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Jean Weissenbach

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Procedures

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Chemicals & Drugs

Genes & Molecular Sequences

Devices

Chromosomes, Artificial, Yeast

Living Beings

Tetraodontiformes

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Publications

TOP 3
de Berardinis Véronique; Durot Maxime; Weissenbach Jean; Salanoubat Marcel
Acinetobacter baylyi ADP1 as a model for metabolic system biology.
Rivière Delphine; Desvignes Virginie; Pelletier Eric; Chaussonnerie Sébastien; Guermazi Sonda; Weissenbach Jean; Li Tianlun; Camacho Patricia; Sghir Abdelghani
Towards the definition of a core of microorganisms involved in anaerobic digestion of sludge.
Fonknechten Nuria; Perret Alain; Perchat Nadia; Tricot Sabine; Lechaplais Christophe; Vallenet David; Vergne Carine; Zaparucha Anne; Le Paslier Denis; Weissenbach Jean; Salanoubat Marcel
A conserved gene cluster rules anaerobic oxidative degradation of L-ornithine.

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All Publications

2009: de Berardinis Véronique; Durot Maxime; Weissenbach Jean; Salanoubat Marcel
Acinetobacter baylyi ADP1 as a model for metabolic system biology.
Current opinion in microbiology 2009;12(5):568-76.
2009: Rivière Delphine; Desvignes Virginie; Pelletier Eric; Chaussonnerie Sébastien; Guermazi Sonda; Weissenbach Jean; Li Tianlun; Camacho Patricia; Sghir Abdelghani
Towards the definition of a core of microorganisms involved in anaerobic digestion of sludge.
The ISME journal 2009;3(6):700-14.
2009: Fonknechten Nuria; Perret Alain; Perchat Nadia; Tricot Sabine; Lechaplais Christophe; Vallenet David; Vergne Carine; Zaparucha Anne; Le Paslier Denis; Weissenbach Jean; Salanoubat Marcel
A conserved gene cluster rules anaerobic oxidative degradation of L-ornithine.
Journal of bacteriology 2009;191(9):3162-7.
2008: Esnault Cécile; Priet Stéphane; Ribet David; Vernochet Cécile; Bruls Thomas; Lavialle Christian; Weissenbach Jean; Heidmann Thierry
A placenta-specific receptor for the fusogenic, endogenous retrovirus-derived, human syncytin-2.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(45):17532-7.
2008: Guermazi Sonda; Daegelen Patrick; Dauga Catherine; Rivière Delphine; Bouchez Théodore; Godon Jean Jacques; Gyapay Gábor; Sghir Abdelghani; Pelletier Eric; Weissenbach Jean; Le Paslier Denis
Discovery and characterization of a new bacterial candidate division by an anaerobic sludge digester metagenomic approach.
Environmental microbiology 2008;10(8):2111-23.
2008: Pelletier Eric; Kreimeyer Annett; Bocs Stéphanie; Rouy Zoé; Gyapay Gábor; Chouari Rakia; Rivière Delphine; Ganesan Akila; Daegelen Patrick; Sghir Abdelghani; Cohen Georges N; Médigue Claudine; Weissenbach Jean; Le Paslier Denis
"Candidatus Cloacamonas acidaminovorans": genome sequence reconstruction provides a first glimpse of a new bacterial division.
Journal of bacteriology 2008;190(7):2572-9.
2008: Chantret Nathalie; Salse Jérôme; Sabot François; Bellec Arnaud; Laubin Bastien; Dubois Ivan; Dossat Carole; Sourdille Pierre; Joudrier Philippe; Gautier Marie-Françoise; Cattolico Laurence; Beckert Michel; Aubourg Sébastien; Weissenbach Jean; Caboche Michel; Leroy Philippe; Bernard Michel; Chalhoub Boulos
Contrasted microcolinearity and gene evolution within a homoeologous region of wheat and barley species.
Journal of molecular evolution 2008;66(2):138-50.
2008: Lapidus Alla; Goltsman Eugene; Auger Sandrine; Galleron Nathalie; Ségurens Béatrice; Dossat Carole; Land Miriam L; Broussolle Veronique; Brillard Julien; Guinebretiere Marie-Helene; Sanchis Vincent; Nguen-The Christophe; Lereclus Didier; Richardson Paul; Wincker Patrick; Weissenbach Jean; Ehrlich S Dusko; Sorokin Alexei
Extending the Bacillus cereus group genomics to putative food-borne pathogens of different toxicity.
Chemico-biological interactions 2008;171(2):236-49.
2008: Vallenet David; Nordmann Patrice; Barbe Valérie; Poirel Laurent; Mangenot Sophie; Bataille Elodie; Dossat Carole; Gas Shahinaz; Kreimeyer Annett; Lenoble Patricia; Oztas Sophie; Poulain Julie; Segurens Béatrice; Robert Catherine; Abergel Chantal; Claverie Jean-Michel; Raoult Didier; Médigue Claudine; Weissenbach Jean; Cruveiller Stéphane
Comparative analysis of Acinetobacters: three genomes for three lifestyles.
PloS one 2008;3(3):e1805.
2008: de Berardinis Véronique; Vallenet David; Castelli Vanina; Besnard Marielle; Pinet Agnès; Cruaud Corinne; Samair Sumitta; Lechaplais Christophe; Gyapay Gabor; Richez Céline; Durot Maxime; Kreimeyer Annett; Le Fèvre François; Schächter Vincent; Pezo Valérie; Döring Volker; Scarpelli Claude; Médigue Claudine; Cohen Georges N; Marlière Philippe; Salanoubat Marcel; Weissenbach Jean
A complete collection of single-gene deletion mutants of Acinetobacter baylyi ADP1.
Molecular systems biology 2008;4():174.
2007: Fraser-Liggett Claire M; Weissenbach Jean
Genomics.
Current opinion in microbiology 2007;10(5):479-80.
2007: Stevanin G; Paternotte C; Coutinho P; Klebe S; Elleuch N; Loureiro J L; Denis E; Cruz V T; Dürr A; Prud'homme J-F; Weissenbach J; Brice A; Hazan J
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21.
Neurology 2007;68(21):1837-40.
2007: Kreimeyer Annett; Perret Alain; Lechaplais Christophe; Vallenet David; Médigue Claudine; Salanoubat Marcel; Weissenbach Jean
Identification of the last unknown genes in the fermentation pathway of lysine.
The Journal of biological chemistry 2007;282(10):7191-7.
2007: Fierro Ana C; Thuret Raphaël; Coen Laurent; Perron Muriel; Demeneix Barbara A; Wegnez Maurice; Gyapay Gabor; Weissenbach Jean; Wincker Patrick; Mazabraud André; Pollet Nicolas
Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis.
BMC genomics 2007;8():118.
2006: Lebofsky Ronald; Heilig Roland; Sonnleitner Max; Weissenbach Jean; Bensimon Aaron
DNA replication origin interference increases the spacing between initiation events in human cells.
Molecular biology of the cell 2006;17(12):5337-45.
