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2011, A Social History of England, ISBN 9780521713238, xv, 454
The years between 900 and 1200 saw transformative social change in Europe, including the creation of extensive town-dwelling populations and the proliferation... 
England | Social conditions | Economic conditions
Book
by Loos, Ruth J F and Lindgren, Cecilia M and Li, Shengxu and Wheeler, Eleanor and Zhao, Jing Hua and Prokopenko, Inga and Inouye, Michael and Freathy, Rachel M and Attwood, Antony P and Beckmann, Jacques S and Berndt, Sonja I and Bergmann, Sven and Bennett, Amanda J and Bingham, Sheila A and Bochud, Murielle and Brown, Morris and Cauchi, Stéphane and Connell, John M and Cooper, Cyrus and Smith, George Davey and Day, Ian and Dina, Christian and De, Subhajyoti and Dermitzakis, Emmanouil T and Doney, Alex S F and Elliott, Katherine S and Elliott, Paul and Evans, David M and Sadaf Farooqi, I and Froguel, Philippe and Ghori, Jilur and Groves, Christopher J and Gwilliam, Rhian and Hadley, David and Hall, Alistair S and Hattersley, Andrew T and Hebebrand, Johannes and Heid, Iris M and Herrera, Blanca and Hinney, Anke and Hunt, Sarah E and Jarvelin, Marjo-Riitta and Johnson, Toby and Jolley, Jennifer D M and Karpe, Fredrik and Keniry, Andrew and Khaw, Kay-Tee and Luben, Robert N and Mangino, Massimo and Marchini, Jonathan and McArdle, Wendy L and McGinnis, Ralph and Meyre, David and Munroe, Patricia B and Morris, Andrew D and Ness, Andrew R and Neville, Matthew J and Nica, Alexandra C and Ong, Ken K and O'Rahilly, Stephen and Owen, Katharine R and Palmer, Colin N A and Papadakis, Konstantinos and Potter, Simon and Pouta, Anneli and Qi, Lu and Randall, Joshua C and Rayner, Nigel W and Ring, Susan M and Sandhu, Manjinder S and Scherag, André and Sims, Matthew A and Song, Kijoung and Soranzo, Nicole and Speliotes, Elizabeth K and Syddall, Holly E and Teichmann, Sarah A and Timpson, Nicholas J and Tobias, Jonathan H and Uda, Manuela and Ganz Vogel, Carla I and Wallace, Chris and Waterworth, Dawn M and Weedon, Michael N and Willer, Cristen J and Wraight, Vicki L and Yuan, Xin and Zeggini, Eleftheria and Hirschhorn, Joel N and Strachan, David P and Ouwehand, Willem H and Caulfield, Mark J and Samani, Nilesh J and Frayling, Timothy M and Vollenweider, Peter and Waeber, Gerard and Mooser, Vincent and Deloukas, Panos and McCarthy, Mark I and Wareham, Nicholas J and ... and Diabetes Genetics Initiative and The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and FUSION and The Wellcome Trust Case Control Consortium and KORA and The SardiNIA Study and Nurses' Health Study and SardiNIA Study and Prostate Lung Colorectal Ovarian and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial
Nature genetics, ISSN 1546-1718, 2008, Volume 40, Issue 6, pp. 768 - 775
To identify common variants influencing body mass index (BMI), we analyzed genome-wide association data from 16,876 individuals of European descent. After... 
FTO GENE | GENETICS & HEREDITY | MELANOCORTIN-4 RECEPTOR GENE | EARLY-ONSET OBESITY | FRAMESHIFT MUTATION | DOMINANT | ADULT OBESITY | EXPRESSION | CHILDHOOD | DEFICIENCY | GENOME-WIDE ASSOCIATION | Meta-Analysis as Topic | Humans | Middle Aged | Alpha-Ketoglutarate-Dependent Dioxygenase FTO | Male | Body Weight - genetics | Obesity - genetics | Case-Control Studies | Genetic Variation | Proteins | Adult | Female | Child | Body Mass Index | Genetic Predisposition to Disease | Cross-Sectional Studies | Receptor, Melanocortin, Type 4 - genetics | Adiposity - genetics | Linkage Disequilibrium | Obesity - pathology | Randomized Controlled Trials as Topic | Obesity - epidemiology | Adolescent | Alleles | Aged | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 18 - genetics | Genome, Human | Quantitative Trait Loci | Cohort Studies | Obesity | Body mass index | Genetic variation | Physiological aspects | Genetic aspects | Diagnosis | Research | Risk factors | Medical research | Biomedical research | Body fat | Health services | Genetics | Birth weight | Adults | Progeny | Integration | Pedigree | Data processing | Melanocortin MC4 receptors | Single-nucleotide polymorphism | Children | Mutation | Population levels | Clinical Medicine | Näringslära | Hälsovetenskap | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Nutrition and Dietetics | Endocrinology and Diabetes | Health Sciences
