Estella S. Poloni

1.6k total citations
33 papers, 1.1k citations indexed

About

Estella S. Poloni is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, Estella S. Poloni has authored 33 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 11 papers in Molecular Biology and 5 papers in Pharmacology. Recurrent topics in Estella S. Poloni's work include Forensic and Genetic Research (14 papers), Genetic diversity and population structure (10 papers) and Epigenetics and DNA Methylation (6 papers). Estella S. Poloni is often cited by papers focused on Forensic and Genetic Research (14 papers), Genetic diversity and population structure (10 papers) and Epigenetics and DNA Methylation (6 papers). Estella S. Poloni collaborates with scholars based in Switzerland, France and Czechia. Estella S. Poloni's co-authors include Audrey Sabbagh, Pierre Darlu, Mathias Currat, Alicia Sanchez‐Mazas, Brigitte Crouau‐Roy, Laurent Excoffier, Ornella Semino, A. Langaney, André Langaney and A. Silvana Santachiara‐Benerecetti and has published in prestigious journals such as PLoS ONE, The Journal of Infectious Diseases and The American Journal of Human Genetics.

In The Last Decade

Estella S. Poloni

32 papers receiving 1.1k citations

Peers

Estella S. Poloni

GENET

ARCHE

PHARM

Denise Carvalho‐Silva United Kingdom

Badal Dey India

В. П. Пузырев Russia

Esther Esteban Spain

Ana María López‐Parra Spain

Rodrigo Rubí‐Castellanos Mexico

Burkhard Rolf Germany

Danai Tiwawech Thailand

Nourdin Harich Morocco

Nilmani Saha Singapore

Denise Carvalho‐Silva United Kingdom

Estella S. Poloni

667 ×1.1

GENET

488 ×1.7

76 ×0.4

ARCHE

29 ×0.2

PHARM

16 ×0.2

Citations per year, relative to Estella S. Poloni Estella S. Poloni (= 1×) peers Denise Carvalho‐Silva

Countries citing papers authored by Estella S. Poloni

Since Specialization

Citations

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

Fields of papers citing papers by Estella S. Poloni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Estella S. Poloni. 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 Estella S. Poloni. The network helps show where Estella S. Poloni may publish in the future.

Co-authorship network of co-authors of Estella S. Poloni

This figure shows the co-authorship network connecting the top 25 collaborators of Estella S. Poloni. A scholar is included among the top collaborators of Estella S. Poloni 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 Estella S. Poloni. Estella S. Poloni 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

Poloni, Estella S., et al.. (2022). From dietary adaptation in the past to drug metabolism of today: An example of NAT genes in the Croatian Roma. American Journal of Biological Anthropology. 178(1). 140–153.

Mouterde, Médéric, Youssef Daali, Victoria Rollason, et al.. (2022). Joint Analysis of Phenotypic and Genomic Diversity Sheds Light on the Evolution of Xenobiotic Metabolism in Humans. Genome Biology and Evolution. 14(12). 1 indexed citations

Gloor, Yvonne, Alain Matthey, Komla Sobo, et al.. (2022). Uncovering a Genetic Polymorphism Located in Huntingtin Associated Protein 1 in Modulation of Central Pain Sensitization Signaling Pathways. Frontiers in Neuroscience. 16. 807773–807773. 7 indexed citations

Mouterde, Médéric, et al.. (2021). Demographic history was a formative mechanism of the genetic structure for the taste receptor TAS2R16 in human populations inhabiting Africa's Sahel/Savannah Belt. American Journal of Biological Anthropology. 177(3). 540–555. 3 indexed citations

Vangenot, Christelle, José Manuel Nunes, Gaby M. Doxiadis, et al.. (2020). Similar patterns of genetic diversity and linkage disequilibrium in Western chimpanzees (Pan troglodytes verus) and humans indicate highly conserved mechanisms of MHC molecular evolution. BMC Evolutionary Biology. 20(1). 119–119. 3 indexed citations

