Rheinische Friedrich-Wilhelms-Universität Bonn
Medizinische Fakultät
Institut für Humangenetik
Address
Venusberg-Campus 1
53127 Bonn
Deutschland
GERiT
This institution in GERiT
53127 Bonn
Projects
Research Units
Completed projects
Administration
(Applicant
Baur, Max Peter
)
Central genotyping services, coordination and quality control
(Applicant
Wienker, Thomas F.
)
Central genotyping services, coordination and quality control
(Applicant
Schreiber, Stefan
)
FOR 423: Genetic Epidemiology and Medical Genetics of Complex Diseases
(Spokesperson
Baur, Max Peter
)
FOR 2107: Neurobiology of Affective Disorders: A Translational Perspective on Brain Structure and Function
(Spokesperson
Kircher, Tilo
)
Functional studies of the human hairless-Protein
(Applicant
Nöthen, Markus M.
)
Genetic analysis of androgenetic alopecia
(Applicant
Kruse, Roland
)
Genetic analysis of androgenetic alopecia
(Applicant
Propping, Peter
)
Genetic investigation of androgenetic alopecia
(Applicant
Nöthen, Markus M.
)
Genetic studies in patients with nonsyndromic orofacial clefts
(Applicant
Mangold, Elisabeth
)
Genetic studies in patients with nonsyndromic orofacial clefts
(Applicant
Kramer, Franz-Josef
)
Indetification of disease genes in familial febrile convulsions
(Applicant
Heils, Armin
)
Integrative analyses of genetic, epigenetic, transcriptomic, and environmental vulnerability factors of affective disorders
(Applicants
Nöthen, Markus M.
;
Rietschel, Marcella
;
Witt, Stephanie
)
Research Fellowships
Completed projects
Etablierung einer Multi-Colour-Fluoreszenz-in situ-Hybridisierungs-Methode zur Untersuchung sämtlicher subtelomerischer Regionen des menschlichen Karyotyps und deren Anwendung zum Nachweis von subtelomerischen Chromosomenaberrationen als Ursache mentaler Retardierung
(Applicant
Engels, Hartmut
)
Genome-wide identification of genetic interactions in human cells using CRISPR/Cas9
(Applicant
Billmann, Maximilian
)
Mapping, cloning and characterization of a gene for Hypotrichosis simplex
(Applicant
Betz, Regina Christine
)
Research Grants
Current projects
Deciphering epigenetic changes related to the SARS-CoV-2 pandemic in a genetically informative, longitudinal twin family study: The TwinLife Epigenetic Change Satellite (TECS) project
(Applicants
Binder, Elisabeth
;
Diewald, Martin
;
Forstner, Andreas J.
;
Kandler, Christian
;
Nöthen, Markus M.
;
Spinath, Frank M.
)
Genetic and social causes of life chances: Improved parametrization of educational attainment and social mobility models through molecular genetic information in a longitudinal twin family study (TWINLIFE)
(Applicants
Diewald, Martin
;
Krawitz, Peter
;
Nöthen, Markus M.
;
Riemann, Rainer
;
Spinath, Frank M.
)
Identification of causal genes for nonsyndromic cleft palate via targeted resequencing of candidate genes and functional analysis within the zebrafish model.
(Applicants
Ishorst, Nina
;
Mangold, Elisabeth
)
Unraveling the molecular causes of alopecia areata (AA): whole-genome sequencing in patients with AA plus other autoimmune diseases
(Applicants
Basmanav, Ph.D., Buket
;
Betz, Regina Christine
;
Krawitz, Peter
)
Completed projects
Genetic aspects of brain activity patterns during cognitive load
(Applicant
Propping, Peter
)
Genetische Grundlagen des Phantomschmerzes: Aufbau einer nationalen Forschungsressource
(Applicant
Wüst, Stefan
)
Identification of causal genes and cellular pathways for idiopathic achalasia on the basis of genome-wide association studies (GWAS)
(Applicants
Knapp, Michael
;
Nöthen, Markus M.
)
Identification of causal genes for dyslexia on the basis of genome-wide association studies
(Applicants
Müller-Myhsok, Bertram
;
Nöthen, Markus M.
;
Schulte-Körne, Gerd
)
Identification of causal genes for nonsyndromic cleft palate only using whole exome sequencing
(Applicant
Mangold, Elisabeth
)
Identification of causal genes for nonsyndromic orofacial clefts using Whole Exome Sequencing
(Applicants
Becker, Tim
;
Ludwig, Kerstin
;
Mangold, Elisabeth
)
Identification of disease genes for esophageal atresia with or without tracheoesophageal fistula (EA/TEF)
(Applicants
Nöthen, Markus M.
;
Reutter, Heiko
)
Identification of rare and penetrant gene mutations for bicuspid aortic valve (BAV)
(Applicants
Krawitz, Peter
;
Nöthen, Markus M.
