Bcl11a is essential for normal lymphoid development

Notch Signaling: Cell Fate Control and Signal Integration in Development

Artavanis-Tsakonas, S., Rand, M. D., & Lake, R. J. (1999) · Science · doi:10.1126/science.284.5415.770 · Cited by 5,909 · see citing works

A clonogenic common myeloid progenitor that gives rise to all myeloid lineages

Akashi, K., Traver, D., Miyamoto, T., & Weissman, I. L. (2000) · Nature · doi:10.1038/35004599 · Cited by 2,617 · see citing works

Identification of Clonogenic Common Lymphoid Progenitors in Mouse Bone Marrow

Kondo, M., Weissman, I. L., & Akashi, K. (1997) · Cell · doi:10.1016/s0092-8674(00)80453-5 · Cited by 2,253 · see citing works

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis.

Okuda, T., van Deursen, J., Hiebert, S. W., Grosveld, G., & Downing, J. R. (1996) · Cell · doi:10.1016/s0092-8674(00)80986-1 · Cited by 1,856 · see citing works

TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms

Ellisen, L. W., Bird, J., West, D. C., Soreng, A. L., Reynolds, T. C., Smith, S. D., & Sklar, J. (1991) · Cell · doi:10.1016/0092-8674(91)90111-b · Cited by 1,691 · see citing works

Requirement of transcription factor PU.1 in the development of multiple hematopoietic lineages

Scott, E. W., Simon, M. C., Anastasi, J., & Singh, H. (1994) · Science · doi:10.1126/science.8079170 · Cited by 1,532 · see citing works

Deficient T Cell Fate Specification in Mice with an Induced Inactivation of Notch1

Radtke, F., Wilson, A., Stark, G., Bauer, M., van Meerwijk, J. P. M., MacDonald, H. R., & Aguet, M. (1999) · Immunity · doi:10.1016/s1074-7613(00)80054-0 · Cited by 1,393 · see citing works

B Cell Development Pathways

Hardy, R. R., & Hayakawa, K. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.595 · Cited by 1,236 · see citing works

Commitment to the B-lymphoid lineage depends on the transcription factor Pax5

Nutt, S. L., Heavey, B., Rolink, A. G., & Busslinger, M. (1999) · Nature · doi:10.1038/44076 · Cited by 1,179 · see citing works

Targeted disruption of the PU.1 gene results in multiple hematopoietic abnormalities

McKercher, S. R., Torbett, B. E., Anderson, K. L., Henkel, G. W., Vestal, D. J., Baribault, H., Klemsz, M., Feeney, A. J., Wu, G. E., Paige, C. J., et al. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00949.x · Cited by 1,130 · see citing works

The ikaros gene is required for the development of all lymphoid lineages

Georgopoulos, K., Bigby, M., Wang, J.-H., Molnar, A., Wu, P., Winandy, S., & Sharpe, A. (1994) · Cell · doi:10.1016/0092-8674(94)90407-3 · Cited by 985 · see citing works

Control of Inflammation, Cytokine Expression, and Germinal Center Formation by BCL-6

Dent, A. L., Shaffer, A. L., Yu, X., Allman, D., & Staudt, L. M. (1997) · Science · doi:10.1126/science.276.5312.589 · Cited by 945 · see citing works

Notch1 Expression in Early Lymphopoiesis Influences B versus T Lineage Determination

Pui, J. C., Allman, D., Xu, L., DeRocco, S. E., Karnell, F. G., Bakkour, S., Lee, J. Y., Kadesch, T. R., Hardy, R. R., Aster, J. C., et al. (1999) · Immunity · doi:10.1016/s1074-7613(00)80105-3 · Cited by 943 · see citing works

α-lnhibin is a tumour-suppressor gene with gonadal specificity in mice

Matzuk, M. M., Finegold, M. J., Su, J.-G. J., Hsueh, A. J. W., & Bradley, A. (1992) · Nature · doi:10.1038/360313a0 · Cited by 890 · see citing works

Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP

Urbánek, P. (1994) · Cell · doi:10.1016/0092-8674(94)90079-5 · Cited by 795 · see citing works

E2A proteins are required for proper B cell development and initiation of immunoglobulin gene rearrangements

Bain, G. (1994) · Cell · doi:10.1016/0092-8674(94)90077-9 · Cited by 779 · see citing works

Exclusive development of T cell neoplasms in mice transplanted with bone marrow expressing activated Notch alleles.

Pear, W. S., Aster, J. C., Scott, M. L., Hasserjian, R. P., Soffer, B., Sklar, J., & Baltimore, D. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.5.2283 · Cited by 708 · see citing works

Failure of B-cell differentiation in mice lacking the transcription factor EBF

Lin, H., & Grosschedl, R. (1995) · Nature · doi:10.1038/376263a0 · Cited by 692 · see citing works

The helix-loop-helix gene E2A is required for B cell formation

Zhuang, Y. (1994) · Cell · doi:10.1016/0092-8674(94)90076-0 · Cited by 675 · see citing works

Transcription factor GATA-3 is required for development of the T-cell lineage

Ting, C.-N., Olson, M. C., Barton, K., & Leiden, J. M. (1996) · Nature · doi:10.1038/384474a0 · Cited by 607 · see citing works

A developmental switch in thymic lymphocyte maturation potential occurs at the level of hematopoietic stem cells

Ikuta, K., Kina, T., MacNeil, I., Uchida, N., Peault, B., Chien, Y.-H., & Weissman, I. L. (1990) · Cell · doi:10.1016/0092-8674(90)90262-d · Cited by 583 · see citing works

Diversification of haematopoietic stem cells to specific lineages

Orkin, S. H. (2000) · Nature Reviews Genetics · doi:10.1038/35049577 · Cited by 564 · see citing works

