N. Avidan

发表

High-resolution linkage analysis and physical characterization of the EIX-responding locus in tomato

G. Martin, A. Avni, D. Zamir, 2000, Theoretical and Applied Genetics.

Loss of antigenic epitopes as the result of env gene recombination in retrovirus-induced leukemia in immunocompetent mice.

B. Overmoyer, N. Avidan, K. Tumas, 1993, Virology.

Personalized Medicine and Theranostics

E. Staun-ram, N. Avidan, I. Lejbkowicz, 2016 .

USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses

Tsviya Olender, Doron Lancet, Shmuel Pietrokovski, 2002, European Journal of Human Genetics.

Integrative analysis of methylome and transcriptome in human blood identifies extensive sex- and immune cell-specific differentially methylated regions

Ariel Miller, E. Staun-ram, N. Avidan, 2015, Epigenetics.

Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis.

O. Sarig, M. Indelman, R. Bergman, 2010, The Journal of investigative dermatology.

Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy.

J. R. MacDonald, S. Scherer, J. Beckmann, 2005, American journal of human genetics.

Identification of the gene causing mucolipidosis type IV

Gustavo Glusman, D. Lancet, A. Frumkin, 2000, Nature Genetics.

Genetic Basis of Thoracic Aortic Aneurysms and Dissections

D. Milewicz, N. Avidan, V. Tran-Fadulu, 2006, Annals of the New York Academy of Sciences.

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.

Robert K. Yu, E. Boerwinkle, J. Grotta, 2009, American journal of human genetics.

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (vol 39, pg 1488, 2007)

Robert K. Yu, S. Shete, D. Milewicz, 2008 .

Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Robert K. Yu, S. Shete, D. Milewicz, 2007, Nature Genetics.

Corrigendum: Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Robert K. Yu, S. Shete, D. Milewicz, 2008, Nature Genetics.

Involvement of ethylene in growth induction of stationary tobacco pith tissue in vitro

S. Lavee, N. Avidan, A. Parnes, 2010, Plant Cell, Tissue and Organ Culture (PCTOC).

heterogeneity in congenital dyserythropoietic anemia type I gene reveals genetic CDAN1 Linkage and mutational analysis of the

P. Vyas, D. Higgs, H. Tamary, 2011 .

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.

P. Vyas, D. Higgs, H. Tamary, 2006, Blood.

We Also Investigated 6 Sporadic Cases with Cda I for Cdan1

H. Tamary, W. Wood, N. Avidan, 2006 .

Glutamine synthetase protects against neuronal degeneration in injured retinal tissue

R. Gorovits, N. Avidan, L. Vardimon, 1997, Neuroscience Letters.

Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1.

M. Hattori, Y. Sakaki, Gustavo Glusman, 2001, Gene.

Role of T-cell subsets in acute and persistent E-55+ murine leukemia virus infection in susceptible progressor and resistant long-term nonprogressor mouse strains

N. Avidan, K. Blank, T. Sieck, 1997 .

Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers

J. Beckmann, I. Pe’er, D. Lancet, 2007, Pharmacogenetics and genomics.

Chlorogenic acid - an independent morphgenesis regulator or a cofactor.

R. Pierik, S. Lavee, N. Avidan, 1994 .

Molecular Characterization of Common Olive Varieties in Israel and the West Bank Using Randomly Amplified Polymorphic DNA (RAPD) Markers

B. Quebedeaux, S. Lavee, Z. Wiesman, 1998 .

Genomic profiling of interpopulation diversity guides prioritization of candidate-genes for autoimmunity

J. Beckmann, D. Lancet, Ariel Miller, 2004, Genes and Immunity.

Opposing effects of the HLA-DRB1*0301-DQB1*0201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel

J. Oksenberg, J. Wang, N. Avidan, 2010, Genes and Immunity.

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Tsviya Olender, Doron Lancet, Jacques S. Beckmann, 2001, Nature Genetics.

Genetic basis of myasthenia gravis - a comprehensive review.

Ariel Miller, N. Avidan, S. Berrih-Aknin, 2014, Journal of autoimmunity.

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.

J. Beckmann, D. Lancet, H. Tamary, 2002, American journal of human genetics.

Sequence, structure, and evolution of a complete human olfactory receptor gene cluster.

G Glusman, D. Lancet, S. Clifton, 2000, Genomics.

Recruitment of transcriptional effectors by Cas9 creates cis regulatory elements and demonstrates distance-dependent transcriptional regulation

Noam Kaplan, N. Avidan, I. Kehat, 2022, bioRxiv.

Analysis of genetic polymorphisms in acetylcholinesterase as reflected in different populations.

J. Beckmann, J. Sussman, A. Korczyn, 2005, Current Alzheimer research.

HUMAN MUTATION 24:408^416 (2004) RESEARCH ARTICLE A Paradigm for Single Nucleotide Polymorphism Analysis: The Case of the Acetylcholinesterase

J. Beckmann, J. Sussman, A. Korczyn, 2022 .

Exome Sequencing Identifies SMAD3 Mutations as a Cause of Familial Thoracic Aortic Aneurysm and Dissection With Intracranial and Other Arterial Aneurysms

M. Rieder, J. Shendure, D. Nickerson, 2011, Circulation research.

Mechanisms for evolving hypervariability: the case of conopeptides.

