Hasil Pencarian - Dan Spiegelman

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  1. 1
    Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype

    Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotype oleh Mehrdad A. Estiar, Etienne Leveille, Dan Spiegelman, Nicolas Dupre, Jean-François Trempe, Guy A. Rouleau, Ziv Gan‐Or

    Diterbitkan 2020-03-01
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  2. 2
    Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes

    Transcriptome-wide association study of attention deficit hyperactivity disorder identifies associated genes and phenotypes oleh Calwing Liao, Alexandre D. Laporte, Dan Spiegelman, Fulya Akçimen, Ridha Joober, Patrick A. Dion, Guy A. Rouleau

    Diterbitkan 2019-10-01
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  3. 3
    Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study

    Investigation of the causal relationship between ALS and autoimmune disorders: a Mendelian randomization study oleh Paria Alipour, Konstantin Senkevich, Jay P. Ross, Dan Spiegelman, Despoina Manousaki, Patrick A. Dion, Guy A. Rouleau

    Diterbitkan 2022-11-01
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  4. 4
    598 Local radiation in combination with CpG and anti-OX40 induces enhanced T cell activation and proliferation

    598 Local radiation in combination with CpG and anti-OX40 induces enhanced T cell activation and proliferation oleh Paul Sondel, Alexander Rakhmilevich, Anna Hoefges, Mildred Felder, Zachary Morris, Amy Erbe, Arika Feils, Luke Zangl, Ravi Patel, Jacquelyn Hank, Dan Spiegelman, Alexander Pieper, Sritha Moram

    Diterbitkan 2021-11-01
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  5. 5
    Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

    Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report oleh Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C. Elalaoui, Maria Mansouri, Lamia Boualla, Alexandre DIonne-Laporte, Dan Spiegelman, Patrick A. Dion, Patrick Cossette, Guy A. Rouleau, Abdelaziz Sefiani

    Diterbitkan 2018-04-01
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  6. 6
    Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report

    Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report oleh Jaber Lyahyai, Bouchra Ouled Amar Bencheikh, Siham C. Elalaoui, Maria Mansouri, Lamia Boualla, Alexandre DIonne-Laporte, Dan Spiegelman, Patrick A. Dion, Patrick Cossette, Guy A. Rouleau, Abdelaziz Sefiani

    Diterbitkan 2018-02-01
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  7. 7
    Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population.

    Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population. oleh Sirui Zhou, Lan Xiong, Pingxing Xie, Amirthagowri Ambalavanan, Cynthia V Bourassa, Alexandre Dionne-Laporte, Dan Spiegelman, Maude Turcotte Gauthier, Edouard Henrion, Ousmane Diallo, Patrick A Dion, Guy A Rouleau

    Diterbitkan 2015-01-01
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  8. 8
    Global characterization of copy number variants in epilepsy patients from whole genome sequencing.

    Global characterization of copy number variants in epilepsy patients from whole genome sequencing. oleh Jean Monlong, Simon L Girard, Caroline Meloche, Maxime Cadieux-Dion, Danielle M Andrade, Ron G Lafreniere, Micheline Gravel, Dan Spiegelman, Alexandre Dionne-Laporte, Cyrus Boelman, Fadi F Hamdan, Jacques L Michaud, Guy Rouleau, Berge A Minassian, Guillaume Bourque, Patrick Cossette

    Diterbitkan 2018-04-01
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  9. 9
    De novo mutations in moderate or severe intellectual disability.

    De novo mutations in moderate or severe intellectual disability. oleh Fadi F Hamdan, Myriam Srour, Jose-Mario Capo-Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, Christine Massicotte, Amirthagowri Ambalavanan, Dan Spiegelman, Ousmane Diallo, Edouard Henrion, Alexandre Dionne-Laporte, Anne Fougerat, Alexey V Pshezhetsky, Sunita Venkateswaran, Guy A Rouleau, Jacques L Michaud

    Diterbitkan 2014-10-01
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  10. 10
    Fine mapping of the HLA locus in Parkinson’s disease in Europeans

