Publication List

JACQUES S. BECKMANN

PUBLICATION LIST

A. In Refereed Journals

1Daniel, V., S. Sarid, J.S. Beckmann and U.Z. Littauer (1970). In vitro transcription of a transfer RNA gene. Proc. Natl. Acad. Sci. U.S.A. 66: 2160-2166.

2Beckmann, J.S., V. Daniel, Y. Tichauer and U.Z. Littauer (1971). Binding of the termination factor rho to DNA. Biochem. Biophys. Res. Comm. 43: 806-813.

3Daniel, V., J.S. Beckmann, S. Sarid, J.I. Grimberg, M. Herzberg and U.Z. Littauer (1971). Purification and in vitro transcription of a tRNA gene. Proc. Natl. Acad. Sci. U.S.A. 68: 2268-2272.

4Schmitt, H., J.S. Beckmann and U.Z. Littauer (1973). Transcription of supercoiled mitochondrial DNA by bacterial RNA polymerase. Eur. J. Biochem. 47: 225-234.

5Beckmann, J.S. and V. Daniel (1974). Transcriptional control of in vitro tRNATyrsynthesis. Biochem. 13: 4058-4062.

6Mergeay, M., D. Gigot, J.S. Beckmann, N. Glansdorff and A. Piérard (1974). Physiology and genetics of carbamoyl phosphate synthesis in E. coli K12. Mol. gen. Genet. 133: 299-316.

7Beckmann, J.S. (1974). The isolation and transcription of a tRNA gene. Ph. D. Thesis, The Weizmann Inst. of Sciences, Rehovot, Israël.

8Beckmann, J.S. and V. Daniel (1974). Relative stabilities of RNA/DNA hybrids. J. mol. Biol. 89: 355-362.

9Bishop, J.O., J.S. Beckmann, M.S. Campo, N.D. Hastie, M. Izquierdo and S. Perlman (1975). DNA-RNA hybridizations. Proceed. Royal Society, London 272: 147-157.

10Beckmann, J.S., P.F. Johnson and J. Abelson (1977). Cloning of Yeast Transfer RNA Genes in E. coli. Science 196: 205-208.

11Knapp, G., J.S. Beckmann, P.F. Johnson, S.A. Fuhrman and J. Abelson (1978). Transcription and Processing of Intervening Sequences in Yeast tRNA Genes. Cell 14: 221-236.

12Ogden, R.C., J.S. Beckmann, J. Abelson, H.S. Kang, D. Söll and O. Schmidt (1979). Transcription and Processing of a Yeast tRNA Gene Containing an Intervening Sequence. Cell 17: 399-406.

13Schmidt, O., J. Mao, R. Ogden, J.S. Beckmann, H. Sakano, J. Abelson and D. Söll (1980). Dimeric tRNA precursor in yeast. Nature 287: 750-752.

14Salts, Y. and J.S. Beckmann (1981). Chloroplast DNA isolation from Petunia and Nicotiana. Plant Mol. Biol. Newslett. 2: 73-76.

15Lifshitz, I., S. Izhar and J.S. Beckmann (1982). Isolation of circular mitochondrial DNA from suspension culture cells in Petunia. Plant Mol. Biol. Newslett. 3: 6-7.

16Bawnik, N., J.S. Beckmann, S. Sarid and V. Daniel (1983). Isolation and nucleotide sequence of a plant tRNA gene. Nucl. Ac. Research 11: 1117-1122.

17Burr, B., S.V. Evola, F.A. Burr and J.S. Beckmann (1983). The Application of Restriction Fragment Length Polymorphism to Plant Breeding. in: Genetic Engineering: Principles and Methods (Eds J.K. Setlow and A. Hollaender, Plenum Press, New York, NY), Vol 5: 45-59.

18Soller, M. and J.S. Beckmann (1983). Genetic Polymorphism in Varietal Identification and Genetic Improvement. Theor. appl. Genet. 67: 25-33.

19Beckmann, J.S. and M. Soller (1983). Restriction Fragment Length Polymorphisms in Genetic Improvement: Methodologies, Mapping and Costs. Theor. appl. Genet. 67: 35-43.