An Activated Form of Notch Influences the Choice between CD4 and CD8 T Cell Lineages

Robey, E. A., Chang, D., Itano, A. A., Cado, D., Alexander, H., Lans, D., Weinmaster, G., & Salmon, P. (1996) · Cell · doi:10.1016/s0092-8674(00)81368-9 · Cited by 482 · see citing works

Selective Events in T Cell Development

Robey, E. A., & Fowlkes, B. J. (1994) · Annual Review of Immunology · doi:10.1146/annurev.iy.12.040194.003331 · Cited by 480 · see citing works

Early T Lymphocyte Progenitors

Shortman, K., & Wu, L. (1996) · Annual Review of Immunology · doi:10.1146/annurev.immunol.14.1.29 · Cited by 448 · see citing works

New genes involved in cancer identified by retroviral tagging

Suzuki, T., Shen, H., Akagi, K., Morse, H. C., Malley, J. D., Naiman, D. Q., Jenkins, N. A., & Copeland, N. G. (2002) · Nature Genetics · doi:10.1038/ng949 · Cited by 420 · see citing works

Notch 1–Deficient Common Lymphoid Precursors Adopt a B Cell Fate in the Thymus

Wilson, A., MacDonald, H. R., & Radtke, F. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.194.7.1003 · Cited by 399 · see citing works

Notch Activity Influences the αβ versus γδ T Cell Lineage Decision

Washburn, T., Schweighoffer, E., Gridley, T., Chang, D., Fowlkes, B. J., Cado, D., & Robey, E. A. (1997) · Cell · doi:10.1016/s0092-8674(00)81929-7 · Cited by 398 · see citing works

Long-term in vivo reconstitution of T-cell development by Pax5-deficient B-cell progenitors

Rolink, A. G., Nutt, S. L., Melchers, F., & Busslinger, M. (1999) · Nature · doi:10.1038/44164 · Cited by 386 · see citing works

Identification of the Earliest B Lineage Stage in Mouse Bone Marrow

Li, Y. S., Wasserman, R., Hayakawa, K., & Hardy, R. R. (1996) · Immunity · doi:10.1016/s1074-7613(00)80268-x · Cited by 376 · see citing works

Notch1 Signaling Promotes the Maturation of CD4 and CD8 SP Thymocytes

Deftos, M. L., Huang, E. Y., Ojala, E. W., Forbush, K. A., & Bevan, M. J. (2000) · Immunity · doi:10.1016/s1074-7613(00)00009-1 · Cited by 315 · see citing works

The BCL11 gene family: involvement of BCL11A in lymphoid malignancies

Satterwhite, E., Sonoki, T., Willis, T. G., Harder, L., Nowak, R., Arriola, E. L., Liu, H., Price, H. P., Gesk, S., Steinemann, D., et al. (2001) · Blood · doi:10.1182/blood.v98.12.3413 · Cited by 314 · see citing works

Deltex1 Redirects Lymphoid Progenitors to the B Cell Lineage by Antagonizing Notch1

Izon, D. J., Aster, J. C., He, Y., Weng, A. P., Karnell, F. G., Patriub, V., Xu, L., Bakkour, S., Rodríguez, C. E., Allman, D., et al. (2002) · Immunity · doi:10.1016/s1074-7613(02)00271-6 · Cited by 243 · see citing works

Leukaemia disease genes: large-scale cloning and pathway predictions

Li, J., Shen, H., Himmel, K. L., Dupuy, A. J., Largaespada, D. A., Nakamura, T., Shaughnessy, J. D., Jenkins, N. A., & Copeland, N. G. (1999) · Nature Genetics · doi:10.1038/15531 · Cited by 237 · see citing works

Cutting Edge: Protective Effects of Notch-1 on TCR-Induced Apoptosis

Jehn, B. M., Bielke, W., Pear, W. S., & Osborne, B. A. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.2.635 · Cited by 218 · see citing works

Isolation of a Novel Family of C2H2 Zinc Finger Proteins Implicated in Transcriptional Repression Mediated by Chicken Ovalbumin Upstream Promoter Transcription Factor (COUP-TF) Orphan Nuclear Receptors

Avram, D., Fields, A. J., Top, K. P. O., Nevrivy, D. J., Ishmael, J. E., & Leid, M. E. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10315 · Cited by 213 · see citing works

Expression pattern of Notch1, 2 and 3 and Jagged1 and 2 in lymphoid and stromal thymus components: distinct ligand–receptor interactions in intrathymic T cell development

Felli, M. P., Maroder, M., Mitsiadis, T. A., Campese, A. F., Bellavia, D., Vacca, A., Mann, R. S., Frati, L., Lendahl, U., Gulino, A., et al. (1999) · International Immunology · doi:10.1093/intimm/11.7.1017 · Cited by 198 · see citing works

Subversion of the T/B Lineage Decision in the Thymus by Lunatic Fringe-Mediated Inhibition of Notch-1

Koch, U., Lacombe, T. A., Holland, D., Bowman, J. L., Cohen, B. L., Egan, S. E., & Guidos, C. J. (2001) · Immunity · doi:10.1016/s1074-7613(01)00189-3 · Cited by 193 · see citing works

The status of Ig loci rearrangements in single cells from different stages of B cell development

ten Boekel, E., Melchers, F., & Rolink, A. (1995) · International Immunology · doi:10.1093/intimm/7.6.1013 · Cited by 189 · see citing works

Rearrangement and transcription of the β-chain genes of the T-cell antigen receptor in different types of murine lymphocytes

Kronenberg, M., Goverman, J. M., Haars, R., Malissen, M., Kraig, E., Phillips, L., Delovitch, T. L., Suciu‐Foca, N., & Hood, L. (1985) · Nature · doi:10.1038/313647a0 · Cited by 169 · see citing works

