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2002, Wiley reference series in biostatistics, ISBN 9780471486312, xxiv, 831
Book
The Lancet, ISSN 0140-6736, 2003, Volume 361, Issue 9357, pp. 598 - 604
Journal Article
Original Communication - Lack of association of NAT2 (N-acetyl transferase 2) gene polymorphism with atopic asthma in Turkish subjects, 12/2004
It has been shown that slow acetylation may be a risk factor that influences the development of allergic diseases. N-acetyltransferase2 (NAT2), an enzyme that... 
NAT2 (N-acetyl transferase2), asthma, genetics, Turkey
Journal
2008, Studies in comparative social science, ISBN 9781594515651, xi, 253
Book
Lancet, The, ISSN 0140-6736, 2007, Volume 369, Issue 9578, pp. 1980 - 1982
Journal Article
by Randall, Joshua C and Winkler, Thomas W and Kutalik, Zoltán and Berndt, Sonja I and Jackson, Anne U and Monda, Keri L and Kilpeläinen, Tuomas O and Esko, Tõnu and Mägi, Reedik and Li, Shengxu and Workalemahu, Tsegaselassie and Feitosa, Mary F and Croteau-Chonka, Damien C and Day, Felix R and Fall, Tove and Ferreira, Teresa and Gustafsson, Stefan and Locke, Adam E and Mathieson, Iain and Scherag, Ane and Vedantam, Sailaja and Wood, Anew R and Liang, Liming and Steinthorsdottir, Valgerdur and Thorleifsson, Gudmar and Dermitzakis, Emmanouil T and Dimas, Antigone S and Karpe, Freik and Min, Josine L and Nicholson, George and Clegg, Deborah J and Person, Thomas and Krohn, Jon P and Bauer, Sabrina and Buechler, Christa and Eisinger, Kristina and Bonnefond, Amélie and Froguel, Philippe and Hottenga, Jouke-Jan and Prokopenko, Inga and Waite, Lindsay L and Harris, Tamara B and Smith, Albert Vernon and Shuldiner, Alan R and McArdle, Wendy L and Caulfield, Mark J and Munroe, Patricia B and Grönberg, Henrik and Chen, Yii-Der Ida and Li, Guo and Beckmann, Jacques S and Johnson, Toby and Thorsteinsdottir, Unnur and Teder-Laving, Maris and Khaw, Kay-Tee and Wareham, Nicholas J and Zhao, Jing Hua and Amin, Najaf and Oostra, Ben A and Kraja, Aldi T and Province, Michael A and Cupples, L. Aienne and Heard-Costa, Nancy L and Kaprio, Jaakko and Ripatti, Samuli and Surakka, Ida and Collins, Francis S and Saramies, Jouko and Tuomilehto, Jaakko and Jula, Antti and Salomaa, Veikko and Erdmann, Jeanette and Hengstenberg, Christian and Loley, Christina and Schunkert, Heribert and Lamina, Claudia and Wichmann, H. Erich and Albrecht, Eva and Gieger, Christian and Hicks, Anew A and Johansson, Asa and Pramstaller, Peter P and Kathiresan, Sekar and Speliotes, Elizabeth K and Penninx, Brenda and Hartikainen, Anna-Liisa and Jarvelin, Marjo-Riitta and Gyllensten, Ulf and Boomsma, Dorret I and Campbell, Harry and Wilson, James F and Chanock, Stephen J and Farrall, Martin and Goel, Anuj and Medina-Gomez, Carolina and Rivadeneira, Fernando and Estrada, Karol and Uitterlinden, Ané G and Hofman, Albert and Zillikens, M. Carola and ... and DIAGRAM Consortium and MAGIC Investigators and Medicinska fakulteten and Umeå universitet and Medicin and Institutionen för folkhälsa och klinisk medicin and Institutionen för odontologi and Enheten för biobanksforskning and Näringsforskning
PLoS genetics, ISSN 1553-7390, 2013, Volume 9, Issue 6, p. e1003500
Journal Article
Journal Article
The Lancet, ISSN 0140-6736, 2005, Volume 366, Issue 9492, pp. 1223 - 1234
Much effort and expense are being spent internationally to detect genetic polymorphisms contributing to susceptibility to complex human disease. Concomitantly,... 