20Bar-Nun, S., Y. Shneyour and J.S. Beckmann (1983). G-418, an elongation inhibitor of 80S ribosomes. Biochem. Biophys. Acta 741: 123-127.

21Shneyour, Y., A. Zelcer, S. Izhar and J.S. Beckmann (1984). A simple feeder-layer technique for the plating of plant cells and protoplasts at low density. Plant Sci. Letters 33: 293-302.

22Salts, Y., R. Herrmann, N. Peleg, U. Lavi, S. Izhar, R. Frankel and J.S. Beckmann (1984). Physical mapping of chloroplast DNA variation among ten Nicotiana species. Theor. appl. Genet. 69: 1-14.

23Barg, R., N. Peleg, M. Perl and J.S. Beckmann (1984). Isolation of methotrexate-resistant cell lines in Petuniahybrida upon stepwise selection procedure. Plant mol. Biol. 3: 303-311.

24Beckmann, J.S. (1984). Germ-line gene therapy: a misnomer. Nature 312: 408.

25Rom, M. and J.S. Beckmann (1985). Genetic engineering: DNA polymorphisms, a new tool for genetic identification and mapping. Mada (Science, in Hebrew) 29: 123-128.

26Schwartzberg, D., S. Izhar and J.S. Beckmann (1985). Tobacco callus line tolerant to amitrole: selection, regeneration of plants and genetic analysis. J. Plant Physiol. 121: 29-35.

27Salts, Y., J.S. Beckmann, A. Loyter and U. Lavi (1985). Interactions of Sendai Viruses with Plant Protoplasts. Plant Sci. 41: 141-149.

28Beckmann, J.S. and M. Soller (1986). Restriction Fragment Length Polymorphisms and Genetic Improvement of Agricultural Species. Euphytica 35: 111-124.

29Beckmann, J.S. (1986). Intransigence in 'Genetic Engineering': Transgenics or Generics. Trends in Biotechnol. 4: 32.

30Beckmann, J.S., Y. Kashi, E.M. Hallerman, A. Nave and M. Soller (1986). Restriction Fragment Length Polymorphism among Israeli Holstein-Friesian Dairy Bulls. Anim. Genet. 17: 25-38.

31Soller, M. and J.S. Beckmann (1986). Restriction Fragment Length Polymorphisms in Poultry Breeding. Poultry Science 65: 1474-1488.

32Brendel, V., J.S. Beckmann and E.N. Trifonov (1986). Linguistics of Nucleotide Sequences: Morphology and Comparison of Vocabularies. J. of Biomol. Struct. & Dynamics 4: 11-21.

33Beckmann, J.S.,V. Brendel and E.N. Trifonov (1986). Intervening Sequences Exhibit their own Vocabularies. J. of Biomol. Struct. & Dynamics 4: 391-400.

34Lebowitz, R.J., M. Soller and J.S. Beckmann (1986). Trait-Based Analyses for the Detection of Linkage between Marker Loci and Quantitative Trait Loci in Crosses between Inbred Lines. Theor. appl. Genet. 72: 556-562.

35Beckmann, J.S. and M. Bar-Joseph (1986). The use of synthetic DNA probes in breeders' rights protection: a proposal to superimpose an alpha-numerical code on the DNA. Trends in Biotechnol. 4: 230-232.

36Hallerman, E., Y. Kashi, A. Nave, J.S. Beckmann and M. Soller (1986). Restriction Fragment Length Polymorphisms in Dairy Cattle and Their Utilization for Genetic Improvement. World Rev. Anim. Prod. 22: 31-38.

37Barg, R., M. Perl and J.S. Beckmann (1987). Elevated amounts of methotrexate-binding protein, different from normal dihydrofolate reductase, in a petunia MTXR-cell line. Plant mol. Biol. 8: 87-94.

38Hallerman, E., A. Nave, Y. Kashi, M. Soller and J.S. Beckmann (1987). Restriction Fragment Length Polymorphisms in Dairy and Beef Cattle at the Growth Hormone and Prolactin Loci. Anim. Genet. 18: 213-222.