2006: Marlétaz Ferdinand; Martin Elise; Perez Yvan; Papillon Daniel; Caubit Xavier; Lowe Christopher J; Freeman Bob; Fasano Laurent; Dossat Carole; Wincker Patrick; Weissenbach Jean; Le Parco Yannick
Chaetognath phylogenomics: a protostome with deuterostome-like development.
Current biology : CB 2006;16(15):R577-8.
2006: Danchin Antoine; Fujiyama Asao; Matsubara Ken-ichi; Roberts Richard; Sugano Sumio; Weissenbach Jean
Re: request from the International Advisory Committee to DDBJ/EMBL/GenBank.
Journal of medical virology 2006;78(7):995.
2006: Duret Laurent; Chureau Corinne; Samain Sylvie; Weissenbach Jean; Avner Philip
The Xist RNA gene evolved in eutherians by pseudogenization of a protein-coding gene.
Science (New York, N.Y.) 2006;312(5780):1653-5.
2006: van de Guchte M; Penaud S; Grimaldi C; Barbe V; Bryson K; Nicolas P; Robert C; Oztas S; Mangenot S; Couloux A; Loux V; Dervyn R; Bossy R; Bolotin A; Batto J-M; Walunas T; Gibrat J-F; Bessières P; Weissenbach J; Ehrlich S D; Maguin E
The complete genome sequence of Lactobacillus bulgaricus reveals extensive and ongoing reductive evolution.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(24):9274-9.
2006: Vodovar Nicolas; Vallenet David; Cruveiller Stéphane; Rouy Zoé; Barbe Valérie; Acosta Carlos; Cattolico Laurence; Jubin Claire; Lajus Aurélie; Segurens Béatrice; Vacherie Benoît; Wincker Patrick; Weissenbach Jean; Lemaitre Bruno; Médigue Claudine; Boccard Frédéric
Complete genome sequence of the entomopathogenic and metabolically versatile soil bacterium Pseudomonas entomophila.
Nature biotechnology 2006;24(6):673-9.
2006: Thill Gilbert; Castelli Vanina; Pallud Sophie; Salanoubat Marcel; Wincker Patrick; de la Grange Pierre; Auboeuf Didier; Schächter Vincent; Weissenbach Jean
ASEtrap: a biological method for speeding up the exploration of spliceomes.
Genome research 2006;16(6):776-86.
2006: Sanlaville D; Etchevers H C; Gonzales M; Martinovic J; Clément-Ziza M; Delezoide A-L; Aubry M-C; Pelet A; Chemouny S; Cruaud C; Audollent S; Esculpavit C; Goudefroye G; Ozilou C; Fredouille C; Joye N; Morichon-Delvallez N; Dumez Y; Weissenbach J; Munnich A; Amiel J; Encha-Razavi F; Lyonnet S; Vekemans M; Attié-Bitach T
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.
Journal of medical genetics 2006;43(3):211-217.
2006: Fournier Pierre-Edouard; Vallenet David; Barbe Valérie; Audic Stéphane; Ogata Hiroyuki; Poirel Laurent; Richet Hervé; Robert Catherine; Mangenot Sophie; Abergel Chantal; Nordmann Patrice; Weissenbach Jean; Raoult Didier; Claverie Jean-Michel
Comparative genomics of multidrug resistance in Acinetobacter baumannii.
PLoS genetics 2006;2(1):e7.
2006: Bourdet A; Ciaudo C; Zakin L; Elalouf J-M; Rusniok C; Weissenbach J; Avner P
A SAGE approach to identifying novel trans-acting factors involved in the X inactivation process.
Cytogenetic and genome research 2006;113(1-4):325-35.
2005: Roest Crollius Hugues; Weissenbach Jean
Fish genomics and biology.
Genome research 2005;15(12):1675-82.
2005: Raible Florian; Tessmar-Raible Kristin; Osoegawa Kazutoyo; Wincker Patrick; Jubin Claire; Balavoine Guillaume; Ferrier David; Benes Vladimir; de Jong Pieter; Weissenbach Jean; Bork Peer; Arendt Detlev
Vertebrate-type intron-rich genes in the marine annelid Platynereis dumerilii.
Science (New York, N.Y.) 2005;310(5752):1325-6.
2005: Chouari Rakia; Le Paslier Denis; Daegelen Patrick; Ginestet Philippe; Weissenbach Jean; Sghir Abdelghani
Novel predominant archaeal and bacterial groups revealed by molecular analysis of an anaerobic sludge digester.
Environmental microbiology 2005;7(8):1104-15.
2005: Eiglmeier Karin; Wincker Patrick; Cattolico Laurence; Anthouard Veronique; Holm Inge; Eckenberg Ralph; Quesneville Hadi; Jaillon Olivier; Collins Frank H; Weissenbach Jean; Brey Paul T; Roth Charles W
Comparative analysis of BAC and whole genome shotgun sequences from an Anopheles gambiae region related to Plasmodium encapsulation.
Insect biochemistry and molecular biology 2005;35(8):799-814.
2005: Chouari Rakia; Le Paslier Denis; Dauga Catherine; Daegelen Patrick; Weissenbach Jean; Sghir Abdelghani
Novel major bacterial candidate division within a municipal anaerobic sludge digester.
Applied and environmental microbiology 2005;71(4):2145-53.
2005: Chantret Nathalie; Salse Jérôme; Sabot François; Rahman Sadequr; Bellec Arnaud; Laubin Bastien; Dubois Ivan; Dossat Carole; Sourdille Pierre; Joudrier Philippe; Gautier Marie-Françoise; Cattolico Laurence; Beckert Michel; Aubourg Sébastien; Weissenbach Jean; Caboche Michel; Bernard Michel; Leroy Philippe; Chalhoub Boulos
Molecular basis of evolutionary events that shaped the hardness locus in diploid and polyploid wheat species (Triticum and Aegilops).
The Plant cell 2005;17(4):1033-45.
2005: Edvardsen Rolf B; Seo Hee-Chan; Jensen Marit F; Mialon Antoine; Mikhaleva Jana; Bjordal Marianne; Cartry Jérome; Reinhardt Richard; Weissenbach Jean; Wincker Patrick; Chourrout Daniel
Remodelling of the homeobox gene complement in the tunicate Oikopleura dioica.
Current biology : CB 2005;15(1):R12-3.
2005: Fischer C; Bouneau L; Coutanceau J-P; Weissenbach J; Ozouf-Costaz C; Volff J-N
Diversity and clustered distribution of retrotransposable elements in the compact genome of the pufferfish Tetraodon nigroviridis.
Cytogenetic and genome research 2005;110(1-4):522-36.
2005: Gomez Shawn M; Eiglmeier Karin; Segurens Beatrice; Dehoux Pierre; Couloux Arnaud; Scarpelli Claude; Wincker Patrick; Weissenbach Jean; Brey Paul T; Roth Charles W
Pilot Anopheles gambiae full-length cDNA study: sequencing and initial characterization of 35,575 clones.
Genome biology 2005;6(4):R39.
2004: Abel Annette; Fonknechten Nuria; Hofer Anne; Dürr Alexandra; Cruaud Corinne; Voit Thomas; Weissenbach Jean; Brice Alexis; Klimpe Sven; Auburger Georg; Hazan Jamilé
Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A.
Neurogenetics 2004;5(4):239-43.
