M.L. Martínez‐Fernández

600 total citations
20 papers, 196 citations indexed

About

M.L. Martínez‐Fernández is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, M.L. Martínez‐Fernández has authored 20 papers receiving a total of 196 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in M.L. Martínez‐Fernández's work include Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (8 papers) and Prenatal Screening and Diagnostics (6 papers). M.L. Martínez‐Fernández is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (8 papers) and Prenatal Screening and Diagnostics (6 papers). M.L. Martínez‐Fernández collaborates with scholars based in Spain, Italy and Germany. M.L. Martínez‐Fernández's co-authors include Elena Mansilla, Laura Rodríguez, M. L. Martínez‐Frías, Alexandra MacDonald, María Luisa Martínez‐Frías, Marina Murdolo, María Luisa Martínez‐Frías, Marcella Zollino, Eva Bermejo and Thomas Liehr and has published in prestigious journals such as Journal of Medical Genetics, Frontiers in Genetics and Contact Dermatitis.

In The Last Decade

M.L. Martínez‐Fernández

19 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M.L. Martínez‐Fernández Spain	9	154	78	58	48	18	20	196
Imma Rost Germany	9	212 1.4×	157 2.0×	74 1.3×	45 0.9×	10 0.6×	24	322
Soumaya Mougou-Zerelli Tunisia	8	164 1.1×	108 1.4×	21 0.4×	78 1.6×	13 0.7×	23	337
Vera Ayres Meloni Brazil	9	233 1.5×	122 1.6×	50 0.9×	59 1.2×	5 0.3×	26	272
Carla S. D’Angelo Brazil	10	229 1.5×	156 2.0×	27 0.5×	42 0.9×	28 1.6×	15	302
Catherine Ozilou France	10	273 1.8×	118 1.5×	67 1.2×	72 1.5×	7 0.4×	11	319
Emanuela Ponzi Italy	7	93 0.6×	87 1.1×	17 0.3×	22 0.5×	16 0.9×	14	182
Conny van Ravenswaaij Netherlands	7	204 1.3×	124 1.6×	53 0.9×	95 2.0×	7 0.4×	8	278
Angharad M. Roberts United Kingdom	7	99 0.6×	69 0.9×	14 0.2×	57 1.2×	6 0.3×	15	199
Gordon S. Stephen United Kingdom	8	171 1.1×	100 1.3×	62 1.1×	66 1.4×	5 0.3×	15	239
Amelia Villa Spain	9	176 1.1×	83 1.1×	50 0.9×	75 1.6×	10 0.6×	12	241

Countries citing papers authored by M.L. Martínez‐Fernández

Since Specialization

Citations

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

Fields of papers citing papers by M.L. Martínez‐Fernández

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.L. Martínez‐Fernández. 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.L. Martínez‐Fernández. The network helps show where M.L. Martínez‐Fernández may publish in the future.

Co-authorship network of co-authors of M.L. Martínez‐Fernández

This figure shows the co-authorship network connecting the top 25 collaborators of M.L. Martínez‐Fernández. A scholar is included among the top collaborators of M.L. Martínez‐Fernández 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.L. Martínez‐Fernández. M.L. Martínez‐Fernández 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

Nevado, Julián, Adolfo Hernández, M.L. Martínez‐Fernández, et al.. (2021). Deep Phenotyping and Genetic Characterization of a Cohort of 70 Individuals With 5p Minus Syndrome. Frontiers in Genetics. 12. 645595–645595. 8 indexed citations

Bermejo, Eva, et al.. (2015). Deletion 1q43‐44 in a patient with clinical diagnosis of Warburg–Micro syndrome. American Journal of Medical Genetics Part A. 167(6). 1243–1251. 4 indexed citations

Martínez‐Fernández, M.L., et al.. (2015). Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date. American Journal of Medical Genetics Part A. 167(9). 2034–2041. 4 indexed citations

Martínez‐Frías, María Luisa, J. Gonzalo Ocejo‐Vinyals, Rosa Arteaga, et al.. (2013). Interstitial deletion 14q22.3‐q23.2: Genotype–phenotype correlation. American Journal of Medical Genetics Part A. 164(3). 639–647. 6 indexed citations

