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Refinado por: assunto: Genetics remover
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1
Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents
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Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents

Docherty, Anna R ; Shabalin, Andrey A ; DiBlasi, Emily ; Monson, Eric ; Mullins, Niamh ; Adkins, Daniel E ; Bacanu, Silviu-Alin ; Bakian, Amanda V ; Crowell, Sheila ; Chen, Danli ; Darlington, Todd M ; Callor, William B ; Christensen, Erik D ; Gray, Douglas ; Keeshin, Brooks ; Klein, Michael ; Anderson, John S ; Jerominski, Leslie ; Hayward, Caroline ; Porteous, David J ; McIntosh, Andrew ; Li, Qingqin ; Coon, Hilary

The American journal of psychiatry, 2020-10, Vol.177 (10), p.917-927 [Periódico revisado por pares]

United States: American Psychiatric Association

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2
A meta-analysis of genome-wide association studies of epigenetic age acceleration
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A meta-analysis of genome-wide association studies of epigenetic age acceleration

Gibson, Jude ; Russ, Tom C ; Clarke, Toni-Kim ; Howard, David M ; Hillary, Robert F ; Evans, Kathryn L ; Walker, Rosie M ; Bermingham, Mairead L ; Morris, Stewart W ; Campbell, Archie ; Hayward, Caroline ; Murray, Alison D ; Porteous, David J ; Horvath, Steve ; Lu, Ake T ; McIntosh, Andrew M ; Whalley, Heather C ; Marioni, Riccardo E Greally, John M.

PLoS genetics, 2019-11, Vol.15 (11), p.e1008104-e1008104 [Periódico revisado por pares]

United States: Public Library of Science

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3
Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course
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Differential effects of the APOE e4 allele on different domains of cognitive ability across the life-course

Marioni, Riccardo E ; Campbell, Archie ; Scotland, Generation ; Hayward, Caroline ; Porteous, David J ; Deary, Ian J

European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.919-923 [Periódico revisado por pares]

England: Nature Publishing Group

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4
Complement C3 Variant and the Risk of Age-Related Macular Degeneration
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Complement C3 Variant and the Risk of Age-Related Macular Degeneration

Yates, John R.W ; Sepp, Tiina ; Matharu, Baljinder K ; Khan, Jane C ; Thurlby, Deborah A ; Shahid, Humma ; Clayton, David G ; Hayward, Caroline ; Morgan, Joanne ; Wright, Alan F ; Armbrecht, Ana Maria ; Dhillon, Baljean ; Deary, Ian J ; Redmond, Elizabeth ; Bird, Alan C ; Moore, Anthony T

The New England journal of medicine, 2007-08, Vol.357 (6), p.553-561 [Periódico revisado por pares]

Boston, MA: Massachusetts Medical Society

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5
Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation
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Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

Xia, Charley ; Amador, Carmen ; Huffman, Jennifer ; Trochet, Holly ; Campbell, Archie ; Porteous, David ; Hastie, Nicholas D ; Hayward, Caroline ; Vitart, Veronique ; Navarro, Pau ; Haley, Chris S Gibson, Greg

PLoS genetics, 2016-02, Vol.12 (2), p.e1005804-e1005804 [Periódico revisado por pares]

United States: Public Library of Science

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6
Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway
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Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway

Benedetti, Elisa ; Pučić-Baković, Maja ; Keser, Toma ; Wahl, Annika ; Hassinen, Antti ; Yang, Jeong-Yeh ; Liu, Lin ; Trbojević-Akmačić, Irena ; Razdorov, Genadij ; Štambuk, Jerko ; Klarić, Lucija ; Ugrina, Ivo ; Selman, Maurice H J ; Wuhrer, Manfred ; Rudan, Igor ; Polasek, Ozren ; Hayward, Caroline ; Grallert, Harald ; Strauch, Konstantin ; Peters, Annette ; Meitinger, Thomas ; Gieger, Christian ; Vilaj, Marija ; Boons, Geert-Jan ; Moremen, Kelley W ; Ovchinnikova, Tatiana ; Bovin, Nicolai ; Kellokumpu, Sakari ; Theis, Fabian J ; Lauc, Gordan ; Krumsiek, Jan

Nature communications, 2017-11, Vol.8 (1), p.1483-15, Article 1483 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Generation Scotland: an update on Scotland’s longitudinal family health study
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Generation Scotland: an update on Scotland’s longitudinal family health study

Milbourn, Hannah ; McCartney, Daniel ; Richmond, Anne ; Campbell, Archie ; Flaig, Robin ; Robertson, Sarah ; Fawns-Ritchie, Chloe ; Hayward, Caroline ; Marioni, Riccardo E ; McIntosh, Andrew M ; Porteous, David J ; Whalley, Heather C ; Sudlow, Cathie

BMJ open, 2024-06, Vol.14 (6), p.e084719 [Periódico revisado por pares]

London: British Medical Journal Publishing Group

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8
The genetic landscape of Scotland and the Isles
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The genetic landscape of Scotland and the Isles

Gilbert, Edmund ; O’Reilly, Seamus ; Merrigan, Michael ; McGettigan, Darren ; Vitart, Veronique ; Joshi, Peter K. ; Clark, David W. ; Campbell, Harry ; Hayward, Caroline ; Ring, Susan M. ; Golding, Jean ; Goodfellow, Stephanie ; Navarro, Pau ; Kerr, Shona M. ; Amador, Carmen ; Campbell, Archie ; Haley, Chris S. ; Porteous, David J. ; Cavalleri, Gianpiero L. ; Wilson, James F.

Proceedings of the National Academy of Sciences - PNAS, 2019-09, Vol.116 (38), p.19064-19070 [Periódico revisado por pares]

United States: National Academy of Sciences

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9
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants
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Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

Nagy, Reka ; Boutin, Thibaud S ; Marten, Jonathan ; Huffman, Jennifer E ; Kerr, Shona M ; Campbell, Archie ; Evenden, Louise ; Gibson, Jude ; Amador, Carmen ; Howard, David M ; Navarro, Pau ; Morris, Andrew ; Deary, Ian J ; Hocking, Lynne J ; Padmanabhan, Sandosh ; Smith, Blair H ; Joshi, Peter ; Wilson, James F ; Hastie, Nicholas D ; Wright, Alan F ; McIntosh, Andrew M ; Porteous, David J ; Haley, Chris S ; Vitart, Veronique ; Hayward, Caroline

Genome medicine, 2017-03, Vol.9 (1), p.23-23, Article 23 [Periódico revisado por pares]

England: BioMed Central

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10
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits
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Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traits

Bretherick, Andrew D ; Canela-Xandri, Oriol ; Joshi, Peter K ; Clark, David W ; Rawlik, Konrad ; Boutin, Thibaud S ; Zeng, Yanni ; Amador, Carmen ; Navarro, Pau ; Rudan, Igor ; Wright, Alan F ; Campbell, Harry ; Vitart, Veronique ; Hayward, Caroline ; Wilson, James F ; Tenesa, Albert ; Ponting, Chris P ; Baillie, J Kenneth ; Haley, Chris Davey Smith, George

PLoS genetics, 2020-07, Vol.16 (7), p.e1008785-e1008785 [Periódico revisado por pares]

United States: Public Library of Science

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