39Soller, M. and J.S. Beckmann (1987). Cloning of Quantitative Trait Loci by Means of Insertional Mutagenesis. Theor. appl. Genet. 74: 369-378.

40Soller, M. and J.S. Beckmann (1988). Genomic Genetics and the Utilization for Breeding Purposes of Genetic Variation between Populations. In: Proceedings of the Second International Conference on Quantitative Genetics (Eds: B.S. Weir, E.J. Eisen, M.M. Goodman and G. Namkoong). Sinauer, Sunderland, Massachusetts, Pp 161-188.

41Hallerman, E.M., J.S. Beckmann and M. Soller (1987). Statistical Power of the North Carolina Experiment III Design in Determining the Likelihood of Success of Pedigree Breeding Programs in Selfing Plants. Heredity 59: 431-440.

42Beckmann, J.S. and M. Soller (1988). Detection of linkage between marker loci and loci affecting quantitative traits in crosses between segregating populations. Theor. appl. Genet. 76: 228-236.

43Delarbre, C., Y. Kashi, P. Boursot, J.S. Beckmann,P. Kourilsky, F. Bonhomme and G. Gachelin (1988). Phylogenetic distribution in the genus Mus of t-complex-specific DNA and protein markers: inferences on the origin of t-haplotypes. Mol. Biol. & Evol. 5: 120-133.

44Hallerman, E.M., J.L. Theilmann, J.S. Beckmann, M. Soller and J.E. Womack (1988). Mapping of Bovine Prolactin and Rhodopsin Genes in Hybrid Somatic Cells. Anim. Genet. 19: 123-132.

45Hallerman, E.M. and J.S. Beckmann (1988). DNA Polymorphism as a tool in fisheries science. Can. J. of Fish. and Aquat. Sci. 45: 1075-1087.

46Hallerman, E., A. Nave, M. Soller and J.S. Beckmann (1988). Screening of Israeli Holstein-Friesian Cattle for RFLPs Using Homologous and Heterologous DNA Probes. J. Dairy Sci. 71: 3378-3389.

47Beckmann, J.S. (1988). Oligonucleotide Polymorphisms: A New Tool in Genomic Genetics. Bio/Technology 6: 1061-1064.

48Fries, R., J.S.Beckmann, M. Georges, M. Soller and J. Womack (1989). The Bovine Gene Map. Animal Genetics 20: 3-30.

49Soller, M. and J.S. Beckmann (1990). On the Usefulness of Replicated Progenies in Marker-based Mapping of QTL. Theor appl. Genet. 80: 205-208.

50Kashi, Y., F. Iraqi, Y. Tikochinksy, B. Ruzitski, A. Nave, J.S. Beckmann, A. Friedmann, M. Soller and Y. Gruenbaum (1990). (TG)n uncovers a sex-specific hybridization pattern in cattle. Genomics 6: 31-36.

51Livneh, O., Y. Nagler, Y. Tal, S. Ben Hanish, Y. Gafni, J.S. Beckmann and I. Sela (1990). RFLP analysis of a hybrid cultivar (Capsicum annum) and its use in distinguishing between parental lines and in hybrid identification. Seed Sci. technol. 18: 209-214.

52Barg, R., J.S. Beckmann and M. Perl (1990). The effect of nicotinamide dinucleotides on methotrexate binding to protein in a methotrexate-resistant cell line of Petunia hybrida. J. Plant Physiol. 136: 611-614.

53Beckmann, J.S. (1990). Genetic and Physical Mapping of the Human Genome. Science 248: 18.

54Kashi, Y., Y. Tikoschinksy, F. Iraqi, E. Genislav, A. Nave, J.S. Beckmann, Y. Gruenbaum and M. Soller (1990). Large restriction fragments containing poly-TG are highly polymorphic in a variety of vertebrates. Nucl. Ac. Res. 18: 1129-1132.