    Fine mapping of the HLA locus in Parkinson’s disease in Europeans oleh Eric Yu, Aditya Ambati, Maren Stolp Andersen, Lynne Krohn, Mehrdad A. Estiar, Prabhjyot Saini, Konstantin Senkevich, Yuri L. Sosero, Ashwin Ashok Kumar Sreelatha, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Mathias Toft, Marte K. Viken, Manu Sharma, Cornelis Blauwendraat, Lasse Pihlstrøm, Emmanuel Mignot, Ziv Gan-Or

    Diterbitkan 2021-09-01
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  11. 11
    Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor

    Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor oleh Calwing Liao, Calwing Liao, Faezeh Sarayloo, Faezeh Sarayloo, Veikko Vuokila, Daniel Rochefort, Fulya Akçimen, Fulya Akçimen, Simone Diamond, Gabrielle Houle, Gabrielle Houle, Alexandre D. Laporte, Dan Spiegelman, Qin He, Hélène Catoire, Patrick A. Dion, Patrick A. Dion, Guy A. Rouleau, Guy A. Rouleau, Guy A. Rouleau

    Diterbitkan 2020-07-01
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  12. 12
    A population genetic approach to mapping neurological disorder genes using deep resequencing.

    A population genetic approach to mapping neurological disorder genes using deep resequencing. oleh Rachel A Myers, Ferran Casals, Julie Gauthier, Fadi F Hamdan, Jon Keebler, Adam R Boyko, Carlos D Bustamante, Amelie M Piton, Dan Spiegelman, Edouard Henrion, Martine Zilversmit, Julie Hussin, Jacklyn Quinlan, Yan Yang, Ronald G Lafrenière, Alexander R Griffing, Eric A Stone, Guy A Rouleau, Philip Awadalla

    Diterbitkan 2011-02-01
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  13. 13
    Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases

    Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases oleh Wejdan M. Alenezi, Wejdan M. Alenezi, Wejdan M. Alenezi, Caitlin T. Fierheller, Caitlin T. Fierheller, Corinne Serruya, Timothée Revil, Timothée Revil, Kathleen K. Oros, Deepak N. Subramanian, Jeffrey Bruce, Dan Spiegelman, Dan Spiegelman, Trevor Pugh, Trevor Pugh, Trevor Pugh, Ian G. Campbell, Ian G. Campbell, Anne-Marie Mes-Masson, Anne-Marie Mes-Masson, Diane Provencher, Diane Provencher, William D. Foulkes, William D. Foulkes, William D. Foulkes, William D. Foulkes, William D. Foulkes, William D. Foulkes, Zaki El Haffaf, Zaki El Haffaf, Guy Rouleau, Guy Rouleau, Luigi Bouchard, Luigi Bouchard, Luigi Bouchard, Celia M. T. Greenwood, Celia M. T. Greenwood, Celia M. T. Greenwood, Celia M. T. Greenwood, Jiannis Ragoussis, Jiannis Ragoussis, Patricia N. Tonin, Patricia N. Tonin, Patricia N. Tonin

    Diterbitkan 2023-03-01
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  14. 14
    HLA in isolated REM sleep behavior disorder and Lewy body dementia

    HLA in isolated REM sleep behavior disorder and Lewy body dementia oleh Eric Yu, Lynne Krohn, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Zalak Shah, Ruth Chia, Isabelle Arnulf, Michele T. M. Hu, Jacques Y. Montplaisir, Jean‐François Gagnon, Alex Desautels, Yves Dauvilliers, Gian Luigi Gigli, Mariarosaria Valente, Francesco Janes, Andrea Bernardini, Birgit Högl, Ambra Stefani, Abubaker Ibrahim, Anna Heidbreder, Karel Sonka, Petr Dusek, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Elena Antelmi, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel‐Döring, Valérie Cochen De Cock, Luigi Ferini‐Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, Guy A. Rouleau, Ronald B. Postuma, The International LBD Genomics Consortium, Sonja W. Scholz, Ziv Gan‐Or

    Diterbitkan 2023-09-01
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