Fabienne Parente

578 total citations
12 papers, 174 citations indexed

About

Fabienne Parente is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Fabienne Parente has authored 12 papers receiving a total of 174 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Fabienne Parente's work include Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Fabienne Parente is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Fabienne Parente collaborates with scholars based in France, Canada and United States. Fabienne Parente's co-authors include Claude Turc‐Carel, Jean‐Michel Coindre, Nicholas Ah Mew, Jaak Jaeken, Philippe Terrier, Josiane Grosgeorge, Brian M. Gilfix, Georges F. Carle, Patrick Gaudray and Laura Russell and has published in prestigious journals such as Journal of Biological Chemistry, Clinica Chimica Acta and Journal of Medical Genetics.

In The Last Decade

Fabienne Parente

12 papers receiving 173 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fabienne Parente France	8	76	60	39	29	20	12	174
Rosaria Polci Italy	7	152 2.0×	22 0.4×	32 0.8×	15 0.5×	22 1.1×	14	228
Nazanin Kabgani Germany	6	115 1.5×	23 0.4×	22 0.6×	25 0.9×	16 0.8×	8	315
Gaia Roversi Italy	10	112 1.5×	54 0.9×	19 0.5×	33 1.1×	16 0.8×	26	225
Adam C. Gunning United Kingdom	7	179 2.4×	151 2.5×	14 0.4×	36 1.2×	27 1.4×	12	291
Lynette S. Penney Canada	7	143 1.9×	112 1.9×	45 1.2×	22 0.8×	12 0.6×	13	273
Jessica J. Y. Lee Canada	5	102 1.3×	52 0.9×	16 0.4×	44 1.5×	33 1.6×	7	205
Patroula Smpokou United States	9	195 2.6×	29 0.5×	18 0.5×	6 0.2×	9 0.5×	12	279
Noelia Lozano‐Vidal Netherlands	5	85 1.1×	74 1.2×	89 2.3×	65 2.2×	5 0.3×	7	226
Karen Ouyang United States	7	113 1.5×	143 2.4×	35 0.9×	54 1.9×	36 1.8×	17	244

Countries citing papers authored by Fabienne Parente

Since Specialization

Citations

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

Fields of papers citing papers by Fabienne Parente

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabienne Parente

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

All Works

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12 of 12 papers shown

Demaret, Tanguy, et al.. (2024). Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis. Molecular Genetics and Metabolism Reports. 39. 101073–101073. 1 indexed citations

Wiedemann, Arnaud, et al.. (2024). Hyperosmolarity in children with hyperammonemia: a risk of brain herniation at the start of renal replacement therapy. Frontiers in Pediatrics. 12. 1431008–1431008. 1 indexed citations

Zhao, Chen, Youlin Wang, Hao Yang, et al.. (2021). Propionic acidemia in mice: Liver acyl-CoA levels and clinical course. Molecular Genetics and Metabolism. 135(1). 47–55. 9 indexed citations

Accogli, Andrea, et al.. (2018). Diagnostic Yield of Intellectual Disability Gene Panels. Pediatric Neurology. 92. 32–36. 22 indexed citations

Parente, Fabienne, et al.. (2016). An unusual cause of Achilles tendon xanthoma. Journal of clinical lipidology. 10(4). 1040–1044. 7 indexed citations

Briand, Gilbert, Stéphanie Lemaire‐Ewing, Fabienne Parente, & Roselyne Garnotel. (2015). Mass spectrometry and inherited metabolic diseases diagnosis. Annales de biologie clinique. 73(1). 93–106. 2 indexed citations

Ye, Maoqing, Fabienne Parente, Xiaodong Li, et al.. (2014). Gene‐targeted deletion of OPCML and Neurotrimin in mice does not yield congenital heart defects. American Journal of Medical Genetics Part A. 164(4). 966–974. 9 indexed citations

Parente, Fabienne, Nicholas Ah Mew, Jaak Jaeken, & Brian M. Gilfix. (2009). A new Capillary Zone Electrophoresis method for the screening of Congenital Disorders of Glycosylation (CDG). Clinica Chimica Acta. 411(1-2). 64–66. 32 indexed citations

Tvrdík, Petr, Abolfazl Asadi, Leslie P. Kozak, et al.. (1999). Cig30 and Pitx3 Genes Are Arranged in a Partially Overlapping Tail-to-Tail Array Resulting in Complementary Transcripts. Journal of Biological Chemistry. 274(37). 26387–26392. 10 indexed citations

10.

Parente, Fabienne, et al.. (1999). Comparative Genomic Hybridization Reveals Novel Chromosome Deletions in 90 Primary Soft Tissue Tumors. Cancer Genetics and Cytogenetics. 115(2). 89–95. 45 indexed citations

11.

Parente, Fabienne, Patrick Gaudray, Georges F. Carle, & Claude Turc‐Carel. (1997). Experimental assessment of the detection limit of genomic amplification by comparative genomic hybridization CGH. Cytogenetic and Genome Research. 78(1). 65–68. 29 indexed citations

12.

Mignon, C., Fabienne Parente, Patrick Collignon, et al.. (1997). Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.. Journal of Medical Genetics. 34(3). 217–222. 7 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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