Djihad Hadjadj

Paris, France

Last Updated: 09/26/2026

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Found 12 publications

Insights Into the FOXE3 Transcriptional Network and Disease Mechanisms From the Investigation of a Regulatory Variant Driving Complex Microphthalmia.

Insights Into the FOXE3 Transcriptional Network and Disease Mechanisms From the Investigation of a Regulatory Variant Driving Complex Microphthalmia.

Journal: Investigative ophthalmology & visual science

Published: August 20, 2025

PRKACA constitutional duplication: a specific cause of primary pigmented nodular adrenocortical disease.

PRKACA constitutional duplication: a specific cause of primary pigmented nodular adrenocortical disease.

Journal: European journal of endocrinology

Published: August 19, 2025

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with NF1 point variants.

Refined genotype-phenotype correlations in neurofibromatosis type 1 patients with NF1 point variants.

Journal: Journal of medical genetics

Published: March 14, 2025

Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics.

Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics.

Journal: NPJ genomic medicine

Published: January 24, 2024

Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.

Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.

Journal: American journal of human genetics

Published: January 12, 2024

Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1.

Identification of potential common genetic modifiers of neurofibromas: a genome-wide association study in 1333 patients with neurofibromatosis type 1.

Journal: The British journal of dermatology

Published: April 28, 2023

Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1.

Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1.

Journal: European journal of human genetics : EJHG

Published: January 19, 2023

Biology and Management of High-Grade Chondrosarcoma: An Update on Targets and Treatment Options.

Biology and Management of High-Grade Chondrosarcoma: An Update on Targets and Treatment Options.

Journal: International journal of molecular sciences

Published: November 17, 2022

Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1.

Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1.

Journal: Human genetics

Published: June 11, 2022

Efficient, quick and easy-to-use DNA replication timing analysis with START-R suite.

Efficient, quick and easy-to-use DNA replication timing analysis with START-R suite.

Journal: NAR genomics and bioinformatics

Published: February 20, 2020

A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomas.

A hypothesis-driven approach identifies CDK4 and CDK6 inhibitors as candidate drugs for treatments of adrenocortical carcinomas.

Journal: Aging

Published: March 31, 2017

Characterization of the replication timing program of 6 human model cell lines.

Characterization of the replication timing program of 6 human model cell lines.

Journal: Genomics data

Published: June 27, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026