Tjakko W van Ham

26PUBLICATIONS
157CO-AUTHORS
Data models, storage and indexingGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Cancer geneticsCell and nuclear division
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Publications (26)

|Oct 31, 2026
MetaDome 2027: a comprehensively updated resource for aggregating missense variant evidence across homologous human protein domains.

|Oct 24, 2026
MetaDome 2027: a comprehensively updated resource for aggregating missense variant evidence across homologous human protein domains.

|Mar 11, 2026
HiFi long-read RNA sequencing enhances clinical diagnostics in rare disorders.

Carolina Jaramillo Oquendo, Federico Ferraro, Htoo A Wai

|Feb 04, 2026
Two siblings with CCDC32-related cardiofacioneurodevelopmental syndrome diagnosed by clinical RNA-sequencing and review of literature.

Fatimah Albuainain, Myrrhe Venema, Rachel Schot

|Jan 16, 2026
An accurate cellular assay to determine pathogenicity of coding and noncoding variants in Lynch syndrome genes.

Iris E Glykofridis, Marleen Dekker, Chantal Stoepker

|Oct 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making.

Daphne J Smits, Federico Ferraro, Mark Drost

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Frequent Collaborators

5 joint publications

Tahsin Stefan Barakat

5 joint publications

Federico Ferraro

3 joint publications

Lies H Hoefsloot

3 joint publications

Rachel Schot