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    1. Bolotin, A; Wincker, P; Mauger, S; Jaillon, O; Malarme, K; Weissenbach, J; Ehrlich, SD; Sorokin, A
      The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp lactis IL1403

      GENOME RESEARCH
    2. Charlier, C; Segers, K; Wagenaar, D; Karim, L; Berghams, S; Jaillon, O; Shay, T; Weissenbach, J; Cockett, N; Gyapay, G; Georges, M
      Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8

      GENOME RESEARCH
    3. Peyret, P; Katinka, MD; Duprat, S; Duffieux, F; Barbe, V; Barbazanges, M; Weissenbach, J; Saurin, W; Vivares, CP
      Sequence and analysis of chromosome I of the amitochondriate intracellularparasite Encephalitozoon cuniculi (Microspora)

      GENOME RESEARCH
    4. Avner, P; Bruis, T; Poras, I; Eley, L; Ruiz, P; Wiles, MV; Sousa-Nunes, R; Kettleborough, R; Rana, A; Morrisette, J; Bentley, L; Goldsworthy, M; Haynes, A; Herbert, E; Southam, L; Lehrach, H; Weissenbach, J; Manenti, G; Rodriguez-Tome, P; Beddington, R; Dunwoodie, S; Cox, RD
      A radiation hybrid transcript map of the mouse genome (vol 29, pg 194, 2001)

      NATURE GENETICS
    5. Avner, P; Bruls, T; Poras, I; Eley, L; Gas, S; Ruiz, P; Wiles, MV; Sousa-Nunes, R; Kettleborough, R; Rana, A; Morissette, J; Bentley, L; Goldsworthy, M; Haynes, A; Herbert, E; Southam, L; Lehrach, H; Weissenbach, J; Manenti, G; Rodriguez-Tome, P; Beddington, R; Dunwoodie, S; Cox, RD
      A radiation hybrid transcript map of the mouse genome

      NATURE GENETICS
    6. Fischer, J; Bouadjar, B; Heilig, R; Huber, M; Lefevre, C; Jobard, F; Macari, F; Bakija-Konsuo, A; Ait-Belkacem, F; Weissenbach, J; Lathrop, M; Hohl, D; Prud'homme, JF
      Mutations in the gene encoding SLURP-1 in Mel de Meleda

      HUMAN MOLECULAR GENETICS
    7. Weissenbach, J
      Plethoric data and shortage of concepts?

      M S-MEDECINE SCIENCES
    8. Balzergue, S; Dubreucq, B; Chauvin, S; Le-Clainche, I; Le Boulaire, F; de Rose, R; Samson, F; Biaudet, V; Lecharny, A; Cruaud, C; Weissenbach, J; Caboche, M; Lepiniec, L
      Improved PCR-walking for large-scale isolation of plant T-DNA borders

      BIOTECHNIQUES
    9. Weissenbach, J; Esnault, Y
      First lessons from the human genome

      BIOFUTUR
    10. Ogata, H; Audic, S; Renesto-Audiffren, P; Fournier, PE; Barbe, V; Samson, D; Roux, V; Cossart, P; Weissenbach, J; Claverie, JM; Raoult, D
      Mechanisms of evolution in Rickettsia conorii and R. prowazekii

      SCIENCE
    11. Katinka, MD; Duprat, S; Cornillot, E; Metenier, G; Thomarat, F; Prensier, G; Barbe, V; Peyretaillade, E; Brottier, P; Wincker, P; Delbac, F; El Alaoui, H; Peyret, P; Saurin, W; Gouy, M; Weissenbach, J; Vivares, CP
      Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi

      NATURE
    12. Lander, ES; Linton, LM; Birren, B; Nusbaum, C; Zody, MC; Baldwin, J; Devon, K; Dewar, K; Doyle, M; FitzHugh, W; Funke, R; Gage, D; Harris, K; Heaford, A; Howland, J; Kann, L; Lehoczky, J; LeVine, R; McEwan, P; McKernan, K; Meldrim, J; Mesirov, JP; Miranda, C; Morris, W; Naylor, J; Raymond, C; Rosetti, M; Santos, R; Sheridan, A; Sougnez, C; Stange-Thomann, N; Stojanovic, N; Subramanian, A; Wyman, D; Rogers, J; Sulston, J; Ainscough, R; Beck, S; Bentley, D; Burton, J; Clee, C; Carter, N; Coulson, A; Deadman, R; Deloukas, P; Dunham, A; Dunham, I; Durbin, R; French, L; Grafham, D; Gregory, S; Hubbard, T; Humphray, S; Hunt, A; Jones, M; Lloyd, C; McMurray, A; Matthews, L; Mercer, S; Milne, S; Mullikin, JC; Mungall, A; Plumb, R; Ross, M; Shownkeen, R; Sims, S; Waterston, RH; Wilson, RK; Hillier, LW; McPherson, JD; Marra, MA; Mardis, ER; Fulton, LA; Chinwalla, AT; Pepin, KH; Gish, WR; Chissoe, SL; Wendl, MC; Delehaunty, KD; Miner, TL; Delehaunty, A; Kramer, JB; Cook, LL; Fulton, RS; Johnson, DL; Minx, PJ; Clifton, SW; Hawkins, T; Branscomb, E; Predki, P; Richardson, P; Wenning, S; Slezak, T; Doggett, N; Cheng, JF; Olsen, A; Lucas, S; Elkin, C; Uberbacher, E; Frazier, M; Gibbs, RA; Muzny, DM; Scherer, SE; Bouck, JB; Sodergren, EJ; Worley, KC; Rives, CM; Gorrell, JH; Metzker, ML; Naylor, SL; Kucherlapati, RS; Nelson, DL; Weinstock, GM; Sakaki, Y; Fujiyama, A; Hattori, M; Yada, T; Toyoda, A; Itoh, T; Kawagoe, C; Watanabe, H; Totoki, Y; Taylor, T; Weissenbach, J; Heilig, R; Saurin, W; Artiguenave, F; Brottier, P; Bruls, T; Pelletier, E; Robert, C; Wincker, P; Rosenthal, A; Platzer, M; Nyakatura, G; Taudien, S; Rump, A; Yang, HM; Yu, J; Wang, J; Huang, GY; Gu, J; Hood, L; Rowen, L; Madan, A; Qin, SZ; Davis, RW; Federspiel, NA; Abola, AP; Proctor, MJ; Myers, RM; Schmutz, J; Dickson, M; Grimwood, J; Cox, DR; Olson, MV; Kaul, R; Raymond, C; Shimizu, N; Kawasaki, K; Minoshima, S; Evans, GA; Athanasiou, M; Schultz, R; Roe, BA; Chen, F; Pan, HQ; Ramser, J; Lehrach, H; Reinhardt, R; McCombie, WR; de la Bastide, M; Dedhia, N; Blocker, H; Hornischer, K; Nordsiek, G; Agarwala, R; Aravind, L; Bailey, JA; Bateman, A; Batzoglou, S; Birney, E; Bork, P; Brown, DG; Burge, CB; Cerutti, L; Chen, HC; Church, D; Clamp, M; Copley, RR; Doerks, T; Eddy, SR; Eichler, EE; Furey, TS; Galagan, J; Gilbert, JGR; Harmon, C; Hayashizaki, Y; Haussler, D; Hermjakob, H; Hokamp, K; Jang, WH; Johnson, LS; Jones, TA; Kasif, S; Kaspryzk, A; Kennedy, S; Kent, WJ; Kitts, P; Koonin, EV; Korf, I; Kulp, D; Lancet, D; Lowe, TM; McLysaght, A; Mikkelsen, T; Moran, JV; Mulder, N; Pollara, VJ; Ponting, CP; Schuler, G; Schultz, JR; Slater, G; Smit, AFA; Stupka, E; Szustakowki, J; Thierry-Mieg, D; Thierry-Mieg, J; Wagner, L; Wallis, J; Wheeler, R; Williams, A; Wolf, YI; Wolfe, KH; Yang, SP; Yeh, RF; Collins, F; Guyer, MS; Peterson, J; Felsenfeld, A; Wetterstrand, KA; Patrinos, A; Morgan, MJ
      Initial sequencing and analysis of the human genome

