Publications Genoscope de 1998 à 2004

Les collaborateurs du Genoscope sont indiqués en gras parmi les auteurs. Vous pouvez aussi accéder à la liste plus restreinte des publications signées par les chercheurs de l'UMR CNRS 8030 "Génomique Métabolique".

1998 - 1999 - 2000 - 2001 - 2002 - 2003 - 2004

1998

Bernot A., Da Silva C., Petit J.L., Cruaud C., Caloustian C., Castet V., Ahmed-Arab 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. and Touitou I.,

Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF). Hum. Mol. Genet. 7:1317-25 (1998).

Bernot A., Heilig R., Clepet C., Smaoui N., Da Silva C., Petit J.L., Devaud C., Chiannilkulchai N., Fizames C., Samson D., Cruaud C., Caloustian C., Gyapay G., Delpech M. and Weissenbach J.,

A transcriptional Map of the FMF region. Genomics 50:147-60 (1998).

Deloukas P., Schuler G.D., Gyapay G., Beasley E.M., Soderlund C., Rodriguez-Tomé P., Hui L., Matise T.C., McKusick K.B., Bentolila S., Bihoreau M.T., Birren B.B., Browne J., Butler A., Castle A.B., Chiannilkulchai N., Clee C., Day P.J.R., Dehejia A., Bibling 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., Louis-Dit-Sully C., Ma J., Mendis A., Miller J., Morissette J., Muselet D., Nusbaum H.C., Peck A., Rozen S., Simon D., Slonim D.K., Staples R., Stein L.D., Stewart E.A., Suchard M.A., Thangarajah T., Vega-Czarny N., Webber C., Wu X., Hudson J., Auffray C., Nomura N., Sikela J.M., Polymeropoulos M.H., James M.R., Lander E.S., Hudson T.J., Myers R.M., Cox D.R., Weissenbach J., Boguski M.S. and Bentley D.R.,

A physical map of 30,000 human genes. Science 282:744-746 (1998).

Dewalle M., Domingo C., Rozenbaum M., Ben-Chétrit E., Cattan D., Bernot A., Dross C., Dupont M., Notarnicola C., Levy M., Rosner I., Demaille J. and Touitou I.,

Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF). Eur. J. Human Genet. 6:95-97 (1998).

Fischer J., Bouadjar B., Heilig R., Fizames C., Prud'homme J.F. and Weissenbach J.,

Genetic linkage of Meleda disease to chromosome 8qter. Eur. J. Human Genet. 6:542-547 (1998).

Fischer J., Urtizberea J.A., Pavek S., Vandiedonck C., Brüls T., Saker S., Alkatip Y., Prud'homme J.F. and Weissenbach J.,

Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22. Hum. Genet. 103:60-64 (1998).

Mustapha M., Chardenoux S., Nieder A., Salem N., Weissenbach J., El-Zir E., Loiselet J. and Petit C.,

A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36. Eur. J. Human Genet. 6:245-250 (1998).

Paternotte C., Rudnicki D., Fizames C., Davoine C.S., 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. and Hazan J.,

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q. Genome Res. 8:1216-1227 (1998).

Pawlak A., Chiannikulchai N., Ansorge W., Bulle F., Weissenbach J., Gyapay G. and Guellaën G.,

Identification and mapping of 26 human testis mRNAs containing CAG/CTG repeats. Mamm. Genome 9:745-8 (1998).

Salomon-Nguyen F., Le Coniat-Busson M., Heilig R., Campion D., Weissenbach J. and Berger R.,

Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA. C. R. Acad. Sci. III 321:447-52 (1998).

Weissenbach J.,

Human genome mapping and sequencing: perspectives for toxicology. Toxicol. Lett. 102-103:1-4 (1998).

Weissenbach J.,

The Human Genome Project: from mapping to sequencing. Clin. Chem. Lab. Med. 36:511-4 (1998).

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1999

Bentolila S., Bach J.M., Kessler J.L., Bordelais I., Cruaud C., Weissenbach J. and Panthier J.J.,

Analysis of major repetitive DNA sequences in the dog (Canis familiaris) genome. Mamm. Genome 10:699-705 (1999).

