eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

Browse by Topic

  1. Biochemistry
  2. Bioethics & Philosophy
  3. Cell Biology
  4. Developmental Biology
  5. Ecology
  6. Evolution & Diversity of Life
  7. Genetics & Disease
    1. Bioinformatics and Genetic Disease
    2. Cancer Genetics
    3. Chromosomal Disorders
    4. Epigenetics and Disease
    5. Forensic Genetics
    6. Gene and Genome Structure and Organisation
    7. Gene Expression Profiling of Genetic Disease
    8. Gene Mapping by Disease Association
    9. Gene Therapy
    10. General Genetics and Disease
    11. Genetic Counseling
    12. Genetic Models
    13. Genetics of Intelligence and Cognition
    14. Genomic Disorders
    15. Inter-Individual Variation and Polymorphism
      1. Absolute Pitch: Genetics
      2. Addiction and Genes: Animal Models
      3. Adoption Strategies
      4. Allele Spectrum of Human Genetic Disease
      5. Allelic and Locus Heterogeneity
      6. Analysis of Gene–Gene Interactions Underlying Human Disease
      7. Anticipation
      8. Assessing Genetic Variants of Uncertain Significance: The Example of Breast Cancer
      9. Assessing Genetic Variants of Uncertain Significance: The Example of Lynch Syndrome
      10. Balancing Selection in Human Evolution
      11. Balancing Selection in the Human Genome
      12. Behaviour Genetics – Human
      13. Behavioural Genetics in the Postgenomics Era
      14. Bioethics: ELSI
      15. You have free access to this content
        Bioinformatics
      16. Blood Group Genetics
      17. Blood Groups: Molecular Genetic Basis
      18. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      19. Characterising Structural Variation by Means of Next-Generation Sequencing
      20. Chromosome 2
      21. Chromosome 3
      22. Chromosome 4
      23. Chromosome 5
      24. Chromosome 6
      25. Chromosome 7
      26. Chromosome 9
      27. Chromosome 1
      28. Chromosome 10
      29. Chromosome 11
      30. Chromosome 12
      31. Chromosome 13
      32. Chromosome 14
      33. Chromosome 16
      34. Chromosome 17
      35. Chromosome 18
      36. Chromosome 19
      37. Chromosome 20
      38. Chromosome 22
      39. Clinical and Phenotypic Relevance of cis-Acting Regulatory Polymorphisms
      40. Comparative Genomic Hybridization in the Study of Human Disease
      41. CpG Dinucleotides and Human Disorders
      42. Cytochrome P450 (CYP) Gene Superfamily
      43. Development and Role of the Human Reference Sequence in Personal Genomics
      44. Direct-to-Consumer Genetic Testing
      45. Disability, Human Rights and Contemporary Genetics
      46. Disease Associations: Human Leukocyte Antigen (HLA) and Apolipoprotein E (APOE) Gene
      47. Dopamine D4 Receptor (DRD4) Box Score
      48. Drug-Metabolising Enzymes: Genetic Polymorphisms
      49. Dysmorphic Syndromes
      50. Electroencephalogram (EEG) and Evoked Potentials
      51. Ethnicity and Disease
      52. Evolution of Genetic Resistance/Susceptibility to Malaria Infection
      53. Evolution of Skin Pigmentation Differences in Humans
      54. An Evolutionary Genetic Framework for Heritable Disorders
      55. Family-based Association Test (FBAT)
      56. Forensic Genetics
      57. Genetic Determinants of Human Life-Span
      58. Genetic Disease in the Ashkenazim: Role of a Founder Effect
      59. Genetic Disease: Prevalence
      60. Genetic Factors Involved in Human Susceptibility to Infection by Schistosomiasis
      61. Genetic Isolates and Behavioral Gene Searches
      62. Genetic Risk
      63. Genetic Screening and Testing
      64. Genetic Susceptibility to Autoimmune Disorders
