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Hashem Shahin

Observed names: H Shahin, H. Shahin
OpenAlex ID: A5001035421
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
2013 · Suleyman Gulsuner, Tom Walsh, et al. · Cell · 548
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A novel deletion involving the connexin-30 gene, del( GJB6 -d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment
2005 · F J del Castillo, M Rodríguez-Ballesteros, et al. · Journal of Medical Genetics · 337
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Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82
2010 · Tom Walsh, Hashem Shahin, et al. · The American Journal of Human Genetics · 291
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From flies' eyes to our ears: Mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30
2002 · Tom Walsh, Vanessa Walsh, et al. · Proceedings of the National Academy of Sciences · 253
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families
2011 · Zippora Brownstein, Lilach M Friedman, et al. · Genome biology · 197
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The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population
2000 · T. Sobe, S. Vreugde, et al. · Human Genetics · 149
Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East
2002 · Hashem Shahin, Tom Walsh, et al. · Human Genetics · 138
Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
2014 · Hilal Unal Gulsuner, Suleyman Gulsuner, et al. · Proceedings of the National Academy of Sciences · 137
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Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss
2012 · Kemal O. Yariz, Duygu Duman, et al. · The American Journal of Human Genetics · 135
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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome
2012 · Dan Doherty, Albert E. Chudley, et al. · The American Journal of Human Genetics · 123
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Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss
2005 · Hashem Shahin, Tom Walsh, et al. · The American Journal of Human Genetics · 123
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Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51
2010 · Tom Walsh, Sarah B. Pierce, et al. · The American Journal of Human Genetics · 112
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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families
2009 · Hashem Shahin, Tom Walsh, et al. · European Journal of Human Genetics · 91
Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation
2010 · Amiel A. Dror, Yael Politi, et al. · Journal of Biological Chemistry · 90
A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
2010 · Aslı Sırmacı, Seyra Erbek, et al. · The American Journal of Human Genetics · 69
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Genomic analysis of inherited hearing loss in the Palestinian population
2020 · Amal Abu Rayyan, Lara Kamal, et al. · Proceedings of the National Academy of Sciences · 66
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Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population
2006 · Tom Walsh, Amal Abu Rayan, et al. · Human Genomics · 58
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Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84: Figure 1
2010 · Hashem Shahin, Michael Rahil, et al. · Journal of Medical Genetics · 45
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A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA
2010 · Vanessa L. Walsh, Dorith Raviv, et al. · Mammalian Genome · 42
Demographics of consanguinity in Palestinians with orofacial clefts: a non-randomised longitudinal study
2019 · Hassan J Zawahrah, Meredith G Moore, et al. · The Lancet · 5
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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome
2012 · Dan Doherty, Albert E. Chudley, et al. · The American Journal of Human Genetics · 3
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Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor
2015 · Hilal Unal Gulsuner, Suleyman Gulsuner, et al. · Proceedings of the National Academy of Sciences · 1
Works count: 22
Citation count: 3,013
H-index: 19
I10-index: 19
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