| ID
Numbers for Cross Referencing : Volume
1 Genetics |
| This
list will help you include cross references
to other articles in GGPB. Find the article
that you wish to cross refer to, note its
corresponding unique ID number e.g (g203206)
and then insert that unique ID number into
your text. Please do not insert the article
title, just its unique ID number. This makes
your work easier (less typing) and it gives
us a unique identifier to ensure that accurate
and unambiguous cross-referencing is obtained.
Thank you for using the unique ID numbers.
Please remember you can cross reference to
articles outside the section in which your
article appears. |
| Genetic
Variation and Evolution |
| Cytogenetics
|
| Epigenetics |
| Gene
Mapping |
| Complex
Traits and Diseases |
| Genetic
Medicine and Clinical Genetics |
| Gene
Therapy |
 |
| Section 1 Genetic Variation & Evolution |
| ID |
Title |
| g101105 |
Population genomics: patterns of genetic variation within populations |
| g101201 |
Modeling human genetic history |
| g101209 |
Homeobox gene repertoires: implications for the evolution of diversity |
| g101304 |
The genetic structure of human pathogens |
| g101306 |
The role of gene regulation in evolution |
| g101308 |
Studies of human genetic history using the Y chromosome |
| g101311 |
Modeling protein evolution |
| g101312 |
Genetic signatures of natural selection |
| g101314 |
Studies of human genetic history using mtDNA variation |
| g101403 |
Measuring variation in natural populations: a primer |
|
|
| Section 2 Cytogenetics |
| ID |
Title |
| g102105 |
Human cytogenetics and human chromosome abnormalities |
| g102114 |
Visualising human chromosomes |
| g102201 |
Human X chromosome inactivation |
| g102204 |
Acquired chromosome abnormalities: the cytogenetics of cancer |
| g102206 |
Cytogenetic aspects of meiosis |
| g102302 |
Microdeletions |
| g102307 |
Nondisjunction |
| g102309 |
Cytogenetics of infertility |
| g102310 |
Preimplantation genetic diagnosis for chromosome abnormalities |
| g102313 |
Mosaicism |
| g102315 |
Uniparental disomy |
| g102403 |
Cytogenetic analysis of lymphomas |
| g102408 |
Comparative genomic hybridization |
| g102411 |
FISH |
| g102417 |
Human sperm--FISH for identifying potential paternal
risk factors for chromosomally abnormal reproductive outcomes |
|
|
| Section 3 Epigenetics |
| ID |
Title |
| g103106 |
Imprinting and epigenetic inheritance in human disease |
| g103201 |
The histone code and epigenetic inheritance |
| g103203 |
Imprinting at the GNAS locus and endocrine disease |
| g103207 |
Imprinting and epigenetics in mouse models and embryogenesis: understanding
the requirement for both parental genomes |
| g103213 |
Beckwith-Wiedemann syndrome |
| g103214 |
Imprinting in Prader-Willi and Angelman syndromes |
| g103304 |
DNA methylation in epigenetics, development, and imprinting |
| g103308 |
Mechanisms of epigenetic loss of chromosomes in insects |
| g103311 |
Imprinted QTL in farm animals: A fortuity or a common phenomenon? |
| g103312 |
Evolution of genomic imprinting in mammals |
| g103315 |
Imprinting and behavior |
| g103316 |
Initiation of X-chromosome inactivation (or X-chromosome inactivation:
counting, choosing, inactivating) |
| g103317 |
Epigenetics and imprint resetting in cloned animals |
| g103320 |
Epigenetic reprogramming in germ cells and preimplantation embryos |
| g103321 |
Rapidly evolving imprinted loci |
| g103322 |
Epigenetic inheritance and RNAi at the centromere and heterochromatin |
| g103324 |
Variable expressivity and epigenetics |
| g103325 |
Spreading of X chromosome inactivation |
| g103409 |
Techniques in genomic imprinting research |
