Sonia Canún

1.2k total citations
15 papers, 171 citations indexed

About

Sonia Canún is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sonia Canún has authored 15 papers receiving a total of 171 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sonia Canún's work include Congenital limb and hand anomalies (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Chromosomal and Genetic Variations (3 papers). Sonia Canún is often cited by papers focused on Congenital limb and hand anomalies (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Chromosomal and Genetic Variations (3 papers). Sonia Canún collaborates with scholars based in Mexico, Brazil and United Kingdom. Sonia Canún's co-authors include Alessandra Carnevale, Victoria del Castillo, Antonio Ysunza, James F. Reynolds, Ma. Carmen Pamplona, Susana Kofman‐Alfaro, Alicia Cervantes, Marisol López, Nancy Monroy‐Jaramillo and Fernando Regla Vargas and has published in prestigious journals such as Human Genetics, American Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Sonia Canún

14 papers receiving 163 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sonia Canún Mexico	8	97	86	31	30	19	15	171
J M Cantú Mexico	10	93 1.0×	72 0.8×	23 0.7×	45 1.5×	7 0.4×	17	220
M. L. Guion‐Almeida Brazil	10	164 1.7×	83 1.0×	27 0.9×	61 2.0×	5 0.3×	28	234
M Atasu Türkiye	13	244 2.5×	186 2.2×	47 1.5×	45 1.5×	6 0.3×	40	414
Isabel Cordeiro Portugal	7	162 1.7×	146 1.7×	18 0.6×	22 0.7×	25 1.3×	14	296
Nancy Mizue Kokitsu‐Nakata Brazil	11	210 2.2×	130 1.5×	7 0.2×	54 1.8×	20 1.1×	35	285
Lee Osterman United States	5	119 1.2×	83 1.0×	14 0.5×	141 4.7×	8 0.4×	8	278
José Carlos Cabral de Almeida Brazil	9	112 1.2×	72 0.8×	24 0.8×	67 2.2×	2 0.1×	17	281
Gerald I. Sugarman United States	9	152 1.6×	162 1.9×	25 0.8×	48 1.6×	2 0.1×	16	293
Valérie Raclin France	8	110 1.1×	196 2.3×	10 0.3×	54 1.8×		9	276
Jacques Battin France	7	91 0.9×	76 0.9×	36 1.2×	34 1.1×		13	249

Countries citing papers authored by Sonia Canún

Since Specialization

Citations

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

Fields of papers citing papers by Sonia Canún

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Canún

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

All Works

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15 of 15 papers shown

Canún, Sonia, Martin B. Delatycki, Gabriele Gillessen‐Kaesbach, et al.. (2008). No mutation in genes of the WNT signaling pathway in patients with Zimmermann–Laband syndrome. Clinical Dysmorphology. 17(3). 181–185. 10 indexed citations

Ysunza, Antonio, et al.. (2005). [Sensitivity and specificity of endoscopy for the detection of velocardiofacial syndrome].. PubMed. 56(4). 454–9. 6 indexed citations

Ysunza, Antonio, et al.. (2003). Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome). International Journal of Pediatric Otorhinolaryngology. 67(8). 911–915. 17 indexed citations

Canún, Sonia, et al.. (2002). Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: A new distinct entity. American Journal of Medical Genetics Part A. 116A(3). 278–283. 21 indexed citations

Monroy‐Jaramillo, Nancy, Marisol López, Alicia Cervantes, et al.. (2001). Microsatellite analysis in Turner syndrome: Parental origin of X chromosomes and possible mechanism of formation of abnormal chromosomes. American Journal of Medical Genetics. 107(3). 181–189. 17 indexed citations

Cervantes, Alicia, Marisol López, Mónica Aguinaga‐Ríos, et al.. (2001). PCR–PRINS–FISH analysis of structurally abnormal sex chromosomes in eight patients with Turner phenotype. Clinical Genetics. 60(5). 385–392. 6 indexed citations

Canún, Sonia, et al.. (1999). Blepharo‐cheilo‐dontic (BCD) syndrome in two Mexican patients. American Journal of Medical Genetics. 85(2). 157–159. 6 indexed citations

Vargas, Fernando Regla, Erich Roessler, Karin Gaudenz, et al.. (1998). Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly. Human Genetics. 102(4). 387–392. 35 indexed citations

Canún, Sonia, Osvaldo M. Mutchinick, Lisa G. Shaffer, & Carlos Fernández. (1998). Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.. PubMed. 80(3). 199–203. 8 indexed citations

10.

Felix, Robert J., et al.. (1995). [Epilepsy and pregnancy. Risks and benefits of anticonvulsant treatment].. PubMed. 63. 282–6. 2 indexed citations

11.

Domínguez, Luis Carlos, et al.. (1995). Epilepsia y embarazo. Riesgos y beneficios del tratamiento anticonvulsivo. 1 indexed citations

12.

Carnevale, Alessandra, et al.. (1987). Idiopathic multicentric osteolysis with facial anomalies and nephropathy. American Journal of Medical Genetics. 26(4). 877–886. 22 indexed citations

13.

Canún, Sonia. (1986). Absent tibiae, triphalangeal thumbs, Polydactyly and non‐penetrance. Clinical Genetics. 29(4). 347–347. 1 indexed citations

14.

Canún, Sonia, et al.. (1984). Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis. Clinical Genetics. 25(2). 182–186. 16 indexed citations

15.

Arroyo, Pedro, et al.. (1979). Variability between and within laboratories in the analysis of structural chromosomal abnormalities. Clinical Genetics. 15(5). 377–381. 3 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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