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For:	Zhou X, Feliciano P, Wang T, Astrovskaya I, Shu C, Hall JB, Obiajulu JU, Wright J, Murali S, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey W, Nishida A, O’roak BJ, Geschwind DH, Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK, The SPARK Consortium. Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes.. [DOI: 10.1101/2021.10.08.21264256] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]

For:

Zhou X, Feliciano P, Wang T, Astrovskaya I, Shu C, Hall JB, Obiajulu JU, Wright J, Murali S, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey W, Nishida A, O’roak BJ, Geschwind DH, Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK, The SPARK Consortium. Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes.. [DOI: 10.1101/2021.10.08.21264256] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]

Number	Citing Articles
1	Zhong G, Choi YA, Shen Y. Integration of single cell gene expression data in Bayesian association analysis of rare variants.. [DOI: 10.1101/2022.05.13.491893] [Reference Citation Analysis]
2	Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Klei L, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, Dodge S, Gabriel SB, Gauthier L, Lee SK, Liang L, Ljungdahl A, Mahjani B, Sloofman L, Smirnov A, Barbosa M, Brusco A, Chung BH, Cuccaro ML, Domenici E, Ferrero GB, Gargus JJ, Herman GE, Hertz-picciotto I, Maciel P, Manoach DS, Passos-bueno MR, Persico AM, Renieri A, Tassone F, Trabetti E, Campos G, Chan MC, Fallerini C, Giorgio E, Girard AC, Hansen-kiss E, Lee SL, Lintas C, Ludena Y, Nguyen R, Pavinato L, Pericak-vance M, Pessah I, Riberi E, Schmidt R, Smith M, Souza CI, Trajkova S, Wang JY, Yu MH, Cutler DJ, De Rubeis S, Buxbaum JD, Daly MJ, Devlin B, Roeder K, Sanders SJ, Talkowski ME, The Autism Sequencing Consoritum (ASC), Broad Institute Center for Common Disease Genomics (Broad-CCDG), iPSYCH-BROAD Consortium. Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism.. [DOI: 10.1101/2021.12.20.21267194] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 9.5] [Reference Citation Analysis]
3	Rolland T, Cliquet F, Anney RJ, Moreau C, Traut N, Mathieu A, Huguet G, Duan J, Warrier V, Portalier S, Dry L, Leblond CS, Douard E, Amsellem F, Malesys S, Maruani A, Toro R, Børglum AD, Grove J, Baron-cohen S, Packer A, Chung WK, Jacquemont S, Delorme R, Bourgeron T. Sub-diagnostic effects of genetic variants associated with autism.. [DOI: 10.1101/2021.02.12.21251621] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]