55Kashi, Y., E. Lipkin, A. Darvasi, A. Nave, Y. Gruenbaum, J. S. Beckmann and M. Soller (1990). Parentage Identification in the Bovine Using “Deoxyribonucleic Acid Fingerprints”. J. Dairy Sciences 73: 3306-3311.

56Beckmann, J.S. and M. Soller (1990). Toward a unified approach to genetic mapping of Eukaryotes Based on Sequence Tagged Microsatellite Sites. Bio/Technology 8: 930-932.

57Striem, M.J., P. Spiegel-Roy, G. Ben-Hayyim, J. Beckmann and D. Gidoni (1990). Genomic DNA fingerprinting of Vitis vinifera by the use of multi-loci probes. Vitis 29: 223-227.

58Iraqi, F., M. Soller and J.S. Beckmann (1991). Endogenous viruses in commercial poultry layer populations. Poultry Sci 70: 665-679.

59Beckmann, J.S. and J.L. Weber (1991). Microsatellite loci in human DNA sequences. in: Cytogenetics and Cell Genetics 55: 707-722.

60Beckmann, J.S. and E.N. Trifonov (1991). Splice junctions follow a 205 base ladder. Proc. Natl. Acad. Sci. USA 88: 2380-2383.

61Beckmann, J.S, I. richard, D. Hillaire, O. Broux, C. Antignac, E. Bois, H. Cann, R. W. Cottingham Jr., N. Feingold, J. Feingold, J. Kalil, G. M. Lathrop, A. marcadet, M. Masset, C. Mignard, M.-R. Passos-Bueno, N. Pellerain, M. Zatz, J. Dausset, M. Fardeau and D. Cohen (1991). A Gene for Limb-Girdle Muscular Dystrophy Maps to Chromosome 15 by Linkage. C. r. Acad. Sci. 312,Série III: 141-148.

62Ebers, G.C., A.L. Georges, R.L. Barchi, S.S. Ting-Passador, R.G. Kallen, G.M. Lathrop, J.S. Beckmann, A.F. Hahn, W.F. Brown, R.D. Campbell and A.J. Hudson (1991) Paramyotonia Congenita and Hyperkalemic Periodic Paralysis are Linked to the Adult Muscle Sodium Channel Gene. Ann. Neurol. 30: 810-816.

63Hilbert, P., K. Lindpaintner, J.S. Beckmann, T. Serikawa, F. Soubrier, C. Dubay, P. Cartwright, B. De Gouyon, C. Julier, S. Takahasi, M. Vincent, D. Ganten, M. Georges and G.M. Lathrop (1991). Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats. Nature 353: 521-529.

64Williamson, R.W., A. Bowcock, K. Kidd, P. Pearson, J. Schmidtke, P. Ceverha, M. Chipperfield, D.N. Cooper, C. Coutelle, J. Hewitt, K. Klinger, K. Langley, J.S. Beckmann, M. Tolley and B. Maidak (1991). Report of the DNA Committee and Catalogues of Cloned and Mapped Genes, Markers Formatted for PCR and DNA Polymorphisms. Cytogenetics and Cell Genetics 58: 1190-1832.

65Beckmann, J.S. and J.L. Weber (1992). Survey of Human and Rat Microsatellites. Genomics 12: 627-631.

66Speer, M.C., L.H. Yamaoka, J.M. Gilchrist, C.P. Gaskell, J.M. Stajich, J.M. Vance, A. Kazantzev, A. Lastra, C.S. Haynes, J.S. Beckmann, D. Cohen, J.L. Weber, A.D. Roses and M.A. Pericak-Vance. (1992). Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: Linkage of an autosomal dominant form of limb-girdle muscular dystrophy to chromosome 5q. Am. J. Hum. Genetics 50: 1211-1217.

67Fougerousse, F., I. Richard, O. Broux, D. Cohen and J.S. Beckmann (1992). Mapping of two chromosome 15 microsatellites. Genomics 13: 903-904.

68Kashi, Y., Y. Tikochinski, A. Nave, J.S. Beckmann, M. Soller and Y. Gruenbaum (1992). A new minisatellite probe shows highly polymorphic hybridization pattern in human. Nucl. Ac. Res. 20: 926.

