Resultados de Procura por Autor :: APM

1

A Role for AMP-Activated Protein Kinase in Contraction- and Hypoxia-Regulated Glucose Transport in Skeletal Muscle por James Mu, Joseph T. Brozinick, Otto Valladares, Maja Bućan, Morris J. Birnbaum

Publicado 2001

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2

DASHR 2.0: integrated database of human small non-coding RNA genes and mature products por Pavel P. Kuksa, Alexandre Amlie‐Wolf, Živadin Katanić, Otto Valladares, Li‐San Wang, Yuk Yee Leung

Publicado 2018

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3

An Automated System for Recording and Analysis of Sleep in Mice por Sigrid C. Veasey, Otto Valladares, Polina Fenik, David Kapfhamer, Larry D. Sanford, Joel H. Benington, Maja Bućan

Publicado 2000

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4

Genome-Wide Double-Stranded RNA Sequencing Reveals the Functional Significance of Base-Paired RNAs in Arabidopsis por Qi Zheng, Paul Ryvkin, Fan Li, Isabelle Dragomir, Otto Valladares, Jamie Yang, Kajia Cao, Li‐San Wang, Brian D. Gregory

Publicado 2010

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5

HAMR: high-throughput annotation of modified ribonucleotides por Paul Ryvkin, Yuk Yee Leung, Ian M. Silverman, Micah Childress, Otto Valladares, Isabelle Dragomir, Brian D. Gregory, Li‐San Wang

Publicado 2013

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6

HIPPIE: a high-throughput identification pipeline for promoter interacting enhancer elements por Yih-Chii Hwang, Chiao‐Feng Lin, Otto Valladares, John Malamon, Pavel P. Kuksa, Qi Zheng, Brian D. Gregory, Li‐San Wang

Publicado 2014

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7

DASHR: database of small human noncoding RNAs por Yuk Yee Leung, Pavel P. Kuksa, Alexandre Amlie‐Wolf, Otto Valladares, Lyle Ungar, Sampath Kannan, Brian D. Gregory, Li‐San Wang

Publicado 2015

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8

Sleep Behaviors and Sleep Quality in Children with Autism Spectrum Disorders por Margaret C. Souders, Thorton B. A. Mason, Otto Valladares, Maja Bućan, Susan E. Levy, David S. Mandell, Terri E. Weaver, Jennifer Pinto‐Martin

Publicado 2009

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9

INFERNO: inferring the molecular mechanisms of noncoding genetic variants por Alexandre Amlie‐Wolf, Mitchell Tang, Elisabeth E. Mlynarski, Pavel P. Kuksa, Otto Valladares, Živadin Katanić, Debby W. Tsuang, Christopher D. Brown, Gerard D. Schellenberg, Li‐San Wang

Publicado 2018

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10

VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project por Yuk Yee Leung, Otto Valladares, Yi‐Fan Chou, Han‐Jen Lin, Amanda B Kuzma, Laura B. Cantwell, Liming Qu, Prabhakaran Gangadharan, William Salerno, Gerard D. Schellenberg, Li‐San Wang

Publicado 2018

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11

Reassessment of Risk Genotypes (<i>GRN</i>,<i>TMEM106B</i>, and<i>ABCC9</i>Variants) Associated With Hippocampal Sclerosis of Aging Pathology por Peter T. Nelson, Wang‐Xia Wang, Amanda Partch, Sarah E. Monsell, Otto Valladares, Sally R. Ellingson, Bernard R. Wilfred, Adam C. Naj, Li-San Wang, Walter A. Kukull, David W. Fardo

Publicado 2014

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12

Global Analysis of RNA Secondary Structure in Two Metazoans por Fan Li, Qi Zheng, Paul Ryvkin, Isabelle Dragomir, Yaanik Desai, Subhadra Aiyer, Otto Valladares, Jamie Yang, Shelly Bambina, Leah R. Sabin, John I. Murray, Todd Lamitina, Arjun Raj, Sara Cherry, Li‐San Wang, Brian D. Gregory

Publicado 2012

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13

NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge por Emily Greenfest‐Allen, Otto Valladares, Pavel P. Kuksa, Prabhakaran Gangadharan, Wan‐Ping Lee, Jeffrey Cifello, Živadin Katanić, Amanda B Kuzma, Nicholas R. Wheeler, William S. Bush, Yuk Yee Leung, Gerard D. Schellenberg, Christian J. Stoeckert, Li‐San Wang

Publicado 2023

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14

Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders por Elaine T. Lim, Soumya Raychaudhuri, Stephan Sanders, Christine Stevens, Aniko Sabo, Daniel G. MacArthur, Benjamin M. Neale, Andrew Kirby, Douglas M. Ruderfer, Menachem Fromer, Monkol Lek, Li Liu, Jason Flannick, Stephan Ripke, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Alicia Hawes, Irene Newsham, Yuanqing Wu, Lora Lewis, Huyen Dinh, Shannon Gross, Li-San Wang, Chiao‐Feng Lin, Otto Valladares, Stacey B. Gabriel, Mark A. DePristo, David Altshuler, Shaun Purcell, Matthew W. State, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Richard A. Gibbs, Gerard D. Schellenberg, James S. Sutcliffe, Bernie Devlin, Kathryn Roeder, Mark J. Daly

