BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Özbek U, Lin HM, Lin Y, Weeks DE, Chen W, Shaffer JR, Purcell SM, Feingold E. Statistics for X-chromosome associations. Genet Epidemiol 2018;42:539-50. [PMID: 29900581 DOI: 10.1002/gepi.22132] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Yang ZY, Liu W, Yuan YX, Kong YF, Zhao PZ, Fung WK, Zhou JY. Robust association tests for quantitative traits on the X chromosome. Heredity (Edinb) 2022. [PMID: 36085362 DOI: 10.1038/s41437-022-00560-y] [Reference Citation Analysis]
2 Keur N, Ricaño-Ponce I, Kumar V, Matzaraki V. A systematic review of analytical methods used in genetic association analysis of the X-chromosome. Brief Bioinform 2022:bbac287. [PMID: 35901513 DOI: 10.1093/bib/bbac287] [Reference Citation Analysis]
3 Wang Z, Sun L, Paterson AD. Major sex differences in allele frequencies for X chromosomal variants in both the 1000 Genomes Project and gnomAD. PLoS Genet 2022;18:e1010231. [PMID: 35639794 DOI: 10.1371/journal.pgen.1010231] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Barbier M, Camuzat A, Hachimi KE, Guegan J, Rinaldi D, Lattante S, Houot M, Sánchez-Valle R, Sabatelli M, Antonell A, Molina-Porcel L, Clot F, Couratier P, van der Ende E, van der Zee J, Manzoni C, Camu W, Cazeneuve C, Sellal F, Didic M, Golfier V, Pasquier F, Duyckaerts C, Rossi G, Bruni AC, Alvarez V, Gómez-Tortosa E, de Mendonça A, Graff C, Masellis M, Nacmias B, Oumoussa BM, Jornea L, Forlani S, Van Deerlin V, Rohrer JD, Gelpi E, Rademakers R, Van Swieten J, Le Guern E, Van Broeckhoven C, Ferrari R, Génin E, Brice A, Le Ber I; French clinical and genetic Research network on FTLD/FTLD-ALS and PREVDEMALS, The International Frontotemporal Dementia Genomics Consortium, The European Early Onset Dementia (EU -EOD) Consortium, Brainbank Neuro-CEB Neuropathology Network, Neurological Tissue Bank of the Biobank Hospital Clinic-IDIBAPS. SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration. Brain 2021;144:2798-811. [PMID: 34687211 DOI: 10.1093/brain/awab171] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
5 Chen B, Craiu RV, Strug LJ, Sun L. The X factor: A robust and powerful approach to X-chromosome-inclusive whole-genome association studies. Genet Epidemiol 2021. [PMID: 34224641 DOI: 10.1002/gepi.22422] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
6 Hong EP, Chao MJ, Massey T, McAllister B, Lobanov S, Jones L, Holmans P, Kwak S, Orth M, Ciosi M, Monckton DG, Long JD, Lucente D, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease. J Huntingtons Dis 2021. [PMID: 34180418 DOI: 10.3233/JHD-210485] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Song Y, Biernacka JM, Winham SJ. Testing and estimation of X-chromosome SNP effects: Impact of model assumptions. Genet Epidemiol 2021;45:577-92. [PMID: 34082482 DOI: 10.1002/gepi.22393] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
8 Smith SM, Douaud G, Chen W, Hanayik T, Alfaro-Almagro F, Sharp K, Elliott LT. An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Nat Neurosci 2021;24:737-45. [PMID: 33875891 DOI: 10.1038/s41593-021-00826-4] [Cited by in Crossref: 70] [Cited by in F6Publishing: 77] [Article Influence: 35.0] [Reference Citation Analysis]
9 Turkmen AS, Lin S. Detecting X-linked common and rare variant effects in family-based sequencing studies. Genet Epidemiol 2021;45:36-45. [PMID: 32864779 DOI: 10.1002/gepi.22352] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
10 Smith SM, Douaud G, Chen W, Hanayik T, Alfaro-almagro F, Sharp K, Elliott LT. Enhanced Brain Imaging Genetics in UK Biobank.. [DOI: 10.1101/2020.07.27.223545] [Cited by in Crossref: 21] [Cited by in F6Publishing: 22] [Article Influence: 7.0] [Reference Citation Analysis]
11 Deng WQ, Mao S, Kalnapenkis A, Esko T, Mägi R, Paré G, Sun L. Analytical strategies to include the X-chromosome in variance heterogeneity analyses: Evidence for trait-specific polygenic variance structure. Genet Epidemiol 2019;43:815-30. [PMID: 31332826 DOI: 10.1002/gepi.22247] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
12 Deng WQ, Mao S, Kalnapenkis A, Esko T, Mägi R, Paré G, Sun L. Analytical strategies to include the X-chromosome in variance heterogeneity analyses: evidence for trait-specific polygenic variance structure.. [DOI: 10.1101/306654] [Reference Citation Analysis]