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Journal Article
by Kanoni, Stavroula and Masca, Nicholas G.D and Stirrups, Kathleen E and Varga, Tibor V and Warren, Helen R and Scott, Robert A and Southam, Lorraine and Zhang, Weihua and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Alves, Alexessander Couto and Strawbridge, Rona J and Lataniotis, Lazaros and Hashim, Nikman An and Besse, Céline and Boland, Anne and Braund, Peter S and Connell, John M and Dominiczak, Anna and Farmaki, Aliki-Eleni and Franks, Stephen and Grallert, Harald and Jansson, Jan-Håkan and Karaleftheri, Maria and Keinänen-Kiukaanniemi, Sirkka and Matchan, Angela and Pasko, Dorota and Peters, Annette and Poulter, Neil and Rayner, Nigel W and Renström, Frida and Rolandsson, Olov and Sabater-Lleal, Maria and Sennblad, Bengt and Sever, Peter and Shields, Denis and Silveira, Angela and Stanton, Alice V and Strauch, Konstantin and Tomaszewski, Maciej and Tsafantakis, Emmanouil and Waldenberger, Melanie and Blakemore, Alexandra I.F and Dedoussis, George and Escher, Stefan A and Kooner, Jaspal S and McCarthy, Mark I and Palmer, Colin N.A and Hamsten, Anders and Caulfield, Mark J and Frayling, Timothy M and Tobin, Martin D and Jarvelin, Marjo-Riitta and Zeggini, Eleftheria and Gieger, Christian and Chambers, John C and Wareham, Nick J and Munroe, Patricia B and Franks, Paul W and Samani, Nilesh J and Deloukas, Panos and Wellcome Trust Case Control Consor and Wellcome Trust Case Control Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Enheten för biobanksforskning and Allmänmedicin and Umeå universitet and Medicin
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 18, pp. 4094 - 4106
Journal Article
by Kanoni, Stavroula and Masca, Nicholas G D and Stirrups, Kathleen E and Varga, Tibor V and Warren, Helen R and Scott, Robert A and Southam, Lorraine and Zhang, Weihua and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Alves, Alexessander Couto and Strawbridge, Rona J and Lataniotis, Lazaros and Hashim, Nikman An and Besse, Céline and Boland, Anne and Braund, Peter S and Connell, John M and Dominiczak, Anna and Farmaki, Aliki-Eleni and Franks, Stephen and Grallert, Harald and Jansson, Jan-Håkan and Karaleftheri, Maria and Keinänen-Kiukaanniemi, Sirkka and Matchan, Angela and Pasko, Dorota and Peters, Annette and Poulter, Neil and Rayner, Nigel W and Renström, Frida and Rolandsson, Olov and Sabater-Lleal, Maria and Sennblad, Bengt and Sever, Peter and Shields, Denis C and Silveira, Angela and Stanton, Alice V and Strauch, Konstantin and Tomaszewski, Maciej and Tsafantakis, Emmanouil and Waldenberger, Melanie and Blakemore, Alexandra I. F and Dedoussis, George and Escher, Stefan A and Kooner, Jaspal S and McCarthy, Mark I and Palmer, Colin N. A and Hamsten, Anders and Caulfield, Mark J and Frayling, Timothy M and Tobin, Martin D and Jarvelin, Marjo Riitta and Zeggini, Eleftheria and Gieger, Christian and Chambers, John C and Wareham, Nick J and Munroe, Patricia B and Franks, Paul W and Samani, Nilesh J and Deloukas, Panos and EpiHealth: Epidemiology for Health and Lund University and Genetic and Molecular Epidemiology and Genetisk och molekylär epidemiologi and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 18, p. 4094
It has been hypothesized that low frequency (1-5% minor allele frequency (MAF)) and rare (<1% MAF) variants with large effect sizes may contribute to the... 
Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
Indian Journal of Clinical Biochemistry, ISSN 0970-1915, 4/2015, Volume 30, Issue 2, pp. 134 - 139
Genome-wide association studies have discovered multiple single nucleotide polymorphisms (SNPs) associated with the risk of common diseases. The objective of... 
Life Sciences | Biochemistry, general | Risk prediction model | Pathology | Association | Microbiology | SNP | Chemistry/Food Science, general | Breast cancer | Case–control study | Prevention | Hospitals | Analysis | Business parks | Genomics | Genetic research | Genetic aspects | Single nucleotide polymorphisms | Chromosomes | Risk factors | Cancer | Genetics | Polymorphism | Original
Journal Article
The Indian Journal of Medical Research, ISSN 0971-5916, 12/2014, Volume 140, Issue 6, pp. 873 - 882
Background & objectives: Colorectal cancer (CRC) is second only to breast cancer as the leading cause of cancer-related deaths in Malaysia. In the Asia-Pacific... 
Sample size | Bias | Colorectal cancer | Family medical history | Metastasis | Gene expression | Meat | Cell adhesion & migration | Studies | Ethnicity | Hospitals | Questionnaires | Age | Polymorphism
Journal Article
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2012, Volume 13, Issue 12, pp. 6005 - 6010
Background: Nasopharyngeal carcinoma (NPC) is endemic in Southern Chinese and Southeast Asian populations. Geographical and ethnic clustering of the cancer is... 
Nasopharyngeal carcinoma | Association study | Southeast Asia | SNP | Cancer risk | nasopharyngeal carcinoma | GUANGXI | MODEL | PRESERVED FOODS | CANCER | PREDICTION | ONCOLOGY | association study | cancer risk | SALTED FISH | SUSCEPTIBILITY LOCUS | EPSTEIN-BARR-VIRUS | EPIDEMIOLOGY | GENOME-WIDE ASSOCIATION
Journal Article
Asian Pacific journal of cancer prevention : APJCP, ISSN 1513-7368, 2012, Volume 13, Issue 12, pp. 6005 - 6010
Background: Nasopharyngeal carcinoma (NPC) is endemic in Southern Chinese and Southeast Asian populations. Geographical and ethnic clustering of the cancer is... 
Journal Article
Asian Pacific journal of cancer prevention : APJCP, 2012, Volume 13, Issue 12, p. 6005
Nasopharyngeal carcinoma (NPC) is endemic in Southern Chinese and Southeast Asian populations. Geographical and ethnic clustering of the cancer is due to... 
Genome-Wide Association Study | Humans | Risk Factors | Asian Continental Ancestry Group - genetics | Polymorphism, Single Nucleotide | Case-Control Studies
Journal Article
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