A. Oppenheim

发表

Tracing European founder lineages in the Near Eastern mtDNA pool.

A. Di Rienzo, R. Villems, T. Kivisild, 2000, American journal of human genetics.

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

M. Faerman, A. Oppenheim, C. Greenblatt, 1995, Gene.

DNA methylation pattern is determined by the intracellular level of the methylase.

M. Szyf, A. Razin, A. Oppenheim, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Intrinsic potential for high fetal hemoglobin production in a Druze family with β-thalassemia is due to an unlinked genetic determinant

H. Kazazian, A. Oppenheim, Corinne Wong, 1990, Human Genetics.

Hypomethylation of DNA derived from purified human erythroid cells correlates with gene activity of the beta-globin cluster.

A. Oppenheim, E. Fibach, A. Goldfarb, 1985, Blood.

Molecular Studies of β‐Thalassemia in Israel

H. Kazazian, A. Oppenheim, D. Filon, 1990 .

Beta-thalassemia: analysis of mRNA precursors of a mutant human globin gene with defective splicing using peripheral blood nucleated red blood cells.

R. Treisman, T. Maniatis, A. Oppenheim, 1986, Hemoglobin.

Two mutations in the beta-globin polyadenylylation signal reveal extended transcripts and new RNA polyadenylylation sites.

H. Kazazian, A. Oppenheim, E. Rachmilewitz, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Genetic analysis of β‐thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype

A. Oppenheim, D. Filon, E. Rachmilewitz, 1997, American journal of hematology.

Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.

H. Kazazian, A. Oppenheim, D. Filon, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Mean corpuscular volume of heterozygotes for beta-thalassemia correlates with the severity of mutations.

A. Oppenheim, D. Filon, E. Rachmilewitz, 1992, Blood.

Proliferation and maturation of human erythroid progenitors in liquid culture.

A. Oppenheim, E. Fibach, A. Oppenheim, 1989, Blood.

The origin of sickle cell alleles in Israel

A. Oppenheim, O. Shalev, D. Rund, 1990, Human Genetics.

Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.

A. Oppenheim, L. Luzzatto, P. Mason, 1990, American journal of human genetics.

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

A. Oppenheim, D. Filon, D. Rund, 2000 .

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

A. Oppenheim, D. Filon, D. Rund, 1998 .

The Y chromosome pool of Jews as part of the genetic landscape of the Middle East.

P. Majumder, M. Faerman, A. Oppenheim, 2001, American journal of human genetics.

From a dry bone to a genetic portrait: A case study of sickle cell anemiaThe contribution of the first and the second authors is equal.

Mark George Thomas, N. Bradman, M. Faerman, 2000 .

From a dry bone to a genetic portrait: a case study of sickle cell anemia.

N. Bradman, M. Faerman, A. Oppenheim, 2000, American journal of physical anthropology.

Severe thalassaemia intermedia caused by interaction of homozygosity for α‐globin gene triplication with heterozygosity for β thalassaemia

A. Oppenheim, D. Filon, D. Rund, 1994 .

Adult and neonatal patterns of human globin gene expression are recapitulated in liquid cultures.

A. Oppenheim, E. Fibach, E. Rachmilewitz, 1992, Experimental hematology.

G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews

T. Vulliamy, A. Oppenheim, L. Luzzatto, 1993, Human Genetics.

Spectrum of β‐thalassemia mutations in the Gaza area

A. Oppenheim, T. Tulchinsky, D. Filon, 1995 .

Sickle cell trait in a white Jewish family presenting as splenic infarction at high altitude

A. Oppenheim, C. Levene, O. Shalev, 1988, American journal of hematology.

Expression of beta-globin in primary erythroid progenitors of beta-thalassemia patients using an SV40-based gene delivery system.

A. Oppenheim, N. Dalyot-Herman, D. Rund, 1999, Journal of hematotherapy & stem cell research.

Erythropoietin triggers a burst of GATA-1 in normal human erythroid cells differentiating in tissue culture.

