| human | Q5 |
| P2013 | Facebook username | noam.shomron |
| P227 | GND ID | 1236372212 |
| P2671 | Google Knowledge Graph ID | /g/1hlgfwh3_ |
| P1960 | Google Scholar author ID | BdJzVV4AAAAJ |
| P269 | IdRef ID | 171808975 |
| P244 | Library of Congress authority ID | nb2013021558 |
| P6634 | LinkedIn personal profile ID | nshomron |
| P2798 | Loop ID | 24418 |
| P8189 | National Library of Israel J9U ID | 987007359989205171 |
| P856 | official website | http://www.tau.ac.il/~nshomron |
| https://med.tau.ac.il/profile/nshomron | ||
| P496 | ORCID iD | 0000-0001-9913-6124 |
| P8159 | SciProfiles ID | 676727 |
| P1153 | Scopus author ID | 14020403700 |
| P214 | VIAF ID | 305260330 |
| P69 | educated at | Hebrew University of Jerusalem | Q174158 |
| Massachusetts Institute of Technology | Q49108 | ||
| Tel Aviv University | Q319239 | ||
| Macquarie University | Q741082 | ||
| P108 | employer | Tel Aviv University | Q319239 |
| Rare Genomics Institute | Q30271814 | ||
| P735 | given name | Noam | Q1994678 |
| Noam | Q1994678 | ||
| P106 | occupation | researcher | Q1650915 |
| P5008 | on focus list of Wikimedia project | WikiProject COVID-19 | Q87748614 |
| P21 | sex or gender | male | Q6581097 |
| Q92917866 | A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC) |
| Q64113675 | A novel intronic mutation of is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews |
| Q87051193 | A personal perspective on personalized medicine |
| Q33844376 | A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism |
| Q49865252 | A splice variant of ADAMTS13 is expressed in human hepatic stellate cells and cancerous tissues. |
| Q43012647 | Ab initio identification of functionally interacting pairs of cis-regulatory elements |
| Q36098646 | Actionable clinical decisions based on comprehensive genomic evaluation in asymptomatic adults |
| Q37598535 | An evolutionary perspective of animal microRNAs and their targets |
| Q30581758 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge. |
| Q34307443 | Analysis of insertion-deletion from deep-sequencing data: software evaluation for optimal detection |
| Q55301278 | Analysis of microRNAs in familial Mediterranean fever. |
| Q34843753 | Assembly algorithms for deep sequencing data: basics and pitfalls |
| Q112303719 | Axonal TDP-43 condensates drive neuromuscular junction disruption through inhibition of local synthesis of nuclear encoded mitochondrial proteins |
| Q64077212 | Bayesian-based noninvasive prenatal diagnosis of single-gene disorders |
| Q112643278 | Behavioral aspects and neurobiological properties underlying medical cannabis treatment in Shank3 mouse model of autism spectrum disorder |
| Q33307791 | Biased exonization of transposed elements in duplicated genes: A lesson from the TIF-IA gene |
| Q48226856 | Biased hosting of intronic microRNA genes |
| Q40572207 | Bioactivation of carbamate-based 20(S)-camptothecin prodrugs |
| Q51231785 | Biomaterials for Abrogating Metastasis: Bridging the Gap between Basic and Translational Research. |
| Q52640771 | Boric acid reversibly inhibits the second step of pre‐mRNA splicing |
| Q95601914 | Breast cancer genomics in the deep sequencing era |
| Q95600612 | COVID-19 diagnosis prediction by symptoms of tested individuals: a machine learning approach |
| Q39260466 | Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis |
| Q36493258 | Canalization of development by microRNAs |
| Q38791536 | Cancer, senescence, and aging: translation from basic research to clinics |
| Q64887596 | Characterization of MicroRNA and Gene Expression Profiles Following Ricin Intoxication. |
| Q34328026 | Characterization of coding synonymous and non-synonymous variants in ADAMTS13 using ex vivo and in silico approaches |
| Q89146315 | Circulating MicroRNAs: a Potential Biomarker for Cardiac Damage, Inflammatory Response, and Left Ventricular Function Recovery in Pediatric Viral Myocarditis |
| Q37217072 | Cole Disease Results from Mutations in ENPP1. |
| Q57283075 | Comparison of breast cancer metastasis models reveals a possible mechanism of tumor aggressiveness |
| Q42382135 | Correction: MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease Phenotypes |
| Q49644932 | Corrigendum to "X-linked elliptocytosis with impaired growth is related to mutated AMMECR1" [Gene 606C (2017) 47-52]. |
| Q86773948 | Crowdfunding effort identifies the causative mutation in a patient with nystagmus, microcephaly, dystonia and hypomyelination |
