Jacques Demaille - Publications, H-index & Citations

Jacques Demaille

universite de montpellier

57H指数

246论文数

1.2W被引数

收录论文 29

发表时间

Genome analysis of the smallest free-living eukaryote Ostreococcus tauri unveils many unique features

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2006-08-01

807

OAAI

Derelle, Evelyne; Ferraz, Conchita; Rombauts, Stephane; Rouze, Pierre; Worden, Alexandra Z.; Robbens, Steven; Partensky, Frederic; Degroeve, Sven; Echeynie, Sophie; Cooke, Richard; Saeys, Yvan; Wuyts, Jan; Jabbari, Kamel; Bowler, Chris; Panaud, Olivier; Piegu, Benoit; Ball, Steven G.; Ral, Jean-Philippe; Bouget, Francois-Yves; Piganeau, Gwenael; De Baets, Bernard; Picard, Andre; Delseny, Michel; Demaille, Jacques; Van de Peer, Yves; Moreau, Herve

Renal toxicogenomic response to chronic uranyl nitrate insult in mice

ENVIRONMENTAL HEALTH PERSPECTIVES

IF9.8

2004-11-01

OAAI

Taulan, M; Paquet, F; Maubert, C; Delissen, O; Demaille, J; Romey, MC

Infevers: An evolving mutation database for auto-inflammatory syndromes

HUMAN MUTATION

IF3.7

2004-01-01

262

OAAI

Touitou, I; Lesage, S; McDermott, M; Cuisset, L; Hoffman, H; Dode, C; Shoham, N; Aganna, E; Hugot, JP; Wise, C; Waterham, H; Pugnere, D; Demaille, J; de Menthiere, CS

Maternal aging and chromosomal abnormalities:: new data drawn from in vitro unfertilized human oocytes

HUMAN GENETICS

IF3.6

2003-02-01

300

PREAI

Pellestor, F; Andréo, B; Arnal, F; Humeau, C; Demaille, J

Transcriptome analysis of monocytic leukemia cell differentiation

GENOMICS

IF3

2002-09-01

PREAI

Piquemal, D; Commes, T; Manchon, L; Lejeune, M; Ferraz, C; Pugnère, D; Demaille, J; Elalouf, JM; Marti, J

Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean fever

GENES AND IMMUNITY

IF4.5

2002-02-21

PREAI

Notarnicola, C; Didelot, MN; Seguret, F; Demaille, J; Touitou, I

Mapping and identification of essential gene functions on the X chromosome of Drosophila

EMBO REPORTS

IF6.2

2002-01-01

111

OAAI

Peter, A; Schöttler, P; Werner, M; Beinert, N; Dowe, G; Burkert, P; Mourkioti, F; Dentzer, L; He, YC; Deak, P; Benos, PV; Gatt, MK; Murphy, L; Harris, D; Barrell, B; Ferraz, C; Vidal, S; Brun, C; Demaille, J; Cadieu, E; Dreano, S; Gloux, S; Lelaure, V; Mottier, S; Galibert, F; Borkova, D; Miñana, B; Kafatos, FC; Bolshakov, S; Sidén-Kiamos, I; Papagiannakis, G; Spanos, L; Louis, C; Madueño, E; de Pablos, B; Modolell, J; Bucheton, A; Callister, D; Campbell, L; Henderson, NS; McMillan, PJ; Salles, C; Tait, E; Valenti, P; Saunders, RDC; Billaud, A; Pachter, L; Klapper, R; Janning, W; Glover, DM; Ashburner, M; Bellen, HJ; Jäckle, H; Schäfer, U

Comparative genomics of the SOX9 region in human and Fugu rubripes:: Conservation of short regulatory sequence elements within large intergenic regions

GENOMICS

IF3

2001-11-01

PREAI

Bagheri-Fam, S; Ferraz, C; Demaille, J; Scherer, G; Pfeifer, D

The myosin light chain kinase gene is not duplicated in mouse:: Partial structure and chromosomal localization of Mylk

GENOMICS

IF3

2001-07-01

PREAI

Giorgi, D; Ferraz, C; Mattéi, MG; Demaille, J; Rouquier, S

From first base:: The sequence of the tip of the X chromosome of Drosophila melanogaster, a comparison of two sequencing strategies

GENOME RESEARCH

IF5.5

2001-05-01

OAAI

Benos, PV; Gatt, MK; Murphy, L; Harris, D; Barrell, B; Ferraz, C; Vidal, S; Brun, C; Demaille, J; Cadieu, E; Dreano, S; Gloux, S; Lelaure, V; Mottier, S; Galibert, F; Borkova, D; Miñana, B; Kafatos, FC; Bolshakov, S; Sidén-Kiamos, I; Papagiannakis, G; Spanos, L; Louis, C; Madueño, E; de Pablos, B; Modolell, J; Peter, A; Schöttler, P; Werner, M; Mourkioti, F; Beinert, N; Dowe, G; Schäfer, U; Jäckle, H; Bucheton, A; Callister, D; Campbell, L; Henderson, NS; McMillan, PJ; Salles, C; Tait, E; Valenti, P; Saunders, RDC; Billaud, A; Pachter, L; Glover, DM; Ashburner, M

Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa

HUMAN GENETICS

IF3.6

2001-04-24

105

PREAI

Bareil, C; Hamel, CP; Delague, V; Arnaud, B; Demaille, J; Claustres, M

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

JOURNAL OF MEDICAL GENETICS

IF3.7

2001-01-01

OAAI

Lefort, G; Blanchet, P; Chaze, AM; Girardet, A; Sarda, P; Demaille, J; Pellestor, F

Lattice corneal dystrophy

OPHTHALMOLOGY

IF9.5

2000-09-01

OAAI

Schmitt-Bernard, CF; Claustres, M; Arnaud, B; Demaille, J; Argiles, A

Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneity

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2000-06-15

OAAI

Domingo, C; Touitou, I; Bayou, A; Ozen, S; Notarnicola, C; Dewalle, M; Demaille, J; Buades, R; Sayadat, C; Levy, M; Ben-Chetrit, E

A naturally occurring sequence variation that creates a YY1 element is associated with increased cystic fibrosis transmembrane conductance regulator gene expression

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2000-02-01

OAAI

Romey, MC; Pallares-Ruiz, N; Mange, A; Mettling, C; Peytavi, R; Demaille, J; Claustres, M

MEFV Mutations in Behcet's Disease

HUMAN MUTATION

IF3.7

2000-01-01

140

OAAI

Touitou, Isabelle; Magne, Xavier; Molinari, Nicolas; Navarro, Andre; Le Quellec, Alain; Picco, Paolo; Seri, Marco; Ozen, Seza; Bakkaloglu, Aysin; Karaduman, Aysen; Garnier, Jean Marc; Demaille, Jacques; Kone-Paut, Isabelle

Sequence, structure, and evolution of a complete human olfactory receptor gene cluster

GENOMICS

IF3

2000-01-01

113

PREAI

Glusman, G; Sosinsky, A; Ben-Asher, E; Avidan, N; Sonkin, D; Bahar, A; Rosenthal, A; Clifton, S; Roe, B; Ferraz, C; Demaille, J; Lancet, D

Point mutations in the dystrophin gene: Evidence for frequent use of cryptic splice sites as a result of splicing defects

HUMAN MUTATION

IF3.7

1999-11-01

OAAI