Genetics of Tinnitus: Still in its Infancy

por Vona, Barbara, Nanda, Indrajit, Shehata-Dieler, Wafaa, Haaf, Thomas
Publicado 2017

Detection of pericentric inversion with breakpoint in DMD by whole genome sequencing

por Zaum, Ann‐Kathrin, Nanda, Indrajit, Kress, Wolfram, Rost, Simone
Publicado 2022

Confirmation of GRHL2 as the gene for the DFNA28 locus

por Vona, Barbara, Nanda, Indrajit, Neuner, Cordula, Müller, Tobias, Haaf, Thomas
Publicado 2013

Analysis of global DNA methylation changes in primary human fibroblasts in the early phase following X-ray irradiation

por Maierhofer, Anna, Flunkert, Julia, Dittrich, Marcus, Müller, Tobias, Schindler, Detlev, Nanda, Indrajit, Haaf, Thomas
Publicado 2017

Epigenetic signatures of gestational diabetes mellitus on cord blood methylation

por Haertle, Larissa, El Hajj, Nady, Dittrich, Marcus, Müller, Tobias, Nanda, Indrajit, Lehnen, Harald, Haaf, Thomas
Publicado 2017

Hereditary hearing loss SNP-microarray pilot study

por Vona, Barbara, Hofrichter, Michaela A. H., Schröder, Jörg, Shehata-Dieler, Wafaa, Nanda, Indrajit, Haaf, Thomas
Publicado 2018

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature

por Vona, Barbara, Nanda, Indrajit, Neuner, Cordula, Schröder, Jörg, Kalscheuer, Vera M, Shehata-Dieler, Wafaa, Haaf, Thomas
Publicado 2014

Rat Hepatic Stellate Cell Line CFSC-2G: Genetic Markers and Short Tandem Repeat Profile Useful for Cell Line Authentication

por Nanda, Indrajit, Schröder, Sarah K., Steinlein, Claus, Haaf, Thomas, Buhl, Eva M., Grimm, Domink G., Weiskirchen, Ralf
Publicado 2022

Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes

por Maierhofer, Anna, Flunkert, Julia, Oshima, Junko, Martin, George M., Poot, Martin, Nanda, Indrajit, Dittrich, Marcus, Müller, Tobias, Haaf, Thomas
Publicado 2019

Evolution of the Degenerated Y-Chromosome of the Swamp Guppy, Micropoecilia picta

por Nanda, Indrajit, Schories, Susanne, Simeonov, Ivan, Adolfi, Mateus Contar, Du, Kang, Steinlein, Claus, Alsheimer, Manfred, Haaf, Thomas, Schartl, Manfred
Publicado 2022

Genetic Characterization of Rat Hepatic Stellate Cell Line PAV-1

por Gäberlein, Kiara, Schröder, Sarah K., Nanda, Indrajit, Steinlein, Claus, Haaf, Thomas, Buhl, Eva M., Sauvant, Patrick, Sapin, Vincent, Abergel, Armand, Weiskirchen, Ralf
Publicado 2023

Whole-Genome Sequencing Identified New Structural Variations in the DMD Gene That Cause Duchenne Muscular Dystrophy in Two Girls

por Pluta, Natalie, von Moers, Arpad, Pechmann, Astrid, Stenzel, Werner, Goebel, Hans-Hilmar, Atlan, David, Wolf, Beat, Nanda, Indrajit, Zaum, Ann-Kathrin, Rost, Simone
Publicado 2023

Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report

por Lekszas, Caroline, Nanda, Indrajit, Vona, Barbara, Böck, Julia, Ashrafzadeh, Farah, Donyadideh, Nahid, Ebrahimzadeh, Farnoosh, Ahangari, Najmeh, Maroofian, Reza, Karimiani, Ehsan Ghayoor, Haaf, Thomas
Publicado 2019

Genetic Characterization of Rat Hepatic Stellate Cell Line HSC-T6 for In Vitro Cell Line Authentication

por Nanda, Indrajit, Steinlein, Claus, Haaf, Thomas, Buhl, Eva M., Grimm, Domink G., Friedman, Scott L., Meurer, Steffen K., Schröder, Sarah K., Weiskirchen, Ralf
Publicado 2022

Biallelic TANGO1 mutations cause a novel syndromal disease due to hampered cellular collagen secretion

por Lekszas, Caroline, Foresti, Ombretta, Raote, Ishier, Liedtke, Daniel, König, Eva-Maria, Nanda, Indrajit, Vona, Barbara, De Coster, Peter, Cauwels, Rita, Malhotra, Vivek, Haaf, Thomas
Publicado 2020

Epigenetic dysregulation in the developing Down syndrome cortex

por 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
Publicado 2016

Widespread differences in cortex DNA methylation of the “language gene” CNTNAP2 between humans and chimpanzees

por Schneider, Eberhard, El Hajj, Nady, Richter, Steven, Roche-Santiago, Justin, Nanda, Indrajit, Schempp, Werner, Riederer, Peter, Navarro, Bianca, Bontrop, Ronald E, Kondova, Ivanela, Scholz, Claus Jürgen, Haaf, Thomas
Publicado 2014

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations

por Vona, Barbara, Müller, Tobias, Nanda, Indrajit, Neuner, Cordula, Hofrichter, Michaela A. H., Schröder, Jörg, Bartsch, Oliver, Läßig, Anne, Keilmann, Annerose, Schraven, Sebastian, Kraus, Fabian, Shehata-Dieler, Wafaa, Haaf, Thomas
Publicado 2014

High tandem repeat content in the genome of the short-lived annual fish Nothobranchius furzeri: a new vertebrate model for aging research

por Reichwald, Kathrin, Lauber, Chris, Nanda, Indrajit, Kirschner, Jeanette, Hartmann, Nils, Schories, Susanne, Gausmann, Ulrike, Taudien, Stefan, Schilhabel, Markus B, Szafranski, Karol, Glöckner, Gernot, Schmid, Michael, Cellerino, Alessandro, Schartl, Manfred, Englert, Christoph, Platzer, Matthias
Publicado 2009

Roles of brca2 (fancd1) in Oocyte Nuclear Architecture, Gametogenesis, Gonad Tumors, and Genome Stability in Zebrafish

por Rodríguez-Marí, Adriana, Wilson, Catherine, Titus, Tom A., Cañestro, Cristian, BreMiller, Ruth A., Yan, Yi-Lin, Nanda, Indrajit, Johnston, Adam, Kanki, John P., Gray, Erin M., He, Xinjun, Spitsbergen, Jan, Schindler, Detlev, Postlethwait, John H.
Publicado 2011