69Fougerousse, F., R. Meloni, C. Roudaut and J.S. Beckmann (1992). Dinucleotide repeat polymorphism at the human hemoglobin alpha-1 pseudo-gene (HBAP1). Nucl. Ac. Res. 20: 1165.

70Fougerousse, F., R. Meloni, C. Roudaut and J.S. Beckmann (1992). Tetranucleotide repeat polymorphism at the human N-MYC gene (MYCN). Nucl. Ac. Res. 20: 1165.

71Fougerousse, F., R. Meloni, C. Roudaut and J.S. Beckmann (1992). Dinucleotide repeat polymorphism at the human Poly (ADP-Ribose) polymerase gene (PPOL). Nucl. Ac. Res. 20: 1166.

72Meloni, R., F. Fougerousse, C. Roudaut and J.S. Beckmann (1992). Dinucleotide repeat polymorphism at the human liver arginase gene (ARG1). Nucl. Ac. Res. 20: 1166.

73Meloni, R., F. Fougerousse, C. Roudaut and J.S. Beckmann (1992). Trinucleotide repeat polymorphism at the human insulin-like growth factor I receptor gene (IGF1R). Nucl. Ac. Res. 20: 1427.

74Kashi, Y., A. Nave, Y. Gruenbaum, M. Soller and J.S. Beckmann (1992). A minisatellite probe from bovine uncovers highly polymorphic DNA fingerprint patterns in mammals and chickens. Anim. Genet. 23: 570.

75Froguel, Ph., M. Vaxillaire, F. Sun, G. Velho, H. Zouali, M.O. Butel, S. Lesage, N. Vionnet, K. Clément, F. Fougerousse, Y. Tanizawa, J. Weissenbach, J.S. Beckmann, G.M. Lathrop, Ph. Passa, M.A. Permutt and D. Cohen (1992). The glucokinase locus on chromosome 7p is closely linked to early onset non-insulin dependent diabetes mellitus. Nature 356: 162-164.

76Schwartz, K., J.S. Beckmann, C. Dufour, L. Faure, F. Fougerousse, L. Carrier, C. Hengstenberg, D. Cohen, H.-P. Vosberg, A. Sacrez, M. Ferrière, M. Desnos, F. Cambien, O. Dubourg and M. Komajda (1992). Exclusion of myosin heavy chain and cardiac actin gene involvement in hypertrophic cardiomyopathies of several french families. Circ. Research 71: 3-8.

77Serikawa, T., T. Kuramoto, P. Hilbert, M. Mori, J. Yamada, C.J. Dubay, J.-L. Guenet, G.M. Lathrop, and J.S. Beckmann (1992). Rat gene mapping using PCR-analyzed microsatellites. Genetics 131: 701-721.

78Young, K., T. Foroud, P. Williams, C.E. Jackson, J.S. Beckmann, D. Cohen, P.M. Conneally, J. Tischfield and M.E. Hodes (1992). Confirmation of Linkage of Limb-Girdle Muscular Dystrophy to Chromosome 15. Genomics 13: 1370-71.

79Watkins, C., D. Warne, D. Kelsell, J. Beckmann, K. Nyberg and N. Spurr (1992). The use of PCR and ethidium bromide staining to detect length variation in short repeat units. Technique 3: 175-178.

80Belal, S., K. Panayides, G. Sirugo, C. Ben Hamida, P. Ioannou, F. Hentati, J.S. Beckmann, M. Koenig, J.L. Mandel, M. Ben Hamida and L. Middleton (1992). Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. Am. J. Hum. Genet. 51: 1372-1376.

81Fougerousse, F., C. Dufour, C. Roudaut and J.S. Beckmann (1992). Dinucleotide repeat polymorphism at the human gene for cardiac beta-myosin heavy chain (MYH6). Hum. mol. Genet. 1: 64.

82Richard, I., O. Broux, D. Hillaire, D. Cherif, F. Fougerousse, D. Cohen, and J.S. Beckmann.(1992). Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of Limb-Girdle Muscular Dystrophy. Hum. molec. Genet. 1: 621-624.

