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Human Placental Transcriptome Reveals Critical Alterations in Inflammation and Energy Metabolism with Fetal Sex Differences in Spontaneous Preterm Birth.
Int J Mol Sci. 2021 Jul 23;22(15):7899. doi: 10.3390/ijms22157899.
Int J Mol Sci. 2021.
PMID: 34360662
Free PMC article.
Lifelong pulmonary sequelae of bronchopulmonary dysplasia.
Sillers L, Alexiou S, Jensen EA.
Sillers L, et al.
Curr Opin Pediatr. 2020 Apr;32(2):252-260. doi: 10.1097/MOP.0000000000000884.
Curr Opin Pediatr. 2020.
PMID: 32084032
Review.
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Pulseless Electrical Activity Complicating Neonatal Resuscitation.
Sillers L, Handley SC, James JR, Foglia EE.
Sillers L, et al.
Neonatology. 2019;115(2):95-98. doi: 10.1159/000493357. Epub 2018 Oct 23.
Neonatology. 2019.
PMID: 30352434
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Survival and decannulation across indications for infant tracheostomy: a twelve-year single-center cohort study.
Sillers L, Lioy J, Moran K, Stow J, Jacobs IN, DeMauro SB.
Sillers L, et al.
J Perinatol. 2022 Jan;42(1):72-78. doi: 10.1038/s41372-021-01181-9. Epub 2021 Aug 17.
J Perinatol. 2022.
PMID: 34404923
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Clinical and Molecular Analysis in 2 Families With Novel Compound Heterozygous SBP2 (SECISBP2) Mutations.
Fu J, Korwutthikulrangsri M, Gönç EN, Sillers L, Liao XH, Alikaşifoğlu A, Kandemir N, Menucci MB, Burman KD, Weiss RE, Dumitrescu AM.
Fu J, et al. Among authors: sillers l.
J Clin Endocrinol Metab. 2020 Mar 1;105(3):e6-e11. doi: 10.1210/clinem/dgz169.
J Clin Endocrinol Metab. 2020.
PMID: 32084277
Free PMC article.
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Neonatal Thrombocytopenia: Etiology and Diagnosis.
Sillers L, Van Slambrouck C, Lapping-Carr G.
Sillers L, et al.
Pediatr Ann. 2015 Jul;44(7):e175-80. doi: 10.3928/00904481-20150710-11.
Pediatr Ann. 2015.
PMID: 26171707
Free PMC article.
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The Atoh1-lineage gives rise to hair cells and supporting cells within the mammalian cochlea.
Driver EC, Sillers L, Coate TM, Rose MF, Kelley MW.
Driver EC, et al. Among authors: sillers l.
Dev Biol. 2013 Apr 1;376(1):86-98. doi: 10.1016/j.ydbio.2013.01.005. Epub 2013 Jan 11.
Dev Biol. 2013.
PMID: 23318633
Free PMC article.
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Cytokine gene polymorphisms as risk and severity factors for juvenile dermatomyositis.
Mamyrova G, O'Hanlon TP, Sillers L, Malley K, James-Newton L, Parks CG, Cooper GS, Pandey JP, Miller FW, Rider LG; Childhood Myositis Heterogeneity Collaborative Study Group.
Mamyrova G, et al. Among authors: sillers l.
Arthritis Rheum. 2008 Dec;58(12):3941-50. doi: 10.1002/art.24039.
Arthritis Rheum. 2008.
PMID: 19035492
Free PMC article.
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