Ali Entezam

1.6k total citations
17 papers, 1.2k citations indexed

About

Ali Entezam is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Ali Entezam has authored 17 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Plant Science. Recurrent topics in Ali Entezam's work include Genetics and Neurodevelopmental Disorders (9 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ali Entezam is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Ali Entezam collaborates with scholars based in United States, United Kingdom and South Africa. Ali Entezam's co-authors include Karen Usdin, Anthony V. Furano, Stéphane Boissinot, Daman Kumari, Gloria E. Hoffman, Erick Greene, Lata Mahishi, Robert L. Nussbaum, Jerel C. Davis and Tapas Saha and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Genome Research.

In The Last Decade

Ali Entezam

17 papers receiving 1.2k citations

Peers

Ali Entezam

GENET

CMN

Melissa Kramer United States

Ryan N. Doan United States

Alex Plocik United States

Michael Wittig Germany

Yingcong Zheng China

Toshiaki Hino Japan

Scott V. Dindot United States

Elissa D. Pastuzyn United States

Archana N. Raja United States

Chun‐Chieh Lin United States

Melissa Kramer United States

Ali Entezam

980 ×1.0

835 ×1.4

GENET

448 ×1.3

75 ×0.3

CMN

108 ×0.6

Citations per year, relative to Ali Entezam Ali Entezam (= 1×) peers Melissa Kramer

Countries citing papers authored by Ali Entezam

Since Specialization

Citations

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

Fields of papers citing papers by Ali Entezam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Entezam

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

All Works

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17 of 17 papers shown

Winder, Thomas, Christopher Tan, Hannah L. White, et al.. (2020). Clinical utility of multigene analysis in over 25,000 patients with neuromuscular disorders. Neurology Genetics. 6(2). e412–e412. 28 indexed citations

Truty, Rebecca, Nila Patil, Raman Sankar, et al.. (2019). Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy. Epilepsia Open. 4(3). 397–408. 72 indexed citations

Aradhya, Swaroop, Nila Patil, Rebecca Truty, et al.. (2017). Deep sequencing multi-gene panel analysis is a useful first-tier test with a high diagnostic yield and broad mutation spectrum detection in childhood epilepsy. Journal of the Neurological Sciences. 381. 85–85. 1 indexed citations

Lokanga, Rachel, Xiaoning Zhao, Ali Entezam, & Karen Usdin. (2014). X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion. Human Molecular Genetics. 23(18). 4985–4994. 26 indexed citations

Hoffman, Gloria E., Wei Wei Le, Ali Entezam, et al.. (2012). Ovarian Abnormalities in a Mouse Model of Fragile X Primary Ovarian Insufficiency. Journal of Histochemistry & Cytochemistry. 60(6). 439–456. 56 indexed citations

Lokanga, Rachel, Ali Entezam, Daman Kumari, et al.. (2012). Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles. Human Mutation. 34(1). 157–166. 63 indexed citations

Qin, Mei, Ali Entezam, Karen Usdin, et al.. (2011). A mouse model of the fragile X premutation: Effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. Neurobiology of Disease. 42(1). 85–98. 67 indexed citations

Entezam, Ali, et al.. (2010). Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model. Human Mutation. 31(5). n/a–n/a. 54 indexed citations

Entezam, Ali & Karen Usdin. (2009). ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice. Nucleic Acids Research. 37(19). 6371–6377. 32 indexed citations

10.

Godiska, Ronald, David A. Mead, Vinay K. Dhodda, et al.. (2009). Linear plasmid vector for cloning of repetitive or unstable sequences in Escherichia coli. Nucleic Acids Research. 38(6). e88–e88. 79 indexed citations

11.

Entezam, Ali, Bonnie M. Orrison, Tapas Saha, et al.. (2007). Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model. Gene. 395(1-2). 125–134. 148 indexed citations

12.

Greene, Erick, Lata Mahishi, Ali Entezam, Daman Kumari, & Karen Usdin. (2007). Repeat-induced epigenetic changes in intron 1 of the frataxin gene and its consequences in Friedreich ataxia. Nucleic Acids Research. 35(10). 3383–3390. 166 indexed citations

13.

Entezam, Ali & Karen Usdin. (2007). ATR protects the genome against CGG{middle dot}CCG-repeat expansion in Fragile X premutation mice. Nucleic Acids Research. 36(3). 1050–1056. 47 indexed citations

14.

Boissinot, Stéphane, et al.. (2006). Fitness cost of LINE-1 (L1) activity in humans. Proceedings of the National Academy of Sciences. 103(25). 9590–9594. 109 indexed citations

15.

Boissinot, Stéphane, Ali Entezam, Lynn Young, Peter J. Munson, & Anthony V. Furano. (2004). The Insertional History of an Active Family of L1 Retrotransposons in Humans. Genome Research. 14(7). 1221–1231. 85 indexed citations

16.

Greene, Eriko, Ali Entezam, Daman Kumari, & Karen Usdin. (2004). Ancient repeated DNA elements and the regulation of the human frataxin promoter. Genomics. 85(2). 221–230. 18 indexed citations

17.

Boissinot, Stéphane, Ali Entezam, & Anthony V. Furano. (2001). Selection Against Deleterious LINE-1-Containing Loci in the Human Lineage. Molecular Biology and Evolution. 18(6). 926–935. 145 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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