Transcriptional control of B-cell development

Schebesta, M., Heavey, B., & Busslinger, M. (2002) · Current Opinion in Immunology · doi:10.1016/s0952-7915(02)00324-2 · Cited by 155 · see citing works

c-Myb is essential for early T cell developmentPreprint

ALLEN, R. D., Bender, T. P., & Siu, G. (1999) · Genes & Development · doi:10.1101/gad.13.9.1073 · Cited by 153 · see citing works

An Invitation to T and More

Allman, D., Punt, J. A., Izon, D. J., Aster, J. C., & Pear, W. S. (2002) · Cell · doi:10.1016/s0092-8674(02)00689-x · Cited by 143 · see citing works

Changes in frequencies of clonable pre B cells during life in different lymphoid organs of mice

Rolink, A. G., Haasner, D., Nishikawa, S., & Melchers, F. (1993) · Blood · doi:10.1182/blood.v81.9.2290.2290 · Cited by 136 · see citing works

Evi9 Encodes a Novel Zinc Finger Protein That Physically Interacts with BCL6, a Known Human B-Cell Proto-Oncogene Product

Nakamura, T., Yamazaki, Y., Saiki, Y., Moriyama, M., Largaespada, D. A., Jenkins, N. A., & Copeland, N. G. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.9.3178-3186.2000 · Cited by 100 · see citing works

Enumeration and characterization of DJH structures in mouse fetal liver.

Chang, Y., Paige, C. J., & Wu, G. E. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05241.x · Cited by 96 · see citing works

On the brink of becoming a T cell

Borowski, C., Martin, C. H., Gounari, F., Haughn, L., Aifantis, I., Grassi, F., & von Boehmer, H. (2002) · Current Opinion in Immunology · doi:10.1016/s0952-7915(02)00322-9 · Cited by 84 · see citing works

In vitro development of B cells and macrophages from early mouse fetal thymocytes

Péault, B., Khazaal, I., & Weissman, I. L. (1994) · European Journal of Immunology · doi:10.1002/eji.1830240345 · Cited by 61 · see citing works

Human EVI9, a Homologue of the Mouse Myeloid Leukemia Gene, Is Expressed in the Hematopoietic Progenitors and Down-Regulated during Myeloid Differentiation of HL60 Cells

Saiki, Y., Yamazaki, Y., Yoshida, M. C., Katoh, O., & Nakamura, T. (2000) · Genomics · doi:10.1006/geno.2000.6385 · Cited by 38 · see citing works

Notch1 Perturbation of Hemopoiesis Involves Non-Cell- Autonomous Modifications

Kawamata, S., Du, C., Li, K., & Lavau, C. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.4.1738 · Cited by 29 · see citing works

The fetal thymus stores immature hemopoietic cells capable of differentiating into non-T lineage cells constituting the thymus stromal element

Kimoto, H., Kitamura, K., Sudo, T., Suda, T., Ogawa, Y., Kitagawa, H., Taniguchi, M., & Takemori, T. (1993) · International Immunology · doi:10.1093/intimm/5.12.1535 · Cited by 8 · see citing works

Human Fetal Hemoglobin Expression Is Regulated by the Developmental Stage-Specific Repressor <i>BCL11A</i>

Sankaran, V. G., Menne, T. F., Xu, J., Akie, T. E., Lettre, G., Van Handel, B., Mikkola, H. K. A., Hirschhorn, J. N., Cantor, A. B., & Orkin, S. H. (2008) · Science · doi:10.1126/science.1165409 · Cited by 919 · see citing works

BCL11A enhancer dissection by Cas9-mediated in situ saturating mutagenesis

Canver, M. C., Smith, E. C., Sher, F., Pinello, L., Sanjana, N. E., Shalem, O., Chen, D. D., Schupp, P. G., Vinjamur, D. S., Garcia, S. P., et al. (2015) · Nature · doi:10.1038/nature15521 · Cited by 886 · see citing works

Genome-wide association study shows <i>BCL11A</i> associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

Uda, M., Galanello, R., Sanna, S., Lettre, G., Sankaran, V. G., Chen, W., Usala, G., Busonero, F., Maschio, A., Albai, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711566105 · Cited by 672 · see citing works

An Erythroid Enhancer of <i>BCL11A</i> Subject to Genetic Variation Determines Fetal Hemoglobin Level

Bauer, D. E., Kamran, S. C., Lessard, S., Xu, J., Fujiwara, Y., Lin, C., Shao, Z., Canver, M. C., Smith, E. C., Pinello, L., et al. (2013) · Science · doi:10.1126/science.1242088 · Cited by 653 · see citing works

DNA polymorphisms at the BCL11A , HBS1L-MYB , and β- globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

Lettre, G., Sankaran, V. G., Bezerra, M., Araujo, A. S., Uda, M., Sanna, S., Cao, A., Schlessinger, D., Costa, F. F., Hirschhorn, J. N., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804799105 · Cited by 560 · see citing works

Cancer biology and NuRD: a multifaceted chromatin remodelling complex

Lai, A. Y., & Wade, P. A. (2011) · Nature reviews. Cancer · doi:10.1038/nrc3091 · Cited by 541 · see citing works

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

Menzel, S., Garner, C., Gut, I., Matsuda, F., Yamaguchi, M., Heath, S., Foglio, M., Zelenika, D., Boland, A., Rooks, H., et al. (2007) · Nature Genetics · doi:10.1038/ng2108 · Cited by 529 · see citing works

A global network of transcription factors, involving E2A, EBF1 and Foxo1, that orchestrates B cell fate

Lin, Y. C., Jhunjhunwala, S., Benner, C. W., Heinz, S., Welinder, E., Månsson, R., Sigvardsson, M., Hagman, J. R., Espinoza, C. A., Dutkowski, J., et al. (2010) · Nature Immunology · doi:10.1038/ni.1891 · Cited by 502 · see citing works