A. Oppenheim, S. Ottolenghi, A. Ronchi, 1993, Nucleic acids research.

Molecular Analysis of β-Thalassemia in Vietnam

A. Oppenheim, D. Filon, E. Rachmilewitz, 2000, Hemoglobin.

Evolution of a genetic disease in an ethnic isolate : ,-Thalassemia in the Jews of Kurdistan ( mutations / human I-globin gene / polymerase chain reaction / malarial selection )

H. Kazazian, A. Oppenheim, D. Filon, 2022 .

Diversity of alpha-globin mutations and clinical presentation of alpha-thalassemia in Israel.

A. Oppenheim, D. Filon, D. Rund, 2000, American journal of hematology.

Spectrum of beta-thalassemia mutations in the Gaza area.

A. Oppenheim, T. Tulchinsky, D. Filon, 1995, Human mutation.

Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.

H. Ostrer, M. Hammer, M. Jobling, 2000, Proceedings of the National Academy of Sciences of the United States of America.

A novel mechanism generating short deletion/insertions following slippage is suggested by a mutation in the human alpha2-globin gene.

A. Oppenheim, D. Filon, D. Rund, 1997, Human molecular genetics.

Analysis of beta-globin mutations shows stable mixed chimerism in patients with thalassemia after bone marrow transplantation.

A. Nagler, A. Oppenheim, D. Filon, 1995, Blood.

Analysis of & Globin Mutations Shows Stable Mixed Chimerism in Patients With Thalassemia After Bone Marrow Transplantation

A. Nagler, A. Oppenheim, J. Kapelushnik, 2002 .

Second transplantation using allogeneic peripheral blood stem cells in a β‐thalassaemia major patient featuring stable mixed chimaerism

A. Nagler, A. Oppenheim, D. Filon, 1996, British journal of haematology.

A patient of German descent with (delta beta)0-thalassemia carrying the Sicilian type deletion of the delta and beta globin genes.

A. Shenhav, A. Oppenheim, G. Glaser, 1988, Hemoglobin.

The Relevance of Mean Corpuscular Volume of Heterozygotes to Prenatal Diagnosis of β‐Thalassemia a

A. Oppenheim, D. Filon, E. Rachmilewitz, 1990 .

Improved single-step PCR assay for sex identification post-allogeneic sex-mismatched BMT.

A. Oppenheim, S. Slavin, T. Pugatsch, 1996, Bone marrow transplantation.

Detection of Specific Bglobin Mutations in Kurdish Jews with β-Thalassmia

A. Oppenheim, J. Katzhendler, J. Deutsch, 1988 .

Hypercholesterolemia in five Israeli Christian-Arab kindreds is caused by the “Lebanese” allele at the low density lipoprotein receptor gene locus and by an additional independent major factor

Y. Friedlander, A. Oppenheim, E. Leitersdorf, 1991, Human Genetics.

An unexpectedly high frequency of heterozygosity for α-thalassemia in Ashkenazi Jews

A. Oppenheim, D. Filon, T. Sacha, 2004 .

An unexpectedly high frequency of heterozygosity for alpha-thalassemia in Ashkenazi Jews.

A. Oppenheim, D. Filon, T. Sacha, 2004, Blood cells, molecules & diseases.

Rapid detection of the common Mediterranean alpha-globin deletions/rearrangements using PCR.

A. Oppenheim, D. Filon, D. Rund, 1998, American journal of hematology.

Isolation of Bacillus anthracis, the agent of anthrax, in the Etosha National Park

A. Oppenheim, B. Turnbull, Hofmeyer, 1986 .

Isolation, Migration and Health: Genetic distance analyses in Israeli groups using classical markers and DNA polymorphisms in the β globin gene

A. Oppenheim, A. Ticher, A. Zoossmann-Diskin, 1992 .

A frameshift mutation in codon 10 of the β‐globin gene

A. Oppenheim, D. Filon, D. Rund, 1995 .

Silent carrier β-thalassaemia due to a severe β-globin mutation interacting with other genetic elements

A. Oppenheim, D. Filon, D. Rund, 1993, European Journal of Pediatrics.

Diversity of beta-globin mutations in Israeli ethnic groups reflects recent historic events.

H. Kazazian, A. Oppenheim, A. Shaag, 1994, American journal of human genetics.