1. A familial GLI2 deletion (2q14.2) not associated with the holoprosencephaly syndrome phenotype. (28th March 2015) Authors: Kordaß, Ulrike; Schröder, Carmen; Elbracht, Miriam; Soellner, Lukas; Eggermann, Thomas Journal: American journal of medical genetics Issue: Volume 167:Number 5(2015:May) Page Start: 1121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acute effect of intravenously applied alcohol in the human striatal and extrastriatal D2/D3 dopamine system. (11th July 2016) Authors: Pfeifer, Philippe; Tüscher, Oliver; Buchholz, Hans Georg; Gründer, Gerhard; Vernaleken, Ingo; Paulzen, Michael; Zimmermann, Ulrich S.; Maus, Stephan; Lieb, Klaus; Eggermann, Thomas; Fehr, Christoph; Schreckenberger, Mathias Journal: Addiction biology Issue: Volume 22:Number 5(2017) Page Start: 1449 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Adult phenotype of Russell‐Silver syndrome: A molecular support for Barker‐Brenner's theory. (August 2015) Authors: Takenouchi, Toshiki; Awazu, Midori; Eggermann, Thomas; Kosaki, Kenjiro Journal: Congenital anomalies Issue: Volume 55:Number 3(2015:Sep.) Page Start: 167 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations. Issue 3 (9th July 2016) Authors: Rudnik‐Schöneborn, Sabine; Deden, Florian; Eggermann, Katja; Eggermann, Thomas; Wieczorek, Dagmar; Sellhaus, Bernd; Yamoah, Alfred; Goswami, Anand; Claeys, Kristl G.; Weis, Joachim; Zerres, Klaus Journal: Muscle & nerve Issue: Volume 54:Issue 3(2016) Page Start: 496 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings. Issue 6 (5th June 2007) Authors: Elbracht, Miriam; Senderek, Jan; Eggermann, Thomas; Thürmer, Christian; Park, Jonas; Westhofen, Martin; Zerres, Klaus Journal: Journal of medical genetics Issue: Volume 44:Issue 6(2007) Page Start: e81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. 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) ↗
7. Clinical significance of copy number variations in the 11p15.5 imprinting control regions: new cases and review of the literature. Issue 9 (26th July 2012) Authors: Begemann, Matthias; Spengler, Sabrina; Gogiel, Magdalena; Grasshoff, Ute; Bonin, Michael; Betz, Regina C; Dufke, Andreas; Spier, Isabel; Eggermann, Thomas Journal: Journal of medical genetics Issue: Volume 49:Issue 9(2012) Page Start: 547 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives. Issue 11 (10th October 2022) Authors: van der Kaay, Danielle Christine Maria; Rochtus, Anne; Binder, Gerhard; Kurth, Ingo; Prawitt, Dirk; Netchine, Irène; Johannsson, Gudmundur; Hokken-Koelega, Anita C S; Elbracht, Miriam; Eggermann, Thomas Journal: Endocrine connections Issue: Volume 11:Issue 11(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. 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) ↗
10. Cortico‐limbic connectivity in MAOA‐L carriers is vulnerable to acute tryptophan depletion. Issue 3 (9th December 2016) Authors: Eisner, Patrick; Klasen, Martin; Wolf, Dhana; Zerres, Klaus; Eggermann, Thomas; Eisert, Albrecht; Zvyagintsev, Mikhail; Sarkheil, Pegah; Mathiak, Krystyna A.; Zepf, Florian; Mathiak, Klaus Journal: Human brain mapping Issue: Volume 38:Issue 3(2017) Page Start: 1622 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