Transcriptional Control of Early B Cell Development

Busslinger, M. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104807 · Cited by 482 · see citing works

Direct promoter repression by BCL11A controls the fetal to adult hemoglobin switch

Liu, N., Hargreaves, V. V., Zhu, Q., Kurland, J. V., Hong, J., Kim, W., Sher, F., Macias-Trevino, C., Rogers, J. M., Kurita, R., et al. (2018) · Cell · doi:10.1016/j.cell.2018.03.016 · Cited by 478 · see citing works

Single-Cell Analyses Identify Brain Mural Cells Expressing CD19 as Potential Off-Tumor Targets for CAR-T Immunotherapies

Parker, K. R., Migliorini, D., Perkey, E., Yost, K. E., Bhaduri, A., Bagga, P., Haris, M., Wilson, N. E., Liu, F., Gabunia, K., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.022 · Cited by 451 · see citing works

Post-Transcriptional Genetic Silencing of <i>BCL11A</i> to Treat Sickle Cell Disease

Esrick, E. B., Lehmann, L. E., Biffi, A., Achebe, M., Brendel, C., Ciuculescu, M. F., Daley, H., MacKinnon, B., Morris, E., Federico, A., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2029392 · Cited by 449 · see citing works

The Transcriptional Regulation of B Cell Lineage Commitment

Nutt, S. L., & Kee, B. L. (2007) · Immunity · doi:10.1016/j.immuni.2007.05.010 · Cited by 384 · see citing works

Developmental and species-divergent globin switching are driven by BCL11A

Sankaran, V. G., Xu, J., Ragoczy, T., Ippolito, G. C., Walkley, C. R., Maika, S. D., Fujiwara, Y., Ito, M., Groudine, M., Bender, M. A., et al. (2009) · Nature · doi:10.1038/nature08243 · Cited by 379 · see citing works

Bcl11b is required for differentiation and survival of αβ T lymphocytes

Wakabayashi, Y., Watanabe, H., Inoue, J., Takeda, N., Sakata, J., Mishima, Y., Hitomi, J., Yamamoto, T., Utsuyama, M., Niwa, O., et al. (2003) · Nature Immunology · doi:10.1038/ni927 · Cited by 356 · see citing works

Developmental gene networks: a triathlon on the course to T cell identity

Yui, M. A., & Rothenberg, E. V. (2014) · Nature Reviews Immunology · doi:10.1038/nri3702 · Cited by 342 · see citing works

Revealing the Critical Regulators of Cell Identity in the Mouse Cell Atlas

(2018) · doi:10.1016/j.celrep.2018.10.045 · Cited by 341 · see citing works

The α‐gal epitope and the anti‐Gal antibody in xenotransplantation and in cancer immunotherapy

Galili, U. (2005) · Immunology and Cell Biology · doi:10.1111/j.1440-1711.2005.01366.x · Cited by 335 · see citing works

Correction of Sickle Cell Disease in Adult Mice by Interference with Fetal Hemoglobin Silencing

Xu, J., Peng, C., Sankaran, V. G., Shao, Z., Esrick, E. B., Chong, B. G., Ippolito, G. C., Fujiwara, Y., Ebert, B. L., Tucker, P. W., et al. (2011) · Science · doi:10.1126/science.1211053 · Cited by 326 · see citing works

Foxp1 is an essential transcriptional regulator of B cell development

Hu, H., Wang, B., Borde, M., Nardone, J., Maika, S. D., Allred, L., Tucker, P. W., & Rao, A. (2006) · Nature Immunology · doi:10.1038/ni1358 · Cited by 326 · see citing works

Coupled Single-Cell CRISPR Screening and Epigenomic Profiling Reveals Causal Gene Regulatory Networks

Rubin, A. J., Parker, K. R., Satpathy, A. T., Qi, Y., Wu, B., Ong, A. J., Mumbach, M. R., Ji, A. L., Kim, D. S., Cho, S. W., et al. (2019) · Cell · doi:10.1016/j.cell.2018.11.022 · Cited by 314 · see citing works

The 8;21 translocation in leukemogenesis

Peterson, L. F., & Zhang, D. (2004) · Oncogene · doi:10.1038/sj.onc.1207727 · Cited by 301 · see citing works

The functional interactome landscape of the human histone deacetylase family

Joshi, P., Greco, T. M., Guise, A. J., Luo, Y., Yu, F., Nesvizhskii, A. I., & Cristea, I. M. (2013) · Molecular Systems Biology · doi:10.1038/msb.2013.26 · Cited by 289 · see citing works

Continuous Expression of the Transcription Factor E2-2 Maintains the Cell Fate of Mature Plasmacytoid Dendritic Cells

Ghosh, H. S., Cisse, B., Bunin, A., Lewis, K. L. T., & Reizis, B. (2010) · Immunity · doi:10.1016/j.immuni.2010.11.023 · Cited by 275 · see citing works

Sex differences in the genome-wide DNA methylation pattern and impact on gene expression, microRNA levels and insulin secretion in human pancreatic islets

Hall, E., Volkov, P., Dayeh, T., Esguerra, J. L. S., Salö, S., Eliasson, L., Rönn, T., Bacos, K., & Ling, C. (2014) · Genome Biology · doi:10.1186/s13059-014-0522-z · Cited by 249 · see citing works

Early B Cell Factor 1 Regulates B Cell Gene Networks by Activation, Repression, and Transcription- Independent Poising of Chromatin

Treiber, T., Mandel, E. M., Pott, S., Győry, I., Firner, S., Liu, E. T., & Grosschedl, R. (2010) · Immunity · doi:10.1016/j.immuni.2010.04.013 · Cited by 235 · see citing works

