Year |
Citation |
Score |
2023 |
Lei W, Zhu H, Cao M, Zhang F, Lai Q, Lu S, Dong W, Sun J, Ru D. From genomics to metabolomics: Deciphering sanguinarine biosynthesis in Dicranostigma leptopodum. International Journal of Biological Macromolecules. 128727. PMID 38092109 DOI: 10.1016/j.ijbiomac.2023.128727 |
0.354 |
|
2023 |
Yan B, Di X, Yang M, Wu H, Yu X, Zhang F. Chromosome-Scale Genome Assembly of The Solitary Parasitoid Wasp Microplitis manilae Ashmead, 1904 (Braconidae: Microgastrinae). Genome Biology and Evolution. PMID 37515590 DOI: 10.1093/gbe/evad144 |
0.309 |
|
2023 |
Kumar J, Char SN, Weiss T, Liu H, Liu B, Yang B, Zhang F. Efficient protein tagging and cis-regulatory element engineering via precise and directional oligonucleotide-based targeted insertion in plants. The Plant Cell. PMID 37191128 DOI: 10.1093/plcell/koad139 |
0.343 |
|
2023 |
Bustos FJ, Pandian S, Haensgen H, Zhao JP, Strouf H, Heidenreich M, Swiech L, Deverman B, Gradinaru V, Zhang F, Constantine-Paton M. Removal of a genomic duplication by double-nicking CRISPR restores synaptic transmission and behavior in the MyosinVA mutant mouse Flailer. Biorxiv : the Preprint Server For Biology. PMID 37163068 DOI: 10.1101/2023.04.28.538685 |
0.317 |
|
2023 |
Chamness JC, Kumar J, Cruz AJ, Rhuby E, Holum MJ, Cody JP, Tibebu R, Gamo ME, Starker CG, Zhang F, Voytas DF. An extensible vector toolkit and parts library for advanced engineering of plant genomes. The Plant Genome. e20312. PMID 36896468 DOI: 10.1002/tpg2.20312 |
0.606 |
|
2022 |
An Y, Zhang X, Jiang S, Zhao J, Zhang F. TeaPVs: a comprehensive genomic variation database for tea plant (Camellia sinensis). Bmc Plant Biology. 22: 513. PMID 36324064 DOI: 10.1186/s12870-022-03901-5 |
0.359 |
|
2022 |
Quan ZJ, Li SA, Yang ZX, Zhao JJ, Li GH, Zhang F, Wen W, Cheng T, Zhang XB. GREPore-seq: A robust workflow to detect changes after gene editing through long-range PCR and nanopore sequencing. Genomics, Proteomics & Bioinformatics. PMID 35752289 DOI: 10.1016/j.gpb.2022.06.002 |
0.332 |
|
2022 |
Read A, Weiss T, Crisp PA, Liang Z, Noshay J, Menard CC, Wang C, Song M, Hirsch CN, Springer NM, Zhang F. Genome-wide loss of CHH methylation with limited transcriptome changes in Setaria viridis domains rearranged methyltransferase (DRM) mutants. The Plant Journal : For Cell and Molecular Biology. PMID 35436373 DOI: 10.1111/tpj.15781 |
0.301 |
|
2022 |
Patil GB, Stupar RM, Zhang F. Protoplast Isolation, Transfection, and Gene Editing for Soybean (Glycine max ). Methods in Molecular Biology (Clifton, N.J.). 2464: 173-186. PMID 35258833 DOI: 10.1007/978-1-0716-2164-6_13 |
0.34 |
|
2022 |
Banakar R, Rai KM, Zhang F. CRISPR DNA- and RNP-Mediated Genome Editing via Nicotiana benthamiana Protoplast Transformation and Regeneration. Methods in Molecular Biology (Clifton, N.J.). 2464: 65-82. PMID 35258825 DOI: 10.1007/978-1-0716-2164-6_5 |
0.306 |
|
2022 |
Fu J, Fu YW, Zhao JJ, Yang ZX, Li SA, Li GH, Quan ZJ, Zhang F, Zhang JP, Zhang XB, Sun CK. Improved and Flexible HDR Editing by Targeting Introns in iPSCs. Stem Cell Reviews and Reports. PMID 35089463 DOI: 10.1007/s12015-022-10331-1 |
0.322 |
|
2021 |
Cable J, Ronald PC, Voytas D, Zhang F, Levy AA, Takatsuka A, Arimura SI, Jacobsen SE, Toki S, Toda E, Gao C, Zhu JK, Boch J, Van Eck J, Mahfouz M, et al. Plant genome engineering from lab to field-a Keystone Symposia report. Annals of the New York Academy of Sciences. PMID 34435370 DOI: 10.1111/nyas.14675 |
0.556 |
|
2020 |
Gao L, Altae-Tran H, Böhning F, Makarova KS, Segel M, Schmid-Burgk JL, Koob J, Wolf YI, Koonin EV, Zhang F. Diverse enzymatic activities mediate antiviral immunity in prokaryotes. Science (New York, N.Y.). 369: 1077-1084. PMID 32855333 DOI: 10.1126/Science.Aba0372 |
0.363 |
|
2020 |
MacKay MJ, Hooker AC, Afshinnekoo E, Salit M, Kelly J, Feldstein JV, Haft N, Schenkel D, Nambi S, Cai Y, Zhang F, Church G, Dai J, Wang CL, Levy S, et al. The COVID-19 XPRIZE and the need for scalable, fast, and widespread testing. Nature Biotechnology. PMID 32820257 DOI: 10.1038/S41587-020-0655-4 |