2004: Bernot Alain; Weissenbach Jean
Estimation of the extent of synteny between Tetraodon nigroviridis and Homo sapiens genomes.
Journal of molecular evolution 2004;59(4):556-69.
2004: Seo Hee-Chan; Edvardsen Rolf Brudvik; Maeland Anne Dorthea; Bjordal Marianne; Jensen Marit Flo; Hansen Anette; Flaat Mette; Weissenbach Jean; Lehrach Hans; Wincker Patrick; Reinhardt Richard; Chourrout Daniel
Hox cluster disintegration with persistent anteroposterior order of expression in Oikopleura dioica.
Nature 2004;431(7004):67-71.
2004: Fischer Cécile; Bouneau Laurence; Coutanceau Jean-Pierre; Weissenbach Jean; Volff Jean-Nicolas; Ozouf-Costaz Catherine
Global heterochromatic colocalization of transposable elements with minisatellites in the compact genome of the pufferfish Tetraodon nigroviridis.
Gene 2004;336(2):175-83.
2004: Weissenbach Jean
Genome sequencing: differences with the relatives.
Nature 2004;429(6990):353-5.
2004: Castelli Vanina; Aury Jean-Marc; Jaillon Olivier; Wincker Patrick; Clepet Christian; Menard Manuella; Cruaud Corinne; Quétier Francis; Scarpelli Claude; Schächter Vincent; Temple Gary; Caboche Michel; Weissenbach Jean; Salanoubat Marcel
Whole genome sequence comparisons and "full-length" cDNA sequences: a combined approach to evaluate and improve Arabidopsis genome annotation.
Genome research 2004;14(3):406-13.
2004: Porcel Betina M; Delfour Olivier; Castelli Vanina; De Berardinis Veronique; Friedlander Lucie; Cruaud Corinne; Ureta-Vidal Abel; Scarpelli Claude; Wincker Patrick; Schächter Vincent; Saurin William; Gyapay Gabor; Salanoubat Marcel; Weissenbach Jean
Numerous novel annotations of the human genome sequence supported by a 5'-end-enriched cDNA collection.
Genome research 2004;14(3):463-71.
2004: Barbe Valérie; Vallenet David; Fonknechten Nuria; Kreimeyer Annett; Oztas Sophie; Labarre Laurent; Cruveiller Stéphane; Robert Catherine; Duprat Simone; Wincker Patrick; Ornston L Nicholas; Weissenbach Jean; Marlière Philippe; Cohen Georges N; Médigue Claudine
Unique features revealed by the genome sequence of Acinetobacter sp. ADP1, a versatile and naturally transformation competent bacterium.
Nucleic acids research 2004;32(19):5766-79.
2003: Chouari Rakia; Le Paslier Denis; Daegelen Patrick; Ginestet Philippe; Weissenbach Jean; Sghir Abdelghani
Molecular evidence for novel planctomycete diversity in a municipal wastewater treatment plant.
Applied and environmental microbiology 2003;69(12):7354-63.
2003: Chabardès-Garonne Danielle; Mejéan Arnaud; Aude Jean-Christophe; Cheval Lydie; Di Stefano Antonio; Gaillard Marie-Claude; Imbert-Teboul Martine; Wittner Monika; Balian Chanth; Anthouard Véronique; Robert Catherine; Ségurens Beatrice; Wincker Patrick; Weissenbach Jean; Doucet Alain; Elalouf Jean-Marc
A panoramic view of gene expression in the human kidney.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(23):13710-5.
2003: Lefévre Caroline; Audebert Stéphanie; Jobard Florence; Bouadjar Bakar; Lakhdar Hakima; Boughdene-Stambouli Omar; Blanchet-Bardon Claudine; Heilig Roland; Foglio Mario; Weissenbach Jean; Lathrop Mark; Prud'homme Jean-François; Fischer Judith
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.
Human molecular genetics 2003;12(18):2369-78.
2003: Dufresne Alexis; Salanoubat Marcel; Partensky Frédéric; Artiguenave François; Axmann Ilka M; Barbe Valérie; Duprat Simone; Galperin Michael Y; Koonin Eugene V; Le Gall Florence; Makarova Kira S; Ostrowski Martin; Oztas Sophie; Robert Catherine; Rogozin Igor B; Scanlan David J; Tandeau de Marsac Nicole; Weissenbach Jean; Wincker Patrick; Wolf Yuri I; Hess Wolfgang R
Genome sequence of the cyanobacterium Prochlorococcus marinus SS120, a nearly minimal oxyphototrophic genome.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(17):10020-5.
2003: Silar Philippe; Barreau Christian; Debuchy Robert; Kicka Sébastien; Turcq Béatrice; Sainsard-Chanet Annie; Sellem Carole H; Billault Alain; Cattolico Laurence; Duprat Simone; Weissenbach Jean
Characterization of the genomic organization of the region bordering the centromere of chromosome V of Podospora anserina by direct sequencing.
Fungal genetics and biology : FG & B 2003;39(3):250-63.
2003: Jaillon Olivier; Dossat Carole; Eckenberg Ralph; Eiglmeier Karin; Segurens Béatrice; Aury Jean-Marc; Roth Charles W; Scarpelli Claude; Brey Paul T; Weissenbach Jean; Wincker Patrick
Assessing the Drosophila melanogaster and Anopheles gambiae genome annotations using genome-wide sequence comparisons.
Genome research 2003;13(7):1595-9.
2003: Bouneau Laurence; Fischer Cécile; Ozouf-Costaz Catherine; Froschauer Alexander; Jaillon Olivier; Coutanceau Jean-Pierre; Körting Cornelia; Weissenbach Jean; Bernot Alain; Volff Jean-Nicolas
An active non-LTR retrotransposon with tandem structure in the compact genome of the pufferfish Tetraodon nigroviridis.
Genome research 2003;13(7):1686-95.
2003: Abifadel Marianne; Varret Mathilde; Rabès Jean-Pierre; Allard Delphine; Ouguerram Khadija; Devillers Martine; Cruaud Corinne; Benjannet Suzanne; Wickham Louise; Erlich Danièle; Derré Aurélie; Villéger Ludovic; Farnier Michel; Beucler Isabel; Bruckert Eric; Chambaz Jean; Chanu Bernard; Lecerf Jean-Michel; Luc Gerald; Moulin Philippe; Weissenbach Jean; Prat Annick; Krempf Michel; Junien Claudine; Seidah Nabil G; Boileau Catherine
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.
Nature genetics 2003;34(2):154-6.
2003: Roth Charles W; Holm Inge; Graille Marine; Dehoux Pierre; Rzhetsky Andrey; Wincker Patrick; Weissenbach Jean; Brey Paul T
Identification of the Anopheles gambiae ATP-binding cassette transporter superfamily genes.
Molecules and cells 2003;15(2):150-8.
2003: Jobard Florence; Bouadjar Bakar; Caux Frédéric; Hadj-Rabia Smail; Has Christina; Matsuda Fumi; Weissenbach Jean; Lathrop Mark; Prud'homme Jean-François; Fischer Judith
Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.
Human molecular genetics 2003;12(8):925-35.
