X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (10) 10
index medicus (10) 10
genetics & heredity (8) 8
research (6) 6
article (5) 5
genetic variation (5) 5
genetics (5) 5
risk factors (5) 5
chromosome mapping (4) 4
dk/atira/pure/subjectarea/asjc/1300/1311 (4) 4
genetic aspects (4) 4
genome, human (4) 4
linkage disequilibrium (4) 4
adult (3) 3
european continental ancestry group - genetics (3) 3
expression (3) 3
female (3) 3
gene frequency (3) 3
genomics (3) 3
male (3) 3
medical and health sciences (3) 3
medical research (3) 3
medicin och hälsovetenskap (3) 3
physiological aspects (3) 3
polymorphism, single nucleotide (3) 3
polymorphism, single nucleotide - genetics (3) 3
quantitative trait loci (3) 3
risk (3) 3
studies (3) 3
aged (2) 2
alleles (2) 2
biochemistry & molecular biology (2) 2
case-control studies (2) 2
chromosomes (2) 2
diagnosis (2) 2
europe (2) 2
gene (2) 2
genetic predisposition to disease (2) 2
genome-wide association (2) 2
genome-wide association study (2) 2
genotype (2) 2
genotype & phenotype (2) 2
haplotype diversity (2) 2
haplotypes (2) 2
human genome (2) 2
inflammatory bowel disease (2) 2
medicin (2) 2
medicine (2) 2
meta-analysis (2) 2
middle aged (2) 2
models, genetic (2) 2
multidisciplinary sciences (2) 2
multiple (2) 2
mutation (2) 2
polymorphism (2) 2
single nucleotide polymorphisms (2) 2
21 breast cancers (1) 1
adaptation, biological (1) 1
adiposity - genetics (1) 1
adolescent (1) 1
adult obesity (1) 1
adults (1) 1
africa (1) 1
african americans - genetics (1) 1
age of onset (1) 1
aged, 80 and over (1) 1
algorithms (1) 1
alpha-ketoglutarate-dependent dioxygenase fto (1) 1
angiosarcoma (1) 1
animals (1) 1
anticoagulants - administration & dosage (1) 1
anticoagulants - adverse effects (1) 1
anticoagulants - pharmacokinetics (1) 1
anticoagulants - pharmacology (1) 1
apolipoprotein-e apoe (1) 1
asian continental ancestry group - genetics (1) 1
association (1) 1
autoimmune diseases (1) 1
autophagy (1) 1
bartters-syndrome (1) 1
biomedical research (1) 1
biomedicine (1) 1
biosynthetic pathways - drug effects (1) 1
biosynthetic pathways - genetics (1) 1
biotechnology & applied microbiology (1) 1
birth weight (1) 1
blocks (1) 1
blood pressure (1) 1
blood pressure - genetics (1) 1
body fat (1) 1
body mass index (1) 1
body weight - genetics (1) 1
bowel disease (1) 1
breast neoplasms (1) 1
c431 medical genetics (1) 1
caco-2 cells (1) 1
cardiovascular disease (1) 1
cardiovascular diseases (1) 1
cardiovascular diseases - genetics (1) 1
cardiovascular diseases - physiopathology (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Genetics, ISSN 0340-6717, 3/2007, Volume 121, Issue 1, pp. 23 - 34
Journal Article
by Fisher, Sheila A and Regueiro, Miguel D and Anderson, Carl A and Prescott, Natalie J and Mathew, Christopher G and Rutgeerts, Paul and Parkes, Miles and Steinhart, A Hillary and Drummond, Hazel and Bitton, Alain and Georges, Michel and Gut, Ivo and Jewell, Derek and Barrett, Jeffrey C and Daly, Mark J and Dewit, Olivier and Bumpstead, Suzannah and Hansoul, Sarah and Hugot, Jean-Pierre and Barmada, M Michael and Xavier, Ramnik J and Libioulle, Cécile and Tremelling, Mark and Laukens, Debby and Datta, Lisa Wu and Kistner, Emily O and Onnie, Clive M and Griffiths, Anne M and Franchimont, Denis and Lathrop, Mark and Nimmo, Elaine and Green, Todd and Mansfield, John and Zelenika, Diana and Deloukas, Panos and Taylor, Kent D and Ahmad, Tariq and de Vos, Martine and Van Gossum, André and Duerr, Richard H and Silverberg, Mark S and Nicolae, Dan L and Rotter, Jerome I and Schumm, L Philip and Cardon, Lon R and Ghori, Jilur and Heath, Simon and Dassopoulos, Themistocles and Vermeire, Severine and Sandor, Cynthia and Satsangi, Jack and Marchini, Jonathan and Gwilliam, Rhian and Louis, Edouard and Rioux, John D and Mni, Myriam and Belaiche, Jacques and Targan, Stephan R and Brant, Steven R and Murtha, Michael T and Cho, Judy H and Wellcome Trust Case Control and NIDDK IBD Genetics Consortium and Belgian-French IBD Consortium and Wellcome Trust Case Control Consortium and the NIDDK IBD Genetics Consortium and the Belgian-French IBD Consortium and the Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 08/2008, Volume 40, Issue 8, pp. 955 - 962