Corepressor-dependent silencing of fetal hemoglobin expression by BCL11A

Xu, J., Bauer, D. E., Kerenyi, M. A., Vo, T. D., Hou, S., Hsu, Y.-J., Yao, H., Trowbridge, J. J., Mandel, G., & Orkin, S. H. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303976110 · Cited by 233 · see citing works

Transcriptional Control of Early T and B Cell Developmental Choices

Rothenberg, E. V. (2014) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-100024 · Cited by 232 · see citing works

The transcriptional architecture of early human hematopoiesis identifies multilevel control of lymphoid commitment

Laurenti, E., Doulatov, S. R., Zandi, S., Plumb, I., Chen, J., April, C., Fan, J., & Dick, J. E. (2013) · Nature Immunology · doi:10.1038/ni.2615 · Cited by 224 · see citing works

Bcl11a is essential for lymphoid development and negatively regulates p53

Yu, Y., Wang, J., Khaled, W. T., Burke, S., Li, P., Chen, X., Yang, W., Jenkins, N. A., Copeland, N. G., Zhang, S., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121846 · Cited by 223 · see citing works

Advances in the understanding of haemoglobin switching

Sankaran, V. G., Xu, J., & Orkin, S. H. (2010) · British Journal of Haematology · doi:10.1111/j.1365-2141.2010.08105.x · Cited by 216 · see citing works

Advances in the biology and therapy of diffuse large B-cell lymphoma: moving toward a molecularly targeted approach

Abramson, J. S., & Shipp, M. A. (2005) · Blood · doi:10.1182/blood-2005-02-0687 · Cited by 206 · see citing works

Erythropoiesis: Model systems, molecular regulators, and developmental programs

Tsiftsoglou, A. S., Vizirianakis, I. S., & Strouboulis, J. (2009) · IUBMB Life · doi:10.1002/iub.226 · Cited by 199 · see citing works

Differentiation of human embryonic stem cells to HOXA+ hemogenic vasculature that resembles the aorta-gonad-mesonephros

Ng, E. S., Azzola, L., Bruveris, F., Calvanese, V., Phipson, B., Vlahos, K., Hirst, C. E., Jokubaitis, V. J., Yu, Q. C., Maksimovic, J., et al. (2016) · Nature Biotechnology · doi:10.1038/nbt.3702 · Cited by 196 · see citing works

Genetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease

Hoban, M. D., Orkin, S. H., & Bauer, D. E. (2016) · Blood · doi:10.1182/blood-2015-09-618587 · Cited by 194 · see citing works

Insertional mutagenesis identifies genes that promote the immortalization of primary bone marrow progenitor cells

Du, Y., Jenkins, N. A., & Copeland, N. G. (2005) · Blood · doi:10.1182/blood-2005-03-1113 · Cited by 188 · see citing works

Contingent gene regulatory networks and B cell fate specification

Singh, H., Medina, K. L., & Pongubala, J. M. R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500480102 · Cited by 185 · see citing works

CRISPR–Cas9-mediated gene editing of the BCL11A enhancer for pediatric β0/β0 transfusion-dependent β-thalassemia

Fu, B., Liao, J., Chen, S., Li, W., Wang, Q., Hu, J., Yang, F., Hsiao, S., Jiang, Y., Wang, L., et al. (2022) · Nature Medicine · doi:10.1038/s41591-022-01906-z · Cited by 181 · see citing works

Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders

Bauer, D. E., Kamran, S. C., & Orkin, S. H. (2012) · Blood · doi:10.1182/blood-2012-06-292078 · Cited by 177 · see citing works

BCL11B functionally associates with the NuRD complex in T lymphocytes to repress targeted promoter

Cismasiu, V. B., Adamo, K., Gecewicz, J., Duque, J., Lin, Q., & Avram, D. (2005) · Oncogene · doi:10.1038/sj.onc.1208904 · Cited by 175 · see citing works

TrkB phosphorylation by Cdk5 is required for activity-dependent structural plasticity and spatial memory

Lai, K., Wong, A. S. L., Cheung, M. C., Xu, P., Liang, Z., Lok, K.-C., Xie, H., Palko, M. E., Yung, W., Tessarollo, L., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3237 · Cited by 172 · see citing works

MicroRNA targets in immune genes and the Dicer/Argonaute and ARE machinery components

Asirvatham, A. J., Gregorie, C. J., Hu, Z., Magner, W. J., & Tomasi, T. B. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.10.035 · Cited by 170 · see citing works

Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype.

Brendel, C., Guda, S., Renella, R., Bauer, D. E., Canver, M. C., Kim, Y.-J., Heeney, M. M., Klatt, D., Fogel, J., Milsom, M. D., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci87885 · Cited by 167 · see citing works

Characterization of Early Stages of Human B Cell Development by Gene Expression Profiling

Hystad, M. E., Myklebust, J. H., Bø, T. H., Sivertsen, E. A., Rian, E., Forfang, L., Munthe, E., Rosenwald, A., Chiorazzi, M., Jonassen, I., et al. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.6.3662 · Cited by 166 · see citing works

Transcriptional Regulation of Innate and Adaptive Lymphocyte Lineages

Obaldia, M. E. D., & Bhandoola, A. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112032 · Cited by 163 · see citing works

BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription

Dias, C., Estruch, S. B., Graham, S. A., McRae, J. F., Sawiak, S. J., Hurst, J. A., Joss, S. K., Holder, S., Morton, J. E. V., Turner, C., et al. (2016) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2016.05.030 · Cited by 162 · see citing works

CTIP1 and CTIP2 are differentially expressed during mouse embryogenesis

Leid, M., Ishmael, J. E., Avram, D., Shepherd, D., Fraulob, V., & Dollé, P. (2004) · Gene Expression Patterns · doi:10.1016/j.modgep.2004.03.009 · Cited by 156 · see citing works