2003: Cohen Georges N; Barbe Valérie; Flament Didier; Galperin Michael; Heilig Roland; Lecompte Odile; Poch Olivier; Prieur Daniel; Quérellou Joël; Ripp Raymond; Thierry Jean-Claude; Van der Oost John; Weissenbach Jean; Zivanovic Yvan; Forterre Patrick
An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi.
Molecular microbiology 2003;47(6):1495-512.
2003: Bouneau Laurence; Lardier Guillaume; Fischer Cécile; Ronsin Muriel; Weissenbach Jean; Bernot Alain
Analysis of 148 kb of genomic DNA of Tetraodon nigroviridis covering an amylase gene family.
DNA sequence : the journal of DNA sequencing and mapping 2003;14(1):1-13.
2003: Jaillon O; Aury J M; Roest Crollius H; Salanoubat M; Wincker P; Dossat C; Castelli V; Boudet N; Samair S; Eckenberg R; Bonneval S; Saurin W; Scarpelli C; Schächter V; Weissenbach J
Genome-wide analyses based on comparative genomics.
Cold Spring Harbor symposia on quantitative biology 2003;68():275-82.
2002: De Lonlay Pascale; Mugnier Claude; Sanlaville Damien; Chantrel-Groussard Karine; Bénit Paule; Lebon Sophie; Chrétien Dominique; Kadhom Noman; Saker Safa; Gyapay Gabor; Romana Serge; Weissenbach Jean; Munnich Arnold; Rustin Pierre; Rötig Agnès
Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes.
Human molecular genetics 2002;11(26):3273-81.
2002: Dasilva Corinne; Hadji Hajer; Ozouf-Costaz Catherine; Nicaud Sophie; Jaillon Olivier; Weissenbach Jean; Roest Crollius Hugues
Remarkable compartmentalization of transposable elements and pseudogenes in the heterochromatin of the Tetraodon nigroviridis genome.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(21):13636-41.
2002: Grützner Frank; Roest Crollius Hugues; Lütjens Götz; Jaillon Olivier; Weissenbach Jean; Ropers Hans-Hilger; Haaf Thomas
Four-hundred million years of conserved synteny of human Xp and Xq genes on three Tetraodon chromosomes.
Genome research 2002;12(9):1316-22.
2002: Coimbra Roney S; Weil Dominique; Brottier Phillipe; Blanchard Stéphane; Levi Michael; Hardelin Jean-Pierre; Weissenbach Jean; Petit Christine
A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear.
Genome research 2002;12(6):1007-11.
2002: Fischer Cécile; Bouneau Laurence; Ozouf-Costaz Catherine; Crnogorac-Jurcevic Tatjana; Weissenbach Jean; Bernot Alain
Conservation of the T-cell receptor alpha/delta linkage in the teleost fish Tetraodon nigroviridis.
Genomics 2002;79(2):241-8.
2002: Salanoubat M; Genin S; Artiguenave F; Gouzy J; Mangenot S; Arlat M; Billault A; Brottier P; Camus J C; Cattolico L; Chandler M; Choisne N; Claudel-Renard C; Cunnac S; Demange N; Gaspin C; Lavie M; Moisan A; Robert C; Saurin W; Schiex T; Siguier P; Thébault P; Whalen M; Wincker P; Levy M; Weissenbach J; Boucher C A
Genome sequence of the plant pathogen Ralstonia solanacearum.
Nature 2002;415(6871):497-502.
2002: Jobard Florence; Lefèvre Caroline; Karaduman Aysen; Blanchet-Bardon Claudine; Emre Serap; Weissenbach Jean; Ozgüc Meral; Lathrop Mark; Prud'homme Jean-François; Fischer Judith
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1.
Human molecular genetics 2002;11(1):107-13.
2002: Roest Crollius H; Jaillon O; Bernot A; Pelletier E; Dasilva C; Bouneau L; Burge C; Yeh R-F; Quetier F; Saurin W; Weissenbach J
Genome-wide comparisons between human and tetraodon.
Ernst Schering Research Foundation workshop 2002;(36):11-29.
2001: Vigneau S; Levillayer F; Crespeau H; Cattolico L; Caudron B; Bihl F; Robert C; Brahic M; Weissenbach J; Bureau J F
Homology between a 173-kb region from mouse chromosome 10, telomeric to the Ifng locus, and human chromosome 12q15.
Genomics 2001;78(3):206-13.
2001: Katinka M D; Duprat S; Cornillot E; Méténier 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; Vivarès C P
Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi.
Nature 2001;414(6862):450-3.
2001: Lefèvre C; Jobard F; Caux F; Bouadjar B; Karaduman A; Heilig R; Lakhdar H; Wollenberg A; Verret J L; Weissenbach J; Ozgüc M; Lathrop M; Prud'homme J F; 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 2001;69(5):1002-12.
2001: Ogata H; Audic S; Renesto-Audiffren P; Fournier P E; Barbe V; Samson D; Roux V; Cossart P; Weissenbach J; Claverie J M; Raoult D
Mechanisms of evolution in Rickettsia conorii and R. prowazekii.
Science (New York, N.Y.) 2001;293(5537):2093-8.
2001: Charlier C; Segers K; Wagenaar D; Karim L; Berghmans 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 2001;11(5):850-62.
2001: Bolotin A; Wincker P; Mauger S; Jaillon O; Malarme K; Weissenbach J; Ehrlich S D; Sorokin A
The complete genome sequence of the lactic acid bacterium Lactococcus lactis ssp. lactis IL1403.
Genome research 2001;11(5):731-53.
2001: Fischer J; Bouadjar B; Heilig R; Huber M; Lefèvre C; Jobard F; Macari F; Bakija-Konsuo A; Ait-Belkacem F; Weissenbach J; Lathrop M; Hohl D; Prud'homme J F
Mutations in the gene encoding SLURP-1 in Mal de Meleda.
Human molecular genetics 2001;10(8):875-80.
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; Lepiniec L
Improved PCR-walking for large-scale isolation of plant T-DNA borders.
BioTechniques 2001;30(3):496-8, 502, 504.
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; Heilig R
A physical map of human chromosome 14.
Nature 2001;409(6822):947-8.
2001: Peyret P; Katinka M D; Duprat S; Duffieux F; Barbe V; Barbazanges M; Weissenbach J; Saurin W; Vivarès C P
Sequence and analysis of chromosome I of the amitochondriate intracellular parasite Encephalitozoon cuniculi (Microspora).
Genome research 2001;11(2):198-207.
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; Lépingle A; Malpertuy A; Neuvéglise C; Ozier-Kalogéropoulos O; Potier S; Saurin W; Termier M; Wésolowski-Louvel M; Wincker P; Souciet J; Weissenbach J
Genomic exploration of the hemiascomycetous yeasts: 21. Comparative functional classification of genes.
FEBS letters 2000;487(1):134-49.
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; Lépingle A; Neuvéglise C; Ozier-Kalogeropoulos O; Potier S; Saurin W; Tekaia F; Toffano-Nioche C; Wésolowski-Louvel M; Wincker P; Weissenbach J; Souciet J; Gaillardin C
Genomic exploration of the hemiascomycetous yeasts: 20. Evolution of gene redundancy compared to Saccharomyces cerevisiae.