Publicado 2013

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15

Alzheimer's Disease Sequencing Project release 4 whole genome sequencing dataset por Yuk Yee Leung, Wan‐Ping Lee, Amanda Kuzma, Heather Nicaretta, Otto Valladares, Prabhakaran Gangadharan, Liming Qu, Yi Zhao, Youli Ren, Po‐Liang Cheng, Pavel P. Kuksa, Hui Wang, Heather White, Živadin Katanić, Lauren Bass, Naveen Saravanan, Emily Greenfest‐Allen, Maureen Kirsch, Laura B. Cantwell, Taha Iqbal, Nicholas R. Wheeler, John Farrell, Congcong Zhu, F. S. Turner, Tamil Iniyan Gunasekaran, Pedro Mena, Yumi Jin, Luke Carter, Xiaoling Zhang, Badri N. Vardarajan, Arthur W. Toga, Michael L. Cuccaro, Timothy J. Hohman, William S. Bush, Adam C. Naj, Eden R. Martin, Clifton L. Dalgard, Brian W. Kunkle, Lindsay A. Farrer, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Li‐San Wang

Publicado 2025

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16

Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ϵ4, and the Risk of Late-Onset Alzheimer Disease in African Americans por Christiane Reitz, Gyungah Jun, Adam C. Naj, Ruchita Rajbhandary, Badri N. Vardarajan, Li San Wang, Otto Valladares, Chiao‐Feng Lin, Eric B. Larson, Neill R. Graff‐Radford, Denis A. Evans, Philip L. De Jager, Paul K. Crane, Joseph D. Buxbaum, Jill R. Murrell, Towfique Raj, Nilüfer Ertekin‐Taner, Mark W. Logue, Clinton T. Baldwin, Robert C. Green, Lisa L. Barnes, Laura B. Cantwell, M. Daniele Fallin, Rodney C.P. Go, Patrick Griffith, Thomas O. Obisesan, Jennifer J. Manly, Kathryn L. Lunetta, M. Ilyas Kamboh, Oscar L. López, David A. Bennett, Hugh C. Hendrie, Kathleen Hall, Alison Goate, Goldie S. Byrd, Walter A. Kukull, Tatiana Foroud, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Richard Mayeux

Publicado 2013

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17

The role of <i>TREM2</i> R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease por Christina M. Lill, Aina Rengmark, Lasse Pihlstrøm, Isabella Fogh, Aleksey Shatunov, Patrick Sleiman, Li‐San Wang, Tian Liu, Christina Funch Lassen, Esther Meissner, Panagiotis Alexopoulos, Andrea Calvo, Adriano Chió, Nil Dizdar, Frank Faltraco, Lars Forsgren, Julia Kirchheiner, Alexander Kurz, Jan Larsen, Maria Liebsch, Jan Linder, Karen Morrison, Hans Nissbrandt, Markus Otto, Jens Pahnke, Amanda Partch, Gabriella Restagno, Dan Rujescu, Cathrin Schnack, Christopher E. Shaw, Pamela J. Shaw, Hayrettin Tumani, Ole‐Bjørn Tysnes, Otto Valladares, Vincenzo Silani, Leonard H. van den Berg, Wouter van Rheenen, Jan H. Veldink, Ulman Lindenberger, Elisabeth Steinhagen‐Thiessen, Stefan Teipel, Robert Perneczky, Hákon Hákonarson, Harald Hampel, Christine A. F. Von Arnim, Jørgen H. Olsen, Vivianna M. Van Deerlin, Ammar Al‐Chalabi, Mathias Toft, Beate Ritz, Lars Bertram

Publicado 2015

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18

Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes por Kurt Farrell, Jack Humphrey, Timothy S. Chang, Yi Zhao, Yuk Yee Leung, Pavel P. Kuksa, Vishakha Patil, Wan‐Ping Lee, Amanda B Kuzma, Otto Valladares, Laura B. Cantwell, Hui Wang, Ashvin Ravi, Claudia De Sanctis, Natalia Han, Thomas D. Christie, Robina Afzal, Shrishtee Kandoi, Kristen Whitney, Margaret M. Krassner, Hadley W. Ressler, SoongHo Kim, Diana K. Dangoor, Megan A. Iida, Alicia Casella, Ruth H. Walker, Melissa J. Nirenberg, Alan E. Renton, Bergan Babrowicz, Giovanni Coppola, Towfique Raj, Günter U. Höglinger, Ulrich Müller, Lawrence I. Golbe, Huw R. Morris, John Hardy, Tamás Révész, Thomas T. Warner, Zane Jaunmuktane, Kin Y. Mok, Rosa Rademakers, Dennis W. Dickson, Owen A. Ross, Li‐San Wang, Alison Goate, Daniela Berg, Daniel H. Geschwind, John F. Crary, Adam C. Naj

Publicado 2024

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19

ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology por Peter T. Nelson, Steven Estus, Erin L. Abner, Ishita Parikh, Manasi Malik, Janna H. Neltner, Eseosa T. Ighodaro, Wang‐Xia Wang, Bernard R. Wilfred, Li‐San Wang, Walter A. Kukull, Kannabiran Nandakumar, Mark Farman, Wayne W. Poon, María M. Corrada, Claudia H. Kawas, David H. Cribbs, David A. Bennett, Julie A. Schneider, Eric B. Larson, Paul K. Crane, Otto Valladares, Frederick A. Schmitt, Richard J. Kryscio, Gregory A. Jicha, Charles D. Smith, Stephen W. Scheff, Joshua A. Sonnen, Jonathan L. Haines, Margaret A. Pericak‐Vance, Richard Mayeux, Lindsay A. Farrer, Linda J. Van Eldik, Craig Horbinski, Robert C. Green, Marla Gearing, Leonard W. Poon, Patricia L. Kramer, Randall L. Woltjer, Thomas J. Montine, Amanda Partch, Alexander J. Rajic, KatieRose Richmire, Sarah E. Monsell, Gerard D. Schellenberg, David W. Fardo

Publicado 2014

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20

Patterns and rates of exonic de novo mutations in autism spectrum disorders por Benjamin M. Neale, Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo, Chiao‐Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L. Crawford, Nicholas G. Campbell, Evan Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly

Publicado 2012

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