0.481 |
|
2020 |
Li P, Ning Y, Wang W, Guo X, Poulet B, Wang X, Wen Y, Han J, Hao J, Liang X, Liu L, Du Y, Cheng B, Cheng S, Zhang L, ... Zhang F, et al. The integrative analysis of DNA methylation and mRNA expression profiles confirmed the role of selenocompound metabolism pathway in Kashin-Beck disease. Cell Cycle (Georgetown, Tex.). 1-16. PMID 32816579 DOI: 10.1080/15384101.2020.1807665 |
0.316 |
|
2020 |
Weiss T, Wang C, Kang X, Zhao H, Gamo ME, Starker CG, Crisp PA, Zhou P, Springer NM, Voytas DF, Zhang F. Optimization of multiplexed CRISPR/Cas9 system for highly efficient genome editing in Setaria viridis. The Plant Journal : For Cell and Molecular Biology. PMID 32786122 DOI: 10.1111/Tpj.14949 |
0.65 |
|
2020 |
Jin S, Fei H, Zhu Z, Luo Y, Liu J, Gao S, Zhang F, Chen YH, Wang Y, Gao C. Rationally Designed APOBEC3B Cytosine Base Editors with Improved Specificity. Molecular Cell. PMID 32721385 DOI: 10.1016/J.Molcel.2020.07.005 |
0.398 |
|
2020 |
Schmid-Burgk JL, Gao L, Li D, Gardner Z, Strecker J, Lash B, Zhang F. Highly Parallel Profiling of Cas9 Variant Specificity. Molecular Cell. PMID 32187529 DOI: 10.1016/J.Molcel.2020.02.023 |
0.383 |
|
2020 |
Sun X, Ding Y, Orr MC, Zhang F. Streamlining universal single-copy ortholog and ultraconserved element design: a case study in Collembola. Molecular Ecology Resources. PMID 32065730 DOI: 10.1111/1755-0998.13146 |
0.391 |
|
2019 |
Zhang F, Voytas DF. Modulating gene translational control through genome editing. National Science Review. 6: 391. PMID 34691885 DOI: 10.1093/nsr/nwy123 |
0.571 |
|
2019 |
Liu C, He X, Liu W, Yang S, Wang L, Li W, Wu H, Tang S, Ni X, Wang J, Gao Y, Tian S, Zhang L, Cong J, Zhang Z, ... Zhang F, et al. Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice. American Journal of Human Genetics. PMID 31735294 DOI: 10.1016/J.Ajhg.2019.10.010 |
0.303 |
|
2019 |
Zetsche B, Strecker J, Abudayyeh OO, Gootenberg JS, Scott DA, Zhang F. A Survey of Genome Editing Activity for 16 Cas12a Orthologs. The Keio Journal of Medicine. PMID 31723075 DOI: 10.2302/Kjm.2019-0009-Oa |
0.353 |
|
2019 |
Zhang B, Ma H, Khan T, Ma A, Li T, Zhang H, Gao J, Zhou J, Li Y, Yu C, Bao J, Ali A, Murtaza G, Yin H, Gao Q, ... Zhang F, et al. A missense variant causes flagella destabilization and asthenozoospermia. The Journal of Experimental Medicine. PMID 31658987 DOI: 10.1084/Jem.20182365 |
0.313 |
|
2019 |
Zhang L, Du Y, Wen Y, Ma M, Cheng S, Cheng B, Li P, Qi X, Liang C, Liu L, Liang X, Guo X, Zhang F. Integrating transcriptome-wide association study and mRNA expression profiling identified candidate genes and pathways associated with osteomyelitis. Scandinavian Journal of Rheumatology. 1-6. PMID 31657276 DOI: 10.1080/03009742.2019.1653492 |
0.351 |
|
2019 |
Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, et al. Rare variants in FANCA induce premature ovarian insufficiency. Human Genetics. PMID 31535215 DOI: 10.1007/S00439-019-02059-9 |
0.321 |
|
2019 |
Wang Y, Wu C, Zhang F, Zhang Y, Ren Z, Lammi MJ, Guo X. Screening for Differentially Expressed Circular RNAs in the Cartilage of Osteoarthritis Patients for Their Diagnostic Value. Genetic Testing and Molecular Biomarkers. PMID 31502887 DOI: 10.1089/Gtmb.2019.0108 |
0.314 |
|
2019 |
Chen W, Lin J, Wang L, Li X, Zhao S, Liu J, Akdemir ZC, Zhao Y, Du R, Ye Y, Song X, Zhang Y, Yan Z, Yang X, Lin M, ... ... Zhang F, et al. TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease. Human Mutation. PMID 31471994 DOI: 10.1002/Humu.23907 |
0.341 |
|
2019 |
Hijazi H, Coelho FS, Gonzaga-Jauregui C, Bernardini L, Mar SS, Manning MA, Hanson-Kahn A, Naidu S, Srivastava S, Lee JA, Jones JR, Friez MJ, Alberico T, Torres B, Fang P, ... ... Zhang F, et al. Xq22 deletions and correlation with distinct neurological disease traits in females: further evidence for a contiguous gene syndrome. Human Mutation. PMID 31448840 DOI: 10.1002/Humu.23902 |
