Хайлтын үр дүнгүүд - Frédéric Reinier

  • 7-н 1 - 7 үр дүнгүүдийг харуулж байна
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  1. 1
    Population- and individual-specific regulatory variation in Sardinia

    Population- and individual-specific regulatory variation in Sardinia -н Mauro Pala, Zachary Zappala, Mara Marongiu, Xin Li, Joe R. Davis, Roberto Cusano, Francesca Crobu, Kimberly R. Kukurba, Michael J. Gloudemans, Frédéric Reinier, Riccardo Berutti, Maria Grazia Piras, Antonella Mulas, Magdalena Żołędziewska, Michele Marongiu, Elena P. Sorokin, Gaelen T. Hess, Kevin S. Smith, Fabio Busonero, Andrea Maschio, Maristella Steri, Carlo Sidore, Serena Sanna, Edoardo Fiorillo, Michael C. Bassik, Stephen Sawcer, Alexis Battle, John Novembre, Chris Jones, Andrea Angius, Gonçalo R. Abecasis, David Schlessinger, Francesco Cucca, Stephen B. Montgomery

    Хэвлэсэн 2017
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    Artigo
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  2. 2
    Low-Pass DNA Sequencing of 1200 Sardinians Reconstructs European Y-Chromosome Phylogeny

    Low-Pass DNA Sequencing of 1200 Sardinians Reconstructs European Y-Chromosome Phylogeny -н Paolo Francalacci, Laura Morelli, Andrea Angius, Riccardo Berutti, Frédéric Reinier, Rossano Atzeni, Rosella Pilu, Fabio Busonero, Andrea Maschio, Ilenia Zara, Daria Sanna, Antonella Useli, Maria Francesca Urru, Marco Marcelli, Roberto Cusano, Manuela Oppo, Magdalena Żołędziewska, Maristella Pitzalis, Francesca Deidda, Eleonora Porcu, Fausto Poddie, Hyun Min Kang, Robert Lyons, Brendan Tarrier, Jennifer Bragg Gresham, Bingshan Li, Sergio Tofanelli, Santos Alonso, Mariano Dei, Sandra Lai, Antonella Mulas, Michael B. Whalen, Sergio Uzzau, Chris Jones, David Schlessinger, Gonçalo R. Abecasis, Serena Sanna, Carlo Sidore, Francesco Cucca

    Хэвлэсэн 2013
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    Artigo
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  3. 3
    Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

    Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers -н Carlo Sidore, Fabio Busonero, Andrea Maschio, Eleonora Porcu, Silvia Naitza, Magdalena Żołędziewska, Antonella Mulas, Giorgio Pistis, Maristella Steri, Fabrice Danjou, Alan Kwong, Diego Ortega‐Del Vecchyo, Charleston W. K. Chiang, Jennifer L. Bragg‐Gresham, Maristella Pitzalis, Ramaiah Nagaraja, Brendan Tarrier, Christine Brennan, Sergio Uzzau, Christian Fuchsberger, Rossano Atzeni, Frédéric Reinier, Riccardo Berutti, Jie Huang, Nicholas J. Timpson, Daniela Toniolo, Paolo Gasparini, Giovanni Malerba, George Dedoussis, Eleftheria Zeggini, Nicole Soranzo, Chris Jones, Robert Lyons, Andrea Angius, Hyun Min Kang, John Novembre, Serena Sanna, David Schlessinger, Francesco Cucca, Gonçalo R. Abecasis

    Хэвлэсэн 2015
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    Artigo
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  4. 4
    The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

    The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities -н Jessica X. Chong, Kati J. Buckingham, Shalini N. Jhangiani, Corinne D. Boehm, Nara Sobreira, Joshua D. Smith, Tanya M. Harrell, Margaret J. McMillin, Wojciech Wiszniewski, Tomasz Gambin, Zeynep H. Coban Akdemir, Kimberly F. Doheny, Alan F. Scott, Dimitri Avramopoulos, Aravinda Chakravarti, Julie Hoover‐Fong, Debra Mathews, P. Dane Witmer, Hua Ling, Kurt N. Hetrick, Lee Watkins, Karynne Patterson, Frédéric Reinier, Elizabeth Blue, Donna M. Muzny, Martin Kircher, Kaya Bilgüvar, Francesc López‐Giráldez, V. Reid Sutton, Holly K. Tabor, Suzanne M. Leal, Murat Günel, Shrikant Mane, Richard A. Gibbs, Eric Boerwinkle, Ada Hamosh, Jay Shendure, James R. Lupski, Richard P. Lifton, David Valle, Deborah A. Nickerson, Michael J. Bamshad

    Хэвлэсэн 2015
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    Revisão
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  5. 5
    Genetic Variants Regulating Immune Cell Levels in Health and Disease

