Nicolas Borot

2.0k total citations · 1 hit paper
19 papers, 1.4k citations indexed

About

Nicolas Borot is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Nicolas Borot has authored 19 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Hematology, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Nicolas Borot's work include Iron Metabolism and Disorders (8 papers), Trace Elements in Health (5 papers) and Hemoglobinopathies and Related Disorders (5 papers). Nicolas Borot is often cited by papers focused on Iron Metabolism and Disorders (8 papers), Trace Elements in Health (5 papers) and Hemoglobinopathies and Related Disorders (5 papers). Nicolas Borot collaborates with scholars based in France, Germany and United States. Nicolas Borot's co-authors include Alain Hovnanian, Christine Lonjou, Maja Mockenhaupt, Martin Schumacher, Claudia de Toma, Laure Thomas, Marie‐Paule Roth, Hélène Coppin, Peggy Sekula and Jean‐Claude Roujeau and has published in prestigious journals such as The Journal of Immunology, Gastroenterology and Genetics.

In The Last Decade

Nicolas Borot

19 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs

2008 460 citations Christine Lonjou, Nicolas Borot et al. Pharmacogenetics and Genomics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicolas Borot France	15	715	391	374	271	231	19	1.4k
George Moxley United States	20	115 0.2×	507 1.3×	80 0.2×	91 0.3×	661 2.9×	37	1.5k
Jean‐Denis Franssen Italy	9	152 0.2×	86 0.2×	69 0.2×	80 0.3×	668 2.9×	10	1.5k
M. Lorini Italy	21	161 0.2×	748 1.9×	346 0.9×	20 0.1×	395 1.7×	80	1.4k
Nicole Pezous Switzerland	11	149 0.2×	243 0.6×	124 0.3×	174 0.6×	807 3.5×	20	1.5k
Ilan Goldberg Israel	18	104 0.1×	246 0.6×	336 0.9×	58 0.2×	99 0.4×	53	753
Ji‐Chen Ho Taiwan	15	176 0.2×	182 0.5×	194 0.5×	47 0.2×	276 1.2×	41	909
J.J. Twomey United States	18	44 0.1×	72 0.2×	156 0.4×	94 0.3×	502 2.2×	32	1.0k
María Isidoro‐García Spain	18	68 0.1×	61 0.2×	47 0.1×	87 0.3×	185 0.8×	90	1.1k
Keith M. Hull United States	14	114 0.2×	225 0.6×	54 0.1×	419 1.5×	808 3.5×	29	1.7k
William E. Pullman United States	13	29 0.0×	259 0.7×	195 0.5×	178 0.7×	201 0.9×	18	942

Countries citing papers authored by Nicolas Borot

Since Specialization

Citations

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

Fields of papers citing papers by Nicolas Borot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolas Borot

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

All Works

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19 of 19 papers shown

Lonjou, Christine, Nicolas Borot, Peggy Sekula, et al.. (2008). A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs. Pharmacogenetics and Genomics. 18(2). 99–107. 460 indexed citations breakdown →

Vitezica, Zulma G., et al.. (2008). HLA-DRB1 * 01 associated with cutaneous hypersensitivity induced by nevirapine and efavirenz. AIDS. 22(4). 540–541. 99 indexed citations

Lonjou, Christine, Laure Thomas, Nicolas Borot, et al.. (2006). A marker for Stevens-Johnson syndrome …: ethnicity matters. The Pharmacogenomics Journal. 6(4). 265–268. 294 indexed citations

Fruchon, Séverine, Mounia Bensaid, Nicolas Borot, Marie‐Paule Roth, & Hélène Coppin. (2003). Use of Denaturing HPLC and a Heteroduplex Generator to Detect the HFE C282Y Mutation Associated with Genetic Hemochromatosis. Clinical Chemistry. 49(5). 822–824. 3 indexed citations

Fruchon, Séverine, Mounia Bensaid, Nicolas Borot, et al.. (2002). Inactivation of the hemochromatosis gene differentially regulates duodenal expression of iron-related mRNAs between mouse strains. Gastroenterology. 122(3). 745–751. 88 indexed citations

Bauduer, Frédéric, et al.. (2001). Genetic hemochromatosis is a rare disease entity among French Basques: a center-based study from the General Hospital of Basque Country. Annals of Hematology. 80(8). 472–473. 8 indexed citations

Roth, Marie‐Paule, Maxence Delverdier, Nicolas Borot, et al.. (1999). A Genome-Wide Search Identifies Two Susceptibility Loci for Experimental Autoimmune Encephalomyelitis on Rat Chromosomes 4 and 10. The Journal of Immunology. 162(4). 1917–1922. 48 indexed citations

Totaro, Antonio, A. Grifa, Massimo Carella, et al.. (1997). Hereditary hemochromatosis: aHpal polymorphism within the HLA-H gene. Molecular and Cellular Probes. 11(3). 229–230. 14 indexed citations

Roth, M.P., et al.. (1997). Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex. Genomics. 43(2). 226–231. 57 indexed citations

10.

Borot, Nicolas, et al.. (1997). Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients. Immunogenetics. 45(5). 320–324. 114 indexed citations

11.

Coppin, Hélène, et al.. (1996). A new microsatellite marker at the RFP locus on chromosome 6p22 locates the haemochromatosis gene at least one megabase telomeric to HLA-A. Human Immunology. 47(1-2). 29–29. 1 indexed citations

12.

Roth, Marie‐Paule, Nicolas Borot, Claire Amadou, et al.. (1995). Three highly polymorphic microsatellites at the human myelin oligodendrocyte glycoprotein locus, 100 kb telomeric to HLA-F. Human Immunology. 43(4). 276–282. 30 indexed citations

13.

Roth, Marie‐Paule, et al.. (1995). Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG. Journal of Neuroimmunology. 61(2). 117–122. 21 indexed citations

14.

Coppin, Hélène, et al.. (1995). Polymorphic tri and tetranucleotide repeats in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene. Human Genetics. 96(6). 737–738. 15 indexed citations

15.

Roth, Marie‐Paule, et al.. (1995). The Human Myelin Oligodendrocyte Glycoprotein (MOG) Gene: Complete Nucleotide Sequence and Structural Characterization. Genomics. 28(2). 241–250. 29 indexed citations

16.

Thomsen, Mogens, M. Neugebauer, J. Arnaud, et al.. (1994). RECOMBINATION FRACTIONS IN THE HLA SYSTEM BASED ON THE DATA SET ‘PROVINCES FRANÇAISES’: INDICATIONS OF HAPLOTYPE‐SPECIFIC RECOMBINATION RATES. International Journal of Immunogenetics. 21(1). 33–43. 25 indexed citations

17.

Boretto, Joëlle, Anne‐Marie Jouanolle, Jacqueline Yaouanq, et al.. (1992). Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis. Human Genetics. 89(1). 33–36. 22 indexed citations

18.

Robinson, Wendy P., Anne Cambon‐Thomsen, Nicolas Borot, William Klitz, & G. Thomson. (1991). Selection, hitchhiking and disequilibrium analysis at three linked loci with application to HLA data.. Genetics. 129(3). 931–948. 24 indexed citations

19.

Borot, Nicolas, et al.. (1991). Phosphoglucomutase-1 Subtypes in Two Populations in Adriatic Islands: Presence of PGM1*W3 (PGM1*7+) Allele. Human Heredity. 41(5). 309–315. 6 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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