A predominantly neolithic origin for European paternal lineages
Balaresque, Patricia, Bowden, Georgina R, Adams, Susan M, Leung, Ho-Yee, King, Turi E, Rosser, Zoë H, Goodwin, Jane, Moisan, Jean-Paul, Richard, Christelle, Millward, Ann, Demaine, Andrew G, Barbujani, Guido, Previderè, Carlo, Wilson, Ian J, Tyler-Smith, Chris, Jobling, Mark A
Published in PLoS biology (01.01.2010)
Published in PLoS biology (01.01.2010)
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Identification of SLC39A4 , a gene involved in acrodermatitis enteropathica
Küry, Sébastien, Giraudet, Stéphanie, Bézieau, Stéphane, Dréno, Brigitte, Kharfi, Monia, Kamoun, Ridha, Moisan, Jean-Paul
Published in Nature genetics (01.07.2002)
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Divorcing the Late Upper Palaeolithic demographic histories of mtDNA haplogroups M1 and U6 in Africa
Pennarun, Erwan, Kivisild, Toomas, Metspalu, Ene, Metspalu, Mait, Reisberg, Tuuli, Moisan, Jean-Paul, Behar, Doron M, Jones, Sacha C, Villems, Richard
Published in BMC evolutionary biology (03.12.2012)
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High incidence of N and K-Ras activating mutations in multiple myeloma and primary plasma cell leukemia at diagnosis
Bezieau, Stéphane, Devilder, Marie-Claire, Avet-Loiseau, Hervé, Mellerin, Marie-Paule, Puthier, Denis, Pennarun, Erwan, Rapp, Marie-José, Harousseau, Jean-Luc, Moisan, Jean-Paul, Bataille, Régis
Published in Human mutation (01.09.2001)
Published in Human mutation (01.09.2001)
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Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica
Küry, Sébastien, Kharfi, Monia, Kamoun, Ridha, Taïeb, Alain, Mallet, Eric, Baudon, Jean-Jacques, Glastre, Catherine, Michel, Bruno, Sebag, Francis, Brooks, David, Schuster, Volker, Scoul, Catherine, Dréno, Brigitte, Bézieau, Stéphane, Moisan, Jean-Paul
Published in Human mutation (01.10.2003)
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X-chromosome lineages and the settlement of the Americas
Bourgeois, Stephane, Yotova, Vania, Wang, Sijia, Bourtoumieu, Sylvie, Moreau, Claudia, Michalski, Roman, Moisan, Jean-Paul, Hill, Kim, Hurtado, Ana M., Ruiz-Linares, Andres, Labuda, Damian
Published in American journal of physical anthropology (01.11.2009)
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Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity
Ziętkiewicz, Ewa, Yotova, Vania, Gehl, Dominik, Wambach, Tina, Arrieta, Isabel, Batzer, Mark, Cole, David E.C., Hechtman, Peter, Kaplan, Feige, Modiano, David, Moisan, Jean-Paul, Michalski, Roman, Labuda, Damian
Published in American journal of human genetics (01.11.2003)
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Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28
Kyndt, Florence, Schott, Jean-Jacques, Trochu, Jean-Noël, Baranger, Florence, Herbert, Odile, Scott, Valérie, Fressinaud, Edith, David, Albert, Moisan, Jean-Paul, Bouhour, Jean-Brieuc, Le Marec, Hervé, Bénichou, Bernard
Published in American journal of human genetics (01.03.1998)
Published in American journal of human genetics (01.03.1998)
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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large french family
KYNDT, Florence, PROBST, Vincent, LE MAREC, Hervé, POTET, Franck, DEMOLOMBE, Sophie, CHEVALLIER, Jean-Christophe, BARO, Isabelle, MOISAN, Jean-Paul, BOISSEAU, Pierre, SCHOTT, Jean-Jacques, ESCANDE, Denis
Published in Circulation (New York, N.Y.) (18.12.2001)
Published in Circulation (New York, N.Y.) (18.12.2001)
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Phylogeography of Y-Chromosome Haplogroup I Reveals Distinct Domains of Prehistoric Gene Flow in Europe
Rootsi, Siiri, Kivisild, Toomas, Benuzzi, Giorgia, Help, Hela, Bermisheva, Marina, Kutuev, Ildus, Barać, Lovorka, Peričić, Marijana, Balanovsky, Oleg, Pshenichnov, Andrey, Dion, Daniel, Grobei, Monica, Zhivotovsky, Lev A., Battaglia, Vincenza, Achilli, Alessandro, Al-Zahery, Nadia, Parik, Jüri, King, Roy, Cinnioğlu, Cengiz, Khusnutdinova, Elsa, Rudan, Pavao, Balanovska, Elena, Scheffrahn, Wolfgang, Simonescu, Maya, Brehm, Antonio, Goncalves, Rita, Rosa, Alexandra, Moisan, Jean-Paul, Chaventre, Andre, Ferak, Vladimir, Füredi, Sandor, Oefner, Peter J., Shen, Peidong, Beckman, Lars, Mikerezi, Ilia, Terzić, Rifet, Primorac, Dragan, Cambon-Thomsen, Anne, Krumina, Astrida, Torroni, Antonio, Underhill, Peter A., Santachiara-Benerecetti, A. Silvana, Villems, Richard, Magri, Chiara, Semino, Ornella
Published in American journal of human genetics (01.07.2004)
Published in American journal of human genetics (01.07.2004)
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Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?