Journal Article
by Willer, Cristen and Speliotes, Elizabeth and Loos, Ruth and Li, Shengxu and Lindgren, Cecilia and Heid, Iris and Berndt, Sonja and Elliott, Amanda and Jackson, Anne and Lamina, Claudia and Lettre, Guillaume and Lim, Noha and Lyon, Helen and McCarroll, Steven and Papadakis, Konstantinos and Qi, Lu and Randall, Joshua and Roccasecca, R.M and Sanna, Serena and Scheet, Paul and Weedon, Michael and Wheeler, Eleanor and Zhao, Jing Hua and Jacobs, Leonie and Prokopenko, Inga and Soranzo, Nicole and Tanaka, Toshiko and Timpson, Nicholas and Almgren, Peter and Bennett, Amanda and Bergman, Richard and Bingham, Sheila and Bonnycastle, Lori and Brown, Morris and Burtt, Noël and Chines, Peter and Coin, Lachlan and Collins, Francis and Connell, John and Cooper, Charles and Smith, Davey and Dennison, Elaine and Deodhar, Parimal and Erdos, Michael and Estrada Gil, Karol and Evans, David and Gianniny, Lauren and Gieger, Christian and Gillson, Christopher and Guiducci, Candace and Hackett, Rachel and Hadley, David and Hall, Alistair and Havulinna, Aki and Hebebrand, Johannes and Hofman, Albert and Isomaa, Bo and Johnson, Toby and Jousilahti, Pekka and Jovanovic, Zorica and Khaw, Kay-Tee and Kraft, Peter and Kuokkanen, Mikko and Kuusisto, Johanna and Laitinen, Jaana and Lakatta, Edward and Luan, J and Luben, Robert and Mangino, Massimo and McArdle, Wendy and Meitinger, Thomas and Mulas, Antonella and Munroe, Patricia and Narisu, Narisu and Ness, Anew and Northstone, Kate and O'Rahilly, Stephen and Purmann, Carolin and Rees, Matthew and Ridderstråle, Martin and Ring, Susan and Rivadeneira Ramirez, Fernando and Ruokonen, Aimo and Sandhu, Manjinder and Saramies, Jouko and Scott, Laura and Scuteri, Angelo and Silander, Kaisa and Sims, Matthew and Song, Kijoung and Stephens, Jonathan and Stevens, Suzanne and Stringham, Heather and Tung, Loraine and Valle, Timo and Tikka-Kleemola, Päivi and Vimaleswaran, Karani and Vollenweider, Peter and Waeber, Gérard and Wallace, Chris and ... and the GIANT Consortium and Wellcome Trust Case Control and Giant Consortium and Wellcome Trust Case Control Consortium and Genetic Investigation of ANthropometric Traits Consortium
Nature genetics, ISSN 1546-1718, 2008, Volume 41, Issue 1, pp. 25 - 34
Journal Article
Nature communications, ISSN 2041-1723, 2019, Volume 10, Issue 1, pp. 3935 - 11
Journal Article
by Lindgren, Cecilia and Heid, Iris and Randall, Joshua and Lamina, Claudia and Steinthorsdottir, Valgerdur and Qi, Lu and Speliotes, Elizabeth and Thorleifsson, Gudmar and Willer, Cristen and Herrera, Blanca and Jackson, Anne and Lim, Noha and Scheet, Paul and Soranzo, Nicole and Amin, Najaf and Aulchenko, Yurii and Chambers, John and ng, Alexander and Luan, J and Lyon, Helen and Rivadeneira Ramirez, Fernando and Sanna, Serena and Timpson, Nicholas and Zillikens, Carola and Jing, H.Z and Almgren, Peter and Bandinelli, Stefania and Bennett, Amanda and Bergman, Richard and Bonnycastle, Lori and Bumpstead, Suzannah and Chanock, Stephen and Cherkas, Lynn and Chines, Peter and Coin, Lachlan and Cooper, Charles and Crawford, Gabe and Doering, Angela and Dominiczak, Anna and Doney, Alex and Ebrahim, Shanil and Elliott, Paul and Erdos, Michael and Estrada Gil, Karol and Ferrucci, Luigi and Fischer, Guido and Forouhi, Nita and Gieger, Christian and Grallert, Harald and Groves, Christopher and Grundy, Scott and Guiducci, Candace and Hadley, David and Hamsten, Anders and Havulinna, Aki and Hofman, Albert and Holle, Rolf and Holloway, John and Illig, Thomas and Isomaa, Bo and Jacobs, Leonie and Jameson, Karen and Jousilahti, Pekka and Karpe, Freik and Kuusisto, Johanna and Laitinen, Jaana and Lathrop, Mark and Lawlor, Debbie and Mangino, Massimo and McArdle, Wendy and Meitinger, Thomas and Morken, Mario and Morris, Anew and Munroe, Patricia and Narisu, Narisu and Nordström, Anna and Oostra, Ben and Palmer, Colin and Payne, Felicity and Peden, John and Prokopenko, Inga and Renström, Frida and Ruokonen, Aimo and Salomaa, Veikko and Sandhu, Manjinder and Scott, Laura and Scuteri, Angelo and Silander, Kaisa and Song, Kijoung and Yuan, Xin and Stringham, Heather and Swift, Amy and Tuomi, Tiinamaija and Uda, Manuela and Vollenweider, Peter and Waeber, Gérard and Wallace, Chris and Walters, Bragi and Weedon, Michael and Witteman, Jacqueline and ... and Wellcome Trust Case Control Consor and GIANT Consortium and PROCARDIS Consortia and Wellcome Trust Case Control Consortium and Giant Consortium and Procardis Consortia and The Wellcome Trust Case Control Consortium
