Stefan Mundlos

Affiliations: 
RG development and disease Max Planck Institute for Molecular Genetics, Berlin, Berlin, Germany 
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"Stefan Mundlos"

Parents

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Bjorn R. Olsen post-doc (Anatomy Tree)

Children

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Daniel Murad Ibrahim grad student (Evolution Tree)
Ivana Jerković grad student
Katerina Kraft grad student
Sigmar Stricker grad student
Lila Allou post-doc (Evolution Tree)
Michael Robson post-doc 2016- (Evolution Tree)
Guillaume Andrey post-doc 2014-2018 Max Planck Institute for Molecular Genetics
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Publications

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Elsner J, Mensah MA, Holtgrewe M, et al. (2021) Genome sequencing in families with congenital limb malformations. Human Genetics
Butscheidt S, Tsourdi E, Rolvien T, et al. (2021) Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations. Bone. 115911
Allou L, Balzano S, Magg A, et al. (2021) Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator. Nature
Rodríguez de Los Santos M, Rivalan M, David FS, et al. (2021) A CRISPR-Cas9-engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions. Proceedings of the National Academy of Sciences of the United States of America. 118
Vogt G, El Choubassi N, Herczegfalvi Á, et al. (2020) Expanding the clinical and molecular spectrum of ATP6V1A related metabolic cutis laxa. Journal of Inherited Metabolic Disease
Helmsauer K, Valieva ME, Ali S, et al. (2020) Enhancer hijacking determines extrachromosomal circular MYCN amplicon architecture in neuroblastoma. Nature Communications. 11: 5823
Stürznickel J, Rolvien T, Delsmann A, et al. (2020) Clinical phenotype and relevance of LRP5 and LRP6 variants in patients with early-onset osteoporosis (EOOP). Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research
Pantel JT, Hajjir N, Danyel M, et al. (2020) Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study. Journal of Medical Internet Research. 22: e19263
M Real F, Haas SA, Franchini P, et al. (2020) The mole genome reveals regulatory rearrangements associated with adaptive intersexuality. Science (New York, N.Y.). 370: 208-214
Suter AA, Santos-Simarro F, Toerring PM, et al. (2020) Variable pulmonary manifestations in Chitayat syndrome: Six additional affected individuals. American Journal of Medical Genetics. Part A
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