Works matching AU McCarthy, Mark I.
Results: 216
An effector index to predict target genes at GWAS loci.
- Published in:
- Human Genetics, 2022, v. 141, n. 8, p. 1431, doi. 10.1007/s00439-022-02434-z
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- Article
HIV infection and anaemia do not affect HbA<sub>1c</sub> for the detection of diabetes in black South Africans: Evidence from the Durban Diabetes Study.
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- Diabetic Medicine, 2021, v. 38, n. 11, p. 1, doi. 10.1111/dme.14605
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- Article
Human disease genomics: from variants to biology.
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- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1160-z
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- Article
Genetic Risk Scores for Diabetes Diagnosis and Precision Medicine.
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- Endocrine Reviews, 2019, v. 40, n. 6, p. 1500, doi. 10.1210/er.2019-00088
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- Article
Sex Differences in the Risk of Coronary Heart Disease Associated With Type 2 Diabetes: A Mendelian Randomization Analysis.
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- 2021
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- journal article
Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD).
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- 2020
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- journal article
Variation in the Plasma Membrane Monoamine Transporter (PMAT) (Encoded by ) and Organic Cation Transporter 1 (OCT1) (Encoded by ) and Gastrointestinal Intolerance to Metformin in Type 2 Diabetes: An IMI DIRECT Study.
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- 2019
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- Publication type:
- journal article
Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes.
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- 2019
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- journal article
Validation of Plasma Biomarker Candidates for the Prediction of eGFR Decline in Patients With Type 2 Diabetes.
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- 2018
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- journal article
Systematic assessment of etiology in adults with a clinical diagnosis of young-onset type 2 diabetes is a successful strategy for identifying maturity-onset diabetes of the young.
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- 2012
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- journal article
Systematic Assessment of Etiology in Adults With a Clinical Diagnosis of Young-Onset Type 2 Diabtets Is a Succesful Strategy for Identifying Maturity-Onset Diabetes of the Young.
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- Diabetes Care, 2012, v. 35, n. 6, p. 1206, doi. 10.2337/dc11-1243
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- Article
Assessment of high-sensitivity C-reactive protein levels as diagnostic discriminator of maturity-onset diabetes of the young due to HNF1A mutations.
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- 2010
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- journal article
Assessment of High-Sensitivity C-Reactive Protein Levels as-Diagnostic Discriminator of Maturity-Onset Diabetes of the Young Due to HNF1A Mutations.
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- Diabetes Care, 2010, v. 33, n. 9, p. 1919, doi. 10.2337/dc10-0288
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- Article
Evaluation of serum 1,5 anhydroglucitol levels as a clinical test to differentiate subtypes of diabetes.
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- 2010
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- journal article
Evaluation of Serum 1, 5 Anhydroglucitol Levels as a Clinical Test to Differentiate Subtypes of Diabetes.
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- Diabetes Care, 2010, v. 33, n. 2, p. 252, doi. 10.2337/dc09-1246
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- Article
Ethnic variation in the activity of lipid desaturases and their relationships with cardiovascular risk factors in control women and an at-risk group with previous gestational diabetes mellitus: a cross-sectional study.
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- Lipids in Health & Disease, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1476-511X-12-25
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- Article
PASSIM -- an open source software system for managing information in biomedical studies.
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- BMC Bioinformatics, 2007, v. 8, p. 1, doi. 10.1186/1471-2105-8-52
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- Article
Association of vitamin D with risk of type 2 diabetes: A Mendelian randomisation study in European and Chinese adults.
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- 2018
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- journal article
Finding the missing heritability of complex diseases.
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- Nature, 2009, v. 461, n. 7265, p. 747, doi. 10.1038/nature08494
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- Article
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
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- Nature, 2007, v. 447, n. 7145, p. 661, doi. 10.1038/nature05911
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- Article
Type 2 diabetes and obesity: genomics and the clinic.
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- Human Genetics, 2011, v. 130, n. 1, p. 41, doi. 10.1007/s00439-011-1023-8
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- Article
SLC16A8 is a causal contributor to age-related macular degeneration risk.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00442-8
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- Article
Increased 5α-Reductase Activity and Adrenocortical Drive in Women with Polycystic Ovary Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3558, doi. 10.1210/jc.2009-0837
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- Article
What Will Genome-Wide Association Studies Mean to the Clinical Endocrinologist?
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 7, p. 2245, doi. 10.1210/jc.2009-0403
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- Article
Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries.
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- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 9, p. 3396, doi. 10.1210/jc.2008-0369
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- Article
Serum levels of retinol-binding protein 4 and adiponectin in women with polycystic ovary syndrome: associations with visceral fat but no evidence for fat mass-independent effects on pathogenesis in this condition.
