M. Sandalinas

3.1k total citations
30 papers, 1.9k citations indexed

About

M. Sandalinas is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Plant Science. According to data from OpenAlex, M. Sandalinas has authored 30 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pediatrics, Perinatology and Child Health, 15 papers in Genetics and 8 papers in Plant Science. Recurrent topics in M. Sandalinas's work include Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (12 papers) and Chromosomal and Genetic Variations (8 papers). M. Sandalinas is often cited by papers focused on Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (12 papers) and Chromosomal and Genetic Variations (8 papers). M. Sandalinas collaborates with scholars based in United States, Spain and Serbia. M. Sandalinas's co-authors include S. Munné, Jacques Cohen, Tomás Escudero, Carmen Márquez, Sasha Sadowy, Luca Gianaroli, Mina Alikani, Gloria Calderón, Muhterem Bahçe and David Sable and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Molecular Human Reproduction.

In The Last Decade

M. Sandalinas

30 papers receiving 1.7k citations

Peers

M. Sandalinas

PPCH

GENET

PHEOH

M. Katz-Jaffe United States

Sasha Sadowy United States

E. Velilla Spain

J. Fischer United States

John Garrisi United States

L. Spizzichino Italy

Claude-Edouard Michel United Kingdom

Paula C. Morton United States

Steven J. McArthur Switzerland

C. Márquez Spain

M. Katz-Jaffe United States

M. Sandalinas

1.3k ×0.8

PPCH

441 ×0.5

GENET

817 ×1.1

PHEOH

331 ×0.9

316 ×1.1

Citations per year, relative to M. Sandalinas M. Sandalinas (= 1×) peers M. Katz-Jaffe

Countries citing papers authored by M. Sandalinas

Since Specialization

Citations

This map shows the geographic impact of M. Sandalinas'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. Sandalinas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Sandalinas more than expected).

Fields of papers citing papers by M. Sandalinas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Sandalinas. 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. Sandalinas. The network helps show where M. Sandalinas may publish in the future.

Co-authorship network of co-authors of M. Sandalinas

This figure shows the co-authorship network connecting the top 25 collaborators of M. Sandalinas. A scholar is included among the top collaborators of M. Sandalinas 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. Sandalinas. M. Sandalinas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Blanco, Joan, et al.. (2015). Altered segregation pattern and numerical chromosome abnormalities interrelate in spermatozoa from Robertsonian translocation carriers. Reproductive BioMedicine Online. 31(1). 79–88. 35 indexed citations

Martínez-Pasarell, O., et al.. (2014). Chromosome 16 Abnormalities in Embryos and in Sperm from a Male with a Fragile Site at 16q22.1. Cytogenetic and Genome Research. 142(2). 134–139. 16 indexed citations

Sandalinas, M., et al.. (2009). Prognostic value of sperm fluorescence in situ hybridization analysis over PGD. Human Reproduction. 24(6). 1516–1521. 26 indexed citations

Munné, S., M. Sandalinas, M. Cristina Magli, et al.. (2004). Increased rate of aneuploid embryos in young women with previous aneuploid conceptions. Prenatal Diagnosis. 24(8). 638–643. 85 indexed citations

Colls, P., M. Sandalinas, Kelly Pagidas, & S. Munné. (2004). PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16 (16qh−). Prenatal Diagnosis. 24(9). 741–744. 19 indexed citations

Munné, S., Muhterem Bahçe, M. Sandalinas, et al.. (2004). Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reproductive BioMedicine Online. 8(1). 81–90. 97 indexed citations

Munné, S., M. Sandalinas, Tomás Escudero, et al.. (2003). Improved implantation after preimplantation genetic diagnosis of aneuploidy. Reproductive BioMedicine Online. 7(1). 91–97. 232 indexed citations

Escudero, Tomás, et al.. (2003). Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations. Fertility and Sterility. 79. 1528–1534. 86 indexed citations

Colls, P., et al.. (2003). Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes. Reproductive BioMedicine Online. 6(2). 226–231. 27 indexed citations

10.

Werlin, L.B., T. Escudero, E. Velilla, et al.. (2002). Preimplantation genetic diagnosis (PGD) as both a diagnostic and therapeutic tool in women with advanced maternal age (AMA) undergoing IVF. Fertility and Sterility. 77. S13–S14. 4 indexed citations

11.

Sandalinas, M.. (2002). Spectral karyotyping of fresh, non-inseminated oocytes. Molecular Human Reproduction. 8(6). 580–585. 96 indexed citations

12.

Munné, S., M. Sandalinas, Tomás Escudero, Carmen Márquez, & Jacques Cohen. (2002). Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect. Reproductive BioMedicine Online. 4(3). 223–232. 168 indexed citations

13.

Escudero, Tomás, Michael Lee, John Stevens, M. Sandalinas, & S. Munné. (2001). Preimplantation genetic diagnosis of pericentric inversions. Prenatal Diagnosis. 21(9). 760–766. 34 indexed citations

14.

Sandalinas, M., Sasha Sadowy, Mina Alikani, et al.. (2001). Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. Human Reproduction. 16(9). 1954–1958. 257 indexed citations

15.

Magli, M.C., M. Sandalinas, T. Escudero, et al.. (2001). Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy. Prenatal Diagnosis. 21(12). 1080–1085. 41 indexed citations

16.

Munné, S., M. Sandalinas, Tomás Escudero, et al.. (2000). Outcome of preimplantation genetic diagnosis of translocations. Fertility and Sterility. 73(6). 1209–1218. 215 indexed citations

17.

Márquez, Carmen, et al.. (2000). Chromosome abnormalities in 1255 cleavage-stage human embryos. Reproductive BioMedicine Online. 1(1). 17–26. 160 indexed citations

18.

Boada, Montserrat, et al.. (1998). Successful Use of a Laser for Human Embryo Biopsy in Preimplantation Genetic Diagnosis: Report of Two Cases. Journal of Assisted Reproduction and Genetics. 15(5). 302–307. 67 indexed citations

19.

Veiga, Anna, M. Sandalinas, M. Benkhalifa, et al.. (1997). Laser blastocyst biopsy for preimplantation diagnosis in the human. Zygote. 5(4). 351–354. 90 indexed citations

20.

Veiga, Anna, et al.. (1995). Optimization of implantation in the in-vitro fertilization laboratory. Human Reproduction. 10(suppl 2). 98–106. 8 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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