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Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators. [electronic resource] by
- Keavney, B
- McKenzie, C
- Parish, S
- Palmer, A
- Clark, S
- Youngman, L
- Delépine, M
- Lathrop, M
- Peto, R
- Collins, R
Producer: 20000725
In:
Lancet (London, England) vol. 355
Availability: No items available.
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11.
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Multiple DNA variant association analysis: application to the insulin gene region in type I diabetes. [electronic resource] by
- Julier, C
- Lucassen, A
- Villedieu, P
- Delepine, M
- Levy-Marchal, C
- Danzé, P M
- Bianchi, F
- Boitard, C
- Froguel, P
- Bell, J
Producer: 19941227
In:
American journal of human genetics vol. 55
Availability: No items available.
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12.
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Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q. [electronic resource] by
- Hashimoto, L
- Habita, C
- Beressi, J P
- Delepine, M
- Besse, C
- Cambon-Thomsen, A
- Deschamps, I
- Rotter, J I
- Djoulah, S
- James, M R
Producer: 19940927
In:
Nature vol. 371
Availability: No items available.
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13.
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Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6. [electronic resource] by
- Delépine, M
- Pociot, F
- Habita, C
- Hashimoto, L
- Froguel, P
- Rotter, J
- Cambon-Thomsen, A
- Deschamps, I
- Djoulah, S
- Weissenbach, J
- Nerup, J
- Lathrop, M
- Julier, C
Producer: 19970123
In:
American journal of human genetics vol. 60
Availability: No items available.
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14.
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Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. [electronic resource] by
- Julier, C
- Delépine, M
- Keavney, B
- Terwilliger, J
- Davis, S
- Weeks, D E
- Bui, T
- Jeunemaître, X
- Velho, G
- Froguel, P
- Ratcliffe, P
- Corvol, P
- Soubrier, F
- Lathrop, G M
Producer: 19971219
In:
Human molecular genetics vol. 6
Availability: No items available.
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16.
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Genetic analysis of chromosome 2 in type 1 diabetes: analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster. IMDIAB Group. [electronic resource] by
- Esposito, L
- Hill, N J
- Pritchard, L E
- Cucca, F
- Muxworthy, C
- Merriman, M E
- Wilson, A
- Julier, C
- Delepine, M
- Tuomilehto, J
- Tuomilehto-Wolf, E
- Ionesco-Tirgoviste, C
- Nistico', L
- Buzzetti, R
- Pozzilli, P
- Ferrari, M
- Bosi, E
- Pociot, F
- Nerup, J
- Bain, S C
- Todd, J A
Producer: 19981110
In:
Diabetes vol. 47
Availability: No items available.
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17.
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Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy. [electronic resource] by
- Van Maldergem, L
- Magré, J
- Khallouf, T E
- Gedde-Dahl, T
- Delépine, M
- Trygstad, O
- Seemanova, E
- Stephenson, T
- Albott, C S
- Bonnici, F
- Panz, V R
- Medina, J L
- Bogalho, P
- Huet, F
- Savasta, S
- Verloes, A
- Robert, J J
- Loret, H
- De Kerdanet, M
- Tubiana-Rufi, N
- Mégarbané, A
- Maassen, J
- Polak, M
- Lacombe, D
- Kahn, C R
- Silveira, E L
- D'Abronzo, F H
- Grigorescu, F
- Lathrop, M
- Capeau, J
- O'Rahilly, S
Producer: 20021213
In:
Journal of medical genetics vol. 39
Availability: No items available.
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18.
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CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. [electronic resource] by
- Mercati, O
- Huguet, G
- Danckaert, A
- André-Leroux, G
- Maruani, A
- Bellinzoni, M
- Rolland, T
- Gouder, L
- Mathieu, A
- Buratti, J
- Amsellem, F
- Benabou, M
- Van-Gils, J
- Beggiato, A
- Konyukh, M
- Bourgeois, J-P
- Gazzellone, M J
- Yuen, R K C
- Walker, S
- Delépine, M
- Boland, A
- Régnault, B
- Francois, M
- Van Den Abbeele, T
- Mosca-Boidron, A L
- Faivre, L
- Shimoda, Y
- Watanabe, K
- Bonneau, D
- Rastam, M
- Leboyer, M
- Scherer, S W
- Gillberg, C
- Delorme, R
- Cloëz-Tayarani, I
- Bourgeron, T
Producer: 20171010
In:
Molecular psychiatry vol. 22
Availability: No items available.
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19.
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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. [electronic resource] by
- Magré, J
- Delépine, M
- Khallouf, E
- Gedde-Dahl, T
- Van Maldergem, L
- Sobel, E
- Papp, J
- Meier, M
- Mégarbané, A
- Bachy, A
- Verloes, A
- d'Abronzo, F H
- Seemanova, E
- Assan, R
- Baudic, N
- Bourut, C
- Czernichow, P
- Huet, F
- Grigorescu, F
- de Kerdanet, M
- Lacombe, D
- Labrune, P
- Lanza, M
- Loret, H
- Matsuda, F
- Navarro, J
- Nivelon-Chevalier, A
- Polak, M
- Robert, J J
- Tric, P
- Tubiana-Rufi, N
- Vigouroux, C
- Weissenbach, J
- Savasta, S
- Maassen, J A
- Trygstad, O
- Bogalho, P
- Freitas, P
- Medina, J L
- Bonnicci, F
- Joffe, B I
- Loyson, G
- Panz, V R
- Raal, F J
- O'Rahilly, S
- Stephenson, T
- Kahn, C R
- Lathrop, M
- Capeau, J
Producer: 20010816
In:
Nature genetics vol. 28
Availability: No items available.
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20.
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Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. [electronic resource] by
- Lambert, J-C
- Grenier-Boley, B
- Harold, D
- Zelenika, D
- Chouraki, V
- Kamatani, Y
- Sleegers, K
- Ikram, M A
- Hiltunen, M
- Reitz, C
- Mateo, I
- Feulner, T
- Bullido, M
- Galimberti, D
- Concari, L
- Alvarez, V
- Sims, R
- Gerrish, A
- Chapman, J
- Deniz-Naranjo, C
- Solfrizzi, V
- Sorbi, S
- Arosio, B
- Spalletta, G
- Siciliano, G
- Epelbaum, J
- Hannequin, D
- Dartigues, J-F
- Tzourio, C
- Berr, C
- Schrijvers, E M C
- Rogers, R
- Tosto, G
- Pasquier, F
- Bettens, K
- Van Cauwenberghe, C
- Fratiglioni, L
- Graff, C
- Delepine, M
- Ferri, R
- Reynolds, C A
- Lannfelt, L
- Ingelsson, M
- Prince, J A
- Chillotti, C
- Pilotto, A
- Seripa, D
- Boland, A
- Mancuso, M
- Bossù, P
- Annoni, G
- Nacmias, B
- Bosco, P
- Panza, F
- Sanchez-Garcia, F
- Del Zompo, M
- Coto, E
- Owen, M
- O'Donovan, M
- Valdivieso, F
- Caffarra, P
- Caffara, P
- Scarpini, E
- Combarros, O
- Buée, L
- Campion, D
- Soininen, H
- Breteler, M
- Riemenschneider, M
- Van Broeckhoven, C
- Alpérovitch, A
- Lathrop, M
- Trégouët, D-A
- Williams, J
- Amouyel, P
Producer: 20140421
In:
Molecular psychiatry vol. 18
Availability: No items available.
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