V.K. Maloney

549 total citations
12 papers, 304 citations indexed

About

V.K. Maloney is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, V.K. Maloney has authored 12 papers receiving a total of 304 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in V.K. Maloney's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (3 papers). V.K. Maloney is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers) and Prenatal Screening and Diagnostics (3 papers). V.K. Maloney collaborates with scholars based in United Kingdom, United States and Denmark. V.K. Maloney's co-authors include John A. Crolla, N. Simon Thomas, Shuwen Huang, Sara Benito‐Sanz, Ángel Campos‐Barros, Valérie Cormier‐Daire, Jesús Argente, Karen E. Heath, Darya Gorbenko del Blanco and Miriam Aza‐Carmona and has published in prestigious journals such as The American Journal of Human Genetics, British Journal of Cancer and Vaccine.

In The Last Decade

V.K. Maloney

12 papers receiving 286 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
V.K. Maloney United Kingdom	9	263	174	54	46	19	12	304
Gianna Carvalheira Brazil	14	144 0.5×	182 1.0×	99 1.8×	21 0.5×	36 1.9×	25	381
Chiara Chianese Italy	13	401 1.5×	363 2.1×	57 1.1×	85 1.8×	24 1.3×	16	611
Marjorie Newton United Kingdom	7	280 1.1×	179 1.0×	113 2.1×	81 1.8×	8 0.4×	9	409
K. Gardiner United States	8	147 0.6×	218 1.3×	61 1.1×	50 1.1×	17 0.9×	15	350
Olga Žilina Estonia	12	242 0.9×	132 0.8×	54 1.0×	92 2.0×	19 1.0×	23	314
Moe Tamano Japan	12	201 0.8×	379 2.2×	19 0.4×	24 0.5×	23 1.2×	17	452
Sally Martell Canada	10	178 0.7×	131 0.8×	24 0.4×	83 1.8×	11 0.6×	12	289
Maud Borensztein France	10	271 1.0×	583 3.4×	73 1.4×	53 1.2×	96 5.1×	19	656
Anne Dodd United States	7	248 0.9×	159 0.9×	31 0.6×	15 0.3×	12 0.6×	12	343
Christine Yang Canada	9	118 0.4×	300 1.7×	30 0.6×	15 0.3×	52 2.7×	16	351

Countries citing papers authored by V.K. Maloney

Since Specialization

Citations

This map shows the geographic impact of V.K. 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.K. 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.K. Maloney more than expected).

Fields of papers citing papers by V.K. Maloney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of V.K. Maloney. A scholar is included among the top collaborators of V.K. 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.K. Maloney. V.K. 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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12 of 12 papers shown

Bunyan, David J., et al.. (2014). Homozygosity for a novel deletion downstream of the SHOX gene provides evidence for an additional long range regulatory region with a mild phenotypic effect. American Journal of Medical Genetics Part A. 164(11). 2764–2768. 16 indexed citations

Bunyan, David J., David Robinson, Anthony G. Tyers, et al.. (2014). X-Linked Dominant Congenital Ptosis Cosegregating with an Interstitial Insertion of a Chromosome 1p21.3 Fragment into a Quasipalindromic Sequence in Xq27.1. 4(6). 415–425. 8 indexed citations

Jacobs, P. A., V.K. Maloney, Rosie Cooke, et al.. (2013). Male breast cancer, age and sex chromosome aneuploidy. British Journal of Cancer. 108(4). 959–963. 15 indexed citations

Barber, John, Charlotte Brasch‐Andersen, V.K. Maloney, et al.. (2012). A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q. Cytogenetic and Genome Research. 139(1). 59–64. 3 indexed citations

Mercer, Catherine L., C.E. Browne, John Barber, et al.. (2009). A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH. Cytogenetic and Genome Research. 124(2). 179–186. 8 indexed citations

Tatton‐Brown, Katrina, Daniela T. Pilz, Karen Helene Ørstavik, et al.. (2009). 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A. 149A(2). 147–154. 55 indexed citations

Thomas, N. Simon, Victoria Bryant, V.K. Maloney, Annette E. Cockwell, & Patricia A. Jacobs. (2008). Investigation of the origins of human autosomal inversions. Human Genetics. 123(6). 607–616. 17 indexed citations

Wilson, Heather L., John A. Crolla, Lina Artifoni, et al.. (2008). Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development. European Journal of Human Genetics. 16(11). 1301–1310. 55 indexed citations

Maloney, V.K., et al.. (2006). The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population. ePrints Soton (University of Southampton). 1 indexed citations

10.

Barber, John, Shuai Zhang, Amanda Collins, et al.. (2006). Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenetic and Genome Research. 114(3-4). 351–358. 18 indexed citations

11.

Benito‐Sanz, Sara, N. Simon Thomas, Céline Huber, et al.. (2005). A Novel Class of Pseudoautosomal Region 1 Deletions Downstream of SHOX Is Associated with Léri-Weill Dyschondrosteosis. The American Journal of Human Genetics. 77(4). 533–544. 96 indexed citations

12.

Jones, David H., Brian W. McBride, Marilynn A. Roff, V.K. Maloney, & Graham H. Farrar. (1994). Purification and characterization of simian immunodeficiency virus (SIVmac) envelope glycoprotein GP130 from virus-infected cells. Vaccine. 12(3). 250–258. 12 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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