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Items: 14

1.

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).

Riggs ER, Andersen EF, Cherry AM, Kantarci S, Kearney H, Patel A, Raca G, Ritter DI, South ST, Thorland EC, Pineda-Alvarez D, Aradhya S, Martin CL.

Genet Med. 2019 Nov 6. doi: 10.1038/s41436-019-0686-8. [Epub ahead of print]

PMID:
31690835
2.

A Novel Homozygous Deletion within the FRY Gene Associated with Nonsyndromic Developmental Delay.

Paulraj P, Bosworth M, Longhurst M, Hornbuckle C, Gotway G, Lamb AN, Andersen EF.

Cytogenet Genome Res. 2019;159(1):19-25. doi: 10.1159/000502598. Epub 2019 Sep 6.

PMID:
31487712
3.

Pediatric acute myeloid leukemia with t(7;21)(p22;q22).

Paulraj P, Diamond S, Razzaqi F, Ozeran JD, Longhurst M, Andersen EF, Toydemir RM, Hong B.

Genes Chromosomes Cancer. 2019 Aug;58(8):551-557. doi: 10.1002/gcc.22740. Epub 2019 Feb 14.

PMID:
30706625
4.

Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type.

Zhou XA, Louissaint A Jr, Wenzel A, Yang J, Martinez-Escala ME, Moy AP, Morgan EA, Paxton CN, Hong B, Andersen EF, Guitart J, Behdad A, Cerroni L, Weinstock DM, Choi J.

J Invest Dermatol. 2018 Nov;138(11):2365-2376. doi: 10.1016/j.jid.2018.04.038. Epub 2018 May 30.

5.

Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumors.

Herriges JC, Brown S, Longhurst M, Ozmore J, Moeschler JB, Janze A, Meck J, South ST, Andersen EF.

Eur J Med Genet. 2019 Jan;62(1):9-14. doi: 10.1016/j.ejmg.2018.04.011. Epub 2018 Apr 24.

PMID:
29698806
6.

Genetic evaluation of juvenile xanthogranuloma: genomic abnormalities are uncommon in solitary lesions, advanced cases may show more complexity.

Paxton CN, O'Malley DP, Bellizzi AM, Alkapalan D, Fedoriw Y, Hornick JL, Perkins SL, South ST, Andersen EF.

Mod Pathol. 2017 Sep;30(9):1234-1240. doi: 10.1038/modpathol.2017.50. Epub 2017 Jul 28.

7.

Genomic analysis of follicular dendritic cell sarcoma by molecular inversion probe array reveals tumor suppressor-driven biology.

Andersen EF, Paxton CN, O'Malley DP, Louissaint A Jr, Hornick JL, Griffin GK, Fedoriw Y, Kim YS, Weiss LM, Perkins SL, South ST.

Mod Pathol. 2017 Sep;30(9):1321-1334. doi: 10.1038/modpathol.2017.34. Epub 2017 Jun 16.

8.

Xq28 duplication overlapping the int22h-1/int22h-2 region and including RAB39B and CLIC2 in a family with intellectual and developmental disability.

Andersen EF, Baldwin EE, Ellingwood S, Smith R, Lamb AN.

Am J Med Genet A. 2014 Jul;164A(7):1795-801. doi: 10.1002/ajmg.a.36524. Epub 2014 Apr 3.

PMID:
24700761
9.

Elements of the polycomb repressor SU(Z)12 needed for histone H3-K27 methylation, the interface with E(Z), and in vivo function.

Rai AN, Vargas ML, Wang L, Andersen EF, Miller EL, Simon JA.

Mol Cell Biol. 2013 Dec;33(24):4844-56. doi: 10.1128/MCB.00307-13. Epub 2013 Oct 7.

10.

Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome.

Andersen EF, Carey JC, Earl DL, Corzo D, Suttie M, Hammond P, South ST.

Eur J Hum Genet. 2014 Apr;22(4):464-70. doi: 10.1038/ejhg.2013.192. Epub 2013 Aug 21.

11.

Centrosome movements in vivo correlate with specific neurite formation downstream of LIM homeodomain transcription factor activity.

Andersen EF, Halloran MC.

Development. 2012 Oct;139(19):3590-9. doi: 10.1242/dev.081513. Epub 2012 Aug 16.

12.
13.

Alternative ESC and ESC-like subunits of a polycomb group histone methyltransferase complex are differentially deployed during Drosophila development.

Wang L, Jahren N, Vargas ML, Andersen EF, Benes J, Zhang J, Miller EL, Jones RS, Simon JA.

Mol Cell Biol. 2006 Apr;26(7):2637-47.

14.

Subunit contributions to histone methyltransferase activities of fly and worm polycomb group complexes.

Ketel CS, Andersen EF, Vargas ML, Suh J, Strome S, Simon JA.

Mol Cell Biol. 2005 Aug;25(16):6857-68.

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