Author

Abdelkader Heddar

Assistance Publique – Hôpitaux de ParisORCID 0000-0002-1966-5462Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bernard S. LópeziD· 1 shared Elodie DardillaciD· 1 shared Gabriel LiveraiD· 1 shared Helene Creux· 1 shared Marie Lambert· 1 shared Micheline MisrahiiD· 1 shared Sandrine CaburetiD· 1 shared Sébastien Messiaen· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetics

Bernard S. LópezORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

GeneticsJournal of Medical GeneticsPeer-reviewedJun 1, 2020

A homozygous hypomorphic BRCA2 variant causes primary ovarian insufficiency without cancer or Fanconi anemia traits.

Sandrine Caburet, Abdelkader Heddar, Elodie Dardillac…·Micheline Misrahi

This study identifies a BRCA2 variant causing primary ovarian insufficiency without cancer or Fanconi anemia, showing residual HR function in patient cells.

47 citationstop 5%

humanwhole-exome sequencing

𝕏 PostBluesky