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American Journal of Medical Genetics. Part A|September 12, 2012
Overgrowth with increased proliferation of fibroblast and matrix metalloproteinase activity related to reduced TIMP1: a newly recognized syndrome?Brian Chung, Aleksander Hinek, Sarah Keating, et al.
American Journal of Perinatology|September 21, 2016
Placental Pathology in Relation to Uterine Artery Doppler Findings in Pregnancies with Severe Intrauterine Growth Restriction and Abnormal Umbilical Artery Doppler ChangesKhrystyna Levytska, Mary Higgins, Sarah Keating, et al.
Pediatric Radiology|July 18, 2008
MRI of the fetal eyes: morphologic and biometric assessment for abnormal development with ultrasonographic and clinicopathologic correlationAshley J Robinson, Susan Blaser, Ants Toi, et al.
Nature Reviews. Nephrology|October 27, 2009
Angiogenic factor abnormalities and fetal demise in a twin pregnancyMichelle A Hladunewich, Guy Steinberg, S Ananth Karumanchi, et al.
Clinical Epigenetics|June 23, 2016
Genome-wide placental DNA methylation analysis of severely growth-discordant monochorionic twins reveals novel epigenetic targets for intrauterine growth restrictionMaian Roifman, Sanaa Choufani, Andrei L Turinsky, et al.
Placenta|May 27, 2020
Placental histopathology in sickle cell disease: A descriptive and hypothesis-generating studyAnn Kinga Malinowski, Claudia Dziegielewski, Sarah Keating, et al.
Prenatal Diagnosis|February 27, 2009
Cornelia de Lange syndrome (CdLS): prenatal and autopsy findingsKaren Chong, Sarah Keating, Stephanie Hurst, et al.
Prenatal Diagnosis|November 7, 2006
X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findingsShalini Umranikar, Phyllis Glanc, Sheila Unger, et al.
Cellular & Molecular Immunology|August 18, 2015
Human dNK cell function is differentially regulated by extrinsic cellular engagement and intrinsic activating receptors in first and second trimester pregnancyJianhong Zhang, Caroline E Dunk, Melissa Kwan, et al.
American Journal of Medical Genetics. Part A|May 29, 2013
Broadening the ciliopathy spectrum: motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 geneSharon Moalem, Sarah Keating, Patrick Shannon, et al.
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