0.386 |
|
2019 |
Qi X, Guan F, Wen Y, Li P, Ma M, Cheng S, Zhang L, Liang C, Cheng B, Zhang F. Integrating genome-wide association study and methylation functional annotation data identified candidate genes and pathways for schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 109736. PMID 31425724 DOI: 10.1016/J.Pnpbp.2019.109736 |
0.307 |
|
2019 |
Wu J, Du Y, Song J, Dang X, Wang K, Wen Y, Zhang F, Liu R. Genome-wide DNA methylation profiling of hip articular cartilage identifies differentially methylated loci associated with osteonecrosis of the femoral head. Bone. PMID 31233934 DOI: 10.1016/J.Bone.2019.06.021 |
0.304 |
|
2019 |
Li P, Wu C, Guo X, Wen Y, Liu L, Liang X, Du Y, Zhang L, Ma M, Cheng S, Cheng B, Wang S, Zhang F. Integrative Analysis of Genome-Wide Association Studies and DNA Methylation Profile Identified Genetic Control Genes of DNA Methylation for Kashin-Beck Disease. Cartilage. 1947603519858748. PMID 31220921 DOI: 10.1177/1947603519858748 |
0.324 |
|
2019 |
Strecker J, Ladha A, Gardner Z, Schmid-Burgk JL, Makarova KS, Koonin EV, Zhang F. RNA-guided DNA insertion with CRISPR-associated transposases. Science (New York, N.Y.). PMID 31171706 DOI: 10.1126/Science.Aax9181 |
0.31 |
|
2019 |
Zhang L, Liu L, Ma M, Cheng S, Cheng B, Li P, Wen Y, Du Y, Liang X, Zhao Y, Ding M, Xin Q, Liang C, Huang H, Zhang F. Integrative analysis of transcriptome-wide association study data and mRNA expression profiles identified candidate genes and pathways associated with atrial fibrillation. Heart and Vessels. PMID 31065785 DOI: 10.1007/S00380-019-01418-W |
0.331 |
|
2019 |
Hirano S, Abudayyeh OO, Gootenberg JS, Horii T, Ishitani R, Hatada I, Zhang F, Nishimasu H, Nureki O. Structural basis for the promiscuous PAM recognition by Corynebacterium diphtheriae Cas9. Nature Communications. 10: 1968. PMID 31036811 DOI: 10.1038/s41467-019-09741-6 |
0.301 |
|
2019 |
Cheng B, Liang X, Wen Y, Li P, Zhang L, Ma M, Cheng S, Du Y, Liu L, Ding M, Zhao Y, Zhang F. Integrative analysis of transcriptome-wide association study data and messenger RNA expression profiles identified candidate genes and pathways for inflammatory bowel disease. Journal of Cellular Biochemistry. PMID 31009124 DOI: 10.1002/Jcb.28744 |
0.316 |
|
2019 |
Ma M, Huang DG, Liang X, Zhang L, Cheng S, Cheng B, Qi X, Li P, Du Y, Liu L, Zhao Y, Ding M, Wen Y, Guo X, Zhang F. Integrating transcriptome-wide association study and mRNA expression profiling identifies novel genes associated with bone mineral density. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. PMID 30993394 DOI: 10.1007/S00198-019-04958-Z |
0.311 |
|
2019 |
Liu W, He X, Yang S, Zouari R, Wang J, Wu H, Kherraf ZE, Liu C, Coutton C, Zhao R, Tang D, Tang S, Lv M, Fang Y, Li W, ... ... Zhang F, et al. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice. American Journal of Human Genetics. PMID 30929735 DOI: 10.1016/J.Ajhg.2019.02.020 |
0.315 |
|
2019 |
Jin S, Zong Y, Gao Q, Zhu Z, Wang Y, Qin P, Liang C, Wang D, Qiu JL, Zhang F, Gao C. Cytosine, but not adenine, base editors induce genome-wide off-target mutations in rice. Science (New York, N.Y.). PMID 30819931 DOI: 10.1126/Science.Aaw7166 |
0.396 |
|
2019 |
Coutton C, Martinez G, Kherraf ZE, Amiri-Yekta A, Boguenet M, Saut A, He X, Zhang F, Cristou-Kent M, Escoffier J, Bidart M, Satre V, Conne B, Fourati Ben Mustapha S, Halouani L, et al. Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. American Journal of Human Genetics. PMID 30686508 DOI: 10.1016/J.Ajhg.2018.12.013 |
0.322 |
|
2019 |
Strecker J, Jones S, Koopal B, Schmid-Burgk J, Zetsche B, Gao L, Makarova KS, Koonin EV, Zhang F. Engineering of CRISPR-Cas12b for human genome editing. Nature Communications. 10: 212. PMID 30670702 DOI: 10.1038/S41467-018-08224-4 |
0.378 |
|
2019 |
Zhang F, Ding Y, Zhou QS, Wu J, Luo A, Zhu CD. A high-quality draft genome assembly of Sinella curviseta, a soil model organism (Collembola). Genome Biology and Evolution. PMID 30668671 DOI: 10.1093/Gbe/Evz013 |
