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The Atlantic salmon genome provides insights into rediploidization
The Atlantic salmon genome provides insights into rediploidization
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The Atlantic salmon genome provides insights into rediploidization

Lien, Sigbjørn ; Koop, Ben F ; Sandve, Simen R ; Miller, Jason R ; Kent, Matthew P ; Nome, Torfinn ; Hvidsten, Torgeir R ; Leong, Jong S ; Minkley, David R ; Zimin, Aleksey ; Grammes, Fabian ; Grove, Harald ; Gjuvsland, Arne ; Walenz, Brian ; Hermansen, Russell A ; von Schalburg, Kris ; Rondeau, Eric B ; Di Genova, Alex ; Samy, Jeevan K A ; Olav Vik, Jon ; Vigeland, Magnus D ; Caler, Lis ; Grimholt, Unni ; Jentoft, Sissel ; Våge, Dag Inge ; de Jong, Pieter ; Moen, Thomas ; Baranski, Matthew ; Palti, Yniv ; Smith, Douglas R ; Yorke, James A ; Nederbragt, Alexander J ; Tooming-Klunderud, Ave ; Jakobsen, Kjetill S ; Jiang, Xuanting ; Fan, Dingding ; Hu, Yan ; Liberles, David A ; Vidal, Rodrigo ; Iturra, Patricia ; Jones, Steven J M ; Jonassen, Inge ; Maass, Alejandro ; Omholt, Stig W ; Davidson, William S

Nature (London), 2016-05, Vol.533 (7602), p.200-205 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview
Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview
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Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview

Knoester, Marjolein ; Helfferich, Jelte ; Poelman, Randy ; Van Leer-Buter, Coretta ; Brouwer, Oebele F ; Niesters, Hubert G M

The Pediatric infectious disease journal, 2019-01, Vol.38 (1), p.16-21 [Periódico revisado por pares]

United States: Copyright Wolters Kluwer Health, Inc. All rights reserved

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3
Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes
Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes
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Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes

Fan, Chun Chieh ; Schork, Andrew J ; Brown, Timothy T ; Spencer, Barbara E ; Akshoomoff, Natacha ; Chen, Chi-Hua ; Kuperman, Joshua M ; Hagler, Jr, Donald J ; Steen, Vidar M ; Le Hellard, Stephanie ; Håberg, Asta Kristine ; Espeseth, Thomas ; Andreassen, Ole A ; Dale, Anders M ; Jernigan, Terry L ; Halgren, Eric

Translational psychiatry, 2018-06, Vol.8 (1), p.114-8, Article 114 [Periódico revisado por pares]

United States: Nature Publishing Group

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4
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
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Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

Pardiñas, Antonio F ; Smart, Sophie E ; Willcocks, Isabella R ; Holmans, Peter A ; Dennison, Charlotte A ; Lynham, Amy J ; Legge, Sophie E ; Baune, Bernhard T ; Bigdeli, Tim B ; Cairns, Murray J ; Corvin, Aiden ; Fanous, Ayman H ; Frank, Josef ; Kelly, Brian ; McQuillin, Andrew ; Melle, Ingrid ; Mortensen, Preben B ; Mowry, Bryan J ; Pato, Carlos N ; Periyasamy, Sathish ; Rietschel, Marcella ; Rujescu, Dan ; Simonsen, Carmen ; St Clair, David ; Tooney, Paul ; Wu, Jing Qin ; Andreassen, Ole A ; Kowalec, Kaarina ; Sullivan, Patrick F ; Murray, Robin M ; Owen, Michael J ; MacCabe, James H ; O’Donovan, Michael C ; Walters, James T. R ; Ajnakina, Olesya ; Alameda, Luis ; Barnes, Thomas R. E ; Berardi, Domenico ; Bonora, Elena ; Camporesi, Sara ; Cleusix, Martine ; Conus, Philippe ; Crespo-Facorro, Benedicto ; D’Andrea, Giuseppe ; Demjaha, Arsime ; Do, Kim Q ; Doody, Gillian A ; Eap, Chin B ; Ferchiou, Aziz ; Di Forti, Marta ; Guidi, Lorenzo ; Homman, Lina ; Jenni, Raoul ; Joyce, Eileen M ; Kassoumeri, Laura ; Khadimallah, Inès ; Lastrina, Ornella ; Muratori, Roberto ; Noyan, Handan ; O’Neill, Francis A ; Pignon, Baptiste ; Restellini, Romeo ; Richard, Jean-Romain ; Schürhoff, Franck ; Španiel, Filip ; Szöke, Andrei ; Tarricone, Ilaria ; Tortelli, Andrea ; Üçok, Alp ; Vázquez-Bourgon, Javier

JAMA psychiatry (Chicago, Ill.), 2022-03, Vol.79 (3), p.260-269 [Periódico revisado por pares]

United States: American Medical Association

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5
Patterns of pharmacotherapy for bipolar disorder: A GBC survey
Patterns of pharmacotherapy for bipolar disorder: A GBC survey
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Patterns of pharmacotherapy for bipolar disorder: A GBC survey