      NATURE
    13. McPherson, JD; Marra, M; Hillier, L; Waterston, RH; Chinwalla, A; Wallis, J; Sekhon, M; Wylie, K; Mardis, ER; Wilson, RK; Fulton, R; Kucaba, TA; Wagner-McPherson, C; Barbazuk, WB; Gregory, SG; Humphray, SJ; French, L; Evans, RS; Bethel, G; Whittaker, A; Holden, JL; McCann, OT; Dunham, A; Soderlund, C; Scott, CE; Bentley, DR; Schuler, G; Chen, HC; Jang, WH; Green, ED; Idol, JR; Maduro, VVB; Montgomery, KT; Lee, E; Miller, A; Emerling, S; Kucherlapati, R; Gibbs, R; Scherer, S; Gorrell, JH; Sodergren, E; Clerc-Blankenburg, K; Tabor, P; Naylor, S; Garcia, D; de Jong, PJ; Catanese, JJ; Nowak, N; Osoegawa, K; Qin, SZ; Rowen, L; Madan, A; Dors, M; Hood, L; Trask, B; Friedman, C; Massa, H; Cheung, VG; Kirsch, IR; Reid, T; Yonescu, R; Weissenbach, J; Bruls, T; Heilig, R; Branscomb, E; Olsen, A; Doggett, N; Cheng, JF; Hawkins, T; Myers, RM; Shang, J; Ramirez, L; Schmutz, J; Velasquez, O; Dixon, K; Stone, NE; Cox, DR; Haussler, D; Kent, WJ; Furey, T; Rogic, S; Kennedy, S; Jones, S; Rosenthal, A; Wen, GP; Schilhabel, M; Gloeckner, G; Nyakatura, G; Siebert, R; Schlegelberger, B; Korenburg, J; Chen, XN; Fujiyama, A; Hattori, M; Toyoda, A; Yada, T; Park, HS; Sakaki, Y; Shimizu, N; Asakawa, S; Kawasaki, K; Sasaki, T; Shintani, A; Shimizu, A; Shibuya, K; Kudoh, J; Minoshima, S; Ramser, J; Seranski, P; Hoff, C; Poustka, A; Reinhardt, R; Lehrach, H
      A physical map of the human genome

      NATURE
    14. Bruls, T; Gyapay, G; Petit, JL; Artiguenave, F; Vico, V; Qin, SZ; Tin-Wollam, AM; Da Silva, C; Muselet, D; Mavel, D; Pelletier, E; Levy, M; Fujiyama, A; Matsuda, F; Wilson, R; Rowen, L; Hood, L; Weissenbach, J; Saurin, W; Heilig, R
      A physical map of human chromosome 14

      NATURE
    15. Lefevre, C; Jobard, F; Caux, F; Bouadjar, B; Karaduman, A; Heilig, R; Lakhdar, H; Wollenberg, A; Verret, JL; Weissenbach, J; Ozguc, M; Lathrop, M; Prud'homme, JF; Fischer, J
      Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. Crollius, HR; Jaillon, O; Dasilva, C; Ozouf-Costaz, C; Fizames, C; Fischer, C; Bouneau, L; Billault, A; Quetier, F; Saurin, W; Bernot, A; Weissenbach, J
      Characterization and repeat analysis of the compact genome of the freshwater pufferfish Tetraodon nigroviridis

      GENOME RESEARCH
    17. Nicole, S; Davoine, CS; Topaloglu, H; Cattolico, L; Barral, D; Beighton, P; Ben Hamida, C; Hammouda, H; Cruaud, C; White, PS; Samson, D; Urtizberea, JA; Lehmann-Horn, F; Weissenbach, J; Hentati, F; Fontaine, B
      Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)

      NATURE GENETICS
    18. Tullio-Pelet, A; Salomon, R; Hadj-Rabia, S; Mugnier, C; de Laet, MH; Chaouachi, B; Bakiri, F; Brottier, P; Cattolico, L; Penet, C; Begeot, M; Naville, D; Nicolino, M; Chaussain, JL; Weissenbach, J; Munnich, R; Lyonnet, S
      Mutant WD-repeat protein in triple-A syndrome

      NATURE GENETICS
    19. Crollius, HR; Jaillon, O; Bernot, A; Dasilva, C; Bouneau, L; Fischer, C; Fizames, C; Wincker, P; Brottier, P; Quetier, F; Saurin, W; Weissenbach, J
      Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence

      NATURE GENETICS
    20. Fonknechten, N; Mavel, D; Byrne, P; Davoine, CS; Cruaud, C; Boentsch, D; Samson, D; Coutinho, P; Hutchinson, M; McMonagle, P; Burgunder, JM; Tartaglione, A; Heinzlef, O; Feki, I; Deufel, T; Parfrey, N; Brice, A; Fontaine, B; Prud'homme, JF; Weissenbach, J; Durr, A; Hazan, J
      Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

      HUMAN MOLECULAR GENETICS
    21. Tiret, L; Kessler, JL; Bentolila, S; Faure, S; Bach, JM; Weissenbach, J; Panthier, JJ
      Assignation of highly polymorphic markers on a canine purebred pedigree

      MAMMALIAN GENOME
    22. Escary, JL; Bottius, E; Prince, N; Reyes, C; Fiawoumo, Y; Caloustian, C; Bruls, T; Fujiyama, A; Cooper, RS; Adeyemo, AA; Lathrop, GM; Weissenbach, J; Gyapay, G; Foglio, M; Beckmann, JS
      A first high-density map of 981 biallelic markers on human chromosome 14

      GENOMICS
    23. Weissenbach, J; Salanoubat, M
      Genome sequencing: the big bang

      M S-MEDECINE SCIENCES
    24. Fischer, C; Ozouf-Costaz, C; Crollius, HR; Dasilva, C; Jaillon, O; Bouneau, L; Bonillo, C; Weissenbach, J; Bernot, A
      Karyotype and chromosome location of characteristic tandem repeats in the pufferfish Tetraodon nigroviridis

      CYTOGENETICS AND CELL GENETICS
    25. Weissenbach, J; Esnault, Y
      The first draft of the human genome

      BIOFUTUR
    26. Desaix, A; Marliere, P; Watenberg, P; Weissenbach, J
      Should genes be patented?

