1. A RAD-Tag Genetic Map for the Platyfish (Xiphophorus maculatus) Reveals Mechanisms of Karyotype Evolution Among Teleost Fish. Issue 2 (1st June 2014) Authors: Amores, Angel; Catchen, Julian; Nanda, Indrajit; Warren, Wesley; Walter, Ron; Schartl, Manfred; Postlethwait, John H Journal: Genetics Issue: Volume 197:Issue 2(2014) Page Start: 625 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗
3. Detection of pericentric inversion with breakpoint in DMD by whole genome sequencing. Issue 10 (1st August 2022) Authors: Zaum, Ann‐Kathrin; Nanda, Indrajit; Kress, Wolfram; Rost, Simone Journal: Molecular genetics & genomic medicine Issue: Volume 10:Issue 10(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Epigenetic dysregulation in the developing Down syndrome cortex. Issue 8 (2nd August 2016) Authors: El Hajj, Nady; Dittrich, Marcus; Böck, Julia; Kraus, Theo F. J.; Nanda, Indrajit; Müller, Tobias; Seidmann, Larissa; Tralau, Tim; Galetzka, Danuta; Schneider, Eberhard; Haaf, Thomas Journal: Epigenetics Issue: Volume 11:Issue 8(2016) Page Start: 563 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes. Issue 5 (1st July 2019) Authors: Maierhofer, Anna; Flunkert, Julia; Oshima, Junko; Martin, George M.; Poot, Martin; Nanda, Indrajit; Dittrich, Marcus; Müller, Tobias; Haaf, Thomas Journal: Aging cell Issue: Volume 18:Issue 5(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genome‐wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine‐phosphate‐guanine methylation and histological subtypes. Issue 11 (10th August 2019) Authors: Fiedler, David; Hirsch, Daniela; El Hajj, Nady; Yang, Howard H.; Hu, Yue; Sticht, Carsten; Nanda, Indrajit; Belle, Sebastian; Rueschoff, Josef; Lee, Maxwell P.; Ried, Thomas; Haaf, Thomas; Gaiser, Timo Journal: Genes, chromosomes & cancer Issue: Volume 58:Issue 11(2019) Page Start: 783 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Independent Origin of XY and ZW Sex Determination Mechanisms in Mosquitofish Sister Species. Issue 1 (1st January 2020) Authors: Kottler, Verena A; Feron, Romain; Nanda, Indrajit; Klopp, Christophe; Du, Kang; Kneitz, Susanne; Helmprobst, Frederik; Lamatsch, Dunja K; Lopez-Roques, Céline; Lluch, Jerôme; Journot, Laurent; Parrinello, Hugues; Guiguen, Yann; Schartl, Manfred Journal: Genetics Issue: Volume 214:Issue 1(2020) Page Start: 193 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Non-syndromic hearing loss gene identification: A brief history and glimpse into the future. Issue 5 (October 2015) Authors: Vona, Barbara; Nanda, Indrajit; Hofrichter, Michaela A.H.; Shehata-Dieler, Wafaa; Haaf, Thomas Journal: Molecular and cellular probes Issue: Volume 29:Issue 5(2015) Page Start: 260 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Partial trisomy 1q41‐qter and partial trisomy 9pter‐9q21.32 in a newborn infant: An array CGH analysis and review. Issue 2 (5th December 2013) Authors: Akalin, Ibrahim; Bozdag, Senol; Spielmann, Malte; Basaran, Sarenur Yilmaz; Nanda, Indrajit; Klopocki, Eva Journal: American journal of medical genetics Issue: Volume 164:Issue 2(2014.) Page Start: 490 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. SLC2A3 single‐nucleotide polymorphism and duplication influence cognitive processing and population‐specific risk for attention‐deficit/hyperactivity disorder. (22nd February 2017) Authors: Merker, Sören; Reif, Andreas; Ziegler, Georg C.; Weber, Heike; Mayer, Ute; Ehlis, Ann‐Christine; Conzelmann, Annette; Johansson, Stefan; Müller‐Reible, Clemens; Nanda, Indrajit; Haaf, Thomas; Ullmann, Reinhard; Romanos, Marcel; Fallgatter, Andreas J.; Pauli, Paul; Strekalova, Tatyana; Jansch, Cha... Journal: Journal of child psychology and psychiatry and allied disciplines Issue: Volume 58:Number 7(2017) Page Start: 798 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