M.-F. de Tand

454 total citations
10 papers, 346 citations indexed

About

M.-F. de Tand is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, M.-F. de Tand has authored 10 papers receiving a total of 346 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Immunology. Recurrent topics in M.-F. de Tand's work include CRISPR and Genetic Engineering (2 papers), Chromosomal and Genetic Variations (2 papers) and Pancreatic function and diabetes (2 papers). M.-F. de Tand is often cited by papers focused on CRISPR and Genetic Engineering (2 papers), Chromosomal and Genetic Variations (2 papers) and Pancreatic function and diabetes (2 papers). M.-F. de Tand collaborates with scholars based in France and United States. M.-F. de Tand's co-authors include J Frézal, Odile Cohen‐Haguenauer, N. Van Cong, Marie‐Geneviève Mattéi, Daniel Guerrier, Stéphane Serero, Nathalie Josso, M. C. Hors‐Cayla, Jean‐Yves Picard and Marie‐Sylvie Gross and has published in prestigious journals such as Nature Genetics, Human Genetics and Cytogenetic and Genome Research.

In The Last Decade

M.-F. de Tand

10 papers receiving 331 citations

Peers

M.-F. de Tand

MB

GENET

RM

PHEOH

IMMUN

Renée Bernstein South Africa

Chris Bennett United Kingdom

Th. Hecht Germany

Miyuri Kawasumi Japan

Guus Hamers Netherlands

Paolo Guanciali‐Franchi Italy

Keqin Zheng Canada

Hisayo Nishida‐Fukuda Japan

J. P. M. Geraedts Netherlands

G. Bourrouillou France

Renée Bernstein South Africa

M.-F. de Tand

241 ×1.2

MB

195 ×1.5

GENET

27 ×0.4

RM

62 ×1.1

PHEOH

22 ×0.5

IMMUN

Citations per year, relative to M.-F. de Tand M.-F. de Tand (= 1×) peers Renée Bernstein

Countries citing papers authored by M.-F. de Tand

Since Specialization

Citations

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

Fields of papers citing papers by M.-F. de Tand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.-F. de Tand. 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 M.-F. de Tand. The network helps show where M.-F. de Tand may publish in the future.

Co-authorship network of co-authors of M.-F. de Tand

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

All Works

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10 of 10 papers shown

1.

Chumakov, Ilya, I Le Gall, Alain Billault, et al.. (1992). Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library. Nature Genetics. 1(3). 222–225. 70 indexed citations

2.

J, Jos, Daniel L. Farkas, M.-F. de Tand, et al.. (1991). DNA polymorphism analysis of HLA class II genes in unrelated children and in first-degree relatives with type I diabetes.. PubMed. 18(2). 53–9. 5 indexed citations

3.

Cong, N. Van, Ray D, Marie‐Sylvie Gross, et al.. (1990). Localization of the human oncogene SPI1 on chromosome 11, region p11.22. Human Genetics. 84(6). 542–546. 21 indexed citations

4.

Fichelson, Serge, Mitchell Gross, Brigitte Sola, et al.. (1989). The human homologues of Fim1, Fim2/c-Fms, and Fim3, three retroviral integration regions involved in mouse myeloblastic leukemias, are respectively located on chromosomes 6p23, 5q33, and 3q27. Human Genetics. 81(3). 257–263. 24 indexed citations

5.

Cohen‐Haguenauer, Odile, Paul J.R. Barton, Andrés Buonanno, et al.. (1989). Localization of the acetylcholine receptor γ subunit gene to human chromosome 2q32→qter. Cytogenetic and Genome Research. 52(3-4). 124–127. 15 indexed citations

6.

Cohen‐Haguenauer, Odile, N. Van Cong, Robert G. Knowlton, et al.. (1989). Chromosomal assignment of 14 genomic probes for highly polymorphic loci. Cytogenetic and Genome Research. 50(2-3). 78–83. 2 indexed citations

7.

Serero, Stéphane, Pascal Maire, N. Van Cong, et al.. (1988). Localization of the active gene of aldolase on chromosome 16, and two aldolase A pseudogenes on chromosomes 3 and 10. Human Genetics. 78(2). 167–174. 6 indexed citations

8.

Tosi, Mario, Marie‐Sylvie Gross, Odile Cohen‐Haguenauer, et al.. (1988). Assignment of the complement serine protease genes C1r and C1s to chromosome 12 region 12p13. Human Genetics. 78(4). 363–368. 32 indexed citations

9.

Cohen‐Haguenauer, Odile, Jean‐Yves Picard, Marie‐Geneviève Mattéi, et al.. (1987). Mapping of the gene for anti-Müllerian hormone to the short arm of human chromosome 19. Cytogenetic and Genome Research. 44(1). 2–6. 146 indexed citations

10.

Cong, N. Van, Dominique Weil, C. Finaz, et al.. (1986). Panel of twenty-five independent man-rodent hybrids for human genetic marker mapping.. PubMed. 29(1). 20–6. 25 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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