Carmen Esmer

412 total citations
16 papers, 225 citations indexed

About

Carmen Esmer is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Carmen Esmer has authored 16 papers receiving a total of 225 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Physiology and 4 papers in Genetics. Recurrent topics in Carmen Esmer's work include Glycogen Storage Diseases and Myoclonus (3 papers), Lysosomal Storage Disorders Research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Carmen Esmer is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (3 papers), Lysosomal Storage Disorders Research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Carmen Esmer collaborates with scholars based in Mexico, United States and Panama. Carmen Esmer's co-authors include Nora Urraca, Victoria E. Brewer, Ronald L. Thibert, Kathryn McVicar, Lawrence T. Reiter, N. Carolyn Schanen, Enikö K. Pivnick, Alessandra Carnevale, Sílvia Sánchez and Bertha Molina and has published in prestigious journals such as American Journal of Medical Genetics, Autism Research and American Journal of Medical Genetics Part A.

In The Last Decade

Carmen Esmer

16 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Carmen Esmer Mexico	5	157	116	46	33	17	16	225
Diane Hu‐Lince United States	7	144 0.9×	143 1.2×	24 0.5×	22 0.7×	13 0.8×	7	253
Daniel Amsallem France	10	222 1.4×	173 1.5×	81 1.8×	29 0.9×	19 1.1×	21	335
Margarida Venâncio Portugal	10	233 1.5×	140 1.2×	29 0.6×	23 0.7×	13 0.8×	22	297
Dima El‐Khechen United States	8	208 1.3×	125 1.1×	49 1.1×	26 0.8×	11 0.6×	10	294
Benjamin Kamien Australia	9	128 0.8×	124 1.1×	14 0.3×	42 1.3×	9 0.5×	19	228
Emma McCann United Kingdom	6	177 1.1×	153 1.3×	14 0.3×	80 2.4×	34 2.0×	10	315
Shashidhar Pai United States	8	237 1.5×	278 2.4×	61 1.3×	49 1.5×	35 2.1×	13	391
Michèle Mathieu‐Dramard France	9	170 1.1×	200 1.7×	11 0.2×	44 1.3×	22 1.3×	15	363
Mariana Moysés‐Oliveira Brazil	11	206 1.3×	130 1.1×	29 0.6×	53 1.6×	35 2.1×	45	300
Louise Christie Australia	10	294 1.9×	197 1.7×	68 1.5×	73 2.2×	40 2.4×	14	409

Countries citing papers authored by Carmen Esmer

Since Specialization

Citations

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

Fields of papers citing papers by Carmen Esmer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmen Esmer

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

All Works

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16 of 16 papers shown

Espinosa‐Tanguma, Ricardo, et al.. (2021). Lipofuscinosis ceroidea neuronal. Variante infantil tardía de tipo 6 en dos hermanos heterocigotos compuestos con mutaciones nuevas. Revista de Neurología. 73(10). 368–368. 3 indexed citations

Esmer, Carmen, Sandra Romero‐Hidalgo, Arturo Rojo-Domı́nguez, et al.. (2017). Prevalence and ancestral origin of the c.1987delC GAA gene mutation causing Pompe disease in Central Mexico. Meta Gene. 15. 60–64. 2 indexed citations

Esmer, Carmen, et al.. (2017). Asociación entre la mutación homocigota c.318A>T en el exón 2 del gen EIF2B5 y la forma infantil de la leucoencefalopatía con sustancia blanca evanescente. Boletín Médico del Hospital Infantil de México. 74(5). 364–369. 3 indexed citations

Esmer, Carmen, et al.. (2017). Estandarización de la prueba de marcha de seis minutos en niños mexicanos sanos. 18(3). 11–23. 1 indexed citations

Esmer, Carmen, et al.. (2016). Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 Mutation. Revista de investigaci�n Cl�nica. 68(3). 143–146. 4 indexed citations

Esmer, Carmen, et al.. (2016). Presentación atípica de la enfermedad de Alexander infantil sin macrocefalia. Boletín Médico del Hospital Infantil de México. 73(3). 196–201. 1 indexed citations

Cerda‐Flores, Ricardo M., et al.. (2015). Frequency of SMN1 deletion carriers in a Mestizo population of central and northeastern Mexico: A pilot study. Experimental and Therapeutic Medicine. 9(6). 2053–2058. 1 indexed citations

Lurie, Iosif W., et al.. (2015). A novel interstitial deletion of 2q22.3 q23.3 in a patient with dysmorphic features, epilepsy, aganglionosis, pure red cell aplasia, and skeletal malformations. American Journal of Medical Genetics Part A. 167(8). 1865–1871. 6 indexed citations

Esmer, Carmen, et al.. (2013). A novel homozygous mutation at the GAA gene in Mexicans with early-onset Pompe disease.. PubMed. 32(2). 95–9. 4 indexed citations

10.

Urraca, Nora, Victoria E. Brewer, Enikö K. Pivnick, et al.. (2013). The Interstitial Duplication 15q11.2‐q13 Syndrome Includes Autism, Mild Facial Anomalies and a Characteristic EEG Signature. Autism Research. 6(4). 268–279. 116 indexed citations

11.

Esmer, Carmen, et al.. (2013). Neuropatía sensitiva autonómica hereditaria tipo IIA: manifestaciones neurológicas y esqueléticas tempranas. Anales de Pediatría. 80(4). 254–258. 2 indexed citations

12.

Hernandez, David J., et al.. (2011). Severe consequences of carbamazepine exposure in utero: Figure 1. BMJ Case Reports. 2011. bcr0520114243–bcr0520114243. 3 indexed citations

13.

Villarreal, L., et al.. (2008). Tamiz metabólico neonatal por espectrometría de masas en tándem: dos años de experiencia en Nuevo León, México. Salud Pública de México. 50(3). 200–6. 18 indexed citations

14.

Esmer, Carmen, Nora Urraca, Alessandra Carnevale, & Victoria del Castillo. (2003). Patient follow‐up is a major problem at genetics clinics. American Journal of Medical Genetics Part A. 125A(2). 162–166. 8 indexed citations

15.

Esmer, Carmen, et al.. (2003). DEB test for Fanconi anemia detection in patients with atypical phenotypes. American Journal of Medical Genetics Part A. 124A(1). 35–39. 49 indexed citations

16.

Esmer, Carmen, et al.. (2001). Liver fibrocystic disease and polydactyly: Proposal of a new syndrome. American Journal of Medical Genetics. 101(1). 12–16. 4 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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