Hashem Shahin
Hashem Shahin
Professor of Human Genetics and Molecular Medicine
Verified email at bethlehem.edu
Title
Cited by
Cited by
Year
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
4742013
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
3512005
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
3162010
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
2532002
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
2142011
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
2072000
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
1872002
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
1202014
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
1182006
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
992012
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
872010
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
852012
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
682010
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
602010
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
542006
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
402011
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
402010
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
52020
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
52000
The prevalence of connexin 26 mutations among the Palestinian deaf population
H Shahin
Tel Aviv University, 2000
12000
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Articles 1–20