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Results: 1-25/45
Authors:
de Cid, R
Chomel, JC
Lazaro, C
Sunyer, J
Baudis, M
Casals, T
Le Moual, N
Kitzis, A
Feingold, J
Anto, J
Estivill, X
Kauffmann, F
Citation: R. De Cid et al., CFTR and asthma in the French EGEA study, EUR J HUM G, 9(1), 2001, pp. 67-69
Authors:
Levy, M
Gubler, MC
Feingold, J
Citation: M. Levy et al., Contribution of genetics to knowledge and management of hereditary renal diseases progressing to renal failure, ARCH PED, 8(10), 2001, pp. 1086-1098
Authors:
Kauffmann, F
Dizier, MH
Annesi-Maesano, I
Bousquet, J
Charpin, D
Demenais, F
Ecochard, D
Feingold, J
Gormand, F
Grimfeld, A
Lathrop, M
Matran, R
Neukirch, F
Paty, E
Pison, C
Scheinmann, P
Vervloet, D
Lockhart, A
Citation: F. Kauffmann et al., Epidemiological study of the Genetics and Environment of Asthma, bronchialhyperresponsiveness and atopy (EGEA). Protocol and potential selection factors, REV EPIDEM, 49(4), 2001, pp. 343-356
Authors:
Baulac, S
Picard, F
Herman, A
Feingold, J
Genin, E
Hirsch, E
Prud'homme, JF
Baulac, M
Brice, A
LeGuern, E
Citation: S. Baulac et al., Evidence for digenic inheritance in a family with both febrile convulsionsand temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31, ANN NEUROL, 49(6), 2001, pp. 786-792
Authors:
Fang, LJ
Chalhoub, N
Li, WT
Feingold, J
Ortenberg, J
Lemieux, B
Thirion, JP
Citation: Lj. Fang et al., Genotype analysis of the NF1 gene in the French Canadians from the Quebec population, AM J MED G, 104(3), 2001, pp. 189-198
Authors:
Gabolde, M
Hubert, D
Guilloud-Bataille, M
Lenaerts, C
Feingold, J
Besmond, C
Citation: M. Gabolde et al., The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis, J MED GENET, 38(5), 2001, pp. 310-311
Authors:
Benlounis, A
Nabbout, R
Feingold, J
Parmeggiani, A
Guerrini, R
Kaminska, A
Dulac, O
Citation: A. Benlounis et al., Genetic predisposition to severe myoclonic epilepsy in infancy, EPILEPSIA, 42(2), 2001, pp. 204-209
Authors:
Frebourg, T
Ebel, A
Bonaiti-Pellie, C
Brugieres, L
Berthet, P
Bressac-De Paillerets, B
Chevrier, A
Chompret, A
Cohen-Haguenauer, O
Delattre, O
Feingold, J
Feunteun, J
Frappaz, D
Fricker, JP
Gesta, P
Jonveaux, P
Kalifa, C
Lasset, C
Leheup, B
Limacher, JM
Longy, M
Nogues, C
Oppenheim, D
Sommelet, D
Soubrier, F
Stoll, C
Stoppa-Lyonnet, D
Tristant, H
Citation: T. Frebourg et al., Li-Fraumeni syndrome: update, new data and guidelines for clinical management, B CANCER, 88(6), 2001, pp. 581-587
Authors:
Sylvius, N
Tesson, F
Gayet, C
Charron, P
Benaiche, A
Mangin, L
Peuchmaurd, M
Duboscq-Bidot, L
Feingold, J
Beckmann, JS
Bouchier, C
Komajda, M
Citation: N. Sylvius et al., A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q14, AM J HU GEN, 68(1), 2001, pp. 241-246
Authors:
Dizier, MH
Besse-Schmittler, C
Guilloud-Bataille, M
Annesi-Maesano, I
Boussaha, M
Bousquet, J
Charpin, D
Degioanni, A
Gormand, F
Grimfeld, A
Hochez, J
Hyne, G
Lockhart, A
Luillier-Lacombe, M
Matran, R
Meunier, F
Neukirch, F
Pacheco, Y
Parent, V
Paty, E
Pin, I
Pison, C
Scheinmann, P
Thobie, N
Vervloet, D
Kauffmann, F
Feingold, J
Lathrop, M
Demenais, F
Citation: Mh. Dizier et al., Genome screen for asthma and related phenotypes in the French EGEA study, AM J R CRIT, 162(5), 2000, pp. 1812-1818
Authors:
Gorwood, P
Batel, P
Gouya, L
Courtois, F
Feingold, J
Ades, J
Citation: P. Gorwood et al., Reappraisal of the association between the DRD2 gene, alcoholism and addiction, EUR PSYCHIA, 15(2), 2000, pp. 90-96
Authors:
Neonato, MG
Guilloud-Bataille, M
Beauvais, P
Begue, P
Belloy, M
Benkerrou, M
Ducrocq, R
