Literature DB >> 9012420

Improved set of short-tandem-repeat polymorphisms for screening the human genome.

B Yuan, D Vaske, J L Weber, J Beck, V C Sheffield.   

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Year:  1997        PMID: 9012420      PMCID: PMC1712401     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  5 in total

1.  Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

Authors:  J L Weber; Z Wang; K Hansen; M Stephenson; C Kappel; S Salzman; P J Wilkie; B Keats; N C Dracopoli; B F Brandriff
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

2.  A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Authors:  C Dib; S Fauré; C Fizames; D Samson; N Drouot; A Vignal; P Millasseau; S Marc; J Hazan; E Seboun; M Lathrop; G Gyapay; J Morissette; J Weissenbach
Journal:  Nature       Date:  1996-03-14       Impact factor: 49.962

3.  A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps.

Authors:  V C Sheffield; J L Weber; K H Buetow; J C Murray; D A Even; K Wiles; J M Gastier; J C Pulido; C Yandava; S L Sunden
Journal:  Hum Mol Genet       Date:  1995-10       Impact factor: 6.150

4.  Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mapping.

Authors:  P W Reed; J L Davies; J B Copeman; S T Bennett; S M Palmer; L E Pritchard; S C Gough; Y Kawaguchi; H J Cordell; K M Balfour
Journal:  Nat Genet       Date:  1994-07       Impact factor: 38.330

5.  Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome.

Authors:  J Dubovsky; V C Sheffield; G M Duyk; J L Weber
Journal:  Hum Mol Genet       Date:  1995-03       Impact factor: 6.150

  5 in total
  37 in total

1.  Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

Authors:  M C Lanasa; W A Hogge; C Kubik; J Blancato; E P Hoffman
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

Authors:  A H Kissebah; G E Sonnenberg; J Myklebust; M Goldstein; K Broman; R G James; J A Marks; G R Krakower; H J Jacob; J Weber; L Martin; J Blangero; A G Comuzzie
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

3.  Model-free linkage analysis with covariates confirms linkage of prostate cancer to chromosomes 1 and 4.

Authors:  K A Goddard; J S Witte; B K Suarez; W J Catalona; J M Olson
Journal:  Am J Hum Genet       Date:  2001-04-13       Impact factor: 11.025

4.  A genome screen of multiplex sibships with prostate cancer.

Authors:  B K Suarez; J Lin; J K Burmester; K W Broman; J L Weber; T K Banerjee; K A Goddard; J S Witte; R C Elston; W J Catalona
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

5.  DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24.

Authors:  C C Greene; P M McMillan; S E Barker; P Kurnool; M I Lomax; M Burmeister; M M Lesperance
Journal:  Am J Hum Genet       Date:  2000-12-11       Impact factor: 11.025

6.  A genome screen of families with multiple cases of prostate cancer: evidence of genetic heterogeneity.

Authors:  C L Hsieh; I Oakley-Girvan; R R Balise; J Halpern; R P Gallagher; A H Wu; L N Kolonel; L E O'Brien; I G Lin; D J Van Den Berg; C Z Teh; D W West; A S Whittemore
Journal:  Am J Hum Genet       Date:  2001-06-12       Impact factor: 11.025

7.  Evidence for a gene influencing serum bilirubin on chromosome 2q telomere: a genomewide scan in the Framingham study.

Authors:  Jing-Ping Lin; L Adrienne Cupples; Peter W F Wilson; Nancy Heard-Costa; Christopher J O'Donnell
Journal:  Am J Hum Genet       Date:  2003-02-28       Impact factor: 11.025

Review 8.  The genetics of Tourette syndrome.

Authors:  D L Pauls
Journal:  Curr Psychiatry Rep       Date:  2001-04       Impact factor: 5.285

9.  Genetic and physical mapping of the locus for autosomal dominant renal Fanconi syndrome, on chromosome 15q15.3.

Authors:  U Lichter-Konecki; K W Broman; E B Blau; D S Konecki
Journal:  Am J Hum Genet       Date:  2000-11-22       Impact factor: 11.025

10.  A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study.

Authors:  C I M Panhuysen; L A Cupples; P W F Wilson; A G Herbert; R H Myers; J B Meigs
Journal:  Diabetologia       Date:  2003-03-21       Impact factor: 10.122

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