Genomics
22AMY1A Polymorphism
- 2007.10 - Diet and the evolution of human amylase gene copy number variation.pdf
- 2012.01 - Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos.pdf
- 2013.11 - Plant foods in the Upper Palaeolithic at DolniÌ Vӗstonice.pdf
- 2014.01 - The complete genome sequence of a Neandertal from the Altai Mountains.pdf
- 2016.11 - Selective sweep on human amylase genes postdates the split with Neanderthals.pdf
- 2017.06 - Starch Digestion–Related Amylase Genetic Variant Affects 2-Year Changes in Adiposity in Response to Weight-Loss Diets.pdf
- 2018.12 - Perspective - DNA Copy Number Variations in Cardiovascular Diseases.pdf
- 2019.04 - Human Salivary Amylase Gene Copy Number Impacts Oral and Gut Microbiomes.pdf
- 2019.04 - Human Salivary Amylase Gene Copy Number Impacts Oral and Gut Microbiomes.pdf
- 2020.04 - Salivary AMY1 Copy Number Variation Modifies Age-Related Type 2 Diabetes Risk.pdf
- 2020.11 - Alpha-amylase 1A copy number variants and the association with memory performance and Alzheimer’s dementia.pdf
- 2021.01 - Interaction Effect Between Copy Number Variation in Salivary Amylase Locus (AMY1) and Starch Intake on Glucose Homeostasis in the Malmö Diet and Cancer Cohort.pdf
- 2021.02 - DNA copy number variation - Main characteristics, evolutionary significance, and pathological aspects.pdf
- 2021.06 - Influence of AMY1A copy number variations on obesity and other cardiometabolic risk factors - A review of the evidence - abstract.pdf
- 2021.07 - VariabiliteÌ et eÌvolution du pheÌnotype quantiteÌ d’amylase salivaire.pdf
- 2022.05 - Impact of salivary and pancreatic amylase gene copy numbers on diabetes, obesity, and functional profiles of microbiome in Northern Japanese population.pdf
- 2023.12 - Dental caries prevalence and severity positively associate with AMY1 gene copy number - abstract.pdf
- 2024.09 - Recurrent evolution and selection shape structural diversity at the amylase locus.pdf
- 2024.10 - Global diversity, recurrent evolution, and recent selection on amylase structural haplotypes in humans.pdf
- 2024.10 - Reconstruction of the human amylase locus reveals ancient duplications seeding modern-day variation.pdf
- 2025.02 - AMY1 gene copy number associated with xerostomia and Sjögren’s syndrome - A cross-sectional study.pdf
- 2025.07 - The association between salivary amylase gene copy number and enzyme activity with type 2 diabetes status | PLOS One.pdf
1ApoC3 Polymorphism
60ApoE Polymorphism
- 1995.01 - O. Apolipoprotein E Isoform Phenotype and LDL Subclass Response to a Reduced-Fat Diet.pdf
- 1995.11 - Apolipoprotein E allele frequencies in a South African Indian female population - abstract - edited.pdf
- 1996.11 - The apolipoprotein E polymorphism in Greenland Inuit in its global perspective - abstract.pdf
- 1997.08 - High Frequency of the Apolipoprotein E *4 Allele in African Pygmies and Most of the African Populations in Sub-Saharan Africa.pdf
- 1997.12 - Absence of the E2 allele of apolipoprotein in Amerindians.pdf
- 1999.08 - Heterogeneity of the frequency of the apolipoprotein E-epsilon 4 allele in the European population - abstract - edited.pdf
- 2004.03 - U. Meat-adaptive genes and the evolution of slower aging in humans - abstract edited.pdf
- 2004.10 - A. The effect of dietary fat on LDL size is influenced by apolipoprotein E genotype in healthy subjects.pdf
- 2006.01 - D. APOE epsilon4 is not associated with Alzheimer's disease in elderly Nigerians.pdf
- 2006.01 - E. Cholesterol, APOE genotype, and Alzheimer disease.pdf
- 2006.12 - H. Apolipoprotein E e4 Allele Affects Risk of Hyperhomocysteinemia in the Elderly.pdf
- 2010.04 - B. Selection on Alleles Affecting Human Longevity and Late-Life Disease - The Example of Apolipoprotein E.pdf
- 2010.05 - R. Apolipoprotein E Allelic Frequency Altered in Women with Early-onset Breast Cancer.pdf
