D. Cohen

发表

Identification and characterization of a spinal muscular atrophy-determining gene

J. Weissenbach, D. Paslier, A. Munnich, 1995, Cell.

A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatellite

D. Paslier, D. Schlessinger, G. Sirugo, 1992, Human Genetics.

Integrated YAC contig containing the 3pl4.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B

D. Paslier, T. Glover, D. Cohen, 1994, Genes, chromosomes & cancer.

A first-generation physical map of the human genome

J. Weissenbach, I. Chumakov, Daniel Cohen, 1993, Nature.

Continuum of overlapping clones spanning the entire human chromosome 21q

X. Estivill, D. Cox, J. Weissenbach, 1992, Nature.

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

D. Paslier, D. Ward, E. Barillot, 1992, Cell.

Genetic and physiological data implicating the new human gene G72 and the gene for d-amino acid oxidase in schizophrenia

P. Sham, L. Cavarec, R. Straub, 2002, Proceedings of the National Academy of Sciences of the United States of America.

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

J. Weissenbach, D. Paslier, J. Claverie, 1991, Cell.

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Isabelle Richard, Charles E Jackson, Mayana Zatz, 1995, Cell.

A systematic study of HLA class II-beta DNA restriction fragments in insulin-dependent diabetes mellitus.

J. Dausset, J. Lalouel, D. Cohen, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Standardized Southern Blot Workshop Technique

P. O'Connell, D. Cohen, A. Marcadet, 1989 .

The gene for creatine kinase, mitochondrial 2 (sarcomeric; CKMT2), maps to chromosome 5q13.3.

J. Beckmann, I. Richard, D. Cohen, 1993, Genomics.

PP2A-Bgamma subunit and KCNQ2 K+ channels in bipolar disorder.

L. Cavarec, M. Lazdunski, F. Macciardi, 2007, The pharmacogenomics journal.

CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: outcome in searching for new dynamic mutations.

J. Weissenbach, H. Cann, S. Meier-Ewert, 1998, Genomics.

Correlation between an HLA-DQα length polymorphism of messenger RNA and serologically defined specificities (DQwl, DRw53, DR3 + 5)

J. Dausset, D. Cohen, F. Dautry, 2004, Immunogenetics.

Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21. 1 by fluorescence in situ hybridization.

H. Heng, L. Tsui, R. Pearlman, 1997, Genomics.

Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

J. Mandel, D. Cohen, V. Biancalana, 1995, American journal of human genetics.

Rearranging Gene “ y : Diversity and mRNA Expression in Fresh Cells From T Cell Acute Lymphoblastic Leukemia

D. Paslier, D. Cohen, P. Loiseau, 2005 .

Exuberant restriction fragment length polymorphism associated with the DQ alpha-chain gene and the DX alpha-chain gene.

C. Auffray, J. Dausset, J. Strominger, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Analysis of HLA class I genes with restriction endonuclease fragments: implications for polymorphism of the human major histocompatibility complex.

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

Exuberant restriction fragment length polymorphism associated with the DQ a-chain gene and the DX a-chain gene

J. Lalouel, D. Cohen, Jack, 2022 .

Human T cell gamma genes are frequently rearranged in B-lineage acute lymphoblastic leukemias but not in chronic B cell proliferations

D. Le Paslier, D. Paslier, J. Dausset, 1987, The Journal of experimental medicine.

Genetic mapping of a human class II antigen beta-chain cDNA clone to the SB region of the HLA complex.

C. Auffray, J. Seidman, J. Strominger, 1983, Proceedings of the National Academy of Sciences of the United States of America.

MOLECULAR GENETIC ANALYSES OF THE MAJOR HISTOCOMPATIBILITY COMPLEX IN PIG FAMILIES AND RECOMBINANTS

P. Chardon, D. Cohen, M. Vaiman, 1985, Journal of immunogenetics.

HLA-DR2-associated Dw subtypes correlate with RFLP clusters: most DR2 IDDM patients belong to one of these clusters

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

Polymorphism of the HLA DR1 haplotype in the Israeli population investigated at the serological, cellular, and genomic levels

D. Cohen, A. Friedmann, C. Brautbar, 2004, Immunogenetics.

DNA polymorphism in the major histocompatibility complex of man and various farm animals.

