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Items: 23

1.

Psychosocial Stress and Adversity: Effects from the Perinatal Period to Adulthood.

Barrero-Castillero A, Morton SU, Nelson CA 3rd, Smith VC.

Neoreviews. 2019 Dec;20(12):e686-e696. doi: 10.1542/neo.20-12-e686.

PMID:
31792156
2.

Maternal Dietary Intake of Omega-3 Fatty Acids Correlates Positively with Regional Brain Volumes in 1-Month-Old Term Infants.

Morton SU, Vyas R, Gagoski B, Vu C, Litt J, Larsen RJ, Kuchan MJ, Lasekan JB, Sutton BP, Grant PE, Ou Y.

Cereb Cortex. 2019 Nov 11. pii: bhz222. doi: 10.1093/cercor/bhz222. [Epub ahead of print]

PMID:
31711132
3.

Paternal-age-related de novo mutations and risk for five disorders.

Taylor JL, Debost JPG, Morton SU, Wigdor EM, Heyne HO, Lal D, Howrigan DP, Bloemendal A, Larsen JT, Kosmicki JA, Weiner DJ, Homsy J, Seidman JG, Seidman CE, Agerbo E, McGrath JJ, Mortensen PB, Petersen L, Daly MJ, Robinson EB.

Nat Commun. 2019 Jul 10;10(1):3043. doi: 10.1038/s41467-019-11039-6.

4.

Abnormal Left-Hemispheric Sulcal Patterns Correlate with Neurodevelopmental Outcomes in Subjects with Single Ventricular Congenital Heart Disease.

Morton SU, Maleyeff L, Wypij D, Yun HJ, Newburger JW, Bellinger DC, Roberts AE, Rivkin MJ, Seidman JG, Seidman CE, Grant PE, Im K.

Cereb Cortex. 2019 Jun 19. pii: bhz101. doi: 10.1093/cercor/bhz101. [Epub ahead of print]

PMID:
31216004
5.

ORE identifies extreme expression effects enriched for rare variants.

Richter F, Hoffman GE, Manheimer KB, Patel N, Sharp AJ, McKean D, Morton SU, DePalma S, Gorham J, Kitaygorodksy A, Porter GA, Giardini A, Shen Y, Chung WK, Seidman JG, Seidman CE, Schadt EE, Gelb BD.

Bioinformatics. 2019 Oct 15;35(20):3906-3912. doi: 10.1093/bioinformatics/btz202.

PMID:
30903145
6.

Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.

O'Connell AE, Gerashchenko MV, O'Donohue MF, Rosen SM, Huntzinger E, Gleeson D, Galli A, Ryder E, Cao S, Murphy Q, Kazerounian S, Morton SU, Schmitz-Abe K, Gladyshev VN, Gleizes PE, Séraphin B, Agrawal PB.

PLoS Genet. 2019 Feb 1;15(2):e1007917. doi: 10.1371/journal.pgen.1007917. eCollection 2019 Feb.

7.

Response to Brodehl et al.

Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D.

Genet Med. 2019 May;21(5):1248-1249. doi: 10.1038/s41436-018-0292-1. Epub 2018 Sep 28. No abstract available.

PMID:
30262924
8.

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect.

Shaaban S, MacKinnon S, Andrews C, Staffieri SE, Maconachie GDE, Chan WM, Whitman MC, Morton SU, Yazar S, MacGregor S, Elder JE, Traboulsi EI, Gottlob I, Hewitt AW; Strabismus Genetics Research Consortium, Hunter DG, Mackey DA, Engle EC.

Invest Ophthalmol Vis Sci. 2018 Aug 1;59(10):4054-4064. doi: 10.1167/iovs.18-24082.

9.

Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.

Minoche AE, Horvat C, Johnson R, Gayevskiy V, Morton SU, Drew AP, Woo K, Statham AL, Lundie B, Bagnall RD, Ingles J, Semsarian C, Seidman JG, Seidman CE, Dinger ME, Cowley MJ, Fatkin D.

Genet Med. 2019 Mar;21(3):650-662. doi: 10.1038/s41436-018-0084-7. Epub 2018 Jul 2.

PMID:
29961767
10.

Reducing time to initiation and advancement of enteral feeding in an all-referral neonatal intensive care unit.

Morton SU, Belfort MB, Kahlon PS, Hajizadeh Barfjani S, Rudie C, Hashim E, Hansen A, Huh SY.

J Perinatol. 2018 Jul;38(7):936-943. doi: 10.1038/s41372-018-0110-2. Epub 2018 May 8.