Boeddrich A., Burgtorf C., Roest Crollius H., Hennig S., Bernot A., Clark M., Reinhardt R., Lehrach H. and Francis F.,

Analysis of the spermine synthase gene region in Fugu rubripes, Tetraodon fluviatilis and Danio rerio. Genomics 164-168 (1999).

Galio L., Bouquet C. and Brooks P.,

ATP hydrolysis-dependent formation of a dynamic ternary nucleoprotein complex with MutS and MutL. Nucl. Acid Res. 27:2325-2331 (1999).

Hazan J., Davoine C.S., 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. and Weissenbach J.,

A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant Spastic Paraplegia. Genomics 60:309-319 (1999).

Hazan J., Fonknechten N., Mavel D., Paternotte C., Samson D., Artiguenave F., Davoine C.S., Cruaud C., Dürr A., Wincker P., Brottier P., Cattolico L., Barbe V., Burgunder J.M., Prud'homme J.F., Brice A., Fontaine B., Heilig R. and Weissenbach J.,

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nature Genet. 23:296-303 (1999).

Korenberg J.R., Chen X.N., Sun Z., Shi Z.Y., Ma S., Vataru E., Yimlamai D., Weissenbach J., Shizuya H., Simon M.I., Gerety S.S., Nguyen H., Zemsteva I.S., Hui L., Silva J., Wu X., Birren B.W. and Hudson T.J.,

Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine. Genome Res. 9:994-1001 (1999).

Morissette J., Villeneuve A., Bordeleau L., Rochette D., Laberge C., Gagne B., Laprise C., Bouchard G., Plante M., Gobeil L., Shink E., Weissenbach J. and 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. Am. J. Med. Genet. 88:567-587 (1999).

Roest Crollius H.,

Des clusters de gènes HOX surnuméraires révèlent une duplication du génome chez les poissons. Med. Sci. 15:411-413 (1999).

Tiret L., Kessler J.L., Bentolila S., Fauré S., Bach J.M., Weissenbach J. and Panthier J.J.,

Characterization and mapping of canine polymorphic markers. Animal Genet. 30:475-476 (1999).

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2000

Adams M.D., Celniker S.E., Holt R.A., Evans C.A., Gocayne J.D., Amanatides P.G., Scherer S., Li P.W., Hoskins R.A., Galle R.F., George R.A., Lewis S., Richards S., Ashburner M., Henderson S.N., Sutton G.G., Wortman J.R., Yandell M.D., Zhang Q., Chen L.X., Brandon R.C., Rogers Y.H.C., Blazej R.G., Champe M., Pfeiffer B.D., Wan K.H., Doyle C., Baxter E.G., Nelson C.R., Miklos G.L.G., Ferrando J.F.A., Agbayani A., An H.J., Ballew R.M., Basu A., Baxendale J., Bayraktaroglu L., Beasley E.M., Beeson K.Y., Benos P.V., Berman B.P., Bhandari D., Bolshakov S., Borkova D., Botchan M.R., Bouck J., Brokstein P., Brottier P., Burtis K.C., Busam D., Butler H., Cadieu E., Cherry J.M., Dahlke C., Davies P., de Pablos B., Delcher A., Deng Z., Deslattes Mays A., Dew I., Dietz S.M., Dodson K., Doup L., Downes M., Dugan-Rocha S., Dunkov B.C., Dunn P., Durbin K.J., Evangelista C.C., Ferraz C., Fleischmann W., Fosler C., Gabrielian A.E., Garg N., Gelbart W.M., Glasser K., Glodek A., Gong F., Gorrell J.H., Gu Z., Guan P., Harris M., Harris N.L., Harvey D., Heiman T.J., Helt G., Hernandez J.R., Houck J., Houston K.A., Howland T.J., Kalush F., Karpen G.H., Ke P., Kennison J.A., Ketchum K.A., Kimmel B., Kodira C.D., Kraft C., Kravitz S., Kulp D., Lai Z., Lasko P., Lei Y., Levitsky A.A., Li J., Li Z., Liang Y., Lin X., Liu X., Mattei B., McIntosh T.C., McLeod M.P., McPherson D., Merkulov G., Milshina N.V., Mobarry C., Morris J., Moshrefi A., Mount S.M., Moy M., Murphy B., Murphy L., Muzny D.M., Nelson D.L., Nelson D.R., Nelson K.A., Nixon K., Nusskern D.R., Pacleb J.M., Palazzolo M., Pittman G.S., Pan S., Pollard J., Puri V., Reese M.G., Reinert K., Remington K., Saunders R.D., Scheeler F., Shen H., Shue B.C., Siden-Kiamos I., Simpson M., Skupski M.P., Smith T., Spier E., Spradling A.C., Stapleton M., Strong R., Sun E., Svirskas R., Tector C., Turner R., Venter E., Wang A.H., Wang X., Wang Z.Y., Wassarman D.A., Weinstock G.M., Weissenbach J., Williams S.M., WoodageT., Worley K.C., Wu D., Yang S., Yao Q.A., Ye J., Yeh R.F., Zaveri J.S., Zhan M., Zhang G., Zhao Q., Zheng L., Zheng X.H., Zhong F.N., Zhong W., Zhou X., Zhu S., Zhu X., Smith H.O., Gibbs R.A., Myers E.W., Rubin G.M. and Venter J.C.,

