Gijs Santen

Department head

Leiden University Medical Center

Netherlands

Research Interests

Explore related searches

Professors in Netherlands Professors in Medical Science Medical Science professors in Netherlands

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Gijs Santen is the Department Head at Leiden University Medical Center in the Netherlands. His research areas include pediatric cardiomyopathy, bone marrow failure, genetic neurodevelopmental disorders, and the epigenetic landscapes of Mendelian disorders. Recent publications reflect his focus on understanding rare genetic diseases and improving diagnostic methodologies. He is actively involved in addressing the clinical implications of genetic variations in various health conditions.

Articles (10)

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (2)

Renske Oegema

UMC Utrecht

NETHERLANDS

View details

Anita Rauch

SWITZERLAND

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Gijs Santen

Research Interests

Explore related searches

Contact this professor

About

Articles (10)

Biallelic loss of <i>LDB3</i> leads to a lethal pediatric dilated cardiomyopathy

Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders

Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders

PhenoScore: AI-based phenomics to quantify rare disease and genetic variation

Diagnostic Value of a Protocolized In-Depth Evaluation of Pediatric Bone Marrow Failure: A Multi-Center Prospective Cohort Study

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Gene-disease relationship evidence: A clinical perspective focusing on ultra-rare diseases

Hearing loss, cleft palate, and congenital hip dysplasia in female carriers of an intragenic deletion of AMMECR1

Missense variants in <i>ANKRD11</i> cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Population pharmacokinetics of clonazepam in saliva and plasma: Steps towards noninvasive pharmacokinetic studies in vulnerable populations

Collaborators (2)

Renske Oegema

Anita Rauch

Make your next move.