      65. Genetic Variation: Human
      66. You have free access to this content
        Genetic Variation: Polymorphisms and Mutations
      67. Genetic, Epigenetic and Environmental Influences on Human Tooth Size, Shape and Number
      68. Genetics and Genomics of Human Longevity
      69. Genetics and the Origin of the Finns
      70. Genetics of Adaptation to High Altitude
      71. Genetics of Adult Antisocial Behaviour
      72. Genetics of Adverse Drug Reactions
      73. Genetics of Age at Menarche
      74. Genetics of Athletic Performance
      75. Genetics of Birth Weight
      76. Genetics of Disordered Gambling
      77. Genetics of Eye Colour
      78. The Genetics of Human Aggressive Behaviour
      79. Genetics of Human Social Behaviour
      80. Genetics of Nicotine Addiction
      81. Genetics of Preterm Birth
      82. Genetics of Suicidality
      83. Genetics of Susceptibility to Leprosy
      84. Genetics of Susceptibility to Mycobacterial Disease
      85. Genetics of Taste Perception
      86. Genome Organization: Human
      87. Genome-Wide Association Studies in Asthma
      88. Genome-wide Association Studies of Cancers
      89. Genotype–Phenotype Relationships
      90. Genotype–Phenotype Relationships: Fatal Familial Insomnia and Creutzfeldt–Jakob Disease
      91. Germline Copy Number Variation and Cancer Risk
      92. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      93. HapMap Project
      94. Heritability
      95. Heritability Wars
      96. Higher Order Genetic Interactions and Complex Trait Variation
      97. Human Genetics: Online Resources
      98. Human Genome Diversity Project (HGDP)
      99. Human Genome Diversity Studies: Impact on Indigenous Communities
      100. Human Genome Project, Personalised Medicine and Future Health Care
      101. Human Genome Project: Importance in Clinical Genetics
      102. Human Immunodeficiency Virus (HIV) Infection: Genetics
      103. Human Leukocyte Antigen (HLA) System and Human Disorders
      104. Human Variation Databases
      105. You have free access to this content
        Immunoglobulin Gene Construction: Human
      106. Impact of Missense Variants on Protein–Protein Interactions
      107. Imprinting (Mammals)
      108. Infectious Diseases: Predisposition
      109. Intelligence and Cognition
      110. Intelligence, Heredity and Genes: A Historical Perspective
      111. Interpreting Disease Relevance of Amino Acid Substitutions
      112. Is There a Role for Genetic Testing in Sports?
      113. Language and Genes
      114. Longevity: Genetics
      115. Major Histocompatibility Complex (MHC)
      116. Major Histocompatibility Complex (MHC) Genes
      117. Major Histocompatibility Complex: Human
      118. Malarial Resistance and Susceptibility, Genetics of
      119. Markov Chain Monte Carlo Methods
      120. Metabolism: Hereditary Errors
      121. Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping
      122. Microdeletion Syndromes
      123. MicroRNA Polymorphisms
      124. Microsatellite Instability
      125. Mitochondrial DNA Polymorphisms
      126. Molecular Basis of Complex Traits
      127. Molecular Genetic Causes of Discordance in Monozygotic Twins
      128. Molecular Genetics of Anxiety
      129. Molecular Genetics of Hyperuricaemia and Gout
      130. Molecular Genetics of Hypophosphatasia
      131. Molecular Genetics of Type 1 Diabetes
      132. Molecular Genetics of Variability in Human Pain
      133. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      134. Multidrug Resistance in Cancer: Genetics of ABC Transporters