The genome sequence of Drosophila melanogaster, Science 287:2185-2195 (2000).

Artiguenave F., Wincker P., Brottier P., Duprat S., Jovelin F., Scarpelli C., Verdier J., Vico V., Weissenbach J. and Saurin W.,

Genomic exploration of the hemiascomycetous yeasts: 2. Data generation and processing. FEBS Lett. 487:13-16 (2000).

Blandin G., Llorente B., Malpertuy A., Wincker P., Artiguenave F. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 13. Pichia angusta. FEBS Lett. 487:76-81 (2000).

Blandin G., Ozier-Kalogeropoulos O., Wincker P., Artiguenave F. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 16. Candida tropicalis. FEBS Lett. 487:91-94 (2000).

Bolotin-Fukuhara M., Toffano-Nioche C., Artiguenave F., Duchateau-Nguyen G., Lemaire M., Marmeisse R., Montrocher R., Robert C., Termier M., Wincker P. and Wesolowski-Louvel M.,

Genomic exploration of the hemiascomycetous yeasts: 11. Kluyveromyces lactis. FEBS Lett. 487:66-70 (2000).

Bon E., Neuveglise C., Casaregola S., Artiguenave F., Wincker P., Aigle M. and Durrens P.,

Genomic exploration of the hemiascomycetous yeasts: 5. Saccharomyces bayanus var. uvarum. FEBS Lett. 487:37-41 (2000).

Bon E., Neuveglise C., Lepingle A., Wincker P., Artiguenave F., Gaillardin C. and Casaregola S.,

Genomic exploration of the hemiascomycetous yeasts: 6. Saccharomyces exiguus. FEBS Lett. 487:42-46 (2000).

Bürger J., Fonknechten N., Hoeltzenbein M., Neumann L., Bratanoff E., Hazan J. and Reis A.,

Hereditary spastic paraplegia caused by mutations in the SPG4 gene. Eur. J. Human Genet. 8:771-776 (2000).

Casaregola S., Lepingle A., Bon E., Neuveglise C., Nguyen H., Artiguenave F., Wincker P. and Gaillardin C.,

Genomic exploration of the hemiascomycetous yeasts: 7. Saccharomyces servazzii. FEBS Lett. 487:47-51 (2000).

Casaregola S., Neuveglise C., Lepingle A., Bon E., Feynerol C., Artiguenave F., Wincker P. and Gaillardin C.,

Genomic exploration of the hemiascomycetous yeasts: 17. Yarrowia lipolytica. FEBS Lett. 487:95-100 (2000).

de Montigny J., Spehner C., Souciet J., Tekaia F., Dujon B., Wincker P., Artiguenave F. and Potier S.,

Genomic exploration of the hemiascomycetous yeasts: 15. Pichia sorbitophila. FEBS Lett. 487:87-90 (2000).

de Montigny J., Straub M., Potier S., Tekaia F., Dujon B., Wincker P., Artiguenave F. and Souciet J.,

Genomic exploration of the hemiascomycetous yeasts: 8. Zygosaccharomyces rouxii (1). FEBS Lett. 487:52-55 (2000).

