| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HUMU.10107 |
| P698 | PubMed publication ID | 12203988 |
| P2093 | author name string | Jan Aerts | |
| Jeroen Aerssens | |||
| Nadine Cohen | |||
| Yves Wetzels | |||
| P2860 | cites work | Single nucleotide polymorphisms as tools in human genetics | Q22066046 |
| HGBASE: a database of SNPs and other variations in and around human genes | Q24515305 | ||
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| Polymorphisms of CYP2A6 and its practical consequences | Q28362536 | ||
| Repbase update: a database and an electronic journal of repetitive elements | Q29614368 | ||
| Genetic dissection of complex traits | Q29618312 | ||
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| Database analysis and gene discovery in pharmacogenetics | Q34093087 | ||
| A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? | Q34385362 | ||
| A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity | Q42540064 | ||
| Single-nucleotide polymorphisms in the public domain: how useful are they? | Q53327084 | ||
| In silico identification of transcripts and SNPs from a region of 4p linked with bipolar affective disorder | Q57416193 | ||
| Polymorphisms of human aryl hydrocarbon receptor (AhR) gene in a French population: relationship with CYP1A1 inducibility and lung cancer | Q58408666 | ||
| Haplotype tagging for the identification of common disease genes | Q59200321 | ||
| P433 | issue | 3 | |
| P921 | main subject | data mining | Q172491 |
| P304 | page(s) | 162-173 | |
| P577 | publication date | 2002-09-01 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | Data mining of public SNP databases for the selection of intragenic SNPs | |
| P478 | volume | 20 |
| Q30365147 | A gentle introduction to SNP analysis: resources and tools. |
| Q34286236 | Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database |
| Q21283795 | Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis |
| Q35691099 | Defining "mutation" and "polymorphism" in the era of personal genomics |
| Q30838832 | Effective screening of informative single nucleotide polymorphisms using the novel method of restriction fragment mass polymorphism |
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| Q33536458 | Identification of single nucleotide polymorphism in ginger using expressed sequence tags |
| Q30398454 | New approaches to making the microenvironment of the female reproductive tract hostile to HIV. |
| Q60915109 | Risk Factor Genes in Patients with Dystonia: A Comprehensive Review |
| Q45115362 | Single-nucleotide polymorphisms in genes relating to homocysteine metabolism: how applicable are public SNP databases to a typical European population? |
| Q58431065 | The Development of Genetic Markers from Fungal Genome Initiatives |
| Q36683908 | The necessity for in vivo functional analysis in human medical genetics |
| Q34173777 | UASIS: Universal Automatic SNP Identification System. |
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