- 2011.03 - I. The emergence of human-evolutionary medical genomics.pdf
- 2011.03 - J. How evolutionary principles improve the understanding of human health and disease.pdf
- 2012.05 - K. Exercise Engagement as a Moderator of the Effects of APOE Genotype on Amyloid Deposition.pdf
- 2012.10 - S. The Apolipoprotein E (APOE) Gene Appears Functionally Monomorphic in Chimpanzees (Pan troglodytes).pdf
- 2013.05 - G. APOE genotype modifies the association between plasma omega-3 fatty acids and plasma lipids in the Multi-Ethnic Study of Atherosclerosis (MESA).pdf
- 2014.05 - T. Exercise, APOE genotype, and the evolution of the human lifespan.pdf
- 2014.09 - Q. Dietary fat composition and dementia risk.pdf
- 2016.02 - L. High-Fat Diet Changes Hippocampal Apolipoprotein E (apoE).pdf
- 2016.03 - F. Impact of Genotype on EPA and DHA Status and Responsiveness to Increased Intakes.pdf
- 2016.06 - Apolipoprotein E - From cardiovascular disease to neurodegenerative disorders.pdf
- 2016.10 - Apolipoprotein E Gene Variants and Risk of Coronary Heart Disease - A Meta-Analysis.pdf
- 2017.03 - C. Apolipoprotein E4 and Insulin Resistance Interact to Impair Cognition and Alter the Epigenome and Metabolome.pdf
- 2017.06 - Evolution of human apolipoprotein E (APOE) isoforms-Gene structure, protein function and interaction with dietary factors.pdf
- 2017.06 - M. Apolipoprotein E - A Multifunctional Protein with Implications in Various Pathologies.pdf
- 2017.07 - N. ApoE Genotype Influences Insulin Resistance.pdf
- 2017.12 - P. Apolipoprotein E4 mediates insulin resistance-associated cerebrovascular dysfunction.pdf
- 2018.04 - V. Association of apolipoprotein E gene polymorphisms with blood lipids and their interaction with dietary factors.pdf
- 2018.10 - W. Clinical Application of APOE in Alzheimer's Prevention - A Precision Medicine Approach.pdf
- 2019.01 - Ketogenic diet rescues cognition in ApoE4þ patient with mild Alzheimer's disease - A case study (K).pdf
- 2019.01 - X. The ApoE ε4 Isoform - Can the Risk of Diseases be Reduced by Environmental Factors?.pdf
- 2019.01 - Y. Modulating Effect of Diet on Alzheimer’s Disease.pdf
- 2019.03 - The Genetic Variability of APOE in Different Human Populations and Its Implications for Longevity (Burkina Faso).pdf
- 2019.04 - APOE genotype influences the gut microbiome structure and function in humans and mice.pdf
- 2019.11 - ApoE4-Induced Cholesterol Dysregulation and Its Brain Cell Type-Specific Implications in the Pathogenesis of Alzheimer’s Disease (K).pdf
- 2020.06 - Cholesterol and Alzheimer’s Disease Risk - A Meta-Meta-Analysis (K).pdf
- 2020.06 - Refined carbohydrate-rich diet is associated with long-term risk of dementia and Alzheimer’s disease in apolipoprotein E 4 allele carriers.pdf
- 2020.08 - ApolipoproteinE (APOE) genotype-associated disease risks- aphenome-wide, registry-based, case-control study utilising the UK Biobank.pdf
- 2020.10 - APOE2 is associated with longevity independent of Alzheimer’s disease.pdf
- 2020.11 - APOE e4 Genotype Predicts Severe COVID-19 in the UK Biobank Community Cohort.pdf
- 2021.04 - Age and sex specific effects of APOE genotypes on ischemic heart disease and its risk factors in the UK Biobank.pdf
- 2021.04 - Precision Nutrition for Alzheimer’s Prevention in ApoE4 Carriers (K).pdf
- 2021.04 - Precision Nutrition for Alzheimer’s Prevention in ApoE4 Carriers.pdf
- 2021.06. Cholesterol and Alzheimer’s Disease; From Risk Genes to Pathological Effects (K).pdf
- 2021.07 - APOE Genotype and Alzheimer’s Disease - The Influence of Lifestyle and Environmental Factors.pdf
- 2021.10 - Apolipoprotein E and Alzheimer’s disease.pdf
- 2022.11 - Associations of Alzheimer Disease–Protective APOE Variants With Age-Related Macular Degeneration.pdf
- 2023.06 - Contribution of APOE Genetic Variants to Dyslipidemia (K).pdf
