M. A. Mori
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Cellular and Molecular Neuroscience
- Psychiatry and Mental health
- Co-authors
- Pablo LapunzinaAdriana MimbacasRichard J. UriarteAlicia DelicadoI. López PajaresMaría TorresMaría Palomares‐BraloLuís Fernández
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Prenatal Screening and Diagnostics (4 papers)Chromosomal and Genetic Variations (3 papers)
In The Last Decade
M. A. Mori
15 papers receiving 342 citations
Peers
Comparison fields: 5 of 56
- Genetics 216
- Molecular Biology 156
- Pediatrics, Perinatology and Child Health 82
- Cellular and Molecular Neuroscience 63
- Psychiatry and Mental health 53
Countries citing papers authored by M. A. Mori
This map shows the geographic impact of M. A. Mori'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 M. A. Mori with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. A. Mori more than expected).
Fields of papers citing papers by M. A. Mori
This network shows the impact of papers produced by M. A. Mori. 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 M. A. Mori. The network helps show where M. A. Mori may publish in the future.
Co-authorship network of co-authors of M. A. Mori
This figure shows the co-authorship network connecting the top 25 collaborators of M. A. Mori. A scholar is included among the top collaborators of M. A. Mori 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 M. A. Mori. M. A. Mori is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Dysgammaglobulinemia Associated With Glu349del, a Hypomorphic XIAP Mutation. | 9 |
| 2 | 27 | |
| 3 | 16 | |
| 4 | 28 | |
| 5 | 15 | |
| 6 | 59 | |
| 7 | 61 | |
| 8 | 17 | |
| 9 | 8 | |
| 10 | 1 | |
| 11 | 101 | |
| 12 | 12 | |
| 13 | Partial monosomy 15q due to de novo t(15;22)(q15;p11). | 7 |
| 14 | 15 | |
| 15 | Unusual extra chromosomes in the mother of a 18-trisomy newborn. | 2 |
About M. A. Mori
M. A. Mori is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 15 papers that have together received 378 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Genetics (216 citations), Pediatrics, Perinatology and Child Health (82 citations) and Biological Psychiatry (10 citations). M. A. Mori has collaborated with scholars based in Spain, Argentina and Germany. Frequent co-authors include Pablo Lapunzina, Adriana Mimbacas, Richard J. Uriarte, Alicia Delicado, I. López Pajares, María Torres, María Palomares‐Bralo, Luís Fernández, Alfredo García‐Alix and Dolores Arjona. Their work appears in journals such as Human Molecular Genetics, Gene and Journal of Medical 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.