0.348 |
|
2019 |
Dong S, Wang C, Li X, Shen Q, Fu X, Wu M, Song C, Yang N, Wu Y, Wang H, Jin L, Xu H, Zhang F. Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract. Molecular Genetics and Genomics : Mgg. PMID 30604070 DOI: 10.1007/S00438-018-1522-6 |
0.311 |
|
2019 |
Wang Q, Li D, Cai B, Chen Q, Li C, Wu Y, Jin L, Wang X, Zhang X, Zhang F. Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations. Human Genetics. PMID 30603774 DOI: 10.1007/S00439-018-1962-4 |
0.34 |
|
2019 |
Zhang F. Biology and Application of Genome Editing Blood. 134. DOI: 10.1182/Blood-2019-121282 |
0.331 |
|
2018 |
Huang H, Cheng S, Ding M, Wen Y, Ma M, Zhang L, Li P, Cheng B, Liang X, Liu L, Du Y, Zhao Y, Kafle OP, Han B, Zhang F. Integrative Analysis of Transcriptome-Wide Association Study and mRNA Expression Profiles Identifies Candidate Genes Associated With Autism Spectrum Disorders. Autism Research : Official Journal of the International Society For Autism Research. PMID 30561910 DOI: 10.1002/Aur.2048 |
0.329 |
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2018 |
Ji X, Si X, Zhang Y, Zhang H, Zhang F, Gao C. Conferring DNA virus resistance with high specificity in plants using virus-inducible genome-editing system. Genome Biology. 19: 197. PMID 30442181 DOI: 10.1186/S13059-018-1580-4 |
0.322 |
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2018 |
He X, Li W, Wu H, Lv M, Liu W, Liu C, Zhu F, Li C, Fang Y, Yang C, Cheng H, Zhang J, Tan J, Chen T, Tang D, ... ... Zhang F, et al. Novel homozygous mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. Journal of Medical Genetics. PMID 30415212 DOI: 10.1136/Jmedgenet-2018-105486 |
0.315 |
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2018 |
Gao K, Zhang Y, Zhang L, Kong W, Xie H, Wang J, Wu Y, Wu X, Liu X, Zhang Y, Zhang F, Yu AC, Jiang Y. Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology Analysis. Advances in Neurobiology. 21: 247-266. PMID 30334225 DOI: 10.1007/978-3-319-94593-4_9 |
0.32 |
|
2018 |
Li W, He X, Yang S, Liu C, Wu H, Liu W, Lv M, Tang D, Tan J, Tang S, Chen Y, Wang J, Zhang Z, Wang H, Jin L, ... Zhang F, et al. Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility. Journal of Human Genetics. PMID 30310178 DOI: 10.1038/S10038-018-0520-1 |
0.334 |
|
2018 |
Yang N, Wu N, Zhang L, Zhao Y, Liu J, Liang X, Ren X, Li W, Chen W, Dong S, Zhao S, Lin J, Xiang H, Xue H, Chen L, ... ... Zhang F, et al. TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice. Human Molecular Genetics. PMID 30307510 DOI: 10.1093/Hmg/Ddy358 |
0.315 |
|
2018 |
Nishimasu H, Shi X, Ishiguro S, Gao L, Hirano S, Okazaki S, Noda T, Abudayyeh OO, Gootenberg JS, Mori H, Oura S, Holmes B, Tanaka M, Seki M, Hirano H, ... ... Zhang F, et al. Engineered CRISPR-Cas9 nuclease with expanded targeting space. Science (New York, N.Y.). PMID 30166441 DOI: 10.1126/Science.Aas9129 |
0.341 |
|
2018 |
Zhang F, Voytas DF. Synthetic genomes engineered by SCRaMbLEing. Science China. Life Sciences. PMID 29951952 DOI: 10.1007/S11427-018-9325-1 |
0.579 |
|
2018 |
He A, Ning Y, Wen Y, Cai Y, Xu K, Cai Y, Han J, Liu L, Du Y, Liang X, Li P, Fan Q, Hao J, Wang X, Guo X, ... Zhang F, et al. Use of integrative epigenetic and mRNA expression analyses to identify significantly changed genes and functional pathways in osteoarthritic cartilage. Bone & Joint Research. 7: 343-350. PMID 29922454 DOI: 10.1302/2046-3758.75.Bjr-2017-0284.R1 |
0.352 |
|
2018 |
Ding M, Li P, Wen Y, Zhao Y, Cheng B, Zhang L, Ma M, Cheng S, Liu L, Du Y, Liang X, He A, Guo X, Zhang F. Integrative analysis of genome-wide association study and brain region related enhancer maps identifies biological pathways for insomnia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. PMID 29883697 DOI: 10.1016/J.Pnpbp.2018.05.026 |
0.331 |
|
2018 |
