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Funded by an IRDiRC member =

Research projects

GERMANY

Bayern
ERLANGEN

Funded by an IRDiRC memberCHROMATIN-Net: Dissecting the molecular mechanisms of cognitive disorders with mutations in the SWI/SNF complex
Humangenetisches Institut am Universitätsklinikum Erlangen
Humangenetisches Institut

GERMANY

Bayern
ERLANGEN

Funded by an IRDiRC memberCHROMATIN-Net: Establishing human disease specific cortical neurons
Humangenetisches Institut am Universitätsklinikum Erlangen
Humangenetisches Institut

GERMANY

Bayern
ERLANGEN

Funded by an IRDiRC memberCHROMATIN-Net: Network on cognitive impairment disorders with defective chromatin (coordination)
Humangenetisches Institut am Universitätsklinikum Erlangen
Humangenetisches Institut

GERMANY

Bayern
MÜNCHEN

Funded by an IRDiRC memberCHROMATIN-Net: Whole Genome Sequencing and Analysis
Helmholtz Zentrum München
Institut für Humangenetik

GERMANY

Nordrhein-Westfalen
DÜSSELDORF

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberClinical characterization and molecular genetic analysis of the BAF complex related syndromes
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Genética Clínica y Dismorfología

FRANCE

PAYS DE LA LOIRE
NANTES

In vivo modeling for the genetic diagnosis of intellectual disabilities
CHU de Nantes - Institut de Biologie
Laboratoire de génétique moléculaire

SPAIN

Comunidad Valenciana
VALENCIA

SWITZERLAND

Suisse Alémanique
SCHLIEREN

Identification of novel autosomal genes causing mental retardation
Universität Zürich
Institut für Medizinische Genetik

FRANCE

PAYS DE LA LOIRE
ANGERS

SPAIN

Madrid
MADRID

Funded by an IRDiRC memberWhole exome sequencing for the study of 30 children with developmental delay or moderate to severe
INGEMM - Instituto de Genética Médica y Molecular (IdiPAZ)
Sección de Genómica Estructural y Funcional

SWITZERLAND

Suisse Alémanique
BASEL

Massively parallel sequencing for gene discovery in lethal fetal disorders
Universitätsspital Basel
Abteilung für Medizinische Genetik

UNITED KINGDOM

Cambridgeshire
HINXTON

The Deciphering Developmental Disorders (the DDD study)
Wellcome Trust Sanger Institute
DECIPHER

UNITED KINGDOM

Devon
EXETER

Exploring the Genetics of Renal Developmental Disease
Royal Devon and Exeter Hospital - Wonford site
Department of Urology

UNITED KINGDOM

Lothian
EDINBURGH

Genetic disorders of human brain development
Western General Hospital
MRC Human Genetics Unit

ITALY

CAMPANIA
NAPOLI

Funded by an IRDiRC memberTelethon Undiagnosed Disease Program - Revised Proposal
Azienda Ospedaliera Universitaria - Seconda Università degli Studi di Napoli
Laboratorio di Genetica Medica

Multicentric Research projects