Escary J.L., Bottius E., Prince N., Reyes C., Fiawoumo Y., Caloustian C., Brüls T., Fujiyama A., Cooper R.S., Adeyemo A.A., Lathrop G.M., Weissenbach J., Gyapay G., Foglio M. and Beckmann J.S.,

A first high-density map of 981 biallelic markers on human chromosome 14. Genomics 70:153-164 (2000).

Fischer C., Ozouf-Costaz C., Roest-Crollius H., Da Silva C., Jaillon O., Bouneau L., Bonillo C., Weissenbach J. and Bernot A.,

Karyotype and chromosome location of characteristic tandem repeats in the pufferfish Tetraodon nigroviridis. Cytogenet. Cell Genet. 88:50-55 (2000).

Fischer J., Faure A., Bouadjar B., Blanchet-Bardon C., Karaduman A., Thomas I., Emre S., Cure S., Özgüc M., Weissenbach J. and Prud'homme J.F.,

Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity. Am. J. Hum. Genet. 66:904-913 (2000).

Fonknechten N., Mavel D., Byrne P., Davoine C.S., Cruaud C., Boentsch D., Samson D., Coutinho P., Hutchinson M., McMonagle P., Burgunder J.M., Tartaglione A., Heinzlef O., Feki I., Deufel T., Parfrey N., Brice A., Fontaine B., Prud'homme J.F., Weissenbach J., DÃ¼rr A. and Hazan J.,

Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. Hum. Mol. Genet. 9:637-644 (2000).

Fontaine B., Davoine C.S., Durr A., Paternotte C., Feki I., Weissenbach J., Hazan J. and Brice A.,

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34. Am. J. Hum. Genet. 66:702-7 (2000).

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 J. and Weissenbach J.,

Genomic exploration of the hemiascomycetous yeasts: 21. Comparative functional classification of genes. FEBS Lett 487:134-149 (2000).

Garcia V., Salanoubat M., Choisne N. and Tissier A.,

An ATM homologue from Arabidopsis thaliana: complete genomic organisation and expression analysis. Nucl. Acids Res. 28:1692-9 (2000).

Lepingle A., Casaregola S., Neuveglise C., Bon E., Nguyen H., Artiguenave F., Wincker P. and Gaillardin C.,

Genomic exploration of the hemiascomycetous yeasts: 14. Debaryomyces hansenii var. hansenii. FEBS Lett. 487:82-86 (2000).

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 J. and Gaillardin C.,

Genomic exploration of the hemiascomycetous yeasts: 20. Evolution of gene redundancy compared to Saccharomyces cerevisiae. FEBS Lett. 487:122-133 (2000).

Llorente B., Malpertuy A., Blandin G., Artiguenave F., Wincker P. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 12. Kluyveromyces marxianus var. marxianus. FEBS Lett 487:71-75 (2000).

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 J. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 18. Comparative analysis of chromosome maps and synteny with Saccharomyces cerevisiae. FEBS Lett. 487:101-112 (2000).

Malpertuy A., Llorente B., Blandin G., Artiguenave F., Wincker P. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 10. Kluyveromyces thermotolerans. FEBS Lett. 487:61-65 (2000).

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 J. and Dujon B.,

Genomic exploration of the hemiascomycetous yeasts: 19. Ascomycetes-specific genes. FEBS Lett. 487:113-121 (2000).

Myllykallio H., Lopez P., Lopez-Garcia P., Heilig R., Saurin W., Zivanovic Y., Philippe H. and Forterre P.,

Bacterial mode of replication with eukaryotic-like machinery in a hyperthermophilic archaeon. Science 288:2212-5 (2000).

Neuveglise C., Bon E., Lepingle A., Wincker P., Artiguenave F., Gaillardin C. and Casaregola S.,

Genomic exploration of the hemiascomycetous yeasts: 9. Saccharomyces kluyveri. FEBS Lett. 487:56-60 (2000).

Nicole S., Davoine C.S., Topaloglu H., Cattolico L., Barral D., Beighton P., Hamida C.B., Hammouda H., Cruaud C., White P.S., Samson D., Urtizberea J.A., Lehmann-Horn F., Weissenbach J., Hentati F. and Fontaine B.,

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nature Genet. 26:480-483 (2000).

