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Institut des Maladies Génétiques Imagine | Researchclopedia

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Institut des Maladies Génétiques Imagine

Paris, Île-de-Francefacility

5,922

Works

1,020,903

Citations

360

h-index

Top Research Topics

Immunodeficiency and Autoimmune Disorders Immune Cell Function and Interaction interferon and immune responses

Top Researchers

Tom Maniatis Allen Institute for Brain Science

367 works231,740 citationsh-index: 153

Recent Research

Dietary Lycopene Intake and Gastric Cancer Risk: Findings from a Case-Control Study

Ngoan Tran Le,Y. Chan N. Pham,et al.

20260 citations

Genomics and Rare Diseases

Blood disorders and treatments

Hemoglobinopathies and Related Disorders

Genetics and Neurodevelopmental Disorders

T-cell and B-cell Immunology

RNA modifications and cancer

COVID-19 Clinical Research Studies

Genetic and Kidney Cyst Diseases

Inflammasome and immune disorders

Didier Raoult Aix-Marseille Université

4,035 works225,024 citationsh-index: 198

Jean‐Laurent Casanova Uppsala University

1,394 works119,012 citationsh-index: 171

Michel C. Nussenzweig Howard Hughes Medical Institute

614 works117,758 citationsh-index: 183

Marta Gut Universitat Pompeu Fabra

976 works111,304 citationsh-index: 157

1,208 works101,430 citationsh-index: 157

Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus cases

Maud Tusseau,Samira Khaldi-Plassart,et al.

20260 citations

Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins)

Danièle Dubois-Laforgue,Bruno Donadille,et al.

20260 citations

Longitudinal information extraction from clinical notes in rare diseases: an efficient approach with small language models

Xiaomeng Wang,Carole Faviez,et al.

20260 citations

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies

Elsa Leitão,Amandine Santini,et al.

20260 citations

Homozygous Loss‐of‐Function Variant in <scp> <i>SLC20A1</i> </scp> Coding for Ubiquitous Phosphate Transporter <scp>PiT1</scp> Is Associated With Multiple Developmental Abnormalities

Eugénie Koumakis,Céline Huber,et al.

20260 citations