F. Marlhens

1.0k total citations
15 papers, 347 citations indexed

About

F. Marlhens is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, F. Marlhens has authored 15 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in F. Marlhens's work include Genomic variations and chromosomal abnormalities (4 papers), Retinal Development and Disorders (3 papers) and DNA and Nucleic Acid Chemistry (2 papers). F. Marlhens is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Retinal Development and Disorders (3 papers) and DNA and Nucleic Acid Chemistry (2 papers). F. Marlhens collaborates with scholars based in France and Netherlands. F. Marlhens's co-authors include Annie Nicole, Bernard Dutrillaux, Corinne Bareil, Jean‐Michel Griffoin, Bernard Arnaud, Mireille Claustres, Alain Aurias, Christian P. Hamel, Anne Bernard and J.‐C. Kaplan and has published in prestigious journals such as Nucleic Acids Research, Biochemical and Biophysical Research Communications and Human Mutation.

In The Last Decade

F. Marlhens

15 papers receiving 338 citations

Peers

F. Marlhens

GENET

OPHTH

Michol Crist United States

Arnold E. Cuenca United States

Victoria Pye Australia

Sandrine Siffroi‐Fernandez France

Kathryn Louie United States

Naseebullah Kakar Pakistan

P Eversole-Cire United States

Shorafidinkhuja Dadakhujaev South Korea

Wataru Otsu Japan

Karen E. Roth United States

Michol Crist United States

F. Marlhens

160 ×0.6

98 ×1.1

GENET

41 ×0.8

OPHTH

13 ×0.3

15 ×0.4

Citations per year, relative to F. Marlhens F. Marlhens (= 1×) peers Michol Crist

Countries citing papers authored by F. Marlhens

Since Specialization

Citations

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

Fields of papers citing papers by F. Marlhens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Marlhens

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

All Works

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15 of 15 papers shown

Griffoin, Jean‐Michel, Corinne Bareil, Sarah Bonnet, et al.. (2000). [Molecular genetics of pigmentary retinopathies: identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes].. Journal Français d Ophtalmologie. 23(10). 985–95. 18 indexed citations

Marlhens, F., et al.. (1999). X-linked retinoschisis with a novel substitutive amino acid (P193S) in XLRS1. Human Mutation. 13(3). 259–259. 1 indexed citations

Marlhens, F., Jean‐Michel Griffoin, Corinne Bareil, et al.. (1998). Autosomal recessive retinal dystrophy associated with two novel mutations in the RPE65 gene. European Journal of Human Genetics. 6(5). 527–531. 53 indexed citations

Marlhens, F., et al.. (1998). Des mutations de gènes contrôlant le métabolisme des rétinoïdes 11-cis responsables de dystrophies rétiniennes sévères.. médecine/sciences. 14(6-7). 754–754. 3 indexed citations

Delattre, Olivier, Anne Bernard, Bernard Malfoy, et al.. (1988). Studies on the Human Chromosome 3 Centromere with a Newly Cloned Alphoid DNA Probe. Human Heredity. 38(3). 156–167. 14 indexed citations

Chelly, Jamel, F. Marlhens, Bernard Dutrillaux, et al.. (1988). Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia. Human Genetics. 78(3). 222–227. 15 indexed citations

Marlhens, F., Claude Saint‐Ruf, Christian Lavialle, et al.. (1988). Karyotype evolution of the human HBL-100 cell line and mapping of the integration site of SV40 DNA.. PubMed. 31(2). 81–6. 8 indexed citations

Marlhens, F., Jamel Chelly, J.‐C. Kaplan, et al.. (1987). Familial deletion of Xp21.2 with glycerol kinase deficiency and congenital adrenal hypoplasia. Human Genetics. 77(4). 379–383. 12 indexed citations

Marlhens, F., Olivier Delattre, Anne Bernard, et al.. (1987). RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM do. D18S8). Nucleic Acids Research. 15(3). 1348–1348. 20 indexed citations

10.

Delattre, Olivier, et al.. (1987). RFLP identified by the anonymous DNA segment OL VII A8 at 18q11 (HGM8 do. D18S7). Nucleic Acids Research. 15(3). 1343–1343. 13 indexed citations

11.

Delattre, Olivier, Anne Bernard, Bernard Malfoy, et al.. (1987). Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3.. PubMed. 15(20). 8561–8561. 8 indexed citations

12.

Huret, J. L., Jean‐Maurice Delabar, F. Marlhens, et al.. (1987). Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality. Human Genetics. 75(3). 251–257. 44 indexed citations

13.

Chelly, Jamel, F. Marlhens, B. Le Marec, et al.. (1986). De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy. Human Genetics. 74(2). 193–196. 35 indexed citations

14.

Marlhens, F., Walid Al Achkar, Alain Aurias, et al.. (1986). The rate of chromosome breakage is age dependent in lymphocytes of adult controls. Human Genetics. 73(4). 290–297. 62 indexed citations

15.

Marlhens, F., et al.. (1985). Lowered level of translatable messenger RNAs for manganese superoxide dismutase in human fibroblasts transformed by SV 40. Biochemical and Biophysical Research Communications. 129(1). 300–305. 41 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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