FEBS letters 2000;487(1):122-33.
2000: Malpertuy A; Tekaia F; Casarégola S; Aigle M; Artiguenave F; Blandin G; Bolotin-Fukuhara M; Bon E; Brottier P; de Montigny J; Durrens P; Gaillardin C; Lépingle A; Llorente B; Neuvéglise C; Ozier-Kalogeropoulos O; Potier S; Saurin W; Toffano-Nioche C; Wésolowski-Louvel M; Wincker P; Weissenbach J; Souciet J; Dujon B
Genomic exploration of the hemiascomycetous yeasts: 19. Ascomycetes-specific genes.
FEBS letters 2000;487(1):113-21.
2000: Llorente B; Malpertuy A; Neuvéglise C; de Montigny J; Aigle M; Artiguenave F; Blandin G; Bolotin-Fukuhara M; Bon E; Brottier P; Casaregola S; Durrens P; Gaillardin C; Lépingle A; Ozier-Kalogéropoulos O; Potier S; Saurin W; Tekaia F; Toffano-Nioche C; Wésolowski-Louvel M; Wincker P; Weissenbach J; Souciet J; Dujon B
Genomic exploration of the hemiascomycetous yeasts: 18. Comparative analysis of chromosome maps and synteny with Saccharomyces cerevisiae.
FEBS letters 2000;487(1):101-12.
2000: 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 and processing.
FEBS letters 2000;487(1):13-6.
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; Lépingle A; Llorente B; Malpertuy A; Neuvéglise C; Ozier-Kalogéropoulos O; Potier S; Saurin W; Tekaia F; Toffano-Nioche C; Wésolowski-Louvel M; Wincker P; Weissenbach J
Genomic exploration of the hemiascomycetous yeasts: 1. A set of yeast species for molecular evolution studies.
FEBS letters 2000;487(1):3-12.
2000: Escary J L; Bottius E; Prince N; Reyes C; Fiawoumo Y; Caloustian C; Bruls T; Fujiyama A; Cooper R S; Adeyemo A A; Lathrop G M; Weissenbach J; Gyapay G; Foglio M; Beckmann J S
A first high-density map of 981 biallelic markers on human chromosome 14.
Genomics 2000;70(2):153-64.
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; Fontaine B
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).
Nature genetics 2000;26(4):480-3.
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; Bégeot M; Naville D; Nicolino M; Chaussain J L; Weissenbach J; Munnich A; Lyonnet S
Mutant WD-repeat protein in triple-A syndrome.
Nature genetics 2000;26(3):332-5.
2000: Roest Crollius H; 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 2000;10(7):939-49.
2000: Roest Crollius H; Jaillon O; Bernot A; Dasilva C; Bouneau L; Fischer C; Fizames C; Wincker P; Brottier P; Quétier F; Saurin W; Weissenbach J
Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence.
Nature genetics 2000;25(2):235-8.
2000: Fischer J; Faure A; Bouadjar B; Blanchet-Bardon C; Karaduman A; Thomas I; Emre S; Cure S; Ozgüc M; Weissenbach J; Prud'homme J F
Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneity.
American journal of human genetics 2000;66(3):904-13.
2000: 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 2000;66(3):778-89.
2000: Fonknechten N; Mavel D; Byrne P; Davoine C S; Cruaud C; Bönsch 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; Dürr A; Hazan J
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
Human molecular genetics 2000;9(4):637-44.
2000: Fontaine B; Davoine C S; Dürr 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 2000;66(2):702-7.
2000: Fischer C; Ozouf-Costaz C; Roest Crollius H; 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 2000;88(1-2):50-5.
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 B; Weissenbach J
Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.
Nature genetics 1999;23(3):296-303.
1999: Seboun E; Oksenberg J R; Rombos A; Usuku K; Goodkin D E; Lincoln R R; Wong M; Pham-Dinh D; Boesplug-Tanguy O; Carsique R; Fitoussi R; Gartioux C; Reyes C; Ribierre F; Faure S; Fizames C; Gyapay G; Weissenbach J; Dautigny A; Rimmler J B; Garcia M E; Pericak-Vance M A; Haines J L; Hauser S L
Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Neurogenetics 1999;2(3):155-62.
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; Weissenbach J
A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.
Genomics 1999;60(3):309-19.
1999: Pineau P; Nagai H; Prigent S; Wei Y; Gyapay G; Weissenbach J; Tiollais P; Buendia M A; Dejean A
Identification of three distinct regions of allelic deletions on the short arm of chromosome 8 in hepatocellular carcinoma.
Oncogene 1999;18(20):3127-34.
1999: 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 of the chromosome 2 candidate locus.
European journal of human genetics : EJHG 1999;7(1):77-87.
1998: Fischer J; Bouadjar B; Heilig R; Fizames C; Prud'homme J F; Weissenbach J
Genetic linkage of Meleda disease to chromosome 8qter.
European journal of human genetics : EJHG 1998;6(6):542-7.
1998: Paternotte C; Rudnicki D; Fizames C; Davoine C S; Mavel D; Dürr 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 1998;8(11):1216-27.
1998: Pawlak A; Chiannikulchai N; Ansorge W; Bulle F; Weissenbach J; Gyapay G; Guellaën G
Identification and mapping of 26 human testis mRNAs containing CAG/CTG repeats.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(9):745-8.
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; Dodé C; Pêcheux C; Nédelec 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 1998;7(8):1317-25.
1998: Fischer J; Urtizberea J A; Pavek S; Vandiedonck C; Bruls T; Saker S; Alkatip Y; Prud'homme J F; Weissenbach J
Genetic linkage of progressive pseudorheumatoid dysplasia to a 3-cM interval of chromosome 6q22.
Human genetics 1998;103(1):60-4.
1998: Salomon-Nguyen F; Le Coniat-Busson 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'Académie des sciences. Série III, Sciences de la vie 1998;321(6):447-52.
1998: von Fellenberg J; Paternotte C; Prud'homme J F; Weissenbach J; Hazan J; Burgunder J M
[Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis]
Schweizerische medizinische Wochenschrift 1998;128(26):1043-50.
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; Weissenbach J
A transcriptional Map of the FMF region.
Genomics 1998;50(2):147-60.
1998: Heinzlef O; Paternotte C; Mahieux F; Prud'homme J F; Dien J; Madigand M; Pouget J; Weissenbach J; Roullet E; Hazan J
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
Journal of medical genetics 1998;35(2):89-93.
1997: Saunier S; Calado J; Heilig R; Silbermann F; Benessy F; Morin G; Konrad M; Broyer M; Gubler M C; 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 1997;6(13):2317-23.
1997: Abdelhak S; Kalatzis V; Heilig R; Compain S; Samson D; Vincent C; Levi-Acobas F; Cruaud C; Le Merrer M; Mathieu M; König R; Vigneron J; Weissenbach J; Petit C; Weil D
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.
Human molecular genetics 1997;6(13):2247-55.
1997: Simmler M C; 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 : official journal of the International Mammalian Genome Society 1997;8(10):760-6.
1997: Bulle F; Chiannilkulchai N; Pawlak A; Weissenbach J; Gyapay G; Guellaën G
Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain.
Genome research 1997;7(7):705-15.
