1. Basal plate plaque: a novel organising placental thrombotic process. Issue 8 (20th January 2011) Authors: Fitzgerald, Brendan; Shannon, Patrick; Kingdom, John; Keating, Sarah Journal: Journal of clinical pathology Issue: Volume 64:Issue 8(2011) Page Start: 725 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Broadening the ciliopathy spectrum: Motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 gene. Issue 7 (24th May 2013) Authors: Moalem, Sharon; Keating, Sarah; Shannon, Patrick; Thompson, Megan; Millar, Kathryn; Nykamp, Keith; Forster, Adam; Noor, Abdul; Chitayat, David Journal: American journal of medical genetics Issue: Volume 161:Issue 7(2013:Jul.) Page Start: 1792 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Chronic Histiocytic Intervillositis – Clinical, Biochemical and Radiological Associations [30F]. Issue 1 (May 2017) Authors: Koby, Lawrence; Keating, Sarah; Malinowski, Ann; Murphy, Kellie; D'Souza, Rohan Journal: Obstetrics and gynecology Issue: Volume 129:Issue 1(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Chronic histiocytic intervillositis – Clinical, biochemical and radiological findings: An observational study. (April 2018) Authors: Koby, Lawrence; Keating, Sarah; Malinowski, Ann Kinga; D'Souza, Rohan Journal: Placenta Issue: Volume 64(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Diagnostic accuracy of fetal growth charts for placenta-related fetal growth restriction. (February 2021) Authors: Melamed, Nir; Hiersch, Liran; Aviram, Amir; Mei-Dan, Elad; Keating, Sarah; Kingdom, John C. Journal: Placenta Issue: Volume 105(2021) Page Start: 70 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Diagnostic Utility of Pathological Investigations in Late Gestation Stillbirth: A Cohort Study. (April 2020) Authors: Lou, Si Kei; Keating, Sarah; Kolomietz, Elena; Shannon, Patrick Journal: Pediatric and developmental pathology Issue: Volume 23:Number 2(2020) Page Start: 96 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Dyssegmental dysplasia, Silverman‐Handmaker type: prenatal ultrasound findings and molecular analysis. (4th August 2013) Authors: Ladhani, Noor Niyar N.; Chitayat, David; Nezarati, Marjan M.; Laureane, Mittaz Crettol; Keating, Sarah; Silver, Rachel J.; Unger, Sheila; Velsher, Lea; Sirkin, Wilma; Toi, Ants; Glanc, Phyllis Journal: Prenatal diagnosis Issue: Volume 33:Number 11(2013:Nov.) Page Start: 1039 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome-wide placental DNA methylation analysis of severely growth-discordant monochorionic twins reveals novel epigenetic targets for intrauterine growth restriction. Issue 1 (December 2016) Authors: Roifman, Maian; Choufani, Sanaa; Turinsky, Andrei; Drewlo, Sascha; Keating, Sarah; Brudno, Michael; Kingdom, John; Weksberg, Rosanna Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Maternal Vascular Malperfusion and Adverse Perinatal Outcomes in Low-Risk Nulliparous Women. Issue 5 (November 2017) Authors: Wright, Emily; Audette, Melanie C.; Ye, Xiang Y.; Keating, Sarah; Hoffman, Barry; Lye, Stephen J.; Shah, Prakesh S.; Kingdom, John C. Journal: Obstetrics and gynecology Issue: Volume 130:Issue 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. MG-105 Facial dysmorphism, skeletal abnormalities and central nervous system abnormalities in two sibs born to a consanguineous couple: A new autosomal recessive condition. (4th December 2015) Authors: Chad, Lauren; Thompson, Megan; Miron, Ioana; Shannon, Patrick; Keating, Sarah; Chitayat, David Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 1 Page Start: A1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