      135. Mutations in Human Genetic Disease
      136. Mutations: Penetrance
      137. Next-generation Sequencing in Clinical Molecular Diagnostics
      138. Nutrigenetics
      139. Personal Identity: Genetics and Determinism
      140. Pharmacogenetics and Pharmacogenomics
      141. Pharmacogenetics of Pain
      142. Polymorphism of TNF Genes and Disease Susceptibility
      143. Polymorphisms: Origins and Maintenance
      144. Population Genetics: Historical Aspects
      145. Population History and Linkage Disequilibrium
      146. Prediction of Human Pigmentation Traits from DNA Polymorphisms
      147. Protein Kinases in the Era of Precision Medicine
      148. Psychiatric Disorders: The Search for Genes
      149. Quantitative Genetics
      150. ‘Race’: What Biology Can Tell Us about a Social Construct
      151. Recent Insights into the Genetics of Plasma Triglycerides and Possible Causal Mechanisms in Cardiovascular Disease
      152. Reconstructing Human History Using Autosomal, Y-Chromosomal and Mitochondrial Markers
      153. Restriction Fragment Length Polymorphism (RFLP)
      154. Rhesus Haemolytic Disease of the Newborn
      155. Selection and Common Monogenic Disease
      156. Selective Constraints and Human Disease Genes: Evolutionary and Bioinformatics Approaches
      157. Sexual Orientation
      158. Sexual Orientation: Genetics
      159. Single Nucleotide Polymorphism (SNP)
      160. Single Nucleotide Polymorphisms (SNPs): Identification and Scoring
      161. Single Nucleotide Polymorphisms in Human Disease and Evolution: Phylogenies and Genealogies
      162. Somatic Hypermutation in Antibody Evolution
      163. Spectrum of Point Mutations in the Human Genome and Major Subpopulations
      164. Structural Diversity of the Human Genome and Disease Susceptibility
      165. Susceptibility to Human Infectious Diseases, Genetics of
      166. Susceptibility to Malaria, Genetics of
      167. Synonymous Mutations as a Cause of Human Genetic Disease
      168. Thalassaemias
      169. The Genetics of Facial Morphology
      170. The Genetics of Stuttering
      171. Twin Methodology
      172. Twin Studies
      173. Twin Studies: Software and Algorithms
      174. Unravelling the Mystery of Sudden Cardiac Death Through Genetic Approaches
      175. Use of DNA Identification in Human Rights Work to Reunite Families in Latin America
      176. Use of Personalized Genomic Information
      177. Using Evolutionary Biology in the Medical Sciences
      178. Variable Drug Response: Genetic Evaluation
      179. Variation: Measures
      180. Absolute Pitch: Genetics
      181. Addiction and Genes: Animal Models
      182. Adoption Strategies
      183. Allele Spectrum of Human Genetic Disease
      184. Allelic and Locus Heterogeneity
      185. Analysis of Gene–Gene Interactions Underlying Human Disease
      186. Anticipation
      187. Assessing Genetic Variants of Uncertain Significance: The Example of Breast Cancer
      188. Assessing Genetic Variants of Uncertain Significance: The Example of Lynch Syndrome
      189. Balancing Selection in Human Evolution
      190. Balancing Selection in the Human Genome
      191. Behaviour Genetics – Human
      192. Behavioural Genetics in the Postgenomics Era
      193. Bioethics: ELSI
      194. You have free access to this content
        Bioinformatics
      195. Blood Group Genetics
      196. Blood Groups: Molecular Genetic Basis
      197. Causes and Consequences of Structural Genomic Alterations in the Human Genome
      198. Characterising Structural Variation by Means of Next-Generation Sequencing
      199. Chromosome 2
      200. Chromosome 3
      201. Chromosome 4
      202. Chromosome 5
      203. Chromosome 6
      204. Chromosome 7
      205. Chromosome 9
      206. Chromosome 1
      207. Chromosome 10
      208. Chromosome 11
      209. Chromosome 12
      210. Chromosome 13
      211. Chromosome 14
      212. Chromosome 16
      213. Chromosome 17
      214. Chromosome 18
      215. Chromosome 19
      216. Chromosome 20
      217. Chromosome 22
      218. Clinical and Phenotypic Relevance of cis-Acting Regulatory Polymorphisms