| g103410 |
Bioinformatics and identification of imprinted genes in mammals |
| g103419 |
UPD in human and mouse and role in identification of imprinted loci |
|
|
| Section 4 Gene Mapping |
| ID |
Title |
| g104102 |
Introduction to gene mapping: Linkage at a crossroads |
| g104104 |
Parametric vs. non-parametric and two-point vs. multipoint: controversies
in gene mapping |
| g104206 |
Gene mapping and the transition from STRPs to SNPs |
| g104209 |
Gene mapping, imprinting and epigenetics |
| g104301 |
Algorithmic improvements in gene mapping |
| g104305 |
Sex-specific maps and consequences for linkage mapping |
| g104307 |
Information content in gene mapping |
| g104308 |
Choices in gene mapping: populations and family structures |
| g104310 |
Polymorphic inversions, deletions, and duplications in gene mapping |
| g104411 |
Computation of LOD scores |
|
|
| Section 5 Complex Traits & Diseases |
| ID |
Title |
| g105108 |
Genetics of complex diseases: Lessons from type 2 diabetes |
| g105205 |
The common disease common variant concept |
| g105209 |
Population selection in complex disease gene mapping |
| g105211 |
Concept of complex trait genetics |
| g105303 |
Allergy and asthma |
| g105313 |
Complexity of cancer as a genetic disease |
| g105314 |
Genetics of cognitive disorders |
| g105315 |
Hypertension genetics: under pressure |
| g105316 |
Inflammation and inflammatory bowel disease |
| g105317 |
The mitochondrial genome |
|
|
| Section 6 Genetic medicine & clinical genetics |
| ID |
Title |
| g106117 |
Approach to common chronic disorders of adulthood |
| g106123 |
Approach to rare monogenic and chromosomal disorders |
| g106206 |
Current approaches to prenatal screening and diagnosis |
| g106209 |
Advances in newborn screening for biochemical genetic disorders |
| g106210 |
Advances in cytogenetic diagnosis |
| g106211 |
Current approaches to molecular diagnosis |
| g106225 |
The clinical and economic implications of pharmacogenomics |
| g106303 |
Molecular dysmorphology |
| g106314 |
Ethical and legal issues in medical genetics |
| g106318 |
Changing paradigms of genetic counseling |
| g106401 |
Mechanisms of inheritance |
| g106402 |
Family history, pedigree analysis, risk assessment |
| g106404 |
Genetic testing and genotype--phenotype correlations |
| g106405 |
Treatment of monogenic disorders |
| g106407 |
Tutorial: carrier screening |
| g106408 |
Tutorial: Gene identification in common disorders |
| g106413 |
Uses of databases |
| g106415 |
Familial adenomatous polyposis |
| g106416 |
The physical examination in clinical genetics |
| g106419 |
Genetic counseling process |
| g106420 |
Cancer genetics |
| g106422 |
Prenatal aneuploidy screening |
| g106424 |
The microdeletion syndromes |
|
|
| Section 7 Gene Therapy |
| ID |
Title |
| g107115 |
Gene therapy I: principles and clinical applications |
| g107118 |
Gene therapy II: Viral vectors and treatment modalities |
| g107201 |
Gene therapy in the central nervous system |
| g107206 |
Haematopoietic stem cell gene therapy |
| g107216 |
Cardiovascular gene therapy |
| g107304 |
Gene transfer vectors as medicinal products: risks and benefits |
| g107305 |
Immunity and tolerance induction in gene therapy |
| g107309 |
Artificial self-assembling systems for gene therapy |
| g107310 |
Adenovirus vectors |
| g107313 |
Adeno-associated viral vectors: depend(o)ble stability |
| g107314 |
Retro/lentiviral vectors |
| g107402 |
Control of transgene expression in mammalian cells |
| g107403 |
Gene transfer to skeletal muscle |
| g107407 |
Gene transfer to the liver |
| g107411 |
Gene transfer to the skin |
|
|
| |
|
|