| Q41378628 | Deep sequencing analysis of viral infection and evolution allows rapid and detailed characterization of viral mutant spectrum |
| Q37218675 | Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting |
| Q42611158 | Determinants of targeting by endogenous and exogenous microRNAs and siRNAs |
| Q38787257 | Differential analysis of mutations in the Jewish population and their implications for diseases. |
| Q37204742 | Distinctive pattern of let-7 family microRNAs in aggressive carcinoma of the oral tongue in young patients |
| Q42068405 | Does base-pairing strength play a role in microRNA repression? |
| Q31055456 | Downregulation of miR-31, miR-155, and miR-564 in chronic myeloid leukemia cells |
| Q64104796 | Dual inhibition of ABCE1 and LCP1 by microRNA-96 results in an additive effect in breast cancer mouse model |
| Q50318619 | Early Detection of Preeclampsia Using Circulating Small non-coding RNA. |
| Q90192296 | Early diagnosis of gestational diabetes mellitus using circulating microRNAs |
| Q39176758 | Emergence and transmission of arbovirus evolutionary intermediates with epidemic potential |
| Q33850381 | Epidermolytic Ichthyosis Sine Epidermolysis |
| Q99603105 | Ethnic differences in alpha-1 antitrypsin deficiency allele frequencies may partially explain national differences in COVID-19 fatality rates |
| Q43163886 | Evaluation of optimization techniques for variable selection in logistic regression applied to diagnosis of myocardial infarction |
| Q38123052 | Exome sequencing analysis: a guide to disease variant detection |
| Q47239489 | Exosomal microRNAs derived from colorectal cancer-associated fibroblasts: role in driving cancer progression. |
| Q36096111 | Familial pityriasis rubra pilaris is caused by mutations in CARD14. |
| Q34058182 | Feed-forward microprocessing and splicing activities at a microRNA-containing intron |
| Q60549442 | Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A |
| Q36560522 | Fluid consumption and taste novelty determines transcription temporal dynamics in the gustatory cortex |
| Q86496840 | Genetics research: jumping into the deep end of the pool |
| Q39293823 | Genome-wide miRNA expression profiling of human lymphoblastoid cell lines identifies tentative SSRI antidepressant response biomarkers |
| Q100416514 | Genome-wide noninvasive prenatal diagnosis of monogenic disorders: Current and future trends |
| Q38319500 | Genome-wide transcriptomic variations of human lymphoblastoid cell lines: insights from pairwise gene-expression correlations |
| Q34322663 | GenomeGems: evaluation of genetic variability from deep sequencing data |
| Q27320149 | Group Selection and Contribution of Minority Variants during Virus Adaptation Determines Virus Fitness and Phenotype |
| Q61809755 | HIV-1 infection increases microRNAs that inhibit Dicer1, HRB and HIV-EP2, thereby reducing viral replication |
| Q104495374 | How I embrace diversity in my lab |
| Q38799182 | Identification of Dormancy-Associated MicroRNAs for the Design of Osteosarcoma-Targeted Dendritic Polyglycerol Nanopolyplexes |
| Q28276555 | Identification of let-7-regulated oncofetal genes |
| Q112728631 | Improved noninvasive fetal variant calling using standardized benchmarking approaches |
| Q28469075 | Inference of splicing regulatory activities by sequence neighborhood analysis |
| Q38381474 | Influence of population diversity on neurovirulence potential of plaque purified L-Zagreb variants |
| Q38903498 | Insulin-like Growth Factor 1 Differentially Affects Lithium Sensitivity of Lymphoblastoid Cell Lines from Lithium Responder and Non-responder Bipolar Disorder Patients |
| Q35710097 | Insulin-like growth factor-I receptor (IGF-IR) translocates to nucleus and autoregulates IGF-IR gene expression in breast cancer cells |
| Q42593884 | Intercellular transfer of small RNAs from astrocytes to lung tumor cells induces resistance to chemotherapy |
| Q38735502 | Interplay between pre-mRNA splicing and microRNA biogenesis within the supraspliceosome |
| Q44477999 | Involvement of IGF-1R regulation by miR-515-5p modifies breast cancer risk among BRCA1 carriers |
| Q37273646 | Local microRNA delivery targets Palladin and prevents metastatic breast cancer. |
| Q64962393 | Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome. |
| Q91568812 | Loss-of-function variants in SERPINA12 underlie autosomal recessive palmoplantar keratoderma |
