G. Glóver
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
- Congenital Ear and Nasal Anomalies 2
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- Congenital heart defects research 3
- Co-authors
- Pablo Carbonell (8 shared papers)Montserrat Milà (3 shared papers)I. López (4 shared papers)H. Kruyer (2 shared papers)F Ballesta (2 shared papers)Xavier Estivill (2 shared papers)Ana Luisa Jiménez (3 shared papers)John C. Mulley (1 shared paper)
In The Last Decade
G. Glóver
25 papers receiving 468 citations
Peers
Comparison fields: 5 of 53
- Genetics 364
- Cognitive Neuroscience 126
- Reproductive Medicine 38
- Pediatrics, Perinatology and Child Health 86
- Molecular Biology 257
Countries citing papers authored by G. Glóver
This map shows the geographic impact of G. Glóver'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 G. Glóver with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G. Glóver more than expected).
Fields of papers citing papers by G. Glóver
This network shows the impact of papers produced by G. Glóver. 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 G. Glóver. The network helps show where G. Glóver may publish in the future.
Co-authors
The 25 scholars most cited alongside G. Glóver, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins. | 1994 | 79 |
| 2 | 1995 | 78 | |
| 3 | 2000 | 53 | |
| 4 | 2003 | 44 | |
| 5 | 2008 | 39 | |
| 6 | 1986 | 30 | |
| 7 | 1994 | 21 | |
| 8 | 1996 | 20 | |
| 9 | 2004 | 16 | |
| 10 | 1988 | 15 | |
| 11 | 1988 | 14 | |
| 12 | 2014 | 11 | |
| 13 | 2010 | 10 | |
| 14 | 1992 | 8 | |
| 15 | 2009 | 8 | |
| 16 | 1987 | 8 | |
| 17 | 2009 | 7 | |
| 18 | 2003 | 7 | |
| 19 | 1985 | 4 | |
| 20 | 2005 | 3 |
About G. Glóver
G. Glóver is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cognitive Neuroscience and Plant Science, having authored 26 papers that have together received 484 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (4 papers), Chromosomal and Genetic Variations (4 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (3 papers), Congenital Ear and Nasal Anomalies (2 papers) and Cystic Fibrosis Research Advances (2 papers). The work is most often cited by research in Genetics (364 citations), Cognitive Neuroscience (126 citations), Reproductive Medicine (38 citations), Pediatrics, Perinatology and Child Health (86 citations) and Molecular Biology (257 citations). G. Glóver has collaborated with scholars based in Spain, Australia and Portugal. Frequent co-authors include Pablo Carbonell, Montserrat Milà, I. López, H. Kruyer, F Ballesta, Xavier Estivill, Ana Luisa Jiménez, John C. Mulley, David Hay and Andrew J. Donnelly. Their work appears in journals such as Clinical Genetics, Journal of Cystic Fibrosis, Human Genetics, Annals of Human Genetics and NMR in Biomedicine.
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.