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American Journal of Human Genetics|June 19, 2012
Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type VChristian Beetz, Thomas R Pieber, Nicole Hertel, et al.
Journal of Neurology|September 6, 2011
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth diseaseCarina Fischer, Slave Trajanoski, Lea Papić, et al.
Nature Communications|December 14, 2017
A miR-327-FGF10-FGFR2-mediated autocrine signaling mechanism controls white fat browningCarina Fischer, Takahiro Seki, Sharon Lim, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 26, 2022
Generation of mega brown adipose tissue in adults by controlling brown adipocyte differentiation in vivoQiqiao Du, Jieyu Wu, Carina Fischer, et al.
Scientific Reports|March 13, 2019
Human melanoma brain metastases cell line MUG-Mel1, isolated clones and their detailed characterizationEllen Heitzer, Arwin Groenewoud, Katharina Meditz, et al.
Journal of the Neurological Sciences|July 31, 2007
Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndromeBarbara Rohkamm, Mary M Reilly, Hanns Lochmüller, et al.
JCI Insight|February 28, 2017
Switching harmful visceral fat to beneficial energy combustion improves metabolic dysfunctionsXiaoyan Yang, Wenhai Sui, Meng Zhang, et al.
Nature Genetics|December 29, 2009
Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2CMichaela Auer-Grumbach, Andrea Olschewski, Lea Papić, et al.
The EMBO Journal|September 29, 2021
DNA hypomethylation leads to cGAS-induced autoinflammation in the epidermisMirjam A Beck, Heinz Fischer, Lisa M Grabner, et al.
Neurology|November 4, 2020
The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on <i>MME</i>Jan Senderek, Petra Lassuthova, Dagmara Kabzińska, et al.
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