      BIOFUTUR
    27. Adams, MD; Celniker, SE; Holt, RA; Evans, CA; Gocayne, JD; Amanatides, PG; Scherer, SE; Li, PW; Hoskins, RA; Galle, RF; George, RA; Lewis, SE; Richards, S; Ashburner, M; Henderson, SN; Sutton, GG; Wortman, JR; Yandell, MD; Zhang, Q; Chen, LX; Brandon, RC; Rogers, YHC; Blazej, RG; Champe, M; Pfeiffer, BD; Wan, KH; Doyle, C; Baxter, EG; Helt, G; Nelson, CR; Miklos, GLG; Abril, JF; Agbayani, A; An, HJ; Andrews-Pfannkoch, C; Baldwin, D; Ballew, RM; Basu, A; Baxendale, J; Bayraktaroglu, L; Beasley, EM; Beeson, KY; Benos, PV; Berman, BP; Bhandari, D; Bolshakov, S; Borkova, D; Botchan, MR; Bouck, J; Brokstein, P; Brottier, P; Burtis, KC; Busam, DA; Butler, H; Cadieu, E; Center, A; Chandra, I; Cherry, JM; Cawley, S; Dahlke, C; Davenport, LB; Davies, A; de Pablos, B; Delcher, A; Deng, ZM; Mays, AD; Dew, I; Dietz, SM; Dodson, K; Doup, LE; Downes, M; Dugan-Rocha, S; Dunkov, BC; Dunn, P; Durbin, KJ; Evangelista, CC; Ferraz, C; Ferriera, S; Fleischmann, W; Fosler, C; Gabrielian, AE; Garg, NS; Gelbart, WM; Glasser, K; Glodek, A; Gong, FC; Gorrell, JH; Gu, ZP; Guan, P; Harris, M; Harris, NL; Harvey, D; Heiman, TJ; Hernandez, JR; Houck, J; Hostin, D; Houston, DA; Howland, TJ; Wei, MH; Ibegwam, C; Jalali, M; Kalush, F; Karpen, GH; Ke, ZX; Kennison, JA; Ketchum, KA; Kimmel, BE; Kodira, CD; Kraft, C; Kravitz, S; Kulp, D; Lai, ZW; Lasko, P; Lei, YD; Levitsky, AA; Li, JY; Li, ZY; Liang, Y; Lin, XY; Liu, XJ; Mattei, B; McIntosh, TC; McLeod, MP; McPherson, D; Merkulov, G; Milshina, NV; Mobarry, C; Morris, J; Moshrefi, A; Mount, SM; Moy, M; Murphy, B; Murphy, L; Muzny, DM; Nelson, DL; Nelson, DR; Nelson, KA; Nixon, K; Nusskern, DR; Pacleb, JM; Palazzolo, M; Pittman, GS; Pan, S; Pollard, J; Puri, V; Reese, MG; Reinert, K; Remington, K; Saunders, RDC; Scheeler, F; Shen, H; Shue, BC; Siden-Kiamos, I; Simpson, M; Skupski, MP; Smith, T; Spier, E; Spradling, AC; Stapleton, M; Strong, R; Sun, E; Svirskas, R; Tector, C; Turner, R; Venter, E; Wang, AHH; Wang, X; Wang, ZY; Wassarman, DA; Weinstock, GM; Weissenbach, J; Williams, SM; Woodage, T; Worley, KC; Wu, D; Yang, S; Yao, QA; Ye, J; Yeh, RF; Zaveri, JS; Zhan, M; Zhang, GG; Zhao, Q; Zheng, LS; Zheng, XQH; Zhong, FN; Zhong, WY; Zhou, XJ; Zhu, SP; Zhu, XH; Smith, HO; Gibbs, RA; Myers, EW; Rubin, GM; Venter, JC
      The genome sequence of Drosophila melanogaster

      SCIENCE
    28. Kaul, S; Koo, HL; Jenkins, J; Rizzo, M; Rooney, T; Tallon, LJ; Feldblyum, T; Nierman, W; Benito, MI; Lin, XY; Town, CD; Venter, JC; Fraser, CM; Tabata, S; Nakamura, Y; Kaneko, T; Sato, S; Asamizu, E; Kato, T; Kotani, H; Sasamoto, S; Ecker, JR; Theologis, A; Federspiel, NA; Palm, CJ; Osborne, BI; Shinn, P; Conway, AB; Vysotskaia, VS; Dewar, K; Conn, L; Lenz, CA; Kim, CJ; Hansen, NF; Liu, SX; Buehler, E; Altafi, H; Sakano, H; Dunn, P; Lam, B; Pham, PK; Chao, QM; Nguyen, M; Yu, GX; Chen, HM; Southwick, A; Lee, JM; Miranda, M; Toriumi, MJ; Davis, RW; Wambutt, R; Murphy, G; Dusterhoft, A; Stiekema, W; Pohl, T; Entian, KD; Terryn, N; Volckaert, G; Choisne, N; Rieger, M; Ansorge, W; Unseld, M; Fartmann, B; Valle, G; Artiguenave, F; Weissenbach, J; Quetier, F; Wilson, RK; de la Bastide, M; Sekhon, M; Huang, E; Spiegel, L; Gnoj, L; Pepin, K; Murray, J; Johnson, D; Habermann, K; Dedhia, N; Parnell, L; Preston, R; Hillier, L; Chen, E; Marra, M; Martienssen, R; McCombie, WR; Mayer, K; White, O; Bevan, M; Lemcke, K; Creasy, TH; Bielke, C; Haas, B; Haase, D; Maiti, R; Rudd, S; Peterson, J; Schoof, H; Frishman, D; Morgenstern, B; Zaccaria, P; Ermolaeva, M; Pertea, M; Quackenbush, J; Volfovsky, N; Wu, DY; Lowe, TM; Salzberg, SL; Mewes, HW; Rounsley, S; Bush, D; Subramaniam, S; Levin, I; Norris, S; Schmidt, R; Acarkan, A; Bancroft, I; Quetier, F; Brennicke, A; Eisen, JA; Bureau, T; Legault, BA; Le, QH; Agrawal, N; Yu, Z; Martienssen, R; Copenhaver, GP; Luo, S; Pikaard, CS; Preuss, D; Paulsen, IT; Sussman, M; Britt, AB; Eisen, JA; Selinger, DA; Pandey, R; Mount, DW; Chandler, VL; Jorgensen, RA; Pikaard, C; Juergens, G; Meyerowitz, EM; Ecker, JR; Theologis, A; Dangl, J; Jones, JDG; Chen, M; Chory, J; Somerville, C
      Analysis of the genome sequence of the flowering plant Arabidopsis thaliana