Long-Term Engraftment and Fetal Globin Induction upon BCL11A Gene Editing in Bone-Marrow-Derived CD34 + Hematopoietic Stem and Progenitor Cells

Chang, K.-H., Smith, S. E., Sullivan, T., Chen, K., Zhou, Q., West, J. A., Liu, M., Liu, Y., Vieira, B. F., Sun, C., et al. (2017) · Molecular Therapy - Methods &amp; Clinical Development · doi:10.1016/j.omtm.2016.12.009 · Cited by 155 · see citing works

BCL11A is a triple-negative breast cancer gene with critical functions in stem and progenitor cells

Khaled, W. T., Lee, S. C., Stingl, J., Chen, X., Ali, H. R., Rueda, O. M., Hadi, F., Wang, J., Yu, Y., Chin, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms6987 · Cited by 154 · see citing works

The c-Rel transcription factor and B-cell proliferation: a deal with the devil

Gilmore, T. D., Kalaitzidis, D., Liang, M., & Starczynowski, D. T. (2004) · Oncogene · doi:10.1038/sj.onc.1207410 · Cited by 147 · see citing works

Involvement of the Histone Deacetylase SIRT1 in Chicken Ovalbumin Upstream Promoter Transcription Factor (COUP-TF)-interacting Protein 2-mediated Transcriptional Repression

Senawong, T., Peterson, V. J., Avram, D., Shepherd, D. M., Frye, R. A., Minucci, S., & Leid, M. E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307477200 · Cited by 145 · see citing works

Hemoglobin switching’s surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobin.

Bauer, D. E., & Orkin, S. H. (2015) · Current Opinion in Genetics &amp; Development · doi:10.1016/j.gde.2015.08.001 · Cited by 143 · see citing works

Immunological Tolerance During Fetal Development

Mold, J. E., & McCune, J. M. (2012) · Advances in immunology · doi:10.1016/b978-0-12-394299-9.00003-5 · Cited by 138 · see citing works

Cooperating cancer-gene identification through oncogenic-retrovirus-induced insertional mutagenesis.

Du, Y., Spence, S., Jenkins, N., & Copeland, N. (2005) · Blood · doi:10.1182/blood-2004-12-4840 · Cited by 145 · see citing works

The regulatory network of B‐cell differentiation: a focused view of early B‐cell factor 1 function

Boller, S., & Grosschedl, R. (2014) · Immunological Reviews · doi:10.1111/imr.12206 · Cited by 127 · see citing works

DiRE: identifying distant regulatory elements of co-expressed genes

Gotea, V., & Ovcharenko, I. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn300 · Cited by 127 · see citing works

Long noncoding RNAs in B-cell development and activation

Brazão, T. F., Johnson, J. S., Müller, J., Heger, A., Ponting, C. P., & Tybulewicz, V. L. J. (2016) · Blood · doi:10.1182/blood-2015-11-680843 · Cited by 126 · see citing works

Dendritic cell fate is determined by BCL11A

Ippolito, G. C., Dekker, J. D., Wang, Y., Lee, B., Shaffer, A. L., Lin, J. X., Wall, J. K., Lee, B.-S., Staudt, L. M., Liu, Y., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1319228111 · Cited by 126 · see citing works

Transcription control of early B cell differentiation

Mandel, E. M., & Grosschedl, R. (2010) · Current Opinion in Immunology · doi:10.1016/j.coi.2010.01.010 · Cited by 125 · see citing works

Bcl11a Deficiency Leads to Hematopoietic Stem Cell Defects with an Aging-like Phenotype

Luc, S., Huang, J., McEldoon, J. L., Somuncular, E., Li, D., Rhodes, C., Mamoor, S., Hou, S., Xu, J., & Orkin, S. H. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.064 · Cited by 125 · see citing works

BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells

Lessel, D., Gehbauer, C., Bramswig, N. C., Schluth‐Bolard, C., Venkataramanappa, S., van Gassen, K. L. I., Hempel, M., Haack, T. B., Barešić, A., Genetti, C. A., et al. (2018) · Brain · doi:10.1093/brain/awy173 · Cited by 121 · see citing works

Fate Decisions Regulating Bone Marrow and Peripheral B Lymphocyte Development

Monroe, J. G., & Dorshkind, K. A. (2007) · Advances in immunology · doi:10.1016/s0065-2776(07)95001-4 · Cited by 121 · see citing works

MicroRNA-486-3p Regulates γ-Globin Expression in Human Erythroid Cells by Directly Modulating BCL11A

Lulli, V., Romania, P., Morsilli, O., Cianciulli, P., Gabbianelli, M., Testa, U., Giuliani, A., & Marziali, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060436 · Cited by 121 · see citing works

miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction

Guda, S., Brendel, C., Renella, R., Du, P., Bauer, D. E., Canver, M. C., Grenier, J. K., Grimson, A., Kamran, S. C., Thornton, J. E., et al. (2015) · Molecular Therapy · doi:10.1038/mt.2015.113 · Cited by 120 · see citing works

Emerging genetic therapy for sickle cell disease

Orkin, S. H., & Bauer, D. E. (2019) · Annual Review of Medicine · doi:10.1146/annurev-med-041817-125507 · Cited by 119 · see citing works

Critical roles of Bcl11b in T‐cell development and maintenance of T‐cell identity

Liu, P., Li, P., & Burke, S. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00953.x · Cited by 118 · see citing works

Recent progress in understanding and manipulating haemoglobin switching for the haemoglobinopathies

Vinjamur, D. S., Bauer, D. E., & Orkin, S. H. (2018) · British Journal of Haematology · doi:10.1111/bjh.15038 · Cited by 114 · see citing works

Single-cell transcriptomic reconstruction reveals cell cycle and multi-lineage differentiation defects in Bcl11a-deficient hematopoietic stem cells

