Progetti di ricerca terminati = Finanziato da un ente associato a IRDiRC = Membro di una ERN =

Progetti di ricerca

GERMANIA

Saarland
HOMBURG

German Renal Cell Tumor Network: Molecular and clinical characterization of papillary renal cell carcinoma type II

Universitätsklinikum des Saarlandes

Klinik für Urologie und Kinderurologie

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GERMANIA

Baden-Württemberg
HEIDELBERG

Li-Fraumeni syndrome-cancer predisposition syndrome registry

Deutsches Krebsforschungszentrum

KITZ - Hopp-Kindertumorzentrum Heidelberg

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GERMANIA

Niedersachsen
HANNOVER

Li-Fraumeni syndrome-cancer predisposition syndrome registry

Medizinische Hochschule Hannover

Klinik für Pädiatrische Hämatologie und Onkologie

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CANADA

Colombie-Britannique
VICTORIA

Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations

University of Victoria

Community Genetics Research Program/Island Medical Program

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CANADA

Ontario
TORONTO

Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer

Hospital for Sick Children, Research Institute

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SPAGNA

Cataluña
BARCELONA

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases

Centro de Regulación Genómica

Archivo europeo de genomas y fenomas del CRG

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SPAGNA

Cataluña
BARCELONA

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases

Hospital Clínic de Barcelona

Servicio de Inmunologia

Ulteriori dettagli

SPAGNA

Cataluña
BARCELONA

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases

Hospital Universitari Vall d'Hebron

Laboratorio de Genética

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SPAGNA

Cataluña
BARCELONA

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases

Hospital de la Santa Creu i Sant Pau

Servicio de Genética

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SPAGNA

Cataluña
L'HOSPITALET DE LLOBREGAT

Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases

Hospital Universitari de Bellvitge

Unidad de Genética Molecular

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SPAGNA

Madrid
MADRID

Mechanistic models using Machine Learning for therapeutic targets discovery and drug repurposing in Rare Diseases

ISCIII - Instituto de Salud Carlos III

Centro de Investigación Biomédica en Red de Enfermedades Raras

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SPAGNA

Madrid
MADRID

Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine

Instituto de Investigación Hospital 12 de Octubre

Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares

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STATI UNITI

Washington
ADDRESS: NOT PROVIDED - US

A powerful web-based discovery platform for rare disease genetics

Institution: Information not provided - US

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Progetti di ricerca multicentrici

FRANCIA
ILE-DE-FRANCE
ORSAY
CAMINEMS: Integrated Micro-Nano-Opto Fluidic systems for high-content diagnosis and studies of rare cancer cells
Institut Curie
Macromolécules et Microsystèmes en Biologie et en Medecine
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