Myers SA, Wright J, Peckner R, Kalish BT, Zhang F, Carr SA. Discovery of proteins associated with a predefined genomic locus via dCas9-APEX-mediated proximity labeling. Nature Methods. PMID 29735997 DOI: 10.1038/S41592-018-0007-1 |
0.388 |
|
2018 |
Canver MC, Haeussler M, Bauer DE, Orkin SH, Sanjana NE, Shalem O, Yuan GC, Zhang F, Concordet JP, Pinello L. Integrated design, execution, and analysis of arrayed and pooled CRISPR genome-editing experiments. Nature Protocols. 13: 946-986. PMID 29651054 DOI: 10.1038/Nprot.2018.005 |
0.333 |
|
2018 |
Wang G, Chow RD, Ye L, Guzman CD, Dai X, Dong MB, Zhang F, Sharp PA, Platt RJ, Chen S. Mapping a functional cancer genome atlas of tumor suppressors in mouse liver using AAV-CRISPR-mediated direct in vivo screening. Science Advances. 4: eaao5508. PMID 29503867 DOI: 10.1126/Sciadv.Aao5508 |
0.322 |
|
2018 |
Fan C, Cai X, Zhang F, Hochstetler C, Chen X, Guo F, Tian W, Zheng Y. Precision Assessment of on- and Off-Target Effects of mTOR Kinase Inhibitors in a Mouse Model Blood. 132: 2632-2632. DOI: 10.1182/Blood-2018-99-115225 |
0.311 |
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2018 |
Zhang F, Voytas DF. Modulating gene translational control through genome editing National Science Review. 6: 391-391. DOI: 10.1093/Nsr/Nwy123 |
0.612 |
|
2017 |
Fan H, Lv P, Huo X, Wu J, Wang Q, Cheng L, Liu Y, Tang Q, Zhang L, Zhang F, Zheng X, Wu H, Wen B. The nuclear matrix protein HNRNPU maintains 3D genome architecture globally in mouse hepatocytes. Genome Research. PMID 29273625 DOI: 10.1101/Gr.224576.117 |
0.339 |
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2017 |
He A, Wang W, Prakash NT, Tinkov AA, Skaln AV, Wen Y, Hao J, Guo X, Zhang F. Integrating genome-wide association study summaries and element-gene interaction datasets identified multiple associations between elements and complex diseases. Genetic Epidemiology. PMID 29265413 DOI: 10.1002/Gepi.22106 |
0.318 |
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2017 |
Jiang Q, Liu F, Miao C, Li Q, Zhang Z, Xiao P, Su L, Yu K, Chen X, Zhang F, Chakravarti A, Li L. RET somatic mutations are underrecognized in Hirschsprung disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29261189 DOI: 10.1038/Gim.2017.178 |
0.32 |
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2017 |
Cox DBT, Gootenberg JS, Abudayyeh OO, Franklin B, Kellner MJ, Joung J, Zhang F. RNA editing with CRISPR-Cas13. Science (New York, N.Y.). PMID 29070703 DOI: 10.1126/Science.Aaq0180 |
0.31 |
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2017 |
Zhao Y, He A, Zhu F, Ding M, Hao J, Fan Q, Li P, Liu L, Du Y, Liang X, Guo X, Zhang F, Ma X. Integrating genome-wide association study and expression quantitative trait locus study identifies multiple genes and gene sets associated with schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. PMID 29024729 DOI: 10.1016/J.Pnpbp.2017.10.003 |
0.324 |
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2017 |
Yang L, Briggs AW, Chew WL, Mali P, Guell M, Aach J, Goodman DB, Cox D, Kan Y, Lesha E, Soundararajan V, Zhang F, Church G. Corrigendum: Engineering and optimising deaminase fusions for genome editing. Nature Communications. 8: 16169. PMID 28991237 DOI: 10.1038/Ncomms16169 |
0.304 |
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2017 |
Wang W, Huang S, Hou W, Liu Y, Fan Q, He A, Wen Y, Hao J, Guo X, Zhang F. Integrative analysis of GWAS, eQTLs and meQTLs data suggests that multiple gene sets are associated with bone mineral density. Bone & Joint Research. 6: 572-576. PMID 28978616 DOI: 10.1302/2046-3758.610.Bjr-2017-0113.R1 |
0.367 |
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2017 |
Abudayyeh OO, Gootenberg JS, Essletzbichler P, Han S, Joung J, Belanto JJ, Verdine V, Cox DBT, Kellner MJ, Regev A, Lander ES, Voytas DF, Ting AY, Zhang F. RNA targeting with CRISPR-Cas13. Nature. PMID 28976959 DOI: 10.1038/Nature24049 |
0.525 |
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2017 |