Tsang, J. C. H., Yu, Y., Burke, S., Buettner, F., Wang, C., Kolodziejczyk, A., Teichmann, S., Lu, L.-M., & Liu, P. (2015) · Genome Biology · doi:10.1186/s13059-015-0739-5 · Cited by 98 · see citing works

Evolving views on the genealogy of B cells

Welner, R. S., Pelayo, R., & Kincade, P. W. (2008) · Nature reviews. Immunology · doi:10.1038/nri2234 · Cited by 108 · see citing works

GATA-3 promotes T-cell specification by repressing B-cell potential in pro–T cells in mice

García‐Ojeda, M. E., Wolterink, R. G. J. K., Lemaı̂tre, F., Goff, O. R.-L., Hasan, M., Hendriks, R. W., Cumano, A., & Santo, J. P. D. (2013) · Blood · doi:10.1182/blood-2012-06-440065 · Cited by 105 · see citing works

Fetal haemoglobin in sickle-cell disease: from genetic epidemiology to new therapeutic strategies

Lettre, G., & Bauer, D. E. (2016) · The Lancet · doi:10.1016/s0140-6736(15)01341-0 · Cited by 104 · see citing works

Functional interactors of three genome-wide association study genes are differentially expressed in severe chronic obstructive pulmonary disease lung tissue

Morrow, J. D., Zhou, X., Lao, T., Jiang, Z., DeMeo, D. L., Cho, M. H., Qiu, W., Cloonan, S. M., Pinto-Plata, V., Celli, B., et al. (2017) · Scientific Reports · doi:10.1038/srep44232 · Cited by 104 · see citing works

Clinicopathologic Significance and Prognostic Value of Chromosomal Imbalances in Diffuse Large B-Cell Lymphomas

Beà, S., Colomo, L., López‐Guillermo, A., Salaverría, I., Puig, X., Pinyol, M., Rives, S., Montserrat, E., & Campo, E. (2004) · Journal of Clinical Oncology · doi:10.1200/jco.2004.11.025 · Cited by 99 · see citing works

Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer

Wilber, A. C., Hargrove, P. W., Kim, Y., Riberdy, J. M., Sankaran, V. G., Papanikolaou, E., Georgomanoli, M., Anagnou, N. P., Orkin, S. H., Nienhuis, A. W., et al. (2010) · Blood · doi:10.1182/blood-2010-08-300723 · Cited by 98 · see citing works

Comprehensive analysis and accurate quantification of unintended large gene modifications induced by CRISPR-Cas9 gene editing

Park, S. H., Cao, M., Pan, Y., Davis, T., Saxena, L., Deshmukh, H., Fu, Y., Treangen, T. J., Sheehan, V., & Bao, G. (2022) · Science Advances · doi:10.1126/sciadv.abo7676 · Cited by 92 · see citing works

Functional studies of BCL11A: characterization of the conserved BCL11A-XL splice variant and its interaction with BCL6 in nuclear paraspeckles of germinal center B cells

Liu, H., Ippolito, G. C., Wall, J. K., Niu, T., Probst, L., Lee, B.-S., Pulford, K. A. F., Banham, A. H., Stockwin, L. H., Shaffer, A. L., et al. (2006) · Molecular Cancer · doi:10.1186/1476-4598-5-18 · Cited by 89 · see citing works

Fetal haemoglobin induction in sickle cell disease

Paikari, A., & Sheehan, V. (2017) · British Journal of Haematology · doi:10.1111/bjh.15021 · Cited by 87 · see citing works

Gene therapy of hemoglobinopathies: progress and future challenges

Ikawa, Y., Miccio, A., Magrin, E., Kwiatkowski, J. L., Rivella, S., & Cavazzana, M. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz172 · Cited by 86 · see citing works

ZNF410 represses fetal globin by singular control of CHD4

Vinjamur, D. S., Yao, Q., Cole, M. A., McGuckin, C., Ren, C., Zeng, J., Hossain, M. A., Luk, K., Wolfe, S. A., Pinello, L., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00843-w · Cited by 82 · see citing works

Multilayered specification of the T-cell lineage fate.

Rothenberg, E. V., Zhang, J., & Li, L. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00964.x · Cited by 81 · see citing works

Machine learning assisted analysis of breast cancer gene expression profiles reveals novel potential prognostic biomarkers for triple-negative breast cancer

Thalor, A., Joon, H. K., Singh, G., Roy, S., & Gupta, D. K. (2022) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2022.03.019 · Cited by 80 · see citing works

RUNX1 and the endothelial origin of blood

Gao, L., Tober, J. M., Gao, P., Chen, C., Tan, K., & Speck, N. A. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.10.009 · Cited by 78 · see citing works

BCL11A-dependent recruitment of SIRT1 to a promoter template in mammalian cells results in histone deacetylation and transcriptional repression

Senawong, T., Peterson, V. J., & Leid, M. E. (2004) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2004.10.028 · Cited by 76 · see citing works

Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11AXL protein are frequent in primary mediastinal B-cell lymphoma

Weniger, M. A., Pulford, K. A. F., Gesk, S., Ehrlich, S., Banham, A. H., Lyne, L., Martín-Subero, J. I., Siebert, R., Dyer, M. J. S., Mӧller, P., et al. (2006) · Leukemia · doi:10.1038/sj.leu.2404324 · Cited by 73 · see citing works

Ctip1 Regulates the Balance between Specification of Distinct Projection Neuron Subtypes in Deep Cortical Layers

Woodworth, M. B., Greig, L. C., Liu, K. X., Ippolito, G. C., Tucker, H. O., & Macklis, J. D. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.03.064 · Cited by 73 · see citing works

Preclinical evaluation of a novel lentiviral vector driving lineage-specific BCL11A knockdown for sickle cell gene therapy

