Xin Wang

12PUBLICATIONS
148CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Haematological tumoursVision scienceEpigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)
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Publications (12)

|May 18, 2026
Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

|Apr 20, 2026
Genomic evolution and natural history of myeloproliferative neoplasms on therapy.

|May 03, 2025
Rare genetic variation in PTPRB is associated with central serous chorioretinopathy, varicose veins and glaucoma.

Joel T Rämö, Bryan R Gorman, Lu-Chen Weng

|Apr 09, 2025
Timing and trajectory of BCR::ABL1-driven chronic myeloid leukaemia.

Aleksandra E Kamizela, Daniel Leongamornlert, Nicholas Williams

|Mar 06, 2025
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk.

Seung Hoan Choi, Sean J Jurgens, Ling Xiao

|Jan 02, 2025
The impact of common and rare genetic variants on bradyarrhythmia development.

Lu-Chen Weng, Joel T Rämö, Sean J Jurgens

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Frequent Collaborators

9 joint publications

Sean Jurgens

7 joint publications

Patrick T Ellinor

6 joint publications

Connie R Bezzina

6 joint publications

Mark D Chaffin