Lisi EC[au] - Search Results

Year	Number of Results
2007	1
2008	1
2009	1
2011	1
2015	1
2016	2
2020	1
2021	4
2022	1
2024	0

1

Genomics Integration Into Nephrology Practice.

Pinto E Vairo F, Prochnow C, Kemppainen JL, Lisi EC, Steyermark JM, Kruisselbrink TM, Pichurin PN, Dhamija R, Hager MM, Albadri S, Cornell LD, Lazaridis KN, Klee EW, Senum SR, El Ters M, Amer H, Baudhuin LM, Moyer AM, Keddis MT, Zand L, Sas DJ, Erickson SB, Fervenza FC, Lieske JC, Harris PC, Hogan MC. Pinto E Vairo F, et al. Among authors: lisi ec. Kidney Med. 2021 Jun 29;3(5):785-798. doi: 10.1016/j.xkme.2021.04.014. eCollection 2021 Sep-Oct. Kidney Med. 2021. PMID: 34746741 Free PMC article.

2

Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature.

Lisi EC, Cohn RD. Lisi EC, et al. Dev Med Child Neurol. 2011 Jul;53(7):586-99. doi: 10.1111/j.1469-8749.2011.03918.x. Epub 2011 Mar 21. Dev Med Child Neurol. 2011. PMID: 21418198 Free article. Review.

3

Clinically Actionable Findings Derived From Predictive Genomic Testing Offered in a Medical Practice Setting.

Anderson JL, Kruisselbrink TM, Lisi EC, Hughes TM, Steyermark JM, Winkler EM, Berg CM, Vierkant RA, Gupta R, Ali AH, Faubion SS, Aoudia SL, McAllister TM, Farrugia G, Stewart AK, Lazaridis KN. Anderson JL, et al. Among authors: lisi ec. Mayo Clin Proc. 2021 Jun;96(6):1407-1417. doi: 10.1016/j.mayocp.2020.08.051. Epub 2020 Oct 21. Mayo Clin Proc. 2021. PMID: 33890576

4

Opinions of adults affected with later-onset lysosomal storage diseases regarding newborn screening: A qualitative study.

Lisi EC, Ali N. Lisi EC, et al. J Genet Couns. 2021 Dec;30(6):1544-1558. doi: 10.1002/jgc4.1421. Epub 2021 May 3. J Genet Couns. 2021. PMID: 33938615

5

Expanding insurance coverage for in vitro fertilisation with preimplantation genetic testing: putting the cart before the horse.

Lisi EC. Lisi EC. J Med Ethics. 2022 Mar;48(3):202-204. doi: 10.1136/medethics-2020-106940. Epub 2021 Feb 19. J Med Ethics. 2022. PMID: 33608448

6

Patients' perspectives on newborn screening for later-onset lysosomal storage diseases.

Lisi EC, Gillespie S, Laney D, Ali N. Lisi EC, et al. Mol Genet Metab. 2016 Sep;119(1-2):109-14. doi: 10.1016/j.ymgme.2016.07.009. Epub 2016 Jul 21. Mol Genet Metab. 2016. PMID: 27591925

7

Newborn Screening for Lysosomal Storage Disorders: Views of Genetic Healthcare Providers.

Lisi EC, McCandless SE. Lisi EC, et al. J Genet Couns. 2016 Apr;25(2):373-84. doi: 10.1007/s10897-015-9879-8. Epub 2015 Aug 29. J Genet Couns. 2016. PMID: 26315880

8

3q29 interstitial microduplication: a new syndrome in a three-generation family.

Lisi EC, Hamosh A, Doheny KF, Squibb E, Jackson B, Galczynski R, Thomas GH, Batista DA. Lisi EC, et al. Am J Med Genet A. 2008 Mar 1;146A(5):601-9. doi: 10.1002/ajmg.a.32190. Am J Med Genet A. 2008. PMID: 18241066

9

3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.

Li F, Lisi EC, Wohler ES, Hamosh A, Batista DA. Li F, et al. Among authors: lisi ec. Eur J Med Genet. 2009 Sep-Oct;52(5):349-52. doi: 10.1016/j.ejmg.2009.05.001. Epub 2009 May 19. Eur J Med Genet. 2009. PMID: 19460468

10

Albinism and developmental delay: the need to test for 15q11-q13 deletion.

Saadeh R, Lisi EC, Batista DA, McIntosh I, Hoover-Fong JE. Saadeh R, et al. Among authors: lisi ec. Pediatr Neurol. 2007 Oct;37(4):299-302. doi: 10.1016/j.pediatrneurol.2007.06.024. Pediatr Neurol. 2007. PMID: 17903679 Free PMC article.

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