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Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing
Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing
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Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing

Harries, Lorna W. ; Hernandez, Dena ; Henley, William ; Wood, Andrew R. ; Holly, Alice C. ; Bradley‐Smith, Rachel M. ; Yaghootkar, Hanieh ; Dutta, Ambarish ; Murray, Anna ; Frayling, Timothy M. ; Guralnik, Jack M. ; Bandinelli, Stefania ; Singleton, Andrew ; Ferrucci, Luigi ; Melzer, David

Aging cell, 2011-10, Vol.10 (5), p.868-878 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Cell Specific eQTL Analysis without Sorting Cells
Cell Specific eQTL Analysis without Sorting Cells
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Cell Specific eQTL Analysis without Sorting Cells

Westra, Harm-Jan ; Arends, Danny ; Esko, Tõnu ; Peters, Marjolein J ; Schurmann, Claudia ; Schramm, Katharina ; Kettunen, Johannes ; Yaghootkar, Hanieh ; Fairfax, Benjamin P ; Andiappan, Anand Kumar ; Li, Yang ; Fu, Jingyuan ; Karjalainen, Juha ; Platteel, Mathieu ; Visschedijk, Marijn ; Weersma, Rinse K ; Kasela, Silva ; Milani, Lili ; Tserel, Liina ; Peterson, Pärt ; Reinmaa, Eva ; Hofman, Albert ; Uitterlinden, André G ; Rivadeneira, Fernando ; Homuth, Georg ; Petersmann, Astrid ; Lorbeer, Roberto ; Prokisch, Holger ; Meitinger, Thomas ; Herder, Christian ; Roden, Michael ; Grallert, Harald ; Ripatti, Samuli ; Perola, Markus ; Wood, Andrew R ; Melzer, David ; Ferrucci, Luigi ; Singleton, Andrew B ; Hernandez, Dena G ; Knight, Julian C ; Melchiotti, Rossella ; Lee, Bernett ; Poidinger, Michael ; Zolezzi, Francesca ; Larbi, Anis ; Wang, De Yun ; van den Berg, Leonard H ; Veldink, Jan H ; Rotzschke, Olaf ; Makino, Seiko ; Salomaa, Veikko ; Strauch, Konstantin ; Völker, Uwe ; van Meurs, Joyce B J ; Metspalu, Andres ; Wijmenga, Cisca ; Jansen, Ritsert C ; Franke, Lude Pastinen, Tomi

PLoS genetics, 2015-05, Vol.11 (5), p.e1005223 [Periódico revisado por pares]

United States: Public Library of Science

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3
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.

PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]

United States: Public Library of Science

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4
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers
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Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers

Pilling, Luke C ; Atkins, Janice L ; Duff, Michael O ; Beaumont, Robin N ; Jones, Samuel E ; Tyrrell, Jessica ; Kuo, Chia-Ling ; Ruth, Katherine S ; Tuke, Marcus A ; Yaghootkar, Hanieh ; Wood, Andrew R ; Murray, Anna ; Weedon, Michael N ; Harries, Lorna W ; Kuchel, George A ; Ferrucci, Luigi ; Frayling, Timothy M ; Melzer, David Arking, Dan E.

PloS one, 2017-09, Vol.12 (9), p.e0185083-e0185083 [Periódico revisado por pares]

United States: Public Library of Science

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5
A reference panel of 64,976 haplotypes for genotype imputation
A reference panel of 64,976 haplotypes for genotype imputation
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A reference panel of 64,976 haplotypes for genotype imputation

Das, Sayantan ; Delaneau, Olivier ; Wood, Andrew R ; Teumer, Alexander ; Kang, Hyun Min ; Danecek, Petr ; Luo, Yang ; Sidore, Carlo ; Kwong, Alan ; Timpson, Nicholas ; Koskinen, Seppo ; Vrieze, Scott ; Scott, Laura J ; Zhang, He ; Mahajan, Anubha ; Veldink, Jan ; Peters, Ulrike ; Pato, Carlos ; van Duijn, Cornelia M ; Gillies, Christopher E ; Gandin, Ilaria ; Mezzavilla, Massimo ; Gilly, Arthur ; Cocca, Massimiliano ; Traglia, Michela ; Angius, Andrea ; Barrett, Jeffrey C ; Boomsma, Dorrett ; Branham, Kari ; Breen, Gerome ; Brummett, Chad M ; Busonero, Fabio ; Campbell, Harry ; Chen, Sai ; Chew, Emily ; Collins, Francis S ; Corbin, Laura J ; Smith, George Davey ; Dedoussis, George ; Dorr, Marcus ; Farmaki, Aliki-Eleni ; Ferrucci, Luigi ; Forer, Lukas ; Fraser, Ross M ; Gabriel, Stacey ; Levy, Shawn ; Groop, Leif ; Harrison, Tabitha ; Hattersley, Andrew ; Holmen, Oddgeir L ; Hveem, Kristian ; Kretzler, Matthias ; Lee, James C ; McGue, Matt ; Meitinger, Thomas ; Vincent, John B ; Nauck, Matthias ; Nickerson, Deborah ; Palotie, Aarno ; Pato, Michele ; Pirastu, Nicola ; McInnis, Melvin ; Richards, J Brent ; Sala, Cinzia ; Salomaa, Veikko ; Schlessinger, David ; Schoenherr, Sebastian ; Slagboom, P Eline ; Small, Kerrin ; Spector, Timothy ; Tuke, Marcus ; Tuomilehto, Jaakko ; Van den Berg, Leonard H ; Van Rheenen, Wouter ; Volker, Uwe ; Wijmenga, Cisca ; Toniolo, Daniela ; Zeggini, Eleftheria ; Gasparini, Paolo ; Sampson, Matthew G ; Wilson, James F ; Frayling, Timothy ; de Bakker, Paul I W ; Swertz, Morris A ; McCarroll, Steven ; Kooperberg, Charles ; Dekker, Annelot ; Altshuler, David ; Willer, Cristen ; Iacono, William ; Ripatti, Samuli ; Soranzo, Nicole ; Walter, Klaudia ; Swaroop, Anand ; Cucca, Francesco ; Anderson, Carl A ; Myers, Richard M ; Boehnke, Michael ; McCarthy, Mark I ; Durbin, Richard

