1. A novel missense variant in MYO3A is associated with autosomal dominant high‐frequency hearing loss in a German family. Issue 8 (10th June 2020) Authors: Doll, Julia; Hofrichter, Michaela A. H.; Bahena, Paulina; Heihoff, Alfred; Segebarth, Dennis; Müller, Tobias; Dittrich, Marcus; Haaf, Thomas; Vona, Barbara Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 8(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors. (October 2018) Authors: Potabattula, Ramya; Dittrich, Marcus; Böck, Julia; Haertle, Larissa; Müller, Tobias; Hahn, Thomas; Schorsch, Martin; Hajj, Nady El; Haaf, Thomas Journal: Epigenomics Issue: Volume 10:Number 10(2018) Page Start: 1315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function. Issue 10 (21st July 2022) Authors: Lin, Sheng‐Jia; Vona, Barbara; Porter, Hillary M.; Izadi, Mahmoud; Huang, Kevin; Lacassie, Yves; Rosenfeld, Jill A.; Khan, Saadullah; Petree, Cassidy; Ali, Tayyiba A.; Muhammad, Nazif; Khan, Sher A.; Muhammad, Noor; Liu, Pengfei; Haymon, Marie‐Louise; Rüschendorf, Franz; Kong, Il‐Keun; Schnapp, L... Journal: Human mutation Issue: Volume 43:Issue 10(2022) Page Start: 1472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. CAF-like state in primary skin fibroblasts with constitutional BRCA1 epimutation sheds new light on tumor suppressor deficiency-related changes in healthy tissue. Issue 2 (1st February 2016) Authors: Etzold, Anna; Galetzka, Danuta; Weis, Eva; Bartsch, Oliver; Haaf, Thomas; Spix, Claudia; Itzel, Timo; Schweiger, Susann; Strand, Dennis; Strand, Susanne; Zechner, Ulrich Journal: Epigenetics Issue: Volume 11:Issue 2(2016) Page Start: 120 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cell Type and Species-specific Patterns in Neuronal and Non-neuronal Methylomes of Human and Chimpanzee Cortices. (6th August 2018) Authors: Böck, Julia; Remmele, Christian W; Dittrich, Marcus; Müller, Tobias; Kondova, Ivanela; Persengiev, Stephan; Bontrop, Ronald E; Ade, Carsten P; Kraus, Theo F J; Giese, Armin; El Hajj, Nady; Schneider, Eberhard; Haaf, Thomas Journal: Cerebral cortex Issue: Volume 28:Number 10(2018) Page Start: 3724 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Chromosomes Today. Issue 12 (December 1997) Authors: Haaf, Thomas Journal: Journal of medical genetics Issue: Volume 34:Issue 12(1997) Page Start: 1038 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Confirmation of GRHL2 as the gene for the DFNA28 locus. Issue 8 (27th June 2013) Authors: Vona, Barbara; Nanda, Indrajit; Neuner, Cordula; Müller, Tobias; Haaf, Thomas Journal: American journal of medical genetics Issue: Volume 161:Issue 8(2013:Aug.) Page Start: 2060 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene. Issue 4 (July 2016) Authors: Vona, Barbara; Lechno, Stanislav; Hofrichter, Michaela A. H.; Hopf, Susanne; Läßig, Anne K.; Haaf, Thomas; Keilmann, Annerose; Zechner, Ulrich; Bartsch, Oliver Journal: Ear and hearing Issue: Volume 37:Issue 4(2016:Jul./Aug.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DNA methylation and mRNA expression of developmentally important genes in bovine oocytes collected from donors of different age categories. Issue 9 (20th September 2016) Authors: Mattern, Felix; Herrmann, Doris; Heinzmann, Julia; Hadeler, Klaus Gerd; Bernal‐Ulloa, Sandra Milena; Haaf, Thomas; Niemann, Heiner Journal: Molecular reproduction and development Issue: Volume 83:Issue 9(2016) Page Start: 802 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome. Issue 2 (19th January 2022) Authors: Bejaoui, Yosra; Razzaq, Aleem; Yousri, Noha A.; Oshima, Junko; Megarbane, Andre; Qannan, Abeer; Potabattula, Ramya; Alam, Tanvir; Martin, George M.; Horn, Henning F.; Haaf, Thomas; Horvath, Steve; El Hajj, Nady Journal: Aging cell Issue: Volume 21:Issue 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