| Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography P Normand, P Lapierre, LS Tisa, JP Gogarten, N Alloisio, E Bagnarol, ... Genome research 17 (1), 7-15, 2007 | 418 | 2007 |
| Phylogenomics reveals multiple losses of nitrogen-fixing root nodule symbiosis M Griesmann, Y Chang, X Liu, Y Song, G Haberer, MB Crook, ... Science 361 (6398), eaat1743, 2018 | 355 | 2018 |
| Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3 ML Ribeiro, N Alloisio, H Almeida, C Gomes, P Texier, C Lemos, ... Blood, The Journal of the American Society of Hematology 96 (4), 1602-1604, 2000 | 211 | 2000 |
| Evidence that red blood cell protein p55 may participate in the skeleton-membrane linkage that involves protein 4.1 and glycophorin C N Alloisio, N Dalla Venezia, A Rana, K Andrabi, P Texier, F Gilsanz, ... | 162 | 1993 |
| Transcriptomics of actinorhizal symbioses reveals homologs of the whole common symbiotic signaling cascade V Hocher, N Alloisio, F Auguy, P Fournier, P Doumas, P Pujic, H Gherbi, ... Plant Physiology 156 (2), 700-711, 2011 | 146 | 2011 |
| The Frankia alni Symbiotic Transcriptome N Alloisio, C Queiroux, P Fournier, P Pujic, P Normand, D Vallenet, ... Molecular Plant-Microbe Interactions 23 (5), 593-607, 2010 | 113 | 2010 |
| Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46. R Wilmotte, J Marechal, L Morle, F Baklouti, N Philippe, R Kastally, ... The Journal of clinical investigation 91 (5), 2091-2096, 1993 | 113 | 1993 |
| Hereditary spherocytosis: from clinical to molecular defects A Iolascon, EM Del Giudice, S Perrotta, N Alloisio, L Morlé, J Delaunay Haematologica 83 (3), 240-257, 1998 | 109 | 1998 |
| Spectrin beta-chain variant associated with hereditary elliptocytosis. D Dhermy, MC Lecomte, M Garbarz, O Bournier, C Galand, H Gautero, ... The Journal of Clinical Investigation 70 (4), 707-715, 1982 | 96 | 1982 |
| A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss L Morlé, M Bozon, N Alloisio, P Latour, A Vandenberghe, H Plauchu, ... Journal of medical genetics 37 (5), 368-370, 2000 | 95 | 2000 |
| The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum N Alloisio, P Texier, L Denoroy, C Berger, E Miraglia del Giudice, ... | 93 | 1996 |
| Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin … N Alloisio, L Morlé, J Maréchal, AF Roux, MT Ducluzeau, D Guetarni, ... The Journal of clinical investigation 87 (6), 2169-2177, 1991 | 82 | 1991 |
| Differential Effects of Rare Specific Flavonoids on Compatible and Incompatible Strains in the Myrica gale-Frankia Actinorhizal Symbiosis J Popovici, G Comte, É Bagnarol, N Alloisio, P Fournier, F Bellvert, ... Applied and Environmental Microbiology 76 (8), 2451-2460, 2010 | 77 | 2010 |
| Red cell membrane sialoglycoptein β in homozygous and heterozygous 4.1 (−) hereditary elliptocytosis N Alloisio, L Morle, D Bachir, D Guetarni, P Colonna, J Delaunay Biochimica et Biophysica Acta (BBA)-Biomembranes 816 (1), 57-62, 1985 | 77 | 1985 |
| Mutation in the zonadhesin-like domain of α-tectorin associated with autosomal dominant non-syndromic hearing loss N Alloisio, L Morle, M Bozon, J Godet, K Verhoeven, G Van Camp, ... European journal of human genetics 7 (2), 255-258, 1999 | 74 | 1999 |
| Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis N Alloisio, P Texier, A Vallier, ML Ribeiro, L Morle, M Bozon, E Bursaux, ... Blood, The Journal of the American Society of Hematology 90 (1), 414-420, 1997 | 69 | 1997 |
| Hereditary spherocytosis with band 3 deficiency. Association with a nonsense mutation of the band 3 gene (allele Lyon), and aggravation by a low-expression allele occurring in … N Alloisio, P Maillet, G Carre, P Texier, A Vallier, F Baklouti, N Philippe, ... | 59 | 1996 |
| Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis. J Delaunay, N Alloisio, L Morle, F Baklouti, N Dalla Venezia, P Maillet, ... Annales de Genetique 39 (4), 209-221, 1996 | 58 | 1996 |
| Homozygous 4.1 (-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene. N Dalla Venezia, F Gilsanz, N Alloisio, MT Ducluzeau, EJ Benz, ... The Journal of clinical investigation 90 (5), 1713-1717, 1992 | 57 | 1992 |
| Gerbich reactivity in 4.1 (—) hereditary elliptocytosis and protein 4.1 level in blood group Gerbich deficiency D Sondag, N Alloisio, D Blanchard, MT Ducluzeau, P Colonna, D Bachir, ... British journal of haematology 65 (1), 43-50, 1987 | 57 | 1987 |
