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1.
Risk interaction of obesity, insulin resistance and hormone-sensitive lipase promoter polymorphisms (LIPE-60 C > G) in the development of fatty liver
Pi-Jung Hsiao, Zhih-Cherg Chen, Wei-Wen Hung, Yi-Hsin Yang, Mei-Yueh Lee, Jee-Fu Huang, Kung-Kai Kuo BMC Medical Genetics 2013, 14 :54 (20 May 2013)
Abstract | Full text | PDF | ePUB | PubMed
2.
Study design of DIACORE (DIAbetes COhoRtE) – a cohort study of patients with diabetes mellitus type 2
Lena Dörhöfer, Alexander Lammert, Vera Krane, Mathias Gorski, Bernhard Banas, Christoph Wanner, Bernhard K Krämer, Iris M Heid, Carsten A Böger, for the DIACORE Study Group BMC Medical Genetics 2013, 14 :25 (14 February 2013)
Abstract | Full text | PDF | PubMed
3.
A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ ) and its receptors (ADIPOR1/R2 ), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome
Kirsten E Peters, John Beilby, Gemma Cadby, Nicole M Warrington, David G Bruce, Wendy A Davis, Timothy ME Davis, Steven Wiltshire, Matthew Knuiman, Brendan M McQuillan, Lyle J Palmer, Peter L Thompson, Joseph Hung BMC Medical Genetics 2013, 14 :15 (25 January 2013)
Abstract | Full text | PDF | PubMed
4.
Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes
Natalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, Chiara Viviani-Anselmi, Francesca De Micco, Alessandra Mezzelani, Werner Koch, Petra Hoppmann, Adnan Kastrati, Alexandre FR Stewart, Li Chen, Robert Roberts, Lennart C Karssen, Najaf Amin, Valentina Trimarco, Raffaele Izzo, Guido Iaccarino, Gerolama Condorelli, Annibale A Puca, Paolo Pagnotta, Flavio Airoldi, Bruno Trimarco, Cornelia M van Duijn, Gianluigi Condorelli, Carlo Briguori BMC Medical Genetics 2013, 14 :11 (23 January 2013)
Abstract | Full text | PDF | PubMed
5.
Meta-analysis of associations between TCF7L2 polymorphisms and risk of type 2 diabetes mellitus in the Chinese population
Jinjin Wang, Fulan Hu, Tianping Feng, Jingzhi Zhao, Lei Yin, Linlin Li, Yan Wang, Qian Wang, Dongsheng Hu BMC Medical Genetics 2013, 14 :8 (12 January 2013)
Abstract | Full text | PDF | PubMed
6.
APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
Catalina Dussaillant, Valentina Serrano, Alberto Maiz, Susana Eyheramendy, Luis Cataldo, Matías Chavez, Susan V Smalley, Marcela Fuentes, Attilio Rigotti, Lorena Rubio, Carlos F Lagos, José Martinez, José Santos BMC Medical Genetics 2012, 13 :106 (15 November 2012)
Abstract | Full text | PDF | PubMed
7.
Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: The Athero Gene Study
Choumous Kallel, William Cohen, Noémie Saut, Stefan Blankenberg, Renate Schnabel, Hans J Rupprecht, Christoph Bickel, Thomas Munzel, David-Alexandre Tregouet, Pierre-Emmanuel Morange BMC Medical Genetics 2012, 13 :103 (8 November 2012)
Abstract | Full text | PDF | PubMed
8.
The contribution of FTO and UCP -1 SNPs to extreme obesity, diabetes and cardiovascular risk in Brazilian individuals
Adauto V Ramos, Luciana Bastos-Rodrigues, Bruna A Resende, Eitan Friedman, Luciana Campanha-Versiani, Debora M Miranda, Marta Sarquis, Luiz De Marco BMC Medical Genetics 2012, 13 :101 (7 November 2012)
Abstract | Full text | PDF | PubMed
9.
Maternal and offspring fasting glucose and type 2 diabetes-associated genetic variants and cognitive function at age 8: a Mendelian randomization study in the Avon Longitudinal Study of Parents and Children
Carolina Bonilla, Debbie A Lawlor, Yoav Ben–Shlomo, Andrew R Ness, David Gunnell, Susan M Ring, George Smith, Sarah J Lewis BMC Medical Genetics 2012, 13 :90 (27 September 2012)
Abstract | Full text | PDF | ePUB | PubMed
10.
Expression analyses of the genes harbored by the type 2 diabetes and pediatric BMI associated locus on 10q23
Jianhua Zhao, Sandra Deliard, Ali Aziz, Struan FA Grant BMC Medical Genetics 2012, 13 :89 (24 September 2012)
Abstract | Full text | PDF | PubMed
11.
Association of ALOX5AP gene single nucleotide polymorphisms and cerebral infarction in the Han population of northern China
Shuang-yan Zhang, Mei-ling Xu, Cui-e Zhang, Zheng-yi Qu, Bin-bin Zhang, Zu-yan Zheng, Li-ming Zhang BMC Medical Genetics 2012, 13 :61 (31 July 2012)
Abstract | Full text | PDF | PubMed
12.
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Rinki Murphy, Lourdes Ibáñez, Andrew Hattersley, Jörg Tost BMC Medical Genetics 2012, 13 :42 (30 May 2012)
Abstract | Full text | PDF | PubMed
13.