Brendel, C., Negre, O., Rothe, M., Guda, S., Parsons, G., Harris, C., McGuinness, M., Abriss, D., Tsytsykova, A., Klatt, D., et al. (2020) · Molecular Therapy - Methods &amp; Clinical Development · doi:10.1016/j.omtm.2020.03.015 · Cited by 72 · see citing works

The hidden risks of CRISPR/Cas: structural variations and genome integrity

Aussel, C., Cathomen, T., & Fuster‐García, C. (2025) · Nature Communications · doi:10.1038/s41467-025-62606-z · Cited by 72 · see citing works

Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease

Khosravi, M. A., Abbasalipour, M., Concordet, J., Berg, J. V., Zeinali, S., Arashkia, A., Azadmanesh, K., Buch, T., & Karimipoor, M. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.04.042 · Cited by 71 · see citing works

SWI/SNF complexes in hematological malignancies: biological implications and therapeutic opportunities

Andrades, Á., Peinado, P., Álvarez-Pérez, J. C., Sanjuán‐Hidalgo, J., García, D. J., Arenas, A. M., Matia‐González, A. M., & Medina, P. P. (2023) · Molecular Cancer · doi:10.1186/s12943-023-01736-8 · Cited by 71 · see citing works

Role of the transcription factor Bcl11b in development and lymphomagenesis

Kominami, R. (2012) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.88.72 · Cited by 71 · see citing works

2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment

Funnell, A. P. W., Prontera, P., Ottaviani, V., Piccione, M., Giambona, A., Maggio, A., Ciaffoni, F., Stehling-Sun, S., Marra, M., Masiello, F., et al. (2015) · Blood · doi:10.1182/blood-2015-04-638528 · Cited by 70 · see citing works

B cells and osteoblast and osteoclast development

Horowitz, M. C., Bothwell, A. L. M., Hesslein, D. G. T., Pflugh, D. L., & Schatz, D. G. (2005) · Immunological Reviews · doi:10.1111/j.0105-2896.2005.00328.x · Cited by 70 · see citing works

CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia

Meisel, R. (2021) · New England Journal of Medicine · doi:10.1056/nejmc2103481 · Cited by 70 · see citing works

Bcl11a is required for neuronal morphogenesis and sensory circuit formation in dorsal spinal cord development

John, A., Brylka, H., Wiegreffe, C., Simon, R., Liu, P., Jüttner, R., Crenshaw, E. B., Luyten, F. P., Jenkins, N. A., Copeland, N. G., et al. (2012) · Development · doi:10.1242/dev.072850 · Cited by 69 · see citing works

BCL11A: a potential diagnostic biomarker and therapeutic target in human diseases

Yin, J., Xie, X., Ye, Y., Wang, L., & Che, F. (2019) · Bioscience Reports · doi:10.1042/bsr20190604 · Cited by 68 · see citing works

Interplay between cofactors and transcription factors in hematopoiesis and hematological malignancies

Wang, Z., Wang, P., Li, Y., Peng, H., Zhu, Y., Mohandas, N., & Liu, J. (2021) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00422-1 · Cited by 68 · see citing works

Transcription factor expression dynamics of early T-lymphocyte specification and commitment

David‐Fung, E., Butler, R. R., Buzi, G., Yui, M. A., Diamond, R. A., Anderson, M. K., Rowen, L., & Rothenberg, E. V. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.10.021 · Cited by 68 · see citing works

The role of cerebellar genes in pathology of autism and schizophrenia

Fatemi, S. H., Reutiman, T. J., Folsom, T. D., & Sidwell, R. W. (2008) · The Cerebellum · doi:10.1007/s12311-008-0017-0 · Cited by 68 · see citing works

B-cell development fails in the absence of the Pbx1 proto-oncogene

Sanyal, M., Tung, J. W., Karsunky, H., Zeng, H., Selleri, L., Weissman, I. L., Herzenberg, L. A., & Cleary, M. L. (2007) · Blood · doi:10.1182/blood-2006-10-054213 · Cited by 68 · see citing works

CRISPR/Cas9 for Sickle Cell Disease: Applications, Future Possibilities, and Challenges

Demirci, S., Leonard, A. K., Haro‐Mora, J. J., Uchida, N., & Tisdale, J. F. (2019) · Advances in experimental medicine and biology · doi:10.1007/5584_2018_331 · Cited by 67 · see citing works

Deletion of Bcl11a Gene Reveals Roles in Lymphoid, Myeloid, and Leukemic Cell Development.

Ortiz, M., Liu, P., Tessarollo, L., Rachel, R. A., Nakamura, T., Stull, S. W., Jenkins, N. A., Copeland, N. G., & Keller, J. R. (2004) · Blood · doi:10.1182/blood.v104.11.385.385 · Cited by 1 · see citing works

Bcl11a is essential for lymphoid development and negatively regulates p53

Yu, Y., Wang, J., Khaled, W. T., Burke, S., Li, P., Chen, X., Yang, W., Jenkins, N. A., Copeland, N. G., Zhang, S., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20121846 · Cited by 223 · see citing works

Role of the transcription factor Bcl11b in development and lymphomagenesis

Kominami, R. (2012) · Proceedings of the Japan Academy Series B · doi:10.2183/pjab.88.72 · Cited by 71 · see citing works

Partners in crime

Buckland, J. (2003) · Nature reviews. Immunology · doi:10.1038/nri1119

Haploinsufficiency of Bcl11b suppresses the progression of ATM-deficient T cell lymphomas

Pinkney, K. A., Jiang, W., Lee, B. J., Loredan, D. G., Li, C., Bhagat, G., & Zha, S. (2015) · Journal of Hematology & Oncology · doi:10.1186/s13045-015-0191-8 · Cited by 7 · see citing works