Josef Ekstein

1.4k total citations
27 papers, 851 citations indexed

About

Josef Ekstein is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Josef Ekstein has authored 27 papers receiving a total of 851 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 6 papers in Pulmonary and Respiratory Medicine and 6 papers in Genetics. Recurrent topics in Josef Ekstein's work include RNA regulation and disease (4 papers), Lysosomal Storage Disorders Research (4 papers) and ATP Synthase and ATPases Research (3 papers). Josef Ekstein is often cited by papers focused on RNA regulation and disease (4 papers), Lysosomal Storage Disorders Research (4 papers) and ATP Synthase and ATPases Research (3 papers). Josef Ekstein collaborates with scholars based in United States, Israel and Australia. Josef Ekstein's co-authors include Howard M. Katzenstein, Berish Y. Rubin, Sylvia L. Anderson, Neil Risch, Sabrina A. Volpi, Elizabeth Kichula, Rocco Coli, Hua Tang, Gideon Bach and Dvorah Abeliovich and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Josef Ekstein

24 papers receiving 827 citations

Peers

Josef Ekstein

GENET

CMN

PHYSI

Sebahattin Çırak Germany

Erik-Jan Kamsteeg Netherlands

Ivo Kremensky Bulgaria

Lysanne Patry Canada

Maja Hempel Germany

Si Ho Choi United States

Carol Guy United Kingdom

Saeko Ishida Japan

Delphine Roussel France

Davide Tonduti Italy

Sebahattin Çırak Germany

Josef Ekstein

538 ×1.3

170 ×0.9

GENET

106 ×0.6

CMN

142 ×1.2

157 ×1.5

PHYSI

Citations per year, relative to Josef Ekstein Josef Ekstein (= 1×) peers Sebahattin Çırak

Countries citing papers authored by Josef Ekstein

Since Specialization

Citations

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

Fields of papers citing papers by Josef Ekstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josef Ekstein

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Urano, Fumihiko, Wenjuan Ye, Punn Augsornworawat, et al.. (2022). eP264: Genotype-phenotype correlation analysis and therapeutic development using a patient stem cell-derived disease model of Wolfram syndrome. Genetics in Medicine. 24(3). S167–S167. 1 indexed citations

Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations

Booth, Kevin T., et al.. (2021). Identification of Novel and Recurrent Variants in MYO15A in Ashkenazi Jewish Patients With Autosomal Recessive Nonsyndromic Hearing Loss. Frontiers in Genetics. 12. 737782–737782.

Hirsch, Yoel, et al.. (2019). A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews. Human Genome Variation. 6(1). 45–45. 4 indexed citations

Anderson, Sylvia L., Chaim Jalas, Anastasia Fedick, et al.. (2014). A founder mutation in the TCIRG1 gene causes osteopetrosis in the Ashkenazi Jewish population. Clinical Genetics. 88(1). 74–79. 7 indexed citations

Fedick, Anastasia, Jing Su, Chaim Jalas, et al.. (2013). High-Throughput Carrier Screening Using TaqMan Allelic Discrimination. PLoS ONE. 8(3). e59722–e59722. 20 indexed citations

Fedick, Anastasia, et al.. (2013). Carrier frequency of two BBS2 mutations in the Ashkenazi population. Clinical Genetics. 85(6). 578–582. 9 indexed citations

Li, Rong, Sakkubai Naidu, Edwin H. Kolodny, et al.. (2012). Splice site, frameshift, and chimericGFAPmutations in Alexander disease. Human Mutation. 33(7). 1141–1148. 29 indexed citations

Jalas, Chaim, et al.. (2011). A founder mutation in the MPL gene causes congenital amegakaryocytic thrombocytopenia (CAMT) in the Ashkenazi Jewish population. Blood Cells Molecules and Diseases. 47(1). 79–83. 8 indexed citations

10.

Gläser, Benjamin, Ilana Blech, Josef Ekstein, et al.. (2011). ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia. Genetics in Medicine. 13(10). 891–894. 27 indexed citations

11.

Ekstein, Josef, et al.. (2004). The rabbi's dilemma. The New Scientist. 44–47. 1 indexed citations

12.

Ekstein, Josef. (2004). The rabbi's dilemma. [Interview by Alison George].. PubMed. 181(2434). 44–7. 4 indexed citations

13.

Kornreich, Ruth, Josef Ekstein, Lisa Edelmann, & Robert J. Desnick. (2004). Premarital and prenatal screening for cystic fibrosis: Experience in the Ashkenazi Jewish population. Genetics in Medicine. 6(5). 415–420. 21 indexed citations

14.

Ekstein, Josef, Berish Y. Rubin, Sylvia L. Anderson, et al.. (2004). Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population. American Journal of Medical Genetics Part A. 129A(2). 162–164. 36 indexed citations

15.

Ekstein, Josef, et al.. (2004). Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene. Human Genetics. 115(3). 185–90. 56 indexed citations

16.

Risch, Neil, Hua Tang, Howard M. Katzenstein, & Josef Ekstein. (2003). Geographic Distribution of Disease Mutations in the Ashkenazi Jewish Population Supports Genetic Drift over Selection. The American Journal of Human Genetics. 72(4). 812–822. 97 indexed citations

17.

Anderson, Sylvia L., Rocco Coli, Elizabeth Kichula, et al.. (2001). Familial Dysautonomia Is Caused by Mutations of the IKAP Gene. The American Journal of Human Genetics. 68(3). 753–758. 327 indexed citations

18.

Bach, Gideon, et al.. (2001). Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. American Journal of Medical Genetics. 99(1). 70–75. 52 indexed citations

19.

Ekstein, Josef & Howard M. Katzenstein. (2001). 23. The Dor Yeshorim story: Community-based carrier screening for Tay-Sachs disease. Advances in genetics. 44. 297–310. 87 indexed citations

20.

Bernstine, Hanna, Zvi Bar‐Sever, Josef Ekstein, & Ruth Hardoff. (1999). Ga-67 Scintigraphy in a Rare Case of Primary Pleural Hodgkin’s Lymphoma. Clinical Nuclear Medicine. 24(11). 880–880.

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.

Explore authors with similar magnitude of impact