Suela, Javier, et al.. (2013). A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with marden–walker syndrome. American Journal of Medical Genetics Part A. 161(9). 2281–2290. 4 indexed citations

Martínez‐Fernández, M.L., et al.. (2013). Haploinsufficiency of BMP4 gene may be the underlying cause of Frías syndrome. American Journal of Medical Genetics Part A. 164(2). 338–345. 12 indexed citations

MacDonald, Alexandra, et al.. (2010). Subtelomeric deletion of 12p: Description of a third case and review. American Journal of Medical Genetics Part A. 152A(6). 1561–1566. 15 indexed citations

Martínez‐Fernández, M.L., et al.. (2010). Resumen de la evolución de las técnicas de citogenética y genética molecular para la identificación de las alteraciones genéticas del desarrollo embrionario. Medicina de Familia SEMERGEN. 36(9). 520–525.

Martínez‐Fernández, M.L., Eva Bermejo, & María Luisa Martínez‐Frías. (2010). Ejemplos clínicos de alteraciones crípticas del ADN, y guías para sospechar que un niño pueda tener alguna alteración críptica o molecular. Medicina de Familia SEMERGEN. 36(10). 573–578. 1 indexed citations

10.

Rodríguez, Laura, et al.. (2008). A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1–q12.1 in a healthy man. Molecular Cytogenetics. 1(1). 4–4. 7 indexed citations

11.

Rodríguez, Laura, E. Niebuhr, Andrés M. García, M.L. Martínez‐Fernández, & José Luis Peña Segura. (2008). Be careful with familial unbalanced chromosome abnormalities!. American Journal of Medical Genetics Part A. 146A(15). 2005–2007. 2 indexed citations

12.

Martínez‐Frías, María Luisa, Eva Bermejo, Belén Estébanez, et al.. (2008). Análisis de las frecuencias de todas las combinaciones genotípicas de 4 polimorfismos de genes implicados en el ciclo del folato en la población española. Medicina Clínica. 131(3). 81–88. 1 indexed citations

13.

Rodríguez, Laura, M.L. Martínez‐Fernández, Elena Mansilla, et al.. (2008). Screening for subtelomeric chromosome alteration in a consecutive series of newborns with congenital defects. Clinical Dysmorphology. 17(1). 5–12. 8 indexed citations

14.

Rodríguez, Laura, et al.. (2008). A small and active ring x chromosome in a female with features of Kabuki syndrome. American Journal of Medical Genetics Part A. 146A(21). 2816–2821. 15 indexed citations

15.

Rodríguez, Laura, Marcella Zollino, Elena Mansilla, et al.. (2007). The first 4p euchromatic variant in a healthy carrier having an unusual reproductive history. American Journal of Medical Genetics Part A. 143A(9). 995–998. 7 indexed citations

16.

Liehr, Thomas, Kristin Mrasek, Elena Mansilla, et al.. (2007). Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review. American Journal of Medical Genetics Part A. 143A(22). 2727–2732. 23 indexed citations

17.

Chabchoub, Elyes, Enrique Galán, Elena Mansilla, et al.. (2006). Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation. Journal of Medical Genetics. 44(4). 250–256. 31 indexed citations

18.

Pérez-Milena, Alejandro, et al.. (2006). Tabaquismo y adolescentes: ¿buen momento para dejar de fumar? Relación con factores sociofamiliares. Atención Primaria. 37(8). 452–456. 10 indexed citations

19.

Rodríguez, Laura, Marcella Zollino, Elena Mansilla, et al.. (2005). The new Wolf–Hirschhorn syndrome critical region (WHSCR‐2): A description of a second case. American Journal of Medical Genetics Part A. 136A(2). 175–178. 34 indexed citations

20.

Miranda‐Romero, A., et al.. (1998). Delayed local allergic reaction to intralesional paramethasone acetate. Contact Dermatitis. 39(1). 31–32. 4 indexed citations

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