      NATURE
    29. Salanoubat, M; Lemcke, K; Rieger, M; Ansorge, W; Unseld, M; Fartmann, B; Valle, G; Blocker, H; Perez-Alonso, M; Obermaier, B; Delseny, M; Boutry, M; Grivell, LA; Mache, R; Puigdomenech, P; De Simone, V; Choisne, N; Artiguenave, F; Robert, C; Brottier, P; Wincker, P; Cattolico, L; Weissenbach, J; Saurin, W; Quetier, F; Schafer, M; Muller-Auer, S; Gabel, C; Fuchs, M; Benes, V; Wurmbach, E; Drzonek, H; Erfle, H; Jordan, N; Bangert, S; Wiedelmann, R; Kranz, H; Voss, H; Holland, R; Brandt, P; Nyakatura, G; Vezzi, A; D'Angelo, M; Pallavicini, A; Toppo, S; Simionati, B; Conrad, A; Hornischer, K; Kauer, G; Lohnert, TH; Nordsiek, G; Reichelt, J; Scharfe, M; Schon, O; Bargues, M; Terol, J; Climent, J; Navarro, P; Collado, C; Perez-Perez, A; Ottenwalder, B; Duchemin, D; Cooke, R; Laudie, M; Berger-Llauro, C; Purnelle, B; Masuy, D; de Haan, M; Maarse, AC; Alcaraz, JP; Cottet, A; Casacuberta, E; Monfort, A; Argiriou, A; Flores, M; Liguori, R; Vitale, D; Mannhaupt, G; Haase, D; Schoof, H; Rudd, S; Zaccaria, P; Mewes, HW; Mayer, KFX; Kaul, S; Town, CD; Koo, HL; Tallon, LJ; Jenkins, J; Rooney, T; Rizzo, M; Walts, A; Utterback, T; Fujii, CY; Shea, TP; Creasy, TH; Haas, B; Maiti, R; Wu, DY; Peterson, J; Van Aken, S; Pai, G; Militscher, J; Sellers, P; Gill, JE; Feldblyum, TV; Preuss, D; Lin, XY; Nierman, WC; Salzberg, SL; White, O; Venter, JC; Fraser, CM; Kaneko, T; Nakamura, Y; Sato, S; Kato, T; Asamizu, E; Sasamoto, S; Kimura, T; Idesawa, K; Kawashima, K; Kishida, Y; Kiyokawa, C; Kohara, M; Matsumoto, M; Matsuno, A; Muraki, A; Nakayama, S; Nakazaki, N; Shinpo, S; Takeuchi, C; Wada, T; Watanabe, A; Yamada, M; Yasuda, M; Tabata, S
      Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana

      NATURE
    30. Souciet, JL; Aigle, M; Artiguenave, F; Blandin, G; Bolotin-Fukuhara, M; Bon, E; Brottier, P; Casaregola, S; de Montigny, J; Dujon, B; Durrens, P; Gaillardin, C; Lepingle, A; Llorente, B; Malpertuy, A; Neuveglise, C; Ozier-Kalogeropoulos, O; Potier, S; Saurin, W; Tekaia, F; Toffano-Nioche, C; Wesolowski-Louvel, M; Wincker, P; Weissenbach, J
      Genomic Exploration of the Hemiascomycetous Yeasts: 1. A set of yeast species for molecular evolution studies

      FEBS LETTERS
    31. Artiguenave, F; Wincker, P; Brottier, P; Duprat, S; Jovelin, F; Scarpelli, C; Verdier, J; Vico, V; Weissenbach, J; Saurin, W
      Genomic exploration of the hemiascomycetous yeasts: 2. Data generation andprocessing

      FEBS LETTERS
    32. Llorente, B; Malpertuy, A; Neuveglise, C; de Montigny, J; Aigle, M; Artiguenave, F; Blandin, G; Bolotin-Fukuhara, M; Bon, E; Brottier, P; Casaregola, S; Durrens, P; Gaillardin, C; Lepingle, A; Ozier-Kalogeropoulos, O; Potier, S; Saurin, W; Tekaia, F; Toffano-Nioche, C; Wesolowski-Louvel, M; Wincker, P; Weissenbach, J; Souciet, JL; Dujon, B
      Genomic Exploration of the Hemiascomycetous Yeasts: 18. Comparative analysis of chromosome maps and synteny with Saccharomyces cerevisiae

      FEBS LETTERS
    33. Malpertuy, A; Tekaia, F; Casaregola, S; Aigle, M; Artiguenave, F; Blandin, G; Bolotin-Fukuhara, M; Bon, E; Brottier, P; de Montigny, J; Durrens, P; Gaillardin, C; Lepingle, A; Llorente, B; Neuveglise, C; Ozier-Kalogeropoulos, O; Potier, S; Saurin, W; Toffano-Nioche, C; Wesolowski-Louvel, M; Wincker, P; Weissenbach, J; Souciet, JL; Dujon, B
      Genomic Exploration of the Hemiascomycetous Yeasts: 19. Ascomycetes-specific genes

      FEBS LETTERS
    34. Llorente, B; Durrens, P; Malpertuy, A; Aigle, M; Artiguenave, F; Blandin, G; Bolotin-Fukuhara, M; Bon, E; Brottier, P; Casaregola, S; Dujon, B; de Montigny, J; Lepingle, A; Neuveglise, C; Ozier-Kalogeropoulos, O; Potier, S; Saurin, W; Tekaia, F; Toffano-Nioche, C; Wesolowski-Louvel, M; Wincker, P; Weissenbach, J; Souciet, JL; Gaillardin, C
      Genomic Exploration of the Hemiascomycetous Yeasts: 20. Evolution of gene redundancy compared to Saccharomyces cerevisiae

      FEBS LETTERS
    35. Gaillardin, C; Duchateau-Nguyen, G; Tekaia, F; Llorente, B; Casaregola, S; Toffano-Nioche, C; Aigle, M; Artiguenave, F; Blandin, G; Bolotin-Fukuhara, M; Bon, E; Brottier, P; de Montigny, J; Dujon, B; Durrens, P; Lepingle, A; Malpertuy, A; Neuveglise, C; Ozier-Kalogeropoulos, O; Potier, S; Saurin, W; Termier, M; Wesolowski-Louvel, M; Wincker, P; Souciet, JL; Weissenbach, J
      Genomic Exploration of the Hemiascomycetous Yeasts: 21. Comparative functional classification of genes