| Q114564839 | Machine learning-based prediction of COVID-19 diagnosis based on symptoms |
| Q48188602 | Meeting summary: Ethical aspects of whole exome and whole genome sequencing studies (WES/WGS) in rare diseases, Tel Aviv, Israel, January 2013. |
| Q37273430 | MiR-192 directly binds and regulates Dicer1 expression in neuroblastoma |
| Q50629470 | MiR-30e induces apoptosis and sensitizes K562 cells to imatinib treatment via regulation of the BCR-ABL protein. |
| Q42321104 | MicroRNA 10b promotes abnormal expression of the proto-oncogene c-Jun in metastatic breast cancer cells |
| Q35105657 | MicroRNA editing facilitates immune elimination of HCMV infected cells |
| Q42028379 | MicroRNA miR-125a-3p modulates molecular pathway of motility and migration in prostate cancer cells |
| Q37886369 | MicroRNA pharmacogenomics: post-transcriptional regulation of drug response |
| Q33688484 | MicroRNA regulation of progesterone receptor in breast cancer |
| Q50679525 | MicroRNA-34a is dispensable for p53 function as teratogenesis inducer. |
| Q34642754 | MicroRNA-382 expression is elevated in the olfactory neuroepithelium of schizophrenia patients |
| Q47118154 | MicroRNA-Mediated Regulation of ITGB3 and CHL1 Is Implicated in SSRI Action |
| Q37552759 | MicroRNA-biogenesis and Pre-mRNA splicing crosstalk |
| Q35522595 | MicroRNA-mediated regulation of p21 and TASK1 cellular restriction factors enhances HIV-1 infection |
| Q90181942 | MicroRNAs Affect Complement Regulator Expression and Mitochondrial Activity to Modulate Cell Resistance to Complement-Dependent Cytotoxicity |
| Q36106571 | MicroRNAs Expression in the Ileal Pouch of Patients with Ulcerative Colitis Is Robustly Up-Regulated and Correlates with Disease Phenotypes |
| Q33610042 | MicroRNAs and developmental robustness: a new layer is revealed |
| Q37736453 | MicroRNAs and pharmacogenomics |
| Q51925779 | MicroRNAs and their antagonists as novel therapeutics. |
| Q28509271 | MicroRNAs are essential for development and function of inner ear hair cells in vertebrates |
| Q46330068 | MicroRNAs as predictors for CNS relapse of systemic diffuse large B-cell lymphoma |
| Q97551154 | MicroRNAs in Ascending Thoracic Aortic Aneurysms |
| Q62599252 | MicroRNAs in the growth plate are responsive to nutritional cues: association between miR-140 and SIRT1 |
| Q42270340 | MicroRNAs: fundamental regulators of gene expression in major affective disorders and suicidal behavior? |
| Q50719239 | Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism. |
| Q38730554 | Molecular Risk Factors for Schizophrenia |
| Q36162463 | Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. |
| Q35760472 | Mutations in coronavirus nonstructural protein 10 decrease virus replication fidelity |
| Q35885239 | Neuro-Epigenetic Indications of Acute Stress Response in Humans: The Case of MicroRNA-29c |
| Q30435542 | Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways |
| Q35693912 | Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT). |
| Q36008219 | Novel insight into the non-coding repertoire through deep sequencing analysis |
| Q39526055 | Pathogen detection using short-RNA deep sequencing subtraction and assembly |
| Q34629231 | Pax6 regulates gene expression in the vertebrate lens through miR-204 |
| Q33920265 | Pharmaco-miR: linking microRNAs and drug effects |
| Q39557479 | Pharmacogenomics genes show varying perceptibility to microRNA regulation. |
| Q96953996 | Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis |
| Q34445768 | Phylogenetic and genome-wide deep-sequencing analyses of canine parvovirus reveal co-infection with field variants and emergence of a recent recombinant strain |
| Q86510207 | Prioritizing personalized medicine |
| Q45127712 | Privacy, anonymity and subjectivity in genomic research. |
| Q55044678 | Promoter-Associated RNAs Regulate HSPC152 Gene Expression in Malignant Melanoma. |
| Q50588513 | RBM28, a protein deficient in ANE syndrome, regulates hair follicle growth via miR-203 and p63. |
| Q54750921 | RNA-binding protein PTB and microRNA-221 coregulate AdipoR1 translation and adiponectin signaling. |
| Q90852897 | Rare Genetic Variants in Jewish Patients Suffering from Age-Related Macular Degeneration |
| Q39366882 | Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration |
| Q24813203 | Recognition of unknown conserved alternatively spliced exons |
| Q38770633 | Regulation of Complement-Dependent Cytotoxicity by MicroRNAs miR-200b, miR-200c, and miR-217. |
