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ANNUAL REVIEW OF MEDICINE, ISSN 0066-4219, 2005, Volume 56, pp. 443 - 443
Until relatively recently, the small number of identifiable inherited human diseases associated with marked obesity were complex, pleiotropic developmental... 
CONGENITAL LEPTIN DEFICIENCY | ULNAR-MAMMARY SYNDROME | EARLY-ONSET OBESITY | ALSTROM-SYNDROME | NATURAL-HISTORY | leptin | BODY-WEIGHT | MEDICINE, GENERAL & INTERNAL | genetics | BARDET-BIEDL-SYNDROME | MISSENSE MUTATION | syndromes | FRAMESHIFT MUTATION | PRADER-WILLI-SYNDROME
Journal Article
Journal Article
Nature, ISSN 0028-0836, 04/2000, Volume 404, Issue 6778, pp. 632 - 634
Obesity has increased at ale alarming rate in recent years and is now a worldwide public health problem. In addition to suffering poor health and an increased... 
MC4R | BODY-WEIGHT | GENE | MULTIDISCIPLINARY SCIENCES | OB/OB MICE | OVERWEIGHT | HUMANS | LEPTIN LEVELS | EARLY-ONSET OBESITY | FRAMESHIFT MUTATION | Leptin - physiology | Environment | Obesity - etiology | Life Expectancy | Humans | Obesity | Hormones | Molecular biology | Genes | Public health | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 03/2012, Volume 483, Issue 7389, pp. 350 - 354
Journal Article
Journal Article
International Journal of Obesity, ISSN 0307-0565, 09/2002, Volume 26, Issue 2, pp. S12 - S17
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