| Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour C Bacon, M Schneider, C Le Magueresse, H Froehlich, C Sticht, C Gluch, ... Molecular psychiatry 20 (5), 632-639, 2015 | 131 | 2015 |
| Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder E Sollis, SA Graham, A Vino, H Froehlich, M Vreeburg, D Dimitropoulou, ... Human molecular genetics 25 (3), 546-557, 2016 | 94 | 2016 |
| Lactaturia and loss of sodium-dependent lactate uptake in the colon of SLC5A8-deficient mice H Frank, N Groger, M Diener, C Becker, T Braun, T Boettger Journal of Biological Chemistry 283 (36), 24729-24737, 2008 | 77 | 2008 |
| SLC4A11 prevents osmotic imbalance leading to corneal endothelial dystrophy, deafness, and polyuria N Gröger, H Fröhlich, H Maier, A Olbrich, S Kostin, T Braun, T Boettger Journal of biological chemistry 285 (19), 14467-14474, 2010 | 76 | 2010 |
| Foxp1 Regulates Cortical Radial Migration and Neuronal Morphogenesis in Developing Cerebral Cortex X Li, J Xiao, H Fröhlich, X Tu, L Li, Y Xu, H Cao, J Qu, GA Rappold, ... PloS one 10 (5), e0127671, 2015 | 67 | 2015 |
| Rapamycin-induced phosphaturia DS Kempe, M Dërmaku-Sopjani, H Fröhlich, M Sopjani, A Umbach, ... Nephrology Dialysis Transplantation 25 (9), 2938-2944, 2010 | 60 | 2010 |
| Targeted mutation of SLC4A5 induces arterial hypertension and renal metabolic acidosis N Gröger, H Vitzthum, H Fröhlich, M Krüger, H Ehmke, T Braun, T Boettger Human molecular genetics 21 (5), 1025-1036, 2012 | 56 | 2012 |
| Foxp1 expression is essential for sex-specific murine neonatal ultrasonic vocalization H Fröhlich, R Rafiullah, N Schmitt, S Abele, GA Rappold Human molecular genetics 26 (8), 1511-1521, 2017 | 40 | 2017 |
| Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Foxp1+/− mice H Fröhlich, ML Kollmeyer, VC Linz, M Stuhlinger, D Groneberg, A Reigl, ... Proceedings of the National Academy of Sciences 116 (44), 22237-22245, 2019 | 39 | 2019 |
| Hypothyroidism of gene-targeted mice lacking Kcnq1 H Fröhlich, KM Boini, G Seebohm, N Strutz-Seebohm, ON Ureche, ... Pflügers Archiv-European Journal of Physiology 461, 45-52, 2011 | 36 | 2011 |
| Sex Hormones Regulate SHANK Expression S Berkel, A Eltokhi, H Fröhlich, D Porras-Gonzalez, R Rafiullah, ... Frontiers in molecular neuroscience 11, 337, 2018 | 35 | 2018 |
| Inhibition of the heterotetrameric K+ channel KCNQ1/KCNE1 by the AMP-activated protein kinase I Alesutan, M Föller, M Sopjani, M Dermaku-Sopjani, C Zelenak, ... Molecular Membrane Biology 28 (2), 79-89, 2011 | 35 | 2011 |
| Hydration-sensitive gene expression in brain C Tang, C Zelenak, J Völkl, M Eichenmüller, I Regel, H Fröhlich, D Kempe, ... Cellular Physiology and Biochemistry 27 (6), 757-768, 2011 | 29 | 2011 |
| Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome J Wang, H Fröhlich, FB Torres, RL Silva, G Poschet, A Agarwal, ... Proceedings of the National Academy of Sciences 119 (8), e2112852119, 2022 | 20 | 2022 |
| An analgesic pathway from parvocellular oxytocin neurons to the periaqueductal gray in rats M Iwasaki, A Lefevre, F Althammer, E Clauss Creusot, O Łąpieś, ... Nature Communications 14 (1), 1066, 2023 | 17 | 2023 |
| Thrombin-sensitive expression of the store operated Ca2+ channel Orai1 in platelets P Münzer, A Tolios, L Pelzl, E Schmid, EM Schmidt, B Walker, H Fröhlich, ... Biochemical and Biophysical Research Communications 436 (1), 25-30, 2013 | 16 | 2013 |
| Regulation of renal tubular glucose reabsorption by Akt2/PKBβ DS Kempe, G Siraskar, H Fröhlich, AT Umbach, M Stübs, F Weiss, ... American Journal of Physiology-Renal Physiology 298 (5), F1113-F1117, 2010 | 15 | 2010 |
| Regulation of gastric acid secretion by the serum and glucocorticoid inducible kinase isoform SGK3 V Pasham, A Rotte, M Bhandaru, M Eichenmüller, H Fröhlich, AF Mack, ... Journal of gastroenterology 46, 305-317, 2011 | 9 | 2011 |
| Blunted IgE-mediated activation of mast cells in mice lacking the serum-and glucocorticoid-inducible kinase SGK3 IM Zemtsova, N Heise, H Fröhlich, SM Qadri, Y Kucherenko, KM Boini, ... American Journal of Physiology-Cell Physiology 299 (5), C1007-C1014, 2010 | 8 | 2010 |
| Analysis of the hypothalamic oxytocin system and oxytocin receptor‐expressing astrocytes in a mouse model of Prader–Willi syndrome F Althammer, MC Wimmer, Q Krabichler, S Küppers, J Schimmer, ... Journal of Neuroendocrinology 34 (12), e13217, 2022 | 6 | 2022 |
