L Rivat

1.1k total citations
86 papers, 920 citations indexed

About

L Rivat is a scholar working on Hematology, Immunology and Molecular Biology. According to data from OpenAlex, L Rivat has authored 86 papers receiving a total of 920 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Hematology, 27 papers in Immunology and 18 papers in Molecular Biology. Recurrent topics in L Rivat's work include Blood groups and transfusion (26 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Monoclonal and Polyclonal Antibodies Research (15 papers). L Rivat is often cited by papers focused on Blood groups and transfusion (26 papers), Immunodeficiency and Autoimmune Disorders (17 papers) and Monoclonal and Polyclonal Antibodies Research (15 papers). L Rivat collaborates with scholars based in France, Switzerland and Netherlands. L Rivat's co-authors include C Ropartz, C. Rivat, J. Lenoir, Marie‐Paule Lefranc, Maryvonne Daveau, Jacques Loiselet, Erna van Loghem, Danièle Gilbert, Philippe Burtin and Gerda de Lange and has published in prestigious journals such as Nature, JNCI Journal of the National Cancer Institute and The American Journal of Medicine.

In The Last Decade

L Rivat

80 papers receiving 763 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L Rivat France	17	353	318	311	292	180	86	920
C Ropartz France	22	403 1.1×	455 1.4×	367 1.2×	436 1.5×	251 1.4×	157	1.4k
L Amante Italy	6	418 1.2×	72 0.2×	229 0.7×	258 0.9×	67 0.4×	14	771
L. Mårtensson Sweden	13	153 0.4×	183 0.6×	189 0.6×	175 0.6×	74 0.4×	22	475
Andrew G. Hadley United Kingdom	20	300 0.8×	573 1.8×	362 1.2×	270 0.9×	215 1.2×	42	962
Delta E. Uphoff United States	14	281 0.8×	373 1.2×	182 0.6×	204 0.7×	154 0.9×	40	1.1k
J. Folkersen Denmark	16	190 0.5×	188 0.6×	104 0.3×	283 1.0×	64 0.4×	44	845
Vincent Yakulis United States	18	184 0.5×	261 0.8×	153 0.5×	213 0.7×	54 0.3×	44	702
Henri Isliker Switzerland	11	222 0.6×	154 0.5×	160 0.5×	142 0.5×	29 0.2×	23	501
C. R. Barker United Kingdom	19	506 1.4×	142 0.4×	236 0.8×	318 1.1×	83 0.5×	39	1.1k
M Jokinen Finland	12	198 0.6×	351 1.1×	124 0.4×	613 2.1×	107 0.6×	16	1.1k

Countries citing papers authored by L Rivat

Since Specialization

Citations

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

Fields of papers citing papers by L Rivat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L Rivat

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Daveau, Maryvonne, et al.. (1980). Frequencies of Gm and Km Allotypes in the Population of Singapore, Sri Lanka and Punjabis in North India. Human Heredity. 30(4). 237–244. 6 indexed citations

2.

Youinou, Pierre, et al.. (1979). Familial occurrence of monoclonal gammapathies.. PubMed. 28(4). 226–32. 21 indexed citations

3.

Daveau, Maryvonne, et al.. (1978). Immunoglobulin Gm and Km Genetic Markers in Vietnamese. Human Heredity. 28(6). 435–444. 1 indexed citations

4.

Lefranc, Marie‐Paule, L Rivat, J.P. Salier, et al.. (1977). Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemia.. PubMed. 29(5). 523–36. 21 indexed citations

5.

Daveau, Maryvonne, et al.. (1975). Gm and Inv Allotypes in French Guiana Indians. Human Heredity. 25(2). 88–92. 15 indexed citations

6.

Rivat, L, et al.. (1972). Ten Gm Factors and the Inv System in Eskimos in Greenland. Human Heredity. 22(5-6). 519–528. 2 indexed citations

7.

Ropartz, C, et al.. (1972). Frequency of Gm, Inv and ISf Phenotypes in the Population of 4 Yugoslavian Villages. Human Heredity. 22(5-6). 508–518. 10 indexed citations

8.

Ropartz, C, et al.. (1970). Maladie de Kahler familiale. Etude immunologique et caryotypique d'une observation.. La Presse Médicale. 78(40). 5 indexed citations

9.

Steinberg, Arthur G., Alison M. Muir, L Rivat, & C Ropartz. (1970). A pedigree demonstrating the transmission of a Gm2,8,21 phenogroup.. PubMed. 22(4). 378–83. 2 indexed citations

10.

Lebreton, J. P., C. Rivat, L Rivat, & C Ropartz. (1968). Les protéinuries des immunoglobulinopathies. PubMed. 11(4). 331–348. 1 indexed citations

11.

Rivat, C., et al.. (1967). Une immunoglobulinopathie méconnue: la maladie des chaines lourdes.. La Presse Médicale. 75(45). 13 indexed citations

12.

Ropartz, C, et al.. (1966). Seven new Human Serum Factors Presumably Supported by the Gamma‐Globulins*. Vox Sanguinis. 11(1). 99–102. 8 indexed citations

13.

Ropartz, C, et al.. (1965). The Influence of the Anti‐Rh Coat and Red Cells on the Manifestation of the Gm(b) Phenotype. Vox Sanguinis. 10(5). 583–589. 6 indexed citations

14.

Loghem, Erna van, et al.. (1965). Two Families with Gm(b) Types Lacking Part of the Gm(b) Mosaic. Vox Sanguinis. 10(5). 572–582. 4 indexed citations

15.

Ropartz, C, et al.. (1964). On the Frequency of the Gm- and Inv-Serum Groups in South-Western Germany. Human Heredity. 14(3-4). 298–308. 8 indexed citations

16.

Ritter, H., et al.. (1964). [ON THE MORPHOLOGY AND GENETICS OF GM POLYMORPHISM OF GAMMA GLOBULINS (CHARACTERISTICS OF GM(A), GM(B), GM(E); STUDY ON 387 FAMILIES].. PubMed. 14. 4–14. 1 indexed citations

17.

Ropartz, C, et al.. (1964). [2 NEW FACTORS IN THE HEREDITARY GAMMA GLOBULIN SYSTEMS: GM(E) AND INV(I)].. PubMed. 19. 455–8. 3 indexed citations

18.

Ritter, H., et al.. (1964). Studies on the Formal Genetics of the Gammaglobulin Polymorphism Gm (Characters Gm[a], Gm[b], Gm[x]). Vox Sanguinis. 9(3). 340–348. 5 indexed citations

19.

Ropartz, C, et al.. (1963). [THE GM AND INV SYSTEMS IN EUROPE].. PubMed. 13. 109–23. 16 indexed citations

20.

Ropartz, C, et al.. (1962). Un deuxième exemple du Phénotype Gm(a‐ x+) pouvant confirmer l'hypothèse de l'existence d'un alléle Gm^bx. Vox Sanguinis. 7(3). 375–378. 13 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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