Maier-Redelsperger, M
de Montalembert, M
Quinet, B
Elion, J
Feingold, J
Girot, R
Citation: Mg. Neonato et al., Acute clinical events in 299 homozygous sickle cell patients living in France, EUR J HAEMA, 65(3), 2000, pp. 155-164
Authors:
Feingold, J
Citation: J. Feingold, Modifiying genes in hereditary diseases, M S-MED SCI, 16(4), 2000, pp. AR1-AR5
Authors:
Sampogna, F
Demenais, F
Hochez, J
Oryszczyn, MP
Maccario, J
Kauffmann, F
Feingold, J
Dizier, MH
Citation: F. Sampogna et al., Segregation analysis of IgE levels in 335 French families (EGEA) using different strategies to correct for the ascertainment through a correlated trait (asthma), GENET EPID, 18(2), 2000, pp. 128-142
Authors:
Levy, M
Feingold, J
Citation: M. Levy et J. Feingold, Estimating prevalence in single-gene kidney diseases progressing to renal failure, KIDNEY INT, 58(3), 2000, pp. 925-943
beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville
Authors:
Mouele, R
Bodo, JM
Mpele, DMB
Feingold, J
Galacteros, F
Citation: R. Mouele et al., beta-globin gene haplotypes and alpha-thalassemia analysis in Babinga pygmies from Congo-Brazzaville, HUMAN BIOL, 72(2), 2000, pp. 379-383
Authors:
Mouele, R
Pambou, O
Feingold, J
Galacteros, F
Citation: R. Mouele et al., alpha-thalassemia in Bantu population from Congo-Brazzaville: Its interaction with sickle cell anemia, HUMAN HERED, 50(2), 2000, pp. 118-125
Authors:
Guilloud-Bataille, M
De Crozes, D
Rault, G
Degioanni, A
Feingold, J
Citation: M. Guilloud-bataille et al., Cystic fibrosis mutations: Report from the French registry, HUMAN HERED, 50(2), 2000, pp. 142-145
Authors:
Garcia, A
Abel, L
Cot, M
Richard, P
Ranque, S
Feingold, J
Demenais, F
Boussinesq, M
Chippaux, JP
Citation: A. Garcia et al., Genetic epidemiology of host predisposition microfilaraemia in human loiasis, TR MED I H, 4(8), 1999, pp. 565-574
Authors:
Neonato, MG
Lu, CY
Guilloud-Bataille, M
Lapoumeroulie, C
Nabeel-Jassim, H
Dabit, D
Girot, R
Krishnamoorthy, R
Feingold, J
Besmond, C
Elion, J
Citation: Mg. Neonato et al., Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections, EUR J HUM G, 7(6), 1999, pp. 679-686
Authors:
Philippe, A
Martinez, M
Guilloud-Bataille, M
Gillberg, C
Rastam, M
Sponheim, E
Coleman, M
Zappella, M
Aschauer, H
Van Maldergem, L
Penet, C
Feingold, J
Brice, A
Leboyer, M
Citation: A. Philippe et al., Genome-wide scan for autism susceptibility genes (vol 8, pg 805, 1999), HUM MOL GEN, 8(7), 1999, pp. 1353-1353
Authors:
Philippe, A
Martinez, M
Guilloud-Bataille, M
Gillberg, C
Rastam, M
Sponheim, E
Coleman, M
Zappella, M
Aschauer, H
van Malldergerme, L
Penet, C
Feingold, J
Brice, A
Leboyer, M
Citation: A. Philippe et al., Genome-wide scan for autism susceptibility genes, HUM MOL GEN, 8(5), 1999, pp. 805-812
Authors:
Gabolde, M
Guilloud-Bataille, M
Feingold, J
Besmond, C
Citation: M. Gabolde et al., Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study, BR MED J, 319(7218), 1999, pp. 1166-1167
Authors:
Favier, R
Neonato, MG
Maillet, F
Feingold, J
Cayre, Y
Girot, R
Citation: R. Favier et al., Incidence of G20210A mutation in severe vaso-occlusive events complicatingsickle cell anemia, BL COAG FIB, 10(2), 1999, pp. 111-112
Authors:
Kauffmann, F
Dizier, MH
Annesi-Maesano, I
Bousquet, J
Charpin, D
Demenais, F
Ecochard, D
Feingold, J
Gormand, F
Grimfeld, A
Lathrop, M
Matran, R
Neukirch, F
Paty, E
Pin, I
Pison, C
Scheinmann, P
Vervloet, D
Lockhart, A
Citation: F. Kauffmann et al., EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy) - descriptive characteristics, CLIN EXP AL, 29, 1999, pp. 17-21