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A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (6), p.3232-3236

2001

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Opposing effects of the HLA-DRB10301-DQB10201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel

Genes and immunity, 2010-07, Vol.11 (5), p.423-431

2010

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

Genes and immunity, 2004-09, Vol.5 (6), p.493-504

2004

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Immunomodulation by chronobiologically-based glucocorticoids treatment for multiple sclerosis relapses

Journal of neuroimmunology, 2009-05, Vol.210 (1), p.124-127

2009

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Chronotherapy using corticosteroids for multiple sclerosis relapses

Journal of neurology, neurosurgery and psychiatry, 2007-08, Vol.78 (8), p.886-888

2007

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Mutations in CYP11B1 and Congenital Adrenal Hyperplasia in Moroccan Jews

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5463-5465

2005

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A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23

American journal of human genetics, 2000, Vol.66 (1), p.47-68

2000

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HLA immunogenetics of multiple sclerosis in Israeli arabs

Human immunology, 2009-11, Vol.70, p.S111-S111

2009

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Tight junction proteins in immune cells: new players in multiple sclerosis?

Multiple sclerosis, 2008-09, Vol.14, p.S231-S231

2008

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Cathepsins and their endogenous inhibitors cystatins in multiple sclerosis

Multiple sclerosis, 2008-09, Vol.14, p.S126-S126

2008

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Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype

European journal of human genetics : EJHG, 2002-11, Vol.10 (11), p.724-728

2002

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Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome

Genomics (San Diego, Calif.), 1999-04, Vol.57 (2), p.235-248

1999

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Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families

Journal of the American Academy of Dermatology, 2002-04, Vol.46 (4), p.510-516

2002

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Patterns of sensory intermodality relationships in the cerebral cortex of the rat

Journal of comparative neurology (1911), 1991-06, Vol.308 (3), p.432-456

1991

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Genes for the CPE Receptor (CPETR1) and the Human Homolog of RVP1 (CPETR2) Are Localized within the Williams–Beuren Syndrome Deletion

Genomics (San Diego, Calif.), 1998-12, Vol.54 (3), p.453-459

1998

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Functional characterization of mongoose nicotinic acetylcholine receptor α-subunit: resistance to α-bungarotoxin and high sensitivity to acetylcholine

FEBS letters, 1998-07, Vol.431 (3), p.411-414

1998

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How Does the Mongoose Cope with α-Bungarotoxin?: Analysis of the Mongoose Muscle AChR α-Subunit

Annals of the New York Academy of Sciences, 1998-05, Vol.841 (1), p.97-100

1998

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The nicotinic acetylcholine receptor of the mongoose; tricks ofevolution

Neuroscience letters, 1997-11, Vol.237, p.S17-S17

1997

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CDNA cloning of chick brain α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors reveals conservation of structure, function and post-transcriptional processes with mammalian receptors

Brain research. Molecular brain research., 1996-02, Vol.36 (1), p.101-113

1996

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Chapter 26 - Personalized Medicine and Theranostics: Applications to Multiple Sclerosis

Translational Neuroimmunology in Multiple Sclerosis, 2016, p.387-414

2016

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Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis

American journal of medical genetics, 2001-02, Vol.99 (1), p.54-58

2001

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A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4

Journal of human genetics, 2019-06, Vol.64 (6), p.589-595

2019

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Loss of CD55 in Eculizumab-Responsive Protein-Losing Enteropathy

The New England journal of medicine, 2017-07, Vol.377 (1), p.87-89

2017

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Gene expression profiling of the response to interferon beta in Epstein-Barr-transformed and primary B cells of patients with multiple sclerosis

PloS one, 2014-07, Vol.9 (7), p.e102331-e102331

2014

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The ubiquitin-proteasome pathway regulates claudin 5 degradation

Journal of cellular biochemistry, 2012-07, Vol.113 (7), p.2415-2423

2012

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A Single Nucleotide Polymorphism in the RAD51 Gene Modifies Cancer Risk in BRCA2 but Not BRCA1 Carriers

Opposing effects of the HLA-DRB10301-DQB10201 haplotype on the risk for multiple sclerosis in diverse Arab populations in Israel

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

Immunomodulation by chronobiologically-based glucocorticoids treatment for multiple sclerosis relapses

Chronotherapy using corticosteroids for multiple sclerosis relapses

Mutations in CYP11B1 and Congenital Adrenal Hyperplasia in Moroccan Jews

A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23

HLA immunogenetics of multiple sclerosis in Israeli arabs

Tight junction proteins in immune cells: new players in multiple sclerosis?

Cathepsins and their endogenous inhibitors cystatins in multiple sclerosis

Androgen receptor CAG repeat length in Jewish Israeli women who are BRCA1/2 mutation carriers: association with breast/ovarian cancer phenotype

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome

Junctional epidermolysis bullosa in the Middle East: Clinical and genetic studies in a series of consanguineous families

Patterns of sensory intermodality relationships in the cerebral cortex of the rat

Genes for the CPE Receptor (CPETR1) and the Human Homolog of RVP1 (CPETR2) Are Localized within the Williams–Beuren Syndrome Deletion

Functional characterization of mongoose nicotinic acetylcholine receptor α-subunit: resistance to α-bungarotoxin and high sensitivity to acetylcholine

How Does the Mongoose Cope with α-Bungarotoxin?: Analysis of the Mongoose Muscle AChR α-Subunit

The nicotinic acetylcholine receptor of the mongoose; tricks ofevolution

CDNA cloning of chick brain α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors reveals conservation of structure, function and post-transcriptional processes with mammalian receptors

Chapter 26 - Personalized Medicine and Theranostics: Applications to Multiple Sclerosis

Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis

A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4

Loss of CD55 in Eculizumab-Responsive Protein-Losing Enteropathy

Gene expression profiling of the response to interferon beta in Epstein-Barr-transformed and primary B cells of patients with multiple sclerosis

The ubiquitin-proteasome pathway regulates claudin 5 degradation

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