1. Correspondence to: Phase 2a randomized clinical trial of dupilumab (anti‐IL‐4Rα) for alopecia areata patients. Issue 3 (25th February 2022) Authors: Maher, Eamonn; Martiniuk, Frank; Levis, William Journal: Allergy Issue: Volume 77:Issue 3(2022) Page Start: 1073 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes. (4th March 2019) Authors: Mackay, Deborah J.G.; Bliek, Jet; Lombardi, Maria Paola; Russo, Silvia; Calzari, Luciano; Guzzetti, Sara; Izzi, Claudia; Selicorni, Angelo; Melis, Daniela; Temple, Karen; Maher, Eamonn; Brioude, Frédéric; Netchine, Irène; Eggermann, Thomas Journal: Genetical research Issue: Volume 101(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Issue 1 (December 2016) Authors: Eggermann, Thomas; de Nanclares, Guiomar; Maher, Eamonn; Temple, I.; Tümer, Zeynep; Monk, David; Mackay, Deborah; Grønskov, Karen; Riccio, Andrea; Linglart, Agnès; Netchine, Irène 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) ↗
4. Expression and knockdown of zebrafish folliculin suggests requirement for embryonic brain morphogenesis. Issue 1 (December 2016) Authors: Kenyon, Emma; Luijten, Monique; Gill, Harmeet; Li, Nan; Rawlings, Matthew; Bull, James; Hadzhiev, Yavor; van Steensel, Maurice; Maher, Eamonn; Mueller, Ferenc Journal: BMC developmental biology Issue: Volume 16:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Hereditary Tumors. Issue 5 (May 1992) Authors: Maher, Eamonn Journal: Journal of medical genetics Issue: Volume 29:Issue 5(1992) Page Start: 360 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Issue 1 (December 2015) Authors: Eggermann, Thomas; Perez de Nanclares, Guiomar; Maher, Eamonn; Temple, I.; Tümer, Zeynep; Monk, David; Mackay, Deborah; Grønskov, Karen; Riccio, Andrea; Linglart, Agnès; Netchine, Irène Journal: Clinical epigenetics Issue: Volume 7:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci. Issue 1 (December 2015) Authors: Eggermann, Thomas; Perez de Nanclares, Guiomar; Maher, Eamonn; Temple, I.; Tümer, Zeynep; Monk, David; Mackay, Deborah; Grønskov, Karen; Riccio, Andrea; Linglart, Agnès; Netchine, Irène Journal: Clinical epigenetics Issue: Volume 7:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. In Vitro Selection of a Single-Stranded DNA Molecular Recognition Element against Clostridium difficile Toxin B and Sensitive Detection in Human Fecal Matter. (5th February 2015) Authors: Hong, Ka Lok; Maher, Eamonn; Williams, Ryan M.; Sooter, Letha J. Other Names: Berkhout Ben Academic Editor. Journal: Journal of nucleic acids Issue: Volume 2015(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Meeting abstracts from the 64th British Thyroid Association Annual Meeting. Issue 1 (February 2017) Authors: Bartalena, Luigi; Fliers, Eric; Hellen, Nicola; Taylor, Peter; Lacey, Arron; Thayer, Daniel; Yusof, Mohd; Tabasum, Arshiya; Muller, Illaria; Marsh, Luke; Ludgate, Marian; Rees, Alex; Boelaert, Kristien; Chan, Shiao; Nelson, Scott; Rees, Aled; Lazarus, John; Dayan, Colin; Vaidya, Bijay; Okosieme, ... Journal: Thyroid research Issue: Volume 10:Issue 1(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Neuropsychiatric risk in children with intellectual disability of genetic origin: IMAGINE, a UK national cohort study. (September 2022) Authors: Wolstencroft, Jeanne; Wicks, Francesca; Srinivasan, Ramya; Wynn, Sarah; Ford, Tamsin; Baker, Kate; Chawner, Samuel J R A; Hall, Jeremy; van den Bree, Marianne B M; Owen, Michael J; Skuse, David; Raymond, F Lucy; Wolstencroft, Jeanne; Wicks, Francesca; Srinivasan, Ramya; Erwood, Marie; Lafont, Amy... Journal: Lancet Issue: Volume 9:Number 9(2022) Page Start: 715 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