DELPHIN, Nathalie, HANEIN, Sylvain, MUNNICH, Arnold, ROCHE, Olivier, KAPLAN, Josseline, ROZET, Jean-Michel, FARES TAIE, Lucas, ZANLONGHI, Xavier, BONNEAU, Dominique, MOISAN, Jean-Paul, BOYLE, Christine, NITSCHKE, Patrick, PRUVOST, Solenn, BONNEFONT, Jean-Paul
Published in European journal of human genetics : EJHG (01.03.2012)
Published in European journal of human genetics : EJHG (01.03.2012)
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Mapping of a gene for long QT syndrome to chromosome 4q25-27
SCHOTT, J.-J, CHARPENTIER, F, LE MAREC, H, PASCAL, O, PELTIER, S, FOLEY, P, DROUIN, E, BOUHOUR, J.-B, DONNELLY, P, VERGNAUD, G, BACHNER, L, MOISAN, J.-P
Published in American journal of human genetics (01.11.1995)
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Published in American journal of human genetics (01.11.1995)
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An mtDNA perspective of French genetic variation
Richard, Chrystelle, Pennarun, Erwan, Kivisild, Toomas, Tambets, Kristiina, Tolk, Helle-Viivi, Metspalu, Ene, Reidla, Maere, Chevalier, Sylviana, Giraudet, Stéphanie, Lauc, Lovorka Bara, Peri i, Marijana, Rudan, Pavao, Claustres, Mireille, Journel, Hubert, Dorval, Ian, Müller, Claude, Villems, Richard, Chaventré, André, Moisan, Jean-Paul
Published in Annals of human biology (2007)
Published in Annals of human biology (2007)
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Spatial and Temporal Distribution of the Neutral Polymorphisms in the Last ZFX Intron: Analysis of the Haplotype Structure and Genealogy
Jaruzelska, Jadwiga, Zietkiewicz, Ewa, Batzer, Mark, Cole, David E. C, Moisan, Jean-Paul, Scozzari, Rosaria, Tavare, Simon, Labuda, Damian
Published in Genetics (Austin) (01.07.1999)
Published in Genetics (Austin) (01.07.1999)
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Human X-chromosomal lineages in Europe reveal Middle Eastern and Asiatic contacts
XIAO, Feng-Xia, YOTOVA, Vania, LABUDA, Damian, ZIETKIEWICZ, Ewa, LOVELL, Alan, GEHL, Dominik, BOURGEOIS, Stéphane, MOREAU, Claudia, SPANAKI, Cleanthe, PLAITAKIS, Andreas, MOISAN, Jean-Paul
Published in European journal of human genetics : EJHG (01.04.2004)
Published in European journal of human genetics : EJHG (01.04.2004)
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Activating Ras mutations in patients with plasma-cell disorders: a reappraisal
Bezieau, Stéphane, Avet-Loiseau, Hervé, Moisan, Jean-Paul, Bataille, Régis, Norton, John D., Rothwell, Dominic G., Kalakonda, Nagesh
Published in Blood (01.08.2002)
Published in Blood (01.08.2002)
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DNA short tandem repeat profiling of Morocco
Jauffrit, Alban, El Amri, Hamid, Airaud, Fabrice, André, Marie-Thérèse, Herbert, Odile, Landeau-Trottier, Gaëlle, Giraudet, Stéphanie, Richard, Christel, Chaventré, André, Moisan, Jean-Paul
Published in Journal of forensic sciences (01.03.2003)
Published in Journal of forensic sciences (01.03.2003)
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Construction of a 780-kb PAC, BAC, and Cosmid Contig Encompassing the Minimal Critical Deletion Involved in B Cell Chronic Lymphocytic Leukemia at 13q14.3
Bouyge-Moreau, Isabelle, Rondeau, Gaëlle, Avet-Loiseau, Hervé, André, Marie-Thérèse, Bézieau, Stéphane, Chérel, Michel, Saleün, Sylvie, Cadoret, Emmanuelle, Shaikh, Tamim, De Angelis, Margaret M., Arcot, Santosh, Batzer, Mark, Moisan, Jean-Paul, Devilder, Marie-Claire
Published in Genomics (San Diego, Calif.) (01.12.1997)
Published in Genomics (San Diego, Calif.) (01.12.1997)
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Mitochondrial DNA analysis on remains of a putative son of Louis XVI, King of France and Marie-Antoinette
Jehaes, E, Decorte, R, Peneau, A, Petrie, J H, Boiry, P A, Gilissen, A, Moisan, J P, Van den Berghe, H, Pascal, O, Cassiman, J J
Published in European journal of human genetics : EJHG (01.07.1998)
Published in European journal of human genetics : EJHG (01.07.1998)
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