Fatima Abidi

3.9k total citations
40 papers, 1.6k citations indexed

About

Fatima Abidi is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Fatima Abidi has authored 40 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 21 papers in Genetics and 7 papers in Plant Science. Recurrent topics in Fatima Abidi's work include Genetics and Neurodevelopmental Disorders (21 papers), Chromatin Remodeling and Cancer (5 papers) and Ubiquitin and proteasome pathways (5 papers). Fatima Abidi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (21 papers), Chromatin Remodeling and Cancer (5 papers) and Ubiquitin and proteasome pathways (5 papers). Fatima Abidi collaborates with scholars based in United States, France and Canada. Fatima Abidi's co-authors include Charles E. Schwartz, Roger E. Stevenson, David James Young, Albert S. Baldwin, Mark Griffiths, David Schlessinger, Herbert A. Lubs, Randall D. Little, Morimasa Wada and Elizabeth J. Keath and has published in prestigious journals such as Journal of Biological Chemistry, JNCI Journal of the National Cancer Institute and Analytical Biochemistry.

In The Last Decade

Fatima Abidi

40 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatima Abidi United States 21 1.0k 649 269 161 153 40 1.6k
H Sakura Japan 22 1.5k 1.4× 326 0.5× 56 0.2× 138 0.9× 56 0.4× 32 2.2k
John Brennand United Kingdom 20 1.5k 1.4× 431 0.7× 27 0.1× 105 0.7× 84 0.5× 38 2.1k
Cornelis Van Dop United States 24 1.7k 1.7× 492 0.8× 81 0.3× 152 0.9× 29 0.2× 55 2.6k
Daniel J. Sillence United Kingdom 19 1.3k 1.2× 164 0.3× 479 1.8× 77 0.5× 46 0.3× 35 2.3k
Elena Vicini Italy 25 1.2k 1.2× 356 0.5× 55 0.2× 92 0.6× 26 0.2× 43 2.0k
Philipp Oberdoerffer United States 21 2.4k 2.3× 318 0.5× 119 0.4× 398 2.5× 181 1.2× 31 3.3k
Hideto Yonekura Japan 17 506 0.5× 152 0.2× 814 3.0× 209 1.3× 24 0.2× 28 1.5k
Béatrice Conne Switzerland 20 921 0.9× 409 0.6× 32 0.1× 95 0.6× 42 0.3× 30 1.9k
Stefanie Weinert Germany 14 883 0.9× 241 0.4× 109 0.4× 55 0.3× 29 0.2× 18 1.3k
Koji Nata Japan 28 781 0.8× 327 0.5× 1.3k 5.0× 377 2.3× 32 0.2× 52 2.6k

Countries citing papers authored by Fatima Abidi

Since Specialization
Citations

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

Fields of papers citing papers by Fatima Abidi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatima Abidi

