V. Maloney

421 total citations
4 papers, 38 citations indexed

About

V. Maloney is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, V. Maloney has authored 4 papers receiving a total of 38 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 4 papers in Plant Science and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in V. Maloney's work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (2 papers). V. Maloney is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (2 papers). V. Maloney collaborates with scholars based in United Kingdom, Netherlands and Mexico. V. Maloney's co-authors include Ruben van’t Slot, PF Bolton, Margaret Barrow, Mihriban Heval Özgen, Shuwen Huang, F. A. Beemer, Lara Cresswell, Martin Poot, Emma van Daalen and Ron Hochstenbach and has published in prestigious journals such as Cytogenetic and Genome Research and Clinical Genetics.

In The Last Decade

V. Maloney

4 papers receiving 36 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
V. Maloney United Kingdom	3	35	13	11	10	9	4	38
Stefania Rassu Italy	2	31 0.9×	5 0.4×	6 0.5×	19 1.9×	10 1.1×	2	44
Uma Mallya United Kingdom	3	40 1.1×	15 1.2×	4 0.4×	20 2.0×	13 1.4×	3	63
Gea Beunders Netherlands	4	52 1.5×	10 0.8×	5 0.5×	34 3.4×	9 1.0×	5	66
Roseline Caumes France	4	32 0.9×	15 1.2×	3 0.3×	31 3.1×	5 0.6×	12	58
Ksenia Lavrichenko Norway	4	54 1.5×	9 0.7×	6 0.5×	35 3.5×	13 1.4×	5	70
Leigh Anne Flore United States	5	84 2.4×	9 0.7×	16 1.5×	35 3.5×	27 3.0×	8	112
Stephen T.S. Lam China	4	73 2.1×	22 1.7×	7 0.6×	31 3.1×	18 2.0×	8	79
Elyse Mitchell United States	4	45 1.3×	3 0.2×	11 1.0×	20 2.0×	17 1.9×	5	65
Anne‐Laure Mosca‐Boidron France	3	55 1.6×	12 0.9×	3 0.3×	41 4.1×	4 0.4×	3	90
Maria Grazia Tibiletti Italy	2	75 2.1×	43 3.3×	5 0.5×	30 3.0×	14 1.6×	3	106

Countries citing papers authored by V. Maloney

Since Specialization

Citations

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

Fields of papers citing papers by V. Maloney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Maloney

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

All Works

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4 of 4 papers shown

1.

Barber, John, et al.. (2013). Another Family with a Euchromatic Duplication Variant of 9q13-q21.1 Derived from Segmentally Duplicated Pericentromeric Euchromatin. Cytogenetic and Genome Research. 141(1). 64–69. 3 indexed citations

2.

Özgen, Mihriban Heval, Emma van Daalen, PF Bolton, et al.. (2009). Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders. Clinical Genetics. 76(4). 348–356. 31 indexed citations

3.

Rivera, Horacio, et al.. (2006). A highly complex rea(2;3;11) and aniridia by position effect. Cytogenetic and Genome Research. 114(1). 83–88. 2 indexed citations

4.

Cockwell, Annette E., et al.. (2005). Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities. Cytogenetic and Genome Research. 112(1-2). 166–169. 2 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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