- 2023.08 - Alzheimer’s disease phenotype based upon the carrier status of the apolipoprotein E ε4 allele (K).pdf
- 2023.08 - Apolipoprotein-ε4 is associated with higher fecundity in a natural fertility population.pdf
- 2023.12 - APOE Genotype and Alzheimer Disease Risk Across Age, Sex, and Population Ancestry (K).pdf
- 2024.01 - The selection landscape and genetic legacy of ancient Eurasians.pdf
- 2024.02 - Apolipoprotein E-ε2 and Resistance to Atherosclerosis in Midlife- The PESA Observational Study.pdf
- 2024.03 - How are APOE4, changes in body weight, and longevity related? Insights from a causal mediation analysis.pdf
- 2024.05 - Dietary fats and the APOE-e4 risk allele in relation to cognitive decline - A longitudinal investigation in a biracial population sample.pdf
- 2024.07 - Apolipoprotein E and Alzheimer's disease pathology in African American older adults - edited.pdf
- High Cholesterol APOE Gene and Diet.pdf
- Steven Gundry - Dietary Management of the Apo E 4.pdf
2BDNF Polymorphism
2CBS Polymorphism
6COMT Polymorphism
- 2001.09 - C. Cathecol-O-Methyltransfera-mediated metabolism of cathecol estrogens.pdf
- 2005.06 - E. COMT Polymorphisms and Anxiety-Related Personality Traits.pdf
- 2006.06 - F. Associations between the COMT Val Met polymorphism early life stress and personality among healthy adults.pdf
- 2014.05 - B. COMT Val158Met and PPARγ Pro12Ala polymorphisms and susceptibility to Alzheimer's disease.pdf
- 2014.08 - D. Genetic polymorphisms affecting susceptibility to mercury neurotoxicity in children.pdf
- 2016.05 - A. Significant association of catechol-O-methyltransferase Val158Met polymorphism with bladder cancer.pdf
4CPT1A Polymorphism
- 2009.04 - The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations - abstract.pdf
- 2012.01 - Genetic polymorphisms in carnitine palmitoyltransferase 1A gene are associated with variation in body composition and fasting lipid traits in Yup'ik Eskimos.pdf
- 2019.01 - Carnitine Palmitoyl Transferase, Type 1A (CPT1A) - The Arctic Variant - abstract.pdf
- 2023.12 - The CPT1A Arctic variant - Perspectives of community members and providers in two Alaska tribal health settings.pdf
4CTLA-4 Polymorphism
- 2005.09 - A. Genetic susceptibility in thyroid autoimmunity.pdf
- 2015.09 - D. CTLA-4 and MDR1 polymorphisms increase the risk for ulcerative colitis - A meta-analysis.pdf
- 2015.11 - B. Immunogenetics of Autoimmune Thyroid Diseases - A comprehensive Review.pdf
- 2017.01 - C. General and Specific Genetic Polymorphism of Cytokines-Related Gene in AITD.pdf
2CYP19A1 Polymorphism
2CYP1A1 Polymorphism
3CYP1A2 Polymorphism
3CYP1B1 Polymorphism
- 2010.02 - A. Association of CYP1B1 Polymorphisms with Breast Cancer - A Case-Control Study in the Han Population.pdf
- 2015.01 - B. Cytochrome P1B1 (CYP1B1) polymorphisms and cancer risk - A meta-analysis of 52 studies.pdf
- 2017.03 - C. Genetic polymorphisms of phase I metabolizing enzyme genes, their interaction with lifetime grilled and smoked meat intake, and breast cancer incidence.pdf
53DIO2 Polymorphism
- 1997.08 - High Frequency of the Apolipoprotein E*4 Allele in African Pygmies and Most of the African Populations in Sub-Saharan Africa.pdf
- 2002.02 - Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases.pdf
- 2009.04 - Novel insights into thyroid hormones from the study of common genetic variation.pdf
- 2009.05 - Association of genetic polymorphisms in the type II deiodinase gene with bipolar disorder.pdf
- 2009.05 - Common Variation in the DIO2 Gene Predicts Response to Combination Therapy in Hypothyroid Patients.pdf
- 2009.05 - For Some, L-Thyroxine Replacement Might Not Be Enough - A Genetic Rationale.pdf
- 2010.01 - Association of the type 2 deiodinase Thr92Ala polymorphism with type 2 diabetes - Case–control study and meta-analysis.pdf
