Literature DB >> 18473366

A prevalence-based association test for case-control studies.

Kelli K Ryckman1, Lan Jiang, Chun Li, Jacquelaine Bartlett, Jonathan L Haines, Scott M Williams.   

Abstract

Genetic association is often determined in case-control studies by the differential distribution of alleles or genotypes. Recent work has demonstrated that association can also be assessed by deviations from the expected distributions of alleles or genotypes. Specifically, multiple methods motivated by the principles of Hardy-Weinberg equilibrium (HWE) have been developed. However, these methods do not take into account many of the assumptions of HWE. Therefore, we have developed a prevalence-based association test (PRAT) as an alternative method for detecting association in case-control studies. This method, also motivated by the principles of HWE, uses an estimated population allele frequency to generate expected genotype frequencies instead of using the case and control frequencies separately. Our method often has greater power, under a wide variety of genetic models, to detect association than genotypic, allelic or Cochran-Armitage trend association tests. Therefore, we propose PRAT as a powerful alternative method of testing for association.

Mesh:

Year:  2008        PMID: 18473366     DOI: 10.1002/gepi.20342

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  11 in total

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Authors:  Roberto Romero; Digna R Velez Edwards; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Tinnakorn Chaiworapongsa; Brad D Pearce; Lara A Friel; Jacquelaine Bartlett; Madan Kumar Anant; Benjamin A Salisbury; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Scott M Williams; Ramkumar Menon
Journal:  Am J Obstet Gynecol       Date:  2010-05       Impact factor: 8.661

2.  A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).

Authors:  Roberto Romero; Lara A Friel; Digna R Velez Edwards; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Offer Erez; Tinnakorn Chaiworapongsa; Brad D Pearce; Jacquelaine Bartlett; Benjamin A Salisbury; Madan Kumar Anant; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Scott M Williams; Ramkumar Menon
Journal:  Am J Obstet Gynecol       Date:  2010-07-31       Impact factor: 8.661

3.  Polymorphisms in maternal and fetal genes encoding for proteins involved in extracellular matrix metabolism alter the risk for small-for-gestational-age.

Authors:  Digna R Velez Edwards; Roberto Romero; Juan Pedro Kusanovic; Sonia S Hassan; Shali Mazaki-Tovi; Edi Vaisbuch; Chong Jai Kim; Offer Erez; Tinnakorn Chaiworapongsa; Brad D Pearce; Jacquelaine Bartlett; Lara A Friel; Benjamin A Salisbury; Madan Kumar Anant; Gerald F Vovis; Min Seob Lee; Ricardo Gomez; Ernesto Behnke; Enrique Oyarzun; Gerard Tromp; Ramkumar Menon; Scott M Williams
Journal:  J Matern Fetal Neonatal Med       Date:  2010-07-09

4.  Common variants of the G protein-coupled receptor type 4 are associated with human essential hypertension and predict the blood pressure response to angiotensin receptor blockade.

Authors:  H Sanada; M Yoneda; J Yatabe; S M Williams; J Bartlett; M J White; L N Gordon; R A Felder; G M Eisner; I Armando; P A Jose
Journal:  Pharmacogenomics J       Date:  2015-03-03       Impact factor: 3.550

5.  Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth.

Authors:  Kelli K Ryckman; Nils-Halvdan Morken; Marquitta J White; Digna R Velez; Ramkumar Menon; Stephen J Fortunato; Per Magnus; Scott M Williams; Bo Jacobsson
Journal:  PLoS One       Date:  2010-02-03       Impact factor: 3.240

6.  Multi-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBG.

Authors:  Mehmet Agirbasli; Fatih Eren; Deniz Agirbasli; Marquitta J White; Scott M Williams
Journal:  OMICS       Date:  2013-08-29

7.  A single nucleotide polymorphism in SLC7A5 is associated with gastrointestinal toxicity after high-dose melphalan and autologous stem cell transplantation for multiple myeloma.

Authors:  Jennifer L Giglia; Marquitta J White; Andrew J Hart; Juan J Toro; César O Freytes; Cherish C Holt; Ying Cai; Scott M Williams; Stephen J Brandt
Journal:  Biol Blood Marrow Transplant       Date:  2014-04-04       Impact factor: 5.742

8.  Evolving hard problems: Generating human genetics datasets with a complex etiology.

Authors:  Daniel S Himmelstein; Casey S Greene; Jason H Moore
Journal:  BioData Min       Date:  2011-07-07       Impact factor: 2.522

9.  Molecular analyses of circadian gene variants reveal sex-dependent links between depression and clocks.

Authors:  S-q Shi; M J White; H M Borsetti; J S Pendergast; A Hida; C M Ciarleglio; P A de Verteuil; A G Cadar; C Cala; D G McMahon; R C Shelton; S M Williams; C H Johnson
Journal:  Transl Psychiatry       Date:  2016-03-01       Impact factor: 6.222

10.  Epiregulin (EREG) and human V-ATPase (TCIRG1): genetic variation, ethnicity and pulmonary tuberculosis susceptibility in Guinea-Bissau and The Gambia.

Authors:  M J White; A Tacconelli; J S Chen; C Wejse; P C Hill; V F Gomes; D R Velez-Edwards; L J Østergaard; T Hu; J H Moore; G Novelli; W K Scott; S M Williams; G Sirugo
Journal:  Genes Immun       Date:  2014-06-05       Impact factor: 2.676

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