    Genetic Variants Regulating Immune Cell Levels in Health and Disease -н Valeria Orrù, Maristella Steri, Gabriella Sole, Carlo Sidore, Francesca Virdis, Mariano Dei, Sandra Lai, Magdalena Żołędziewska, Fabio Busonero, Antonella Mulas, Matteo Floris, Wieslawa I. Mentzen, Silvana Anna Maria Urru, Stefania Olla, Michele Marongiu, Maria Grazia Piras, Monia Lobina, Andrea Maschio, Maristella Pitzalis, Maria Francesca Urru, Marco Marcelli, Roberto Cusano, Francesca Deidda, Valentina Serra, Manuela Oppo, Rosella Pilu, Frédéric Reinier, Riccardo Berutti, Luca Pireddu, Ilenia Zara, Eleonora Porcu, Alan Kwong, Christine Brennan, Brendan Tarrier, Robert Lyons, Hyun Min Kang, Sergio Uzzau, Rossano Atzeni, Maria Consuelo Valentini, Davide Firinu, Lidia Leoni, Gianluca Rotta, Silvia Naitza, Andrea Angius, Mauro Congia, Michael B. Whalen, Chris M. Jones, David Schlessinger, Gonçalo R. Abecasis, Edoardo Fiorillo, Serena Sanna, Francesco Cucca

    Хэвлэсэн 2013
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    Artigo
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  6. 6
    Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3

    Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3 -н Jessica X. Chong, Lindsay C. Burrage, Anita Beck, Colby T. Marvin, Margaret J. McMillin, Kathryn M. Shively, Tanya M. Harrell, Kati J. Buckingham, Carlos A. Bacino, Mahim Jain, Yasemin Alanay, Susan A. Berry, John C. Carey, Richard A. Gibbs, Brendan H. Lee, Deborah Krakow, Jay Shendure, Deborah A. Nickerson, Michael J. Bamshad, Michael J. Bamshad, Jay Shendure, Deborah A. Nickerson, Gonçalo R. Abecasis, Peter Anderson, Elizabeth Blue, Marcus Annable, Brian L. Browning, Kati J. Buckingham, Christina Chen, Jennifer Chin, Jessica X. Chong, Gregory M. Cooper, Colleen Davis, Christopher Frazar, Tanya M. Harrell, Zongxiao He, Preti Jain, Gail P. Jarvik, Guillaume Jimenez, Eric Johanson, Goo Jun, Martin Kircher, Tom Kolar, Stephanie Krauter, Niklas Krumm, Suzanne M. Leal, Daniel Luksic, Colby T. Marvin, Margaret J. McMillin, Sean McGee, Patrick O’Reilly, Bryan Paeper, Karynne Patterson, M. Lázaro Pérez, Sam W. Phillips, Jessica Pijoan, Christa Poel, Frédéric Reinier, Peggy D. Robertson, Regie Lyn P. Santos‐Cortez, Tristan Shaffer, Cindy Shephard, Kathryn M. Shively, Deborah L. Siegel, Joshua D. Smith, Jeffrey Staples, Holly K. Tabor, Monica Tackett, Jason G. Underwood, Marc Wegener, Gao Wang, Marsha M. Wheeler, Yi Qian

    Хэвлэсэн 2015
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    Artigo
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  7. 7
    De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay

    De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay -н Jessica X. Chong, Margaret J. McMillin, Kathryn M. Shively, Anita Beck, Colby T. Marvin, Jose R. Armenteros, Kati J. Buckingham, Naomi T. Nkinsi, Evan A. Boyle, Margaret N. Berry, Maureen Bocian, Nicola Foulds, Maria Luisa Giovannucci Uzielli, Chad R. Haldeman‐Englert, Raoul C.M. Hennekam, Paige Kaplan, Antonie D. Kline, Catherine L. Mercer, Małgorzata J.M. Nowaczyk, Jolien S. Klein Wassink‐Ruiter, Elizabeth W. McPherson, Regina A. Moreno, Angela E. Scheuerle, Vandana Shashi, Cathy A. Stevens, John C. Carey, Arnaud Monteil, Philippe Lory, Holly K. Tabor, Joshua D. Smith, Jay Shendure, Deborah A. Nickerson, Michael J. Bamshad, Michael J. Bamshad, Jay Shendure, Deborah A. Nickerson, Gonçalo R. Abecasis, Peter Anderson, Elizabeth Blue, Marcus Annable, Brian L. Browning, Kati J. Buckingham, Christina Chen, Jennifer Chin, Jessica X. Chong, Gregory M. Cooper, Colleen Davis, Christopher Frazar, Tanya M. Harrell, Zongxiao He, Preti Jain, Gail P. Jarvik, Guillaume Jimenez, Eric Johanson, Goo Jun, Martin Kircher, Tom Kolar, Stephanie Krauter, Niklas Krumm, Suzanne M. Leal, Daniel Luksic, Colby T. Marvin, Margaret J. McMillin, Sean McGee, Patrick O’Reilly, Bryan Paeper, Karynne Patterson, M. Lázaro Pérez, Sam W. Phillips, Jessica Pijoan, Christa Poel, Frédéric Reinier, Peggy D. Robertson, Regie Lyn P. Santos‐Cortez, Tristan Shaffer, Cindy Shephard, Kathryn M. Shively, Deborah L. Siegel, Joshua D. Smith, Jeffrey Staples, Holly K. Tabor, Monica Tackett, Jason G. Underwood, Marc Wegener, Gao Wang, Marsha M. Wheeler, Yi Qian

    Хэвлэсэн 2015
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    Artigo
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