1997: Fischer J; Blanchet-Bardon C; Prud'homme J F; Pavek S; Steijlen P M; Dubertret L; Weissenbach J
Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region.
European journal of human genetics : EJHG 1997;5(3):156-60.
1997: Abdelhak S; Kalatzis V; Heilig R; Compain S; Samson D; Vincent C; Weil D; Cruaud C; Sahly I; Leibovici M; Bitner-Glindzicz M; Francis M; Lacombe D; Vigneron J; Charachon R; Boven K; Bedbeder P; Van Regemorter N; Weissenbach J; Petit C
A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family.
Nature genetics 1997;15(2):157-64.
1997: Chaïb 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 1997;6(1):27-31.
1996: David G; Giunti P; Abbas N; Coullin P; Stevanin G; Horta W; Gemmill R; Weissenbach J; Wood N; Cunha S; Drabkin H; Harding A E; Agid Y; Brice A
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
American journal of human genetics 1996;59(6):1328-36.
1996: Cox S A; Attwood J; Bryant S P; Bains R; Povey S; Rebello M; Kapsetaki M; Moschonas N K; Grzeschik K H; Otto M; Dixon M; Sudworth H E; Kooy R F; Wright A; Teague P; Terrenato L; Vergnaud G; Monfouilloux S; Weissenbach J; Alibert O; Dib C; Fauré S; Bakker E; Pearson N M; Spurr N K
European Gene Mapping Project (EUROGEM): breakpoint panels for human chromosomes based on the CEPH reference families. Centre d'Etude du Polymorphisme Humain.
Annals of human genetics 1996;60(Pt 6):447-86.
1996: Simmler M C; Cunningham D B; Clerc P; Vermat T; Caudron B; Cruaud C; Pawlak A; Szpirer C; Weissenbach J; Claverie J M; Avner P
A 94 kb genomic sequence 3' to the murine Xist gene reveals an AT rich region containing a new testis specific gene Tsx.
Human molecular genetics 1996;5(11):1713-26.
1996: Dürr A; Davoine C S; Paternotte C; von Fellenberg J; Cogilinicean S; Coutinho P; Lamy C; Bourgeois S; Prud'homme J F; Penet C; Mas J L; Burgunder J M; Hazan J; Weissenbach J; Brice A; Fontaine B
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
Brain : a journal of neurology 1996;119 ( Pt 5)():1487-96.
1996: Schuler G D; Boguski M S; Stewart E A; Stein L D; Gyapay G; Rice K; White R E; Rodriguez-Tomé P; Aggarwal A; Bajorek E; Bentolila S; Birren B B; Butler A; Castle A B; Chiannilkulchai N; Chu A; Clee C; Cowles S; Day P J; Dibling T; Drouot N; Dunham I; Duprat S; East C; Edwards C; Fan J B; Fang N; Fizames C; Garrett C; Green L; Hadley D; Harris M; Harrison P; Brady S; Hicks A; Holloway E; Hui L; Hussain S; Louis-Dit-Sully C; Ma J; MacGilvery A; Mader C; Maratukulam A; Matise T C; McKusick K B; Morissette J; Mungall A; Muselet D; Nusbaum H C; Page D C; Peck A; Perkins S; Piercy M; Qin F; Quackenbush J; Ranby S; Reif T; Rozen S; Sanders C; She X; Silva J; Slonim D K; Soderlund C; Sun W L; Tabar P; Thangarajah T; Vega-Czarny N; Vollrath D; Voyticky S; Wilmer T; Wu X; Adams M D; Auffray C; Walter N A; Brandon R; Dehejia A; Goodfellow P N; Houlgatte R; Hudson J R; Ide S E; Iorio K R; Lee W Y; Seki N; Nagase T; Ishikawa K; Nomura N; Phillips C; Polymeropoulos M H; Sandusky M; Schmitt K; Berry R; Swanson K; Torres R; Venter J C; Sikela J M; Beckmann J S; Weissenbach J; Myers R M; Cox D R; James M R; Bentley D; Deloukas P; Lander E S; Hudson T J
A gene map of the human genome.
Science (New York, N.Y.) 1996;274(5287):540-6.
1996: Vicart P; Dupret J M; Hazan J; Li Z; Gyapay G; Krishnamoorthy R; Weissenbach J; Fardeau M; Paulin D
Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy.
Human genetics 1996;98(4):422-9.
1996: Endo K; Sasaki H; Wakisaka A; Tanaka H; Saito M; Igarashi S; Takiyama Y; Sanpei K; Iwabuchi K; Suzuki Y; Onari K; Suzuki T; Weissenbach J; Weber J L; Nomura Y; Segawa M; Nishizawa M; Tsuji S
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease.
American journal of medical genetics 1996;67(5):437-44.
1996: Fontaine B; Nicole S; Topaloglu H; Ben Hamida C; Beighton P; Spaans F; Cantu J M; Bakouri S; Romero N; Ricker K; Barros-Nunez P; Ponsot G; Ben Hamida M; Weissenbach J; Hentati F; Lehmann-Horn F
Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval.
Human genetics 1996;98(3):380-5.
1996: McDowell G; Isogai T; Tanigami A; Hazelwood S; Ledbetter D; Polymeropoulos M H; Lichter-Konecki U; Konecki D; Town M M; Van't Hoff W V; Weissenbach J; Gahl W A
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 1996;58(2):135-41.
1996: Haines J L; Ter-Minassian M; Bazyk A; Gusella J F; Kim D J; Terwedow H; Pericak-Vance M A; Rimmler J B; Haynes C S; Roses A D; Lee A; Shaner B; Menold M; Seboun E; Fitoussi R P; Gartioux C; Reyes C; Ribierre F; Gyapay G; Weissenbach J; Hauser S L; Goodkin D E; Lincoln R; Usuku K; Oksenberg J R
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
Nature genetics 1996;13(4):469-71.
1996: Chaib H; Place C; Salem N; Dodé C; Chardenoux S; Weissenbach J; el Zir E; Loiselet J; Petit C
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.
Human molecular genetics 1996;5(7):1061-4.
1996: Igarashi S; Takiyama Y; Cancel G; Rogaeva E A; Sasaki H; Wakisaka A; Zhou Y X; Takano H; Endo K; Sanpei K; Oyake M; Tanaka H; Stevanin G; Abbas N; Dürr A; Rogaev E I; Sherrington R; Tsuda T; Ikeda M; Cassa E; Nishizawa M; Benomar A; Julien J; Weissenbach J; Wang G X; Agid Y; St George-Hyslop P H; Brice A; Tsuji S
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.
Human molecular genetics 1996;5(7):923-32.
1996: Polymeropoulos M H; Ide S E; Wright M; Goodship J; Weissenbach J; Pyeritz R E; Da Silva E O; Ortiz De Luna R I; Francomano C A
The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16.
Genomics 1996;35(1):1-5.
1996: Tarttelin E E; Plant C; Weissenbach J; Bird A C; Bhattacharya S S; Inglehearn C F
A new family linked to the RP13 locus for autosomal dominant retinitis pigmentosa on distal 17p.
Journal of medical genetics 1996;33(6):518-20.