Ogata H., Audic S., Barbe V., Artiguenave F., Fournier P.E., Raoult D. and Claverie J.M.,

Selfish DNA in protein-coding genes of rickettsia. Science 290:347-50 (2000).

Roest Crollius H., Jaillon O., Bernot A., Da Silva C., Bouneau L., Fischer C., Fizames C., Wincker P., Brottier P., Quétier F., Saurin W. and Weissenbach J.,

Estimate of gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence. Nature Genet. 25:235-238 (2000).

Roest Crollius H., Jaillon O., Da Silva C., Ozouf-Costaz C., Fizames C., Fischer C., Bouneau L., Billault A., Quétier F., Saurin W., Bernot A. and Weissenbach J.,

Characterization and repeat analysis of the compact genome of the freshwater pufferfish Tetraodon nigroviridis. Genome Res. 10:939-49 (2000).

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 L.A., Mache R., Puigdomenech P., De Simone V., Choisne N., Artiguenave F., Robert C., Brottier P., Wincker P., Cattolico L., Weissenbach J., Saurin W., Quétier 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 T.H., 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 A.C., Alcaraz J.P., 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 H.W., Mayer K.F., Kaul S., Town C.D., Koo H.L., Tallon L.J., Jenkins J., Rooney T., Rizzo M., Walts A., Utterback T., Fujii C.Y., Shea T.P., Creasy T.H., Haas B., Maiti R., Wu D. and Peterson J.,

Sequence and analysis of chromosome 3 of the plant Arabidopsis thaliana. Nature 408:820-822 (2000).

Saunier S., Calado J., Benessy F., Silberman F., Heilig R., Weissenbach J. and Antignac C.,

Characterization of the NPHP1 locus: mechanism involved in deletions in familial juvenile nephronophthisis. Am. J. Hum. Genet. 66:778-789 (2000).

Scimeca J.C., Franchi A., Trojani C., Parrinello H., Grosgeorge J., Robert C., Jaillon O., Poirier C., Gaudray P. and Carle G.F.,

The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants. Bone 26:207-13 (2000).

Souciet J., 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. and Weissenbach J.,

Genomic exploration of the hemiascomycetous yeasts: 1. A set of yeast species for molecular evolution studies (1). FEBS Lett. 487:3-12 (2000).

The Arabidopsis Genome Initiative (Salanoubat M., Choisne N., Artiguenave F., Weissenbach J. and Quétier F. for Genoscope),

Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 408:796-815 (2000).

Tiret L., Kessler J.L., Bentolila S., Faure S., Bach J.M., Weissenbach J. and Panthier J.J.,

Assignation of highly polymorphic markers on a canine purebred pedigree. Mamm. Genome 11:703-5 (2000).

Tullio-Pelet A., Salomon R., Hadj-Rabia S., Mugnier C., de Laet M.H., Chaouachi B., Bakiri F., Brottier P., Cattolico L., Penet C., Begeot M., Naville D., Nicolino M., Chaussain J.L., Weissenbach J., Munnich A. and Lyonnet S.,

Mutant WD-repeat protein in triple-A syndrome. Nature Genet. 26:332-335 (2000).

Weissenbach J. and Salanoubat M.,

Séquence des génomes : le feu d'artifice. Med. Sci. 16:10-16 (2000).

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2001

Avner P., Brüls T., Poras I., Eley L., Gas S., Ruiz P., Wiles M.V., 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. and Cox R.D.,

A radiation hybrid transcript map of the mouse genome. Nat. Genet. 29:194-200 (2001).

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. and Lepiniec L.,

Improved PCR-walking for large-scale isolation of plant T-DNA borders. Biotechniques 30:496-8, 502, 504 (2001).

Bernard O.A., Busson-LeConiat M., Ballerini P., Mauchauffe M., Della Valle V., Monni R., Nguyen Khac F., Mercher T., Penard-Lacronique V., Pasturaud P., Gressin L., Heilig R., Daniel M.T., Lessard M. and Berger R.,

A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia. Leukemia 15:1495-504 (2001).

