55 0.4× 105 0.9× 28 0.5× 38 540
Emmanouil Manolakos Greece 15 342 0.8× 181 0.7× 102 0.8× 312 2.6× 41 0.7× 70 642
Carolina Sismani Cyprus 19 735 1.6× 515 2.0× 184 1.4× 266 2.2× 33 0.6× 75 984
Melanie Babcock United States 10 315 0.7× 333 1.3× 150 1.1× 55 0.5× 29 0.5× 17 497

Countries citing papers authored by Viv Maloney

Since Specialization
Citations

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

Fields of papers citing papers by Viv Maloney

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Viv Maloney

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

All Works

18 of 18 papers shown
1.
Bateman, Mark S., Morag N. Collinson, David J. Bunyan, et al.. (2017). Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities. American Journal of Medical Genetics Part A. 176(2). 319–329. 5 indexed citations
2.
Blyth, Moira, Viv Maloney, Sarah J. Beal, et al.. (2015). Pallister-Killian syndrome: a study of 22 British patients. Journal of Medical Genetics. 52(7). 454–464. 33 indexed citations
3.
Barber, John, Jill A. Rosenfeld, Nicola Foulds, et al.. (2013). 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A. 161(3). 487–500. 33 indexed citations
4.
Jones, Matthew L., Sherina L. Murden, Claire Brooks, et al.. (2013). Disruption of AP3B1by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2. BMC Medical Genetics. 14(1). 42–42. 37 indexed citations
5.
Barber, John, Victoria L. Hall, Viv Maloney, et al.. (2012). 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. European Journal of Human Genetics. 21(2). 182–189. 34 indexed citations
6.
Barber, John, Susanne Morlot, Thomas Liehr, et al.. (2010). 8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families. Molecular Cytogenetics. 3(1). 3–3. 23 indexed citations
7.
Balasubramanian, Meena, et al.. (2009). Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy. American Journal of Medical Genetics Part A. 149A(4). 793–797. 24 indexed citations
8.
Rankin, Julia, et al.. (2009). Distal monosomy 1p36: an atypical case with duodenal atresia and a small interstitial deletion. Clinical Dysmorphology. 18(4). 222–224. 5 indexed citations
9.
Barnicoat, Angela, Shuwen Huang, Viv Maloney, et al.. (2008). Transmitted duplication of 8p23.1–8p23.2 associated with speech delay, autism and learning difficulties. European Journal of Human Genetics. 17(1). 37–43. 61 indexed citations
10.
Baptista, Júlia, Catherine Mercer, Elena Prigmore, et al.. (2008). Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort. The American Journal of Human Genetics. 82(4). 927–936. 127 indexed citations
11.
Blyth, Moira, Shuwen Huang, Viv Maloney, John A. Crolla, & I. Karen Temple. (2008). A 2.3 Mb deletion of 17q24.2–q24.3 associated with ‘Carney Complex plus’. European Journal of Medical Genetics. 51(6). 672–678. 22 indexed citations
12.
Thomas, N. Simon, Viv Maloney, Victoria Bryant, et al.. (2008). Breakpoint mapping and haplotype analysis of three reciprocal translocations identify a novel recurrent translocation in two unrelated families: t(4;11)(p16.2;p15.4). Human Genetics. 125(2). 181–188. 15 indexed citations
13.
Barber, John, Viv Maloney, Shuwen Huang, et al.. (2007). 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH. European Journal of Human Genetics. 16(1). 18–27. 67 indexed citations
14.
Barber, John, et al.. (2007). Transmitted duplication of 12q21.32–12q22 includes 48 genes and has no apparent phenotypic consequences. American Journal of Medical Genetics Part A. 143A(6). 615–618. 3 indexed citations
15.
Barber, John, et al.. (2006). Deletions of 2q14 that include the homeobox engrailed 1 (EN1) transcription factor are compatible with a normal phenotype. European Journal of Human Genetics. 14(6). 739–743. 11 indexed citations
16.
Barber, John, Viv Maloney, Edward J. Hollox, et al.. (2005). Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. European Journal of Human Genetics. 13(10). 1131–1136. 42 indexed citations
17.
Turner, Claire, Katherine Lachlan, Nishani Amerasinghe, et al.. (2005). Kabuki syndrome: new ocular findings but no evidence of 8p22-p23.1 duplications in a clinically defined cohort. European Journal of Human Genetics. 13(6). 716–720. 31 indexed citations
18.
Thomas, N. Simon, et al.. (2004). SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. American Journal of Medical Genetics Part A. 128A(2). 179–184. 14 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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