83Casley, W.L., M. Allon, H.K. Cousin, S.S. Ting, L. Hashimoto, F. Cornelis, J.S. Beckmann, A.J. Hudson and G.C. Ebers (1992). Exclusion of Linkage between Hypokalemic Periodic Paralysis and Three Candidate Muscle Ion Channel Gene Loci. Genomics 14: 493-494.

84Froguel, Ph., H. Zouali, N. Vionnet, G. Velho, M. Vaxillaire, F. Sun, S. Lesage, M.-O. Butel, M. Stoffel, J. Takeda, Ph. Passa, A. Permutt, J.S. Beckmann, G. Bell and D. Cohen. (1993). Familial hyperglycemia due to mutations in glucokinase: Definition of a subtype of diabetes mellitus. N. Engl. J. Med. 328: 697-702.

85Passos-Bueno, M.-R., I. Richard, M. Vainzof, F. Fougerousse, J. Weissenbach, O. Broux, D. Cohen, J. Akiyama, S.K.N. Marie, A.A. Carvalho, L. Guilherme, J. Kalil, A.M. Tsunaclis, M. Zats and J.S. Beckmann.(1993) Evidence of Genetic Heterogeneity for the Adult Form of Limb-Girdle Muscular Dystrophy Following Linkage Analysis with 15q Probes in Brazilian Families. J. Med. Genet. 30: 385-87.

86Dubay, C., M. Vincent, N.J. Samani, P. Hilbert, M.A. Kaiser, J.-P. Beressi, Y. Koteletsev, J.S. Beckmann, F. Soubrier, J. Sassard and G.M. Lathrop (1993). Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats. Nature genetics 3: 354-357.

87Pages, J.-C., C. Drieu, H. Blanché, J.S. Beckmann and H.M. Cann (1993). A short tandem repeat polymorphism at the endothelin 1 (EDN1) locus. Hum. mol. Genet. 2: 90.

88Passos-Bueno, M.-R., E. Bakker, S.K.N. Marie, R.C. Pavanello, M. Vainzof, A.A. Carvalho, D. Cohen, J.S. Beckmann and M. Zats (1993) Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families. Hum. mol. Genet. 2: 201-202.

89Antignac, C., C. Arduy, J.S. Beckmann, F. Benessy, F. Gros, M. Medhioub, F. Hildebrandt, J.-L. Dufier, C. Kleinknecht, M. Broyer, J. Weissenbach, R. Habib, and D. Cohen (1993). A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2p. Nature genetics 3: 342-345.

90Carrier, L., C. Hengstenberg, J.S. Beckmann, P. Guicheney, C. Dufour, J. Bercovici, E. Dausse, I. Berrebi-Bertrand, C. Wisnewsky, D. Pulvenis, L. Fetler, A. Vignal, J. Weissenbach, D. Hillaire, J. Feingold, J.-B. Bouhour, A. Hagege, M. Desnos, R. Isnard, O. Dubourg, M. Komajda and K. Schwartz (1993). Mapping of a Novel Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 11. Nature genetics 4: 311-314.

91Dufour, C., L. Carrier, C. Hengstenberg, J. Bercovici, E. Dausse, J. Weissenbach, O. Dubourg, M. Komajda, K. Schwartz and J.S. Beckmann (1993). Exclusion of genes coding for protein of the cytoskeleton and the extracellular matrix in familial hypertrophic cardiomyopathy using a candidate gene approach. C. r. Acad. Sci. Paris, Sciences de la vie/Life sciences. 316: 474-81.

92Zouali, H., M. Vaxillaire, S. Lesage, F. Sun, G. Velho, N. Vionnet, K. Chiu, Ph. Passa, M.A. Permutt, F. Demenais, D. Cohen, J.S. Beckmann and Ph. Froguel (1993). Linkage analysis and molecular scanning of glucokinase gene in NIDDM families. Diabetes 42: 1238-45.

93Richard, I., C. Devaud, D. Cherif, D. Cohen, J.S. Beckmann.(1993). The Gene for Creatine Kinase - Mitochondrial 2 (Sarcomeric; CKMT2) Maps to Chromosome 5q.13.3. Genomics 18: 134-136.

