检索结果 - Marcus Naymik

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  1. 1
    Maternal choline supplementation ameliorates Alzheimer’s disease pathology by reducing brain homocysteine levels across multiple generations

    Maternal choline supplementation ameliorates Alzheimer’s disease pathology by reducing brain homocysteine levels across multiple generations 由 Ramón Velázquez, Eric Ferreira, Wendy Winslow, Nikhil Dave, Ignazio S. Piras, Marcus Naymik, Matthew J. Huentelman, An Tran, Antonella Caccamo, Salvatore Oddo

    出版 2019
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  2. 2
    Transcriptome response of human skeletal muscle to divergent exercise stimuli

    Transcriptome response of human skeletal muscle to divergent exercise stimuli 由 Jared M. Dickinson, Andrew C. D’Lugos, Marcus Naymik, Ashley L. Siniard, Amanda J. Wolfe, Donald R. Curtis, Matthew J. Huentelman, Chad C. Carroll

    出版 2018
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  3. 3
    DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease

    DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease 由 Adrienne Henderson, Qi Wang, Bessie Meechoovet, Ashley L. Siniard, Marcus Naymik, Matthew De Both, Matthew J. Huentelman, Richard J. Caselli, Erika Driver‐Dunckley, Travis Dunckley

    出版 2021
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  4. 4
    Phenome-wide association of APOE alleles in the All of Us Research Program

    Phenome-wide association of APOE alleles in the All of Us Research Program 由 Ehsan Khajouei, Valentina Ghisays, Ignazio S. Piras, Kiana L. Martinez, A. Vicenti, Marcus Naymik, Preston Ngo, Tam C. Tran, Joshua C. Denny, Travis J. Wheeler, Matthew J. Huentelman, Eric M. Reiman, Jason H. Karnes

    出版 2025
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  5. 5
    Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors

    Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors 由 Joshua S. Talboom, Asta K. Håberg, Matthew De Both, Marcus Naymik, Isabelle Schrauwen, Candace R. Lewis, Stacy F Bertinelli, Callie Hammersland, Mason A Fritz, Amanda Myers, Meredith Hay, Carol A. Barnes, Elizabeth L. Glisky, Lee Ryan, Matthew J. Huentelman

    出版 2019
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  6. 6
    Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

    Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases 由 Francisco M. De La Vega, Shimul Chowdhury, Barry Moore, Erwin Frise, Jeanette McCarthy, Edgar J. Hernández, Terence C. Wong, Kiely N. James, Lucia Guidugli, Pankaj B. Agrawal, Casie A. Genetti, Catherine A. Brownstein, Alan H. Beggs, Britt-Sabina Löscher, André Franke, Braden Boone, Shawn Levy, Katrin Õunap, Sander Pajusalu, Matt Huentelman, Keri Ramsey, Marcus Naymik, Vinodh Narayanan, Narayanan Veeraraghavan, Paul R. Billings, Martin G. Reese, Mark Yandell, Stephen F. Kingsmore

    出版 2021
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  7. 7
    Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

    Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation 由 Chris Balak, Marianne Bénard, Élise Schaefer, Sumaiya Iqbal, Keri Ramsey, Michèle Ernoult‐Lange, Francesca Mattioli, Lorida Llaci, Véronique Geoffroy, Maïté Courel, Marcus Naymik, Kristine Bachman, Rolph Pfundt, Patrick Rump, Johanna ter Beest, Ingrid M. Wentzensen, Kristin G. Monaghan, Kirsty McWalter, Ryan Richholt, Antony Le Béchec, Wayne M. Jepsen, Matt De Both, Newell Belnap, Anne Boland, Ignazio S. Piras, Jean‐François Deleuze, Szabolcs Szelinger, Hélène Dollfus, Jamel Chelly, Jean Muller, Arthur J. Campbell, Dennis Lal, Sampathkumar Rangasamy, Jean‐Louis Mandel, Vinodh Narayanan, Matt Huentelman, Dominique Weil, Amélie Piton

    出版 2019
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  8. 8
    Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report

    Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report 由 Joseph F. Arboleda‐Velásquez, Francisco Lopera, Michael O’Hare, Santiago Delgado‐Tirado, Claudia Mariño, Natalia Chmielewska, Kahira L. Saez‐Torres, Dhanesh Amarnani, Aaron P. Schultz, Reisa A. Sperling, David Leyton-Cifuentes, Kewei Chen, Ana Baena, David Aguillón, Silvia Ríos‐Romenets, Margarita Giraldo, Edmarie Guzmán‐Vélez, Daniel Norton, Enmanuelle Pardilla‐Delgado, Arabiye Artola, Justin S. Sanchez, Juliana Acosta‐Uribe, Matthew A. Lalli, Kenneth S. Kosik, Matthew J. Huentelman, Henrik Zetterberg, Kaj Blennow, Rebecca Reiman, Ji Luo, Yinghua Chen, Pradeep Thiyyagura, Yi Su, Gyungah Jun, Marcus Naymik, Xiaowu Gai, Moiz Bootwalla, Jianling Ji, Li Shen, John B. Miller, Leo A. Kim, Pierre N. Tariot, Keith A. Johnson, Eric M. Reiman, Yakeel T. Quiroz

    出版 2019
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  9. 9
    Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish

    Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish 由 Aleksandra Siekierska, Hannah Stamberger, Tine Deconinck, Stephanie N. Oprescu, Michèle Partoens, Yifan Zhang, Jo Sourbron, Elias Adriaenssens, Patrick Mullen, Patrick Wiencek, Katia Hardies, Jeong-Soo Lee, Hoi-Khoanh Giong, Felix Distelmaier, Orly Elpeleg, Katherine L. Helbig, Joseph H. Hersh, Sedat Işıkay, Elizabeth Jordan, Ender Karaca, Angéla Kecskés, James R. Lupski, Réka Kovács-Nagy, Patrick May, Vinodh Narayanan, Manuela Pendziwiat, Keri Ramsey, Sampathkumar Rangasamy, Deepali N. Shinde, Ronen Spiegel, Vincent Timmerman, Sarah von Spiczak, Ingo Helbig, Chris Balak, Newell Belnap, Ana M. Claasen, Amanda Courtright, Matt De Both, Matthew J. Huentelman, Marcus Naymik, Ryan Richholt, Ashley L. Siniard, Szabolcs Szelinger, David W. Craig, Isabelle Schrauwen, Zaid Afawi, Rudi Balling, Stéphanie Baulac, Nina Barišić, Hande Çağlayan, Dana Craiu, Rosa Guerrero-López, Renzo Guerrini, Helle Hjalgrim, Johanna Jähn, Karl Martin Klein, Eric LeGuern, Johannes R. Lemke, Holger Lerche, Carla Marini, Rikke S. Møller, Hiltrud Muhle, Felix Rosenow, José M. Serratosa, Arvid Suls, Ulrich Stephani, Katalin Štěrbová, Pasquale Striano, Federico Zara, Sarah Weckhuysen, Christopher Francklyn, Anthony Antonellis, Peter de Witte, Peter De Jonghe

    出版 2019
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