Bolotin A., Wincker P., Mauger S., Jaillon O., Malarme K., Weissenbach J., Ehrlich S.D. and A. Sorokin,

The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403. Genome Res. 11:731-753 (2001).

Brüls T., Gyapay G., Petit J.L., Artiguenave F., Vico V., Qin S., Tin-Wollam A.M., 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. and Heilig R.,

A physical map of human chromosome 14. Nature 409:947-948 (2001).

Chambaud I., Heilig R., Ferris S., Barbe V., Samson D., Galisson F., Moszer I., Dybvig K., Wroblewski H., Viari A., Rocha E. and Blanchard A.,

The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis. Nucl. Acid. Res. 29:2145-2153 (2001).

Chardon P., Rogel-Gaillard C., Cattolico L., Duprat S., Vaiman M. and Renard C.,

Sequence of the swine major histocompatibility complex region containing all non-classical class I genes. Tissue Antigens 57:55-65 (2001).

Charlier C., Segers K., Karim L., Shay T., Gyapay G., Cockett N. and Georges M.,

The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status. Nat. Genet. 27:367-369 (2001).

Charlier C., Segers K., Wagenaar D., Karim L., Berghmans S., Jaillon O., Shay T., Weissenbach J., Cockett N., Gyapay G. and Georges M.,

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The genome sequence of the malaria mosquito Anopheles gambiae. Science 298:129-149 (2002).

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A panoramic view of gene expression in the human kidney. Proc. Natl. Acad. Sci. USA 100:13710-13715 (2003).

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Molecular evidence for novel planctomycete diversity in a municipal wastewater treatment plant. Appl. Environ. Microbiol. 69:7354-7363 (2003).

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The DNA sequence and analysis of human chromosome 14. Nature 421:601-607 (2003).

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Assessing the Drosophila melanogaster and Anopheles gambiae genome anotations using genome-wide sequence comparisons. Genome Res. 1595-1599 (2003).

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Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome. Hum. Mol. Genet. 12:925-935 (2003).

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The complete mitochondrial genome sequence of the pathogenic yeast Candida (Torulopsis) glabrata. FEBS Lett. 534:39-48 (2003).

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Comparative genomic analysis reveals independent expansion of a lineage-specific gene family in vertebrates: The class II cytokine receptors and their ligands in mammals and fish. BMC Genomics 4:29 (2003).

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Identification of the Anopheles gambiae ATP-binding cassette transporter superfamily genes. Mol. Cells 15:150-158 (2003).

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Characterization of the genomic organization of the region around the centromere of chomosome V of Podospora anserina by direct sequencing. Fungal Genet. Biol. 250-263 (2003).

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2004

Abel A., Fonknechten N., Hofer A., Durr A., Cruaud C., Voit T., Weissenbach J., Brice A., Klimpe S., Auburger G. and Hazan J.,

Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Neurogenetics (2004).

Barbe V., Vallenet D., Fonknechten N., Kreimeyer A., Oztas S., Labarre L., Cruveiller S., Robert C., Duprat S., Wincker P., Ornston L.N., Weissenbach J., Marlière P., Cohen G.N. and Médigue C.,

Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium. Nucleic Acids Res. 32:5766-5779 (2004).

Castelli V., Aury J.M., Jaillon O., Wincker P., Clepet C., Menard M., Cruaud C., Quétier F., Scarpelli C., Schächter V., Temple G., Caboche M., Weissenbach J. and Salanoubat M.,

Whole genome sequence comparisons and "full-length" cDNA sequences: a combined approach to evaluate and improve Arabidopsis genome annotation. Genome Res. 14:406-413 (2004).

Chabrier N., Chiaverini M., Danos V., Fages F. and Schächter V.,

Modeling and querying biochemical interaction networks Theoretical Computer Science 325: 25-44 (2004).

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Insights into the evolution of Yersinia pestis through whole-genome comparison with Yersinia pseudotuberculosis. Proc. Natl. Acad. Sci. USA. 101: 13826-31 (2004).

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The genome sequence of the entomopathogenic bacterium Photorhabdus luminescens. Nature Biotechnology 11: 1307-1313 (2003).

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