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 at 3p14
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
Published in Molecular psychiatry (01.07.2006)
Published in Molecular psychiatry (01.07.2006)
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Journal Article
Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families
Bouzigon, E, Siroux, V, Dizier, M-H, Lemainque, A, Pison, C, Lathrop, M, Kauffmann, F, Demenais, F, Pin, I
Published in The European respiratory journal (01.08.2007)
Published in The European respiratory journal (01.08.2007)
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Journal Article
Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q
BELL, Christopher G, BENZINOU, Michael, MEYRE, David, FROGUEL, Philippe, SIDDIQ, Afshan, LECOEUR, Cécile, DINA, Christian, LEMAINQUE, Arnaud, CLEMENT, Karine, BASDEVANT, Arnaud, GUY-GRAND, Bernard, MEIN, Charles A
Published in Diabetes (New York, N.Y.) (01.07.2004)
Published in Diabetes (New York, N.Y.) (01.07.2004)
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Journal Article
Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma
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
Published in Genes and immunity (01.03.2005)
Published in Genes and immunity (01.03.2005)
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Journal Article
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families
GRECO, L., BABRON, M. C., CORAZZA, G. R., PERCOPO, S., SICA, R., CLOT, F., FULCHIGNONI-LATAUD, M. C., ZAVATTARI, P., MOMIGLIANO-RICHIARDI, P., CASARI, G., GASPARINI, P., TOSI, R., MANTOVANI, V., DE VIRGILIIS, S., IACONO, G., D'ALFONSO, A., SELINGER-LENEMAN, H., LEMAINQUE, A., SERRE, J. L., CLERGET-DARPOUX, F.
Published in Annals of human genetics (01.01.2001)
Published in Annals of human genetics (01.01.2001)
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Journal Article
SRPX2 mutations in disorders of language cortex and cognition
Roll, Patrice, Rudolf, Gabrielle, Pereira, Sandrine, Royer, Barbara, Scheffer, Ingrid E., Massacrier, Annick, Valenti, Maria-Paola, Roeckel-Trevisiol, Nathalie, Jamali, Sarah, Beclin, Christophe, Seegmuller, Caroline, Metz-Lutz, Marie-Noëlle, Lemainque, Arnaud, Delepine, Marc, Caloustian, Christophe, Martin, Anne de Saint, Bruneau, Nadine, Depétris, Danièle, Mattéi, Marie-Geneviève, Flori, Elisabeth, Robaglia-Schlupp, Andrée, Lévy, Nicolas, Neubauer, Bernd A., Ravid, Rivka, Marescaux, Christian, Berkovic, Samuel F., Hirsch, Edouard, Lathrop, Mark, Cau, Pierre, Szepetowski, Pierre
Published in Human molecular genetics (01.04.2006)
Published in Human molecular genetics (01.04.2006)
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Journal Article
Estimation of the Inbreeding Coefficient through Use of Genomic Data
Leutenegger, Anne-Louise, Prum, Bernard, Génin, Emmanuelle, Verny, Christophe, Lemainque, Arnaud, Clerget-Darpoux, Françoise, Thompson, Elizabeth A.
Published in American journal of human genetics (01.09.2003)
Published in American journal of human genetics (01.09.2003)
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Journal Article
A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection
de Villartay, Jean-Pierre, Lim, Annick, Al-Mousa, Hamoud, Dupont, Sophie, Déchanet-Merville, Julie, Coumau-Gatbois, Edith, Gougeon, Marie-Lise, Lemainque, Arnaud, Eidenschenk, Céline, Jouanguy, Emmanuelle, Abel, Laurent, Casanova, Jean-Laurent, Fischer, Alain, Le Deist, Françoise
Published in The Journal of clinical investigation (01.11.2005)
Published in The Journal of clinical investigation (01.11.2005)
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Journal Article
Invasions Toolkit :Current Methods for Tracking the Spread and Impact of Invasive Species
Kamenova, S., Bartley, T.J., Bohan, David, Boutain, J.R., Colautti, R.I., Domaizon, Isabelle, Fontaine, C., Lemainque, A., Le Viol, I., Mollot, Grégory, Perga, Marie-Elodie, Ravigné, V., Massol, F.
