280 related articles for article (PubMed ID: 29955165)
1. Rediscovering the value of families for psychiatric genetics research.
Glahn DC; Nimgaonkar VL; Raventós H; Contreras J; McIntosh AM; Thomson PA; Jablensky A; McCarthy NS; Charlesworth JC; Blackburn NB; Peralta JM; Knowles EEM; Mathias SR; Ament SA; McMahon FJ; Gur RC; Bucan M; Curran JE; Almasy L; Gur RE; Blangero J
Mol Psychiatry; 2019 Apr; 24(4):523-535. PubMed ID: 29955165
[TBL] [Abstract][Full Text] [Related]
2. DNA sequence-level analyses reveal potential phenotypic modifiers in a large family with psychiatric disorders.
Ryan NM; Lihm J; Kramer M; McCarthy S; Morris SW; Arnau-Soler A; Davies G; Duff B; Ghiban E; Hayward C; Deary IJ; Blackwood DHR; Lawrie SM; McIntosh AM; Evans KL; Porteous DJ; McCombie WR; Thomson PA
Mol Psychiatry; 2018 Dec; 23(12):2254-2265. PubMed ID: 29880880
[TBL] [Abstract][Full Text] [Related]
3. Power of family-based association designs to detect rare variants in large pedigrees using imputed genotypes.
Saad M; Wijsman EM
Genet Epidemiol; 2014 Jan; 38(1):1-9. PubMed ID: 24243664
[TBL] [Abstract][Full Text] [Related]
4. Research designs for the study of gene-environment interactions in psychiatric disorders. Report of a Foundations Fund for Research in Psychiatry Panel.
Kidd KK; Matthysee S
Arch Gen Psychiatry; 1978 Aug; 35(8):925-32. PubMed ID: 678045
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Discovering human germ cell mutagens with whole genome sequencing: Insights from power calculations reveal the importance of controlling for between-family variability.
Webster RJ; Williams A; Marchetti F; Yauk CL
Mutat Res Genet Toxicol Environ Mutagen; 2018 Jul; 831():24-32. PubMed ID: 29875074
[TBL] [Abstract][Full Text] [Related]
7. Whole genome sequencing and rare variant analysis in essential tremor families.
Odgerel Z; Sonti S; Hernandez N; Park J; Ottman R; Louis ED; Clark LN
PLoS One; 2019; 14(8):e0220512. PubMed ID: 31404076
[TBL] [Abstract][Full Text] [Related]
8. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Jun G; Manning A; Almeida M; Zawistowski M; Wood AR; Teslovich TM; Fuchsberger C; Feng S; Cingolani P; Gaulton KJ; Dyer T; Blackwell TW; Chen H; Chines PS; Choi S; Churchhouse C; Fontanillas P; King R; Lee S; Lincoln SE; Trubetskoy V; DePristo M; Fingerlin T; Grossman R; Grundstad J; Heath A; Kim J; Kim YJ; Laramie J; Lee J; Li H; Liu X; Livne O; Locke AE; Maller J; Mazur A; Morris AP; Pollin TI; Ragona D; Reich D; Rivas MA; Scott LJ; Sim X; Tearle RG; Teo YY; Williams AL; Zöllner S; Curran JE; Peralta J; Akolkar B; Bell GI; Burtt NP; Cox NJ; Florez JC; Hanis CL; McKeon C; Mohlke KL; Seielstad M; Wilson JG; Atzmon G; Below JE; Dupuis J; Nicolae DL; Lehman D; Park T; Won S; Sladek R; Altshuler D; McCarthy MI; Duggirala R; Boehnke M; Frayling TM; Abecasis GR; Blangero J
Proc Natl Acad Sci U S A; 2018 Jan; 115(2):379-384. PubMed ID: 29279374
[TBL] [Abstract][Full Text] [Related]
9. Whole-genome characterization in pedigreed non-human primates using genotyping-by-sequencing (GBS) and imputation.
Bimber BN; Raboin MJ; Letaw J; Nevonen KA; Spindel JE; McCouch SR; Cervera-Juanes R; Spindel E; Carbone L; Ferguson B; Vinson A
BMC Genomics; 2016 Aug; 17(1):676. PubMed ID: 27558348
[TBL] [Abstract][Full Text] [Related]
10. Power for genetic association studies with random allele frequencies and genotype distributions.
Ambrosius WT; Lange EM; Langefeld CD
Am J Hum Genet; 2004 Apr; 74(4):683-93. PubMed ID: 15024689
[TBL] [Abstract][Full Text] [Related]
11. Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.
Sul JH; Cade BE; Cho MH; Qiao D; Silverman EK; Redline S; Sunyaev S
Am J Hum Genet; 2016 Oct; 99(4):846-859. PubMed ID: 27666371
[TBL] [Abstract][Full Text] [Related]
12. The effect of rare alleles on estimated genomic relationships from whole genome sequence data.
Eynard SE; Windig JJ; Leroy G; van Binsbergen R; Calus MP
BMC Genet; 2015 Mar; 16():24. PubMed ID: 25887220
[TBL] [Abstract][Full Text] [Related]
13. Design considerations for genetic linkage and association studies.
Nsengimana J; Bishop DT
Methods Mol Biol; 2012; 850():237-62. PubMed ID: 22307702
[TBL] [Abstract][Full Text] [Related]
14. Testing genetic association with rare and common variants in family data.
Chen H; Malzahn D; Balliu B; Li C; Bailey JN
Genet Epidemiol; 2014 Sep; 38 Suppl 1(0 1):S37-43. PubMed ID: 25112186
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases.
Siniscalco M; Robledo R; Bender PK; Carcassi C; Contu L; Beck JC
Cytogenet Cell Genet; 1999; 86(2):148-52. PubMed ID: 10545707
[TBL] [Abstract][Full Text] [Related]
17. Leveraging Identity-by-Descent for Accurate Genotype Inference in Family Sequencing Data.
Li B; Wei Q; Zhan X; Zhong X; Chen W; Li C; Haines J
PLoS Genet; 2015 Jun; 11(6):e1005271. PubMed ID: 26043085
[TBL] [Abstract][Full Text] [Related]
18. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
Rudan I
Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
[TBL] [Abstract][Full Text] [Related]
19. Design of association studies with pooled or un-pooled next-generation sequencing data.
Kim SY; Li Y; Guo Y; Li R; Holmkvist J; Hansen T; Pedersen O; Wang J; Nielsen R
Genet Epidemiol; 2010 Jul; 34(5):479-91. PubMed ID: 20552648
[TBL] [Abstract][Full Text] [Related]
20. Robust rare variant association testing for quantitative traits in samples with related individuals.
Jiang D; McPeek MS
Genet Epidemiol; 2014 Jan; 38(1):10-20. PubMed ID: 24248908
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
