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Shareef A. Nahas, Ph.D. - Publications

Affiliations: 
2008 University of California, Los Angeles, Los Angeles, CA 
Area:
Pathology, Molecular Biology
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27 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Hu H, Nahas S, Gatti RA. Assaying Radiosensitivity of Ataxia-Telangiectasia. Methods in Molecular Biology (Clifton, N.J.). 1599: 1-11. PMID 28477107 DOI: 10.1007/978-1-4939-6955-5_1  0.628
2015 Kwok B, Hall JM, Witte JS, Xu Y, Reddy P, Lin K, Flamholz R, Dabbas B, Yung A, Al Hafidh J, Balmert E, Vaupel C, El Hader C, McGinniss MJ, Nahas SA, et al. MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significance. Blood. PMID 26429975 DOI: 10.1182/Blood-2015-08-667063  0.326
2014 Kwok B, Reddy P, Lin K, Flamholz R, Yung A, Dabbas B, McGinniss M, Nahas S, Kines J, Xu Y. Next-Generation Sequencing (NGS)-Based Profiling of Idiopathic Cytopenia of Undetermined Significance (ICUS) Identifies a Subset of Patients with Genomic Similarities to Lower-Risk Myelodysplastic Syndrome (MDS) Blood. 124: 166-166. DOI: 10.1182/blood.v124.21.166.166  0.307
2013 Du L, Jung ME, Damoiseaux R, Completo G, Fike F, Ku JM, Nahas S, Piao C, Hu H, Gatti RA. A new series of small molecular weight compounds induce read through of all three types of nonsense mutations in the ATM gene. Molecular Therapy : the Journal of the American Society of Gene Therapy. 21: 1653-60. PMID 23774824 DOI: 10.1038/Mt.2013.150  0.57
2013 Martin NT, Nakamura K, Davies R, Nahas SA, Brown C, Tunuguntla R, Gatti RA, Hu H. ATM-dependent MiR-335 targets CtIP and modulates the DNA damage response. Plos Genetics. 9: e1003505. PMID 23696749 DOI: 10.1371/Journal.Pgen.1003505  0.687
2012 Li X, Zhou J, Nahas SA, Wan H, Hu H, Gatti RA. Common copy number variations in fifty radiosensitive cell lines. Genomics. 99: 96-100. PMID 22200558 DOI: 10.1016/J.Ygeno.2011.11.001  0.509
2012 Nahas SA, Davies R, Fike F, Nakamura K, Du L, Kayali R, Martin NT, Concannon P, Gatti RA. Comprehensive profiling of radiosensitive human cell lines with DNA damage response assays identifies the neutral comet assay as a potential surrogate for clonogenic survival. Radiation Research. 177: 176-86. PMID 21962002 DOI: 10.1667/Rr2580.1  0.732
2012 Davies RC, Pettijohn K, Fike F, Wang J, Nahas SA, Tunuguntla R, Hu H, Gatti RA, McCurdy D. Defective DNA double-strand break repair in pediatric systemic lupus erythematosus. Arthritis and Rheumatism. 64: 568-78. PMID 21905016 DOI: 10.1002/Art.33334  0.565
2011 Martin NT, Nahas SA, Tunuguntla R, Fike F, Gatti RA. Assessing 'radiosensitivity' with kinetic profiles of γ-H2AX, 53BP1 and BRCA1 foci. Radiotherapy and Oncology : Journal of the European Society For Therapeutic Radiology and Oncology. 101: 35-8. PMID 21722985 DOI: 10.1016/J.Radonc.2011.05.065  0.721
2011 Devgan SS, Sanal O, Doil C, Nakamura K, Nahas SA, Pettijohn K, Bartek J, Lukas C, Lukas J, Gatti RA. Homozygous deficiency of ubiquitin-ligase ring-finger protein RNF168 mimics the radiosensitivity syndrome of ataxia-telangiectasia. Cell Death and Differentiation. 18: 1500-6. PMID 21394101 DOI: 10.1038/Cdd.2011.18  0.645
2009 Nahas SA, Gatti RA. DNA double strand break repair defects, primary immunodeficiency disorders, and 'radiosensitivity'. Current Opinion in Allergy and Clinical Immunology. 9: 510-6. PMID 19858715 DOI: 10.1097/Aci.0B013E328332Be17  0.608
2009 Du L, Damoiseaux R, Nahas S, Gao K, Hu H, Pollard JM, Goldstine J, Jung ME, Henning SM, Bertoni C, Gatti RA. Nonaminoglycoside compounds induce readthrough of nonsense mutations. The Journal of Experimental Medicine. 206: 2285-97. PMID 19770270 DOI: 10.1084/Jem.20081940  0.731
2009 Nahas SA, Butch AW, Du L, Gatti RA. Rapid flow cytometry-based structural maintenance of chromosomes 1 (SMC1) phosphorylation assay for identification of ataxia-telangiectasia homozygotes and heterozygotes. Clinical Chemistry. 55: 463-72. PMID 19147735 DOI: 10.1373/Clinchem.2008.107128  0.607