Jain A, Zode G, Kasetti RB, Ran FA, Yan W, Sharma TP, Bugge K, Searby CC, Fingert JH, Zhang F, Clark AF, Sheffield VC. CRISPR-Cas9-based treatment of myocilin-associated glaucoma. Proceedings of the National Academy of Sciences of the United States of America. PMID 28973933 DOI: 10.1073/Pnas.1706193114 |
0.336 |
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2017 |
Wang W, Yu Y, Hao J, Wen Y, Han J, Hou W, Liu R, Zhao B, He A, Li P, Fan Q, Wu C, Wang S, Wang X, Ning Y, ... ... Zhang F, et al. Genome-wide DNA methylation profiling of articular cartilage reveals significant epigenetic alterations in Kashin-Beck disease and osteoarthritis. Osteoarthritis and Cartilage. PMID 28818737 DOI: 10.1016/J.Joca.2017.08.002 |
0.307 |
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2017 |
Chow RD, Guzman CD, Wang G, Schmidt F, Youngblood MW, Ye L, Errami Y, Dong MB, Martinez MA, Zhang S, Renauer P, Bilguvar K, Gunel M, Sharp PA, Zhang F, et al. AAV-mediated direct in vivo CRISPR screen identifies functional suppressors in glioblastoma. Nature Neuroscience. PMID 28805815 DOI: 10.1038/Nn.4620 |
0.33 |
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2017 |
Joung J, Engreitz JM, Konermann S, Abudayyeh OO, Verdine VK, Aguet F, Gootenberg JS, Sanjana NE, Wright JB, Fulco CP, Tseng YY, Yoon CH, Boehm JS, Lander ES, Zhang F. Genome-scale activation screen identifies a lncRNA locus regulating a gene neighbourhood. Nature. PMID 28792927 DOI: 10.1038/Nature23451 |
0.376 |
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2017 |
Patel SJ, Sanjana NE, Kishton RJ, Eidizadeh A, Vodnala SK, Cam M, Gartner JJ, Jia L, Steinberg SM, Yamamoto TN, Merchant AS, Mehta GU, Chichura A, Shalem O, Tran E, ... Zhang F, et al. Identification of essential genes for cancer immunotherapy. Nature. PMID 28783722 DOI: 10.1038/Nature23477 |
0.341 |
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2017 |
Yamano T, Zetsche B, Ishitani R, Zhang F, Nishimasu H, Nureki O. Structural Basis for the Canonical and Non-canonical PAM Recognition by CRISPR-Cpf1. Molecular Cell. PMID 28781234 DOI: 10.1016/J.Molcel.2017.06.035 |
0.321 |
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2017 |
Scott DA, Zhang F. Implications of human genetic variation in CRISPR-based therapeutic genome editing. Nature Medicine. PMID 28759051 DOI: 10.1038/Nm.4377 |
0.381 |
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2017 |
Liang X, He A, Wang W, Liu L, Du Y, Fan Q, Li P, Wen Y, Hao J, Guo X, Zhang F. Integrating Genome-Wide Association and eQTLs Studies Identifies the Genes and Gene Sets Associated with Diabetes. Biomed Research International. 2017: 1758636. PMID 28744461 DOI: 10.1155/2017/1758636 |
0.336 |
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2017 |
Lu J, Lou H, Fu R, Lu D, Zhang F, Wu Z, Zhang X, Li C, Fang B, Pu F, Wei J, Wei Q, Zhang C, Wang X, Lu Y, et al. Assessing genome-wide copy number variation in the Han Chinese population. Journal of Medical Genetics. PMID 28705883 DOI: 10.1136/Jmedgenet-2017-104613 |
0.327 |
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2017 |
Wang X, Zhang Y, Zhang X, Wang D, Jin G, Li B, Xu F, Cheng J, Zhang F, Wu S, Rui S, He J, Zhang R, Liu W. The comprehensive liver transcriptome of two cattle breeds with different intramuscular fat content. Biochemical and Biophysical Research Communications. PMID 28669724 DOI: 10.1016/J.Bbrc.2017.06.157 |
0.314 |
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Lupski JR, Reid JG, Gonzaga-Jauregui C, Rio Deiros D, Chen DC, Nazareth L, Bainbridge M, Dinh H, Jing C, Wheeler DA, McGuire AL, Zhang F, Stankiewicz P, Halperin JJ, Yang C, et al. Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. The New England Journal of Medicine. 362: 1181-91. PMID 20220177 DOI: 10.1056/Nejmoa0908094 |
0.38 |
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2010 |