94Gispert, S., R. Twells, G. Orozco, A. Brice, J. Weber, L. Heredero, K. Scheufler, B. Riley, R. Allotey, C. Nothers, R. Hillermann, A. Lunkes, C. Khati, G. Stevanin, A. Hernandez, C. Margarino, T. Klockgether, A. Durr, H. Chneiweiss, J. Enczmann, M. Farrall, J.S. Beckmann, M. Mullan, P. Wernet, Y. Agid, H.-J. Freund, R. Williamson, G. Auburger, and S. Chamberlain. (1993). Chromosomal assignment of the second (Cuban) locus for autosomal dominant ataxia (SCA2) to human chromosome 12q23-24.1. Nature genetics4: 295-299.

95Dausse, E., M. Komajda, L. Fetler, O. Dubourg, C. Dufour, L. Carrier, C. Wisnewsky, J. Bercovici, C. Hengstenberg, S. Al-Mahdawi, R. Isnard, A. Hagege, J.-B. Bouhour, M. Desnos, J.S. Beckmann, J. Weissenbach, K. Schwartz and P. Guicheney (1993). Familial hypertrophic cardiomyopathy: microsatellite haplotyping and identification of a hot-spot for mutations in the beta-myosin heavy chain gene. J. Clin. Invest 92: 2807--2813.

96Azibi, K., L. Bachner, J.S. Beckmann, K. Matsumura, E. Hamouda, M. Chaouch, A. Chaouch, R. Ait-Ouarab, A. Vignal, J. Weissenbach, M.C. Vinet, F. Leturcq, H. Collin, F.M.S. Tomé, A. Reghis, M. Fardeau, K.P. Campbell and J.-C. Kaplan (1993). Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12. Hum. mol. Genet. 2: 1423-28.

97Kondo, K., M. Mori, T. Kuramoto, J. Yamada, J.S. Beckmann, D.S. Chazottes, X. Montagutelli, J.-L. Guénet and T. Serikawa (1993). DNA segments mapped by reciprocal use of microsatellite primers between mouse and rats. Mammalian Genome 4: 571-576.

98Beckmann, J.S.,J Tomfohrde, R.I. Barnes, M. Williams, O. Broux, I. Richard, J. Weissenbach and A.M. Bowcock (1993). A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites. Hum. mol. Genet. 2: 2019-2030.

99Richard, I., N. Bourg and J.S. Beckmann (1993). Dinucleotide repeat at the D15S129 locus. Hum. mol. Genet. 2: 2199.

100Fougerousse, F., P. Pasturaud P.and J.S. Beckmann (1993). Dinucleotide repeat at the D15S222 locus. Hum. mol. Genet. 2: 2200.

101Peral, B., J.L. San Millan, C. Hernandez, A. Valero, G.M. Lathrop, J.S. Beckmann and F. Moreno (1993). Linkage studies on Autosomal Dominant Polycystic Kidney Disease (ADPKD) in Spanish population: evidence of genetic heterogeneity. J. Med. Genet. 30: 910-913.

102Pereira de Souza, A., V. Allamand, I. Richard, L. Brenguier, I. Chumakov, D. Cohen and J.S. Beckmann (1994). Targeted Development of Microsatellite Markers from Inter-Alu Amplification of YAC Clones. Genomics 19: 391-393.

103Fougerousse, F., O. Broux, I. Richard, V. Allamand, A. Perreira de Souza, N. Bourg, L. Brenguier, C. Devaud, P. Pasturaud, C. Roudaut, N. Chiannilkulchaï, D. Hillaire, H. Bui, I. Chumakov, J. Weissenbach, D. Cherif, D. Cohen and J.S. Beckmann (1994). Mapping of a Chromosome 15 Region Involved in Limb Girdle Muscular Dystrophy. Human Mol. Genet. 3: 285-293.

104Pereira de Souza, A., V. Allamand, I. Richard, L. Brenguier and J.S. Beckmann (1994). Three dinucleotide repeats on chromosome 21. Human mol. Genet. 3: 381.

