Dennis Kraemer
Zurich, ZH, Switzerland
Last Updated: 09/26/2026
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Found 8 publications
Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function.
Journal: Nature genetics
Published: June 16, 2024
Variants in IGLL1 cause a broad phenotype from agammaglobulinemia to transient hypogammaglobulinemia.
Journal: The Journal of allergy and clinical immunology
Published: May 22, 2024
SwissGenVar: A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland.
Journal: Journal of personalized medicine
Published: April 04, 2024
Further evidence that the neurodevelopmental gene FBXW7 predisposes to Wilms tumor.
Journal: American journal of medical genetics. Part A
Published: November 20, 2023
Challenges for the implementation of next generation sequencing-based expanded carrier screening: Lessons learned from the ciliopathies.
Journal: European journal of human genetics : EJHG
Published: March 15, 2022
Assessing clinical utility of preconception expanded carrier screening regarding residual risk for neurodevelopmental disorders.
Journal: NPJ genomic medicine
Published: February 21, 2022
Prevalence of genetic susceptibility for breast and ovarian cancer in a non-cancer related study population: secondary germline findings from a Swiss single centre cohort.
Journal: Swiss medical weekly
Published: August 19, 2019
Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 27, 2018
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Last Updated: 09/26/2026