      219. Comparative Genomic Hybridization in the Study of Human Disease
      220. CpG Dinucleotides and Human Disorders
      221. Cytochrome P450 (CYP) Gene Superfamily
      222. Development and Role of the Human Reference Sequence in Personal Genomics
      223. Direct-to-Consumer Genetic Testing
      224. Disability, Human Rights and Contemporary Genetics
      225. Disease Associations: Human Leukocyte Antigen (HLA) and Apolipoprotein E (APOE) Gene
      226. Dopamine D4 Receptor (DRD4) Box Score
      227. Drug-Metabolising Enzymes: Genetic Polymorphisms
      228. Dysmorphic Syndromes
      229. Electroencephalogram (EEG) and Evoked Potentials
      230. Ethnicity and Disease
      231. Evolution of Genetic Resistance/Susceptibility to Malaria Infection
      232. Evolution of Skin Pigmentation Differences in Humans
      233. An Evolutionary Genetic Framework for Heritable Disorders
      234. Family-based Association Test (FBAT)
      235. Forensic Genetics
      236. Genetic Determinants of Human Life-Span
      237. Genetic Disease in the Ashkenazim: Role of a Founder Effect
      238. Genetic Disease: Prevalence
      239. Genetic Factors Involved in Human Susceptibility to Infection by Schistosomiasis
      240. Genetic Isolates and Behavioral Gene Searches
      241. Genetic Risk
      242. Genetic Screening and Testing
      243. Genetic Susceptibility to Autoimmune Disorders
      244. Genetic Variation: Human
      245. You have free access to this content
        Genetic Variation: Polymorphisms and Mutations
      246. Genetic, Epigenetic and Environmental Influences on Human Tooth Size, Shape and Number
      247. Genetics and Genomics of Human Longevity
      248. Genetics and the Origin of the Finns
      249. Genetics of Adaptation to High Altitude
      250. Genetics of Adult Antisocial Behaviour
      251. Genetics of Adverse Drug Reactions
      252. Genetics of Age at Menarche
      253. Genetics of Athletic Performance
      254. Genetics of Birth Weight
      255. Genetics of Disordered Gambling
      256. Genetics of Eye Colour
      257. The Genetics of Human Aggressive Behaviour
      258. Genetics of Human Social Behaviour
      259. Genetics of Nicotine Addiction
      260. Genetics of Preterm Birth
      261. Genetics of Suicidality
      262. Genetics of Susceptibility to Leprosy
      263. Genetics of Susceptibility to Mycobacterial Disease
      264. Genetics of Taste Perception
      265. Genome Organization: Human
      266. Genome-Wide Association Studies in Asthma
      267. Genome-wide Association Studies of Cancers
      268. Genotype–Phenotype Relationships
      269. Genotype–Phenotype Relationships: Fatal Familial Insomnia and Creutzfeldt–Jakob Disease
      270. Germline Copy Number Variation and Cancer Risk
      271. Germline Genomic Copy Number Variation Contribution to Cancer Predisposition
      272. HapMap Project
      273. Heritability
      274. Heritability Wars
      275. Higher Order Genetic Interactions and Complex Trait Variation
      276. Human Genetics: Online Resources
      277. Human Genome Diversity Project (HGDP)
      278. Human Genome Diversity Studies: Impact on Indigenous Communities
      279. Human Genome Project, Personalised Medicine and Future Health Care
      280. Human Genome Project: Importance in Clinical Genetics
      281. Human Immunodeficiency Virus (HIV) Infection: Genetics
      282. Human Leukocyte Antigen (HLA) System and Human Disorders
      283. Human Variation Databases
      284. You have free access to this content
        Immunoglobulin Gene Construction: Human
      285. Impact of Missense Variants on Protein–Protein Interactions
      286. Imprinting (Mammals)
      287. Infectious Diseases: Predisposition
      288. Intelligence and Cognition
      289. Intelligence, Heredity and Genes: A Historical Perspective
      290. Interpreting Disease Relevance of Amino Acid Substitutions
      291. Is There a Role for Genetic Testing in Sports?
      292. Language and Genes
      293. Longevity: Genetics
      294. Major Histocompatibility Complex (MHC)
      295. Major Histocompatibility Complex (MHC) Genes