105Pereira de Souza, A., V. Allamand, I. Richard, L. Brenguier and J.S. Beckmann (1994). Two dinucleotide repeats tightly linked to D12S91. Human mol. Genet. 3: 382.

106Allamand, V., A. Pereira de Souza, I. Richard, L. Brenguier and J.S. Beckmann (1994). Dinucleotide repeat polymorphism at D15S221. Human mol. Genet. 3: 382.

107El Kerch, F., A. Sefiani, K. Azibi, N. Boutaleb, M. Yahyaoui, A. Bentahila, M.C. Vinet, F. Leturcq, L. Bachner, J.S. Beckmann, K.P. Campbell, F.M.S. Tomé, M. Fardeau and J.-C. Kaplan (1994). Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy (SCARMD) in Morocco indicate genetic homogeneity of the disease in North Africa. J. Med. Genet. 31: 342-343.

108Ben Hamida, M., S. Belal, G. Sirugo, C. Ben Hamida, K. Panayides, P. Ioannou, J.S. Beckmann, J.L. Mandel, F. Hentati, M. Koenig, and L. Middleton (1994). Friedreich’s ataxia phenotype not linked to chromosome 9 and associated to selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology 43: 2179-83.

109Medhioub, M., D. Cherif, F. Benessy, F. Silbermann, M.C. Gubler, D. Le Paslier, D. Cohen, J. Weissenbach, J.S. Beckmann and C. Antignac (1994). Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity. Genomics 19: 296-301.

110Imbert, G., Y. Trottier, J.S. Beckmann and J.L. Mandel (1994). The gene for the TATA binding protein (TBP) that contains a highly polymorphic protein coding CAG repeat maps to 6q27. Genomics 19:667-668.

111Richard, I., O. Broux, N. Chiannilkulchaï, F. Fougerousse, V. Allamand, N. Bourg, L. Brenguier, C. Devaud, P. Pasturaud, C. Roudaut, R.A. Schultz, M.H. Polymeropoulos, G. Gyapay and J.S. Beckmann (1994). Regional localisation of human chromosome 15 loci. Genomics. 23:619-627.

112Vaxillaire, M., N. Vionnet, C. Vigouroux, F. Sun, R. Espinoza, III, M.M. Lebeau, M. Stoffel, M. Letho, J.S. Beckmann, M. Detheux, Ph.P. Passa, D. Cohen, E. Van Schaftingen, G. Velho, G.I. Bell and Ph. Froguel (1994). Search for a Third Susceptibility Gene for Maturity-Onset Diabetes of the Young. Diabetes 43: 389-395.

113Kashi, Y., A. Nave, A. Darvasi, Y. Gruenbaum, M. Soller and J.S. Beckmann (1994). How is it that microsatellites and oligomers uncover DNA fingerprint patterns? Mammalian Genome 5: 525-530.

114Iraqi, F., A. Darvasi, G. Zeitlin, J.S. Beckmann and M. Soller (1994). Non-linear effects of chicken endogenous viruses on body weight may be responsible for maintaining these elements in a stable genetic polymorphism. Poultry Science 73: 1625-1632.

115Roberds, S.L., F. Leturcq, V. Allamand, F. Piccolo, M. Jeanpierre, R.D. Anderson, L.E. Lim, J.C. Lee, F.M.S. Tomé, N.B. Romero, M. Fardeau, J.S. Beckmann, J.-C. Kaplan and K.P. Campbell (1994). Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Cell 78: 625-633.

116Hillaire, D., A. Leclerc, S. Fauré, H. Topaloglu, N. Chiannilkuchaï, P. Guicheney, L. Grinas, P. Legos, J. Philpot, T. Evangelista, M.C. Routon, M. Mayer, J.F. Pellissier, B. Estournet, A. Barois, F. Hentati, N. Feingold, J.S. Beckmann, V. Dubowitz, F.M.S. Tomé and M. Fardeau (1994). Localisation of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Human Mol. Genet. 3: 1657-1661.