Hashem Shahin

3.1k total citations
17 papers, 1.2k citations indexed

About

Hashem Shahin is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Hashem Shahin has authored 17 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Sensory Systems and 3 papers in Neurology. Recurrent topics in Hashem Shahin's work include Hearing, Cochlea, Tinnitus, Genetics (11 papers), Connexins and lens biology (6 papers) and Biochemical Analysis and Sensing Techniques (2 papers). Hashem Shahin is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (11 papers), Connexins and lens biology (6 papers) and Biochemical Analysis and Sensing Techniques (2 papers). Hashem Shahin collaborates with scholars based in Palestinian Territory, United States and Israel. Hashem Shahin's co-authors include Karen B. Avraham, Moien Kanaan, Mary‐Claire King, Tom Walsh, Ming K. Lee, Tama Sobe, Sarah Vreugde, Amal Abu Rayyan, Eric D. Lynch and Wendy Roeb and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Hashem Shahin

17 papers receiving 1.2k citations

Peers

Hashem Shahin
Rick A. Friedman United States
Hideki Mutai Japan
Teresa Jaijo Spain
Hao Wu China
Frank J. Probst United States
Hans‐Henrik M. Dahl Australia
Salvatore Melchionda Italy
A. Eliot Shearer United States
Rick A. Friedman United States
Hashem Shahin
Citations per year, relative to Hashem Shahin Hashem Shahin (= 1×) peers Rick A. Friedman

Countries citing papers authored by Hashem Shahin

Since Specialization
Citations

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

Fields of papers citing papers by Hashem Shahin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hashem Shahin

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

All Works

17 of 17 papers shown
1.
Rayyan, Amal Abu, Silvia Casadei, Zippora Brownstein, et al.. (2020). Genomic analysis of inherited hearing loss in the Palestinian population. Proceedings of the National Academy of Sciences. 117(33). 20070–20076. 38 indexed citations
2.
Shahin, Hashem, et al.. (2019). Demographics of consanguinity in Palestinians with orofacial clefts: a non-randomised longitudinal study. The Lancet. 393. S55–S55. 2 indexed citations
3.
Gülsüner, Süleyman, Onur Emre Onat, Tom Walsh, et al.. (2014). Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proceedings of the National Academy of Sciences. 111(51). 18285–18290. 92 indexed citations
4.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 91(1). 209–209. 2 indexed citations
5.
Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 90(6). 1088–1093. 81 indexed citations
6.
Shahin, Hashem, Amal Rayan, Karen B. Avraham, et al.. (2010). Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84. Journal of Medical Genetics. 47(9). 643–645. 34 indexed citations
7.
Walsh, Tom, Hashem Shahin, T. Elkan Miller, et al.. (2010). Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. The American Journal of Human Genetics. 87(1). 90–94. 198 indexed citations
8.
Walsh, Tom, Sarah B. Pierce, Danielle R. Lenz, et al.. (2010). Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51. The American Journal of Human Genetics. 87(1). 101–109. 74 indexed citations
9.
Dror, Amiel A., Yael Politi, Hashem Shahin, et al.. (2010). Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation. Journal of Biological Chemistry. 285(28). 21724–21735. 69 indexed citations
10.
Dror, Amiel A., Hashem Shahin, Tom Walsh, et al.. (2010). A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA. Mammalian Genome. 22(3-4). 170–177. 31 indexed citations
11.
Shahin, Hashem, Tom Walsh, Amal Abu Rayyan, et al.. (2009). Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families. European Journal of Human Genetics. 18(4). 407–413. 69 indexed citations
12.
Walsh, Tom, Amal Rayan, Hashem Shahin, et al.. (2006). Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population. Human Genomics. 2(4). 203–11. 42 indexed citations
13.
Shahin, Hashem, Tom Walsh, Tama Sobe, et al.. (2005). Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss. The American Journal of Human Genetics. 78(1). 144–152. 85 indexed citations
14.
Walsh, Tom, Sarah Vreugde, Ronna Hertzano, et al.. (2002). From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. Proceedings of the National Academy of Sciences. 99(11). 7518–7523. 170 indexed citations
15.
Shahin, Hashem, Tom Walsh, Tama Sobe, et al.. (2002). Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East. Human Genetics. 110(3). 284–289. 105 indexed citations
16.
Sobe, Tama, Sarah Vreugde, Hashem Shahin, et al.. (2000). The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population. Human Genetics. 106(1). 50–57. 128 indexed citations
17.
Sobe, Tama, Sarah Vreugde, Hashem Shahin, et al.. (2000). The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population. Human Genetics. 106(1). 50–57. 22 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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