PMID:
29740193
11.

Homozygous EEF1A2 mutation causes dilated cardiomyopathy, failure to thrive, global developmental delay, epilepsy and early death.

Cao S, Smith LL, Padilla-Lopez SR, Guida BS, Blume E, Shi J, Morton SU, Brownstein CA, Beggs AH, Kruer MC, Agrawal PB.

Hum Mol Genet. 2017 Sep 15;26(18):3545-3552. doi: 10.1093/hmg/ddx239.

12.

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant.

Morton SU, Prabhu SP, Lidov HGW, Shi J, Anselm I, Brownstein CA, Bainbridge MN, Beggs AH, Vargas SO, Agrawal PB.

Cold Spring Harb Mol Case Stud. 2017 Mar;3(2):a001560. doi: 10.1101/mcs.a001560.

13.

Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants.

Morton SU, Neilan EG, Peake RWA, Shi J, Schmitz-Abe K, Towne M, Markianos K, Prabhu SP, Agrawal PB.

JIMD Rep. 2017;35:7-15. doi: 10.1007/8904_2016_17. Epub 2016 Nov 18.

14.

Fetal Physiology and the Transition to Extrauterine Life.

Morton SU, Brodsky D.

Clin Perinatol. 2016 Sep;43(3):395-407. doi: 10.1016/j.clp.2016.04.001. Epub 2016 Jun 11. Review.

15.

Separating Putative Pathogens from Background Contamination with Principal Orthogonal Decomposition: Evidence for Leptospira in the Ugandan Neonatal Septisome.

Schiff SJ, Kiwanuka J, Riggio G, Nguyen L, Mu K, Sproul E, Bazira J, Mwanga-Amumpaire J, Tumusiime D, Nyesigire E, Lwanga N, Bogale KT, Kapur V, Broach JR, Morton SU, Warf BC, Poss M.

Front Med (Lausanne). 2016 Jun 13;3:22. doi: 10.3389/fmed.2016.00022. eCollection 2016.

16.

Treatment options for apnoea of prematurity.

Morton SU, Smith VC.

Arch Dis Child Fetal Neonatal Ed. 2016 Jul;101(4):F352-6. doi: 10.1136/archdischild-2015-310228. Epub 2016 Mar 22. Review.

PMID:
27010019
17.

Skeletal muscle microRNA and messenger RNA profiling in cofilin-2 deficient mice reveals cell cycle dysregulation hindering muscle regeneration.

Morton SU, Joshi M, Savic T, Beggs AH, Agrawal PB.

PLoS One. 2015 Apr 13;10(4):e0123829. doi: 10.1371/journal.pone.0123829. eCollection 2015.

18.

miR-145 and miR-143 regulate smooth muscle cell fate and plasticity.

Cordes KR, Sheehy NT, White MP, Berry EC, Morton SU, Muth AN, Lee TH, Miano JM, Ivey KN, Srivastava D.

Nature. 2009 Aug 6;460(7256):705-10. doi: 10.1038/nature08195. Epub 2009 Jul 5.

19.

microRNA-138 modulates cardiac patterning during embryonic development.

Morton SU, Scherz PJ, Cordes KR, Ivey KN, Stainier DY, Srivastava D.

Proc Natl Acad Sci U S A. 2008 Nov 18;105(46):17830-5. doi: 10.1073/pnas.0804673105. Epub 2008 Nov 12.

20.

miR-126 regulates angiogenic signaling and vascular integrity.

Fish JE, Santoro MM, Morton SU, Yu S, Yeh RF, Wythe JD, Ivey KN, Bruneau BG, Stainier DY, Srivastava D.

Dev Cell. 2008 Aug;15(2):272-84. doi: 10.1016/j.devcel.2008.07.008.

21.

Thioredoxin is required for S-nitrosation of procaspase-3 and the inhibition of apoptosis in Jurkat cells.

Mitchell DA, Morton SU, Fernhoff NB, Marletta MA.

Proc Natl Acad Sci U S A. 2007 Jul 10;104(28):11609-14. Epub 2007 Jul 2.

22.

Maternal mortality and the consequences on infant and child survival in rural Haiti.

Anderson FW, Morton SU, Naik S, Gebrian B.

Matern Child Health J. 2007 Jul;11(4):395-401. Epub 2007 Jan 31.

PMID:
17265193
23.

Design and characterization of an active site selective caspase-3 transnitrosating agent.

Mitchell DA, Morton SU, Marletta MA.

ACS Chem Biol. 2006 Nov 21;1(10):659-65.

PMID:
17168570

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