M. A. Mori

727 total citations
15 papers, 378 citations indexed

About

M. A. Mori is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, M. A. Mori has authored 15 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in M. A. Mori's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). M. A. Mori is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). M. A. Mori collaborates with scholars based in Spain, Argentina and Germany. M. A. Mori's 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 and has published in prestigious journals such as Human Molecular Genetics, Gene and Journal of Medical Genetics.

In The Last Decade

M. A. Mori

15 papers receiving 342 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. A. Mori Spain	10	216	156	82	63	53	15	378
Sylvie Joriot France	10	185 0.9×	219 1.4×	93 1.1×	45 0.7×	57 1.1×	27	509
Tiziana Filippi Italy	9	374 1.7×	207 1.3×	157 1.9×	41 0.7×	51 1.0×	10	539
Flemming Juul Hansen Denmark	13	132 0.6×	465 3.0×	107 1.3×	57 0.9×	87 1.6×	21	716
Kiyokuni Miura Japan	12	141 0.7×	133 0.9×	77 0.9×	30 0.5×	100 1.9×	29	444
Atsushi Ieshima Japan	11	205 0.9×	153 1.0×	66 0.8×	37 0.6×	19 0.4×	29	393
Eve Õiglane‐Shlik Estonia	10	185 0.9×	177 1.1×	76 0.9×	39 0.6×	32 0.6×	17	320
Julie Lauzon Canada	10	228 1.1×	196 1.3×	126 1.5×	29 0.5×	13 0.2×	23	430
Asım Cenani Türkiye	11	161 0.7×	98 0.6×	121 1.5×	16 0.3×	66 1.2×	36	316
Christalena Sofocleous Greece	14	261 1.2×	218 1.4×	81 1.0×	41 0.7×	31 0.6×	45	459
Ignacio Pascual Castroviejo Spain	11	216 1.0×	170 1.1×	182 2.2×	131 2.1×	236 4.5×	67	600

Countries citing papers authored by M. A. Mori

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

1.

Nishida, Naonori, Ichiro Takasaki, Kohsuke Imai, et al.. (2015). Dysgammaglobulinemia Associated With Glu349del, a Hypomorphic XIAP Mutation.. PubMed. 25(3). 205–13. 9 indexed citations

2.

Vallespín, Elena, María Palomares‐Bralo, M. A. Mori, et al.. (2013). Customized high resolution CGH‐array for clinical diagnosis reveals additional genomic imbalances in previous well‐defined pathological samples. American Journal of Medical Genetics Part A. 161(8). 1950–1960. 27 indexed citations

3.

Rodríguez‐Revenga, Laia, Elena Vallespín, Irene Madrigal, et al.. (2013). A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability. Gene. 521(1). 82–86. 16 indexed citations

4.

Romanelli, Valeria, Julián Nevado, Mario F. Fraga, et al.. (2010). Constitutional mosaic genome-wide uniparental disomy due to diploidisation: an unusual cancer-predisposing mechanism. Journal of Medical Genetics. 48(3). 212–216. 28 indexed citations

5.

Pajares, I. López, Olaya Villa, Marta Salido, et al.. (2006). Euchromatic variant 16p+. Implications in prenatal diagnosis. Prenatal Diagnosis. 26(6). 535–538. 15 indexed citations

6.

Fernández, Luís, Pablo Lapunzina, Dolores Arjona, et al.. (2005). Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome. Clinical Genetics. 68(4). 373–378. 59 indexed citations

7.

Lapunzina, Pablo, et al.. (2004). Macrocephaly‐cutis marmorata telangiectatica congenita: Report of six new patients and a review. American Journal of Medical Genetics Part A. 130A(1). 45–51. 61 indexed citations

8.

López‐Pajares, Isidora, et al.. (2003). Tetrasomy 8p: Discordance of amniotic fluid and blood karyotypes. American Journal of Medical Genetics Part A. 118A(4). 353–357. 17 indexed citations

9.

Lapunzina, Pablo, et al.. (2002). Autosomal recessive hydrocephalus due to aqueduct stenosis: report of a further family and implications for genetic counselling. The Journal of Maternal-Fetal & Neonatal Medicine. 12(1). 64–66. 8 indexed citations

10.

Lapunzina, Pablo, et al.. (2002). Autosomal recessive hydrocephalus due to aqueduct stenosis: report of a further family and implications for genetic counselling. The Journal of Maternal-Fetal & Neonatal Medicine. 12(1). 64–66. 1 indexed citations

11.

Mori, M. A., et al.. (1993). A new polymorphic probe on chromosome 22q (XD6) (D22S313). Human Molecular Genetics. 2(3). 338–338. 101 indexed citations

12.

Mori, M. A., et al.. (1988). De novo 10q23 interstitial deletion.. Journal of Medical Genetics. 25(3). 209–210. 12 indexed citations

13.

Mori, M. A., et al.. (1987). Partial monosomy 15q due to de novo t(15;22)(q15;p11).. PubMed. 30(4). 246–8. 7 indexed citations

14.

Mori, M. A., et al.. (1985). Trisomy 13 in the child of two carriers of a 13/15 translocation. American Journal of Medical Genetics. 20(1). 17–20. 15 indexed citations

15.

Mori, M. A., et al.. (1969). Unusual extra chromosomes in the mother of a 18-trisomy newborn.. PubMed. 14(2). 145–50. 2 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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