- 2010.02 - The Type 2 Deiodinase Thr92Ala Polymorphism and Bone Density.pdf
- 2010.06 - Association of the type 2 deiodinase Thr92Ala polymorphism with type 2 diabetes - Case-control study and meta-analysis.pdf
- 2010.11 - The Thr92Ala 5' type 2 deiodinase gene polymorphism is associated with a delayed triiodothyronine secretion.pdf
- 2012.03 - Does Combination T4 and T3 therapy make sense.pdf
- 2012.06 - Thyroid hormone replacement therapy - three 'simple' questions, complex answers.pdf
- 2012.09 - Prevalence of Dio2T92A polymorphism and its association with thyroid autoimmunity.pdf
- 2014.01 - Earliest evidence for caries and exploitation of starchy plant foods in Pleistocene hunter-gatherers from Morocco.pdf
- 2014.03 - Paradigm shifts in thyroid hormone replacement therapies for hypothyroidism.pdf
- 2015.01 - Prevalent polymorphism in thyroid hormone-activating enzyme leaves a genetic fingerprint.pdf
- 2015.04 - Genetic determination of the hypothalamic-pituitary-thyroid axis - Where do we stand?.pdf
- 2015.05 - Type II deiodinase polymorphisms and serum thyroid hormone levels in patients with mild cognitive impairment.pdf
- 2015.06 - Association of the DIO2 gene single nucleotide polymorphisms with recurrent depressive disorder.pdf
- 2015.11 - Scope and limitations of iodothyronine deiodinases in hypothyroidism.pdf
- 2016.01 - The History and Future of Treatment of Hypothyroidism.pdf
- 2016.01 - Update on the treatment of hypothyroidism.pdf
- 2016.09 - The Type 2 Deiodinase Thr92Ala Polymorphism Is Associated with Worse Glycemic Control in Patients with Type 2 Diabetes Mellitus.pdf
- 2016.09 - Type 2 Deiodinase Disruption in Astrocytes Results in Anxiety-Depressive-Like Behavior in Male Mice.pdf
- 2016.10 - Is a Normal TSH Synonymous with Euthyroidism in Levothyroxine Monotherapy?.pdf
- 2016.11 - D2 Thr92Ala thyroid hormone levels and biochemical hypothyroidism in preeclampsia.pdf
- 2017.02 - D2-Thr92Ala, thyroid hormone levels and biochemical hypothyroidism in preeclampsia.pdf
- 2017.05 - DIO2 Thr92Ala Reduces Deiodinase-2 Activity and Serum-T3 Levels in Thyroid-Deficient Patients.pdf
- 2017.07 - Hypothyroid Patients Encoding Combined MCT10 and DIO2 Gene Polymorphisms May Prefer L-T3 L-T4 Combination Treatment.pdf
- 2017.12 - T4 T3 combination therapy - Is there a true effect?.pdf
- 2018.01 - Association between genetic polymorphism and levothyroxine bioavailability in hypothyroid patients.pdf
- 2018.02 - A Common DIO2 Polymorphism And Alzheimer's Disease Dementia in African And European Americans.pdf
- 2018.03 - Association between genetic polymorphism and levothyroxine bioavailability in hypothyroid patients.pdf
- 2018.07 - Pathophysiological relevance of deiodinase polymorphism.pdf
- 2018.08 - Clinical significance of type 2 iodothyronine deiodinase polymorphism.pdf
- 2019.01 - Type 2 deiodinase polymorphism causes ER stress and hypothyroidism in the brain.pdf
- 2019.08 - Individualised requirements for optimum treatment of hypothyroidism - Complex needs, limited options.pdf
- 2019.12 - Evolutionary basis for the human diet- consequences for human health.pdf
- 2020.01 - Iodothyronine deiodinases and reduced sensitivity to thyroid hormones.pdf
- 2020.05 - Thr92Ala polymorphism in the type 2 deiodinase gene- an evolutionary perspective.pdf
- 2020.06 - Targeting the right population for T3 T4 combined therapy- where are we now and where to next?.pdf
- 2021.06 - Comparative Effectiveness of Levothyroxine, Desiccated Thyroid Extract, and Levothyroxine Liothyronine in Hypothyroidism.pdf
- 2022.03 - Improvement of depression in a patient with hypothyroidism and deiodinase polymorphism with LT3 Therapy.pdf
- 2022.05 - Heterozygote Advantage of the Type II Deiodinase Thr92Ala Polymorphism on Intrahospital Mortality of COVID-19.pdf
