D. Cohen

发表

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome.

H. Cann, J. Dausset, M. Lathrop, 1990, Genomics.

Improved control of partial DNA restriction enzyme digest in agarose using limiting concentrations of Mg++.

D. Le Paslier, H. Cann, J. Dausset, 1989, Nucleic acids research.

Non-isotopic and sensitive method for diagnosis of maternally-inherited diabetes and deafness

J. Dausset, P. Froguel, H. Blanché, 1994, Diabetologia.

Heterogeneity of HLA genetic factors in IDDM susceptibility

J. Dausset, D. Cohen, C. Boitard, 2004, Immunogenetics.

Clusters of HLA class II beta restriction fragments describe allelic series.

J. Dausset, J. Lalouel, D. Cohen, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

J. Dausset, D. Cohen, P. White, 1986, Human Genetics.

First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination

J. Dausset, J. Oury, D. Cohen, 1986, Human Genetics.

Association of class II HLA-Dβ chain DNA restriction fragments with multiple sclerosis

J. Dausset, R. Fauchet, D. Cohen, 2004, Immunogenetics.

Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers.

J. Weissenbach, J. McPherson, D. Le Paslier, 1994, American journal of human genetics.

Molecular Genetics of the HLA System: New Tools for the Study of HLA and Disease

J. Dausset, D. Cohen, 1984, Clinics in Immunology and Allergy.

HLA at the Gene Level

J. Dausset, D. Cohen, 1984 .

Recombinant DNA Technology: Its Use in the Study of HLA

J. Dausset, D. Cohen, E. Robbins, 1984 .

Cloning the human major histocompatibility complex in YACs.

D. Le Paslier, J. Dausset, D. Cohen, 1994, Genomics.

Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppression.

D. Le Paslier, D. Israeli, L. Cazes, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.

D. Le Paslier, D. Paslier, H. Cann, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Behavioral alterations associated with apoptosis and down-regulation of presenilin 1 in the brains of p53-deficient mice.

D. Israeli, J. Dausset, D. Cohen, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island.

D. Le Paslier, D. Paslier, D. Cohen, 1991, Science.

The CEPH YAC library.

J Dausset, D. Le Paslier, D. Paslier, 1992, Behring Institute Mitteilungen.

cells from T cell acute lymphoblastic leukemia T cell rearranging gene gamma: diversity and mRNA expression in fresh

D. Paslier, F. Sigaux, D. Cohen, 2011 .

T cell rearranging gene gamma: diversity and mRNA expression in fresh cells from T cell acute lymphoblastic leukemia

D. Paslier, F. Sigaux, D. Cohen, 1987 .

Polymorphic restriction endonuclease fragment segregates and correlates with the gene for HLA-B8.

H. Cann, J. Dausset, D. Cohen, 1983, Proceedings of the National Academy of Sciences of the United States of America.

European Gene Mapping Project (EUROGEM): Genetic Maps based on the CEPH reference families

J. Weissenbach, H. Cann, J. Attwood, 1994, European journal of human genetics : EJHG.

Relationship between Charcot-Marie-Tooth 1A and Smith-Magenis regions. snU3 may be a candidate gene for the Smith-Magenis syndrome.

D. Le Paslier, J. Bachellerie, A. Vignal, 1993, Human molecular genetics.

Isolation of chromosome 21–specific yeast artificial chromosomes from a total human genome library

D. Paslier, E. Barillot, R. Berger, 1992, Nature Genetics.

Genotyping with DNA probes in combined immunodeficiency syndrome with defective expression of HLA.

J. Dausset, D. Cohen, C. Griscelli, 1985, The New England journal of medicine.

A YAC contig in 6p23 based on sequence tagged sites.

J. Weissenbach, D. Le Paslier, H. Cann, 1994, Genomics.

A long-range physical map of human Chromosome 21q22.1 band from the YAC continuum

D. Paslier, A. Shiratori, D. Cohen, 1996, Mammalian Genome.

Different stimulating capacity of B and T lymphocytes in primary and secondary allogeneic reactions: cellular detection of HLA-D products on T lymphocytes.

J. Dausset, D. Cohen, D. Fradelizi, 1980, Journal of immunology.

Two DR beta allelic series defined by exon II-specific synthetic oligonucleotide genomic hybridization: a method of HLA typing?

J. Dausset, D. Cohen, P. Millasseau, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Suppression of the human allogenetic response in vitro with primed lymphocytes and suppressive supernates.

J. Dausset, D. Cohen, D. Fradelizi, 1980, The Journal of experimental medicine.

The CIC library: a large insert YAC library for genome mapping in Arabidopsis thaliana.

D. Le Paslier, D. Paslier, C. Camilleri, 1995, The Plant journal : for cell and molecular biology.

[Alpha genes of the T cell receptor: a possible implication in genetic susceptibility to multiple sclerosis].

J. Dausset, J. Strominger, D. Cohen, 1987, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

G. Gyapay, D. Le Paslier, A. Vignal, 1993, Nature genetics.

1.8-megabases fine physical map encompassing IFNAR and AML1 loci on human chromosome 21q22.1.

D. Le Paslier, A. Shiratori, D. Cohen, 1996, DNA sequence : the journal of DNA sequencing and mapping.

Generation of 28 sequence-tagged sites (STSs) from yeast artificial chromosome (YAC) clones anchored at human chromosome 21q22.1 region.

D. Le Paslier, A. Shiratori, D. Cohen, 1995, DNA sequence : the journal of DNA sequencing and mapping.

Phenotypic and genotypic heterogeneity in large granular lymphocyte expansion.

D. Le Paslier, D. Cohen, G. Flandrin, 1987, Leukemia.

A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.

D. Le Paslier, M. Stoffel, R. Espinosa, 1996, Proceedings of the National Academy of Sciences of the United States of America.

Association of class II HLA-DQ beta chain DNA restriction fragments with multiple sclerosis.

J. Dausset, R. Fauchet, D. Cohen, 1985, Immunogenetics.

Search for DNA sequence variations using a MutS-based technology.

J. Dausset, S. Lesage, D. Cohen, 1997, Mutation research.