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Results: 1 to 20 of 112

1.

Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping.

Schulze TG, McMahon FJ.

Hum Hered. 2004;58(3-4):131-8. Review.

PMID:
15812169
[PubMed - indexed for MEDLINE]
Free Article
2.

Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design.

Terwilliger JD, Göring HH.

Hum Biol. 2000 Feb;72(1):63-132. Review.

PMID:
10721614
[PubMed - indexed for MEDLINE]
3.

Analysis of genetically complex epilepsies.

Ottman R.

Epilepsia. 2005;46 Suppl 10:7-14. Review.

PMID:
16359464
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Analysis of linkage and association for diseases of genetic aetiology.

Sturt E.

Stat Med. 1984 Jan-Mar;3(1):57-72.

PMID:
6587497
[PubMed - indexed for MEDLINE]
5.

Approaches to identify genes for complex human diseases: lessons from Mendelian disorders.

Dean M.

Hum Mutat. 2003 Oct;22(4):261-74. Review.

PMID:
12955713
[PubMed - indexed for MEDLINE]
6.

DNA variation and the future of human genetics.

Schafer AJ, Hawkins JR.

Nat Biotechnol. 1998 Jan;16(1):33-9. Review.

PMID:
9447590
[PubMed - indexed for MEDLINE]
7.

Current molecular techniques and strategies for gene localization.

Verma A, Maheshwari MC.

J Assoc Physicians India. 1992 Jun;40(6):405-8. Review. No abstract available.

PMID:
1452568
[PubMed - indexed for MEDLINE]
8.

The complexity of the genotype-phenotype relationship and the limitations of using genetic "markers" at the individual level.

Templeton AR.

Sci Context. 1998 Autumn-Winter;11(3-4):373-89.

PMID:
15168668
[PubMed - indexed for MEDLINE]
10.

Mining OMIM for insight into complex diseases.

Cantor MN, Lussier YA.

Stud Health Technol Inform. 2004;107(Pt 2):753-7.

PMID:
15360913
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

VAPSE-based analysis: a two-phased candidate gene approach for elucidating genetic predisposition to complex disorders.

Weinshenker BG, Sommer S.

Mutat Res. 2001 Jun;458(1-2):7-17.

PMID:
11406417
[PubMed - indexed for MEDLINE]
12.

Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction network.

Iossifov I, Zheng T, Baron M, Gilliam TC, Rzhetsky A.

Genome Res. 2008 Jul;18(7):1150-62. doi: 10.1101/gr.075622.107. Epub 2008 Apr 16.

PMID:
18417725
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The LQT syndromes--current status of molecular mechanisms.

Schulze-Bahr E, Wedekind H, Haverkamp W, Borggrefe M, Assmann G, Breithardt G, Funke H.

Z Kardiol. 1999 Apr;88(4):245-54. Review.

PMID:
10408028
[PubMed - indexed for MEDLINE]
14.

Identifying genes and genetic variation underlying human diseases and complex phenotypes via recombination mapping.

Broeckel U, Schork NJ.

J Physiol. 2004 Jan 1;554(Pt 1):40-5. Review.

PMID:
14678489
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Copy-number variation and association studies of human disease.

McCarroll SA, Altshuler DM.

Nat Genet. 2007 Jul;39(7 Suppl):S37-42. Review.

PMID:
17597780
[PubMed - indexed for MEDLINE]
16.

Analytic options for asthma genetics.

Rich SS.

Clin Exp Allergy. 1998 Apr;28 Suppl 1:84-7; discussion 108-10.

PMID:
9641599
[PubMed - indexed for MEDLINE]
17.

Analysis of linkage with disease-marker association.

Tai JJ.

Proc Natl Sci Counc Repub China B. 1986 Oct;10(4):250-3.

PMID:
3470816
[PubMed - indexed for MEDLINE]
18.
19.

No post-genetics era in human disease research.

Gusella J, MacDonald M.

Nat Rev Genet. 2002 Jan;3(1):72-9. Review.

PMID:
11823793
[PubMed - indexed for MEDLINE]
20.

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