Singh, Balwinder ; Yocum, Anastasia K. ; Strawbridge, Rebecca ; Burdick, Katherine E. ; Millett, Caitlin E. ; Peters, Amy T. ; Sperry, Sarah H. ; Fico, Giovanna ; Vieta, Eduard ; Verdolini, Norma ; Godin, Ophelia ; Leboyer, Marion ; Etain, Bruno ; Tso, Ivy F. ; Coombes, Brandon J. ; McInnis, Melvin G. ; Nierenberg, Andrew A. ; Young, Allan H. ; Ashton, Melanie M. ; Berk, Michael ; Williams, Lana J. ; Keramatian, Kamyar ; Yatham, Lakshmi N. ; Overs, Bronwyn J. ; Fullerton, Janice M. ; Roberts, Gloria ; Mitchell, Philip B. ; Andreassen, Ole A. ; Andreazza, Ana C. ; Zandi, Peter P. ; Pham, Daniel ; Biernacka, Joanna M. ; Frye, Mark A. ; Aubin, Valérie ; Belzeaux, Raoul ; Dubertret, Caroline ; Gard, Sebastien ; Haffen, Emmanuel ; Olie, Emilie ; Passerieux, Christine ; Polosan, Mircea ; Schwan, Raymund ; Samalin, Ludovic

Bipolar disorders, 2024-02, Vol.26 (1), p.22-32 [Periódico revisado por pares]

Denmark: Wiley Subscription Services, Inc

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6
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease
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Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease

Luo, Jiao ; Thomassen, Jesper Qvist ; Bellenguez, Céline ; Grenier-Boley, Benjamin ; de Rojas, Itziar ; Castillo, Atahualpa ; Parveen, Kayenat ; Küçükali, Fahri ; Nicolas, Aude ; Peters, Oliver ; Schneider, Anja ; Dichgans, Martin ; Rujescu, Dan ; Scherbaum, Norbert ; Jürgen, Deckert ; Riedel-Heller, Steffi ; Hausner, Lucrezia ; Porcel, Laura Molina ; Düzel, Emrah ; Grimmer, Timo ; Wiltfang, Jens ; Heilmann-Heimbach, Stefanie ; Moebus, Susanne ; Tegos, Thomas ; Scarmeas, Nikolaos ; Clarimon, Jordi ; Moreno, Fermin ; Pérez-Tur, Jordi ; Bullido, María J ; Pastor, Pau ; Sánchez-Valle, Raquel ; Álvarez, Victoria ; Boada, Mercè ; García-González, Pablo ; Puerta, Raquel ; Mir, Pablo ; Real, Luis M ; Piñol-Ripoll, Gerard ; García-Alberca, Jose María ; Royo, Jose Luís ; Rodriguez-Rodriguez, Eloy ; Soininen, Hilkka ; Kuulasmaa, Teemu ; de Mendonça, Alexandre ; Mehrabian, Shima ; Hort, Jakub ; Vyhnalek, Martin ; van der Lee, Sven ; Graff, Caroline ; Papenberg, Goran ; Giedraitis, Vilmantas ; Boland, Anne ; Bacq-Daian, Delphine ; Deleuze, Jean-François ; Nicolas, Gael ; Dufouil, Carole ; Pasquier, Florence ; Hanon, Olivier ; Debette, Stéphanie ; Grünblatt, Edna ; Popp, Julius ; Benussi, Luisa ; Galimberti, Daniela ; Arosio, Beatrice ; Mecocci, Patrizia ; Solfrizzi, Vincenzo ; Parnetti, Lucilla ; Squassina, Alessio ; Tremolizzo, Lucio ; Borroni, Barbara ; Nacmias, Benedetta ; Sorbi, Sandro ; Caffarra, Paolo ; Seripa, Davide ; Rainero, Innocenzo ; Daniele, Antonio ; Masullo, Carlo ; Spalletta, Gianfranco ; Williams, Julie ; Amouyel, Philippe ; Jessen, Frank ; Kehoe, Patrick ; Tsolaki, Magda ; Rossi, Giacomina ; Sánchez-Juan, Pascual ; Sleegers, Kristel ; Ingelsson, Martin ; Andreassen, Ole A ; Hiltunen, Mikko ; Van Duijn, Cornelia ; Sims, Rebecca ; van der Flier, Wiesje ; Ruiz, Agustín ; Ramirez, Alfredo ; Lambert, Jean-Charles ; Frikke-Schmidt, Ruth

JAMA network open, 2023-05, Vol.6 (5), p.e2313734 [Periódico revisado por pares]

United States: American Medical Association

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7
Age at first birth in women is genetically associated with increased risk of schizophrenia
Age at first birth in women is genetically associated with increased risk of schizophrenia
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Age at first birth in women is genetically associated with increased risk of schizophrenia

Ni, Guiyan ; Gratten, Jacob ; Wray, Naomi R ; Lee, Sang Hong

Scientific reports, 2018-07, Vol.8 (1), p.10168-14, Article 10168 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)
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Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1)

