Denise Emmerich
Berlin, BE 14195, Germany
Last Updated: 09/26/2026
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Found 8 publications
Electric-Field-Tunable Spin-Orbit Gap in a Bilayer Graphene/WSe2 Quantum Dot.
Journal: Nano letters
Published: June 19, 2025
Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.
Journal: European journal of human genetics : EJHG
Published: April 17, 2015
Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model.
Journal: Human molecular genetics
Published: December 10, 2014
GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting.
Journal: The Journal of investigative dermatology
Published: November 17, 2014
Double NF1 inactivation affects adrenocortical function in NF1Prx1 mice and a human patient.
Journal: PloS one
Published: March 29, 2014
Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.
Journal: European journal of human genetics : EJHG
Published: January 31, 2014
Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient.
Journal: European journal of human genetics : EJHG
Published: January 14, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026