1. Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans. Issue 7 (July 2016) Authors: Sanchez-Delgado, Marta; Riccio, Andrea; Eggermann, Thomas; Maher, Eamonn R.; Lapunzina, Pablo; Mackay, Deborah; Monk, David Journal: Trends in genetics Issue: Volume 32:Issue 7(2016) Page Start: 444 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Congenital imprinting disorders: Application of multilocus and high throughput methods to decipher new pathomechanisms and improve their management. Issue 5 (October 2015) Authors: Soellner, Lukas; Monk, David; Rezwan, Faisal I.; Begemann, Matthias; Mackay, Deborah; Eggermann, Thomas Journal: Molecular and cellular probes Issue: Volume 29:Issue 5(2015) Page Start: 282 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequences. (18th February 2020) Authors: Elbracht, Miriam; Mackay, Deborah; Begemann, Matthias; Kagan, Karl Oliver; Eggermann, Thomas Journal: Human reproduction update Issue: Volume 26:Number 2(2020) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57. Issue 1 (December 2016) Authors: Bak, Mads; Boonen, Susanne; Dahl, Christina; Hahnemann, Johanne; Mackay, Deborah; Tümer, Zeynep; Grønskov, Karen; Temple, I.; Guldberg, Per; Tommerup, Niels Journal: BMC medical genetics 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. 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. Transient Neonatal Diabetes Mellitus followed by recurrent asymptomatic hypoglycaemia: a case report. Issue 1 (December 2015) Authors: Priyadarshi, Archana; Verge, Charles; Vandervliet, Leah; Mackay, Deborah; Bolisetty, Srinivas Journal: BMC pediatrics Issue: Volume 15:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