1. A new biological and clinical resource for research into pregnancy complications: The Baby Bio Bank. (October 2016) Authors: Leon, Lydia J.; Solanky, Nita; Stalman, Susanne E.; Demetriou, Charalambos; Abu-Amero, Sayeda; Stanier, Philip; Regan, Lesley; Moore, Gudrun E. Journal: Placenta Issue: Volume 46(2016:Oct.) Page Start: 31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An analysis of common isodisomic regions in five mUPD 16 probands. Issue 3 (1st March 1999) Authors: Abu-Amero, Sayeda N; Ali, Zehra; Abu-Amero, Khaled K; Stanier, Philip; Moore, Gudrun E Journal: Journal of medical genetics Issue: Volume 36:Issue 3(1999) Page Start: 204 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1. Issue 3 (17th January 2018) Authors: Piard, Juliette; Lespinasse, James; Vlckova, Marketa; Mensah, Martin A.; Iurian, Sorin; Simandlova, Martina; Malikova, Marcela; Bartsch, Oliver; Rossi, Massimiliano; Lenoir, Marion; Nugues, Frédérique; Mundlos, Stefan; Kornak, Uwe; Stanier, Philip; Sousa, Sérgio B.; Van Maldergem, Lionel Journal: American journal of medical genetics Issue: Volume 176:Issue 3(2018) Page Start: 668 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Epigenetic signatures of Silver–Russell syndrome. Issue 3 (19th March 2010) Authors: Abu-Amero, Sayeda; Wakeling, Emma L; Preece, Mike; Whittaker, John; Stanier, Philip; Moore, Gudrun E Journal: Journal of medical genetics Issue: Volume 47:Issue 3(2010) Page Start: 150 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Erratum to: Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models. Issue 1 (December 2016) Authors: Mendioroz, Maite; Do, Catherine; Jiang, Xiaoling; Liu, Chunhong; Darbary, Huferesh; Lang, Charles; Lin, John; Thomas, Anna; Abu-Amero, Sayeda; Stanier, Philip; Temkin, Alexis; Yale, Alexander; Liu, Meng-Min; Li, Yang; Salas, Martha; Kerkel, Kristi; Capone, George; Silverman, Wayne; Yu, Y.; Moore,... Journal: Genome biology Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate. (14th January 2019) Authors: Howe, Laurence J; Richardson, Tom G; Arathimos, Ryan; Alvizi, Lucas; Passos-Bueno, Maria R; Stanier, Philip; Nohr, Ellen; Ludwig, Kerstin U; Mangold, Elisabeth; Knapp, Michael; Stergiakouli, Evie; Pourcain, Beate St; Smith, George Davey; Sandy, Jonathan; Relton, Caroline L; Lewis, Sarah J; Hemani... Journal: Epigenomics Issue: Volume 11:Number 2(2019) Page Start: 133 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Familial Absent Uvula With Velopharyngeal Incompetence—A New Syndrome?. (April 2020) Authors: Sommerlad, Brian; Seselgyte, Rimante; Lees, Melissa; Pauws, Erwin; Stanier, Philip; Sell, Debbie Journal: Cleft palate-craniofacial journal Issue: Volume 57:Number 4(2020) Page Start: 514 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. FGFR2c Signalling Attenuation in Craniosynostosis. (July 2017) Authors: Lee, Kevin K.L.; Peskett, Emma; Stanier, Philip; Pauws, Erwin Journal: Mechanisms of development Issue: Volume 145(2017)Supplement Page Start: S32 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification and validation of loss of function variants in clinical contexts. Issue 1 (11th October 2013) Authors: Lescai, Francesco; Marasco, Elena; Bacchelli, Chiara; Stanier, Philip; Mantovani, Vilma; Beales, Philip Journal: Molecular genetics & genomic medicine Issue: Volume 2:Issue 1(2014:Jan.) Page Start: 58 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Investigation of the Annexin A5 M2 haplotype in 500 white European couples who have experienced recurrent spontaneous abortion. Issue 5 (November 2015) Authors: Demetriou, Charalambos; Abu-amero, Sayeda; White, Shawnelle; Peskett, Emma; Markoff, Arseni; Stanier, Philip; Moore, Gudrun E.; Regan, Lesley Journal: Reproductive biomedicine online Issue: Volume 31:Issue 5(2015) Page Start: 681 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