- 2022.06 - Optimal Hormone Replacement Therapy in Hypothyroidism - A Model Predictive Control Approach.pdf
- 2022.09 - Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children - A Case-Control Study.pdf
- 2023.02 - Type 2 deiodinase Thr92Ala polymorphism and aging are associated with a decreased pituitary sensitivity to thyroid hormone.pdf
- 2023.03 - Association between DIO2 Thr92Ala polymorphism and hypertension in patients with hypothyroidism - Korean Genome and Epidemiology Study.pdf
- 2023.04 - The Physiological Functions and Polymorphisms of Type II Deiodinase.pdf
- 2024.05 - Gene polymorphisms and thyroid hormone signaling - Implication for the treatment of hypothyroidism.pdf
- 2025.03 - A feasibility double-blind trial of levothyroxine vs. levothyroxine-liothyronine in postsurgical hypothyroidism.pdf
- 2025.04 - Combined LT3 and LT4 therapy for precision medicine- easier with TTCombo system.pdf
- Breakthrough Discovery - Need for T3 could be genetic Dr Gary Pepper.pdf
7FADS1-2 Polymorphisms
- 2008.11 - Genetic variants of the FADS1 FADS2 gene cluster are associated with altered (n-6) and (n-3) essential fatty acids in plasma and erythrocyte phospholipids in women during pregnancy and in breast milk during lactation - abstract.png
- 2010.02 - Genetic variants of the FADS1 FADS2 gene cluster as related to essential fatty acid metabolism.pdf
- 2015.09 - Greenlandic Inuit show genetic signatures of diet and climate adaptation.pdf
- 2020.05 - Fatty acid profile and estimated desaturase activities in whole blood are associated with metabolic health.pdf
- 2020.09 - FADS genetic and metabolomic analyses identify the ∆5 desaturase (FADS1) step as a critical control point in the formation of biologically important lipid.pdf
- 2023.01 - The role of FADS gene polymorphic variants in adaptation to the Northern climatic conditions and metabolic disorders.pdf
- 2023.03 - Dietary Fatty Acids and Inflammation - Focus on the n-6 Series.pdf
35FUT2 Polymorphism
- 2010.06 - Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease (CD).pdf
- 2011.05 - Fucosyltransferase 2 non-secretor and low secretor status predicts severe outcomes in premature infants (NEC).pdf
- 2011.05 - Secretor Genotype (FUT2 gene) Is Strongly Associated with the Composition of Bifidobacteria in the Human Intestine (ID)°.pdf
- 2011.10 - FUT2 Nonsecretor Status Links Type 1 Diabetes Susceptibility and Resistance to Infection.pdf
- 2011.11 - FUT2 Nonfunctional Variant - A “Missing Link†Between Genes and Environment in Type 1 Diabetes? (ID)°.pdf
- 2014.06 - ABO histo-blood group might modulate predisposition to Crohn's disease and affect disease behavior.pdf
- 2014.09 - Innate lymphoid cells regulate intestinal epithelial cell glycosylation (ID).pdf
- 2014.11 - Reprograming of gut microbiome energy metabolism by the FUT2 Crohn’s disease risk polymorphism (CD).pdf
- 2015.03 - N. FUT2 - Filling the gap between genes and environment in Behçet's disease? - abstract.pdf
- 2015.04 - Maternal fucosyltransferase 2 status affects the gut bifidobacterial communities of breastfed infants (ID)°.pdf
- 2015.06 - Fucosyltransferase 2 - A genetic risk factor for primary sclerosing cholangitis and Crohn's disease--a comprehensive review - abstract edited (CD)°.pdf
- 2016.05 - Gastric mucin glycosylation is shaped by FUT2 activity and functionally impacts Helicobacter pylori binding (HP).pdf
- 2016.11 - Epithelial glycosylation in gut homeostasis and inflammation (IBD).pdf
- 2017.06 - Recent advances in gut immunology (ID).pdf
- 2017.11 - Infection's sweet tooth - How glycans mediate infection and disease susceptibility (ID)°.pdf
- 2018.09 - FUT2 secretor genotype and susceptibility to infections and chronic conditions in the ALSPAC cohort.pdf
- 2018.09 - Review of the Clinical Experiences of Feeding Infants Formula Containing the Human Milk Oligosaccharide 2′-Fucosyllactose.pdf