P. Chardon, D. Cohen, M. Vaiman, 2009, Animal genetics.

Analysis of the sheep MHC using HLA class I, II, and C4 cDNA probes

C. Auffray, J. Strominger, P. Chardon, 2004, Immunogenetics.

Restriction fragment length polymorphism of the major histocompatibility complex of the pig

P. Chardon, D. Cohen, M. Vaiman, 2004, Immunogenetics.

Extensive genomic polymorphism in mouse 21-hydroxylase region

D. Cohen, M. Pla, L. Degos, 2004, Immunogenetics.

A novel monoclonal antibody, 1B3.1, binds to a new epitope of the VLA-1 molecule.

L. Chess, D. Cohen, M. Brenner, 1989, Cellular immunology.

Nucleotide sequence of the HLA-A26 class I gene: identification of specific residues and molecular mapping of public HLA class I epitopes.

H. Zinszner, D. Cohen, L. Degos, 1990, Human immunology.

Molecular genetic analysis of the major histocompatibility complex in an ELA typed horse family.

P. Chardon, D. Cohen, M. Vaiman, 2009, Animal genetics.

Dense Alu clustering and a potential new member of the NFκB family within a 90 kilobase HLA Class III segment

Lydie Bougueleret, J. Claverie, J. Jurka, 1993, Nature Genetics.

Serological expression after sequential double transfection with purified HLA-11 gene of mouse fibroblasts carrying human beta-2 microglobulin

J. Dausset, D. Cohen, M. Pla, 2004, Immunogenetics.

Isolation from the Human MHC of a Class I Gene Encoding a Nonubiquitous Antigen Expressed on Activated Cells

J. Dausset, R. Fauchet, D. Cohen, 1989 .

Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis.

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

Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35.

J. Weissenbach, D. Le Paslier, D. Ward, 1994, Human molecular genetics.

Nomenclature for HLA-RFLP

J. Lalouel, D. Cohen, B. Dupont, 1989 .

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

P. Sham, L. Cavarec, R. Straub, 2002, Nature Reviews Genetics.

HLA Class II Typing by the Workshop Defined RFLP Specificities in Unrelated Individuals

D. Cohen, M. Martell, A. Marcadet, 1989 .

A Simple Method for Prenatal Diagnosis of Trisomy 21 on Uncultured Amniocytes

R. Berger, D. Cohen, S. Romana, 1993, European journal of human genetics : EJHG.

Isolation of a human major histocompatibility complex class I gene encoding a nonubiquitous molecule expressed on activated lymphocytes.

J. Dausset, R. Fauchet, D. Cohen, 1987, Proceedings of the National Academy of Sciences of the United States of America.

DNA Polymorphism of HLA Class I and Class II Regions

H. Cann, J. Dausset, J. Lalouel, 1985, Immunological reviews.

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

J. Beckmann, T. Foroud, J. Tischfield, 1992, Genomics.

A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p

J. Beckmann, J. Weissenbach, C. Antignac, 1993, Nature Genetics.

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

J. Rommens, R. Sherrington, E. Rogaev, 1995, Nature.

Construction and application of a YAC library

D. Paslier, H. Albertsen, D. Cohen, 1992 .

PP2A-Bγ subunit and KCNQ2 K+ channels in bipolar disorder

L. Cavarec, M. Lazdunski, F. Macciardi, 2007, The Pharmacogenomics Journal.

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

J. Weissenbach, H. Cann, S. Meier-Ewert, 1996, Human molecular genetics.

Identification and characterization of the familial adenomatous polyposis coli gene

Margaret Robertson, Jeff Stevens, Joanna Groden, 1991, Cell.

Mapping of the X-Breakpoint Involved in a Balanced X;12 Translocation in a Female with Mild Mental Retardation

P. Billuart, D. Cohen, J. Chelly, 1997, European journal of human genetics : EJHG.

Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region

A. Monaco, D. Bentley, D. Paslier, 1992, Nature Genetics.

Identification of deletion mutations and three new genes at the familial polyposis locus

J. McPherson, D. Paslier, J. Warrington, 1991, Cell.

Restriction Fragment Length Polymorphism of HLA Genes: Summary of the Tenth International Workshop Southern Blot Analysis

J. Lalouel, D. Cohen, B. Dupont, 1989 .

The V gamma locus of the human T cell receptor gamma gene. Repertoire polymorphism of the first variable gene segment subgroup

H. Cann, J. Dausset, F. Sigaux, 1988, The Journal of experimental medicine.

A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes.

