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Hepatology, ISSN 0270-9139, 09/2013, Volume 58, Issue 3, pp. 966 - 975
Journal Article
PLoS Genetics, ISSN 1553-7390, 09/2014, Volume 10, Issue 9, pp. e1004633 - e1004633
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 15989 - 8
The rs780094 single nucleotide polymorphism (SNP; C/T) of glucokinase regulatory protein gene (GCKR) is a regulatory genetic variant that has been associated... 
SIMPLE-MODEL | HEPATIC GLUCOKINASE | LIPID-METABOLISM | P446L VARIANT | GLUCOKINASE REGULATORY PROTEIN | COMMON VARIANT | LIVER GLUCOKINASE | GLUCOSE | MULTIDISCIPLINARY SCIENCES | TYPE-2 DIABETES RISK | FINNISH MEN | Fasting | Glucagon | Single-nucleotide polymorphism | Glucose | Gene polymorphism | Insulin | Glucose tolerance | Genetic variance | Hyperglycemia | Hepatocytes | Glucokinase | Alleles | Lactic acid
Journal Article
by Mahajan, Anubha and Sim, Xueling and Ng, Hui Jin and Manning, Alisa and Rivas, Manuel A and Highland, Heather M and Locke, Adam E and Grarup, Niels and Im, Hae Kyung and Cingolani, Pablo and Flannick, Jason and Fontanillas, Pierre and Fuchsberger, Christian and Gaulton, Kyle J and Teslovich, Tanya M and Rayner, N. William and Robertson, Neil R and Beer, Nicola L and Rundle, Jana K and Bork-Jensen, Jette and Ladenvall, Claes and Blancher, Christine and Buck, David and Buck, Gemma and Burtt, Noël P and Gabriel, Stacey and Gjesing, Anette P and Groves, Christopher J and Hollensted, Mette and Huyghe, Jeroen R and Jackson, Anne U and Jun, Goo and Justesen, Johanne Marie and Mangino, Massimo and Murphy, Jacquelyn and Neville, Matt and Onofrio, Robert and Small, Kerrin S and Stringham, Heather M and Syvänen, Ann-Christine and Trakalo, Joseph and Abecasis, Goncalo and Bell, Graeme I and Blangero, John and Cox, Nancy J and Duggirala, Ravindranath and Hanis, Craig L and Seielstad, Mark and Wilson, James G and Christensen, Cramer and Brandslund, Ivan and Rauramaa, Rainer and Surdulescu, Gabriela L and Doney, Alex S. F and Lannfelt, Lars and Linneberg, Allan and Isomaa, Bo and Tuomi, Tiinamaija and Jørgensen, Marit E and Jørgensen, Torben and Kuusisto, Johanna and Uusitupa, Matti and Salomaa, Veikko and Spector, Timothy D and Morris, Andrew D and Palmer, Colin N. A and Collins, Francis S and Mohlke, Karen L and Bergman, Richard N and Ingelsson, Erik and Lind, Lars and Tuomilehto, Jaakko and Hansen, Torben and Watanabe, Richard M and Prokopenko, Inga and Dupuis, Josee and Karpe, Fredrik and Groop, Leif and Laakso, Markku and Pedersen, Oluf and Florez, Jose C and Morris, Andrew P and Altshuler, David and Meigs, James B and Boehnke, Michael and McCarthy, Mark I and Lindgren, Cecilia M and Gloyn, Anna L and Abboud, Hanna E and Afzal, Uzma and Aguilar, David and Arya, Rector and Atzmon, Gil and Aung, Tin and Banks, Eric and Barroso, Inês and Barzilai, Nir and Below, Jennifer E and Bharadwaj, Dwaipayan and Blackwell, Thomas W and ... and Go T2D Consortium and T2D-GENES Consortium and T2D-GENES consortium and GoT2D consortium and On Behalf of the T2D-GENES consortium and GoT2D consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
PLoS Genetics, ISSN 1553-7390, 01/2015, Volume 11, Issue 1, p. e1004876
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2018, Volume 13, Issue 10, p. e0206174
Journal Article
DIABETES, ISSN 0012-1797, 03/2013, Volume 62, Issue 3, pp. 987 - 992
The molecular basis of type 2 diabetes predisposition at most established susceptibility loci remains poorly understood. KCNQ1 maps within the 11p15.5... 
ALLELE | CONTROL REGION | DOMAIN | P446L VARIANT | GENE | GLUCOSE | ENDOCRINOLOGY & METABOLISM | PANCREATIC BETA-CELLS | MUTATIONS | EXPRESSION | BINDING
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 05/2019, Volume 30, Issue 5, pp. 855 - 864
Background A family history of urolithiasis is associated with a more than doubling of urolithiasis risk, and a twin study estimating 56% heritability of the... 
NEPHROLITHIASIS | human genetics | METABOLIC SYNDROME | DESIGN | PREVALENCE | P446L VARIANT | REPLICATION | genetics and development | CALCIUM | UROLOGY & NEPHROLOGY | COMMON | KIDNEY-STONES | kidney stones | HYPERTENSION
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