PubMed (OMIM) for id: 2020

Year	Number of Results
1989	3
1991	1
1992	1
1995	1
2004	1
2005	2
2006	1
2007	1
2015	1
2024	0

1

Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior.

Genestine M, Lin L, Durens M, Yan Y, Jiang Y, Prem S, Bailoor K, Kelly B, Sonsalla PK, Matteson PG, Silverman J, Crawley JN, Millonig JH, DiCicco-Bloom E. Genestine M, et al. Hum Mol Genet. 2015 Oct 15;24(20):5805-27. doi: 10.1093/hmg/ddv301. Epub 2015 Jul 28. Hum Mol Genet. 2015. PMID: 26220976 Free PMC article.

2

DNA methylation signatures within the human brain.

Ladd-Acosta C, Pevsner J, Sabunciyan S, Yolken RH, Webster MJ, Dinkins T, Callinan PA, Fan JB, Potash JB, Feinberg AP. Ladd-Acosta C, et al. Am J Hum Genet. 2007 Dec;81(6):1304-15. doi: 10.1086/524110. Epub 2007 Nov 1. Am J Hum Genet. 2007. PMID: 17999367 Free PMC article.

3

Slow progressive degeneration of nigral dopaminergic neurons in postnatal Engrailed mutant mice.

Sgadò P, Albéri L, Gherbassi D, Galasso SL, Ramakers GM, Alavian KN, Smidt MP, Dyck RH, Simon HH. Sgadò P, et al. Proc Natl Acad Sci U S A. 2006 Oct 10;103(41):15242-7. doi: 10.1073/pnas.0602116103. Epub 2006 Oct 2. Proc Natl Acad Sci U S A. 2006. PMID: 17015829 Free PMC article.

4

The transcription factor Engrailed-2 guides retinal axons.

Brunet I, Weinl C, Piper M, Trembleau A, Volovitch M, Harris W, Prochiantz A, Holt C. Brunet I, et al. Nature. 2005 Nov 3;438(7064):94-8. doi: 10.1038/nature04110. Nature. 2005. PMID: 16267555 Free PMC article.

5

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, Dicicco-Bloom E, Brzustowicz LM, Millonig JH. Benayed R, et al. Am J Hum Genet. 2005 Nov;77(5):851-68. doi: 10.1086/497705. Epub 2005 Oct 5. Am J Hum Genet. 2005. PMID: 16252243 Free PMC article.

6

Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.

Gharani N, Benayed R, Mancuso V, Brzustowicz LM, Millonig JH. Gharani N, et al. Mol Psychiatry. 2004 May;9(5):474-84. doi: 10.1038/sj.mp.4001498. Mol Psychiatry. 2004. PMID: 15024396

7

Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2.

Hanks M, Wurst W, Anson-Cartwright L, Auerbach AB, Joyner AL. Hanks M, et al. Science. 1995 Aug 4;269(5224):679-82. doi: 10.1126/science.7624797. Science. 1995. PMID: 7624797

8

Chromosomal localization of the human homeo box-containing genes, EN1 and EN2.

Logan C, Willard HF, Rommens JM, Joyner AL. Logan C, et al. Genomics. 1989 Feb;4(2):206-9. doi: 10.1016/0888-7543(89)90301-7. Genomics. 1989. PMID: 2567700

9

Isolation and chromosomal localization of the human En-2 gene.

Poole SJ, Law ML, Kao FT, Lau YF. Poole SJ, et al. Genomics. 1989 Apr;4(3):225-31. doi: 10.1016/0888-7543(89)90324-8. Genomics. 1989. PMID: 2565873

10

Production of a mutation in mouse En-2 gene by homologous recombination in embryonic stem cells.

Joyner AL, Skarnes WC, Rossant J. Joyner AL, et al. Nature. 1989 Mar 9;338(6211):153-6. doi: 10.1038/338153a0. Nature. 1989. PMID: 2563902

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