Bellini, Angela ; Pötschger, Ulrike ; Bernard, Virginie ; Lapouble, Eve ; Baulande, Sylvain ; Ambros, Peter F ; Auger, Nathalie ; Beiske, Klaus ; Bernkopf, Marie ; Betts, David R ; Bhalshankar, Jaydutt ; Bown, Nick ; de Preter, Katleen ; Clément, Nathalie ; Combaret, Valérie ; Font de Mora, Jaime ; George, Sally L ; Jiménez, Irene ; Jeison, Marta ; Marques, Barbara ; Martinsson, Tommy ; Mazzocco, Katia ; Morini, Martina ; Mühlethaler-Mottet, Annick ; Noguera, Rosa ; Pierron, Gaelle ; Rossing, Maria ; Taschner-Mandl, Sabine ; Van Roy, Nadine ; Vicha, Ales ; Chesler, Louis ; Balwierz, Walentyna ; Castel, Victoria ; Elliott, Martin ; Kogner, Per ; Laureys, Geneviève ; Luksch, Roberto ; Malis, Josef ; Popovic-Beck, Maja ; Ash, Shifra ; Delattre, Olivier ; Valteau-Couanet, Dominique ; Tweddle, Deborah A ; Ladenstein, Ruth ; Schleiermacher, Gudrun

Journal of clinical oncology, 2021-10, Vol.39 (30), p.3377-3390 [Periódico revisado por pares]

United States: American Society of Clinical Oncology

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9
Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System
Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System
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Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System

Goode, Elizabeth C. ; Clark, Allan B. ; Mells, George F. ; Srivastava, Brijesh ; Spiess, Kelly ; Gelson, William T.H. ; Trivedi, Palak J. ; Lynch, Kate D. ; Castren, Edit ; Vesterhus, Mette N. ; Karlsen, Tom H. ; Ji, Sun‐Gou ; Anderson, Carl A. ; Thorburn, Douglas ; Hudson, Mark ; Heneghan, Michael A. ; Aldersley, Mark A. ; Bathgate, Andrew ; Sandford, Richard N. ; Alexander, Graeme J. ; Chapman, Roger W. ; Walmsley, Martine ; Hirschfield, Gideon M. ; Rushbrook, Simon M.

Hepatology (Baltimore, Md.), 2019-05, Vol.69 (5), p.2120-2135 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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10
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Dominguez-Valentin, Mev ; Sampson, Julian R ; Seppälä, Toni T ; ten Broeke, Sanne W ; Plazzer, John-Paul ; Nakken, Sigve ; Engel, Christoph ; Aretz, Stefan ; Jenkins, Mark A ; Sunde, Lone ; Bernstein, Inge ; Capella, Gabriel ; Balaguer, Francesc ; Thomas, Huw ; Evans, D. Gareth ; Burn, John ; Greenblatt, Marc ; Hovig, Eivind ; de Vos tot Nederveen Cappel, Wouter H ; Sijmons, Rolf H ; Bertario, Lucio ; Tibiletti, Maria Grazia ; Cavestro, Giulia Martina ; Lindblom, Annika ; Della Valle, Adriana ; López-Köstner, Francisco ; Gluck, Nathan ; Katz, Lior H ; Heinimann, Karl ; Vaccaro, Carlos A ; Büttner, Reinhard ; Görgens, Heike ; Holinski-Feder, Elke ; Morak, Monika ; Holzapfel, Stefanie ; Hüneburg, Robert ; von Knebel Doeberitz, Magnus ; Loeffler, Markus ; Rahner, Nils ; Schackert, Hans K ; Steinke-Lange, Verena ; Schmiegel, Wolff ; Vangala, Deepak ; Pylvänäinen, Kirsi ; Renkonen-Sinisalo, Laura ; Hopper, John L ; Win, Aung Ko ; Haile, Robert W ; Lindor, Noralane M ; Gallinger, Steven ; Le Marchand, Loïc ; Newcomb, Polly A ; Figueiredo, Jane C ; Thibodeau, Stephen N ; Wadt, Karin ; Therkildsen, Christina ; Okkels, Henrik ; Ketabi, Zohreh ; Moreira, Leticia ; Sánchez, Ariadna ; Serra-Burriel, Miquel ; Pineda, Marta ; Navarro, Matilde ; Blanco, Ignacio ; Green, Kate ; Lalloo, Fiona ; Crosbie, Emma J ; Hill, James ; Denton, Oliver G ; Frayling, Ian M ; Rødland, Einar Andreas ; Vasen, Hans ; Mints, Miriam ; Neffa, Florencia ; Esperon, Patricia ; Alvarez, Karin ; Kariv, Revital ; Rosner, Guy ; Pinero, Tamara Alejandra ; Gonzalez, Maria Laura ; Kalfayan, Pablo ; Tjandra, Douglas ; Winship, Ingrid M ; Macrae, Finlay ; Möslein, Gabriela ; Mecklin, Jukka-Pekka ; Nielsen, Maartje ; Møller, Pål

Genetics in medicine, 2020-01 [Periódico revisado por pares]

Lippincott Williams & Wilkins

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