| Regulation of endoplasmic reticulum turnover by selective autophagy A Khaminets, T Heinrich, M Mari, P Grumati, AK Huebner, M Akutsu, ... Nature 522 (7556), 354-358, 2015 | 819 | 2015 |
| Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibition CA Hübner, V Stein, I Hermans-Borgmeyer, T Meyer, K Ballanyi, ... Neuron 30 (2), 515-524, 2001 | 676 | 2001 |
| Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ... Nature genetics 48 (9), 1043-1048, 2016 | 588 | 2016 |
| Maternal oxytocin triggers a transient inhibitory switch in GABA signaling in the fetal brain during delivery R Tyzio, R Cossart, I Khalilov, M Minlebaev, CA Hübner, A Represa, ... Science 314 (5806), 1788-1792, 2006 | 543 | 2006 |
| Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4 T Boettger, CA Hübner, H Maier, MB Rust, FX Beck, TJ Jentsch Nature 416 (6883), 874-878, 2002 | 440 | 2002 |
| Ion channel diseases CA Hübner, TJ Jentsch Human molecular genetics 11 (20), 2435-2445, 2002 | 409 | 2002 |
| Male germ cells and photoreceptors, both dependent on close cell–cell interactions, degenerate upon ClC‐2 Cl− channel disruption MR Bösl, V Stein, C Hübner, AA Zdebik, SE Jordt, AK Mukhopadhyay, ... The EMBO journal, 2001 | 363 | 2001 |
| Expression of the KCl cotransporter KCC2 parallels neuronal maturation and the emergence of low intracellular chloride V Stein, I Hermans‐Borgmeyer, TJ Jentsch, CA Hübner Journal of Comparative Neurology 468 (1), 57-64, 2004 | 338 | 2004 |
| A de novo gain-of-function mutation in SCN11A causes loss of pain perception E Leipold, L Liebmann, GC Korenke, T Heinrich, S Gießelmann, J Baets, ... Nature genetics 45 (11), 1399-1404, 2013 | 319 | 2013 |
| The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice F Leviel, CA Hübner, P Houillier, L Morla, S El Moghrabi, G Brideau, ... The Journal of clinical investigation 120 (5), 1627-1635, 2010 | 303 | 2010 |
| Cadherins and neuropsychiatric disorders C Redies, N Hertel, CA Hübner Brain research 1470, 130-144, 2012 | 281 | 2012 |
| Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ... Nature genetics 53 (12), 1636-1648, 2021 | 278 | 2021 |
| Ion channels: function unravelled by dysfunction TJ Jentsch, CA Hübner, JC Fuhrmann Nature cell biology 6 (11), 1039-1047, 2004 | 275 | 2004 |
| Loss of K‐Cl co‐transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold T Boettger, MB Rust, H Maier, T Seidenbecher, M Schweizer, DJ Keating, ... The EMBO journal, 2003 | 272 | 2003 |
| Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy AR Janecke, DA Thompson, G Utermann, C Becker, CA Hübner, ... Nature genetics 36 (8), 850-854, 2004 | 265 | 2004 |
| Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy I Kurth, T Pamminger, JC Hennings, D Soehendra, AK Huebner, ... Nature genetics 41 (11), 1179-1181, 2009 | 243 | 2009 |
| Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6 M Poët, U Kornak, M Schweizer, AA Zdebik, O Scheel, S Hoelter, W Wurst, ... Proceedings of the National Academy of Sciences 103 (37), 13854-13859, 2006 | 220 | 2006 |
| GABAergic regulation of cerebellar NG2 cell development is altered in perinatal white matter injury M Zonouzi, J Scafidi, P Li, B McEllin, J Edwards, JL Dupree, L Harvey, ... Nature neuroscience 18 (5), 674-682, 2015 | 191 | 2015 |
| Leukoencephalopathy upon disruption of the chloride channel ClC-2 J Blanz, M Schweizer, M Auberson, H Maier, A Muenscher, CA Hübner, ... Journal of Neuroscience 27 (24), 6581-6589, 2007 | 189 | 2007 |
| Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity E Lausch, A Janecke, M Bros, S Trojandt, Y Alanay, C De Laet, ... Nature genetics 43 (2), 132-137, 2011 | 180 | 2011 |