Zhang L, Guo YF, Liu YZ, Liu YJ, Xiong DH, Liu XG, Wang L, Yang TL, Lei SF, Guo Y, Yan H, Pei YF, Zhang F, Papasian CJ, Recker RR, et al. Pathway-based genome-wide association analysis identified the importance of regulation-of-autophagy pathway for ultradistal radius BMD. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 1572-80. PMID 20200951 DOI: 10.1002/Jbmr.36 |
0.341 |
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2010 |
Zhang F, Potocki L, Sampson JB, Liu P, Sanchez-Valle A, Robbins-Furman P, Navarro AD, Wheeler PG, Spence JE, Brasington CK, Withers MA, Lupski JR. Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS. American Journal of Human Genetics. 86: 462-70. PMID 20188345 DOI: 10.1016/J.Ajhg.2010.02.001 |
0.387 |
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2010 |
Carvalho CM, Zhang F, Lupski JR. Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution. Proceedings of the National Academy of Sciences of the United States of America. 107: 1765-71. PMID 20080665 DOI: 10.1073/Pnas.0906222107 |
0.387 |
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2010 |
Guo Y, Tan LJ, Lei SF, Yang TL, Chen XD, Zhang F, Chen Y, Pan F, Yan H, Liu X, Tian Q, Zhang ZX, Zhou Q, Qiu C, Dong SS, et al. Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. Plos Genetics. 6: e1000806. PMID 20072603 DOI: 10.1371/Journal.Pgen.1000806 |
0.335 |
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2009 |
Naito K, Zhang F, Tsukiyama T, Saito H, Hancock CN, Richardson AO, Okumoto Y, Tanisaka T, Wessler SR. Unexpected consequences of a sudden and massive transposon amplification on rice gene expression. Nature. 461: 1130-4. PMID 19847266 DOI: 10.1038/Nature08479 |
0.787 |
|
2009 |
Zhang F, Gu W, Hurles ME, Lupski JR. Copy number variation in human health, disease, and evolution. Annual Review of Genomics and Human Genetics. 10: 451-481. PMID 19715442 DOI: 10.1146/Annurev.Genom.9.081307.164217 |
0.411 |
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2009 |
Nagamani SC, Zhang F, Shchelochkov OA, Bi W, Ou Z, Scaglia F, Probst FJ, Shinawi M, Eng C, Hunter JV, Sparagana S, Lagoe E, Fong CT, Pearson M, Doco-Fenzy M, et al. Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment. Journal of Medical Genetics. 46: 825-33. PMID 19584063 DOI: 10.1136/Jmg.2009.067637 |
0.349 |
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2009 |
Zhang F, Carvalho CMB, Lupski JR. Complex human chromosomal and genomic rearrangements Trends in Genetics. 25: 298-307. PMID 19560228 DOI: 10.1016/J.Tig.2009.05.005 |
0.355 |
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2009 |
Zhang F, Khajavi M, Connolly AM, Towne CF, Batish SD, Lupski JR. The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans. Nature Genetics. 41: 849-53. PMID 19543269 DOI: 10.1038/Ng.399 |
0.395 |
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2009 |
Carvalho CM, Zhang F, Liu P, Patel A, Sahoo T, Bacino CA, Shaw C, Peacock S, Pursley A, Tavyev YJ, Ramocki MB, Nawara M, Obersztyn E, Vianna-Morgante AM, Stankiewicz P, et al. Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching. Human Molecular Genetics. 18: 2188-203. PMID 19324899 DOI: 10.1093/Hmg/Ddp151 |
0.389 |
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2009 |
Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, et al. Increased LIS1 expression affects human and mouse brain development. Nature Genetics. 41: 168-77. PMID 19136950 DOI: 10.1038/Ng.302 |
0.323 |
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2009 |
Yan J, Zhang F, Brundage E, Scheuerle A, Lanpher B, Erickson RP, Powis Z, Robinson HB, Trapane PL, Stachiw-Hietpas D, Keppler-Noreuil KM, Lalani SR, Sahoo T, Chinault AC, Patel A, et al. Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange. Journal of Medical Genetics. 46: 626-34. PMID 19052029 DOI: 10.1136/Jmg.2008.062471 |
0.41 |
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2008 |
Gu W, Zhang F, Lupski JR. Mechanisms for human genomic rearrangements Pathogenetics. 1: 4-4. PMID 19014668 DOI: 10.1186/1755-8417-1-4 |
0.373 |
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2008 |