      FEBS LETTERS
    36. Russell, SEH; McIlhatton, MA; Burrows, JF; Donaghy, PG; Chanduloy, S; Petty, EM; Kalikin, LM; Church, SW; McIlroy, S; Harkin, DP; Keilty, GW; Cranston, AN; Weissenbach, J; Hickey, I; Johnston, PG
      Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors

      CANCER RESEARCH
    37. Saunier, S; Calado, J; Benessy, F; Silbermann, F; Heilig, R; Weissenbach, J; Antignac, C
      Characterization of the NPHP1 locus: Mutational mechanism involved in deletions in familial juvenile nephronophthisis

      AMERICAN JOURNAL OF HUMAN GENETICS
    38. Fischer, J; Faure, A; Bouadjar, B; Blanchet-Bardon, C; Karaduman, A; Thomas, I; Emre, S; Cure, S; Ozguc, M; Weissenbach, J; Prud'homme, JF
      Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity

      AMERICAN JOURNAL OF HUMAN GENETICS
    39. Fontaine, B; Davoine, CS; Durr, A; Paternotte, C; Feki, I; Weissenbach, J; Hazan, J; Brice, A
      A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34

      AMERICAN JOURNAL OF HUMAN GENETICS
    40. Weissenbach, J
      The human genome project in the year 2000

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    41. Hazan, J; Fonknechten, N; Mavel, D; Paternotte, C; Samson, D; Artiguenave, F; Davoine, CS; Cruaud, C; Durr, A; Wincker, P; Brottier, P; Cattolico, L; Barbe, V; Burgunder, JM; Prud'homme, JF; Brice, A; Fontaine, B; Heilig, R; Weissenbach, J
      Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

      NATURE GENETICS
    42. Parmentier, L; Clepet, C; Boughdene-Stambouli, O; Lakhdar, H; Blanchet-Bardon, C; Dubertret, L; Wunderle, E; Pulcini, F; Fizames, C; Weissenbach, J
      Lamellar ichthyosis: Further narrowing, physical and expression mapping ofthe chromosome 2 candidate locus

      EUROPEAN JOURNAL OF HUMAN GENETICS
    43. Pineau, P; Nagai, H; Prigent, S; Wei, Y; Gyapay, G; Weissenbach, J; Tiollais, P; Buendia, MA; Dejean, A
      Identification of three distinct regions of allelic deletions on the shortarm of chromosome 8 in hepatocellular carcinoma

      ONCOGENE
    44. Bentolila, S; Bach, JM; Kessler, JL; Bordelais, I; Cruaud, C; Weissenbach, J; Panthier, JJ
      Analysis of major repetitive DNA sequences in the dog (Canis familiaris) genome

      MAMMALIAN GENOME
    45. Hazan, J; Davoine, CS; Mavel, D; Fonknechten, N; Paternotte, C; Fizames, C; Cruaud, C; Samson, D; Muselet, D; Vega-Czarny, N; Brice, A; Gyapay, G; Heilig, R; Fontaine, B; Weissenbach, J
      A fine integrated map of the SPG4 locus excludes an expanded CAG repeat inchromosome 2p-linked autosomal dominant spastic paraplegia

      GENOMICS
    46. Tiret, L; Kessler, JL; Bentolila, S; Faure, S; Bach, JM; Weissenbach, J; Panthier, JJ
      Characterization and mapping of canine polymorphic markers

      ANIMAL GENETICS
    47. Morissette, J; Villeneuve, A; Bordeleau, L; Rochette, D; Laberge, C; Gagne, B; Laprise, C; Bouchard, G; Plante, M; Gobeil, L; Shink, E; Weissenbach, J; Barden, N
      Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in Quebec points to a locus of major effect on chromosome 12q23-q24

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Carrie, A; Nepotes, V; Billuart, P; Beldjord, C; Bienvenu, T; Chelly, J; Bruls, T; Heilig, R; Weissenbach, J; Jun, L; Marynen, P
      Construction of a highly annotated cosmid contig spanning 550 kb within the X-linked non-specific mental retardation candidate region at Xp21.3-22.1

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Faure, S; Bordelais, I; Marquette, C; Rittey, C; Campos-Castello, J; Goutieres, F; Ponsot, G; Weissenbach, J; Lebon, P
      Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

      CLINICAL GENETICS
    50. Richter, A; Rioux, JD; Bouchard, JP; Mercier, J; Mathieu, J; Ge, B; Poirier, J; Julien, D; Gyapay, G; Weissenbach, J; Hudson, TJ; Melancon, SB; Morgan, K
      Location score and haplotype analyses of the locus for autosomal recessivespastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11

      AMERICAN JOURNAL OF HUMAN GENETICS
    51. WEISSENBACH J
      THE HUMAN GENOME PROJECT - FROM MAPPING TO SEQUENCING

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    52. Paternotte, C; Rudnicki, D; Fizames, C; Davoine, CS; Mavel, D; Durr, A; Samson, D; Marquette, C; Muselet, D; Vega-Czarny, N; Drouot, N; Voit, T; Fontaine, B; Gyapay, G; Auburger, G; Weissenbach, J; Hazan, J
      Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q

      GENOME RESEARCH
    53. MUSTAPHA M; CHARDENOUX S; NIEDER A; SALEM N; WEISSENBACH J; ELZIR E; LOISELET J; PETIT C
      A SENSORINEURAL PROGRESSIVE AUTOSOMAL RECESSIVE FORM OF ISOLATED DEAFNESS, DFNB13, MAPS TO CHROMOSOME 7Q34-Q36

      European journal of human genetics
    54. Fischer, J; Bouadjar, B; Heilig, R; Fizames, C; Prud'homme, JF; Weissenbach, J
      Genetic linkage of Meleda disease to chromosome 8qter

      EUROPEAN JOURNAL OF HUMAN GENETICS
    55. BERNOT A; DASILVA C; PETIT JL; CRUAUD C; CALOUSTIAN C; CASTET V; AHMEDARAB M; DROSS C; DUPONT M; CATTAN D; SMAOUI N; DODE C; PECHEUX C; NEDELEC B; MEDAXIAN J; ROZENBAUM M; ROSNER I; DELPECH M; GRATEAU G; DEMAILLE J; WEISSENBACH J; TOUITOU I
      NON-FOUNDER MUTATIONS IN THE MEFV GENE ESTABLISH THIS GENE AS THE CAUSE OF FAMILIAL MEDITERRANEAN FEVER (FMF)