| Q33889489 | Regulation of cancer aggressive features in melanoma cells by microRNAs |
| Q24676136 | Regulation of transcription of the RNA splicing factor hSlu7 by Elk-1 and Sp1 affects alternative splicing |
| Q50600078 | Restoration of miR-424 suppresses BCR-ABL activity and sensitizes CML cells to imatinib treatment. |
| Q39698187 | Reversible inhibition of the second step of splicing suggests a possible role of zinc in the second step of splicing |
| Q89341946 | SMYD1 is the underlying gene for the AnWj-negative blood group phenotype |
| Q59133574 | Seasonal Genetic Drift of Human Influenza A Virus Quasispecies Revealed by Deep Sequencing |
| Q39160024 | Sequencing your genome: your future is here, but are you sure you want to know it? |
| Q110616071 | Slow Transcription of the 99a/let-7c/125b-2 Cluster Results in Differential MiRNA Expression and Promotes Melanoma Phenotypic Plasticity |
| Q38810653 | Somatic Mosaicism for a "Lethal" GJB2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement |
| Q38122334 | Species-specific microRNA regulation influences phenotypic variability: perspectives on species-specific microRNA regulation |
| Q34159796 | Species-specific microRNA roles elucidated following astrocyte activation. |
| Q101041342 | Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 |
| Q24295147 | Splicing factor hSlu7 contains a unique functional domain required to retain the protein within the nucleus |
| Q24296455 | Stress alters the subcellular distribution of hSlu7 and thus modulates alternative splicing |
| Q113879204 | Structure-function conservation between the methyltransferases SETD3 and SETD6 |
| Q36130875 | Systematic identification of edited microRNAs in the human brain |
| Q34019466 | Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families |
| Q24621525 | Teratogen-induced alterations in microRNA-34, microRNA-125b and microRNA-155 expression: correlation with embryonic p53 genotype and limb phenotype |
| Q101365503 | The Contribution of MicroRNAs to the Inflammatory and Neoplastic Characteristics of Erdheim-Chester Disease |
| Q38355126 | The U1 snRNP base pairs with the 5' splice site within a penta-snRNP complex |
| Q90168060 | The autism-mutated ADNP plays a key role in stress response |
| Q40645427 | The birth of an alternatively spliced exon: 3' splice-site selection in Alu exons |
| Q92036480 | The black sheep of the family- whole-exome sequencing in family of lithium response discordant bipolar monozygotic twins |
| Q37942571 | The impact of microRNAs on endocrinology |
| Q38161385 | The involvement of microRNAs in major depression, suicidal behavior, and related disorders: a focus on miR-185 and miR-491-3p |
| Q36041191 | The microRNA Transcriptome of Human Cytomegalovirus (HCMV) |
| Q89595735 | The pathogenicity of SLC38A8 in five families with foveal hypoplasia and congenital nystagmus |
| Q38248572 | The possible involvement of microRNAs in preeclampsia and gestational diabetes mellitus |
| Q42632463 | Toxicogenomic analysis of a sustained release local anesthetic delivery system |
| Q112710657 | Transcriptional Profiling of Mouse Eosinophils Identifies Distinct Gene Signatures Following Cellular Activation |
| Q45357123 | Vaccinia virus infection suppresses the cell microRNA machinery |
| Q91577328 | Variant PADI3 in Central Centrifugal Cicatricial Alopecia |
| Q91785371 | Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation |
| Q30432351 | Versatility of MicroRNA biogenesis |
| Q80238946 | Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomia |
| Q35903026 | Whole-Genome Sequencing Analysis from the Chikungunya Virus Caribbean Outbreak Reveals Novel Evolutionary Genomic Elements |
| Q87348440 | Whole-exome sequencing in individuals with multiple cardiovascular risk factors and normal coronary arteries |
| Q47827283 | X-linked elliptocytosis with impaired growth is related to mutated AMMECR1. |
| Q92599047 | [LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION] |
| Q91700460 | [THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES] |
| Q48063210 | miRNAkey: a software for microRNA deep sequencing analysis |
| Q24642140 | miRNAminer: a tool for homologous microRNA gene search |
| Q34157619 | miRviewer: a multispecies microRNA homologous viewer |
| Q39162532 | microRNA-125a-3p reduces cell proliferation and migration by targeting Fyn. |
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