A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23 von Gribaa, M., Salih, M., Anheim, M., Lagier-Tourenne, C., H'mida, D., Drouot, N., Mohamed, A., Elmalik, S., Kabiraj, M., Al-Rayess, M., Almubarak, M., Bétard, C., Goebel, H., Koenig, M.

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Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage... von ETAIN, B, MATHIEU, F, BELLIVIER, F, HENRY, C, DINA, C, GALLINA, S, GURLING, H, MALAFOSSE, A, PREISIG, M, FERRERO, F, CICHON, S, SCHUMACHER, J, RIETSCHEL, M, OHIRAUN, S, BORRMANN-HASSENBACH, M, PROPPING, P, ABOU JAMRA, R, SCHUIZE, T. G, MARUSIC, A, DERNOVSEK, Z. M, GIROS, B, BOURGERON, T, LEMAINQUE, A, MAIER, W, BACQ, D, BETARD, C, CHARON, C, NOTHEN, M. M, LATHROP, M, LEBOYER, M, ALBUS, M, MCKEON, P, ROCHE, S, KEALEY, C, BLACKWOOD, D, MUIR, W

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Mapping susceptibility genes for bipolar disorder : a pharmacogenetic approach based on excellent response to lithium von TURECKI, G, GROF, P, ROBERTSON, C, BREWER, C, HUDSON, T. J, ROULEAU, G. A, ALDA, M, GROF, E, D'SOUZA, V, LEBUIS, L, MARINEAU, C, CAVAZZONI, P, DUFFY, A, BETARD, C, ZVOLSKY, P

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Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7 von Goobie, Sharan, Popovic, Maja, Morrison, Jodi, Ellis, Lynda, Ginzberg, Hedy, Boocock, Graeme R.B., Ehtesham, Nadia, Bétard, Christine, Brewer, Carl G., Roslin, Nicole M., Hudson, Thomas J., Morgan, Kenneth, Fujiwara, T. Mary, Durie, Peter R., Rommens, Johanna M.

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Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31 von LAGIER-TOURENNE, C, TRANEBJAERG, L, CHAIGNE, D, GRIBAA, M, DOLLFUS, H, SILVESTRI, G, BETARD, C, WARTER, J. M, KOENIG, M

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Homozygosity mapping of a third Joubert syndrome locus to 6q23 von Lagier-Tourenne, C, Boltshauser, E, Breivik, N, Gribaa, M, Bétard, C, Barbot, C, Koenig, M

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Genome-wide scan linkage analysis for Parkinson’s disease: the European genetic study of Parkinson’s disease von Martinez, M, Brice, A, Vaughan, J R, Zimprich, A, Breteler, M M B, Meco, G, Filla, A, Farrer, M J, Bétard, C, Hardy, J, De Michele, G, Bonifati, V, Oostra, B, Gasser, T, Wood, N W, Dürr, A

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Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia von Moorjani, S., Torres, A., Gagn, C., Brun, D., Lupien, P., Roy, M., Bétard, C., Davignon, J., Lambert, M.

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Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma von Dizier, M-H, Bouzigon, E, Guilloud-Bataille, M, Bétard, C, Bousquet, J, Charpin, D, Gormand, F, Hochez, J, Just, J, Lemainque, A, Le Moual, N, Matran, R, Neukirch, F, Oryszczyn, M-P, Paty, E, Pin, I, Vervloet, D, Kauffmann, F, Lathrop, M, Demenais, F, Annesi-Maesano, I

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Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases von Chagnon, Pierre, Bétard, Christine, Robitaille, Yves, Cholette, Andrée, Gauvrea, Denis

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Genome Scan for Tourette Disorder in Affected-Sibling-Pair and Multigenerational Families von Anon

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Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13 von KHAU VAN KIEN, Philippe, MATHIEU, Flavie, LIMIN ZHU, LALANDE, Alain, BETARD, Christine, LATHROP, Mark, BRUNOTTE, Francois, WOLF, Jean-Eric, JEUNEMAITRE, Xavier

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Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype von Bétard, Christine, Rasquin-Weber, Andrée, Brewer, Carl, Drouin, Eric, Clark, Suzanne, Verner, Andrei, Darmond-Zwaig, Corinne, Fortin, Julie, Mercier, Jocelyne, Chagnon, Pierre, Fujiwara, T. Mary, Morgan, Kenneth, Richter, Andrea, Hudson, Thomas J., Mitchell, Grant A.

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Apo E allele frequencies in Alzheimerʼs disease, Lewy body dementia, Alzheimerʼs disease with cerebrovascular disease and vascular dementia von Bétard, Christine, Robitaille, Yves, Gee, Mark, Tiberghien, Denis, Larrivée, Denis, Roy, Patrice, Mortimer, James A, Gauvreau, Denis

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Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay (ARSACS): High-Resolution Physical and Transcript Map of the Candidate Region in Chromosome Region 13q11 von Engert, James C., Doré, Carole, Mercier, Jocelyne, Ge, Bing, Bétard, Christine, Rioux, John D., Owen, Carolyn, Bérubé, Pierre, Devon, Keri, Birren, Bruce, Melançon, Serge B., Morgan, Kenneth, Hudson, Thomas J., Richter, Andrea

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Molecular scanning of the human PPARα gene: association of the L162V mutation with hyperapobetalipoproteinemia von Vohl, Marie-Claude, Lepage, Pierre, Gaudet, Daniel, Brewer, Carl G., Bétard, Christine, Perron, Patrice, Houde, Ghislaine, Cellier, Christine, Faith, Janet M., Després, Jean-Pierre, Morgan, Kenneth, Hudson, Thomas J.

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A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24 von Ber, Isabelle Le, Martinez, Maria, Campion, Dominique, Laquerrière, Annie, Bétard, Christine, Bassez, Guillaume, Girard, Carol, Saugier-Veber, Pascale, Raux, Gregory, Sergeant, Nicolas, Magnier, Patrick, Maisonobe, Thierry, Eymard, Bruno, Duyckaerts, Charles, Delacourte, André, Frebourg, Thierry, Hannequin, Didier

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Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families von Bouzigon, Emmanuelle, Dizier, Marie-Hélène, Krähenbühl, Christine, Lemainque, Arnaud, Annesi-Maesano, Isabella, Betard, Christine, Bousquet, Jean, Charpin, Denis, Gormand, Frédéric, Guilloud-Bataille, Michel, Just, Jocelyne, Moual, Nicole Le, Maccario, Jean, Matran, Régis, Neukirch, Françoise, Oryszczyn, Marie-Pierre, Paty, Evelyne, Pin, Isabelle, Rosenberg-Bourgin, Myriam, Vervloet, Daniel, Kauffmann, Francine, Lathrop, Mark, Demenais, Florence

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MOLECULAR GENETIC-EVIDENCE FOR A FOUNDER EFFECT IN FAMILIAL HYPERCHOLESTEROLEMIA AMONG FRENCH-CANADIANS von BETARD, C, KESSLING, AM, ROY, M, CHAMBERLAND, A, LUSSIERCACAN, S, DAVIGNON, J

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Influence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-... von Bétard, Christine, Kessling, A.M., Roy, M., Davignon, J.

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