      Human molecular genetics (Print)
    56. PAWLAK A; CHIANNIKULCHAI N; ANSORGE W; BULLE F; WEISSENBACH J; GYAPAY G; GUELLAEN G
      IDENTIFICATION AND MAPPING OF 26 HUMAN TESTIS MESSENGER-RNAS CONTAINING CAG CTG REPEATS/

      Mammalian genome
    57. Spurr, NK; Cohen, D; Adams, S; Bakker, E; Beckman, EJ; Buys, CHCM; Cann, HM; Cassiman, JJ; Contu, L; Dixon, M; Estivill, X; Ferguson-Smith, MA; Grzeschik, KH; Hansmann, I; Kruse, T; McCarthy, T; Moreno, F; Moschonas, N; Povey, S; Roizes, G; Terrenato, L; Vergnaud, G; Weissenbach, J; Williamson, R; Wright, A
      EUROGEM - Individual reports of all 23 network laboratories

      HUMAN GENOME ANALYSIS
    58. BERNOT A; HEILIG R; CLEPET C; SMAOUI N; DASILVA C; PETIT JL; DEVAUD C; CHIANNILKULCHAI N; FIZAMES C; SAMSON D; CRUAUD C; CALOUSTIAN C; GYAPAY G; DELPECH M; WEISSENBACH J
      A TRANSCRIPTIONAL MAP OF THE FMF REGION

      Genomics
    59. ALBANESE V; HOLBERT S; SAADA C; MEIEREWERT S; LEBRE AS; MORINIERE S; BOUGUELERET L; LEGALL I; WEISSENBACH J; LENNON G; LEHRACH H; COHEN D; CANN HM; NERI C
      CAG CTG AND CGG/GCC REPEATS IN HUMAN BRAIN REFERENCE CDNAS - OUTCOME IN SEARCHING FOR NEW DYNAMIC MUTATIONS/

      Genomics
    60. SALOMONNGUYEN F; LECONIATBUSSON M; HEILIG R; CAMPION D; WEISSENBACH J; BERGER R
      EVIDENCE OF CHROMOSOMAL INVERSION USING FLUORESCENCE IN-SITU HYBRIDIZATION TO STRETCHED DNA

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    61. Weissenbach, J
      Human genome mapping and sequencing: perspectives for toxicology

      TOXICOLOGY LETTERS
    62. FISCHER J; URTIZBEREA JA; PAVEK S; VANDIEDONCK C; BRULS T; SAKER S; ALKATIP Y; PRUDHOMME JF; WEISSENBACH J
      GENETIC-LINKAGE OF PROGRESSIVE PSEUDORHEUMATOID DYSPLASIA TO A 3-CM INTERVAL OF CHROMOSOME 6Q22

      Human genetics
    63. FOLSTERHOLST R; MOISES HW; YANG L; FRITSCH W; WEISSENBACH J; CHRISTOPHERS E
      LINKAGE BETWEEN ATOPY AND THE IGE HIGH-AFFINITY RECEPTOR GENE AT 11Q13 IN ATOPIC-DERMATITIS FAMILIES

      Human genetics
    64. CHAMI M; SAIGO K; GOZUACIK D; POUSSIN K; FALSON P; TORCHARD D; CLEPET C; GYAPAY G; CAUDRON B; URASHIMA T; KEW M; ISONO K; LEMARIE M; BECKMAN J; WEISSENBACH J; BRECHOT C; PATERLINI P
      HBV RELATED INSERTIONAL MUTAGENESIS LEADS TO HYPEREXPRESSION OF A HBV-X SERCA-1 HYBRID PROTEIN IN A HUMAN HEPATOCELLULAR-CARCINOMA

      Hepatology
    65. DELOUKAS P; SCHULER GD; GYAPAY G; BEASLEY EM; SODERLUND C; RODRIGUEZTOME P; HUI L; MATISE TC; MCKUSICK KB; BECKMANN JS; BENTOLILA S; BIHOREAU MT; BIRREN BB; BROWNE J; BUTLER A; CASTLE AB; CHIANNILKULCHAI N; CLEE C; DAY PJR; DEHEJIA A; DIBLING T; DROUOT N; DUPRAT S; FIZAMES C; FOX S; GELLING S; GREEN L; HARRISON P; HOCKING R; HOLLOWAY E; HUNT S; KEIL S; LIJNZAAD P; LOUISDITSULLY C; MA J; MENDIS A; MILLER J; MORISSETTE J; MUSELET D; NUSBAUM HC; PECK A; ROZEN S; SIMON D; SLONIM DK; STAPLES R; STEIN LD; STEWART EA; SUCHARD MA; THANGARAJAH T; VEGACZARNY N; WEBBER C; WU X; HUDSON J; AUFFRAY C; NOMURA N; SIKELA JM; POLYMEROPOULOS MH; JAMES MR; LANDER ES; HUDSON TJ; MYERS RM; COX DR; WEISSENBACH J; BOGUSKI MS; BENTLEY DR
      A PHYSICAL MAP OF 30,000 HUMAN GENES

      Science
    66. VONFELLENBERG J; PATERNOTTE C; PRUDHOMME JF; WEISSENBACH J; HAZAN J; BURGUNDER JM
      CLINICAL AND GENETIC-ANALYSIS OF 4 SWISS FAMILIES WITH THE PURE FORM OF HEREDITARY SPASTIC PARAPLEGIA

      Schweizerische medizinische Wochenschrift
    67. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCEDO D; MAENAUT K; WESTHOVENS R; MIGLIORINI P; TRAN TH; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LIOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAY G; LOPESVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      NEW SUSCEPTIBILITY LOCUS FOR RHEUMATOID-ARTHRITIS SUGGESTED BY A GENOME-WIDE LINKAGE STUDY

      Proceedings of the National Academy of Sciences of the United Statesof America
    68. HEINZLEF O; PATERNOTTE C; MAHIEUX F; PRUDHOMME JF; DIEN J; MADIGAND M; POUGET J; WEISSENBACH J; ROULLET E; HAZAN J
      MAPPING OF A COMPLICATED FAMILIAL SPASTIC PARAPLEGIA TO LOCUS SPG4 ONCHROMOSOME 2P

      Journal of Medical Genetics
    69. PARMENTIER L; BOUGHDENESTAMBOULI O; LAKHDAR H; BLANCHETBARDON C; DUBERTRET L; CLEPET C; WUNDERLE E; PULCINI F; FIZAMES C; WEISSENBACH J
      LAMELLAR ICHTHYOSIS - FURTHER NARROWING, PHYSICAL AND EXPRESSION MAPPING OF THE CHROMOSOME-2 CANDIDATE LOCUS