2009 Mitui M, Nahas SA, Du LT, Yang Z, Lai CH, Nakamura K, Arroyo S, Scott S, Purayidom A, Concannon P, Lavin M, Gatti RA. Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk. Human Mutation. 30: 12-21. PMID 18634022 DOI: 10.1002/Humu.20805  0.682
2008 Ehlayel M, de Beaucoudrey L, Fike F, Nahas SA, Feinberg J, Casanova JL, Gatti RA. Simultaneous presentation of 2 rare hereditary immunodeficiencies: IL-12 receptor beta1 deficiency and ataxia-telangiectasia. The Journal of Allergy and Clinical Immunology. 122: 1217-9. PMID 18718650 DOI: 10.1016/J.Jaci.2008.07.005  0.439
2008 Gatti R, Nahas S, Butch A. F.55. Rapid Flow Cytometry-based SMC1 Phosphorylation Assay for Identification of Ataxia-telangiectasia Homozygotes and Heterozygotes Clinical Immunology. 127. DOI: 10.1016/J.Clim.2008.03.167  0.476
2007 Nahas SA, Duquette A, Roddier K, Gatti RA, Brais B. Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiation. Neuromuscular Disorders : Nmd. 17: 968-9. PMID 17720498 DOI: 10.1016/J.Nmd.2007.06.464  0.574
2007 Landmark H, Nahas SA, Aarøe J, Gatti R, Børresen-Dale AL, Rødningen OK. Transcriptional response to ionizing radiation in human radiation sensitive cell lines Radiotherapy and Oncology. 83: 256-260. PMID 17512073 DOI: 10.1016/J.Radonc.2007.04.017  0.526
2006 Goldstine JV, Nahas S, Gamo K, Gartler SM, Hansen RS, Roelfsema JH, Gatti RA, Marahrens Y. Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activity. Dna Repair. 5: 432-43. PMID 16426903 DOI: 10.1016/J.Dnarep.2005.12.002  0.586
2005 Mitui M, Bernatowska E, Pietrucha B, Piotrowska-Jastrzebska J, Eng L, Nahas S, Teraoka S, Sholty G, Purayidom A, Concannon P, Gatti RA. ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia. Annals of Human Genetics. 69: 657-64. PMID 16266405 DOI: 10.1111/J.1529-8817.2005.00199.X  0.62
2005 Ouyang Y, Salstrom J, Diaz-Perez S, Nahas S, Matsuno Y, Dawson D, Teitell MA, Horvath S, Riggs AD, Gatti RA, Marahrens Y. Inhibition of Atm and/or Atr disrupts gene silencing on the inactive X chromosome. Biochemical and Biophysical Research Communications. 337: 875-80. PMID 16213462 DOI: 10.1016/J.Bbrc.2005.09.122  0.557
2005 Nahas SA, Lai CH, Gatti RA. Post-irradiation phosphorylation of structural maintenance chromosome 1 (SMC1) is independent of the Fanconi protein pathway. International Journal of Radiation Oncology, Biology, Physics. 61: 1167-72. PMID 15752898 DOI: 10.1016/J.Ijrobp.2004.11.023  0.668
2004 Lai CH, Chun HH, Nahas SA, Mitui M, Gamo KM, Du L, Gatti RA. Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons. Proceedings of the National Academy of Sciences of the United States of America. 101: 15676-81. PMID 15498871 DOI: 10.1073/Pnas.0405155101  0.737
2004 Butch AW, Chun HH, Nahas SA, Gatti RA. Immunoassay to measure ataxia-telangiectasia mutated protein in cellular lysates. Clinical Chemistry. 50: 2302-8. PMID 15486025 DOI: 10.1373/Clinchem.2004.039461  0.695
2004 Coutinho G, Mitui M, Campbell C, Costa Carvalho BT, Nahas S, Sun X, Huo Y, Lai CH, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena J, Gatti RA. Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics. Part A. 126: 33-40. PMID 15039971 DOI: 10.1002/Ajmg.A.20570  0.703
2004 Eng L, Coutinho G, Nahas S, Yeo G, Tanouye R, Babaei M, Dörk T, Burge C, Gatti RA. Nonclassical splicing mutations in the coding and noncoding regions of the ATM Gene: maximum entropy estimates of splice junction strengths. Human Mutation. 23: 67-76. PMID 14695534 DOI: 10.1002/Humu.10295  0.579
2003 Chun HH, Sun X, Nahas SA, Teraoka S, Lai CH, Concannon P, Gatti RA. Improved diagnostic testing for ataxia-telangiectasia by immunoblotting of nuclear lysates for ATM protein expression. Molecular Genetics and Metabolism. 80: 437-43. PMID 14654357 DOI: 10.1016/J.Ymgme.2003.09.008  0.733
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