1996: Kelsell D P; Risk J M; Leigh I M; Stevens H P; Ellis A; Hennies H C; Reis A; Weissenbach J; Bishop D T; Spurr N K; Field J K
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).
Human molecular genetics 1996;5(6):857-60.
1996: Stevens H P; Kelsell D P; Bryant S P; Bishop D T; Spurr N K; Weissenbach J; Marger D; Marger R S; Leigh I M
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.
Archives of dermatology 1996;132(6):640-51.
1996: Nissinen M; Helbling-Leclerc A; Zhang X; Evangelista T; Topaloglu H; Cruaud C; Weissenbach J; Fardeau M; Tomé F M; Schwartz K; Tryggvason K; Guicheney P
Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.
American journal of human genetics 1996;58(6):1177-84.
1996: Parmentier L; Lakhdar H; Blanchet-Bardon C; Marchand S; Dubertret L; Weissenbach J
Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35.
Human molecular genetics 1996;5(4):555-9.
1996: Gyapay G; Schmitt K; Fizames C; Jones H; Vega-Czarny N; Spillett D; Muselet D; Prud'homme J F; Dib C; Auffray C; Morissette J; Weissenbach J; Goodfellow P N
A radiation hybrid map of the human genome.
Human molecular genetics 1996;5(3):339-46.
1996: Dib C; Fauré S; Fizames C; Samson D; Drouot N; Vignal A; Millasseau P; Marc S; Hazan J; Seboun E; Lathrop M; Gyapay G; Morissette J; Weissenbach J
A comprehensive genetic map of the human genome based on 5,264 microsatellites.
Nature 1996;380(6570):152-4.
1996: Chaïb H; Place C; Salem N; Chardenoux S; Vincent C; Weissenbach J; El-Zir E; Loiselet J; Petit C
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.
Human molecular genetics 1996;5(1):155-8.
1996: Clépet C; Dauwerse H J; Desmaze C; van Ommen G J; Weissenbach J; Morissette J
A 10-cM YAC contig spanning GLC1A, the primary open-angle glaucoma locus at 1q23-q25.
European journal of human genetics : EJHG 1996;4(5):250-9.
1995: Hudson T J; Stein L D; Gerety S S; Ma J; Castle A B; Silva J; Slonim D K; Baptista R; Kruglyak L; Xu S H; Hu X; Colbert A M; Rosenberg C; Reeve-Daly M P; Rozen S; Hui L; Wu X; Vestergaard C; Wilson K M; Bae J S; Maitra S; Ganiatsas S; Evans C A; DeAngelis M M; Ingalls K A; Nahf R W; Horton L T; Anderson M O; Collymore A J; Ye W; Kouyoumjian V; Zemsteva I S; Tam J; Devine R; Courtney D F; Renaud M T; Nguyen H; O'Connor T J; Fizames C; Fauré S; Gyapay G; Dib C; Morissette J; Orlin J B; Birren B W; Goodman N; Weissenbach J; Hawkins T L; Foote S; Page D C; Lander E S
An STS-based map of the human genome.
Science (New York, N.Y.) 1995;270(5244):1945-54.
1995: Bonne G; Carrier L; Bercovici J; Cruaud C; Richard P; Hainque B; Gautel M; Labeit S; James M; Beckmann J; Weissenbach J; Vosberg H P; Fiszman M; Komajda M; Schwartz K
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy.
Nature genetics 1995;11(4):438-40.
1995: Ferrero G B; Franco B; Roth E J; Firulli B A; Borsani G; Delmas-Mata J; Weissenbach J; Halley G; Schlessinger D; Chinault A C
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.
Human molecular genetics 1995;4(10):1821-7.
1995: Cox S; Bryant S P; Collins A; Weissenbach J; Donis-Keller H; Koeleman B P; Steinkasserer A; Spurr N K
Integrated genetic map of human chromosome 2.
Annals of human genetics 1995;59(Pt 4):413-34.
1995: de Meeus A; Stephan E; Debrus S; Jean M K; Loiselet J; Weissenbach J; Demaille J; Bouvagnet P
An isolated cardiac conduction disease maps to chromosome 19q.
Circulation research 1995;77(4):735-40.
1995: Helbling-Leclerc A; Zhang X; Topaloglu H; Cruaud C; Tesson F; Weissenbach J; Tomé F M; Schwartz K; Fardeau M; Tryggvason K
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
Nature genetics 1995;11(2):216-8.
1995: Nicole S; Ben Hamida C; Beighton P; Bakouri S; Belal S; Romero N; Viljoen D; Ponsot G; Sammoud A; Weissenbach J
Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping.
Human molecular genetics 1995;4(9):1633-6.
1995: Guilford P; Dodé C; Crozet F; Blanchard S; Chaïb H; Levilliers J; Levi-Acobas F; Weil D; Weissenbach J; Cohen D
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).
Genomics 1995;29(1):163-9.
1995: Green E D; Maffei M; Braden V V; Proenca R; DeSilva U; Zhang Y; Chua S C; Leibel R L; Weissenbach J; Friedman J M
The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7.
Genome research 1995;5(1):5-12.
1995: Parmentier L; Blanchet-Bardon C; Nguyen S; Prud'homme J F; Dubertret L; Weissenbach J
Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneity.
Human molecular genetics 1995;4(8):1391-5.
1995: Keen T J; Inglehearn C F; Green E D; Cunningham A F; Patel R J; Peacock R E; Gerken S; White R; Weissenbach J; Bhattacharya S S
A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p.
Genomics 1995;28(3):383-8.
1995: Doerflinger N; Linder C; Ouahchi K; Gyapay G; Weissenbach J; Le Paslier D; Rigault P; Belal S; Ben Hamida C; Hentati F
Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.
American journal of human genetics 1995;56(5):1116-24.
1995: Vincent P; Plauchu H; Hazan J; Fauré S; Weissenbach J; Godet J
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q.
Human molecular genetics 1995;4(5):945-9.
1995: Wang I; Franco B; Ferrero G B; Chinault A C; Weissenbach J; Chumakov I; Le Paslier D; Levilliers J; Klink A; Rappold G A
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).
Genomics 1995;26(2):229-38.
1995: Stevanin G; Cancel G; Dürr A; Chneiweiss H; Dubourg O; Weissenbach J; Cann H M; Agid Y; Brice A
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2.
American journal of human genetics 1995;56(1):193-201.
1995: Gispert S; Santos N; Damen R; Voit T; Schulz J; Klockgether T; Orozco G; Kreuz F; Weissenbach J; Auburger G
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
American journal of human genetics 1995;56(1):183-7.
1994: Gouider R; LeGuern E; Emile J; Tardieu S; Cabon F; Samid M; Weissenbach J; Agid Y; Bouche P; Brice A
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities.
Neurology 1994;44(12):2250-2.
1994: Stevanin G; Sousa P S; Cancel G; Dürr A; Dubourg O; Nicholson G A; Weissenbach J; Jardim E; Agid Y; Cassa E
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q.
Neurobiology of disease 1994;1(1-2):79-82.
1994: Plassart E; Elbaz A; Santos J V; Reboul J; Lapie P; Chauveau D; Jurkat-Rott K; Guimaraes J; Saudubray J M; Weissenbach J
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP).