PLoS genetics, ISSN 1553-7390, 06/2009, Volume 5, Issue 6, p. e1000508
Journal Article
by Newton-Cheh, Christopher and Johnson, Toby and Gateva, Vesela and Tobin, Martin D and Bochud, Murielle and Coin, Lachlan and Najjar, Samer S and Zhao, Jing Hua and Heath, Simon C and Eyheramendy, Susana and Papadakis, Konstantinos and Voight, Benjamin F and Scott, Laura J and Zhang, Feng and Farrall, Martin and Tanaka, Toshiko and Wallace, Chris and Chambers, John C and Khaw, Kay-Tee and Nilsson, Peter and van der Harst, Pim and Polidoro, Silvia and Grobbee, Diederick E and Onland-Moret, N Charlotte and Bots, Michiel L and Wain, Louise V and Elliott, Katherine S and Teumer, Alexander and Luan, Jian'an and Lucas, Gavin and Kuusisto, Johanna and Burton, Paul R and Hadley, David and McArdle, Wendy L and Brown, Morris and Dominiczak, Anna and Newhouse, Stephen J and Samani, Nilesh J and Webster, John and Zeggini, Eleftheria and Beckmann, Jacques S and Bergmann, Sven and Lim, Noha and Song, Kijoung and Vollenweider, Peter and Waeber, Gerard and Waterworth, Dawn M and Yuan, Xin and Groop, Leif and Orho-Melander, Marju and Allione, Alessandra and Di Gregorio, Alessandra and Guarrera, Simonetta and Panico, Salvatore and Ricceri, Fulvio and Romanazzi, Valeria and Sacerdote, Carlotta and Vineis, Paolo and Barroso, Inês and Sandhu, Manjinder S and Luben, Robert N and Crawford, Gabriel J and Jousilahti, Pekka and Perola, Markus and Boehnke, Michael and Bonnycastle, Lori L and Collins, Francis S and Jackson, Anne U and Mohlke, Karen L and Stringham, Heather M and Valle, Timo T and Willer, Cristen J and Bergman, Richard N and Morken, Mario A and Döring, Angela and Gieger, Christian and Illig, Thomas and Meitinger, Thomas and Org, Elin and Pfeufer, Arne and Wichmann, H Erich and Kathiresan, Sekar and Marrugat, Jaume and O'Donnell, Christopher J and Schwartz, Stephen M and Siscovick, David S and Subirana, Isaac and Freimer, Nelson B and Hartikainen, Anna-Liisa and McCarthy, Mark I and O'Reilly, Paul F and Peltonen, Leena and Pouta, Anneli and de Jong, Paul E and Snieder, Harold and van Gilst, Wiek H and Clarke, Robert and Goel, Anuj and Hamsten, Anders and Peden, John F and ... and Wellcome Trust Case Control Consortium and Wellcome Trust Case Control Consor
Nature genetics, ISSN 1546-1718, 2009, Volume 41, Issue 6, pp. 666 - 676
Elevated blood pressure is a common, heritable cause of cardiovascular disease worldwide. To date, identification of common genetic variants influencing blood... 
LOW-RENIN HYPERTENSION | COMMON VARIANTS | POPULATION | PUBLIC-HEALTH | METHYLENETETRAHYDROFOLATE REDUCTASE GENE | RISK | POLYMORPHISM | MUTATIONS | CELL-DIFFERENTIATION | UMCG Approved | BARTTERS-SYNDROME | GENETICS & HEREDITY | Cardiovascular Diseases - physiopathology | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Blood Pressure - genetics | Europe | Humans | Diastole - genetics | Intracellular Signaling Peptides and Proteins | Chromosome Mapping | Systole - genetics | DNA-Binding Proteins - genetics | Fibroblast Growth Factor 5 - genetics | Open Reading Frames - genetics | Cardiovascular Diseases - genetics | India | Genetic Variation | Proteins - genetics | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Cytochrome P-450 CYP1A2 - genetics | Phospholipase C delta - genetics | Steroid 17-alpha-Hydroxylase - genetics | Polymorphism, Single Nucleotide | Hypertension | Physiological aspects | Genetic aspects | Blood pressure | Research | Single nucleotide polymorphisms | Cardiovascular diseases | Risk factors | Studies | Data analysis | Genomics | Cardiovascular disease | Gene loci | Statistics | Meta-analysis | Kardiologi | Clinical Medicine | Other Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Endokrinologi och diabetes | Medicin och hälsovetenskap | Annan klinisk medicin | Klinisk medicin | Endocrinology and Diabetes
Journal Article