Torthaí cuardaigh - Dimitri Avramopoulos

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  1. 1
    Neuroinflammation represents a common theme amongst genetic and environmental risk factors for Alzheimer and Parkinson diseases

    Neuroinflammation represents a common theme amongst genetic and environmental risk factors for Alzheimer and Parkinson diseases de réir Rachel J. Boyd, Dimitri Avramopoulos, Lauren L. Jantzie, Andrew S. McCallion

    Foilsithe / Cruthaithe 2022
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  2. 2
    The DPYSL2 gene connects mTOR and schizophrenia

    The DPYSL2 gene connects mTOR and schizophrenia de réir Phạm Xuân Thắng, Guang Song, Shuxuan Lao, Loyal A. Goff, Hua Zhu, David Valle, Dimitri Avramopoulos

    Foilsithe / Cruthaithe 2016
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  3. 3
    Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics

    Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics de réir Julie A. Jurgens, Hua Ling, Kurt N. Hetrick, Elizabeth Pugh, François Schiettecatte, Kimberly F. Doheny, Ada Hamosh, Dimitri Avramopoulos, David Valle, Nara Sobreira

    Foilsithe / Cruthaithe 2015
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  4. 4
    Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia

    Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia de réir Joseph F. Cubells, Xiangqing Sun, Wenbiao Li, Robert W. Bonsall, John A. McGrath, Dimitri Avramopoulos, Virginia K. Lasseter, Paula Wolyniec, Yi‐lang Tang, Kristina B. Mercer, Ann E. Pulver, Robert C. Elston

    Foilsithe / Cruthaithe 2011
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  5. 5
    Molecular imaging of the association between serotonin degeneration and beta-amyloid deposition in mild cognitive impairment

    Molecular imaging of the association between serotonin degeneration and beta-amyloid deposition in mild cognitive impairment de réir Gwenn S. Smith, Hillary Protas, Hiroto Kuwabara, Alena Savonenko, Najlla Nassery, Neda F Gould, Michael A. Kraut, Dimitri Avramopoulos, Daniel P. Holt, Robert F. Dannals, Ayon Nandi, Yi Su, Eric M. Reiman, Kewei Chen

    Foilsithe / Cruthaithe 2023
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  6. 6
    Escitalopram for agitation in Alzheimer's disease (S‐CitAD): Methods and design of an investigator‐initiated, randomized, controlled, multicenter clinical trial

    Escitalopram for agitation in Alzheimer's disease (S‐CitAD): Methods and design of an investigator‐initiated, randomized, controlled, multicenter clinical trial de réir Stephan Ehrhardt, Anton P. Porsteinsson, Cynthia A. Munro, Paul B. Rosenberg, Bruce G. Pollock, Davangere P. Devanand, Jacobo Mintzer, Tarek K. Rajji, Zahinoor Ismail, Lon S. Schneider, Sheriza Baksh, Lea T. Drye, Dimitri Avramopoulos, David Shade, Constantine G. Lyketsos

    Foilsithe / Cruthaithe 2019
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  7. 7
    Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities

    Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities de réir Jorune Balciuniene, Ningping Feng, Kelly Iyadurai, Betsy Hirsch, Lawrence Charnas, Brent Bill, Mathew C. Easterday, Johan Staaf, LeAnn Oseth, Desiree Czapansky-Beilman, Dimitri Avramopoulos, George H. Thomas, Åke Borg, David Valle‐García, Lisa A. Schimmenti, Scott B. Selleck

    Foilsithe / Cruthaithe 2007
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  8. 8
    Sertraline for the Treatment of Depression in Alzheimer Disease: Genetic Influences

    Sertraline for the Treatment of Depression in Alzheimer Disease: Genetic Influences de réir Peters, Matthew E., Vaidya, Vijay, Drye, Lea T., Rosenberg, Paul B., Martin, Barbara K., Porsteinsson, Anton P., Frangakis, Constantine E., Mintzer, Jacobo, Weintraub, Daniel, Schneider, Lon S., Rabins, Peter V., Munro, Cynthia A., Meinert, Curtis L., Lyketsos, Constantine G., Dimitri, Avramopoulos

    Foilsithe / Cruthaithe 2011
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  9. 9
    Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes

    Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes de réir Michel Guipponi, Federico Santoni, Vincent Setola, Corinne Gehrig, Maud Rothärmel, Macarena Cuenca, Olivier Guillin, Dimitris Dikeos, Georgios Georgantopoulos, George N. Papadimitriou, Logos Curtis, Alexandre Méary, Franck Schürhoff, Stéphane Jamain, Dimitri Avramopoulos, Marion Leboyer, Dan Rujescu, Ann E. Pulver, Dominique Campion, David P. Siderovski, Stylianos E. Antonarakis

    Foilsithe / Cruthaithe 2014
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  10. 10
    Insights into genetics, human biology and disease gleaned from family based genomic studies

    Insights into genetics, human biology and disease gleaned from family based genomic studies de réir Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, Tamar Harel, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, Steven Buyske, Davut Pehli̇van, Claudia M.B. Carvalho, Samantha Baxter, Nara Sobreira, Pengfei Liu, Nan Wu, Jill A. Rosenfeld, Sushant Kumar, Dimitri Avramopoulos, Janson J. White, Kimberly F. Doheny, P. Dane Witmer, Corinne D. Boehm, V. Reid Sutton, Donna M. Muzny, Eric Boerwinkle, Murat Günel, Deborah A. Nickerson, Shrikant Mane, Daniel G. MacArthur, Richard A. Gibbs, Ada Hamosh, Richard P. Lifton, Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski

    Foilsithe / Cruthaithe 2019
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  11. 11
    The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

    The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities de réir 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

    Foilsithe / Cruthaithe 2015
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  12. 12
    GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium

    GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium de réir Joey W. Trampush, M L Z Yang, Jin Yu, Emma Knowles, Gail Davies, David C. Liewald, John M. Starr, Srdjan Djurovic, Ingrid Melle, Kjetil Sundet, A. Christoforou, Ivar Reinvang, Pamela DeRosse, Astri J. Lundervold, Vidar M. Steen, Thomas Espeseth, Katri Räikkönen, Elisabeth Widén, Aarno Palotie, Johan G. Eriksson, Ina Giegling, Bettina Konte, Panos Roussos, Stella G. Giakoumaki, Katherine E. Burdick, Antony Payton, William Ollier, M.A. Horan, Ornit Chiba‐Falek, Deborah K. Attix, Anna C. Need, Elizabeth T. Cirulli, Aristotle N. Voineskos, Nikos C. Stefanis, Dimitri Avramopoulos, Alex Hatzimanolis, Dan E. Arking, Nikolaos Smyrnis, Robert M. Bilder, Nelson B. Freimer, Tyrone D. Cannon, Edythe London, Russell A. Poldrack, Fred W. Sabb, Eliza Congdon, Emily Drabant Conley, Matthew A. Scult, Dwight Dickinson, Richard E. Straub, Gary Donohoe, Derek W. Morris, Aiden Corvin, Michael Gill, Ahmad R. Hariri, Daniel R. Weinberger, Neil Pendleton, Panos Bitsios, Dan Rujescu, Jari Lahti, Stéphanie Le Hellard, Matthew C. Keller, Ole A. Andreassen, Ian J. Deary, David C. Glahn, Anil K. Malhotra, Todd Lencz

    Foilsithe / Cruthaithe 2017
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