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- 2008
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- Publication type:
- journal article
Global Adiposity Rather Than Abnormal Regional Fat Distribution Characterizes Women with Polycystic Ovary Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 3, p. 999, doi. 10.1210/jc.2007-2117
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- Article
Detailed analysis of variation at and around mitochondrial position 16189 in a large Finnish cohort reveals no significant associations with early growth or metabolic phenotypes at age 31 years.
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- 2007
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- journal article
Examining the candidacy of ghrelin as a gene responsible for variation in adult stature in a United Kingdom population with type 2 diabetes.
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- 2007
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- journal article
Analysis of Multiple Data Sets Reveals No Association between the Insulin Gene Variable Number Tandem Repeat Element and Polycystic Ovary Syndrome or Related Traits.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 5, p. 2988, doi. 10.1210/jc.2004-2485
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- Article
Large-Scale Analysis of the Relationship between CYP11A Promoter Variation, Polycystic Ovarian Syndrome, and Serum Testosterone.
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- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 5, p. 2408, doi. 10.1210/jc.2003-031640
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- Article
Metabolic Cardiovascular Disease Risk Factors in Women with Self-Reported Symptoms of Oligomenorrhea and/or Hirsutism: Northern Finland Birth Cohort 1966 Study.
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- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 5, p. 2114, doi. 10.1210/jc.2003-031720
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- Article
Hormonal Profile of Women with Self-Reported Symptoms of Oligomenorrhea and/or Hirsutism: Northern Finland Birth Cohort 1966 Study.
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- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 1, p. 141, doi. 10.1210/jc.2002-020982
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- Article
Delayed Metabolic and Thermogenic Response to a Mixed Meal in Normoglycemic European Women with Previous Gestational Diabetes.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 7, p. 3407, doi. 10.1210/jcem.87.7.8698
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- Article
Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2606, doi. 10.1210/jcem.87.6.8608
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- Article
Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole-Genome Sequencing.
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- 2023
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- Letter to the Editor
Toppar: an interactive browser for viewing association study results.
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- Bioinformatics, 2018, v. 34, n. 11, p. 1922, doi. 10.1093/bioinformatics/btx840
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- Article
Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
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- Nature Reviews Genetics, 2008, v. 9, n. 5, p. 356, doi. 10.1038/nrg2344
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- Article
The circadian rhythm of leptin is preserved in growth hormone deficient hypopituitary adults.
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- Clinical Endocrinology, 1998, v. 48, n. 6, p. 685, doi. 10.1046/j.1365-2265.1998.00498.x
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- Article
Genome-wide association studies: past, present and future.
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- Human Molecular Genetics, 2008, v. 17, n. R2, p. R100, doi. 10.1093/hmg/ddn298
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- Article
Genome-wide association studies: potential next steps on a genetic journey.
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- Human Molecular Genetics, 2008, v. 17, n. R2, p. R156, doi. 10.1093/hmg/ddn289
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- Article
Association between the T-381C polymorphism of the brain natriuretic peptide gene and risk of type 2 diabetes in human populations.
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- Human Molecular Genetics, 2007, v. 16, n. 11, p. 1343, doi. 10.1093/hmg/ddm084
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Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R33
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- Article
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2–q22 linked to type 2 diabetes.
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- Human Molecular Genetics, 2003, v. 12, n. 15, p. 1865, doi. 10.1093/hmg/ddg195
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- Article
The importance of Context: Uncovering Species- and Tissue-Specific Effects of Genetic Risk Variants for Type 2 Diabetes.
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- Frontiers in Endocrinology, 2016, v. 7, p. 1, doi. 10.3389/fendo.2016.00112
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- Article
Detailed Investigation of the Role of Common and Low-Frequency WFS1 Variants in Type 2 Diabetes Risk.
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- Diabetes, 2010, v. 59, n. 3, p. 741, doi. 10.2337/db09-0920
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- Article
Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians.
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- Diabetes, 2009, v. 58, n. 11, p. 2703, doi. 10.2337/db08-1805
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- Article
Interrogating Type 2 Diabetes Genome-Wide Association Data Using a Biological Pathway-Based Approach.
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- Diabetes, 2009, v. 58, n. 6, p. 1463, doi. 10.2337/db08-1378
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- Article
Reduced-Function SLC22A1 Polymorphisms Encoding Organic Cation Transporter 1 and Glycemic Response to Metformin: A GoDARTS Study.
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- Diabetes, 2009, v. 58, n. 6, p. 1434, doi. 10.2337/db08-0896
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- Article
Type 2 Diabetes Risk Alleles Are Associated With Reduced Size at Birth.
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- Diabetes, 2009, v. 58, n. 6, p. 1428, doi. 10.2337/db08-1739
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- Article