eLS

eLS

Online ISBN: 9780470015902

DOI: 10.1002/047001590X

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