- 2018.10 - Impact of carbohydrate substrate complexity on the diversity of the human colonic microbiota.pdf
- 2019.02 - FUT2 gene variants and reported respiratory and gastrointestinal illnesses during infancy.pdf
- 2019.12 - Fucosyltransferase Gene Polymorphisms and Lewisb-Negative Status Are Frequent in Swedish Newborns, With Implications for Infectious Disease Susceptibility and Personalized Medicine.pdf
- 2020.03 - The Impact of Human Genetic Polymorphisms on Rotavirus Susceptibility, Epidemiology, and Vaccine Take.pdf
- 2020.10 - Blends of Human Milk Oligosaccharides Confer Intestinal Epithelial Barrier Protection In Vitro.pdf
- 2020.12 - Can the FUT2 Non-secretor Phenotype Associated With Gut Microbiota Increase the Children Susceptibility for Type 1 Diabetes? A Mini Review.pdf
- 2021.03 - A comparison of the in vitro effects of 2'Fucosyllactose and lactose on the composition and activity of gut microbiota from infants and toddlers.pdf
- 2021.10 - 2'-Fucosyllactose ameliorates chemotherapy-induced intestinal mucositis by protecting intestinal epithelial cells against apoptosis.pdf
- 2021.10 - The Effects of Human Milk Oligosaccharides on Gut Microbiota, Metabolite Profiles and Host Mucosal Response in Patients with Irritable Bowel Syndrome.pdf
- 2022.01 - Recent advances on 2'-fucosyllactose - Physiological properties, applications, and production approaches.pdf
- 2022.06 - 2'-Fucosyllactose increases the abundance of Blautia in the presence of extracellular Fucosidase-possessing bacteria.pdf
- 2022.06 - FUT2 gene as a genetic susceptible marker of infectious diseases - A Review.pdf
- 2022.06 - Human Milk oligosaccharides and lactose differentially affect infant gut microbiota and intestinal barrier in vitro.pdf
- 2022.07 - ABO, secretor, and Lewis carbohydrate histo-blood groups are associated with autoimmune neutropenia of early childhood in Danish patients.pdf
- 2023.01 - Gut Microbiome Composition and Metabolic Capacity Differ by FUT2 Secretor Status in Exclusively Breastfed Infants.pdf
- 2023.03 - Functional effects of human milk oligosaccharides (HMOs).pdf
- 2023.07 - An Extensively Hydrolyzed Formula Supplemented with Two Human Milk Oligosaccharides Modifies the Fecal Microbiome and Metabolome in Infants with Cow’s Milk Protein Allergy.pdf
- 2023.10 - Effects of 2'-fucosyllactose on the composition and metabolic activity of intestinal microbiota from piglets after in vitro fermentation.pdf
6GPX1 Polymorphism
- 2012.05 - A. Inherited variations in the SOD and GPX gene families and cancer risk.pdf
- 2014.10 - B. Polymorphisms of glutathione peroxidase 1 GPX1 Pro198Leu and catalase CAT C 262T in women with spontaneous abortion.pdf
- 2016.07 - C. Functional polymorphisms in antioxidant genes in Hurthle cell thyroid neoplasm - an association of GPX1 polymorphism and recurrent Hurthle cell thyroid carcinoma.pdf
- 2017.08 - D. Glutathione peroxidases as oncotargets.pdf
- 2018.10 - E. Genetic Polymorphisms of Catalase and GlutathionePeroxidase-1 in Keratoconus.pdf
- 2019.11 - F. Association of GPx1 P198L and CAT C-262T Genetic Variations With Polycystic Ovary Syndrome in Chinese Women.pdf
2GSTM1 Polymorphism
2GSTP1 Polymorphism
3GSTT1 Polymorphism
- 2009.11 - A. Functional genetic variants of glutathione S-transferase protect against serum ascorbic acid deficiency.pdf
- 2014.01 - B. GSTT1 genotype interacts with vitamin C intake to influence serum ascorbic acid levels.pdf
- 2018.01 - C. Polymorphism of glutathione S-transferase M1 and T1 genes and susceptibility to psoriasis disease.pdf
12LCT Polymorphism
- 2009.04 - Convergent adaptation of human lactase persistence in Africa and Europe.pdf
- 2009.08 - The Origins of Lactase Persistence in Europe.pdf
- 2011.01 - Lactase Persistence SNPs in African Populations Regulate Promoter Activity in Intestinal Cell Culture.pdf