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

All Works

20 of 20 papers shown
1.
Homan, Claire C., Raman Kumar, Lam Son Nguyen, et al.. (2014). Mutations in USP9X Are Associated with X-Linked Intellectual Disability and Disrupt Neuronal Cell Migration and Growth. The American Journal of Human Genetics. 94(3). 470–478. 100 indexed citations
2.
Grafodatskaya, Daria, Darci T. Butcher, Andrei L. Turinsky, et al.. (2013). Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C. BMC Medical Genomics. 6(1). 1–1. 68 indexed citations
3.
Marco, Elysa J., Fatima Abidi, James Bristow, et al.. (2009). ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal. BMJ Case Reports. 2009. bcr0620091999–bcr0620091999. 5 indexed citations
4.
Abidi, Fatima, David D. Weaver, Richard J. Simensen, et al.. (2008). Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia. Journal of Medical Genetics. 45(12). 787–793. 76 indexed citations
5.
Kesler, Shelli R., Richard J. Simensen, Kytja K. S. Voeller, et al.. (2007). Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin–Lowry syndrome. Neurogenetics. 8(2). 143–147. 23 indexed citations
6.
Zhang, Lilei, Chunfa Jie, Cassandra Obie, et al.. (2007). X chromosome cDNA microarray screening identifies a functional PLP2 promoter polymorphism enriched in patients with X-linked mental retardation. Genome Research. 17(5). 641–648. 13 indexed citations
7.
Ramser, Juliane, Fatima Abidi, Céline Burcklé, et al.. (2005). A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Human Molecular Genetics. 14(8). 1019–1027. 146 indexed citations
8.
Abidi, Fatima, Carlos Cardoso, Anne-Marie Lossi, et al.. (2004). Mutation in the 5′ alternatively spliced region of the XNP/ATR-X gene causes Chudley–Lowry syndrome. European Journal of Human Genetics. 13(2). 176–183. 37 indexed citations
9.
Winnepenninckx, Birgitta, Edwin Reyniers, Peter Paul De Deyn, et al.. (2002). Family MRX9 revisited: Further evidence for locus heterogeneity in MRX. American Journal of Medical Genetics. 112(1). 17–22. 2 indexed citations
10.
Abidi, Fatima, et al.. (2002). Cognitive function in Coffin–Lowry syndrome. Clinical Genetics. 61(4). 299–304. 14 indexed citations
11.
Sundaram, Manickavasagam, Sylvia Y.M. Yao, Jean C. Ingram, et al.. (2001). Topology of a Human Equilibrative, Nitrobenzylthioinosine (NBMPR)-sensitive Nucleoside Transporter (hENT1) Implicated in the Cellular Uptake of Adenosine and Anti-cancer Drugs. Journal of Biological Chemistry. 276(48). 45270–45275. 113 indexed citations
12.
Lubs, Herbert A., Fatima Abidi, Jo‐Ann Blaymore Bier, et al.. (1999). XLMR syndrome characterized by multiple respiratory infections, hypertelorism, severe CNS deterioration and early death localizes to distal Xq28. American Journal of Medical Genetics. 85(3). 243–248. 54 indexed citations
13.
Sossey‐Alaoui, Khalid, Jennifer A. Lyon, Fatima Abidi, et al.. (1999). Molecular Cloning and Characterization of TRPC5 (HTRP5), the Human Homologue of a Mouse Brain Receptor-Activated Capacitative Ca2+ Entry Channel. Genomics. 60(3). 330–340. 61 indexed citations
14.
Abidi, Fatima, Bryan D. Hall, Ronald G. Cadle, et al.. (1999). X-linked mental retardation with variable stature, head circumference, and testicular volume linked to Xq12-q21. American Journal of Medical Genetics. 85(3). 223–229. 13 indexed citations
15.
Abidi, Fatima, et al.. (1997). Involvement of the GLUT 3 transporter in myogenic regulation. IUBMB Life. 43(4). 847–866. 3 indexed citations
16.
Keath, Elizabeth J. & Fatima Abidi. (1994). Molecular cloning and sequence analysis of yps-3, a yeast-phase-specific gene in the dimorphic fungal pathogen Histoplasma capsulatum. Microbiology. 140(4). 759–767. 34 indexed citations
17.
Palmieri, Giuseppe, Giovanna Romano, Amelia Casamassimi, et al.. (1993). 1.5-Mb YAC Contig in Xq28 Formatted with Sequence-Tagged Sites and Including a Region Unstable in the Clones. Genomics. 16(3). 586–592. 12 indexed citations
18.
Schlessinger, David, Diha Freije, Fatima Abidi, et al.. (1991). Yeast artificial chromosome-based genome mapping: Some lessons from Xq24–q28. Genomics. 11(4). 783–793. 58 indexed citations
19.
D’Urso, Michele, Ileana Zucchi, Alfredo Ciccodicola, et al.. (1990). Human glucose-6-phosphate dehydrogenase gene carried on a yeast artificial chromosome encodes active enzyme in monkey cells. Genomics. 7(4). 531–534. 33 indexed citations
20.
Abidi, Fatima, Subal Bishayee, Bimal K. Bachhawat, & Ranjan Bhadra. (1987). Lectin-binding assay by polyethylene glycol 8000. Analytical Biochemistry. 166(2). 257–266. 6 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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