V.K. Maloney
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Genetic and rare skin diseases. 1
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- Genomics and Chromatin Dynamics 2
- Glycosylation and Glycoproteins Research 1
- Co-authors
- John A. Crolla (5 shared papers)N. Simon Thomas (3 shared papers)Shuwen Huang (5 shared papers)Céline Huber (1 shared paper)Darya Gorbenko del Blanco (1 shared paper)Miriam Aza‐Carmona (1 shared paper)Karen E. Heath (1 shared paper)Sara Benito‐Sanz (1 shared paper)
- Journals
- Cytogenetic and Genome Research (3 papers)Human Genetics (1 paper)European Journal of Human Genetics (1 paper)British Journal of Cancer (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
V.K. Maloney
12 papers receiving 292 citations
Peers
Comparison fields: 5 of 35
- Genetics 242
- Pediatrics, Perinatology and Child Health 36
- Molecular Biology 140
- Virology 6
- Plant Science 47
Countries citing papers authored by V.K. Maloney
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
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-authors
The 25 scholars most cited alongside V.K. Maloney, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 98 | |
| 2 | 2008 | 56 | |
| 3 | 2009 | 55 | |
| 4 | 2006 | 18 | |
| 5 | 2014 | 18 | |
| 6 | 2008 | 17 | |
| 7 | 2013 | 15 | |
| 8 | 1994 | 12 | |
| 9 | 2014 | 9 | |
| 10 | 2009 | 8 | |
| 11 | 2012 | 3 | |
| 12 | The use of pyrosequencing to identify copy number variation of 16p11.2 in euchromatic variant carriers and the normal population | 2006 | 1 |
About V.K. Maloney
V.K. Maloney is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 12 papers that have together received 310 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (4 papers), Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Glycosylation and Glycoproteins Research (1 paper) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (242 citations), Pediatrics, Perinatology and Child Health (36 citations), Molecular Biology (140 citations), Virology (6 citations) and Plant Science (47 citations). V.K. Maloney has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include John A. Crolla, N. Simon Thomas, Shuwen Huang, Céline Huber, Darya Gorbenko del Blanco, Miriam Aza‐Carmona, Karen E. Heath, Sara Benito‐Sanz, Ángel Campos‐Barros and Jesús Argente. Their work appears in journals such as Cytogenetic and Genome Research, Human Genetics, European Journal of Human Genetics, British Journal of Cancer and The American Journal of Human Genetics.
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.