Marjan Weiss

7PUBLICATIONS
92CO-AUTHORS
Gene mappingPsychosocial aspects of childbirth and perinatal mental healthCancer therapy (excl. chemotherapy and radiation therapy)Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (7)

|May 15, 2024
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.

Wouter Steyaert, Lydia Sagath, German Demidov

|Dec 09, 2022
Experiences of pregnant women with genome-wide non-invasive prenatal testing in a national screening program.

Karuna R M van der Meij, Qiu Ying F van de Pol, Mireille N Bekker

|Sep 23, 2022
Circulating Tumor DNA-Based Disease Monitoring of Patients with Locally Advanced Esophageal Cancer.

Lisa S M Hofste, Maartje J Geerlings, Daniel von Rhein

|May 16, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseases.

Erika Souche, Sergi Beltran, Erwin Brosens

|May 17, 2020
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity.

Laure Asselin, José Rivera Alvarez, Solveig Heide

|Oct 17, 2019
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

Hui Guo, Elisa Bettella, Paul C Marcogliese

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Frequent Collaborators

2 joint publications

Matthis Synofzik

2 joint publications

Christian Gilissen

2 joint publications

Sergi Beltran

1 joint publications

Alexander Hoischen