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Pediatric Mesothelioma With ALK Fusions: A Molecular and Pathologic Study of 5 Cases

The American journal of surgical pathology, 2021-05, Vol.45 (5), p.653-661

2021

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Design and Multicenter Clinical Validation of a 3-Dimensionally Printed Nasopharyngeal Swab for SARS-CoV-2 Testing

JAMA otolaryngology-- head & neck surgery, 2021-05, Vol.147 (5), p.418

2021

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Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma

BMC cancer, 2022-06, Vol.22 (1), p.1-717, Article 717

2022

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Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene

The Lancet (British edition), 2023-07, Vol.402 (10396), p.141-141

2023

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Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR–CCNB3 gene fusion

Histopathology, 2018-01, Vol.72 (2), p.320-329

2018

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Novel TFG–RET fusion in a spindle cell tumour with S100 and CD34 coexpresssion

Histopathology, 2020-01, Vol.76 (2), p.333-336

2020

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Primary paediatric epidural sarcomas: molecular exploration of three cases

BMC cancer, 2019-02, Vol.19 (1), p.182-182, Article 182

2019

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Curious case of paediatric multiple pancreatic cysts

Journal of paediatrics and child health, 2020-05, Vol.56 (5), p.812-814

2020

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Paediatric actinomycosis: A 16‐year, single‐institution retrospective review of cases

Journal of paediatrics and child health, 2023-06, Vol.59 (6), p.833-839

2023

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Volvariella volvacea brain Abscess in an immunocompromised host—An emerging fungal pathogen in Asia

Journal de mycologie médicale, 2022-08, Vol.32 (3), p.101272, Article 101272

2022

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Post-operative diffusion weighted imaging as a predictor of posterior fossa syndrome permanence in paediatric medulloblastoma

Child's nervous system, 2017-03, Vol.33 (3), p.457-465

2017

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Medulloblastoma with tri-vergent melanocytic, myogenic and cartiligious elements

Journal of clinical neuroscience, 2017-07, Vol.41, p.100-103

2017

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Congenital GATA1 -mutated myeloproliferative disorder in trisomy 21 complicated by placental fetal thrombotic vasculopathy

Human pathology, 2014-11, Vol.45 (11), p.2364-2367

2014

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Concurrent paediatric medulloblastoma and Chiari I malformation with syringomyelia

Child's nervous system, 2017-06, Vol.33 (6), p.881-883

2017

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Primary Adrenal Angiomatoid Fibrous Histiocytoma With Novel EWSR1-ATF1 Gene Fusion Exon–Exon Breakpoint

Pediatric and developmental pathology, 2019-10, Vol.22 (5), p.472-474

2019

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Epidermolysis bullosa with pyloric atresia associated with compound heterozygous ITGB4 pathogenic variants: Minimal skin involvement but severe mucocutaneous disease

Pediatric dermatology, 2021-07, Vol.38 (4), p.908-912

2021

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Anomalous intracranial germinoma with unilateral cerebral peduncle swelling

Child's nervous system, 2017-04, Vol.33 (4), p.563-565

2017

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Clinical, pathological and loss of heterozygosity differences in Wilms tumors between Asian and non‐Asian children

International journal of cancer, 2019-03, Vol.144 (6), p.1234-1242

2019

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Novel Karyotypes and Cyclin D1 Immunoreactivity in Clear Cell Sarcoma of the Kidney

Pediatric and developmental pathology, 2015-07, Vol.18 (4), p.297-304

2015

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Mesothelioma with ALK gene mutations in two pediatric patients: Clinical course and outcome

Pediatric blood & cancer, 2022-07, Vol.69 (7), p.e29544-n/a

2022

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Immune and pathophysiologic profiling of antenatal coronavirus disease 2019 in the GIFT cohort: A Singaporean case-control study

Frontiers in pediatrics, 2022-09, Vol.10, p.949756-949756

2022

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Pseudomembranous trigonitis in a male with Klinefelter syndrome: a case report and evidence of a hormonal etiology

International journal of clinical and experimental pathology, 2014-01, Vol.7 (6), p.3375-3379

2014

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Perceived challenges and opportunities for basic scientists transitioning to basic science educators in medical and health professions education

Discover education, 2024-10, Vol.3 (1), p.1-10, Article 195

2024

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Genomic characterisation of breast fibroepithelial lesions in an international cohort

The Journal of pathology, 2019-12, Vol.249 (4), p.447-460

2019

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The challenges of histology education

Clinical anatomy (New York, N.Y.), 2023-03, Vol.36 (2), p.308-314

2023

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Pediatric Mesothelioma With ALK Fusions: A Molecular and Pathologic Study of 5 Cases

Design and Multicenter Clinical Validation of a 3-Dimensionally Printed Nasopharyngeal Swab for SARS-CoV-2 Testing

Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma

Non-immune hydrops fetalis caused by Diamond-Blackfan anaemia and a mutation of the RPL15 gene

Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR–CCNB3 gene fusion

Novel TFG–RET fusion in a spindle cell tumour with S100 and CD34 coexpresssion

Primary paediatric epidural sarcomas: molecular exploration of three cases

Curious case of paediatric multiple pancreatic cysts

Paediatric actinomycosis: A 16‐year, single‐institution retrospective review of cases

Volvariella volvacea brain Abscess in an immunocompromised host—An emerging fungal pathogen in Asia

Post-operative diffusion weighted imaging as a predictor of posterior fossa syndrome permanence in paediatric medulloblastoma

Medulloblastoma with tri-vergent melanocytic, myogenic and cartiligious elements

Congenital GATA1 -mutated myeloproliferative disorder in trisomy 21 complicated by placental fetal thrombotic vasculopathy

Concurrent paediatric medulloblastoma and Chiari I malformation with syringomyelia

Primary Adrenal Angiomatoid Fibrous Histiocytoma With Novel EWSR1-ATF1 Gene Fusion Exon–Exon Breakpoint

Epidermolysis bullosa with pyloric atresia associated with compound heterozygous ITGB4 pathogenic variants: Minimal skin involvement but severe mucocutaneous disease

Anomalous intracranial germinoma with unilateral cerebral peduncle swelling

Clinical, pathological and loss of heterozygosity differences in Wilms tumors between Asian and non‐Asian children

Novel Karyotypes and Cyclin D1 Immunoreactivity in Clear Cell Sarcoma of the Kidney

Mesothelioma with ALK gene mutations in two pediatric patients: Clinical course and outcome

Immune and pathophysiologic profiling of antenatal coronavirus disease 2019 in the GIFT cohort: A Singaporean case-control study

Pseudomembranous trigonitis in a male with Klinefelter syndrome: a case report and evidence of a hormonal etiology

Perceived challenges and opportunities for basic scientists transitioning to basic science educators in medical and health professions education

Genomic characterisation of breast fibroepithelial lesions in an international cohort

The challenges of histology education

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