Literature DB >> 23594489

Some surprising twists on the road to discovering the contribution of rare variants to complex diseases.

Duncan C Thomas.   

Abstract

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Year:  2013        PMID： 23594489      PMCID： PMC3704173          DOI： 10.1159/000347020

Source DB:  PubMed          Journal:  Hum Hered        ISSN： 0001-5652            Impact factor:   0.444


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  52 in total

Review 1.  Linkage analysis in the next-generation sequencing era.

Authors:  Joan E Bailey-Wilson; Alexander F Wilson
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

2.  Optimal tests for rare variant effects in sequencing association studies.

Authors:  Seunggeun Lee; Michael C Wu; Xihong Lin
Journal:  Biostatistics       Date:  2012-06-14       Impact factor: 5.899

Review 3.  Genomic similarity and kernel methods II: methods for genomic information.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

Review 4.  Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations.

Authors:  Daniel J Schaid
Journal:  Hum Hered       Date:  2010-07-03       Impact factor: 0.444

Review 5.  Analysing biological pathways in genome-wide association studies.

Authors:  Kai Wang; Mingyao Li; Hakon Hakonarson
Journal:  Nat Rev Genet       Date:  2010-12       Impact factor: 53.242

6.  Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.

Authors:  Lucia A Hindorff; Praveen Sethupathy; Heather A Junkins; Erin M Ramos; Jayashri P Mehta; Francis S Collins; Teri A Manolio
Journal:  Proc Natl Acad Sci U S A       Date:  2009-05-27       Impact factor: 11.205

7.  Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles.

Authors:  Aravind Subramanian; Pablo Tamayo; Vamsi K Mootha; Sayan Mukherjee; Benjamin L Ebert; Michael A Gillette; Amanda Paulovich; Scott L Pomeroy; Todd R Golub; Eric S Lander; Jill P Mesirov
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-30       Impact factor: 11.205

8.  Incorporating prior biologic information for high-dimensional rare variant association studies.

Authors:  Melanie A Quintana; Fredrick R Schumacher; Graham Casey; Jonine L Bernstein; Li Li; David V Conti
Journal:  Hum Hered       Date:  2013-04-11       Impact factor: 0.444

9.  Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.

Authors:  Wonkuk Kim; Douglas Londono; Lisheng Zhou; Jinchuan Xing; Alejandro Q Nato; Anthony Musolf; Tara C Matise; Stephen J Finch; Derek Gordon
Journal:  Hum Hered       Date:  2013-04-11       Impact factor: 0.444

10.  A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease.

Authors:  Andrew S Allen; Glen A Satten
Journal:  Genet Epidemiol       Date:  2009-12       Impact factor: 2.135
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  2 in total

Review 1.  Two-phase and family-based designs for next-generation sequencing studies.

Authors:  Duncan C Thomas; Zhao Yang; Fan Yang
Journal:  Front Genet       Date:  2013-12-13       Impact factor: 4.599

2.  Simulating pedigrees ascertained for multiple disease-affected relatives.

Authors:  Christina Nieuwoudt; Samantha J Jones; Angela Brooks-Wilson; Jinko Graham
Journal:  Source Code Biol Med       Date:  2018-10-15
  2 in total

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