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For: Bizzotto S, Dou Y, Ganz J, Doan RN, Kwon M, Bohrson CL, Kim SN, Bae T, Abyzov A, Park PJ, Walsh CA; NIMH Brain Somatic Mosaicism Network. Landmarks of human embryonic development inscribed in somatic mutations. Science 2021;371:1249-53. [PMID: 33737485 DOI: 10.1126/science.abe1544] [Cited by in Crossref: 7] [Cited by in F6Publishing: 19] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Chen C, Liao Y, Peng G. Connecting past and present: single-cell lineage tracing. Protein Cell 2022;13:790-807. [PMID: 35441356 DOI: 10.1007/s13238-022-00913-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
2 Singh SM, Win PW, Castellani CA. Complementary approaches involving monozygotic twins and single neuron genomics support postzygotic somatic mutations in schizophrenia. Schizophr Res 2022;248:228-30. [PMID: 36108467 DOI: 10.1016/j.schres.2022.09.011] [Reference Citation Analysis]
3 Lim Y, Park IH, Lee HH, Baek K, Lee BC, Cho G. Modified Taq polymerase for allele-specific ultra-sensitive detection of genetic variants. J Mol Diagn 2022:S1525-1578(22)00221-5. [PMID: 36058471 DOI: 10.1016/j.jmoldx.2022.08.002] [Reference Citation Analysis]
4 Bae T, Fasching L, Wang Y, Shin JH, Suvakov M, Jang Y, Norton S, Dias C, Mariani J, Jourdon A, Wu F, Panda A, Pattni R, Chahine Y, Yeh R, Roberts RC, Huttner A, Kleinman JE, Hyde TM, Straub RE, Walsh CA, Urban AE, Leckman JF, Weinberger DR, Vaccarino FM, Abyzov A, Walsh CA, Park PJ, Sestan N, Weinberger D, Moran JV, Gage FH, Vaccarino FM, Gleeson J, Mathern G, Courchesne E, Roy S, Chess AJ, Akbarian S, Bizzotto S, Coulter M, Dias C, D'Gama A, Ganz J, Hill R, Huang AY, Khoshkhoo S, Kim S, Lee A, Lodato M, Maury EA, Miller M, Borges-Monroy R, Rodin R, Zhou Z, Bohrson C, Chu C, Cortes-Ciriano I, Dou Y, Galor A, Gulhan D, Kwon M, Luquette J, Sherman M, Viswanadham V, Jones A, Rosenbluh C, Cho S, Langmead B, Thorpe J, Erwin J, Jaffe A, McConnell M, Narurkar R, Paquola A, Shin J, Straub R, Abyzov A, Bae T, Jang Y, Wang Y, Molitor C, Peters M, Linker S, Reed P, Wang M, Urban A, Zhou B, Zhu X, Pattni R, Serres Amero A, Juan D, Lobon I, Marques-Bonet T, Solis Moruno M, Garcia Perez R, Povolotskaya I, Soriano E, Antaki D, Averbuj D, Ball L, Breuss M, Yang X, Chung C, Emery SB, Flasch DA, Kidd JM, Kopera HC, Kwan KY, Mills RE, Moldovan JB, Sun C, Zhao X, Zhou W, Frisbie TJ, Cherskov A, Fasching L, Jourdon A, Pochareddy S, Scuderi S; Brain Somatic Mosaicism Network§. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability. Science 2022;377:511-7. [PMID: 35901164 DOI: 10.1126/science.abm6222] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Huang AY, Lee EA. Identification of Somatic Mutations From Bulk and Single-Cell Sequencing Data. Front Aging 2021;2:800380. [PMID: 35822012 DOI: 10.3389/fragi.2021.800380] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Luijts T, Elliott K, Siaw JT, Van de Velde J, Beyls E, Claeys A, Lammens T, Larsson E, Willaert W, Vral A, Van den Eynden J. A clinically annotated post-mortem approach to study multi-organ somatic mutational clonality in normal tissues. Sci Rep 2022;12:10322. [PMID: 35725896 DOI: 10.1038/s41598-022-14240-8] [Reference Citation Analysis]
7 Franco I, Revêchon G, Eriksson M. Challenges of proving a causal role of somatic mutations in the aging process. Aging Cell 2022;21:e13613. [PMID: 35435316 DOI: 10.1111/acel.13613] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Anderson DJ, Pauler FM, McKenna A, Shendure J, Hippenmeyer S, Horwitz MS. Simultaneous brain cell type and lineage determined by scRNA-seq reveals stereotyped cortical development. Cell Syst 2022:S2405-4712(22)00133-8. [PMID: 35452605 DOI: 10.1016/j.cels.2022.03.006] [Reference Citation Analysis]