      Journal of investigative dermatology
    70. VIGOUROUX C; FAJAS L; KHALLOUF E; MEIER M; GYAPAY G; LASCOLS O; AUWERX J; WEISSENBACH J; CAPEAU J; MAGRE J
      HUMAN PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA-2 - GENETIC-MAPPING, IDENTIFICATION OF A VARIANT IN THE CODING SEQUENCE, AND EXCLUSION AS THE GENE RESPONSIBLE FOR LIPOATROPHIC DIABETES

      Diabetes
    71. MAGRE J; LAURELL H; FIZAMES C; ANTOINE PJ; DIB C; VIGOUROUX C; BOURUT C; CAPEAU J; WEISSENBACH J; LANGIN D
      HUMAN HORMONE-SENSITIVE LIPASE - GENETIC-MAPPING, IDENTIFICATION OF ANEW DINUCLEOTIDE REPEAT, AND ASSOCIATION WITH OBESITY AND NIDDM

      Diabetes
    72. BERNOT A; CLEPET C; DASILVA C; DEVAUD C; PETIT JL; CALOUSTIAN C; CRUAUD C; SAMSON D; PULCINI F; WEISSENBACH J; HEILIG R; NOTANICOLA C; DOMINGO C; ROZENBAUM M; BENCHETRIT E; TOPALOGLU R; DEWALLE M; DROSS C; HADJARI P; DUPONT M; DEMAILLE J; TOUITOU I; SMAOUI N; NEDELEC B; MERY JP; CHAABOUNI H; DELPECH M; GRATEAU G
      A CANDIDATE GENE FOR FAMILIAL MEDITERRANEAN FEVER

      Nature genetics
    73. ABDELHAK S; KALATZIS V; HEILIG R; COMPAIN S; SAMSON D; VINCENT C; WEIL D; CRUAUD C; SAHLY I; LEIBOVICI M; BITNERGLINDZICZ M; FRANCIS M; LACOMBE D; VIGNERON J; CHARACHON R; BOVEN K; BEDBEDER P; VANREGEMORTER N; WEISSENBACH J; PETIT C
      A HUMAN HOMOLOG OF THE DROSOPHILA EYES ABSENT GENE UNDERLIES BRANCHIOOTORENAL (BOR) SYNDROME AND IDENTIFIES A NOVEL GENE FAMILY

      Nature genetics
    74. BOUFFARD GG; IDOL JR; BRADEN VV; IYER LM; CUNNINGHAM AF; WEINTRAUB LA; TOUCHMAN JW; MOHRTIDWELL RM; PELUSO DC; FULTON RS; UELTZEN MS; WEISSENBACH J; MAGNESS CL; GREEN ED
      A PHYSICAL MAP OF HUMAN-CHROMOSOME 7 - AN INTEGRATED YAC CONTIG MAP WITH AVERAGE STS SPACING OF 79 KB

      PCR methods and applications
    75. BULLE F; CHIANNILKULCHAI N; PAWLAK A; WEISSENBACH J; GYAPAY G; GUELLAEN G
      IDENTIFICATION AND CHROMOSOMAL LOCALIZATION OF HUMAN GENES CONTAININGCAG CTG REPEATS EXPRESSED IN TESTIS AND BRAIN/

      PCR methods and applications
    76. FISCHER J; BLANCHETBARDON C; PRUDHOMME JF; PAVEK S; STEIJLEN PM; DUBERTRET L; WEISSENBACH J
      MAPPING OF PAPILLON-LEFEVRE-SYNDROME TO THE CHROMOSOME 11Q14 REGION

      European journal of human genetics
    77. PETERS U; SENGER G; RAHLMANN M; DUCHESNE I; STEC I; KOHLER MR; WEISSENBACH J; LEAL SM; KOCH HG; DEUFEL T; HARMS E
      NEPHROPATHIC CYSTINOSIS (CTNS-LSB) - CONSTRUCTION OF A YAC CONTIG COMPRISING THE REFINED CRITICAL REGION ON CHROMOSOME 17P13

      European journal of human genetics
    78. ABDELHAK S; KALATZIS V; HEILIG R; COMPAIN S; SAMSON D; VINCENT C; LEVIACOBAS F; CRUAUD C; LEMERRER M; MATHIEU M; KONIG R; VIGNERON J; WEISSENBACH J; PETIT C; WEIL D
      CLUSTERING OF MUTATIONS RESPONSIBLE FOR BRANCHIOOTORENAL (BOR) SYNDROME IN THE EYES ABSENT HOMOLOGOUS REGION (EYAHR) OF EYA1

      Human molecular genetics
    79. SAUNIER S; CALADO J; HEILIG R; SILBERMANN F; BENESSY F; MORIN G; KONRAD M; BROYER M; GUBLER MC; WEISSENBACH J; ANTIGNAC C
      A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS

      Human molecular genetics
    80. CHAIB H; KAPLAN J; GERBER S; VINCENT C; AYADI H; SLIM R; MUNNICH A; WEISSENBACH J; PETIT C
      A NEWLY IDENTIFIED LOCUS FOR USHER-SYNDROME TYPE-I, USH1E, MAPS TO CHROMOSOME 21Q21

      Human molecular genetics
    81. SIMMLER MC; HEARD E; ROUGEULLE C; CRUAUD C; WEISSENBACH J; AVNER P
      LOCALIZATION AND EXPRESSION ANALYSIS OF A NOVEL CONSERVED BRAIN EXPRESSED TRANSCRIPT, BRX BRX, LYING WITHIN THE XIC/XIC CANDIDATE REGION/

      Mammalian genome
    82. WEISSENBACH J
      THE HUMAN GENOME PROGRAM

      Pathologie et biologie
    83. WAGNER T; TOMMERUP N; WIRTH J; LEFFERS H; ZIMMER J; BACK E; WEISSENBACH J; SCHERER G
      A SOMATIC-CELL HYBRID PANEL FOR DISTAL 17Q - GDIA1 MAPS TO 17Q25.3

      Cytogenetics and cell genetics
    84. RAYMOND V; PLANTE M; COTE G; ANCTIL JL; AMYOT M; CLEPET C; WEISSENBACH J; MORISSETTE J
      NORMAL HOMOZYGOTES FOR AUTOSOMAL-DOMINANT OPEN-ANGLE GLAUCOMA AT THE GLC1A LOCUS

      Investigative ophthalmology & visual science
    85. JOUTEL A; VAHEDI K; CORPECHOT C; TROESCH A; CHABRIAT H; VAYSSIERE C; CRUAUD C; MACIAZEK J; WEISSENBACH J; BOUSSER MG; BACH JF; TOURNIERLASSERVE E
      STRONG CLUSTERING AND STEREOTYPED NATURE OF NOTCH3 MUTATIONS IN CADASIL PATIENTS

