Climate induced human demographic and cultural change in northern Europe during the mid-Holocene von Warden, L., Moros, M., Neumann, T., Shennan, S., Timpson, A., Manning, K., Sollai, M., Wacker, L., Perner, K., Häusler, K., Leipe, T., Zillén, L., Kotilainen, A., Jansen, E., Schneider, R. R., Oeberst, R., Arz, H., Sinninghe Damsté, J. S.

Volltext

Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms von Yet, Idil, Menni, Cristina, Shin, So-Youn, Mangino, Massimo, Soranzo, Nicole, Adamski, Jerzy, Suhre, Karsten, Spector, Tim D, Kastenmüller, Gabi, Bell, Jordana T

Volltext

A quality improvement project to increase breast milk use in very low birth weight infants von Lee, Henry C, Kurtin, Paul S, Wight, Nancy E, Chance, Kathy, Cucinotta-Fobes, Tracey, Hanson-Timpson, Tara A, Nisbet, Courtney C, Rhine, William D, Risingsun, Kate, Wood, Matthew, Danielsen, Beate H, Sharek, Paul J

Volltext

NetView: a high-definition network-visualization approach to detect fine-scale population structures from genome-wide patterns of variation von Neuditschko, Markus, Khatkar, Mehar S, Raadsma, Herman W

Volltext

Relationship between C-Reactive Protein Level and Diabetic Retinopathy: A Systematic Review and Meta-Analysis von Song, Jian, Chen, Song, Liu, Xiaoting, Duan, Hongtao, Kong, Jiahui, Li, Zedong

Volltext

Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations von Candille, Sophie I, Absher, Devin M, Beleza, Sandra, Bauchet, Marc, McEvoy, Brian, Garrison, Nanibaa' A, Li, Jun Z, Myers, Richard M, Barsh, Gregory S, Tang, Hua, Shriver, Mark D

Volltext

Thyroid function and body weight: a community-based longitudinal study von Bjergved, Lena, Jørgensen, Torben, Perrild, Hans, Laurberg, Peter, Krejbjerg, Anne, Ovesen, Lars, Rasmussen, Lone Banke, Knudsen, Nils

Volltext

FTO is expressed in neurones throughout the brain and its expression is unaltered by fasting von McTaggart, James S, Lee, Sheena, Iberl, Michaela, Church, Chris, Cox, Roger D, Ashcroft, Frances M

Volltext

Effects of 16 genetic variants on fasting glucose and type 2 diabetes in South Asians: ADCY5 and GLIS3 variants may predispose to type 2 diabetes von Rees, Simon D, Hydrie, M Zafar I, O'Hare, J Paul, Kumar, Sudhesh, Shera, A Samad, Basit, Abdul, Barnett, Anthony H, Kelly, M Ann

Volltext

Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood von Rye, Marie S, Warrington, Nicole M, Scaman, Elizabeth S H, Vijayasekaran, Shyan, Coates, Harvey L, Anderson, Denise, Pennell, Craig E, Blackwell, Jenefer M, Jamieson, Sarra E

Volltext

Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population von Gao, Wenjie, Peng, Yan, Liang, Guoyan, Liang, Anjing, Ye, Wei, Zhang, Liangming, Sharma, Swarkar, Su, Peiqiang, Huang, Dongsheng

Volltext

Underestimated effect sizes in GWAS: fundamental limitations of single SNP analysis for dichotomous phenotypes von Stringer, Sven, Wray, Naomi R, Kahn, René S, Derks, Eske M

Volltext

Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity von Walters, Robin G, Coin, Lachlan J M, Ruokonen, Aimo, de Smith, Adam J, El-Sayed Moustafa, Julia S, Jacquemont, Sebastien, Elliott, Paul, Esko, Tõnu, Hartikainen, Anna-Liisa, Laitinen, Jaana, Männik, Katrin, Martinet, Danielle, Meyre, David, Nauck, Matthias, Schurmann, Claudia, Sladek, Rob, Thorleifsson, Gudmar, Thorsteinsdóttir, Unnur, Valsesia, Armand, Waeber, Gerard, Zufferey, Flore, Balkau, Beverley, Pattou, François, Metspalu, Andres, Völzke, Henry, Vollenweider, Peter, Stefansson, Kári, Järvelin, Marjo-Riitta, Beckmann, Jacques S, Froguel, Philippe, Blakemore, Alexandra I F

Volltext

Cervical Neoplasia and Repeated Positivity of Human Papillomavirus Infection In Human Immunodeficiency Virus-seropositive and -seronegative Women von Ahdieh, Linda, Munoz, Alvaro, Vlahov, David, Trimble, Cornelia L., Timpson, Lauren A., Shah, Keerti

Volltext

Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants von Kinnamon, Daniel D, Hershberger, Ray E, Martin, Eden R

Volltext

Association between the interleukin-6 promoter polymorphism -174G/C and serum lipoprotein(a) concentrations in humans von Berthold, Heiner K, Laudes, Matthias, Krone, Wilhelm, Gouni-Berthold, Ioanna

Volltext

Genetic association study of common mitochondrial variants on body fat mass von Yang, Tie-Lin, Guo, Yan, Shen, Hui, Lei, Shu-Feng, Liu, Yong-Jun, Li, Jian, Liu, Yao-Zhong, Yu, Na, Chen, Jia, Xu, Ting, Cheng, Yu, Tian, Qing, Yu, Ping, Papasian, Christopher J, Deng, Hong-Wen

Volltext

AVPR1A and SLC6A4 polymorphisms in choral singers and non-musicians: a gene association study von Morley, Andrew P, Narayanan, Madan, Mines, Rebecca, Molokhia, Ashraf, Baxter, Sebastian, Craig, Gavin, Lewis, Cathryn M, Craig, Ian

Volltext

Analysis of pharmacogenomic variants associated with population differentiation von Yeon, Bora, Ahn, Eunyong, Kim, Kyung-Im, Kim, In-Wha, Oh, Jung Mi, Park, Taesung

Volltext

Chromosome 15q25 (CHRNA3-CHRNA5) variation impacts indirectly on lung cancer risk von Wang, Yufei, Broderick, Peter, Matakidou, Athena, Eisen, Timothy, Houlston, Richard S

Volltext