;
Seyfried, Salim
)
Investigation of the interplay between genetic and environmental risk factors for smoking behaviour
(Applicant
Treutlein, Jens
)
Neurophysiological, psychometric and genetic studies in dyslexia
(Applicant
Remschmidt, Helmut
)
Neurophysiological, psychometric, and genetic studies in dyslexia
(Applicant
Warnke, Andreas
)
Neurophysiologische, psychometrische und genetische Untersuchungen zur Lese-Rechtschreibstörung
(Applicant
Grimm, Tiemo
)
Neurophysiologische, psychometrische und genetische Untersuchungen zur Lese-Rechtschreibstörung
(Applicant
Ziegler, Andreas
)
Neurophysiologische, psychometrische und genetische Untersuchungen zur Lese-Rechtschreibstörung
(Applicant
Müller-Myhsok, Bertram
)
Neurophysiologische, psychometrische und genetische Untersuchungen zur Lese-Rechtschreibstörung
(Applicant
Nöthen, Markus M.
)
Risk factors for congenital malformations of the rectum (anorectal malformations)
(Applicant
Jenetzky, Ekkehart
)
Systematic identification of disease genes for alopecia areata
(Applicant
Betz, Regina Christine
)
Systematische Identifizierung von Krankheitsgenen bei nicht-syndromalen orofazialen Spalten/Lippen-Kiefer-Gaumenspalten
(Applicants
Kramer, Franz-Josef
;
Mangold, Elisabeth
;
Nöthen, Markus M.
;
Wienker, Thomas F.
)
Towards a mechanistic understanding of common and rare genetic risk variants for bipolar disorder: studies in iPSC models and extended families
(Applicants
Brüstle, Oliver
;
Nöthen, Markus M.
)
Untersuchung von Patienten mit mentaler Retardierung auf kryptische subtelomerische Chromosomenaberrationen durch COBRA-Multi-Colour-FISH
(Applicant
Propping, Peter
)
Emmy Noether Independent Junior Research Groups
Completed projects
Integrative craniofacial genomics - From GWAS to function
(Applicant
Ludwig, Kerstin
)
Klonierung und Charakterisierung von Genen für monogene und genetisch komplexe Formen isolierter Alopezien
(Applicant
Betz, Regina Christine
)
Heisenberg Professorships
Completed projects
Professorship for Dermatogenetics: Structure, function, and regulation of the development of hair growth: Elucidation of the bases of monogenic and genetically complex forms of inherited alopecias
(Applicant
Betz, Regina Christine
)
Collaborative Research Centres
Completed projects
Genetische variabilität in Genen zentralnervöser Rezeptor- und Transporterproteine
(Project Head
Nöthen, Markus M.
)
Identifizierung von Krankheitsgenen bei der bipolar affektiven Krankheit
(Project Head
Propping, Peter
)
Identifizierung von schizophrenie-assoziierten Genen
(Project Heads
Maier, Wolfgang
;
Propping, Peter
)
SFB 400: Molecular Basis of CNS Disorders
(Spokesperson
Propping, Peter
)
Major Research Instrumentation
Completed projects
Next-Generation-Sequenzer
CRC/Transregios
Current projects
Dissecting the contribution of immune cell activation dependent neuronal connectivity changes to disease trajectories in depression
(Project Heads
Forstner, Andreas J.
;
Klotz, Luisa
;
Ziller, Michael J.
)
GUARD – Genes Underlying AoRtic valve Disease
(Project Heads
Al-Kassou, Baravan
;
Billmann, Maximilian
;
Nöthen, Markus M.
)
Molecular and immunological characterization of symptom changes and course of illness using intense sampling
(Project Heads
Alferink, Judith
;
Forstner, Andreas J.
;
Pariante, Ph.D., Carmine
)
Transcriptomics and epigenetic data analysis
(Project Heads
Billmann, Maximilian
;
Schmidt, Susanne
)
Completed projects
Genetische Grundlagen von Temporallappen-Epilepsien
(Project Heads
Gu, Wenli
;
Propping, Peter
;
Steinlein, Ortrud Kristina
)
GUARD – Genes Underlying AoRtic valve Disease
(Project Heads
Al-Kassou, Baravan
;
Nöthen, Markus M.
;
Sinning, Jan-Malte
;
Tiyerili, Vedat
)
Research Training Groups
Completed projects
GRK 246: Pathogenesis of Diseases of the Central Nervous System
(Spokesperson
Propping, Peter
)
Clusters of Excellence
Completed projects
EXC 1023: ImmunoSensation: The Immune Sensory System
(Spokesperson
Hartmann, Gunther
)
Clusters of Excellence (ExStra)
Current projects
EXC 2151: ImmunoSensation2 - the immune sensory system
(Spokespersons
Hartmann, Gunther
;
Kolanus, Waldemar
;
Latz, Eicke
;
Schultze, Joachim L.
)
