Tze How Mok

479 total citations
17 papers, 148 citations indexed

About

Tze How Mok is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Tze How Mok has authored 17 papers receiving a total of 148 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 7 papers in Neurology and 4 papers in Neurology. Recurrent topics in Tze How Mok's work include Prion Diseases and Protein Misfolding (17 papers), Neurological diseases and metabolism (7 papers) and Trace Elements in Health (4 papers). Tze How Mok is often cited by papers focused on Prion Diseases and Protein Misfolding (17 papers), Neurological diseases and metabolism (7 papers) and Trace Elements in Health (4 papers). Tze How Mok collaborates with scholars based in United Kingdom, United States and Germany. Tze How Mok's co-authors include Simon Mead, John Collinge, Akın Nihat, Graham S. Jackson, Andrew G.B. Thompson, Jonathan M. Schott, Peter Rudge, Ross W. Paterson, Jonathan D. F. Wadsworth and Nick C. Fox and has published in prestigious journals such as Nature Communications, Scientific Reports and The Lancet Neurology.

In The Last Decade

Tze How Mok

14 papers receiving 146 citations

Peers

Countries citing papers authored by Tze How Mok

Since Specialization

Citations

This map shows the geographic impact of Tze How Mok's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Tze How Mok with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tze How Mok more than expected).

Fields of papers citing papers by Tze How Mok

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tze How Mok. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Tze How Mok. The network helps show where Tze How Mok may publish in the future.

Co-authorship network of co-authors of Tze How Mok

This figure shows the co-authorship network connecting the top 25 collaborators of Tze How Mok. A scholar is included among the top collaborators of Tze How Mok based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tze How Mok. Tze How Mok is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Genetic causes and modifiers of prion diseases 2026 ·The Lancet Neurology ·(unknown), (unknown), Tze How Mok, (unknown), (unknown)	0
2	Advances in biomarkers for diagnosis and prognosis of prion diseases 2026 ·The Lancet Neurology ·(unknown), (unknown), Tze How Mok, (unknown)	1
3	PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features 2025 ·Journal of Neurology ·(unknown), Zane Jaunmuktane, Laszlo L. P. Hosszu, Nour K. Majbour, Fuquan Zhang, Tracy Campbell, Lee Darwent, (unknown), Edgar Chan, (unknown), Tze How Mok, Jonathan D. F. Wadsworth, Jan Bieschke, Kannan Nithi, Sebastian Brandner, Colin Smith, Margaret M. Esiri, John Collinge, Simon Mead	0
4	Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157 2025 ·Journal of Alzheimer s Disease ·(unknown), Tze How Mok, (unknown), (unknown), Peter Rudge, Hawraman Ramadan, Lee Darwent, Tracy Campbell, Thomas E. Murphy, Carl Smith, Diane Ritchie, Sebastian Brandner, Zane Jaunmuktane, John Collinge, Simon Mead	0
5	The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer’s disease 2025 ·Journal of Neurogenetics ·(unknown), (unknown), Tze How Mok, Peter Rudge, Zita Reisz, Claire Troakes, Safa Al‐Sarraj, Tracy Campbell, Laszlo L. P. Hosszu, Jan Bieschke, Fuquan Zhang, Jonathan D. F. Wadsworth, Colin Smith, (unknown), Timothy Rittman, Sebastian Brandner, Zane Jaunmuktane, John Collinge, Simon Mead	2
6	Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease 2022 ·Journal of Neurology Neurosurgery & Psychiatry ·Akın Nihat, Tze How Mok, (unknown), Andrew G.B. Thompson, Diana Caine, (unknown), (unknown), (unknown), Peter Rudge, John Collinge, Simon Mead	5
7	Assessing initial MRI reports for suspected CJD patients 2022 ·Journal of Neurology ·Aaron Jesuthasan, (unknown), Harpreet Hyare, (unknown), Peter Rudge, Tze How Mok, Akın Nihat, John Collinge, Simon Mead	9
8	Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases 2021 ·Molecular Psychiatry ·Andrew G.B. Thompson, (unknown), Ronald Druyeh, (unknown), Annapurna Nayak, Akın Nihat, Tze How Mok, Peter Rudge, Jonathan D. F. Wadsworth, Jonathan D. Rohrer, Jonathan M. Schott, Amanda Heslegrave, Henrik Zetterberg, John Collinge, Graham S. Jackson, Simon Mead	33
9	Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion 2021 ·Viruses ·(unknown), Ignazio Calì, Tze How Mok, Helen E. Speedy, Laszlo L. P. Hosszu, Christiane Stehmann, Laura Cracco, Gianfranco Puoti, Thomas W. Prior, Mark L. Cohen, Steven Collins, Simon Mead, Brian S. Appleby	5
10	Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases 2021 ·Scientific Reports ·Tze How Mok, Akın Nihat, (unknown), (unknown), Mark Batchelor, Simon Mead, John Collinge, Graham S. Jackson	18
11	NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease Progression 2021 ·Cells ·David Mengel, Tze How Mok, Akın Nihat, (unknown), Robert A. Rissman, Douglas Galasko, Henrik Zetterberg, Simon Mead, John Collinge, Dominic M. Walsh	6
12	A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis 2020 ·Nature Communications ·Penny J. Norsworthy, Andrew G.B. Thompson, Tze How Mok, (unknown), (unknown), Akın Nihat, Ross W. Paterson, Jonathan M. Schott, John Collinge, Simon Mead, Emmanuelle Viré	25
13	Preclinical biomarkers of prion infection and neurodegeneration 2020 ·Current Opinion in Neurobiology ·Tze How Mok, Simon Mead	5
14	Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process 2019 ·NeuroImage Clinical ·Liane S. Canas, Carole H. Sudre, Enrico De Vita, Akın Nihat, Tze How Mok, Catherine F. Slattery, Ross W. Paterson, Alexander Foulkes, Harpreet Hyare, M. Jorge Cardoso, John S. Thornton, Jonathan M. Schott, Frederik Barkhof, John Collinge, Sébastien Ourselin, Simon Mead, Marc Modat	4
15	Enteral feeding is associated with longer survival in the advanced stages of prion disease 2019 ·Brain Communications ·(unknown), Akın Nihat, Tze How Mok, (unknown), (unknown), Peter Rudge, John Collinge, Simon Mead	5
16	Evaluating the causality of novel sequence variants in the prion protein gene by example 2018 ·Neurobiology of Aging ·Tze How Mok, (unknown), Zane Jaunmuktane, Tracy Campbell, Susan Joiner, Jonathan D. F. Wadsworth, Laszlo L. P. Hosszu, Sebastian Brandner, (unknown), Thomas Truelsen, Eva Løbner Lund, (unknown), John Collinge, Simon Mead	10
17	Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine 2016 ·JAMA Neurology ·(unknown), Samantha W. Jones, (unknown), Nick C. Fox, Tze How Mok, Simon Mead, John Collinge, Graham S. Jackson	20

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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