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Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6446

2024

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Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease

Transfusion (Philadelphia, Pa.), 2023-05, Vol.63 (5), p.1100-1106

2023

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KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Blood, 2018-11, Vol.132 (Supplement 1), p.3640-3640

2018

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Haplotype analysis of α-thalassemia chromosomes reveals heterogeneity and multiple founders in Ashkenazi Jews

European journal of medical genetics, 2016-11, Vol.59 (11), p.555-558

2016

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Monitoring Minimal Residual Disease in RUNX1-Mutated Acute Myeloid Leukemia

Acta haematologica, 2022, Vol.145 (6), p.642-649

2022

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Hb TAYBE: clinical and morphological findings IN 43 patients

European journal of haematology, 2016-08, Vol.97 (2), p.137-144

2016

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Determining the Sex of Infanticide Victims from the Late Roman Era through Ancient DNA Analysis

Journal of archaeological science, 1998-09, Vol.25 (9), p.861-865

1998

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New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F

Hemoglobin, 2017-03, Vol.41 (2), p.144-146

2017

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The Y Chromosome Pool of Jews as Part of the Genetic Landscape of the Middle East

American journal of human genetics, 2001-11, Vol.69 (5), p.1095-1112

2001

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Haplotype Analysis of -α3.7 Chromosomes in Israeli Ethnic Groups Reveals Unexpected Heterogeneity and Demonstrates Ashkenazi Founder Groups in Carriers of α-Thalassemia

Blood, 2006-11, Vol.108 (11), p.1591-1591

2006

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Y-chromosomal STRs in two populations from Israel and the Palestinian Authority Area: Christian and Muslim Arabs

Forensic science international : genetics, 2011-11, Vol.5 (5), p.561-562

2011

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Y chromosome evidence for a founder effect in Ashkenazi Jews

European journal of human genetics : EJHG, 2005-03, Vol.13 (3), p.388-391

2005

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Genetic Evidence for the Expansion of Arabian Tribes into the Southern Levant and North Africa

American journal of human genetics, 2002-06, Vol.70 (6), p.1594-1596

2002

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Four Novel Deletions in Globin Genes Revealed by Multiplex Ligation Dependent Probe Amplification Assay (MLPA) Technology

Blood, 2006-11, Vol.108 (11), p.1593-1593

2006

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ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia

Clinical chemistry and laboratory medicine, 2010-12, Vol.48 (12), p.1713-1718

2010

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Sickle cell anemia in northern Israel: screening and prevention

The Israel Medical Association journal, 2009-04, Vol.11 (4), p.229-234

2009

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High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews

Human genetics, 2000-12, Vol.107 (6), p.630-641

2000

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Two Novel Mutations in the α-Globin Genes Leading to α-Thalassemia

Blood, 2004-11, Vol.104 (11), p.3773-3773

2004

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Diversity of α‐globin mutations and clinical presentation of α‐thalassemia in Israel

American journal of hematology, 2000-11, Vol.65 (3), p.196-203

2000

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Gaucher-like cells in beta-thalassemia patient after bone marrow transplantation

Journal of pediatric hematology/oncology, 2006-04, Vol.28 (4), p.203-204

2006

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Sequence analysis reveals a β-thalassaemia mutation in the DNA of skeletal remains from the archaeological site of Akhziv, Israel

Nature genetics, 1995-04, Vol.9 (4), p.365-368

1995

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Sex identification of archaeological human remains based on amplification of the X and Y amelogenin alleles

Gene, 1995-12, Vol.167 (1), p.327-332

1995

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Successful treatment with plasma exchange in life-threatening hyperhemolytic syndrome unrelated to sickle cell disease

Transfusion, 2023, Vol.63 (5), p.1100-1106

2023

Volltextzugriff (PDF)

Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.22-26

2001

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Rapid detection of the common mediterranean α‐globin deletions/rearrangements using PCR

American journal of hematology, 1998-08, Vol.58 (4), p.306-310

1998

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Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening

Successful treatment with plasma exchange in life‐threatening hyperhemolytic syndrome unrelated to sickle cell disease

KLF1 Mutations Are Not Common in Israel but Can Explain Occasional Cases of Elevated HbA2 or Very Elevated Fetal Hemoglobin

Haplotype analysis of α-thalassemia chromosomes reveals heterogeneity and multiple founders in Ashkenazi Jews

Monitoring Minimal Residual Disease in RUNX1-Mutated Acute Myeloid Leukemia

Hb TAYBE: clinical and morphological findings IN 43 patients

Determining the Sex of Infanticide Victims from the Late Roman Era through Ancient DNA Analysis

New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F

The Y Chromosome Pool of Jews as Part of the Genetic Landscape of the Middle East

Haplotype Analysis of -α3.7 Chromosomes in Israeli Ethnic Groups Reveals Unexpected Heterogeneity and Demonstrates Ashkenazi Founder Groups in Carriers of α-Thalassemia

Y-chromosomal STRs in two populations from Israel and the Palestinian Authority Area: Christian and Muslim Arabs

Y chromosome evidence for a founder effect in Ashkenazi Jews

Genetic Evidence for the Expansion of Arabian Tribes into the Southern Levant and North Africa

Four Novel Deletions in Globin Genes Revealed by Multiplex Ligation Dependent Probe Amplification Assay (MLPA) Technology

ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia

Sickle cell anemia in northern Israel: screening and prevention

High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews

Two Novel Mutations in the α-Globin Genes Leading to α-Thalassemia

Diversity of α‐globin mutations and clinical presentation of α‐thalassemia in Israel

Gaucher-like cells in beta-thalassemia patient after bone marrow transplantation

Sequence analysis reveals a β-thalassaemia mutation in the DNA of skeletal remains from the archaeological site of Akhziv, Israel

Sex identification of archaeological human remains based on amplification of the X and Y amelogenin alleles

Successful treatment with plasma exchange in life-threatening hyperhemolytic syndrome unrelated to sickle cell disease

Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392

Rapid detection of the common mediterranean α‐globin deletions/rearrangements using PCR

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