Kalish JM - Search Results

1

Allele-specific RNA imaging shows that allelic imbalances can arise in tissues through transcriptional bursting.

Symmons O, Chang M, Mellis IA, Kalish JM, Park J, Suszták K, Bartolomei MS, Raj A. Symmons O, et al. Among authors: kalish jm. PLoS Genet. 2019 Jan 9;15(1):e1007874. doi: 10.1371/journal.pgen.1007874. eCollection 2019 Jan. PLoS Genet. 2019. PMID: 30625149 Free PMC article.

2

Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.

Kalish JM, Conlin LK, Bhatti TR, Dubbs HA, Harris MC, Izumi K, Mostoufi-Moab S, Mulchandani S, Saitta S, States LJ, Swarr DT, Wilkens AB, Zackai EH, Zelley K, Bartolomei MS, Nichols KE, Palladino AA, Spinner NB, Deardorff MA. Kalish JM, et al. Am J Med Genet A. 2013 Aug;161A(8):1929-39. doi: 10.1002/ajmg.a.36045. Epub 2013 Jun 26. Am J Med Genet A. 2013. PMID: 23804593 Free PMC article.

3

Epigenetics and imprinting in human disease.

Kalish JM, Jiang C, Bartolomei MS. Kalish JM, et al. Int J Dev Biol. 2014;58(2-4):291-8. doi: 10.1387/ijdb.140077mb. Int J Dev Biol. 2014. PMID: 25023695 Free article. Review.

4

Visualizing allele-specific expression in single cells reveals epigenetic mosaicism in an H19 loss-of-imprinting mutant.

Ginart P, Kalish JM, Jiang CL, Yu AC, Bartolomei MS, Raj A. Ginart P, et al. Among authors: kalish jm. Genes Dev. 2016 Mar 1;30(5):567-78. doi: 10.1101/gad.275958.115. Genes Dev. 2016. PMID: 26944681 Free PMC article.

5

Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome.

Chang S, Hur SK, Naveh NSS, Thorvaldsen JL, French DL, Gagne AL, Jobaliya CD, Anguera MC, Bartolomei MS, Kalish JM. Chang S, et al. Among authors: kalish jm. Epigenetics. 2021 Dec;16(12):1295-1305. doi: 10.1080/15592294.2020.1861172. Epub 2020 Dec 29. Epigenetics. 2021. PMID: 33300436 Free PMC article.

6

Improved molecular detection of mosaicism in Beckwith-Wiedemann Syndrome.

Baker SW, Duffy KA, Richards-Yutz J, Deardorff MA, Kalish JM, Ganguly A. Baker SW, et al. Among authors: kalish jm. J Med Genet. 2021 Mar;58(3):178-184. doi: 10.1136/jmedgenet-2019-106498. Epub 2020 May 19. J Med Genet. 2021. PMID: 32430359 Free PMC article.

7

Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith-Wiedemann syndrome.

Kalish JM, Boodhansingh KE, Bhatti TR, Ganguly A, Conlin LK, Becker SA, Givler S, Mighion L, Palladino AA, Adzick NS, De León DD, Stanley CA, Deardorff MA. Kalish JM, et al. J Med Genet. 2016 Jan;53(1):53-61. doi: 10.1136/jmedgenet-2015-103394. Epub 2015 Nov 6. J Med Genet. 2016. PMID: 26545876 Free PMC article.

8

Overgrowth Syndromes.

Edmondson AC, Kalish JM. Edmondson AC, et al. Among authors: kalish jm. J Pediatr Genet. 2015 Sep;4(3):136-43. doi: 10.1055/s-0035-1564440. Epub 2015 Sep 25. J Pediatr Genet. 2015. PMID: 27617124 Free PMC article. Review.

9

Altered microRNA expression profiles in large offspring syndrome and Beckwith-Wiedemann syndrome.

Li Y, Hagen DE, Ji T, Bakhtiarizadeh MR, Frederic WM, Traxler EM, Kalish JM, Rivera RM. Li Y, et al. Among authors: kalish jm. Epigenetics. 2019 Sep;14(9):850-876. doi: 10.1080/15592294.2019.1615357. Epub 2019 May 30. Epigenetics. 2019. PMID: 31144574 Free PMC article.

10

Novel variants in CDH2 are associated with a new syndrome including Peters anomaly.

Reis LM, Houssin NS, Zamora C, Abdul-Rahman O, Kalish JM, Zackai EH, Plageman TF Jr, Semina EV. Reis LM, et al. Among authors: kalish jm. Clin Genet. 2020 Mar;97(3):502-508. doi: 10.1111/cge.13660. Epub 2019 Nov 10. Clin Genet. 2020. PMID: 31650526 Free PMC article.

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