תוצאות חיפוש - Marcus Naymik
- Showing 1 - 9 results of 9
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Maternal choline supplementation ameliorates Alzheimer’s disease pathology by reducing brain homocysteine levels across multiple generations מאת Ramón Velázquez, Eric Ferreira, Wendy Winslow, Nikhil Dave, Ignazio S. Piras, Marcus Naymik, Matthew J. Huentelman, An Tran, Antonella Caccamo, Salvatore Oddo
יצא לאור 2019Artigo -
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DNA Methylation and Expression Profiles of Whole Blood in Parkinson’s Disease מאת 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
יצא לאור 2021Artigo -
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Phenome-wide association of APOE alleles in the All of Us Research Program מאת 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
יצא לאור 2025Artigo -
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Family history of Alzheimer’s disease alters cognition and is modified by medical and genetic factors מאת 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
יצא לאור 2019Artigo -
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Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases מאת 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
יצא לאור 2021Artigo -
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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation מאת 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
יצא לאור 2019Artigo -
8
Resistance to autosomal dominant Alzheimer’s disease in an APOE3 Christchurch homozygote: a case report מאת 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
יצא לאור 2019Artigo -
9
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish מאת 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
יצא לאור 2019Artigo
כלי חיפוש:
נושאים קשורים
Biology
Genetics
Medicine
Gene
Disease
Dementia
Internal medicine
Alzheimer's disease
Mutation
Pathology
Allele
Apolipoprotein E
Endocrinology
Gene expression
Neurodegeneration
Phenotype
Amino acid
Amyloid (mycology)
Artificial intelligence
Biochemistry
Bioinformatics
Candidate gene
Choline
Cognition
Cognitive aging
Cognitive decline
Complementation
Computational biology
Computer science
Context (archaeology)