M. A. Mori
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 1
- Genetic and rare skin diseases. 1
-
- Congenital heart defects research 3
- Co-authors
- Pablo Lapunzina (9 shared papers)Adriana Mimbacas (1 shared paper)Richard J. Uriarte (1 shared paper)Alicia Delicado (7 shared papers)I. López Pajares (5 shared papers)María Torres (4 shared papers)Luís Fernández (3 shared papers)Julián Nevado (3 shared papers)
In The Last Decade
M. A. Mori
15 papers receiving 342 citations
Peers
Comparison fields: 5 of 53
- Genetics 193
- Biological Psychiatry 9
- Pediatrics, Perinatology and Child Health 67
- Psychiatry and Mental health 47
- Cellular and Molecular Neuroscience 61
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-authors
The 25 scholars most cited alongside M. A. Mori, 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 | 1993 | 101 | |
| 2 | 2004 | 61 | |
| 3 | 2005 | 59 | |
| 4 | 2010 | 28 | |
| 5 | 2013 | 27 | |
| 6 | 2003 | 17 | |
| 7 | 2013 | 16 | |
| 8 | 1985 | 15 | |
| 9 | 2006 | 15 | |
| 10 | 1988 | 12 | |
| 11 | Dysgammaglobulinemia Associated With Glu349del, a Hypomorphic XIAP Mutation. | 2015 | 9 |
| 12 | 2002 | 8 | |
| 13 | Partial monosomy 15q due to de novo t(15;22)(q15;p11). | 1987 | 7 |
| 14 | Unusual extra chromosomes in the mother of a 18-trisomy newborn. | 1969 | 2 |
| 15 | 2002 | 1 |
About M. A. Mori
M. A. Mori is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 15 papers that have together received 378 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (3 papers), Congenital heart defects research (3 papers), Prenatal Screening and Diagnostics (3 papers), Cerebrospinal fluid and hydrocephalus (2 papers), Genetic factors in colorectal cancer (2 papers), Genetics and Neurodevelopmental Disorders (1 paper) and Genetic and rare skin diseases. (1 paper). The work is most often cited by research in Genetics (193 citations), Biological Psychiatry (9 citations), Pediatrics, Perinatology and Child Health (67 citations), Psychiatry and Mental health (47 citations) and Cellular and Molecular Neuroscience (61 citations). M. A. Mori has collaborated with scholars based in Spain, Germany and Argentina. Frequent co-authors include Pablo Lapunzina, Adriana Mimbacas, Richard J. Uriarte, Alicia Delicado, I. López Pajares, María Torres, Luís Fernández, Julián Nevado, Luis Garcı́a-Guereta and Dolores Elorza. Their work appears in journals such as The Journal of Maternal-Fetal & Neonatal Medicine, Journal of Medical Genetics, Clinical Genetics, Gene and Prenatal Diagnosis.
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.