1 - 25 of 26 results for author:"Feingold J." in Literature citations
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| Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis. Marrakchi S., Guigue P., Renshaw B.R., Puel A., Pei X.Y., Fraitag S., Zribi J., Bal E., Cluzeau C., Chrabieh M. et al. N. Engl. J. Med. 365:620-628(2011) · UniProtKB (1) · Mapped (2) |
| Screening of OPTN in French familial amyotrophic lateral sclerosis. Millecamps S., Boillee S., Chabrol E., Camu W., Cazeneuve C., Salachas F., Pradat P.F., Danel-Brunaud V., Vandenberghe N., Corcia P. et al. Neurobiol. Aging 32:557.e11-3(2011) · Mapped (3) |
| rs5888 variant of SCARB1 gene is a possible susceptibility factor for age-related macular degeneration. Zerbib J., Seddon J.M., Richard F., Reynolds R., Leveziel N., Benlian P., Borel P., Feingold J., Munnich A., Soubrane G. et al. PLoS ONE 4:e7341-e7341(2009) · Mapped (8) |
| Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis. Corvol H., Boelle P.Y., Brouard J., Knauer N., Chadelat K., Henrion-Caude A., Flamant C., Muselet-Charlier C., Boule M., Fauroux B. et al. Pediatr. Pulmonol. 43:1224-1232(2008) · Mapped (49) |
| The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism. Camuzat A., Romana M., Durr A., Feingold J., Brice A., Ruberg M., Lannuzel A. Mov. Disord. 23:2384-2391(2008) · Mapped (6) |
| Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse). Trochet D., de Pontual L., Estevao M.H., Mathieu Y., Munnich A., Feingold J., Goridis C., Lyonnet S., Amiel J. Hum. Mutat. 29:770-770(2008) · Mapped (1) |
| Glucocorticoid receptor gene polymorphisms associated with progression of lung disease in young patients with cystic fibrosis. Corvol H., Nathan N., Charlier C., Chadelat K., Le Rouzic P., Tabary O., Fauroux B., Henrion-Caude A., Feingold J., Boelle P.Y. et al. Respir. Res. 8:88-88(2007) · Mapped (16) |
| Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example. Hanein S., Perrault I., Gerber S., Delphin N., Benezra D., Shalev S., Carmi R., Feingold J., Dufier J.L., Munnich A. et al. Eur. J. Hum. Genet. 16:115-123(2008) · Mapped (1) |
| The incidence of Rett syndrome in France. Bienvenu T., Philippe C., De Roux N., Raynaud M., Bonnefond J.P., Pasquier L., Lesca G., Mancini J., Jonveaux P., Moncla A. et al. Pediatr. Neurol. 34:372-375(2006) · Mapped (15) |
| Prevalence and distribution of MEFV mutations among Arabs from the Maghreb patients suffering from familial Mediterranean fever. Belmahi L., Sefiani A., Fouveau C., Feingold J., Delpech M., Grateau G., Dode C. C. R. Biol. 329:71-74(2006) · Mapped (6) |
| Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency. Tredano M., Cooper D.N., Stuhrmann M., Christodoulou J., Chuzhanova N.A., Roudot-Thoraval F., Boelle P.Y., Elion J., Jeanpierre M., Feingold J. et al. Am. J. Med. Genet. A 140:62-69(2006) · Mapped (5) |
| Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C. Tazir M., Azzedine H., Assami S., Sindou P., Nouioua S., Zemmouri R., Hamadouche T., Chaouch M., Feingold J., Vallat J.M. et al. Brain 127:154-163(2004) · Mapped (6) |
| Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations. Cazeneuve C., Hovannesyan Z., Genevieve D., Hayrapetyan H., Papin S., Girodon-Boulandet E., Boissier B., Feingold J., Atayan K., Sarkisian T. et al. Arthritis Rheum. 48:2324-2331(2003) · Mapped (6) |
| Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population. Fang L.J., Li W., Chalhoub N., Feingold J., Ortenberg J., Thirion J.P. Ann. Genet. 45:39-44(2002) · Mapped (10) |
| Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy. Amiel J., Raclin V., Jouannic J.M., Morichon N., Hoffman-Radvanyi H., Dommergues M., Feingold J., Munnich A., Bonnefont J.P. J. Med. Genet. 38:850-852(2001) · Mapped (10) |
| Genotype analysis of the NF1 gene in the French Canadians from the Quebec population. Fang L., Chalhoub N., Li W., Feingold J., Ortenberg J., Lemieux B., Thirion J.P. Am. J. Med. Genet. 104:189-198(2001) · Mapped (10) |
| The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis. Gabolde M., Hubert D., Guilloud-Bataille M., Lenaerts C., Feingold J., Besmond C. J. Med. Genet. 38:310-311(2001) · Mapped (50) |
| CFTR and asthma in the French EGEA study. de Cid R., Chomel J.C., Lazaro C., Sunyer J., Baudis M., Casals T., Le Moual N., Kitzis A., Feingold J., Anto J. et al. Eur. J. Hum. Genet. 9:67-69(2001) · Mapped (45) |
| Reappraisal of the association between the DRD2 gene, alcoholism and addiction. Gorwood P., Batel P., Gouya L., Courtois F., Feingold J., Ades J. Eur. Psychiatry 15:90-96(2000) · Mapped (4) |
| Lack of association between juvenile myoclonic epilepsy and HLA-DR13. Le Hellard S., Neidhart E., Thomas P., Feingold J., Malafosse A., Tafti M. Epilepsia 40:117-119(1999) · Mapped (297) |
| Lack of association between anorexia nervosa and D3 dopamine receptor gene. Bruins-Slot L., Gorwood P., Bouvard M., Blot P., Ades J., Feingold J., Schwartz J.C., Mouren-Simeoni M.C. Biol. Psychiatry 43:76-78(1998) · Mapped (6) |
| Lack of association of angiotensin I-converting enzyme gene polymorphism and premature myocardial infarction in Mauritian Indians. Ramasawmy R., Manraj M., Kotea N., Shun N.K., Genin E., Feingold J., Krishnamoorthy R., Baligadoo S. Clin. Genet. 50:551-554(1996) · Mapped (8) |
| Lack of association between alcohol-dependence and D3 dopamine receptor gene in three independent samples. Gorwood P., Martres M.P., Ades J., Sokoloff P., Noble E.P., Geijer T., Blum K., Neiman J., Jonsson E., Feingold J. Am. J. Med. Genet. 60:529-531(1995) · Mapped (10) |
| Juvenile limb-girdle muscular dystrophy. Clinical, histopathological and genetic data from a small community living in the Reunion island. Fardeau M., Hillaire D., Mignard C., Feingold N., Feingold J., Mignard D., de Ubeda B., Collin H., Tome F.M.S., Richard I. et al. Brain 119:295-308(1996) · UniProtKB (1) |
| Transforming growth factor-alpha: characterization of the BamHI, RsaI, and TaqI polymorphic regions. Qian J.F., Feingold J., Stoll C., May E. Am. J. Hum. Genet. 53:168-175(1993) · UniProtKB (1) |