Journal Article
by Day, Ian and Dermitzakis, Emmanouil T and Randall, Joshua C and Weedon, Michael N and Hinney, Anke and Evans, David M and Qi, Lu and Bennett, Amanda J and Munroe, Patricia B and Herrera, Blanca and Johnson, Toby and Elliott, Katherine S and Song, Kijoung and Zeggini, Eleftheria and Cauchi, Stéphane and Teichmann, Sarah A and Lindgren, Cecilia M and Brown, Morris and Sims, Matthew A and Karpe, Fredrik and O'Rahilly, Stephen and Hattersley, Andrew T and Scherag, André and Samani, Nilesh J and Keniry, Andrew and Li, Shengxu and Beckmann, Jacques S and Cooper, Cyrus and Caulfield, Mark J and Owen, Katharine R and Luben, Robert N and McGinnis, Ralph and Ghori, Jilur and Ness, Andrew R and Bochud, Murielle and Jarvelin, Marjo-Riitta and Hebebrand, Johannes and Ong, Ken K and Freathy, Rachel M and McArdle, Wendy L and Potter, Simon and Wareham, Nicholas J and Ganz Vogel, Carla I and Mooser, Vincent and Barroso, Inês and Deloukas, Panos and Waterworth, Dawn M and Bergmann, Sven and Elliott, Paul and Gwilliam, Rhian and Tobias, Jonathan H and Jolley, Jennifer D M and Morris, Andrew D and Loos, Ruth J F and Yuan, Xin and Smith, George Davey and Palmer, Colin N A and Groves, Christopher J and Dina, Christian and Syddall, Holly E and Waeber, Gerard and Zhao, Jing Hua and Sandhu, Manjinder S and Doney, Alex S F and Hunt, Sarah E and Pouta, Anneli and Speliotes, Elizabeth K and Connell, John M and Timpson, Nicholas J and Wallace, Chris and Attwood, Antony P and Hall, Alistair S and Khaw, Kay-Tee and Meyre, David and Vollenweider, Peter and Bingham, Sheila A and Berndt, Sonja I and Hadley, David and Rayner, Nigel W and Frayling, Timothy M and Sadaf Farooqi, I and Hirschhorn, Joel N and Strachan, David P and Inouye, Michael and Papadakis, Konstantinos and Ring, Susan M and Wraight, Vicki L and Willer, Cristen J and Marchini, Jonathan and Uda, Manuela and Nica, Alexandra C and Mangino, Massimo and Soranzo, Nicole and McCarthy, Mark I and De, Subhajyoti and Neville, Matthew J and Prokopenko, Inga and Wheeler, Eleanor and Heid, Iris M and Froguel, Philippe and ... and Diabetes Genetics Initiative and SardiNIA Study and FUSION and Prostate Lung Colorectal Ovarian and KORA and Wellcome Trust Case Control Consor and Nurses' Health Study and Wellcome Trust Case Control Consortium and Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial and The Wellcome Trust Case Control Consortium and The SardiNIA Study and Diabetes - klinisk obesitasforskning and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Diabetes - Clinical Obesity and Lunds universitet
Nature Genetics, ISSN 1061-4036, 06/2008, 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 | Index Medicus | 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 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, Alessana and Di Gregorio, Alessana and Guarrera, Simonetta and Panico, Salvatore and Ricceri, Fulvio and Romanazzi, Valeria and Sacerdote, Carlotta and Vineis, Paolo and Barroso, Ines 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 Doering, 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 Consor and Wellcome Trust Case Control Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature Genetics, ISSN 1061-4036, 06/2009, Volume 41, Issue 6, pp. 666 - 676
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2009, Volume 41, Issue 12, pp. 1335 - 1340
Journal Article