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Morphological and biochemical features of obesity are associated with mineralization genes' polymorphisms

International Journal of Obesity, 2010-08, Vol.34 (8), p.1308-1318

2010

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Association of heparanase gene (HPSE) single nucleotide polymorphisms with hematological malignancies

Leukemia, 2007-11, Vol.21 (11), p.2296-2303

2007

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Reply to ‘Lack of association of the heparanase gene single-nucleotide polymorphism Arg307Lys with acute lymphoblastic leukemia in patients from Northern Ireland’ by Winter et al

Leukemia, 2008-08, Vol.22 (8), p.1631-1631

2008

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Reply to Winter et al

Leukemia, 2008-08, Vol.22 (8), p.1632-1633

2008

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Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

American journal of human genetics, 1997-10, Vol.61 (4), p.813-821

1997

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Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2006-01, Vol.141B (1), p.91-95

2006

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HLA-A2 class I antigens in couples with recurrent spontaneous abortions

International Journal of Immunogenetics, 2007-08, Vol.34 (4), p.241-246

2007

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Multilocus consensus genetic maps (MCGM): Formulation, algorithms, and results

Computational biology and chemistry, 2006-02, Vol.30 (1), p.12-20

2006

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Possible Interaction between USH1B and USH3 Gene Products as Implied by Apparent Digenic Deafness Inheritance

American journal of human genetics, 1999-07, Vol.65 (1), p.261-265

1999

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Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis

Biological psychiatry (1969), 2004-08, Vol.56 (3), p.169-176

2004

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The human platelet αIIb gene is not closely linked to its integrin partner β3

Blood, 1999-09, Vol.94 (6), p.2039-2047

1999

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Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

American journal of human genetics, 1996-06, Vol.58 (6), p.1254-1259

1996

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Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor

Annals of human genetics, 2003-03, Vol.67 (2), p.153-164

2003

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Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation

Journal of leukocyte biology, 2009-08, Vol.86 (2), p.445-455

2009

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VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations

Journal of applied genetics, 2014-05, Vol.55 (2), p.163-171

2014

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Morpho-physiological features of human populations in the context of climatic--geographical conditions

Collegium antropologicum, 2012-09, Vol.36 (3), p.729-743

2012

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Genetic Mapping of the Gene for Usher Syndrome: Linkage Analysis in a Large Samaritan Kindred

Genomics (San Diego, Calif.), 1994-03, Vol.20 (1), p.36-42

1994

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Genotype and allele frequencies of C3435T polymorphism of the MDR1 gene in various Jewish populations of Israel

Therapeutic drug monitoring, 2004-12, Vol.26 (6), p.679

2004

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Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders

American journal of physical anthropology, 1997-10, Vol.104 (2), p.193-200

1997

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Pemphigus vulgaris in Jewish patients is associated with HLA-A region genes: mapping by microsatellite markers

Human Immunology, 2003-08, Vol.64 (8), p.771-779

2003

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Temperature Dependence of the Iron-Histidine Resonance Raman Band of Deoxyheme Proteins: Anharmonic Coupling Versus Distribution over Taxonomic Conformational Substates

Biophysical journal, 2004, Vol.86 (1), p.656-659

2004

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Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

The international journal of neuropsychopharmacology, 2007-06, Vol.10 (3), p.301-308

2007

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Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

Human molecular genetics, 1995-09, Vol.4 (9), p.1637-1642

1995

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Erroneous identification in a mixed population: simulation using Israeli STR data

International journal of legal medicine, 2004-04, Vol.118 (2), p.111-114

2004

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Morphological and biochemical features of obesity are associated with mineralization genes' polymorphisms

Association of heparanase gene (HPSE) single nucleotide polymorphisms with hematological malignancies

Reply to ‘Lack of association of the heparanase gene single-nucleotide polymorphism Arg307Lys with acute lymphoblastic leukemia in patients from Northern Ireland’ by Winter et al

Reply to Winter et al

Mutation Profile of All 49 Exons of the Human Myosin VIIA Gene, and Haplotype Analysis, in Usher 1B Families from Diverse Origins

Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel

HLA-A2 class I antigens in couples with recurrent spontaneous abortions

Multilocus consensus genetic maps (MCGM): Formulation, algorithms, and results

Possible Interaction between USH1B and USH3 Gene Products as Implied by Apparent Digenic Deafness Inheritance

Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis

The human platelet αIIb gene is not closely linked to its integrin partner β3

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3

Maternal and Paternal Lineages of the Samaritan Isolate: Mutation Rates and Time to Most Recent Common Male Ancestor

Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations

Morpho-physiological features of human populations in the context of climatic--geographical conditions

Genetic Mapping of the Gene for Usher Syndrome: Linkage Analysis in a Large Samaritan Kindred

Genotype and allele frequencies of C3435T polymorphism of the MDR1 gene in various Jewish populations of Israel

Usher syndrome in the Samaritans: Strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders

Pemphigus vulgaris in Jewish patients is associated with HLA-A region genes: mapping by microsatellite markers

Temperature Dependence of the Iron-Histidine Resonance Raman Band of Deoxyheme Proteins: Anharmonic Coupling Versus Distribution over Taxonomic Conformational Substates

Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population

Erroneous identification in a mixed population: simulation using Israeli STR data

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