147 related articles for article (PubMed ID: 32237178)
1. Gene-based and pathway-based testing for rare-variant association in affected sib pairs.
Romanescu RG; Green J; Andrulis IL; Bull SB
Genet Epidemiol; 2020 Jun; 44(4):368-381. PubMed ID: 32237178
[TBL] [Abstract][Full Text] [Related]
2. Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Bureau A; Begum F; Taub MA; Hetmanski JB; Parker MM; Albacha-Hejazi H; Scott AF; Murray JC; Marazita ML; Bailey-Wilson JE; Beaty TH; Ruczinski I
Genet Epidemiol; 2019 Feb; 43(1):37-49. PubMed ID: 30246882
[TBL] [Abstract][Full Text] [Related]
3. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
DE LA Vega FM; Bustamante CD; Leal SM
Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
[TBL] [Abstract][Full Text] [Related]
4. Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.
He Z; O'Roak BJ; Smith JD; Wang G; Hooker S; Santos-Cortez RL; Li B; Kan M; Krumm N; Nickerson DA; Shendure J; Eichler EE; Leal SM
Am J Hum Genet; 2014 Jan; 94(1):33-46. PubMed ID: 24360806
[TBL] [Abstract][Full Text] [Related]
5. A Rare Variant Nonparametric Linkage Method for Nuclear and Extended Pedigrees with Application to Late-Onset Alzheimer Disease via WGS Data.
Zhao L; He Z; Zhang D; Wang GT; Renton AE; Vardarajan BN; Nothnagel M; Goate AM; Mayeux R; Leal SM
Am J Hum Genet; 2019 Oct; 105(4):822-835. PubMed ID: 31585107
[TBL] [Abstract][Full Text] [Related]
6. Allele sharing and allelic association I: sib pair tests with increased power.
Lazzeroni LC
Genet Epidemiol; 2002 Apr; 22(4):328-44. PubMed ID: 11984865
[TBL] [Abstract][Full Text] [Related]
7. Robust and Powerful Affected Sibpair Test for Rare Variant Association.
Lin KH; Zöllner S
Genet Epidemiol; 2015 Jul; 39(5):325-33. PubMed ID: 25966809
[TBL] [Abstract][Full Text] [Related]
8. Exome Sequencing of Familial Bipolar Disorder.
Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
[TBL] [Abstract][Full Text] [Related]
9. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
Larson NB; McDonnell S; Albright LC; Teerlink C; Stanford J; Ostrander EA; Isaacs WB; Xu J; Cooney KA; Lange E; Schleutker J; Carpten JD; Powell I; Bailey-Wilson J; Cussenot O; Cancel-Tassin G; Giles G; MacInnis R; Maier C; Whittemore AS; Hsieh CL; Wiklund F; Catalona WJ; Foulkes W; Mandal D; Eeles R; Kote-Jarai Z; Ackerman MJ; Olson TM; Klein CJ; Thibodeau SN; Schaid DJ
Genet Epidemiol; 2016 Sep; 40(6):461-9. PubMed ID: 27312771
[TBL] [Abstract][Full Text] [Related]
10. The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.
He Z; Zhang D; Renton AE; Li B; Zhao L; Wang GT; Goate AM; Mayeux R; Leal SM
Am J Hum Genet; 2017 Feb; 100(2):193-204. PubMed ID: 28065470
[TBL] [Abstract][Full Text] [Related]
11. The affected-/discordant-sib-pair design can guarantee validity of multipoint model-free linkage analysis of incomplete pedigrees when there is marker-marker disequilibrium.
Xing C; Sinha R; Xing G; Lu Q; Elston RC
Am J Hum Genet; 2006 Aug; 79(2):396-401. PubMed ID: 16826532
[TBL] [Abstract][Full Text] [Related]
12. Effects of stratification in the analysis of affected-sib-pair data: benefits and costs.
Leal SM; Ott J
Am J Hum Genet; 2000 Feb; 66(2):567-75. PubMed ID: 10677317
[TBL] [Abstract][Full Text] [Related]
13. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Chen R; Wei Q; Zhan X; Zhong X; Sutcliffe JS; Cox NJ; Cook EH; Li C; Chen W; Li B
Bioinformatics; 2015 May; 31(9):1452-9. PubMed ID: 25568282
[TBL] [Abstract][Full Text] [Related]
14. Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
Crawford BD; Gillies CE; Robertson CC; Kretzler M; Otto EA; Vega-Warner V; Sampson MG
Pediatr Nephrol; 2017 Mar; 32(3):467-476. PubMed ID: 27766458
[TBL] [Abstract][Full Text] [Related]
15. GenePy - a score for estimating gene pathogenicity in individuals using next-generation sequencing data.
Mossotto E; Ashton JJ; O'Gorman L; Pengelly RJ; Beattie RM; MacArthur BD; Ennis S
BMC Bioinformatics; 2019 May; 20(1):254. PubMed ID: 31096927
[TBL] [Abstract][Full Text] [Related]
16. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.
Kinnamon DD; Hershberger RE; Martin ER
PLoS One; 2012; 7(2):e30238. PubMed ID: 22363423
[TBL] [Abstract][Full Text] [Related]
17. Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data.
Hu H; Huff CD
Pac Symp Biocomput; 2014; ():51-62. PubMed ID: 24297533
[TBL] [Abstract][Full Text] [Related]
18. Analysis of affected sib pairs, with covariates--with and without constraints.
Greenwood CM; Bull SB
Am J Hum Genet; 1999 Mar; 64(3):871-85. PubMed ID: 10053022
[TBL] [Abstract][Full Text] [Related]
19. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease.
Persyn E; Karakachoff M; Le Scouarnec S; Le Clézio C; Campion D; Consortium FE; Schott JJ; Redon R; Bellanger L; Dina C
PLoS One; 2017; 12(7):e0179364. PubMed ID: 28742119
[TBL] [Abstract][Full Text] [Related]
20. High-resolution HLA allele and haplotype frequencies in several unrelated populations determined by next generation sequencing: 17th International HLA and Immunogenetics Workshop joint report.
Creary LE; Sacchi N; Mazzocco M; Morris GP; Montero-Martin G; Chong W; Brown CJ; Dinou A; Stavropoulos-Giokas C; Gorodezky C; Narayan S; Periathiruvadi S; Thomas R; De Santis D; Pepperall J; ElGhazali GE; Al Yafei Z; Askar M; Tyagi S; Kanga U; Marino SR; Planelles D; Chang CJ; Fernández-Viña MA
Hum Immunol; 2021 Jul; 82(7):505-522. PubMed ID: 34030896
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