      Lancet
    86. JOUTEL A; CORPECHOT C; DUCROS A; VAHEDI K; CHABRIAT H; MOUTON P; ALAMOWITCH S; DOMENGA V; CECILLION M; MARECHAL E; MACIAZEK J; VAYSSIERE C; CRUAUD C; CABANIS EA; RUCHOUX MM; WEISSENBACH J; BACH JF; BOUSSER MG; TOURNIERLASSERVE E
      IDENTIFICATION OF THE CADASIL GENE

      Stroke
    87. JOUTEL A; CORPECHOT C; VAYSSIERE C; VAHEDI K; CHABRIAT H; MARECHAL E; MACIAZEK J; CRUAUD C; RUCHOUX MM; WEISSENBACH J; BOUSSER MG; TOURNIERLASSERVE E
      CHARACTERIZATION OF NOTCH3 MUTATIONS IN CADASIL PATIENTS

      Neurology
    88. ZHOU YX; TAKIYAMA Y; IGARASHI S; LI YF; ZHOU BY; GUI DC; ENDO K; TANAKA H; CHEN ZH; ZHOU LS; FAN MZ; YANG BX; WEISSENBACH J; WANG GX; TSUJI S
      MACHADO-JOSEPH-DISEASE IN 4 CHINESE PEDIGREES - MOLECULAR ANALYSIS OF15 PATIENTS INCLUDING 2 JUVENILE CASES AND CLINICAL CORRELATIONS

      Neurology
    89. NAOM IS; DALESSANDRO M; TOPALOGLU H; SEWRY C; FERLINI A; HELBLINGLECLERC A; GUICHENEY P; WEISSENBACH J; SCHWARTZ K; BUSHBY K; PHILPOT J; DUBOWITZ V; MUNTONI F
      REFINEMENT OF THE LAMININ ALPHA-2 CHAIN LOCUS TO HUMAN-CHROMOSOME 6Q2IN SEVERE AND MILD MEROSIN DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY

      Journal of Medical Genetics
    90. VIGOUROUX C; KHALLOUF E; BOURUT C; ROBERT JJ; DEKERDANET M; TUBIANARUFI N; FAURE S; WEISSENBACH J; CAPEAU J; MAGRE J
      GENETIC EXCLUSION OF 14 CANDIDATE GENES IN LIPOATROPIC DIABETES USINGLINKAGE ANALYSIS IN 10 CONSANGUINEOUS FAMILIES

      The Journal of clinical endocrinology and metabolism
    91. CORNELIS F; FRITZ P; PRUDHOMME JF; LIOTE F; WEISSENBACH J; KUNTZ D; BARDIN T
      DNA RESSOURCE OF AFFECTED SIB PAIR FAMILIES FOR GENETIC-STUDIES OF RHEUMATOID-ARTHRITIS

      Arthritis and rheumatism
    92. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCIDO D; MAENAUT K; WESTHOEVENS B; MIGLIORINI P; TRAN TH; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LLOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAV G; LOPEZVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      RHEUMATOID-ARTHRITIS GENOME SCAN AND PUTATIVE AUTOIMMUNITY LOCUS

      Arthritis and rheumatism
    93. CORNELIS F; HARDWICK L; FLIPO RM; MARTINEZ M; LASBLEIZ S; PRUDHOMME JF; TRAN TH; WALSH S; DELAYE A; NICOD A; LOSTE MN; LEPAGE V; GIBSON K; PILE K; DJOULAH S; DANZE PM; LIOTE F; CHARRON D; WEISSENBACH J; KUNTZ D; BARDIN T; WORDSWORTH BP
      ASSOCIATION OF RHEUMATOID-ARTHRITIS WITH AN AMINO-ACID ALLELIC VARIATION OF THE T-CELL RECEPTOR

      Arthritis and rheumatism
    94. CORNELIS F; FAURE S; MARTINEZ M; PRUDHOMME JF; FRITZ P; DIB C; ALVES H; BARRERA P; DEVRIES N; BALSA A; PASCUALSALCIDO D; MAENAUT K; WESTHOEVENS R; MIGLIORINI P; TRAN T; DELAYE A; PRINCE N; LEFEVRE C; THOMAS G; POIRIER M; SOUBIGOU S; ALIBERT O; LASBLEIZ S; FOUIX S; BOUCHIER C; LIOTE F; LOSTE MN; LEPAGE V; CHARRON D; GYAPAY G; LOPESVAZ A; KUNTZ D; BARDIN T; WEISSENBACH J
      RHEUMATOID-ARTHRITIS GENOME SCAN AND PUTATIVE AUTOIMMUNITY LOCUS

      American journal of human genetics
    95. DELEPINE M; POCIOT F; HABITA C; HASHIMOTO L; FROGUEL P; ROTTER J; CAMBONTHOMSEN A; DESCHAMPS I; DJOULAH S; WEISSENBACH J; NERUP J; LATHROP M; JULIER C
      EVIDENCE OF A NON-MHC SUSCEPTIBILITY LOCUS IN TYPE-I DIABETES LINKED TO HLA ON CHROMOSOME-6

      American journal of human genetics
    96. WEISSENBACH J; BENTOLILA S
      INTEGRATING MAPS REQUIRES INTEGRATED DATA

      Nature biotechnology
    97. MCDOWELL G; ISOGAI T; TANIGAMI A; HAZELWOOD S; LEDBETTER D; POLYMEROPOULOS MH; LICHTERKONECKI U; KONECKI D; TOWN MM; VANTHOFF W; WEISSENBACH J; GAHL WA
      FINE MAPPING OF THE CYSTINOSIS GENE USING AN INTEGRATED GENETIC AND PHYSICAL MAP OF A REGION WITHIN HUMAN-CHROMOSOME BAND 17P13

      Biochemical and molecular medicine
    98. MARQUET S; ABEL L; HILLAIRE D; DESSEIN H; KALIL J; FEINGOLD J; WEISSENBACH J; DESSEIN AJ
      GENETIC LOCALIZATION OF A LOCUS CONTROLLING THE INTENSITY OF INFECTION BY SCHISTOSOMA-MANSONI ON CHROMOSOME 5Q31-Q33

      Nature genetics
    99. HAINES JL; TERMINASSIAN M; BAZYK A; GUSELLA JF; KIM DJ; TERWEDOW H; PERICAKVANCE MA; RIMMLER JB; HAYNES CS; ROSES AD; LEE A; SHANER B; MENOLD M; SEBOUN E; FITOUSSI RP; GARTIOUX C; REYES C; RIBIERRE F; GYAPAY G; WEISSENBACH J; HAUSER SL; GOODKIN DE; LINCOLN R; USUKU K; GARCIAMERINO A; GATTO N; YOUNG S; OKSENBERG JR
      A COMPLETE GENOMIC SCREEN FOR MULTIPLE-SCLEROSIS UNDERSCORES A ROLE FOR THE MAJOR HISTOCOMPATABILITY COMPLEX

      Nature genetics
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 08:06:44