Hashem Shahin
Hashem Shahin
Professor of Human Genetics and Molecular Medicine
Verified email at bethlehem.edu
Cited by
Cited by
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network
S Gulsuner, T Walsh, AC Watts, MK Lee, AM Thornton, S Casadei, ...
Cell 154 (3), 518-529, 2013
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 …
FJ Del Castillo, M Rodriguez-Ballesteros, A Alvarez, T Hutchin, ...
Journal of medical genetics 42 (7), 588-594, 2005
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82
T Walsh, H Shahin, T Elkan-Miller, MK Lee, AM Thornton, W Roeb, ...
The American Journal of Human Genetics 87 (1), 90-94, 2010
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30
T Walsh, V Walsh, S Vreugde, R Hertzano, H Shahin, S Haika, MK Lee, ...
Proceedings of the National Academy of Sciences 99 (11), 7518-7523, 2002
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families
Z Brownstein, LM Friedman, H Shahin, V Oron-Karni, N Kol, AA Rayyan, ...
Genome biology 12 (9), 1-11, 2011
The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population
T Sobe, S Vreugde, H Shahin, M Berlin, N Davis, M Kanaan, Y Yaron, ...
Human genetics 106 (1), 50-57, 2000
Genetics of congenital deafness in the Palestinian population: multiple connexiná26 alleles with shared origins in the Middle East
H Shahin, T Walsh, T Sobe, E Lynch, MC King, KB Avraham, M Kanaan
Human genetics 110 (3), 284-289, 2002
Mitochondrial serine protease HTRA2 p. G399S in a kindred with essential tremor and Parkinson disease
HU Gulsuner, S Gulsuner, FN Mercan, OE Onat, T Walsh, H Shahin, ...
Proceedings of the National Academy of Sciences 111 (51), 18285-18290, 2014
Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss
H Shahin, T Walsh, T Sobe, AA Rayan, ED Lynch, MK Lee, KB Avraham, ...
The American Journal of Human Genetics 78 (1), 144-152, 2006
Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss
KO Yariz, D Duman, CZ Seco, J Dallman, M Huang, TA Peters, A Sirmaci, ...
The American Journal of Human Genetics 91 (5), 872-882, 2012
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families
H Shahin, T Walsh, AA Rayyan, MK Lee, J Higgins, D Dickel, K Lewis, ...
European Journal of Human Genetics 18 (4), 407-413, 2010
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome
D Doherty, AE Chudley, G Coghlan, GE Ishak, AM Innes, EG Lemire, ...
The American Journal of Human Genetics 90 (6), 1088-1093, 2012
Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation*♦
AA Dror, Y Politi, H Shahin, DR Lenz, S Dossena, C Nofziger, H Fuchs, ...
Journal of Biological Chemistry 285 (28), 21724-21735, 2010
A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
A Sırmacı, S Erbek, J Price, M Huang, D Duman, FB Cengiz, G Bademci, ...
The American Journal of Human Genetics 86 (5), 797-804, 2010
Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population
T Walsh, AA Rayan, H Shahin, J Shepshelovich, MK Lee, K Hirschberg, ...
Human genomics 2 (4), 1-9, 2006
A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA
VL Walsh, D Raviv, AA Dror, H Shahin, T Walsh, MN Kanaan, ...
Mammalian Genome 22 (3), 170-177, 2011
Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84
H Shahin, M Rahil, AA Rayan, KB Avraham, MC King, M Kanaan, T Walsh
Journal of medical genetics 47 (9), 643-645, 2010
Genomic analysis of inherited hearing loss in the Palestinian population
AA Rayyan, L Kamal, S Casadei, Z Brownstein, F Zahdeh, H Shahin, ...
Proceedings of the National Academy of Sciences 117 (33), 20070-20076, 2020
DFNB28, a novel locus for prelingual nonsyndromic autosomal recessive hearing loss maps to 22q13 in a large consanguineous Palestinian kindred
T Walsh, H Shahin, J Morrow, MC King, K Avraham, E Lynch, M Kanaan
Bethlehem University Journal 19, 96-96, 2000
The prevalence of connexin 26 mutations among the Palestinian deaf population
H Shahin
Tel Aviv University, 2000
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