Published in Networks of Invasion: A Synthesis of Concepts (01.01.2017)
Published in Networks of Invasion: A Synthesis of Concepts (01.01.2017)
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Book Chapter
A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene
Ferreiro, Ana, Monnier, Nicole, Romero, Norma B., Leroy, Jean-Paul, Bönnemann, Carsten, Haenggeli, Charles-Antoine, Straub, Volker, Voss, Wolfgang D., Nivoche, Yves, Jungbluth, Heinz, Lemainque, Arnaud, Voit, Thomas, Lunardi, Joël, Fardeau, Michel, Guicheney, Pascale
Published in Annals of neurology (01.06.2002)
Published in Annals of neurology (01.06.2002)
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Journal Article
Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31
Laurin, Nancy, Brown, Jacques P., Lemainque, Arnaud, Duchesne, Annie, Huot, Denys, Lacourcière, Yves, Drapeau, Gervais, Verreault, Jean, Raymond, Vincent, Morissette, Jean
Published in American journal of human genetics (01.09.2001)
Published in American journal of human genetics (01.09.2001)
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Journal Article
A novel X-linked recessive form of Mendelian susceptibility to mycobaterial disease
Bustamante, Jacinta, Picard, Capucine, Fieschi, Claire, Filipe-Santos, Orchidée, Feinberg, Jacqueline, Perronne, Christian, Chapgier, Ariane, de Beaucoudrey, Ludovic, Vogt, Guillaume, Sanlaville, Damien, Lemainque, Arnaud, Emile, Jean-François, Abel, Laurent, Casanova, Jean-Laurent
Published in Journal of medical genetics (01.02.2007)
Published in Journal of medical genetics (01.02.2007)
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Journal Article
Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome
Caraballo, Roberto, Pavek, Sylvana, Lemainque, Arnaud, Gastaldi, Marguerite, Echenne, Bernard, Motte, Jacques, Genton, Pierre, Cersósimo, Ricardo, Humbertclaude, Véronique, Fejerman, Natalio, Monaco, Anthony P., Lathrop, Mark G., Rochette, Jacques, Szepetowski, Pierre
Published in American journal of human genetics (01.03.2001)
Published in American journal of human genetics (01.03.2001)
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Journal Article
A Major Susceptibility Locus on Chromosome 22q12 Plays a Critical Role in the Control of Kala-Azar
Bucheton, Bruno, Abel, Laurent, El-Safi, Sayda, Kheir, Musa M., Pavek, Sylvana, Lemainque, Arnaud, Dessein, Alain J.
Published in American journal of human genetics (01.11.2003)
Published in American journal of human genetics (01.11.2003)
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Journal Article
A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1
Vuillaume, Isabelle, Devos, David, Schraen-Maschke, Susanna, Dina, Christian, Lemainque, Arnaud, Vasseur, Francis, Bocquillon, Guy, Devos, Patrick, Kocinski, Carole, Marzys, Christiane, Destée, Alain, Sablonnière, Bernard
Published in Annals of neurology (01.11.2002)
Published in Annals of neurology (01.11.2002)
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Journal Article
Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p
RUF, Rainer G, FUCHSHUBER, Arno, KARLE, Stephanie M, LEMAINQUE, Arnaud, HUCK, Kirsten, WIENKER, Thomas, OTTO, Edgar, HILDEBRANDT, Friedhelm
Published in Journal of the American Society of Nephrology (01.07.2003)
Published in Journal of the American Society of Nephrology (01.07.2003)
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Journal Article
Evidence for linkage of a new region (11p14) to eczema and allergic diseases
Guilloud-Bataille, Michel, Bouzigon, Emmanuelle, Annesi-Maesano, Isabella, Bousquet, Jean, Charpin, Denis, Gormand, Frédéric, Hochez, Joëlle, Just, Jocelyne, Lemainque, Arnaud, Le Moual, Nicole, Matran, Régis, Neukirch, Françoise, Oryszczyn, Marie-Pierre, Paty, Evelyne, Pin, Isabelle, Vervloet, Daniel, Kauffmann, Francine, Lathrop, Mark, Demenais, Florence, Dizier, Marie-Hélène
Published in Human genetics (01.01.2008)
Published in Human genetics (01.01.2008)
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Journal Article
Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families
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
Published in Human molecular genetics (15.12.2004)
Published in Human molecular genetics (15.12.2004)
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Journal Article
Amish brittle hair syndrome gene maps to 7p14.1
Seboun, Eric, Lemainque, Arnaud, Jackson, Charles E.
Published in American journal of medical genetics. Part A (30.04.2005)
Published in American journal of medical genetics. Part A (30.04.2005)
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Journal Article