Doco-Fenzy M, Holder-Espinasse M, Bieth E, Magdelaine C, Vincent M, Khoury M, Andrieux J, Zhang F, Lupski JR, Klink R, Schneider A, Goze-Martineau O, Cuisset J, Vallee L, Manouvrier-Hanu S, et al. The clinical spectrum associated with a chromosome 17 short arm proximal duplication (dup 17p11.2) in three patients. American Journal of Medical Genetics Part A. 146: 917-924. PMID 18327785 DOI: 10.1002/Ajmg.A.32195 |
0.317 |
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2008 |
Zhang F, Xiao P, Yang F, Shen H, Xiong DH, Deng HY, Papasian CJ, Drees BM, Hamilton JJ, Recker RR, Deng HW. A whole genome linkage scan for QTLs underlying peak bone mineral density. Osteoporosis International. 19: 303-310. PMID 17882466 DOI: 10.1007/S00198-007-0468-Z |
0.313 |
|
2007 |
He LN, Xiong DH, Liu YJ, Zhang F, Recker RR, Deng HW. Association study of the oestrogen signalling pathway genes in relation to age at natural menopause. Journal of Genetics. 86: 269-276. PMID 18305346 DOI: 10.1007/S12041-007-0034-7 |
0.313 |
|
2007 |
Yang G, Zhang F, Hancock CN, Wessler SR. Transposition of the rice miniature inverted repeat transposable element mPing in Arabidopsis thaliana. Proceedings of the National Academy of Sciences of the United States of America. 104: 10962-7. PMID 17578919 DOI: 10.1073/Pnas.0702080104 |
0.74 |
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2007 |
Chen Y, Xiong DH, Yang TL, Yang F, Jiang H, Zhang F, Shen H, Xiao P, Recker RR, Deng HW. Variations in RANK gene are associated with adult height in Caucasians. American Journal of Human Biology : the Official Journal of the Human Biology Council. 19: 559-65. PMID 17546619 DOI: 10.1002/Ajhb.20619 |
0.308 |
|
2006 |
Zhang J, Zhang F, Peterson T. Transposition of reversed Ac element ends generates novel chimeric genes in maize. Plos Genetics. 2: e164. PMID 17029561 DOI: 10.1371/Journal.Pgen.0020164 |
0.608 |
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2006 |
Zhang F, Peterson T. Gene conversion between direct noncoding repeats promotes genetic and phenotypic diversity at a regulatory locus of Zea mays (L.). Genetics. 174: 753-62. PMID 16816430 DOI: 10.1534/Genetics.105.053942 |
0.617 |
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2006 |
Zhang F, Li Z, Wen B, Jiang J, Shao M, Zhao Y, He Y, Song X, Qian J, Lu D, Jin L. A frequent partial AZFc deletion does not render an increased risk of spermatogenic impairment in East Asians. Annals of Human Genetics. 70: 304-13. PMID 16674553 DOI: 10.1111/J.1529-8817.2005.00231.X |
0.32 |
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2005 |
Zhang F, Peterson T. Comparisons of maize pericarp color1 alleles reveal paralogous gene recombination and an organ-specific enhancer region. The Plant Cell. 17: 903-14. PMID 15722466 DOI: 10.1105/Tpc.104.029660 |
0.564 |
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2005 |
Yu J, Wang J, Lin W, Li S, Li H, Zhou J, Ni P, Dong W, Hu S, Zeng C, Zhang J, Zhang Y, Li R, Xu Z, Li S, ... ... Zhang F, et al. The Genomes of Oryza sativa: a history of duplications. Plos Biology. 3: e38. PMID 15685292 DOI: 10.1371/Journal.Pbio.0030038 |
0.722 |
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2003 |
Qin E, Zhu Q, Yu M, Fan B, Chang G, Si B, Yang B, Peng W, Jiang T, Liu B, Deng Y, Liu H, Zhang Y, Wang C, Li Y, ... ... Zhang F, et al. A complete sequence and comparative analysis of a SARS-associated virus (Isolate BJ01). Chinese Science Bulletin = Kexue Tongbao. 48: 941-948. PMID 32214698 DOI: 10.1007/Bf03184203 |
0.677 |
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2003 |
Bi S, Qin E, Xu Z, Li W, Wang J, Hu Y, Liu Y, Duan S, Hu J, Han Y, Xu J, Li Y, Yi Y, Zhou Y, Lin W, ... ... Zhang F, et al. Complete genome sequences of the SARS-CoV: the BJ Group (Isolates BJ01-BJ04). Genomics, Proteomics & Bioinformatics. 1: 180-92. PMID 15629030 DOI: 10.1016/S1672-0229(03)01023-4 |
0.64 |
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