Khalil Elbedour

3.1k total citations
31 papers, 2.2k citations indexed

About

Khalil Elbedour is a scholar working on Genetics, Molecular Biology and Sensory Systems. According to data from OpenAlex, Khalil Elbedour has authored 31 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 4 papers in Sensory Systems. Recurrent topics in Khalil Elbedour's work include Genetic and Kidney Cyst Diseases (9 papers), Genetic Syndromes and Imprinting (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Khalil Elbedour is often cited by papers focused on Genetic and Kidney Cyst Diseases (9 papers), Genetic Syndromes and Imprinting (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Khalil Elbedour collaborates with scholars based in Israel, United States and India. Khalil Elbedour's co-authors include Rivka Carmi, Val C. Sheffield, Edwin M. Stone, Darryl Nishimura, Ohad S. Birk, Ginat Narkis, Rivka Ofir, Terry A. Braun, Thomas L. Casavant and Tatiana Rokhlina and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Genome Research.

In The Last Decade

Khalil Elbedour

31 papers receiving 2.2k citations

Peers

Khalil Elbedour

GENET

NEURO

Mordechai Shohat Israel

Célia Bádenas Spain

Yoshihisa Sakai United States

Mohammed Al‐Owain Saudi Arabia

Arnold Munnich France

Rafael C. Caruso United States

Jessica C. Gardner United Kingdom

Nejat Mahdieh Iran

Isabelle Russell‐Eggitt United Kingdom

Guillermo Antiñolo Spain

Mordechai Shohat Israel

Khalil Elbedour

1.7k ×1.2

540 ×0.5

GENET

512 ×2.1

154 ×0.7

237 ×1.2

NEURO

Citations per year, relative to Khalil Elbedour Khalil Elbedour (= 1×) peers Mordechai Shohat

Countries citing papers authored by Khalil Elbedour

Since Specialization

Citations

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

Fields of papers citing papers by Khalil Elbedour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Khalil Elbedour

This figure shows the co-authorship network connecting the top 25 collaborators of Khalil Elbedour. A scholar is included among the top collaborators of Khalil Elbedour 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 Khalil Elbedour. Khalil Elbedour 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

Cohen, Idan, Eldad Silberstein, Yonatan Perez, et al.. (2013). Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase. European Journal of Human Genetics. 22(3). 374–378. 45 indexed citations

Gradstein, Libe, Annika Pasanen, Rivka Ofir, et al.. (2011). High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2. The American Journal of Human Genetics. 89(3). 438–445. 81 indexed citations

Levy, Jaime, et al.. (2010). Congenital Glaucoma. Journal of Glaucoma. 19(1). 35–38. 11 indexed citations

Birnbaum, Ramon Y., Daniella Landau, Khalil Elbedour, et al.. (2008). Deletion of the first pair of fibronectin type III repeats of the integrin β‐4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients. American Journal of Medical Genetics Part A. 146A(8). 1063–1066. 21 indexed citations

Ding, Yuan Chun, Zvi Weizman, Baruch Yerushalmi, et al.. (2007). An autosomal genome-wide screen for celiac disease in Bedouin families. Genes and Immunity. 9(1). 81–86. 2 indexed citations

Narkis, Ginat, Rivka Ofir, Esther Manor, et al.. (2007). Lethal Congenital Contractural Syndrome Type 2 (LCCS2) Is Caused by a Mutation in ERBB3 (Her3), a Modulator of the Phosphatidylinositol-3-Kinase/Akt Pathway. The American Journal of Human Genetics. 81(3). 589–595. 49 indexed citations

Narkis, Ginat, Rivka Ofir, Daniella Landau, et al.. (2007). Lethal Contractural Syndrome Type 3 (LCCS3) Is Caused by a Mutation in PIP5K1C, Which Encodes PIPKIγ of the Phophatidylinsitol Pathway. The American Journal of Human Genetics. 81(3). 530–539. 79 indexed citations

Flusser, Hagit, Rivka Ofir, Ilan Shelef, et al.. (2006). PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy. The American Journal of Human Genetics. 79(5). 942–948. 145 indexed citations

Chiang, Annie, Darryl Nishimura, Charles Searby, et al.. (2004). Comparative Genomic Analysis Identifies an ADP-Ribosylation Factor–like Gene as the Cause of Bardet-Biedl Syndrome (BBS3). The American Journal of Human Genetics. 75(3). 475–484. 175 indexed citations

10.

Narkis, Ginat, Daniella Landau, Esther Manor, et al.. (2004). Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13. American Journal of Medical Genetics Part A. 130A(3). 272–276. 15 indexed citations

11.

Neuhausen, Susan L., Zvi Weizman, Nicola J. Camp, et al.. (2002). HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease. Human Immunology. 63(6). 502–507. 14 indexed citations

12.

Mykytyn, Kirk, Terry A. Braun, Rivka Carmi, et al.. (2001). Identification of the gene that, when mutated, causes the human obesity syndrome BBS4. Nature Genetics. 28(2). 188–191. 200 indexed citations

13.

Weitzman, Dahlia, et al.. (2000). Factors Affecting the Use of Prenatal Testing for Fetal Anomalities in a Traditional Society. Public Health Genomics. 3(2). 61–70. 20 indexed citations

14.

Scott, Daryl A., Stacy S. Drury, D. Timothy Bishop, et al.. (2000). Refining the DFNB7–DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2. Gene. 246(1-2). 265–274. 22 indexed citations

15.

Greinwald, John H., Daryl A. Scott, Jacquie Marietta, et al.. (1997). Construction of P1-Derived Artificial Chromosome and Yeast Artificial Chromosome Contigs Encompassing the DFNB7 andDFNB11 Region of Chromosome 9q13–21. Genome Research. 7(9). 879–886. 7 indexed citations

16.

Carmi, Rivka, Khalil Elbedour, Edwin M. Stone, & Val C. Sheffield. (1995). Phenotypic differences among patients with Bardet‐Biedl syndrome linked to three different chromosome loci. American Journal of Medical Genetics. 59(2). 199–203. 80 indexed citations

17.

Carmi, Rivka, Tatiana Rokhlina, Anne E. Kwitek, et al.. (1995). Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15. Human Molecular Genetics. 4(1). 9–13. 148 indexed citations

18.

Elbedour, Khalil, Nili Zucker, Eli Zalzstein, Y. Barki, & Rivka Carmi. (1994). Cardiac abnormalities in the Bardet‐Biedl syndrome: Echocardiographic studies of 22 patients. American Journal of Medical Genetics. 52(2). 164–169. 78 indexed citations

19.

Sheffield, Val C., Tatiana Rokhlina, Geoffrey M. Duyk, et al.. (1994). Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping. Human Molecular Genetics. 3(8). 1331–1335. 169 indexed citations

20.

Kwitek, Anne E., Rivka Carmi, Geoffrey M. Duyk, et al.. (1993). Linkage of Bardet–Biedl syndrome to chromosome 16q and evidence for non–allelic genetic heterogeneity. Nature Genetics. 5(4). 392–396. 134 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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