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Patrick Edery

Affiliation : Lyon 1 Université · Centre National de la Recherche Scientifique · Inserm · Centre de Recherche en Neurosciences de Lyon · Hospices Civils de Lyon

2Publications (affiliation in France)
282Total publications
11140Citations
56h-index

ORCID OpenAlex

Research profile

Patrick Edery has 2 indexed publications (2015–2018). Their work appears mainly in “Journal of Medical Genetics” and “Clinical Genetics”. Their most cited article, “16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations” (2018), has been cited 85 times. Their work is co-authored with at least 12 researchers, including institutions in United States, Tunisia, United Kingdom.

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Research areas

Genomics and Rare Diseases
Genomic variations and chromosomal abnormalities
Genetics and Neurodevelopmental Disorders
Congenital gastrointestinal and neural anomalies
Connective tissue disorders research

Publications (2)

16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations
2018 · Journal of Medical Genetics · cited 85 times
Whole‐exome sequencing improves the diagnosis yield in sporadic infantile spasm syndrome
2015 · Clinical Genetics · cited 84 times

Publication venues

Journal of Medical Genetics × 1
Clinical Genetics × 1

Publications per year

20181
20151

Collaborations

Partner institutions : Assistance Publique – Hôpitaux de Paris · Sorbonne Paris Cité · CHU Dijon Bourgogne · Hôpital Cochin · Université Paris Descartes

Co-authors’ countries : United States · Tunisia · United Kingdom

Co-authors

Bibliographic data from OpenAlex (open database).