Ngā hua rapu - Dimitri Avramopoulos
- E whakaatu ana i te 1 - 12 hua o te 12
-
1
-
2
The DPYSL2 gene connects mTOR and schizophrenia mā Phạm Xuân Thắng, Guang Song, Shuxuan Lao, Loyal A. Goff, Hua Zhu, David Valle, Dimitri Avramopoulos
I whakaputaina 2016Artigo -
3
Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics mā Julie A. Jurgens, Hua Ling, Kurt N. Hetrick, Elizabeth Pugh, François Schiettecatte, Kimberly F. Doheny, Ada Hamosh, Dimitri Avramopoulos, David Valle, Nara Sobreira
I whakaputaina 2015Artigo -
4
Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia mā 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
I whakaputaina 2011Artigo -
5
Molecular imaging of the association between serotonin degeneration and beta-amyloid deposition in mild cognitive impairment mā 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
I whakaputaina 2023Artigo -
6
Escitalopram for agitation in Alzheimer's disease (S‐CitAD): Methods and design of an investigator‐initiated, randomized, controlled, multicenter clinical trial mā 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
I whakaputaina 2019Artigo -
7
Recurrent 10q22-q23 Deletions: A Genomic Disorder on 10q Associated with Cognitive and Behavioral Abnormalities mā 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
I whakaputaina 2007Artigo -
8
Sertraline for the Treatment of Depression in Alzheimer Disease: Genetic Influences mā 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
I whakaputaina 2011Text -
9
Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes mā 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
I whakaputaina 2014Artigo -
10
Insights into genetics, human biology and disease gleaned from family based genomic studies mā 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
I whakaputaina 2019Revisão -
11
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities mā 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
I whakaputaina 2015Revisão -
12
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium mā 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
I whakaputaina 2017Revisão
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Gene
Medicine
Psychology
Computational biology
Genome
Psychiatry
Disease
Exome sequencing
Mendelian inheritance
Mutation
Neuroscience
Pathology
Phenotype
Alzheimer's disease
Copy-number variation
Endocrinology
Exome
Genomics
Genotype
Internal medicine
Locus (genetics)
Missense mutation
Penetrance
Proband
Single-nucleotide polymorphism
Alternative medicine
Amyloid (mycology)
Antidepressant