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1
Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder
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Artigo
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Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

Tammimies, Kristiina ; Marshall, Christian R ; Walker, Susan ; Kaur, Gaganjot ; Thiruvahindrapuram, Bhooma ; Lionel, Anath C ; Yuen, Ryan K. C ; Uddin, Mohammed ; Roberts, Wendy ; Weksberg, Rosanna ; Woodbury-Smith, Marc ; Zwaigenbaum, Lonnie ; Anagnostou, Evdokia ; Wang, Zhuozhi ; Wei, John ; Howe, Jennifer L ; Gazzellone, Matthew J ; Lau, Lynette ; Sung, Wilson W. L ; Whitten, Kathy ; Vardy, Cathy ; Crosbie, Victoria ; Tsang, Brian ; D’Abate, Lia ; Tong, Winnie W. L ; Luscombe, Sandra ; Doyle, Tyna ; Carter, Melissa T ; Szatmari, Peter ; Stuckless, Susan ; Merico, Daniele ; Stavropoulos, Dimitri J ; Scherer, Stephen W ; Fernandez, Bridget A

JAMA : the journal of the American Medical Association, 2015-09, Vol.314 (9), p.895-903 [Periódico revisado por pares]

United States: American Medical Association

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2
Pharmacogenetic profiling via genome sequencing in children with medical complexity
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Pharmacogenetic profiling via genome sequencing in children with medical complexity

Pan, Amy ; Scodellaro, Sierra ; Khan, Tayyaba ; Ushcatz, Inna ; Wu, Wendy ; Curtis, Meredith ; Cohen, Eyal ; Cohn, Ronald D ; Hayeems, Robin Z ; Meyn, M Stephen ; Orkin, Julia ; Otal, Jaskiran ; Reuter, Miriam S ; Walker, Susan ; Scherer, Stephen W ; Marshall, Christian R ; Cohn, Iris ; Costain, Gregory

Pediatric research, 2023-03, Vol.93 (4), p.905-910 [Periódico revisado por pares]

United States: Nature Publishing Group

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3
Serum levels of endotrophin are associated with nonalcoholic steatohepatitis
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Artigo
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Serum levels of endotrophin are associated with nonalcoholic steatohepatitis

Hagström, Hannes ; Bu, Dawei ; Nasr, Patrik ; Ekstedt, Mattias ; Hegmar, Hannes ; Kechagias, Stergios ; Zhang, Ningyan ; An, Zhiqiang ; Stål, Per ; Scherer, Philipp E.

Scandinavian journal of gastroenterology, 2021-04, Vol.56 (4), p.437-442 [Periódico revisado por pares]

England: Taylor & Francis

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4
Sizing Up a Superstorm: Exploring the Role of Recalled Experience and Attribution of Responsibility in Judgments of Future Hurricane Risk
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Sizing Up a Superstorm: Exploring the Role of Recalled Experience and Attribution of Responsibility in Judgments of Future Hurricane Risk

Rickard, Laura N. ; Yang, Z. Janet ; Schuldt, Jonathon P. ; Eosco, Gina M. ; Scherer, Clifford W. ; Daziano, Ricardo A.

Risk analysis, 2017-12, Vol.37 (12), p.2334-2349 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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5
Climatic controls of decomposition drive the global biogeography of forest-tree symbioses
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Artigo
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Climatic controls of decomposition drive the global biogeography of forest-tree symbioses

Steidinger, B S ; Crowther, T W ; Liang, J ; Van Nuland, M E ; Werner, G D A ; Reich, P B ; Nabuurs, G J ; de-Miguel, S ; Zhou, M ; Picard, N ; Herault, B ; Zhao, X ; Zhang, C ; Routh, D ; Peay, K G

Nature (London), 2019-05, Vol.569 (7756), p.404-408 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Characterization of Caveolin-Rich Membrane Domains Isolated from an Endothelial-Rich Source: Implications for Human Disease
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Characterization of Caveolin-Rich Membrane Domains Isolated from an Endothelial-Rich Source: Implications for Human Disease

Lisanti, Michael P. ; Scherer, Philipp E. ; Vidugiriene, Jolanta ; Tang, ZhaoLan ; Hermanowski-Vosatka, Anne ; Tu, Ya-Huei ; Cook, Richard F. ; Sargiacomo, Massimo

The Journal of cell biology, 1994-07, Vol.126 (1), p.111-126 [Periódico revisado por pares]

New York, NY: Rockefeller University Press

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7
Novel CYP2A6 diplotypes identified through next-generation sequencing are associated with in-vitro and in-vivo nicotine metabolism
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Artigo
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Novel CYP2A6 diplotypes identified through next-generation sequencing are associated with in-vitro and in-vivo nicotine metabolism

Tanner, Julie-Anne ; Zhu, Andy Z ; Claw, Katrina G ; Prasad, Bhagwat ; Korchina, Viktoriya ; Hu, Jianhong ; Doddapaneni, HarshaVardhan ; Muzny, Donna M ; Schuetz, Erin G ; Lerman, Caryn ; Thummel, Kenneth E ; Scherer, Steven E ; Tyndale, Rachel F

Pharmacogenetics and genomics, 2018-01, Vol.28 (1), p.7-16 [Periódico revisado por pares]

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

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8
Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder
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Artigo
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Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder

Liu, Yi ; Zhang, Yanqing ; Zhao, Dongmei ; Dong, Rui ; Yang, Xiaomeng ; Tammimies, Kristiina ; Uddin, Mohammed ; Scherer, Stephen W. ; Gai, Zhongtao

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2015-06, Vol.168B (4), p.258-264 [Periódico revisado por pares]

United States: Blackwell Publishing Ltd

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9
European Guidelines on cardiovascular disease prevention in clinical practice (version 2012): the Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts)
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European Guidelines on cardiovascular disease prevention in clinical practice (version 2012): the Fifth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of nine societies and by invited experts)

Perk, Joep ; De Backer, Guy ; Gohlke, Helmut ; Graham, Ian ; Reiner, Zeljko ; Verschuren, Monique ; Albus, Christian ; Benlian, Pascale ; Boysen, Gudrun ; Cifkova, Renata ; Deaton, Christi ; Ebrahim, Shah ; Fisher, Miles ; Germano, Giuseppe ; Hobbs, Richard ; Hoes, Arno ; Karadeniz, Sehnaz ; Mezzani, Alessandro ; Prescott, Eva ; Ryden, Lars ; Scherer, Martin ; Syvänne, Mikko ; Scholte Op Reimer, Wilma ; Vrints, Christiaan ; Wood, David ; Zamorano, Jose Louis ; Zennad, Faiez

European journal of preventive cardiology, 2012, Vol.19 (4), p.585-667 [Periódico revisado por pares]

England: SAGE Publications Ltd

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10
Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challenges
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Genome sequencing for detection of pathogenic deep intronic variation: A clinical case report illustrating opportunities and challenges

Walker, Susan ; Lamoureux, Sylvia ; Khan, Tayyaba ; Joynt, Alyssa C. M. ; Bradley, Melissa ; Branson, Helen M. ; Carter, Melissa T. ; Hayeems, Robin Z. ; Jagiello, Lukasz ; Marshall, Christian R. ; Meyn, M. Stephen ; Miller, Steven P. ; Wilson, Diane ; Scherer, Stephen W. ; Blaser, Susan ; Mireskandari, Kamiar ; Costain, Gregory

American journal of medical genetics. Part A, 2021-10, Vol.185 (10), p.3129-3135 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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