- 2012.07 - A. Lactose intolerance - Diagnosis, genetic, and clinical factors.pdf
- 2012.12 - An Evolutionary Whodunit - How Did Humans Develop Lactose Tolerance?.pdf
- 2014.04 - Genetic Origins of Lactase Persistence and the Spread of Pastoralism in Africa.pdf
- 2016.02 - B. Lactase persistence versus lactose intolerance - Is there an intermediate phenotype? - abstract edited.pdf
- 2017.06 - C. Lactose Intolerance (LCT-13910C>T) Genotype Is Associated with Plasma 25-Hydroxyvitamin D Concentrations in Caucasians - abstract edited.pdf
- 2017.06 - Country, regional, and global estimates for lactose malabsorption in adults - A systematic review and meta-analysis.pdf
- 2017.09 - The Relationship Between the Human Genome and Microbiome Comes into View.pdf
- 2019.08 - Association of Lactase Persistence Genotypes (rs4988235) and Ethnicity with Dairy Intake in a Healthy U.S. Population***.pdf
- 2020.09 - Genetics of Lactose Intolerance - An Updated Review and Online Interactive World Maps of Phenotype and Genotype Frequencies.pdf
3MAO-A Polymorphism
- 2013.08 - A. MAOA and MAOB polymorphisms and anger-related traits in suicidal participants and controls.pdf
- 2014.12 - C. Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.pdf
- 2017.10 - B. Role of preferentially transmitted monoamine oxidase gene variants in behavioral problems of male ADHD probands.pdf
7MTHFR Polymorphism
- 2007.12 - G. Nutrigenomics - The Genome-Food Interface.pdf
- 2013.06 - F. Use of azathioprine and the risk of cancer in inflammatory bowel disease.pdf
- 2015.01 - A. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism - Epidemiology metabolism and the associated diseases.pdf
- 2016.08 - B. Association of MTHFR A1298C polymorphism with breast cancer and-or ovarian cancer risk - An updated meta-analysis.pdf
- 2016.11 - C. Geographical and ethnic distribution of MTHFR gene polymorphisms and their associations with diseases among Chinese population.pdf
- 2017.01 - D. MTHFR C677T polymorphism and breast ovarian cancer risk - A meta-analysis of 19 - 260 patients and 26364 controls.pdf
- 2017.06 - E. Investigation of Methylenetetrahydrofolate Reductase C677T Polymorphism and Human Papilloma Virus Genotypes in Iranian Breast Cancer.pdf
2MTR-MTRR Polymorphisms
3NQO1 Polymorphism
- 2014.12 - A. A Review of NAD(P)H Quinone Oxidoreductase 1 (NQO1) - A Multifunctional Antioxidant Enzyme.pdf
- 2017.08 - B. Functions of NQO1 in Cellular Protection and CoQ10 Metabolism and its Potential Role as a Redox Sensitive Molecular Switch.pdf
- 2017.09 - C. NQO1 C609T polymorphism and lung cancer susceptibility.pdf
7OGG1 Polymorphism
- 2013.10 - A. Genotype-phenotype analysis of S326C OGG1 polymorphism - Risk factor for oxidative pathologies.pdf
- 2013.10 - G. Alzheimer’s Disease Associated Polymorphisms in Human OGG1 Alter Catalytic Activity and Sensitize Cells to DNA Damage.pdf
- 2015.02 - B. A systematic review and meta-analysis of the association between OGG1 Ser326Cys polymorphism and cancers.pdf
- 2016.02 - C. Association between OGG1 Ser326Cys polymorphism and risk of upper aero-digestive tract and gastrointestinal cancers.pdf
- 2017.06 - D. Association between the 8-oxoguanine DNA glycosylase gene Ser326Cys polymorphism and age-related cataract.pdf
- 2017.07 - E. The hOGG1 Ser326Cys Gene Polymorphism and Breast Cancer Risk in Saudi Population.pdf
- 2018.01 - F. Effects of the Ser326Cys Polymorphism in the DNA Repair OGG1 Gene on Cancer, Cardiovascular, and All-Cause Mortality.pdf
4OLR1 Polymorphism
- 2013.04 - The role of OLR1 polymorphisms in determining the risk and prognosis of ischemic stroke in a Chinese population - abstract.pdf
- 2015.12 - The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke - Evidence from a Meta-Analysis.pdf