Nature genetics, 2016-10, Vol.48 (10), p.1279-1283 [Periódico revisado por pares]

United States: Nature Publishing Group

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6
Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
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Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank

Pilling, Luke C ; Tamosauskaite, Jone ; Jones, Garan ; Wood, Andrew R ; Jones, Lindsay ; Kuo, Chai-Ling ; Kuchel, George A ; Ferrucci, Luigi ; Melzer, David

BMJ (Online), 2019-01, Vol.364, p.k5222-k5222 [Periódico revisado por pares]

England: BMJ Publishing Group LTD

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7
Another explanation for apparent epistasis
Another explanation for apparent epistasis
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Another explanation for apparent epistasis

Wood, Andrew R ; Tuke, Marcus A ; Nalls, Mike A ; Hernandez, Dena G ; Bandinelli, Stefania ; Singleton, Andrew B ; Melzer, David ; Ferrucci, Luigi ; Frayling, Timothy M ; Weedon, Michael N

Nature (London), 2014-10, Vol.514 (7520), p.E3-E5 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies
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Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies

Harlow, Charli E. ; Gandawijaya, Josan ; Bamford, Rosemary A. ; Martin, Emily-Rose ; Wood, Andrew R. ; van der Most, Peter J. ; Tanaka, Toshiko ; Leonard, Hampton L. ; Etheridge, Amy S. ; Innocenti, Federico ; Beaumont, Robin N. ; Tyrrell, Jessica ; Nalls, Mike A. ; Simonsick, Eleanor M. ; Garimella, Pranav S. ; Shiroma, Eric J. ; Verweij, Niek ; van der Meer, Peter ; Gansevoort, Ron T. ; Snieder, Harold ; Gallins, Paul J. ; Jima, Dereje D. ; Wright, Fred ; Zhou, Yi-hui ; Ferrucci, Luigi ; Bandinelli, Stefania ; Hernandez, Dena G. ; van der Harst, Pim ; Patel, Vickas V. ; Waterworth, Dawn M. ; Chu, Audrey Y. ; Oguro-Ando, Asami ; Frayling, Timothy M.

American journal of human genetics, 2022-09, Vol.109 (9), p.1638-1652 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants
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Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants

Pilling, Luke C ; Atkins, Janice L ; Bowman, Kirsty ; Jones, Samuel E ; Tyrrell, Jessica ; Beaumont, Robin N ; Ruth, Katherine S ; Tuke, Marcus A ; Yaghootkar, Hanieh ; Wood, Andrew R ; Freathy, Rachel M ; Murray, Anna ; Weedon, Michael N ; Xue, Luting ; Lunetta, Kathryn ; Murabito, Joanne M ; Harries, Lorna W ; Robine, Jean-Marie ; Brayne, Carol ; Kuchel, George A ; Ferrucci, Luigi ; Frayling, Timothy M ; Melzer, David

Aging (Albany, NY.), 2016-03, Vol.8 (3), p.547-560

United States: Impact Journals

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10
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association
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Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

Wood, Andrew R ; Hernandez, Dena G ; Nalls, Michael A ; Yaghootkar, Hanieh ; Gibbs, J. Raphael ; Harries, Lorna W ; Chong, Sean ; Moore, Matthew ; Weedon, Michael N ; Guralnik, Jack M ; Bandinelli, Stefania ; Murray, Anna ; Ferrucci, Luigi ; Singleton, Andrew B ; Melzer, David ; Frayling, Timothy M

Human molecular genetics, 2011-10, Vol.20 (20), p.4082-4092 [Periódico revisado por pares]

Oxford: Oxford University Press

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