      296. Major Histocompatibility Complex: Human
      297. Malarial Resistance and Susceptibility, Genetics of
      298. Markov Chain Monte Carlo Methods
      299. Metabolism: Hereditary Errors
      300. Microarrays and Single Nucleotide Polymorphism (SNP) Genotyping
      301. Microdeletion Syndromes
      302. MicroRNA Polymorphisms
      303. Microsatellite Instability
      304. Mitochondrial DNA Polymorphisms
      305. Molecular Basis of Complex Traits
      306. Molecular Genetic Causes of Discordance in Monozygotic Twins
      307. Molecular Genetics of Anxiety
      308. Molecular Genetics of Hyperuricaemia and Gout
      309. Molecular Genetics of Hypophosphatasia
      310. Molecular Genetics of Type 1 Diabetes
      311. Molecular Genetics of Variability in Human Pain
      312. Molecular Mechanisms Underlying Pathogenic Missense Mutations
      313. Multidrug Resistance in Cancer: Genetics of ABC Transporters
      314. Mutations in Human Genetic Disease
      315. Mutations: Penetrance
      316. Next-generation Sequencing in Clinical Molecular Diagnostics
      317. Nutrigenetics
      318. Personal Identity: Genetics and Determinism
      319. Pharmacogenetics and Pharmacogenomics
      320. Pharmacogenetics of Pain
      321. Polymorphism of TNF Genes and Disease Susceptibility
      322. Polymorphisms: Origins and Maintenance
      323. Population Genetics: Historical Aspects
      324. Population History and Linkage Disequilibrium
      325. Prediction of Human Pigmentation Traits from DNA Polymorphisms
      326. Protein Kinases in the Era of Precision Medicine
      327. Psychiatric Disorders: The Search for Genes
      328. Quantitative Genetics
      329. ‘Race’: What Biology Can Tell Us about a Social Construct
      330. Recent Insights into the Genetics of Plasma Triglycerides and Possible Causal Mechanisms in Cardiovascular Disease
      331. Reconstructing Human History Using Autosomal, Y-Chromosomal and Mitochondrial Markers
      332. Restriction Fragment Length Polymorphism (RFLP)
      333. Rhesus Haemolytic Disease of the Newborn
      334. Selection and Common Monogenic Disease
      335. Selective Constraints and Human Disease Genes: Evolutionary and Bioinformatics Approaches
      336. Sexual Orientation
      337. Sexual Orientation: Genetics
      338. Single Nucleotide Polymorphism (SNP)
      339. Single Nucleotide Polymorphisms (SNPs): Identification and Scoring
      340. Single Nucleotide Polymorphisms in Human Disease and Evolution: Phylogenies and Genealogies
      341. Somatic Hypermutation in Antibody Evolution
      342. Spectrum of Point Mutations in the Human Genome and Major Subpopulations
      343. Structural Diversity of the Human Genome and Disease Susceptibility
      344. Susceptibility to Human Infectious Diseases, Genetics of
      345. Susceptibility to Malaria, Genetics of
      346. Synonymous Mutations as a Cause of Human Genetic Disease
      347. Thalassaemias
      348. The Genetics of Facial Morphology
      349. The Genetics of Stuttering
      350. Twin Methodology
      351. Twin Studies
      352. Twin Studies: Software and Algorithms
      353. Unravelling the Mystery of Sudden Cardiac Death Through Genetic Approaches
      354. Use of DNA Identification in Human Rights Work to Reunite Families in Latin America
      355. Use of Personalized Genomic Information
      356. Using Evolutionary Biology in the Medical Sciences
      357. Variable Drug Response: Genetic Evaluation
      358. Variation: Measures
    16. Linkage Analysis
    17. Mitochondrial Diseases
    18. Model Organisms and Human Disease
    19. Molecular Genetics of Common and Complex Disease
    20. Mutational Mechanisms of Genetic Disease
    21. Pharmacogenetics and Pharmacogenomics
    22. Proteomic Studies of Genetic Disease
    23. Quantitative Genetics
    24. Specific Genetic Disorders
    25. Statistical Methodology in Genetics
    26. Techniques and Tools in Clinical Genetics
  8. Immunology
  9. Microbiology
  10. Molecular Biology
  11. Neuroscience
  12. Plant Science
  13. Science & Society
  14. Structural Biology
  15. Virology

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