D. Samolyk

1.0k total citations
14 papers, 579 citations indexed

About

D. Samolyk is a scholar working on Cellular and Molecular Neuroscience, Genetics and Molecular Biology. According to data from OpenAlex, D. Samolyk has authored 14 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 5 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in D. Samolyk's work include Genetics and Neurodevelopmental Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). D. Samolyk is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Metabolism and Genetic Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). D. Samolyk collaborates with scholars based in France, Tunisia and Morocco. D. Samolyk's co-authors include Jacques Mallet, A. Lamouroux, Nicole Faucon Biguet, Michel Buda, Claudine Laurent, Dominique Campion, María Martínez, Florence Thibaut, Alain Privat and Jean‐François Pujol and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

D. Samolyk

13 papers receiving 561 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D. Samolyk France	11	301	251	166	108	86	14	579
Alipi V. Naydenov United States	16	381 1.3×	260 1.0×	79 0.5×	148 1.4×	63 0.7×	18	751
Greer S. Kirshenbaum Canada	11	158 0.5×	291 1.2×	81 0.5×	112 1.0×	38 0.4×	14	494
Hélène Becq France	15	673 2.2×	406 1.6×	101 0.6×	125 1.2×	57 0.7×	17	910
Hitomi Takao Japan	9	161 0.5×	386 1.5×	218 1.3×	43 0.4×	46 0.5×	9	585
Alexandre Bacq France	10	179 0.6×	203 0.8×	130 0.8×	92 0.9×	47 0.5×	14	515
Sally Timm Denmark	11	120 0.4×	280 1.1×	106 0.6×	130 1.2×	48 0.6×	16	731
Yoshimi Iwayama‐Shigeno Japan	10	188 0.6×	400 1.6×	235 1.4×	70 0.6×	43 0.5×	10	622
Tamar Chachua United States	12	209 0.7×	130 0.5×	85 0.5×	177 1.6×	46 0.5×	19	412
Bruno Sterlini Italy	11	172 0.6×	208 0.8×	169 1.0×	200 1.9×	28 0.3×	24	521
Jesús Machado‐Salas Mexico	11	188 0.6×	137 0.5×	145 0.9×	223 2.1×	71 0.8×	15	547

Countries citing papers authored by D. Samolyk

Since Specialization

Citations

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

Fields of papers citing papers by D. Samolyk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Samolyk

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

All Works

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14 of 14 papers shown

Chaldée, Michel de, Claudine Laurent, Florence Thibaut, et al.. (1999). Linkage disequilibrium on the COMT gene in French schizophrenics and controls. American Journal of Medical Genetics. 88(5). 452–457. 7 indexed citations

Laurent, Claudine, Florence Thibaut, María Martínez, et al.. (1999). Linkage disequilibrium on theCOMT gene in French schizophrenics and controls. American Journal of Medical Genetics. 88(5). 452–457. 39 indexed citations

Laurent, Claudine, Cecilia Zander, Florence Thibaut, et al.. (1998). Anticipation in schizophrenia: No evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases. American Journal of Medical Genetics. 81(4). 342–346. 12 indexed citations

Zander, Cecilia, Claudine Laurent, Frank Bellivier, et al.. (1998). CAG repeat sequences in bipolar affective disorder: No evidence for association in a french population. American Journal of Medical Genetics. 81(4). 338–341. 33 indexed citations

Laurent, Claudine, Florence Thibaut, Philippe Ravassard, et al.. (1997). Detection of two new polymorphic sites in the human interleukin-1β gene. Psychiatric Genetics. 7(3). 103–106. 20 indexed citations

Zander, Cecilia, Florence Thibaut, María Martínez, et al.. (1996). Anticipation and CAG/CTG repeat expansion detection in schizophrenia. Psychiatric Genetics. 6(3). 154–154. 1 indexed citations

Meloni, Rolando, Claudine Laurent, Dominique Campion, et al.. (1995). A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients.. PubMed. 318(7). 803–9. 40 indexed citations

Laurent, Claudine, Dominique Campion, Thierry d’Amato, et al.. (1994). No major role for the dopamine D2 receptor Ser → Cys311 mutation in schizophrenia. Psychiatric Genetics. 4(4). 229–230. 32 indexed citations

Malafosse, Alain, Marion Leboyer, Olivier Dulac, et al.. (1992). Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20. Human Genetics. 89(1). 54–58. 66 indexed citations

10.

d’Amato, Thierry, Marion Leboyer, Alain Malafosse, et al.. (1989). Two TaqI dimorphk sites at the human β-hydroxylase locus. Nucleic Acids Research. 17(14). 5871–5871. 13 indexed citations

11.

Biguet, Nicole Faucon, Michel Buda, A. Lamouroux, D. Samolyk, & Jacques Mallet. (1986). Time course of the changes of TH mRNA in rat brain and adrenal medulla after a single injection of reserpine.. The EMBO Journal. 5(2). 287–291. 192 indexed citations

12.

Mallet, Jacques, Nicole Faucon Biguet, Michel Buda, A. Lamouroux, & D. Samolyk. (1983). Detection and Regulation of the Tyrosine Hydroxylase mRNA Levels in Rat Adrenal Medulla and Brain Tissues. Cold Spring Harbor Symposia on Quantitative Biology. 48(0). 305–308. 43 indexed citations

13.

Lamouroux, A., Nicole Faucon Biguet, D. Samolyk, et al.. (1982). Identification of cDNA clones coding for rat tyrosine hydroxylase antigen.. Proceedings of the National Academy of Sciences. 79(12). 3881–3885. 80 indexed citations

14.

Privat, Alain, et al.. (1981). [In vitro synthesis of tyrosine hydroxylase].. PubMed. 292(6). 455–60. 1 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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