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Current Diabetes Reports, ISSN 1534-4827, 8/2019, Volume 19, Issue 8, pp. 1 - 9
Journal Article
PLoS Medicine, ISSN 1549-1277, 09/2018, Volume 15, Issue 9, p. e1002654
Background Type 2 diabetes (T2D) is a heterogeneous disease for which (1) disease-causing pathways are incompletely understood and (2) subclassification may... 
COMMON VARIANTS | MEDICINE, GENERAL & INTERNAL | RARE VARIANTS | GENOTYPE IMPUTATION | FATTY LIVER-DISEASE | LOW-FREQUENCY | SUSCEPTIBILITY LOCI | AGING RESEARCH | INSULIN SENSITIVITY | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Diabetes Mellitus, Type 2 - classification | Genetic Predisposition to Disease | Genome-Wide Association Study | Multigene Family | Prospective Studies | Cross-Sectional Studies | Diabetes Mellitus, Type 2 - genetics | Humans | Risk Factors | Databases, Genetic | Male | Genetic Loci | Genetic Markers | Founder Effect | Phenotype | Algorithms | Bayes Theorem | Insulin Resistance - genetics | Insulin - deficiency | Female | Insulin - genetics | Cluster Analysis | Cohort Studies | Type 2 diabetes | Medical research | Genomics | Development and progression | Triglycerides | Research | Coronary heart disease | Genetic markers | Blood cholesterol | Analysis | Physiological aspects | Medicine, Experimental | Genetic research | Insulin resistance | Genetic aspects | Diabetics | Treatment outcome | Care and treatment | Usage | Management | Biological markers | Patients | Cluster analysis | Pediatrics | Identification methods | Lipids | Genomes | Adiponectin | Body mass index | Heterogeneity | Pathways | Genetic analysis | Genetics | Blood pressure | Lipid metabolism | Lipoproteins (high density) | Diabetes mellitus (non-insulin dependent) | Heart diseases | Supervision | Phenotypes | Stroke | Liver diseases | Medical treatment | Diabetes mellitus | Coronary artery | Metabolism | Clustering | Insulin | Coronary artery disease | Loci | Cholesterol | Medicine | Beta cells | Genetic variance | Hospitals | Body mass | Body size | Biomarkers | Lipodystrophy | Gene loci | Diabetes | Bayesian analysis | Metabolic disorders
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 321 - 14
Journal Article
Cancer Epidemiology Biomarkers & Prevention, ISSN 1055-9965, 08/2008, Volume 17, Issue 8, pp. 1843 - 1848
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 5/2009, Volume 18, Issue 9, pp. 1692 - 1703
Journal Article
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2018, Volume 102, Issue 6, pp. 1204 - 1211
There is a limited understanding about the impact of rare protein-truncating variants across multiple phenotypes. We explore the impact of this class of... 
rare variants | constraint genes | exome sequencing | phewas | selection | ultra-rare variants | burden analysis | GENERAL-POPULATION | AUTISM | VARIANT ASSOCIATION | DISEASE | GENETICS & HEREDITY | DISORDERS | RISK | MUTATIONS | SAMPLES | GENOME | Physiological aspects | Phenotype | Genetic aspects | Research | Genetic variation | Report
Journal Article
by Flannick, Jason and Mercader, Josep M and Fuchsberger, Christian and Udler, Miriam S and Mahajan, Anubha and Wessel, Jennifer and Teslovich, Tanya M and Caulkins, Lizz and Koesterer, Ryan and Barajas-Olmos, Francisco and Blackwell, Thomas W and Boerwinkle, Eric and Brody, Jennifer A and Centeno-Cruz, Federico and Chen, Ling and Chen, Siying and Contreras-Cubas, Cecilia and Córdova, Emilio and Correa, Adolfo and Cortes, Maria and DeFronzo, Ralph A and Dolan, Lawrence and Drews, Kimberly L and Elliott, Amanda and Floyd, James S and Gabriel, Stacey and Garay-Sevilla, Maria Eugenia and García-Ortiz, Humberto and Gross, Myron and Han, Sohee and Heard-Costa, Nancy L and Jackson, Anne U and Jørgensen, Marit E and Kang, Hyun Min and Kelsey, Megan and Kim, Bong-Jo and Koistinen, Heikki A and Kuusisto, Johanna and Leader, Joseph B and Linneberg, Allan and Liu, Ching-Ti and Liu, Jianjun and Lyssenko, Valeriya and Manning, Alisa K and Marcketta, Anthony and Malacara-Hernandez, Juan Manuel and Martínez-Hernández, Angélica and Matsuo, Karen and Mayer-Davis, Elizabeth and Mendoza-Caamal, Elvia and Mohlke, Karen L and Morrison, Alanna C and Ndungu, Anne and Ng, Maggie C. Y and O’Dushlaine, Colm and Payne, Anthony J and Pihoker, Catherine and Post, Wendy S and Preuss, Michael and Psaty, Bruce M and Vasan, Ramachandran S and Rayner, N. William and Reiner, Alexander P and Revilla-Monsalve, Cristina and Robertson, Neil R and Santoro, Nicola and Schurmann, Claudia and So, Wing Yee and Soberón, Xavier and Stringham, Heather M and Strom, Tim M and Tam, Claudia H. T and Thameem, Farook and Tomlinson, Brian and Torres, Jason M and Tracy, Russell P and van Dam, Rob M and Vujkovic, Marijana and Wang, Shuai and Welch, Ryan P and Witte, Daniel R and Wong, Tien-Yin and Atzmon, Gil and Barzilai, Nir and Blangero, John and Bonnycastle, Lori L and Bowden, Donald W and Chambers, John C and Chan, Edmund and Cheng, Ching-Yu and Cho, Yoon Shin and Collins, Francis S and de Vries, Paul S and Duggirala, Ravindranath and Glaser, Benjamin and Gonzalez, Clicerio and Gonzalez, Ma Elena and Groop, Leif and Kooner, Jaspal Singh and Kwak, Soo Heon and ... and DiscovEHR Collaboration and ESP and GoT2D and SIGMA-T2D and Broad Genomics Platform and AMP-T2D-GENES and LuCamp and T2D-GENES and CHARGE and ProDiGY
Nature, ISSN 0028-0836, 06/2019, Volume 570, Issue 7759, pp. 71 - 76
Journal Article