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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2013 | 2 |
2014 | 1 |
2015 | 1 |
2024 | 0 |
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5 results
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Page 1
Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder.
PLoS Genet. 2014 May 29;10(5):e1004402. doi: 10.1371/journal.pgen.1004402. eCollection 2014.
PLoS Genet. 2014.
PMID: 24875834
Free PMC article.
Epigenetic silencing of Oct4 by a complex containing SUV39H1 and Oct4 pseudogene lncRNA.
Scarola M, Comisso E, Pascolo R, Chiaradia R, Marion RM, Schneider C, Blasco MA, Schoeftner S, Benetti R.
Scarola M, et al. Among authors: marion rm.
Nat Commun. 2015 Jul 9;6:7631. doi: 10.1038/ncomms8631.
Nat Commun. 2015.
PMID: 26158551
Free PMC article.
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Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Delio M, Guo T, McDonald-McGinn DM, Zackai E, Herman S, Kaminetzky M, Higgins AM, Coleman K, Chow C, Jalbrzikowski M, Bearden CE, Bailey A, Vangkilde A, Olsen L, Olesen C, Skovby F, Werge TM, Templin L, Busa T, Philip N, Swillen A, Vermeesch JR, Devriendt K, Schneider M, Dahoun S, Eliez S, Schoch K, Hooper SR, Shashi V, Samanich J, Marion R, van Amelsvoort T, Boot E, Klaassen P, Duijff SN, Vorstman J, Yuen T, Silversides C, Chow E, Bassett A, Frisch A, Weizman A, Gothelf D, Niarchou M, van den Bree M, Owen MJ, Suñer DH, Andreo JR, Armando M, Vicari S, Digilio MC, Auton A, Kates WR, Wang T, Shprintzen RJ, Emanuel BS, Morrow BE.
Delio M, et al. Among authors: marion r.
Am J Hum Genet. 2013 Mar 7;92(3):439-47. doi: 10.1016/j.ajhg.2013.01.018. Epub 2013 Feb 28.
Am J Hum Genet. 2013.
PMID: 23453669
Free PMC article.
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TRF1 is a stem cell marker and is essential for the generation of induced pluripotent stem cells.
Schneider RP, Garrobo I, Foronda M, Palacios JA, Marión RM, Flores I, Ortega S, Blasco MA.
Schneider RP, et al. Among authors: marion rm.
Nat Commun. 2013;4:1946. doi: 10.1038/ncomms2946.
Nat Commun. 2013.
PMID: 23735977
Free article.
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Fronto-ocular syndrome: newly recognized trigonocephaly syndrome.
Schneider EN, Bogdanow A, Goodrich JT, Marion RW, Cohen MM Jr.
Schneider EN, et al. Among authors: marion rw.
Am J Med Genet. 2000 Jul 17;93(2):89-93. doi: 10.1002/1096-8628(20000717)93:2<89::aid-ajmg2>3.0.co;2-4.
Am J Med Genet. 2000.
PMID: 10869108
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