Haplotypes | Genetics, Population | Gene Frequency | Humans | Genotype | Chromosome Mapping | Polymorphism, Single Nucleotide | Linkage Disequilibrium | Linkage (Genetics) | Human genome | Genetic aspects | Research | Single nucleotide polymorphisms | Australia | Diseases
Journal Article
P L o S Genetics (Print), ISSN 1553-7390, 02/2011, Volume 7, Issue 2, p. e1001307
Journal Article
by Winkler, Thomas W and Justice, Anne E and Graff, Mariaelisa and Barata, Llilda and Feitosa, Mary F and Chu, Su and Czajkowski, Jacek and Esko, Tõnu and Fall, Tove and Kilpeläinen, Tuomas O and Lu, Yingchang and Mägi, Reedik and Mihailov, Evelin and Pers, Tune H and Rüeger, Sina and Teumer, Alexander and Ehret, Georg B and Ferreira, Teresa and Heard-Costa, Nancy L and Karjalainen, Juha and Lagou, Vasiliki and Mahajan, Anubha and Neinast, Michael D and Prokopenko, Inga and Simino, Jeannette and Teslovich, Tanya M and Jansen, Rick and Westra, Harm-Jan and White, Charles C and Absher, Devin and Ahluwalia, Tarunveer S and Ahmad, Shafqat and Albrecht, Eva and Alves, Alexessander Couto and Bragg-Gresham, Jennifer L and de Craen, Anton J. M and Bis, Joshua C and Bonnefond, Amélie and Boucher, Gabrielle and Cadby, Gemma and Cheng, Yu-Ching and Chiang, Charleston W. K and Delgado, Graciela and Demirkan, Ayse and Dueker, Nicole and Eklund, Niina and Eiriksdottir, Gudny and Eriksson, Joel and Feenstra, Bjarke and Fischer, Krista and Frau, Francesca and Galesloot, Tessel E and Geller, Frank and Goel, Anuj and Gorski, Mathias and Grammer, Tanja B and Gustafsson, Stefan and Haitjema, Saskia and Hottenga, Jouke-Jan and Huffman, Jennifer E and Jackson, Anne U and Jacobs, Kevin B and Johansson, Åsa and Kaakinen, Marika and Kleber, Marcus E and Lahti, Jari and Mateo Leach, Irene and Lehne, Benjamin and Liu, Youfang and Lo, Ken Sin and Lorentzon, Mattias and Luan, Jian'an and Madden, Pamela A. F and Mangino, Massimo and McKnight, Barbara and Medina-Gomez, Carolina and Monda, Keri L and Montasser, May E and Müller, Gabriele and Müller-Nurasyid, Martina and Nolte, Ilja M and Panoutsopoulou, Kalliope and Pascoe, Laura and Paternoster, Lavinia and Rayner, Nigel W and Renström, Frida and Rizzi, Federica and Rose, Lynda M and Ryan, Kathy A and Salo, Perttu and Sanna, Serena and Scharnagl, Hubert and Shi, Jianxin and Smith, Albert Vernon and Southam, Lorraine and Stančáková, Alena and Steinthorsdottir, Valgerdur and Strawbridge, Rona J and Sung, Yun Ju and Tachmazidou, Ioanna and ... and DIAGRAM Consortium and CHARGE Consortium and GLGC Consortium and MAGIC Consortium and ICBP Consortium and Global-BPGen Consortium
PLoS genetics, ISSN 1553-7390, 2015, Volume 11, Issue 10, pp. 1 - 42
Genome-wide association studies (GWAS) have identified more than 100 genetic variants contributing to BMI, a measure of body size, or waist-to-hip ratio... 
LIFE-COURSE | BIOLOGICAL PATHWAYS | NATURAL MENOPAUSE | MASS INDEX | COMMON SNPS | GENETICS & HEREDITY | PERIPHERAL-BLOOD | WEIGHT-GAIN | LOCI | FAT DISTRIBUTION | SELF-REPORTED HEIGHT | Body Mass Index | Genetic Predisposition to Disease | Genome-Wide Association Study | Age Factors | Humans | Middle Aged | European Continental Ancestry Group | Male | Chromosome Mapping | Sex Characteristics | Adult | Female | Aged | Body Size - genetics | Polymorphism, Single Nucleotide | Waist-Hip Ratio | Genetic research | Dimorphism (Biology) | Research | Single nucleotide polymorphisms | Samfunnsmedisin, sosialmedisin: 801 | Community medicine, Social medicine: 801 | VDP | Helsefag: 800 | Health sciences: 800 | Medisinske Fag: 700 | Medical disciplines: 700 | Life Sciences | Genetics | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | HNE Voeding en Gezondheid in de Levenscyclus | Wereldvoeding | VLAG | Chair Nutrition and Health over the Lifecourse | Global Nutrition | HNE Nutrition and Health over the Lifecourse | Women | Medical research | Funding | Health care policy | Biology | Genomes | Studies | Consortia | Body mass index | Mens health | Councils | Older people | Gene loci | Adults | Diabetes | Age | Metabolic disorders
Journal Article