Author

Komala Pillay

Observed names: K Pillay, K. Pillay, Pillay, K., Pillay, Komala, Κ Pillay

Institutions: National Health Laboratory Service, University of Cape Town, Red Cross War Memorial Children's Hospital

Observed institutions: National Health Laboratory Service, University of Cape Town, University of Milan, Stellenbosch University, Chris Hani Baragwanath Hospital, Groote Schuur Hospital, Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia, Dana-Farber Cancer Institute, Centro di Riferimento Oncologico, Red Cross War Memorial Children's Hospital, University of Bari Aldo Moro, European Institute of Oncology, University of Brescia, University of KwaZulu-Natal

ORCID: 0000-0003-1971-900X

Observed ORCID: 0000-0003-1971-900X

OpenAlex ID: A5066818968

RYR1 mutations are a common cause of congenital myopathies with central nuclei

2010 · J.M. Wilmshurst, S. Lillis, et al. · Annals of Neurology · 275

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Predictive Value of Tumor Ki-67 Expression in Two Randomized Trials of Adjuvant Chemoendocrine Therapy for Node-Negative Breast Cancer

2008 · Giuseppe Viale, On the behalf of the International Breast Cancer Study Group, et al. · JNCI Journal of the National Cancer Institute · 247

Chemoendocrine Compared With Endocrine Adjuvant Therapies for Node-Negative Breast Cancer: Predictive Value of Centrally Reviewed Expression of Estrogen and Progesterone Receptors—International Breast Cancer Study Group

2008 · Giuseppe Viale, Meredith M. Regan, et al. · Journal of Clinical Oncology · 112

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Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis

2013 · Sandra Mercier, Sébastien Küry, et al. · The American Journal of Human Genetics · 88

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ALK protein expression in rhabdomyosarcomas

2002 · K Pillay, D Govender, et al. · Histopathology · 78

Interdigitating dendritic cell sarcoma: a report of four paediatric cases and review of the literature

2004 · K Pillay, R Solomon, et al. · Histopathology · 64

RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling

2013 · Haiyan Zhou, Ori Rokach, et al. · Human Mutation · 53

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Epigenetic changes as a common trigger of muscle weakness in congenital myopathies

2015 · Ori Rokach, Marijana Sekulic-Jablanovic, et al. · Human Molecular Genetics · 50

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Malakoplakia in association with colorectal carcinoma: a series of four cases

2002 · K. Pillay, R. Chetty · Pathology · 44

Poikiloderma, tendon contracture and pulmonary fibrosis: a new autosomal dominant syndrome?

2006 · N.P. Khumalo, K. Pillay, et al. · British Journal of Dermatology · 43

Clear Cell Sarcoma of the Kidney

2019 · Alessandro Pietro Aldera, Komala Pillay · Archives of Pathology & Laboratory Medicine · 39

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Microbiological yield from induced sputum compared to oropharyngeal swab in young children with cystic fibrosis

2016 · Marco Zampoli, Komala Pillay, et al. · Journal of Cystic Fibrosis · 38

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An evaluation of molecular markers for improved detection of breast cancer metastases in sentinel nodes

2006 · S Abdul-Rasool, S H Kidson, et al. · Journal of Clinical Pathology · 35

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Intussusception as a presenting feature of Burkitt lymphoma: implications for management and outcome

2011 · R. J. England, K. Pillay, et al. · Pediatric Surgery International · 34

Kaposi sarcoma in children with HIV: a clinical series from Red Cross Children's Hospital

2009 · Lydia L. Cairncross, Alan Davidson, et al. · Journal of Pediatric Surgery · 31

Mitochondrial impairment observed in fibroblasts from South African Parkinson’s disease patients with parkin mutations

2014 · Celia van der Merwe, Ben Loos, et al. · Biochemical and Biophysical Research Communications · 30

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Differential impact of antiretroviral therapy initiated before or during pregnancy on placenta pathology in HIV-positive women

2021 · Nadia M Ikumi, Thokozile R Malaba, et al. · AIDS · 29

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Acute ‘relaxer’-associated scarring alopecia: a report of five cases

2007 · N.P. Khumalo, K. Pillay, et al. · British Journal of Dermatology · 29

A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance

2010 · Gianina Ravenscroft, Jo M. Wilmshurst, et al. · Neuromuscular Disorders · 26

Polymyositis in African HIV-infected subjects

2010 · J.M. Heckmann, K. Pillay, et al. · Neuromuscular Disorders · 25

Borderline Serous Cystadenocarcinoma with Coexistent Angiosarcoma: An Unusual Form of Ovarian Carcinosarcoma

2001 · K. Pillay, A. S. Essa, et al. · International Journal of Surgical Pathology · 25

The First Case of Riboflavin Transporter Deficiency in sub-Saharan Africa

2017 · Shaakira Chaya, Marco Zampoli, et al. · Seminars in Pediatric Neurology · 24

Placental pathology in women with HIV

2021 · Nadia M. Ikumi, Mushi Matjila, et al. · Placenta · 23

Identification of a single MPV17 nonsense‐associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy

2018 · S. Meldau, R.J. De Lacy, et al. · Clinical Genetics · 21

Surgical manifestations of gastrointestinal cytomegalovirus infection in children: Clinical audit and literature review

2015 · M. Arnold, R. Itzikowitz, et al. · Journal of Pediatric Surgery · 20

Works count: 111

Citation count: 1,876

H-index: 23

I10-index: 42