NutraHacker University - Curriculum
- Science and Tech
- Are Cavities Genetic?
- Benefits of Breastfeeding
- How to Download Nebula Genomics Whole Genome Sequencing (WGS) Raw Data
- Top 20 Galactogogues
- Understanding Microarray DNA Sequencing vs. Whole Genome Sequencing (WGS) in Nutrigenetics, Nutrigenomics, and Biohacking
- Oxytocin: The Hormone of Connection and Its Genetic Influences
- What Are Amino Acids? A Deep Dive into the Building Blocks of Life
- What Are Coding Regions? A Deep Dive into Genetic Blueprint
- What Are Hormones? A Deep Dive
- What Are Proteins? A Deep Dive
- Understanding Non-Coding Regions: Beyond the Genes
- Whole Genome Sequencing Data Formats Explained
- Whole Genome Sequencing vs. Whole Exome Sequencing: What's the Difference?
- Reviews
- Athletigen vs NutraHacker: An In-Depth Analysis of Genetic Testing Services
- Examine.com vs NutraPedia: An In-Depth Analysis
- GeneFood vs NutraHacker: A Comprehensive Comparison
- GeneticGenie vs NutraHacker. Free Methylation and Detox Report Comparison
- Genetic Lifehacks vs NutraHacker: A Comprehensive Comparison
- GeneSight vs NutraHacker: A Detailed Side-by-Side Review
- Genomind vs NutraHacker: A Comparative Analysis
- GenoPalate vs NutraHacker: A Comprehensive Guide for Personalized Nutrition Enthusiasts
- LiveWello vs NutraHacker: Navigating the World of Genetic Health Reports
- Promethease vs NutraHacker: A Detailed Comparison of Genetic Analysis Services
- Conditions
- Acne
- Adrenal Fatigue
- Asperger's or Autism Spectrum Disorder
- Awake Bruxism
- Benign Prostate Hyperplasia (BPH)
- Biotinidase Deficiency
- Brain Fog / Mild Cognitive Dysfunction
- Chronic Fatigue Syndrome (CFS) / Myalgic Encephalomyelitis
- Chronic Lyme Disease
- Crohn's Disease
- Cushing's Disease
- Depression
- Dry Eyes
- Dry Mouth
- Eczema
- Ehlers-Danlos syndrome, vascular type
- Endometriosis
- Familial adenomatous polyposis
- Familial hypercholesterolemia
- Fibromyalgia
- Generalized Anxiety
- Gout
- Hereditary breast and ovarian cancer
- Hereditary hemochromatosis
- Hereditary hemorrhagic telangiectasia
- Hereditary paraganglioma-pheochromocytoma syndrome
- Irritable Bowel Syndrome (IBS)
- Li-Fraumeni syndrome
- Lynch syndrome
- Malignant hyperthermia susceptibility
- Marfan syndrome, Loeys-Dietz syndromes, and familial thoracic aortic aneurysms and dissections
- Maturity-onset diabetes of the young
- Metabolic Syndrome / Obesity
- Migraines
- Multiple Chemical Sensitivity (MCS) - symptoms from low-level chemical exposure
- Multiple endocrine neoplasia type 2
- MYH-associated polyposis; adenomas, multiple colorectal, FAP type 2; colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas
- Nighttime Urination
- Ornithine transcarbamylase deficiency
- Overactive Bladder
- Peutz-Jeghers syndrome
- Polycystic Ovary Syndrome (PCOS)
- Pompe Disease
- Pre Menstrual Syndrome (PMS)
- Raynaud's Phenomenon
- Restless Legs Syndrome
- Romano-Ward long-QT syndrome types 1, 2, and 3, Brugada syndrome
- Sleep Apnea
- Sleep Bruxism
- Social Anxiety
- Sulfate/Sulfite Sensitivity
- Von Hippel–Lindau syndrome
- Genes
- 5HT1A
- 5HT1B
- 5HT2A
- 5HT3B
- 5-HTTLPR
- ABCB1
- ACE
- ACVRL1
- ADM
- ADRA2A
- ADRB1
- ADRB2
- AMELX
- AMPD1
- APC
- AQP1
- BDNF
- BRCA1
- BRCA2
- BTD
- CA6
- CACNA1S
- CILP
- CKM
- CLOCK
- CNR1
- CNR2
- COL1A1
- COL3A1
- COL5A1
- COL6A1
- COL26A1
- COMT
- CREB1
- CRHBP
- CRHR1
- CRHR2
- CYP1A2
- CYP2C9
- CYP2C19
- DEFB1
- DIO1
- DRD2
- DRD3
- DRD4
- EDN1
- ELOVL5
- ENAM
- FBN1
- FADS1
- FKBP5
- FUT2
- GAA
- GLUT2
- GNB3
- GPX1
- GPX3
- GRIA1
- GRIA3
- GRIK2
- GRIN3A
- GSK3B
- HFE
- HNF1A
- IL6
- IL11
- IL-1beta
- MAOA
- MAOB
- MSH2
- MSH6
- MTHFD1
- MTHFR
- MTR
- MTRR
- MUTYH
- NET
- NOS3
- OTC
- PEMT
- RET
- RGS2
- RYR1
- SCN5A
- SDHAF2
- SLC12A6
- SLC17A5
- SLC26A4
- SLC30A2
- SLC4A1
- SLC5A5
- SLCO1B1
- SMPD1
- SOD2
- STK11
- TGFBR2
- TMPRSS2
- TPH
- TP53
- UST
- VDR
- VHL