Fu W - Search Results

1

New Human Chromosomal Sites with "Safe Harbor" Potential for Targeted Transgene Insertion.

Pellenz S, Phelps M, Tang W, Hovde BT, Sinit RB, Fu W, Li H, Chen E, Monnat RJ Jr. Pellenz S, et al. Among authors: fu w. Hum Gene Ther. 2019 Jul;30(7):814-828. doi: 10.1089/hum.2018.169. Epub 2019 Mar 28. Hum Gene Ther. 2019. PMID: 30793977 Free PMC article.

2

Global and disease-associated genetic variation in the human Fanconi anemia gene family.

Rogers KJ, Fu W, Akey JM, Monnat RJ Jr. Rogers KJ, et al. Among authors: fu w. Hum Mol Genet. 2014 Dec 20;23(25):6815-25. doi: 10.1093/hmg/ddu400. Epub 2014 Aug 7. Hum Mol Genet. 2014. PMID: 25104853 Free PMC article.

3

Human RECQ Helicase Pathogenic Variants, Population Variation and "Missing" Diseases.

Fu W, Ligabue A, Rogers KJ, Akey JM, Monnat RJ Jr. Fu W, et al. Hum Mutat. 2017 Feb;38(2):193-203. doi: 10.1002/humu.23148. Epub 2016 Dec 9. Hum Mutat. 2017. PMID: 27859906 Free PMC article.

4

Present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago.

Wang C, Yan S, Hou Z, Fu W, Xiong M, Han S, Jin L, Li H. Wang C, et al. Among authors: fu w. J Hum Genet. 2012 Mar;57(3):216-8. doi: 10.1038/jhg.2011.147. Epub 2011 Dec 22. J Hum Genet. 2012. PMID: 22189622

5

Y chromosomes of 40% Chinese descend from three Neolithic super-grandfathers.

Yan S, Wang CC, Zheng HX, Wang W, Qin ZD, Wei LH, Wang Y, Pan XD, Fu WQ, He YG, Xiong LJ, Jin WF, Li SL, An Y, Li H, Jin L. Yan S, et al. Among authors: fu wq. PLoS One. 2014 Aug 29;9(8):e105691. doi: 10.1371/journal.pone.0105691. eCollection 2014. PLoS One. 2014. PMID: 25170956 Free PMC article.

6

Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.

Tabor HK, Auer PL, Jamal SM, Chong JX, Yu JH, Gordon AS, Graubert TA, O'Donnell CJ, Rich SS, Nickerson DA; NHLBI Exome Sequencing Project; Bamshad MJ. Tabor HK, et al. Am J Hum Genet. 2014 Aug 7;95(2):183-93. doi: 10.1016/j.ajhg.2014.07.006. Epub 2014 Jul 31. Am J Hum Genet. 2014. PMID: 25087612 Free PMC article.

7

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome.

Peng Z, Zhou W, Fu W, Du R, Jin L, Zhang F. Peng Z, et al. Among authors: fu w. Hum Mol Genet. 2015 Mar 1;24(5):1225-33. doi: 10.1093/hmg/ddu533. Epub 2014 Oct 16. Hum Mol Genet. 2015. PMID: 25324539

8

Robust Inference of Identity by Descent from Exome-Sequencing Data.

Fu W, Browning SR, Browning BL, Akey JM. Fu W, et al. Am J Hum Genet. 2016 Nov 3;99(5):1106-1116. doi: 10.1016/j.ajhg.2016.09.011. Epub 2016 Oct 13. Am J Hum Genet. 2016. PMID: 27745837 Free PMC article.

9

Characteristics of neutral and deleterious protein-coding variation among individuals and populations.

Fu W, Gittelman RM, Bamshad MJ, Akey JM. Fu W, et al. Am J Hum Genet. 2014 Oct 2;95(4):421-36. doi: 10.1016/j.ajhg.2014.09.006. Am J Hum Genet. 2014. PMID: 25279984 Free PMC article.

10

Rare loss of function variants in candidate genes and risk of colorectal cancer.

Rosenthal EA, Shirts BH, Amendola LM, Horike-Pyne M, Robertson PD, Hisama FM, Bennett RL, Dorschner MO, Nickerson DA, Stanaway IB, Nassir R, Vickers KT, Li C, Grady WM, Peters U, Jarvik GP; NHLBI GO Exome Sequencing Project. Rosenthal EA, et al. Hum Genet. 2018 Oct;137(10):795-806. doi: 10.1007/s00439-018-1938-4. Epub 2018 Sep 28. Hum Genet. 2018. PMID: 30267214 Free PMC article. Clinical Trial.

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