Mehdi Keddache

3.2k total citations
43 papers, 1.6k citations indexed

About

Mehdi Keddache is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Mehdi Keddache has authored 43 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Physiology. Recurrent topics in Mehdi Keddache's work include Epilepsy research and treatment (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Lysosomal Storage Disorders Research (4 papers). Mehdi Keddache is often cited by papers focused on Epilepsy research and treatment (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Lysosomal Storage Disorders Research (4 papers). Mehdi Keddache collaborates with scholars based in United States, Germany and Belgium. Mehdi Keddache's co-authors include Lisa J. Martin, David A. Greenberg, Gregory A. Grabowski, Cynthia A. Molloy, Terry F. Davies, Meredith E. Tabangin, Tracy A. Glauser, Giuseppe Barbesino, D. Woodrow Benson and Linda Cripe and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The Journal of Immunology.

In The Last Decade

Mehdi Keddache

41 papers receiving 1.6k citations

Peers

Mehdi Keddache

GENET

PMH

EPIDE

Zühal Yapıcı Türkiye

Laura Bernardini Italy

Julie Evans United Kingdom

Jillian S. Parboosingh Canada

Jac Charlesworth Australia

Junko Nakayama Japan

Michael C. Kruer United States

Jean‐Louis Blouin Switzerland

Byung Chan Lim South Korea

Guntram Borck Germany

Zühal Yapıcı Türkiye

Mehdi Keddache

442 ×0.7

GENET

523 ×1.0

318 ×1.3

PMH

159 ×0.7

EPIDE

119 ×0.6

Citations per year, relative to Mehdi Keddache Mehdi Keddache (= 1×) peers Zühal Yapıcı

Countries citing papers authored by Mehdi Keddache

Since Specialization

Citations

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

Fields of papers citing papers by Mehdi Keddache

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mehdi Keddache

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

All Works

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20 of 20 papers shown

Goswami, Chirayu, Michael Sheldon, Mehdi Keddache, et al.. (2022). Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program. BMC Infectious Diseases. 22(1). 404–404. 23 indexed citations

Dasgupta, Nupur, Yongping Xu, Ronghua Li, et al.. (2015). Neuronopathic Gaucher disease: dysregulated mRNAs and miRNAs in brain pathogenesis and effects of pharmacologic chaperone treatment in a mouse model. Human Molecular Genetics. 24(24). ddv404–ddv404. 42 indexed citations

Trexler, Ryan V., Caroline Solomon, Colin Brislawn, et al.. (2014). Assessing impacts of unconventional natural gas extraction on microbial communities in headwater stream ecosystems in Northwestern Pennsylvania. Frontiers in Microbiology. 5. 522–522. 37 indexed citations

Namjou, Bahram, Mehdi Keddache, Keith Marsolo, et al.. (2013). EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Frontiers in Genetics. 4. 268–268. 39 indexed citations

Dasgupta, Nupur, Yongping Xu, Sunghee Oh, et al.. (2013). Gaucher Disease: Transcriptome Analyses Using Microarray or mRNA Sequencing in a Gba1 Mutant Mouse Model Treated with Velaglucerase alfa or Imiglucerase. PLoS ONE. 8(10). e74912–e74912. 15 indexed citations

Kottyan, Leah C., Jessica G. Woo, Mehdi Keddache, et al.. (2012). Novel variations in the adiponectin gene (ADIPOQ) may affect distribution of oligomeric complexes. SpringerPlus. 1(1). 66–66. 5 indexed citations

Dwork, Andrew J., et al.. (2012). Serotonin 2c receptor RNA editing in major depression and suicide. The World Journal of Biological Psychiatry. 14(8). 590–601. 47 indexed citations

Morrow, Ardythe L., Jareen Meinzen‐Derr, Pengwei Huang, et al.. (2011). Fucosyltransferase 2 Non-Secretor and Low Secretor Status Predicts Severe Outcomes in Premature Infants. The Journal of Pediatrics. 158(5). 745–751. 94 indexed citations

Sheridan, Rachel, Kristin Lampe, Shiva Kumar Shanmukhappa, et al.. (2011). Lampe1: An ENU-Germline Mutation Causing Spontaneous Hepatosteatosis Identified through Targeted Exon-Enrichment and Next-Generation Sequencing. PLoS ONE. 6(7). e21979–e21979. 20 indexed citations

10.

Schorry, Elizabeth K., Mehdi Keddache, Nancy Lanphear, et al.. (2008). Genotype–phenotype correlations in Rubinstein–Taybi syndrome. American Journal of Medical Genetics Part A. 146A(19). 2512–2519. 65 indexed citations

11.

Kardia, Sharon L. R., Reagan Kelly, Mehdi Keddache, et al.. (2008). Multiple interactions between the alpha2C- and beta1-adrenergic receptors influence heart failure survival. BMC Medical Genetics. 9(1). 93–93. 18 indexed citations

12.

Gilbert, Donald L., Elizabeth J. Leslie, Mehdi Keddache, & Nancy D. Leslie. (2008). A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24‐2q31. Movement Disorders. 24(3). 364–370. 10 indexed citations

13.

Martin, Lisa J., Vijaya Ramachandran, Linda Cripe, et al.. (2007). Evidence in favor of linkage to human chromosomal regions 18q, 5q and 13q for bicuspid aortic valve and associated cardiovascular malformations. Human Genetics. 121(2). 275–284. 121 indexed citations

14.

Molloy, Cynthia A., Mehdi Keddache, & Lisa J. Martin. (2005). Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression. Molecular Psychiatry. 10(8). 741–746. 73 indexed citations

15.

Thompson, Susan D., Marta B. Moroldo, Mary Ryan, et al.. (2004). A genome‐wide scan for juvenile rheumatoid arthritis in affected sibpair families provides evidence of linkage. Arthritis & Rheumatism. 50(9). 2920–2930. 55 indexed citations

16.

Lim, Lynne Hsueh Yee, Yingshi Guo, Valentina Pilipenko, et al.. (2003). Genotypic and Phenotypic Correlations of DFNB1-Related Hearing Impairment in the Midwestern United States. Archives of Otolaryngology - Head and Neck Surgery. 129(8). 836–836. 30 indexed citations

17.

Zhao, Haijiao, et al.. (2003). Gaucher's disease: identification of novel mutant alleles and genotype–phenotype relationships. Clinical Genetics. 64(1). 57–64. 21 indexed citations

18.

Buxbaum, Joseph D., Jeremy M. Silverman, Mehdi Keddache, et al.. (2003). Linkage analysis for autism in a subset families with obsessive–compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. Molecular Psychiatry. 9(2). 144–150. 108 indexed citations

19.

Greenberg, David A., Martina Durner, Mehdi Keddache, et al.. (2000). Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy. The American Journal of Human Genetics. 66(2). 508–516. 94 indexed citations

20.

Greenberg, David A., Martina Durner, Shlomo Shinnar, et al.. (1996). Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy. Neurology. 47(3). 750–755. 21 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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