1. Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse‐Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene. Issue 1 (9th September 2013) Authors: Nanda, Arti; Pasternack, Sandra M.; Mahmoudi, Hassnaa; Ishorst, Nina; Grimalt, Ramon; Betz, Regina C. Journal: Pediatric dermatology Issue: Volume 31:Issue 1(2014) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Extending the allelic spectrum at noncoding risk loci of orofacial clefting. Issue 8 (3rd June 2021) Authors: Thieme, Frederic; Henschel, Leonie; Hammond, Nigel L.; Ishorst, Nina; Hausen, Jonas; Adamson, Antony D.; Biedermann, Angelika; Bowes, John; Zieger, Hanna K.; Maj, Carlo; Kruse, Teresa; Buness, Andreas; Hoischen, Alexander; Gilissen, Christian; Kreusch, Thomas; Jäger, Andreas; Gölz, Lina; Braumann... Journal: Human mutation Issue: Volume 42:Issue 8(2021) Page Start: 1066 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Issue 3 (5th December 2022) Authors: Ishorst, Nina; Henschel, Leonie; Thieme, Frederic; Drichel, Dmitriy; Sivalingam, Sugirthan; Mehrem, Sarah L.; Fechtner, Ariane C.; Fazaal, Julia; Welzenbach, Julia; Heimbach, André; Maj, Carlo; Borisov, Oleg; Hausen, Jonas; Raff, Ruth; Hoischen, Alexander; Dixon, Michael; Rada‐Iglesias, Alvaro; B... Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 3(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Nonsyndromic cleft palate: An association study at GWAS candidate loci in a multiethnic sample. Issue 10 (2nd March 2018) Authors: Ishorst, Nina; Francheschelli, Paola; Böhmer, Anne C.; Khan, Mohammad Faisal J.; Heilmann‐Heimbach, Stefanie; Fricker, Nadine; Little, Julian; Steegers‐Theunissen, Regine P.M.; Peterlin, Borut; Nowak, Stefanie; Martini, Markus; Kruse, Teresa; Dunsche, Anton; Kreusch, Thomas; Gölz, Lina; Aldhorae,... Journal: Birth defects research Issue: Volume 110:Issue 10(2018) Page Start: 871 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