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Artificial selection on allometry: change in elevation but not slope
EGSET, C. K., HANSEN, T. F., LE ROUZIC, A., BOLSTAD, G. H., ROSENQVIST, G., PÉLABON, C.
Published in Journal of evolutionary biology (01.05.2012)
Published in Journal of evolutionary biology (01.05.2012)
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Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes
Rosenfeld, Jill A, Traylor, Ryan N, Schaefer, G Bradley, McPherson, Elizabeth W, Ballif, Blake C, Klopocki, Eva, Mundlos, Stefan, Shaffer, Lisa G, Aylsworth, Arthur S
Published in European journal of human genetics : EJHG (01.07.2012)
Published in European journal of human genetics : EJHG (01.07.2012)
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Evolution of Paget's disease of bone in adults inheriting SQSTM1 mutations
Cundy, Tim, Rutland, Michael D., Naot, Dorit, Bolland, Mark
Published in Clinical endocrinology (Oxford) (01.09.2015)
Published in Clinical endocrinology (Oxford) (01.09.2015)
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Patterns of Inheritance of Constitutional Delay of Growth and Puberty in Families of Adolescent Girls and Boys Referred to Specialist Pediatric Care
Wehkalampi, Karoliina, Widén, Elisabeth, Laine, Tiina, Palotie, Aarno, Dunkel, Leo
Published in The journal of clinical endocrinology and metabolism (01.03.2008)
Published in The journal of clinical endocrinology and metabolism (01.03.2008)
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Mimvec: a deep learning approach for analyzing the human phenome
Gan, Mingxin, Li, Wenran, Zeng, Wanwen, Wang, Xiaojian, Jiang, Rui
Published in BMC systems biology (21.09.2017)
Published in BMC systems biology (21.09.2017)
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Previous Estimates of Mitochondrial DNA Mutation Level Variance Did Not Account for Sampling Error: Comparing the mtDNA Genetic Bottleneck in Mice and Humans
Wonnapinij, Passorn, Chinnery, Patrick F., Samuels, David C.
Published in American journal of human genetics (09.04.2010)
Published in American journal of human genetics (09.04.2010)
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Association between the ENPP1 K121Q Polymorphism and Risk of Diabetic Kidney Disease: A Systematic Review and Meta-Analysis
Sortica, Denise Alves, Buffon, Marjorie Piucco, Souza, Bianca Marmontel, Nicoletto, Bruna Bellicanta, Santer, Andressa, Assmann, Tais Silveira, Crispim, Daisy, Canani, Luis Henrique
Published in PloS one (20.03.2015)
Published in PloS one (20.03.2015)
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The T309G MDM2 Gene Polymorphism Is a Novel Risk Factor for Proliferative Vitreoretinopathy
Pastor-Idoate, Salvador, Rodríguez-Hernández, Irene, Rojas, Jimena, Fernández, Itziar, García-Gutiérrez, María T., Ruiz-Moreno, José M., Rocha-Sousa, Amandio, Ramkissoon, Yashin, Harsum, Steven, MacLaren, Robert E., Charteris, David, VanMeurs, Jan C., González-Sarmiento, Rogelio, Pastor, José C.
Published in PloS one (09.12.2013)
Published in PloS one (09.12.2013)
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Discovering Cortical Folding Patterns in Neonatal Cortical Surfaces Using Large-Scale Dataset
Meng, Yu, Li, Gang, Wang, Li, Lin, Weili, Gilmore, John H, Shen, Dinggang
Published in Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention (01.10.2016)
Published in Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention (01.10.2016)
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Familial History of Diabetes is Associated with Poor Glycaemic Control in Type 2 Diabetics: A Cross-sectional Study
Wu, Ming, Wen, Jinbo, Qin, Yu, Zhao, Hailong, Pan, Xiaoqun, Su, Jian, Du, Wencong, Pan, Enchun, Zhang, Qin, Zhang, Ning, Sheng, Hongyan, Liu, Chunlan, Shen, Chong
Published in Scientific reports (03.05.2017)
Published in Scientific reports (03.05.2017)
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The polymorphic inheritance of DIO2 rs225014 may predict body weight variation after Graves’ disease treatment
Comarella, Ana Paula, Vilagellin, Danilo, Bufalo, Natassia Elena, Euflauzino, Jessica Ferreira, Teixeira, Elisangela de Souza, Miklos, Ana Beatriz Pinotti Pedro, Santos, Roberto Bernardo dos, Romaldini, João H., Ward, Laura S.
Published in Archives of Endocrinology and Metabolism (01.11.2021)
Published in Archives of Endocrinology and Metabolism (01.11.2021)
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Gene Genealogies Strongly Distorted by Weakly Interfering Mutations in Constant Environments
Seger, Jon, Smith, Wendy A, Perry, Jarom J, Hunn, Jessalynn, Kaliszewska, Zofia A, Sala, Luciano La, Pozzi, Luciana, Rowntree, Victoria J, Adler, Frederick R
Published in Genetics (Austin) (01.02.2010)
Published in Genetics (Austin) (01.02.2010)
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