9 Breuss MW, Yang X, Schlachetzki JCM, Antaki D, Lana AJ, Xu X, Chung C, Chai G, Stanley V, Song Q, Newmeyer TF, Nguyen A, O'Brien S, Hoeksema MA, Cao B, Nott A, McEvoy-Venneri J, Pasillas MP, Barton ST, Copeland BR, Nahas S, Van Der Kraan L, Ding Y, Glass CK, Gleeson JG; NIMH Brain Somatic Mosaicism Network. Somatic mosaicism reveals clonal distributions of neocortical development. Nature 2022. [PMID: 35444276 DOI: 10.1038/s41586-022-04602-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
10 Kwon SG, Bae GH, Choi JH, Mali NM, Jun MS, Kim DS, Han MH, Park S, Ju YS, Choi SH, Oh JW. Asymmetric Contribution of Blastomere Lineages of First Division of the Zygote to Entire Human Body Using Post-Zygotic Variants. Tissue Eng Regen Med 2022. [PMID: 35438457 DOI: 10.1007/s13770-022-00443-7] [Reference Citation Analysis]
11 Bizzotto S, Walsh CA. Genetic mosaicism in the human brain: from lineage tracing to neuropsychiatric disorders. Nat Rev Neurosci 2022. [PMID: 35322263 DOI: 10.1038/s41583-022-00572-x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
12 Rossant J, Tam PP. Early human embryonic development: Blastocyst formation to gastrulation. Developmental Cell 2022;57:152-65. [DOI: 10.1016/j.devcel.2021.12.022] [Cited by in Crossref: 14] [Cited by in F6Publishing: 8] [Article Influence: 14.0] [Reference Citation Analysis]
13 Kelley KW, Pașca SP. Human brain organogenesis: Toward a cellular understanding of development and disease. Cell 2021:S0092-8674(21)01177-6. [PMID: 34774127 DOI: 10.1016/j.cell.2021.10.003] [Cited by in F6Publishing: 11] [Reference Citation Analysis]
14 Xiang Y, Sugimura R. Single-Cell Approaches to Deconvolute the Development of HSCs. Cells 2021;10:2876. [PMID: 34831099 DOI: 10.3390/cells10112876] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Albertini DF. Genomic insights into human development: time to upgrade reproductive genetics. J Assist Reprod Genet 2021;38:2505-6. [PMID: 34677700 DOI: 10.1007/s10815-021-02343-6] [Reference Citation Analysis]
16 Mitani T, Isikay S, Gezdirici A, Gulec EY, Punetha J, Fatih JM, Herman I, Akay G, Du H, Calame DG, Ayaz A, Tos T, Yesil G, Aydin H, Geckinli B, Elcioglu N, Candan S, Sezer O, Erdem HB, Gul D, Demiral E, Elmas M, Yesilbas O, Kilic B, Gungor S, Ceylan AC, Bozdogan S, Ozalp O, Cicek S, Aslan H, Yalcintepe S, Topcu V, Bayram Y, Grochowski CM, Jolly A, Dawood M, Duan R, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM, Marafi D, Akdemir ZC, Karaca E, Carvalho CMB, Gibbs RA, Posey JE, Lupski JR, Pehlivan D; Baylor-Hopkins Center for Mendelian Genomics. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population. Am J Hum Genet 2021;108:1981-2005. [PMID: 34582790 DOI: 10.1016/j.ajhg.2021.08.009] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
17 Zhu M, Shahbazi M, Martin A, Zhang C, Sozen B, Borsos M, Mandelbaum RS, Paulson RJ, Mole MA, Esbert M, Titus S, Scott RT, Campbell A, Fishel S, Gradinaru V, Zhao H, Wu K, Chen ZJ, Seli E, de Los Santos MJ, Zernicka Goetz M. Human embryo polarization requires PLC signaling to mediate trophectoderm specification. Elife 2021;10:e65068. [PMID: 34569938 DOI: 10.7554/eLife.65068] [Cited by in Crossref: 1] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
18 Naxerova K. Mutation fingerprints encode cellular histories. Nature 2021;597:334-6. [PMID: 34433973 DOI: 10.1038/d41586-021-02269-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 Yang X, Breuss MW, Xu X, Antaki D, James KN, Stanley V, Ball LL, George RD, Wirth SA, Cao B, Nguyen A, McEvoy-Venneri J, Chai G, Nahas S, Van Der Kraan L, Ding Y, Sebat J, Gleeson JG. Developmental and temporal characteristics of clonal sperm mosaicism. Cell 2021:S0092-8674(21)00883-7. [PMID: 34388390 DOI: 10.1016/j.cell.2021.07.024] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
20 Burgess DJ. Human cell-lineage imbalances. Nat Rev Genet 2021;22:266-7. [PMID: 33785896 DOI: 10.1038/s41576-021-00358-4] [Reference Citation Analysis]