Y. Gilad, E. Ben‐Asher, N. Avidan, 2001, Molecular biology and evolution.

Possible juvenile-related proteins in olive tree tissues

S. Lavee, N. Avidan, J. L. Garcia, 2000 .

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia

Doron Lancet, Fabio Macciardi, Daniela Amann-Zalcenstein, 2006, European Journal of Human Genetics.

Fine mapping of a schizophrenia susceptibility locus at chromosome 6q23: increased evidence for linkage and reduced linkage interval

J. Beckmann, K. Kanyas, B. Lerer, 2005, European Journal of Human Genetics.

Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmia.

D. Lancet, D. Bercovich, E. Feldmesser, 2007, Chemical senses.

Gene Expression Profiling of the Response to Interferon Beta in Epstein-Barr-Transformed and Primary B Cells of Patients with Multiple Sclerosis

Ariel Miller, N. Avidan, I. Lejbkowicz, 2014, PloS one.

Clinical and molecular variability in congenital dyserythropoietic anaemia type I

H. Tamary, I. Yaniv, B. Bader-Meunier, 2005, British journal of haematology.

CATSPER2, a human autosomal nonsyndromic male infertility gene

J. Beckmann, D. Lancet, H. Tamary, 2003, European Journal of Human Genetics.

Trick or treat: The effect of placebo on the power of pharmacogenetic association studies

J. Beckmann, I. Pe’er, N. Avidan, 2005, Human Genomics.

VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis

B. Lie, H. Harbo, S. Horn-Saban, 2014, Annals of clinical and translational neurology.

Interferon-Beta Induces Distinct Gene Expression Response Patterns in Human Monocytes versus T cells

Ron Y. Pinter, Ariel Miller, R. Pinter, 2013, PloS one.

Translation towards personalized medicine in Multiple Sclerosis

Ron Y. Pinter, Ariel Miller, R. Pinter, 2008, Journal of the Neurological Sciences.

The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23

D. Lancet, K. Kanyas, B. Lerer, 2006, Molecular Psychiatry.

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

D. Lancet, O. Man, M. Eldar, 2001, American journal of human genetics.

Active and passive immune responses of Yaez (ibex × goat) kids, and their associations with growth performance

N. Avidan, J. Hillel, D. Rattner, 1990 .

Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins.

L. Servais, Ariel Miller, E. Staun-ram, 2017, Journal of autoimmunity.

âMAALOTâ A NEW CULTIVAR FOR OIL EXTRACTION RESISTANT TO SPILOCAEA OLEAGINA (CAST.)

S. Lavee, N. Avidan, A. Trapero, 1999 .

AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia

J. Beckmann, W. Maier, R. Ebstein, 2007, European Journal of Human Genetics.

PROTEIN CONTENT AND COMPOSITION OF LEAVES AND SHOOT BARK IN RELATION TO ALTERNATE BEARING OF OLIVE TREES (OLEA EUROPAEA L.)

S. Lavee, N. Avidan, 1994 .

PHENOLIC ACIDS - POSSIBLE INVOLVEMENT IN REGULATING GROWTH AND ALTERNATE FRUITING IN OLIVE TREES.

S. Lavee, N. Avidan, H. Harshemesh, 1986 .

Mutational analysis of the CDAN1 gene in familial and sporadic congenital dyserythropoietic anaemia type 1

P. Vyas, H. Tamary, W. Wood, 2003 .

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

H. Tamary, I. Yaniv, B. Bader-Meunier, 2004 .

The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition

David M. Eagleman, Suzanne M. Leal, S. Leal, 2011, Behavioural Brain Research.

MTIA: First Generation Silicon Targeting Meta's Recommendation Systems

Martin D. Schatz, Krishna Shankara Narayanan, Jordan Fix, 2023, ISCA.

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

D. Lancet, M. Eldar, T. Olender, 2001, Cold Spring Harbor symposia on quantitative biology.

Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections

Timothy B Sackton, Jay D. Evans, Jay D Evans, 2007, Nature Genetics.

Mucolipidosis type IV: Novel MCOLN1 mutations in Jewish and non‐Jewish patients and the frequency of the disease in the Ashkenazi Jewish population

D. Lancet, A. Frumkin, N. Avidan, 2001, Human mutation.

The genetics of colored sequence synesthesia: Suggestive evidence of linkage to 16q and genetic heterogeneity for the condition

S. Leal, D. Eagleman, D. Milewicz, 2011, Behavioural Brain Research.

The genetics of colored sequence synesthesia: Evidence of linkage to chromosome 16q and genetic heterogeneity for the condition

S. Leal, D. Eagleman, D. Milewicz, 2009 .