- 2017.10 - Scavenger Receptor LOX1 Genotype Predicts Coronary Artery Disease in Patients With Familial Hypercholesterolemia.pdf
- 2018.07 - OLR1 Gene Polymorphism and Oxidized LDL Levels in Metabolic Syndrome in Indian Population.pdf
3PEMT Polymorphism
5PON1 Polymorphism
- 2010.03 - A. Protective Effect of Paraoxonase 1 Gene Variant Gln192Arg in Age-Related Macular Degeneration.pdf
- 2017.03 - B. PON1 L55M polymorphism might contribute to the risk of cancer.pdf
- 2017.10 - C. Organophosphate pesticides and PON1 L55M in Parkinson's disease progression.pdf
- 2017.10 - D. Role of polyphenols and polyphenol-rich foods in the modulation of PON1 activity and expression.pdf
- 2017.12 - E. Joint Effects of PON1 Polymorphisms and VegetableIntake on Ischemic Stroke - A Family-Based Case Control Study.pdf
4SIRT3
- 2011.03 - A. Sirtuins at a glance.pdf
- 2012.07 - B. Sirtuins 1 & 3 - physiological Modulators of Metabolism.pdf
- 2013.04 - The Role of Sirtuins in Alzheimer's Disease.pdf
- 2013.07 - C. Interaction of Sirt3 with OGG1 contributes to repair of mitochondrial DNA and protects from apoptotic cell death under oxidative stress.pdf
6SOD2 Polymorphism
- 2005.04 - A. Is the Val16Ala manganese superoxide dismutase polymorphism associated with the aging process.pdf
- 2009.08 - B. Regulation of superoxide dismutase genes - Implications in disease.pdf
- 2014.08 - Manganese superoxide dismutase in carcinogenesis - Friend or foe?.pdf
- 2015.01 - C. Manganese superoxide dismutase and oxidative stress modulation.pdf
- 2015.09 - D. Superoxide dismutase 2 gene and cancer risk - Evidence from an updated meta-analysis.pdf
- 2019.09 - E. Decoding the role of SOD2 in sickle cell disease.pdf
2SULT1A1 Polymorphism
3SUOX Polymorphism
3TCF7L2 Polymorphism
- 2009.02 - Association between TCF7L2 gene polymorphisms and susceptibility to Type 2 Diabetes Mellitus - A large Human Genome Epidemiology (HuGE) review and meta-analysis.pdf
- 2009.04 - TCF7L2, dietary carbohydrate, and risk of type 2 diabetes in US women.pdf
- 2015.09 - Association of TCF7L2 Genetic Polymorphisms with Type 2 Diabetes Mellitus in the Uygur Population of China.pdf
14VDR Polymorphism
- 2005.01 - M. Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population.pdf
- 2009.11 - A. Vitamin D Receptor gene polymorphism may predict response to vitamin D intake and bone turnover (VD).pdf
- 2013.04 - B. Polymorphisms in the vitamin D receptor gene and risk of autoimmune thyroid diseases - A meta-analysis (HT).pdf
- 2013.05 - C. Vitamin D in the etiopathogenesis of autoimmune thyroiditis (HT).pdf
- 2013.06 - D. Vitamin D receptor gene ApaI, TaqI, FokI and BsmI polymorphisms in a group of Turkish patients with Hashimoto's thyroiditis (HT).pdf
- 2014.01 - L. Vitamin D Levels in Serum, Vitamin D Receptor Polymorphisms and Semen Quality Correlations.pdf
- 2014.07 - E. Environmental, personal, and genetic determinants of response to vitamin D supplementation in older adults (VD).pdf
- 2016.04 - F. Association of vitamin D receptor gene polymorphisms and serum 25-hydroxyvitamin D levels with Crohn's disease in Chinese patients (CD).pdf
- 2016.10 - G. Effects of Genetic and Nongenetic Factors on Total and Bioavailable 25(OH)D Responses to Vitamin D Supplementation (VD).pdf
- 2017.01 - H. Does vitamin D play a role in autoimmune endocrine disorders A proof of concept (HT).pdf
- 2017.01 - I. Vitamin D in Autoimmunity - Molecular Mechanisms and Therapeutic Potential (HT)(CD).pdf
- 2017.02 - J. The association between vitamin D receptor polymorphisms and serum 25-hydroxyvitamin D levels with ulcerative colitis in Chinese Han population (UC).pdf
- 2017.07 - K. Circulating 25-Hydroxy Vitamin D Relative to Vitamin D Receptor Polymorphism after Vitamin D3 Supplementation in Breast Cancer Women.pdf
- 2017.11 - N. Vitamin D Axis in Inflammatory Bowel Diseases - Role, Current Uses and Future Perspectives.pdf
