Dr Pei Dai

Role: PhD Student (No GSA)
Lab/Group: Intravital Microscopy and Gene Expression (IMAGE) Lab

Selected publications

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2024
Frontiers in Immunology10.3389/fimmu.2024.1436733
Paraneoplastic progressive encephalomyelitis with rigidity and myoclonus associated with monoclonal B-cell lymphocytosis in the setting of longstanding methotrexate use: case report.
Fangzhi Frank Jia, Mohammad Ruhul Amin, Gi Tae Kwon, Amir Mousapasandi, Pei Dai, Jed Kitson, Adrian Selim, Jerome Ip
2024
Clinical Journal of the American Society of Nephrology : CJASN10.2215/CJN.0000000000000464
Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study.
Amali C Mallawaarachchi, Lindsay Fowles, Louise Wardrop, Alasdair Wood, Rosie O'Shea, Erik Biros, Trudie Harris, Stephen I Alexander, Simon Bodek, Neil Boudville, Jo Burke, Leslie Burnett, Sarah Casauria, Steve Chadban, Aron Chakera, Sam Crafter, Pei Dai, Paul De Fazio, Randall Faull, Andrew Honda, Vanessa Huntley, Sadia Jahan, Kushani Jayasinghe, Matthew Jose, Anna Leaver, Mandi MacShane, Evanthia Olympia Madelli, Kathy Nicholls, Rhonda Pawlowski, Gopi Rangan, Paul Snelling, Jacqueline Soraru, Madhivanan Sundaram, Michel Tchan, Giulia Valente, Mathew Wallis, Laura Wedd, Matthew Welland, John Whitlam, Ella J Wilkins, Hugh McCarthy, Cas Simons, Catherine Quinlan, Chirag Patel, Zornitza Stark, Andrew J Mallett
2024
Journal of Clinical Immunology10.1007/s10875-023-01637-x
Filaggrin-Associated Atopic Skin, Eye, Airways, and Gut Disease, Modifying the Presentation of X-Linked Reticular Pigmentary Disorder (XLPDR).
Margaret W Y Li, Leslie Burnett, Pei Dai, Danielle T Avery, Tahereh Noori, Ilia Voskoboinik, Parth R Shah, Artiene Tatian, Stuart G Tangye, Paul E Gray, Cindy S Ma
2023
Oxford Medical Case Reports10.1093/omcr/omad005
Hyper-IgM and acquired C1q complement deficiency in a patient with mutation.
Adrian Y S Lee, Pei Dai, Leslie Burnett, Xiumei Wei, Fakhria Kakar, Thomas Ohnesorg, Ming-Wei Lin
2022
Genetics in Medicine : Official Journal of the American College of Medical Genetics10.1016/j.gim.2022.04.021
Recommendations for next generation sequencing data reanalysis of unsolved cases with suspected Mendelian disorders: A systematic review and meta-analysis.
Pei Dai, Andrew Honda, Lisa Ewans, Julie McGaughran, Leslie Burnett, Matthew Law, Tri Giang Phan

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Dr Pei Dai

Selected publications

Paraneoplastic progressive encephalomyelitis with rigidity and myoclonus associated with monoclonal B-cell lymphocytosis in the setting of longstanding methotrexate use: case report.

Genomic Testing in Patients with Kidney Failure of an Unknown Cause: A National Australian Study.

Filaggrin-Associated Atopic Skin, Eye, Airways, and Gut Disease, Modifying the Presentation of X-Linked Reticular Pigmentary Disorder (XLPDR).

Hyper-IgM and acquired C1q complement deficiency in a patient with mutation.

Recommendations for next generation sequencing data reanalysis of unsolved cases with suspected Mendelian disorders: A systematic review and meta-analysis.

Follow-up genetic testing gives patients further chance of diagnosis