Rollason, Victoria, Médéric Mouterde, Youssef Daali, et al.. (2020). Safety of the Geneva Cocktail, a Cytochrome P450 and P-Glycoprotein Phenotyping Cocktail, in Healthy Volunteers from Three Different Geographic Origins. Drug Safety. 43(11). 1181–1189. 12 indexed citations

Vicente, Mário, et al.. (2019). Population history and genetic adaptation of the Fulani nomads: inferences from genome-wide data and the lactase persistence trait. BMC Genomics. 20(1). 915–915. 37 indexed citations

Vangenot, Christelle, et al.. (2015). Variation in NAT2 acetylation phenotypes is associated with differences in food-producing subsistence modes and ecoregions in Africa. BMC Evolutionary Biology. 15(1). 263–263. 30 indexed citations

Dreslerová, Dagmar, et al.. (2014). The place of Slovakian paternal diversity in the clinal European landscape. Annals of Human Biology. 42(6). 511–522. 1 indexed citations

10.

Tréjaut, J., Estella S. Poloni, Ju-Chen Yen, et al.. (2014). Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia. BMC Genetics. 15(1). 77–77. 42 indexed citations

11.

Sabbagh, Audrey, Julie Marin, Charlotte Veyssière, et al.. (2013). Rapid birth-and-death evolution of the xenobiotic metabolizing NAT gene family in vertebrates with evidence of adaptive selection. BMC Evolutionary Biology. 13(1). 62–62. 31 indexed citations

12.

Silva, Nuno, Luı́sa Pereira, Estella S. Poloni, & Mathias Currat. (2012). Human Neutral Genetic Variation and Forensic STR Data. PLoS ONE. 7(11). e49666–e49666. 48 indexed citations

13.

Currat, Mathias, Estella S. Poloni, & Alicia Sanchez‐Mazas. (2010). Human genetic differentiation across the Strait of Gibraltar. BMC Evolutionary Biology. 10(1). 237–237. 49 indexed citations

14.

Sabbagh, Audrey, André Langaney, Pierre Darlu, et al.. (2008). Worldwide distribution of NAT2 diversity: Implications for NAT2 evolutionary history. BMC Genetics. 9(1). 21–21. 113 indexed citations

15.

Sabbagh, Audrey, et al.. (2007). Haplotype tagging efficiency and tagSNP sets portability in worldwide populations in NAT2 gene. Bulletins et Mémoires de la Société d anthropologie de Paris. 19(3-4). 233–241. 3 indexed citations

16.

Arredi, Barbara, Estella S. Poloni, Silvia Paracchini, et al.. (2004). A Predominantly Neolithic Origin for Y-Chromosomal DNA Variation in North Africa. The American Journal of Human Genetics. 75(2). 338–345. 155 indexed citations

17.

Poloni, Estella S., et al.. (2000). Maternal and paternal lineages in Albania and the genetic structure of Indo-European populations. European Journal of Human Genetics. 8(7). 480–486. 30 indexed citations

18.

Malaspina, Andrea, Letizia Mazzini, C. Camana, et al.. (1999). Heterogeneous distribution of amyotrophic lateral sclerosis patients with SOD-1 gene mutations: preliminary data on an Italian survey. Journal of the Neurological Sciences. 162(2). 201–204. 6 indexed citations

19.

Quintana‐Murci, Lluís, Ornella Semino, Estella S. Poloni, et al.. (1999). Y‐chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study. Annals of Human Genetics. 63(2). 153–166. 23 indexed citations

20.

Poloni, Estella S., Ornella Semino, Giuseppe Passarino, et al.. (1997). Human Genetic Affinities for Y-Chromosome P49a,f/TaqI Haplotypes Show Strong Correspondence with Linguistics. The American Journal of Human Genetics. 61(5). 1015–1035. 131 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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