Lilien Chertkoff

742 total citations
31 papers, 479 citations indexed

About

Lilien Chertkoff is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lilien Chertkoff has authored 31 papers receiving a total of 479 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lilien Chertkoff's work include Genetic Syndromes and Imprinting (6 papers), Cystic Fibrosis Research Advances (6 papers) and Prenatal Screening and Diagnostics (4 papers). Lilien Chertkoff is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Cystic Fibrosis Research Advances (6 papers) and Prenatal Screening and Diagnostics (4 papers). Lilien Chertkoff collaborates with scholars based in Argentina, France and Portugal. Lilien Chertkoff's co-authors include Mariana Herrera Piñero, Leonardo Fainboim, María Eugenia Foncuberta, M. Leonardo Satz, Carmen Mazza, Claudio Castaños, Verónica Giubergia, Virginia Fano, Eduardo Chaler and Elisa Vaiani and has published in prestigious journals such as PEDIATRICS, Clinical Endocrinology and Human Mutation.

In The Last Decade

Lilien Chertkoff

30 papers receiving 462 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lilien Chertkoff Argentina 14 194 165 85 76 75 31 479
Gemma Walmsley United Kingdom 11 54 0.3× 146 0.9× 164 1.9× 27 0.4× 53 0.7× 25 465
Ella Sugo Australia 9 74 0.4× 78 0.5× 77 0.9× 46 0.6× 48 0.6× 25 359
Neeraj Kumar India 12 52 0.3× 152 0.9× 67 0.8× 23 0.3× 14 0.2× 58 478
D. C. Moriarty Ireland 8 46 0.2× 64 0.4× 112 1.3× 12 0.2× 24 0.3× 8 355
Derya Erçal Türkiye 11 123 0.6× 135 0.8× 37 0.4× 117 1.5× 37 0.5× 41 341
Wen Ying Chen Hong Kong 5 50 0.3× 139 0.8× 18 0.2× 56 0.7× 192 2.6× 5 469
Laura Sillers United States 8 25 0.1× 65 0.4× 47 0.6× 30 0.4× 77 1.0× 10 300
Sébastien Boni France 9 69 0.4× 115 0.7× 57 0.7× 9 0.1× 10 0.1× 14 319
Christine Reyes United States 13 100 0.5× 165 1.0× 56 0.7× 142 1.9× 83 1.1× 22 586
Xingguang Ye China 11 64 0.3× 92 0.6× 22 0.3× 30 0.4× 18 0.2× 25 296

Countries citing papers authored by Lilien Chertkoff

Since Specialization
Citations

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

Fields of papers citing papers by Lilien Chertkoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lilien Chertkoff

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

All Works

20 of 20 papers shown
1.
Reyes, Gabriela, et al.. (2020). Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients. Epilepsy & Behavior. 111. 107322–107322. 6 indexed citations
2.
Chertkoff, Lilien, et al.. (2020). Molecular analysis of GALT gene in Argentinian population: Correlation with enzyme activity and characterization of a novel Duarte-like allele. Molecular Genetics and Metabolism Reports. 25. 100695–100695. 9 indexed citations
3.
Monges, Soledad, Laura Alías, Sara Bernal, et al.. (2016). Genotype–phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina. European Journal of Paediatric Neurology. 20(6). 910–917. 18 indexed citations
4.
Roisman, Alejandro, et al.. (2016). Gene polymorphism profiles of drug-metabolising enzymes GSTM1, GSTT1 and GSTP1 in an Argentinian population. Annals of Human Biology. 44(4). 379–383. 5 indexed citations
5.
Sen, Luisa, et al.. (2014). Mannose-binding lectin gene as a modifier of the cystic fibrosis phenotype in Argentinean pediatric patients. Journal of Cystic Fibrosis. 14(1). 78–83. 9 indexed citations
6.
Foncuberta, María Eugenia, et al.. (2014). Pharmacogenetic studies in children with acute lymphoblastic leukemia in Argentina. Leukemia & lymphoma. 56(5). 1370–1378. 22 indexed citations
7.
Giubergia, Verónica, et al.. (2013). Influence of β2-adrenergic receptor polymorphisms on asthma exacerbation in children with severe asthma regularly receiving salmeterol. Annals of Allergy Asthma & Immunology. 110(3). 156–160. 9 indexed citations
8.
Vaiani, Elisa, et al.. (2010). Thyroid axis dysfunction in patients with Prader‐Willi syndrome during the first 2 years of life. Clinical Endocrinology. 73(4). 546–550. 41 indexed citations
9.
Giubergia, Verónica, et al.. (2009). β2-Adrenergic polymorphisms and total serum IgE levels in children with asthma from Argentina. Annals of Allergy Asthma & Immunology. 102(4). 308–313. 7 indexed citations
10.
Giubergia, Verónica, et al.. (2008). Influence of β2‐adrenoceptor polymorphisms on the response to chronic use of albuterol in asthmatic children. Pediatric Pulmonology. 43(5). 421–425. 19 indexed citations
11.
Foncuberta, María Eugenia, et al.. (2007). Carrier frequency of the 35delG and A1555G deafness mutations in the Argentinean population. International Journal of Pediatric Otorhinolaryngology. 71(4). 639–643. 29 indexed citations
12.
Chertkoff, Lilien, et al.. (2006). A combination of five short tandem repeats of chromosome 15 significantly improves the identification of Prader-Willi syndrome etiology in the Argentinean population.. PubMed. 5(2). 390–8. 3 indexed citations
13.
Chertkoff, Lilien, et al.. (2006). Characterization of Alterations in Carbohydrate Metabolism in Children with Prader-Willi Syndrome. Journal of Pediatric Endocrinology and Metabolism. 19(7). 911–8. 27 indexed citations
14.
Fano, Virginia, et al.. (2005). High specificity of head circumference to recognize N540K mutation in hypochondroplasia. Annals of Human Biology. 32(6). 782–788. 8 indexed citations
15.
Bonaventure, Gustavo, et al.. (1998). Fragile X founder effects in Argentina. American Journal of Medical Genetics. 79(3). 200–204. 10 indexed citations
16.
Chertkoff, Lilien, et al.. (1997). Spectrum of CFTR mutations in Argentine cystic fibrosis patients. Clinical Genetics. 51(1). 43–47. 21 indexed citations
17.
Piñero, Mariana Herrera, Federico Augustovski, Lilien Chertkoff, et al.. (1994). Molecular characterization of HLA class II genes in celiac disease patients of Latin American caucasian origin. Tissue Antigens. 43(2). 83–87. 24 indexed citations
18.
Chertkoff, Lilien, Mariana Herrera Piñero, Leonardo Fainboim, & M. Leonardo Satz. (1991). Complete nucleotide sequence of a genomic clone encoding HLA-B35 isolated from a Caucasian individual of hispanic origin identification of a new variant of HLA-B35. Human Immunology. 31(3). 153–158. 23 indexed citations
19.
Piñero, Mariana Herrera, et al.. (1989). Restriction fragment length polymorphism in HLA class II genes of Latin-American caucasian celiac disease patients. Human Immunology. 26(4). 272–280. 30 indexed citations
20.
Chertkoff, Lilien, et al.. (1988). DNA polymorphism of the HLA-B35 gene associated to different HLA-C locus alleles. Human Immunology. 23(4). 241–253. 9 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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