Stefan Nicolau - Concepedia

Author

Stefan Nicolau

Also Known As

Alenezi, Raed M, S G NICOLAU, S NICOLAU, S. G. NICOLAU, S. G. Nicolau, S. Gh Nicolau, S. Nicolau, S.G. Nicolau, Stefan Nicolau, Stefan. Nicolau

Publications

704

Citations

H-Index

Concepts

All Affiliations

Mayo Clinic Mayo Clinic in Arizona Mayo Clinic in Florida Nationwide Children's Hospital National Institute of Neurological Disorders and Stroke

About

Stefan Nicolau is an author at Mayo Clinic specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	130
2	Pathology	4	4	130
3	Cell Biology	1	1	19
4	Molecular Genetics	1	1	19
5	Neurology	1	1	18

Stefan Nicolau

Publications

359

Citations

H-Index

Page 1

	Year	Citations
The transcription factor Pitx3 is expressed selectively in midbrain dopaminergic neurons susceptible to neurodegenerative stress Kelvin C. Luk, Vladimir V. Rymar, Pepijn van den Munckhof, Journal of Neurochemistry	2013	55
CHRONIC ACTINIC CHEILITIS AND CANCER OF THE LOWER LIP. Stefan Nicolau, L. Båluş British Journal of Dermatology MedicineThe Lower LipHistopathologyPathologyOncology	1964	54
Congenital myopathies in the adult neuromuscular clinic Stefan Nicolau, Teerin Liewluck, Jennifer A. Tracy, Neurology Genetics	2019	40
A form of muscular dystrophy associated with pathogenic variants in JAG2 Sandra Coppens, Alison M. Barnard, Sanna Puusepp, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesis	2021	39
Immune‐mediated necrotizing myopathy: Unusual presentations of a treatable disease Stefan Nicolau, Margherita Milone, Jennifer A. Tracy, Muscle & Nerve	2021	24
Guidelines for genetic testing of muscle and neuromuscular junction disorders Stefan Nicolau, Margherita Milone, Teerin Liewluck Muscle & Nerve	2021	21
Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies Tatyana A. Vetter, Stefan Nicolau, A. Bradley, Neuropathology and Applied Neurobiology	2021	20
A novel heterozygous mutation in the C-terminal region of HSPB8 leads to limb-girdle rimmed vacuolar myopathy Stefan Nicolau, Teerin Liewluck, Jeffrey L. Elliott, Neuromuscular Disorders Molecular PhysiologyC-terminal RegionMendelian DisorderGenetic DisorderGenetics	2020	19
A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmission Stefan Nicolau, Teerin Liewluck, Xin‐Ming Shen, Neuromuscular Disorders Mitochondrial MyopathyPostsynaptic DefectsMendelian DisorderSkeletal MuscleGenetic Disorder	2019	18
Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy (FSHD) Allison Ducharme‐Smith, Stefan Nicolau, C. Anwar A. Chahal, Frontiers in Neurology	2021	18

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