Apolipoprotein E-∈ A allele and Alzheimer's disease N Anwar, S Lovestone, ME Cheetham, R Levy, JF Powell, P Amouyel, ... The Lancet 342 (8882), 1308-1309, 1993 | 91 | 1993 |
Apolipoprotein E-epsilon 4 allele and Alzheimer's disease G Lucotte, F David, S Visvikis, B Leininger-Müller, G Siest, MC Babron, ... Lancet (London, England) 342 (8882), 1309, 1993 | 76 | 1993 |
Association of apolipoprotein E allele ϵ4 with late‐onset sporadic Alzheimer's disease G Lucotte, S Visvikis, B Leininger‐Möler, F David, S Berriche, ... American journal of medical genetics 54 (3), 286-288, 1994 | 58 | 1994 |
Manic depressive illness is linked to factor IX in a French pedigree. G Lucotte, A Landoulsi, S Berriche, F David, MC Babron Annales de Genetique 35 (2), 93-95, 1992 | 54 | 1992 |
Reduced variability in Y-chromosome-specific haplotypes for some Central African populations G Lucotte, N Gérard, R Krishnamoorthy, F David, A Aouizérate, P Galzot Human biology, 519-526, 1994 | 35 | 1994 |
Nucleotide sequence of p49a, a genomic Y-specific probe with potential utilization in sex determination. G Lucotte, F David, M Mariotti Molecular and cellular probes 5 (5), 359-363, 1991 | 35 | 1991 |
Alzheimer's mutation G Lucotte, S Berriche, F David Nature 351 (6327), 530-530, 1991 | 32 | 1991 |
Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population M Vidaud, A Kitzis, C Ferec, D Bozon, V Dumur, G Giraud, F David, ... Human genetics 81, 183-184, 1989 | 25 | 1989 |
Haplotype VIII of the Y chromosome is the ancestral haplotype in Jews G Lucotte, F David, S Berriche Human Biology, 467-471, 1996 | 24 | 1996 |
Y-chromosome-specific haplotypes of Jews detected by probes 49f and 49a G Lucotte, F David Human biology, 757-761, 1992 | 23 | 1992 |
MHD hypersonic flow control for aerospace applications JP Petit, J Geffray, F David 16th AIAA/DLR/DGLR International Space Planes and Hypersonic Systems and …, 2009 | 21 | 2009 |
Une méthode d'amplification génique isotherme F David, É Turlotte Comptes Rendus de l'Académie des Sciences-Series III-Sciences de la Vie 321 …, 1998 | 20 | 1998 |
HLA‐DRB AND‐DBQ TYPING BY PCR AMPLIFICATION USING SEQUENCE‐SPECIFIC PRIMERS (PCR‐SSP): ASSESSMENT AFTER 1 YEAR OF ROUTINE USE BY THREE LABORATORIES B Mercier, RA Daccak, A Samaan, F David, A Carta, P Cracco, ... International Journal of Immunogenetics 21 (2), 105-123, 1994 | 16 | 1994 |
Familial Alzheimer's disease (FAD): co-segregation between alleles at the D21S11 DNA marker and the FAD gene in a particular pedigree F David, F Clerget, G Lucote Journal of neurology 235, 485-486, 1988 | 8 | 1988 |
An isothermal gene amplification method F David, É Turlotte Comptes Rendus de l'Academie des Sciences Series III Sciences de la Vie 11 …, 1998 | 7 | 1998 |
Absence of a close linkage between Alzheimer's disease and the polymorphic probe coding for superoxide dismutase 1 F David, S Intrator, JF Foncin, D Salmon, G Lucotte Comptes Rendus de L'academie des sciences. Serie III, Sciences de la vie 306 …, 1988 | 7 | 1988 |
Absence of a close linkage between Alzheimer's disease susceptibility gene and a polymorphic DNA probe coding for beta-amyloid. F David, G Lucotte Biomedicine & Pharmacotherapy= Biomedecine & Pharmacotherapie 42 (9), 575-577, 1988 | 5 | 1988 |
Self-polarisation of fusion diodes: from excess energy to energy F David, J Giles Proc. of the ICCF14, 2008 | 4 | 2008 |
Utiliser les propriétés topologiques de l’ADN: une nouvelle arme contre les agents pathogènes F David PDF). Fusion. http://www. lab-rech-associatives. com/pdf/Utiliser% 20la …, 2002 | 4 | 2002 |
Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France. G Lucotte, S Berriche, F David, H Rouquet, JC Turpin Genetic Counseling (Geneva, Switzerland) 4 (4), 285-287, 1993 | 4 | 1993 |