Circulating leukocyte telomere length is highly heritable among families of Arab descent
Omar S Al-Attas, Nasser M Al-Daghri, Majed S Alokail, Khalid M Alkharfy, Assim A Alfadda, Philip McTernan, Greg C Gibson, Shaun B Sabico, George P Chrousos BMC Medical Genetics 2012, 13 :38 (18 May 2012)
Abstract | Full text | PDF | PubMed |
14.
Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III)
Jonna L Grimsby, Bianca C Porneala, Jason L Vassy, Quanhe Yang, José C Florez, Josée Dupuis, Tiebin Liu, Ajay Yesupriya, Man-Huei Chang, Renee M Ned, Nicole F Dowling, Muin J Khoury, James B Meigs, the MAGIC Investigators BMC Medical Genetics 2012, 13 :30 (27 April 2012)
Abstract | Full text | PDF | PubMed
15.
Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity
Johanna Korvala, Harald Jüppner, Outi Mäkitie, Etienne Sochett, Dirk Schnabel, Stefano Mora, Cynthia F Bartels, Matthew L Warman, Donald Deraska, William G Cole, Heini Hartikka, Leena Ala-Kokko, Minna Männikkö BMC Medical Genetics 2012, 13 :26 (10 April 2012)
Abstract | Full text | PDF | PubMed
16.
Genetic variations in APPL2 are associated with overweight and obesity in a Chinese population with normal glucose tolerance
Shan Jiang, Qichen Fang, Weihui Yu, Rong Zhang, Cheng Hu, Kun Dong, Yuqian Bao, Chen Wang, Kunsan Xiang, Weiping Jia BMC Medical Genetics 2012, 13 :22 (30 March 2012)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central
17.
The combined effect of the T2DM susceptibility genes is an important risk factor for T2DM in non-obese Japanese: a population based case-control study
Kimiko Yamakawa-Kobayashi, Maki Natsume, Shingo Aoki, Sachi Nakano, Tomoko Inamori, Nobuhiko Kasezawa, Toshinao Goda BMC Medical Genetics 2012, 13 :11 (24 February 2012)
Abstract | Full text | PDF | PubMed
18.
The effect of FOXA2 rs1209523 on glucose-related phenotypes and risk of type 2 diabetes in Danish individuals
Karina Banasik, Mette Hollensted, Ehm Andersson, Thomas Sparsø, Annelli Sandbæk, Torsten Lauritzen, Torben Jørgensen, Daniel R Witte, Oluf Pedersen, Torben Hansen BMC Medical Genetics 2012, 13 :10 (12 February 2012)
Abstract | Full text | PDF | PubMed
19.
Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial disease
Daniel S Lieber, Scott B Vafai, Laura C Horton, Nancy G Slate, Shangtao Liu, Mark L Borowsky, Sarah E Calvo, Jeremy D Schmahmann, Vamsi K Mootha BMC Medical Genetics 2012, 13 :3 (6 January 2012)
Abstract | Full text | PDF | PubMed
20.
Association of common variants in JAK2 gene with reduced risk of metabolic syndrome and related disorders
Alberto Penas-Steinhardt, Mariana L Tellechea¹, Leonardo Gomez-Rosso, Fernando Brites, Gustavo D Frechtel, Edgardo Poskus BMC Medical Genetics 2011, 12 :166 (20 December 2011)
Abstract | Full text | PDF | PubMed
21.
A non-synonymous coding change in the CYP19A1 gene Arg264Cys (rs700519) does not affect circulating estradiol, bone structure or fracture
Jenny Z Wang, Mandeep S Deogan, Joshua R Lewis, Shelby Chew, Ben H Mullin, Tegan J McNab, Scott G Wilson, Evan Ingley, Richard L Prince BMC Medical Genetics 2011, 12 :165 (20 December 2011)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central
22.
Risk variants in BMP4 promoters for nonsyndromic cleft lip/palate in a Chilean population
José Suazo, Julio C Tapia, José Luis Santos, Víctor G Castro, Alicia Colombo, Rafael Blanco BMC Medical Genetics 2011, 12 :163 (19 December 2011)
Abstract | Full text | PDF | PubMed
23.
Disorder-specific effects of polymorphisms at opposing ends of the Insulin Degrading Enzyme gene
Jasmin Bartl, Claus-Jürgen Scholz, Margareta Hinterberger, Susanne Jungwirth, Ildiko Wichart, Michael K Rainer, Susanne Kneitz, Walter Danielczyk, Karl H Tragl, Peter Fischer, Peter Riederer, Edna Grünblatt BMC Medical Genetics 2011, 12 :151 (22 November 2011)
Abstract | Full text | PDF | PubMed
24.
Comprehensive analysis of RET common and rare variants in a series of Spanish Hirschsprung patients confirms a synergistic effect of both kinds of events
Rocio Núñez-Torres, Raquel M Fernández, Manuel Acosta, Maria del Valle Enguix-Riego, Martina Marbá, Juan Carlos de Agustín, Luis Castaño, Guillermo Antiñolo, Salud Borrego BMC Medical Genetics 2011, 12 :138 (13 October 2011)
Abstract | Full text | PDF | PubMed
25.
Clinical and genetic analyses of three Korean families with hereditary hemorrhagic telangiectasia
Mi-Jung Kim, Seon-Tae Kim, Hyoung-Doo Lee, Kyu-Yong Lee, Jiyoung Seo, Jae-Bom Lee, Young-Jae Lee, Suk P Oh BMC Medical Genetics 2011, 12 :130 (3 October 2011)
Abstract | Full text | PDF | PubMed | Cited on BioMed Central