Human genetics 1994;94(5):551-6.
1994: Le Guern E; Ravise N; Gugenheim M; Vignal A; Penet C; Bouche P; Weissenbach J; Agid Y; Brice A
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene.
Neuromuscular disorders : NMD 1994;4(5-6):463-9.
1994: Jurkat-Rott K; Lehmann-Horn F; Elbaz A; Heine R; Gregg R G; Hogan K; Powers P A; Lapie P; Vale-Santos J E; Weissenbach J
A calcium channel mutation causing hypokalemic periodic paralysis.
Human molecular genetics 1994;3(8):1415-9.
1994: Weil D; Wang I; Dietrich A; Poustka A; Weissenbach J; Petit C
Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness.
Nature genetics 1994;7(3):414-9.
1994: Guilford P; Ayadi H; Blanchard S; Chaib H; Le Paslier D; Weissenbach J; Drira M; Petit C
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
Human molecular genetics 1994;3(6):989-93.
1994: Gyapay G; Morissette J; Vignal A; Dib C; Fizames C; Millasseau P; Marc S; Bernardi G; Lathrop M; Weissenbach J
The 1993-94 Généthon human genetic linkage map.
Nature genetics 1994;7(2 Spec No):246-339.
1994: Kestilä M; Männikkö M; Holmberg C; Gyapay G; Weissenbach J; Savolainen E R; Peltonen L; Tryggvason K
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.
American journal of human genetics 1994;54(5):757-64.
1994: Walter M A; Spillett D J; Thomas P; Weissenbach J; Goodfellow P N
A method for constructing radiation hybrid maps of whole genomes.
Nature genetics 1994;7(1):22-8.
1994: Fontaine B; Vale-Santos J; Jurkat-Rott K; Reboul J; Plassart E; Rime C S; Elbaz A; Heine R; Guimarães J; Weissenbach J
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families.
Nature genetics 1994;6(3):267-72.
1994: Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
Nature genetics 1994;6(1):24-8.
1994: Wunderle V; Dib C; Fizames C; Morisette J; Hazan J; Hansmann I; Whitehouse D; Vergnaud G; Weissenbach J
The EUROGEM map of human chromosome 20.
European journal of human genetics : EJHG 1994;2(3):242-3.
1993: Weissenbach J
A second generation linkage map of the human genome based on highly informative microsatellite loci.
Gene 1993;135(1-2):275-8.
1993: Hazan J; Lamy C; Melki J; Munnich A; de Recondo J; Weissenbach J
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
Nature genetics 1993;5(2):163-7.
1993: Weissenbach J
Microsatellite polymorphisms and the genetic linkage map of the human genome.
Current opinion in genetics & development 1993;3(3):414-7.
1992: Weissenbach J; Gyapay G; Dib C; Vignal A; Morissette J; Millasseau P; Vaysseix G; Lathrop M
A second-generation linkage map of the human genome.
Nature 1992;359(6398):794-801.
1992: Hazan J; Dubay C; Pankowiak M P; Becuwe N; Weissenbach J
A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.
Genomics 1992;12(2):183-9.
1991: Slim R; Weissenbach J; Nguyen V C; Danglot G; Bernheim A
Relative order determination of four Yp cosmids on metaphase and interphase chromosomes by two-color competitive in situ hybridization.
Human genetics 1991;88(1):21-6.
1990: Petit C; Melki J; Levilliers J; Serville F; Weissenbach J; Maroteaux P
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature.
Human genetics 1990;85(2):247-50.
1990: Petit C; Levilliers J; Weissenbach J
Long-range restriction map of the terminal part of the short arm of the human X chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(10):3680-4.
1990: Petit C; Levilliers J; Rouyer F; Simmler M C; Herouin E; Weissenbach J
Isolation of sequences from Xp22.3 and deletion mapping using sex chromosome rearrangements from human X-Y interchange sex reversals.
Genomics 1990;6(4):651-8.
1990: Rouyer F; de la Chapelle A; Weissenbach J
A polymorphic DNA sequence from the terminal part of chromosome 21q [D21S154]
Nucleic acids research 1990;18(6):1663.
1990: Rouyer F; de la Chapelle A; Weissenbach J
A polymorphic DNA sequence from the terminal part of chromosome 20q [D20S26]
Nucleic acids research 1990;18(6):1662.
1990: Rouyer F; de la Chapelle A; Weissenbach J
A polymorphic DNA sequence from the terminal part of chromosome 12q [D12S37]
Nucleic acids research 1990;18(6):1664.
1990: Rouyer F; de la Chapelle A; Weissenbach J
A polymorphic DNA sequence from the terminal part of chromosome 20q [D20S25]
Nucleic acids research 1990;18(6):1661.
1990: Rouyer F; de la Chapelle A; Andersson M; Weissenbach J
An interspersed repeated sequence specific for human subtelomeric regions.
The EMBO journal 1990;9(2):505-14.
1990: Weissenbach J; Rouyer F
[The Y chromosome and sex determination]
Reproduction, nutrition, development 1990;Suppl 1():27s-38s.
1989: Levilliers J; Quack B; Weissenbach J; Petit C
Exchange of terminal portions of X- and Y-chromosomal short arms in human XY females.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(7):2296-300.
1988: Weissenbach J
Mapping the human Y chromosome.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;322(1208):125-31.
1988: Petit C; Levilliers J; Weissenbach J
Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.
The EMBO journal 1988;7(8):2369-76.
1987: Rouyer F; Simmler M C; Page D C; Weissenbach J
A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination.
Cell 1987;51(3):417-25.
1987: Simmler M C; Johnsson C; Petit C; Rouyer F; Vergnaud G; Weissenbach J
Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes.
The EMBO journal 1987;6(4):963-9.
1987: Weissenbach J; Levilliers J; Petit C; Rouyer F; Simmler M C
Normal and abnormal interchanges between the human X and Y chromosomes.
Development (Cambridge, England) 1987;101 Suppl():67-74.
1986: Ngo K Y; Vergnaud G; Johnsson C; Lucotte G; Weissenbach J
A DNA probe detecting multiple haplotypes of the human Y chromosome.
American journal of human genetics 1986;38(4):407-18.
1986: Vergnaud G; Page D C; Simmler M C; Brown L; Rouyer F; Noel B; Botstein D; de la Chapelle A; Weissenbach J
A deletion map of the human Y chromosome based on DNA hybridization.
American journal of human genetics 1986;38(2):109-24.
1986: Rouyer F; Simmler M C; Johnsson C; Vergnaud G; Cooke H J; Weissenbach J
A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes.
Nature 1986;319(6051):291-5.
1986: Rouyer F; Simmler M C; Vergnaud G; Johnsson C; Levilliers J; Petit C; Weissenbach J
The pseudoautosomal region of the human sex chromosomes.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():221-8.
1985: Simmler M C; Rouyer F; Vergnaud G; Nyström-Lahti M; Ngo K Y; de la Chapelle A; Weissenbach J
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes.
Nature 1985;317(6039):692-7.
1983: Rosa F; Berissi H; Weissenbach J; Maroteaux L; Fellous M; Revel M
The beta2-microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon.
The EMBO journal 1983;2(2):239-43.

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