X. Chen, J. Korenberg, D. Cohen, 1995, Genome research.

RFLP Standardization Report for DR Beta/TaqI

D. Cohen, R. Walford, I. Legall, 1989 .

RFLP Standardization Report for DQ Alpha/TaqI

R. Bontrop, D. Cohen, R. Walford, 1989 .

Mapping of two chromosome 15 microsatellites.

J. Beckmann, I. Richard, F. Fougerousse, 1992, Genomics.

RFLP Standardization Report for DQ Beta/TaqI

D. Cohen, R. Walford, M. Martell, 1989 .

Allelic Class II Determinants Defined by PLT Typing

J. Dausset, D. Cohen, J. Hors, 1984 .

HLA-DP genotyping in HLA-A,B, and DR identical intrafamilial bone marrow transplantation.

D. Cohen, E. Gluckman, C. Raffoux, 1990, Leukemia.

Organization and Design of the Southern Blot Component of the Tenth Histocompatibility Workshop

D. Cohen, B. Dupont, A. Marcadet, 1989 .

DNA-RFLP Analysis: HLA-DR Beta Workshop Report

J. Lalouel, D. Cohen, J. Tiercy, 1989 .

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q

M. Lathrop, J. Melki, J. Aicardi, 1990, Nature.

A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C).

J. Weissenbach, F. Crozet, D. Weil, 1995, Genomics.

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families.

J. Beckmann, C. Hengstenberg, F. Fougerousse, 1992, Circulation research.

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families.

J. Weissenbach, M. Passos-Bueno, I. Richard, 1993, Journal of medical genetics.

Targeted development of microsatellite markers from inter-Alu amplification of YAC clones.

J. Beckmann, I. Richard, D. Cohen, 1994, Genomics.

THE Vy LOCUS OF THE HUMAN T CELL RECEPTOR y GENE Repertoire Polymorphism of the First Variable Gene Segment Subgroup

Pascale Fung, D. Cohen, Zhu, 1988 .

Exclusion ofCardiac MyosinHeavyChainand Actin GeneInvolvement inHypertrophic Cardiomyopathy ofSeveral FrenchFamilies

J. Beckmann, C. Hengstenberg, M. Desnos, 2011 .

DNA polymorphism related to the idiopathic hemochromatosis gene: evidence in a recombinant family

I. Gicquel, R. Fauchet, M. Simon, 1986, Human Genetics.

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (vol 99, pg 13675, 2002)

P. Sham, L. Cavarec, R. Straub, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

K H Buetow, J C Murray, J. Weber, 1994, Science.

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.

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

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

"Retroposon" insertion into the cellular oncogene c-myc in canine transmissible venereal tumor.

J. B. Cohen, T. Unger, D. Givol, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Preferential localization of the limb-girdle muscular dystrophy type 2A gene in the proximal part of a 1-cM 15q15.1-q15.3 interval.

J. Beckmann, N. Chiannilkulchai, J. Tischfield, 1995, American journal of human genetics.

Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy.

J. Beckmann, N. Chiannilkulchai, I. Chumakov, 1994, Human molecular genetics.

method for selecting at least one screen for mutations, its application to a method for rapid identification of alleles of polymorphic systems and device for its implementation óoeuvre.

J. Dausset, L. Bougueleret, D. Cohen, 1991 .

The CEPH YAC library.

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

Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

J. Beckmann, N. Chiannilkulchai, F. Duclos, 1996, Neuromuscular Disorders.

Preferential Localization oftheLimb-Girdle Muscular Dystrophy

N. Chiannilkulchai, J. Tischfield, N. Bourg, 1995 .

Exclusion of cardiac myosin heavy chain and actin gene involvement in hypertrophic cardiomyopathy of several French families.

J. Beckmann, C. Hengstenberg, F. Fougerousse, 1992, Circulation research.